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Wu K, Lu L, Chen Y, Peng J, Wu X, Tang G, Ma T, Cheng J, Ran P, Zhou Y. Associations of anxiety and depression with prognosis in chronic obstructive pulmonary disease: A systematic review and meta-analysis. Pulmonology 2025; 31:2438553. [PMID: 39671175 DOI: 10.1080/25310429.2024.2438553] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/29/2024] [Accepted: 09/30/2024] [Indexed: 12/14/2024] Open
Abstract
The associations between anxiety, depression, and the prognosis of COPD remain uncertain. The present study aims to investigate the associations of anxiety and depression with 30-day readmission rates and acute exacerbations of COPD (AECOPD). Four databases were searched to identify relevant studies published before 13 March 2024. Studies that report on the impact of anxiety and depression on the prognosis of AECOPD were included. The pooled effect size and its 95% confidence interval (CI) were calculated using a random effects model. The primary outcomes were 30-day readmission and AECOPD within the first year after discharge in COPD patients. Of the 5,955 studies screened, 14 studies were included in the analysis. Patients with anxiety had a higher risk of AECOPD within the first year after discharge compared to those without anxiety (HR: 2.10, 95% CI: 1.28-3.45, p = 0.003). Patients with depression also had a higher risk of AECOPD within the first year after discharge (HR: 1.36, 95% CI: 1.10-1.69, p = 0.004). Similar results were observed in the associations of anxiety and depression with 30-day readmission. Our results suggested that anxiety and depression were associated with an increased risk of 30-day readmission and AECOPD in patients with COPD.
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Affiliation(s)
- Kefan Wu
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
| | - Lifei Lu
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
| | - Yubiao Chen
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- Guangzhou National Laboratory, Bio-Island, Guangzhou, China
| | - Jieqi Peng
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- Guangzhou National Laboratory, Bio-Island, Guangzhou, China
| | - Xiaohui Wu
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
| | - Gaoying Tang
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
| | - Ting Ma
- The Department of Radiology, The First Hospital of Guangzhou Medical University, Guangzhou, China
| | - Jing Cheng
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
| | - Pixin Ran
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- Guangzhou National Laboratory, Bio-Island, Guangzhou, China
| | - Yumin Zhou
- Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- Guangzhou National Laboratory, Bio-Island, Guangzhou, China
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Ito JT, Alves LHV, Oliveira LDM, Xavier RF, Carvalho-Pinto RM, Tibério IDFLC, Sato MN, Carvalho CRF, Lopes FDTQDS. Effect of exercise training on modulating the TH17/TREG imbalance in individuals with severe COPD: A randomized controlled trial. Pulmonology 2025; 31:2441069. [PMID: 39764722 DOI: 10.1080/25310429.2024.2441069] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/29/2023] [Accepted: 11/13/2024] [Indexed: 01/11/2025] Open
Abstract
BACKGROUND Chronic obstructive pulmonary disease (COPD) induces an imbalance in T helper (Th) 17/regulatory T (Treg) cells that contributes to of the dysregulation of inflammation. Exercise training can modulate the immune response in healthy subjects. OBJECTIVE We aimed to evaluate the effects of exercise training on Th17/Treg responses and the differentiation of Treg phenotypes in individuals with COPD. METHODS This randomized controlled trial included 50 individuals with severe or very severe COPD who were allocated to the Exercise or Control groups. The Exercise group underwent eight weeks of aerobic and muscle strength training, whereas the Control group received usual care. The primary outcome was the change in the phenotypic characteristics of Tregs and Th17 profile differentiation in systemic inflammation. RESULTS Exercise training increased the frequency of total and activated Tregs and decreased the frequency of Th17 cells in between-group comparisons. Additionally, Th17/Treg responses were moderately correlated with improvements in the six-minute walking test, muscle strength of the upper and lower limbs, and daily life physical activity levels. CONCLUSION Exercise training improved functional exercise capacity, muscle strength, and physical fitness, which was associated with a decrease in the Th17 inflammatory response and an increase in Treg cell phenotypes immunosuppressive activity.
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Affiliation(s)
- Juliana Tiyaki Ito
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Luan Henrique Vasconcelos Alves
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Luana de Mendonça Oliveira
- Laboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, Tropical Medicine Institute of Sao Paulo, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | | | - Regina Maria Carvalho-Pinto
- Pulmonary Division, Heart Institute (InCor), Clinics Hospital, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | | | - Maria Notomi Sato
- Laboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, Tropical Medicine Institute of Sao Paulo, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Celso R F Carvalho
- Department of Physical Therapy, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Fernanda Degobbi Tenorio Quirino Dos Santos Lopes
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
- Thoracic Surgery Research Laboratory (LIM-61), Division of Thoracic Surgery, Heart Institute (InCor), Clinics Hospital, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
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3
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Meng Y, Gao R, Yang H, Zhang F, Shang M, Liu Y, Li L, Chen L, Zhong X, Lu H. Health-related quality of life and related factors among esophageal cancer survivors after esophagectomy in the 6-month postoperative period: A multicenter cross-sectional study in north China. Asia Pac J Oncol Nurs 2025; 12:100655. [PMID: 40092139 PMCID: PMC11909444 DOI: 10.1016/j.apjon.2025.100655] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/20/2024] [Accepted: 01/14/2025] [Indexed: 03/19/2025] Open
Abstract
Objective Esophagectomy is a primary curable treatment and a highly challenging procedure for esophageal cancer (EC) survivors. EC survivors experience various unmet needs. This study is aimed to assess unmet needs, health-related quality of life (HRQOL), and psychological distress of postoperative EC survivors. Methods A multicenter cross-sectional study was conducted between December 2023 and March 2024 across 28 hospitals in northern China. The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire, Hospital Anxiety and Depression Scale, and Supportive Care Need Survey - Short Form 34 were utilized to assess the HRQOL, anxiety, depression, and unmet needs. Results A total of 357 postoperative EC survivors were recruited, with a mean age of 63.42 years. Approximately 14.6% exhibited borderline anxiety, and 17.9% showed borderline depression. Unmet needs were highest in health information and patient care domains. HRQOL was lower in global health, social, and physical functions post-surgery. Fatigue, appetite loss, insomnia, and financial difficulties were common. Dysphagia, dry mouth, reflux, and choking negatively impacted HRQOL. Multivariable regression analysis indicated that anxiety and depression levels were higher, and HRQOL was lower in those one week to six months post-surgery compared to one-week post-surgery. Conclusions EC survivors experience significant psychological distress and reduced HRQOL up to six months post-surgery. Dysphagia and unmet needs are prevalent. Compared to immediate post-surgery, EC survivors experienced higher levels of anxiety and depression, and lower level of HRQOL in six months. Future research should focus on developing individualized care strategies to provide optimal support.
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Affiliation(s)
- Yingtao Meng
- Nursing Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
| | - Ruitong Gao
- The Nethersole School of Nursing, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China
| | - Hailing Yang
- Qilu Hospital of Shandong University, Jinan, China
| | - Fang Zhang
- Esophageal Surgical Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
| | - Meimei Shang
- Nursing Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
| | - Yuping Liu
- Nursing Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
| | - Lingjuan Li
- Nursing Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
| | - Lu Chen
- Nursing Department, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China
| | - Xia Zhong
- Qilu Hospital of Shandong University, Jinan, China
| | - Hongmei Lu
- Nursing Department, Henan Cancer Hospital, Zhengzhou, China
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Lennartsson AK, Jonsdottir IH, Jansson PA, Sjörs Dahlman A. Study of glucose homeostasis in burnout cases using an oral glucose tolerance test. Stress 2025; 28:2438699. [PMID: 39688015 DOI: 10.1080/10253890.2024.2438699] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/05/2024] [Accepted: 11/23/2024] [Indexed: 12/18/2024] Open
Abstract
Burnout is caused by long term psychosocial stress and has, besides the fatigue and mental health burden, been associated with increased risk of adverse physical health, such as for example type 2 diabetes. This study aims to investigate the glucose and insulin levels in individuals with stress related burnout, by assessing these metabolic markers in response to a standard oral glucose tolerance test (OGTT). 38 cases with burnout (13 men and 25 women) and 35 healthy controls (13 men and 22 women) in the age 24-55 were included in the study. The burnout group overall did not differ from healthy controls in glucose or insulin levels during the OGTT. However, the burnout cases who reported more severe burnout symptoms exhibited significantly higher levels of both glucose and insulin levels during the OGTT compared to burnout cases reporting lower severity of symptoms. Furthermore, the group of burnout cases who reported symptoms of depression exhibited higher insulin levels during OGTT compared to the burnout cases without depressive symptoms. The observed higher levels in the burnout cases with most severe symptoms indicate an increased diabetic risk in these patients and it may be of importance to follow glucose and insulin levels in individuals with more severe symptoms of burnout i.e. to perform an OGTT.
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Affiliation(s)
- Anna-Karin Lennartsson
- The Institute of Stress Medicine, Region Västra Götaland, Gothenburg, Sweden
- School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden
| | - Ingibjörg H Jonsdottir
- The Institute of Stress Medicine, Region Västra Götaland, Gothenburg, Sweden
- School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden
| | - Per-Anders Jansson
- Wallenberg Laboratory, Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
| | - Anna Sjörs Dahlman
- Swedish National Road and Transport Research Institute (VTI), Linköping, Sweden
- Department of Electrical Engineering, and SAFER Vehicle and Traffic Safety Centre, Chalmers University of Technology, Gothenburg, Sweden
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5
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Jarab AS, Al-Qerem W, Alzoubi KH, Abuzetun NT, Abu Heshmeh S, Momany SM, Al Hamarneh YN, Aburuz S. Determinants of poor chronic obstructive pulmonary disease control. Libyan J Med 2025; 20:2507987. [PMID: 40388607 PMCID: PMC12090273 DOI: 10.1080/19932820.2025.2507987] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/25/2024] [Accepted: 05/14/2025] [Indexed: 05/21/2025] Open
Abstract
Uncontrolled COPD has been associated with reduced health-related quality of life, activity impairment, and increased use of healthcare resources. However, limited research is available on the factors associated with poor disease control in COPD patients. This study aimed to explore the factors associated with poor disease control in patients with COPD. The current cross-sectional study was conducted on patients with COPD who attended outpatient respiratory clinics at two major hospitals in Jordan. Information about disease and medication-related characteristics was collected through patient interviews and medical files. Validated instruments, including the 4-item medication adherence scale and the hospital anxiety and depression scales, were used to assess medication adherence, anxiety, and depression among the study participants. COPD severity was assessed using the GOLD classification criteria. Ordinal regression analysis was conducted to explore the variables associated with poor COPD control. In total, 702 patients participated in the study, with a median (interquartile range) age of 68 years (58-77). According to the GOLD report, most of the participants were in the B group (low risk/high symptoms; 40.2%), followed by the D group (high risk/high symptoms; 28.2%). Older age, higher depression scores, and a higher number of prescribed medications were associated with poorer COPD control, while not receiving LAMA (long-acting muscarinic antagonists) was associated with better control. Future mental health care initiatives should address the prevalence of depression symptoms in COPD patients and manage them effectively to improve COPD control and prevent further complications, with special attention to older patients, those receiving multiple medications, and those using LAMA.
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Affiliation(s)
- Anan S. Jarab
- College of Pharmacy, Al Ain University, Abu Dhabi, United Arab Emirates
| | - Walid Al-Qerem
- Department of Pharmacy, Faculty of Pharmacy, Al-Zaytoonah University of Jordan, Amman, Jordan
| | - Karem H. Alzoubi
- Department of Pharmacy Practice and Pharmacotherapeutics, College of Pharmacy, University of Sharjah, Sharjah, UAE
- Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan
| | - Nid’a T. Abuzetun
- Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan
| | - Shrouq Abu Heshmeh
- Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan
| | - Suleiman M. Momany
- Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan
- Pulmonary and Critical Care Division, King Abdullah University Hospital, Irbid, Jordan
| | - Yazid N Al Hamarneh
- Department of Pharmacology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada
| | - Salah Aburuz
- Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, Al Ain, United Arab Emirates
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6
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Romeo A, Di Tella M, Benfante A, Colonna F, Castelli L. Metacognition and pain in patients with fibromyalgia: the role of psychological distress. J Affect Disord 2025; 382:85-88. [PMID: 40250812 DOI: 10.1016/j.jad.2025.04.062] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/19/2025] [Revised: 04/01/2025] [Accepted: 04/14/2025] [Indexed: 04/20/2025]
Abstract
BACKGROUND Fibromyalgia (FM) is a syndrome characterised by chronic and widespread musculoskeletal pain that is often accompanied by psychological distress. Another psychological aspect associated with FM is metacognition. Metacognition is a process that enables a person to understand themselves and others in terms of intentional mental states. The aim of the present study was to investigate the relationship between metacognitive functioning, psychological distress and pain intensity in a sample of FM patients. METHODS Sixty-one females with FM were asked to complete the following questionnaires after signing informed consent: the pain intensity item of the Fibromyalgia Impact Questionnaire-Revised (FIQ-R), the Hospital Anxiety and Depression Scale (HADS), and the Metacognitive Functions Screening Scale (MFSS-30). RESULTS The pain intensity item of the FIQ-R was negatively associated with metacognitive abilities (MFSS-30) and positively related to psychological distress (HADS total). The mediation analysis showed that the HADS total score mediated the relationship between the MFSS total score and the pain intensity item of the FIQ-R. This result suggests that reduced metacognitive abilities were associated with higher levels of psychological distress, which in turn were associated with greater pain intensity. CONCLUSIONS These findings have important clinical implications. The suggestion of a psychological intervention targeting metacognitive processes could reduce the degree of psychological distress and consequently the intensity of pain.
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Affiliation(s)
| | | | - Agata Benfante
- Department of Psychology, University of Turin, Turin, Italy
| | | | - Lorys Castelli
- Department of Psychology, University of Turin, Turin, Italy
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Lii TR, Flohr JR, Okada RL, Cianfichi LJ, Hack LM, Schatzberg AF, Heifets BD. Opioids diminish the placebo antidepressant response: Observational post hoc findings from a randomized controlled ketamine trial. J Affect Disord 2025; 381:200-204. [PMID: 40185412 DOI: 10.1016/j.jad.2025.04.008] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/19/2024] [Revised: 03/31/2025] [Accepted: 04/01/2025] [Indexed: 04/07/2025]
Abstract
BACKGROUND The endogenous opioid system is thought to play a role in the placebo antidepressant response. A recent trial comparing the rapid antidepressant effects of ketamine versus placebo in surgical patients, some of whom were on chronic opioid therapy, revealed a substantial placebo effect. This finding provided an opportunity to test the hypothesis that opioid agonist exposure interacts with placebo antidepressant responses. METHODS This post hoc analysis utilized data from a previously reported randomized, anesthesia-blinded, placebo-controlled trial of intravenous ketamine in depressed patients undergoing routine surgery. Mixed-effects models were used to determine whether baseline opioid use influenced antidepressant responses to the trial interventions, as measured by the Montgomery-Åsberg Depression Rating Scale (MADRS) over 1 to 14 days post-treatment. RESULTS The analysis showed that baseline opioid use significantly reduced post-treatment depression severity in patients who received placebo, but not in those who received ketamine. This reduction was independent of baseline depression severity, baseline pain intensity, and ethnicity. Additionally, there was negligible correlation between postoperative pain intensity and depression severity. LIMITATIONS This post hoc analysis was conducted on a small sample, and the findings need to be confirmed by prospective controlled studies. CONCLUSIONS Opioid use at baseline attenuated the placebo antidepressant response independently of pain in depressed patients who received the study treatment under general anesthesia for routine surgery. The antidepressant response was preserved in opioid users who received intravenous ketamine.
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Affiliation(s)
- Theresa R Lii
- Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA
| | - Josephine R Flohr
- Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA
| | - Robin L Okada
- Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA
| | - Lisa J Cianfichi
- Department of Radiology, Stanford University School of Medicine, Stanford, CA, USA
| | - Laura M Hack
- Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA; Sierra Pacific Mental Illness Research, Education, and Clinical Center, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USA
| | - Alan F Schatzberg
- Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA
| | - Boris D Heifets
- Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
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Carter E, Banerjee S, Alexopoulos GS, Bingham KS, Marino P, Meyers BS, Mulsant BH, Neufeld NH, Rothschild AJ, Voineskos AN, Whyte EM, Flint AJ. Prediction of remission of pharmacologically treated psychotic depression: A machine learning approach. J Affect Disord 2025; 381:291-297. [PMID: 40187431 DOI: 10.1016/j.jad.2025.04.013] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/19/2025] [Revised: 03/31/2025] [Accepted: 04/01/2025] [Indexed: 04/07/2025]
Abstract
BACKGROUND The combination of antidepressant and antipsychotic medication is an effective treatment for major depressive disorder with psychotic features ('psychotic depression'). The present study aims to identify sociodemographic and clinical predictors of remission of psychotic depression treated with combination pharmacotherapy and determine the accuracy of prediction models. METHODS Two hundred and sixty-nine participants aged 18 to 85 years with psychotic depression were acutely treated with protocolized sertraline plus olanzapine for up to 12 weeks. Three cross-validated machine learning models were implemented to predict remission based on 74 sociodemographic and clinical variables measured at acute baseline. The optimal model for each method was selected by the average fold C-index. Based on the performance of each method, grouped elastic net (cox) regression was chosen to examine the association of each predictor with remission of psychotic depression. RESULTS Of the 269 participants, 145 (53.9 %) experienced full remission of the depressive episode and psychotic features. Multivariable models had 65.1 % to 67.4 % accuracy in predicting remission. In the grouped elastic net (cox) regression model, longer duration of index episode, somatic or tactile hallucinations, higher burden of comorbid physical problems, and single or divorced marital status were independent predictors of longer time to remission. A higher number of lifetime depressive episodes and peripheral vascular or cardiovascular disease were predictors of shorter time to remission. CONCLUSIONS Future research needs to determine whether the addition of biomarkers to clinical and sociodemographic variables can improve model accuracy in predicting remission of pharmacologically-treated psychotic depression.
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Affiliation(s)
- Emily Carter
- Department of Population Health Sciences, Weill Cornell Medicine, New York, USA
| | - Samprit Banerjee
- Department of Population Health Sciences, Weill Cornell Medicine, New York, USA; Department of Psychiatry, Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine, New York, USA
| | - George S Alexopoulos
- Department of Psychiatry, Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine, New York, USA
| | - Kathleen S Bingham
- Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Canada; Centre for Mental Health, University Health Network, Toronto, Canada
| | - Patricia Marino
- Department of Psychiatry, Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine, New York, USA
| | - Barnett S Meyers
- Department of Psychiatry, Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine, New York, USA
| | - Benoit H Mulsant
- Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Canada; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada
| | - Nicholas H Neufeld
- Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Canada; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada
| | - Anthony J Rothschild
- University of Massachusetts Chan Medical School and UMass Memorial Health Care, Worcester, USA
| | - Aristotle N Voineskos
- Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Canada; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada
| | - Ellen M Whyte
- Department of Psychiatry, University of Pittsburgh School of Medicine and UPMC Western Psychiatric Hospital, Pittsburgh, USA
| | - Alastair J Flint
- Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Canada; Centre for Mental Health, University Health Network, Toronto, Canada.
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Dabb C, Dryer R, Brunton RJ, Krägeloh C, Moussa M, Yap K, Roach VJ, Medvedev O. Development of the paternal pregnancy-related anxiety scale (PPrAS) using Rasch analysis with Australian and USA samples of expectant fathers. J Affect Disord 2025; 381:33-43. [PMID: 40180052 DOI: 10.1016/j.jad.2025.03.184] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 09/24/2024] [Revised: 03/28/2025] [Accepted: 03/30/2025] [Indexed: 04/05/2025]
Abstract
Up to 25 % of expectant fathers may experience anxiety symptoms, with potential adverse consequences for themselves and their families. This study developed a psychometrically sound measure of pregnancy-related anxiety for fathers, addressing a current gap in research and practice for psychological scales that specifically assess men's fears, worries, and concerns specific to pregnancy. An item pool encompassing men's pregnancy-related concerns and worries was generated based on findings from a systematic review (Dabb et al., 2023). Following expert panel review, 95 items were evaluated within the framework of the Rasch measurement model, using data from 292 expectant fathers (Mage = 29.9 years, SD = 5.55) from Australia (N = 146) and the USA (N = 146). The resultant 33-item unidimensional scale demonstrated good fit, no evidence for differential item functioning, sound levels of targeting, and excellent internal consistency reliability. The new Paternal Pregnancy-related Anxiety Scale (PPrAS) is a comprehensive measure of pregnancy-related anxiety for expectant fathers, with usefulness in both clinical and research contexts.
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Affiliation(s)
- Carol Dabb
- Australian Catholic University, Strathfield, NSW, Australia.
| | - Rachel Dryer
- Australian Catholic University, Strathfield, NSW, Australia.
| | | | | | - Michele Moussa
- Australian Catholic University, Strathfield, NSW, Australia
| | - Keong Yap
- Australian Catholic University, Strathfield, NSW, Australia
| | - Vijay J Roach
- Past President, Royal Australian and New Zealand College of Obstetricians and Gynaecologists, Australia.
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Cassidy L, Thompson G, Hill L, McGaughey J, Dempster M, Greene E, Donnelly P, Dixon L, Campbell P, Fitzsimons D. Co-design and feasibility testing of the heart failure carer support programme (HELP): A convergent, mixed-method study. PATIENT EDUCATION AND COUNSELING 2025; 136:108760. [PMID: 40187229 DOI: 10.1016/j.pec.2025.108760] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/05/2024] [Revised: 02/25/2025] [Accepted: 03/16/2025] [Indexed: 04/07/2025]
Abstract
OBJECTIVES This study co-designed and feasibility tested a novel psychoeducational intervention delivered online to carers of patients with heart failure (HF) and examined the potential impact on carer-related outcomes. METHODS The HEart faiLure carer support Programme (HELP) was co-designed with carers and healthcare professionals at a large University hospital. This intervention comprises an information booklet and six psychoeducational support group sessions delivered online by a multidisciplinary team. A convergent mixed-method design examined the feasibility, acceptability, and potential impact of HELP. Carers of patients with HF were recruited in the United Kingdom (UK) via clinical teams along with printed and online advertisements. Quantitative measurements included carer-related outcomes (carer burden, carer preparedness, quality of life, anxiety, depression, stress, and social support) and feasibility assessments (recruitment rates, attrition, and intervention usefulness). Focus groups conducted post-intervention qualitatively investigated the acceptability of HELP. Data was collected at baseline, 6 weeks post-intervention, and 3 months post-intervention. Quantitative and qualitative data were analyzed with descriptive and thematic analysis, respectively. The results were integrated to generate a holistic understanding of the findings. RESULTS 51 carers were eligible and 22 (43 %) provided consent. Of those 22, 18 (89 %) participated and 12 (67 %) completed all intervention sessions. Participants highly rated the usefulness of the intervention via a feedback questionnaire (4.7 ± 0.59 out of 5, overall) and positive changes were found across the following carer-related outcomes: anxiety, depression, caregiver burden, stress, preparedness, and social support. Data integration generated three key findings: (1) Improved carer preparedness and knowledge, (2) Support from group environment, and (3) Emotional support and personal wellbeing. CONCLUSIONS HELP delivery to carers of patients with HF is feasible and potentially provides emotional support and empowerment in their caring role. PRACTICE IMPLICATIONS HELP will advance to implementation testing across the UK to inform large-scale adoption in routine clinical practice.
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Affiliation(s)
- Lorna Cassidy
- School of Nursing and Midwifery, Queen's University Belfast, Belfast, United Kingdom.
| | - Gareth Thompson
- School of Nursing and Midwifery, Queen's University Belfast, Belfast, United Kingdom.
| | - Loreena Hill
- School of Nursing and Paramedic Science, Ulster University, Derry/Londonderry, United Kingdom.
| | - Jennifer McGaughey
- School of Nursing and Midwifery, Queen's University Belfast, Belfast, United Kingdom.
| | - Martin Dempster
- School of Psychology, Queen's University Belfast, Belfast, United Kingdom.
| | - Eunice Greene
- School of Nursing and Midwifery, Queen's University Belfast, Belfast, United Kingdom.
| | - Patrick Donnelly
- Ulster Hospital, South Eastern Health and Social Care Trust, Belfast, United Kingdom.
| | - Lana Dixon
- Royal Victoria Hospital, Belfast Health and Social Care Trust, Belfast, United Kingdom.
| | - Patricia Campbell
- Craigavon Area Hospital, Southern Health and Social Care Trust, Portadown, United Kingdom.
| | - Donna Fitzsimons
- School of Nursing and Midwifery, Queen's University Belfast, Belfast, United Kingdom.
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11
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Renner A, Bätge SJ, Filser M, Lau S, Pöttgen J, Penner IK. Non-pharmacological randomized intervention trial for the management of neuropsychological symptoms in outpatients with progressive multiple sclerosis. APPLIED NEUROPSYCHOLOGY. ADULT 2025; 32:1027-1039. [PMID: 37652158 DOI: 10.1080/23279095.2023.2233648] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 09/02/2023]
Abstract
PURPOSE Despite typically more pronounced cognitive and mental health issues in progressive disease courses of multiple sclerosis (PMS), rehabilitation research in this subgroup is rare. The efficacy of two non-pharmacological interventions with positive results from prior investigations was therefore examined in PMS specifically. METHODS Persons with PMS (pwPMS) received either computerized cognitive training (BrainStim), standardized cognitive-behavioral group sessions (Metacognitive Training [MaTiMS]), or a combination of both in an ambulatory setting. Neuropsychological assessment was conducted before and after the four-week intervention. RESULTS 37 participants (13 with primary/24 with secondary PMS, meanage = 52.87, SDage = 7.11, meanEDSS = 4.02, SDEDSS = 1.35) entered analyses. The BrainStim group improved in immediate and delayed verbal memory, recognition, verbal working memory, and perceived cognitive deficits while experiencing increased anxiety post-intervention. MaTiMS participants reported high program satisfaction and less cognitive difficulties at retest. The Combination group performed better in immediate and delayed verbal memory, and in information processing speed after training. Descriptive data further indicated positive effects on anxiety and depression in the MaTiMS and Combination group. CONCLUSIONS While objective cognitive performance improved when explicitly trained, psychoeducative sessions contributed to subjective mental health. The combination of both approaches is thus suggested, considering the specific needs of pwPMS treated in an ambulatory setting.
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Affiliation(s)
- Alina Renner
- Cogito Center for Applied Neurocognition and Neuropsychological Research, Düsseldorf, Germany
| | - Sharon Jean Bätge
- Cogito Center for Applied Neurocognition and Neuropsychological Research, Düsseldorf, Germany
| | - Melanie Filser
- Cogito Center for Applied Neurocognition and Neuropsychological Research, Düsseldorf, Germany
| | - Stephanie Lau
- Institute of Neuroimmunology and Multiple Sclerosis (INIMS), Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
- Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
| | - Jana Pöttgen
- Institute of Neuroimmunology and Multiple Sclerosis (INIMS), Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
- Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
| | - Iris-Katharina Penner
- Cogito Center for Applied Neurocognition and Neuropsychological Research, Düsseldorf, Germany
- Department of Neurology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
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12
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Altay B, Yılmaz Bulut T, Çekiç Y. The Effects of Pulmonary Rehabilitation Applied to Intensive Care Unit Patients on Dyspnea, Quality of Life, Depression, Anxiety, and Daily Living Activities: A Randomized Controlled Study. Dimens Crit Care Nurs 2025; 44:196-203. [PMID: 40408174 DOI: 10.1097/dcc.0000000000000706] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/25/2025] Open
Abstract
PURPOSE The aim of our study was to find out the effects of pulmonary rehabilitation (PR), which was applied to patients with coronavirus disease 2019 (COVID-19) both during their stay in the intensive care unit and also after discharge, on dyspnea, daily living activities, anxiety, depression, and quality of life. METHODS The study was conducted using a randomized, pretest, posttest, follow-up, and control group interventional study design. The data were collected from patients between June and August 2021. A total of 60 patients with COVID-19 in the intensive care unit, including 30 in the intervention and 30 in the control group, were included randomly in the study. The patients in the intervention group were started PR at home and continued with telerehabilitation. RESULTS Pulmonary rehabilitation applied to patients diagnosed with COVID-19 both during their stay in the intensive care unit and following discharge had a positive effect on patients' dyspnea, daily living activities, anxiety, depression, and quality of life. CONCLUSION It was found that PR applied both during the intensive care unit stay and at home by using the telerehabilitation method decreased anxiety, depression, and dyspnea in patients with COVID-19 and affected the quality of life and daily living activities positively. Continuing PR, which was applied to acute respiratory patients in the hospital and with telerehabilitation at home, can ensure the integrity of care and treatment.
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13
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Witten JA, Coetzer R, Rowlands L, Turnbull OH. "Talk and Chalk": An emotion regulation intervention for anger after acquired brain injury. APPLIED NEUROPSYCHOLOGY. ADULT 2025; 32:928-943. [PMID: 37339498 DOI: 10.1080/23279095.2023.2224481] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/22/2023]
Abstract
Uncontrollable anger is a debilitating consequence of acquired brain injury (ABI). This proof-of-concept study investigated the preliminary efficacy of an emotion regulation intervention for managing post-ABI anger. A secondary objective was to determine which participant characteristics were related to intervention gains. With a pre-post intervention design and three-month follow-up, there were five individually administered meetings on Zoom, over a four-month period. 24 adults who had sustained an ABI were enrolled. Participants were mostly males, from 24 to 85 years old. A series of one-way repeated-measures ANOVAs were conducted to determine the intervention's efficacy, and Spearman's rho bivariate correlations for the association between participant characteristics and intervention gains. Significant differences were observed in external anger from baseline to post-treatment; there were no further changes from post-treatment to follow-up. Of the participant characteristics, only readiness to change and anxiety were correlated. The proposed intervention presents a brief, feasible, and preliminary efficacious alternative for regulating post-ABI anger. Intervention gains are associated with readiness to change and anxiety, which has important implications for clinical delivery.
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Affiliation(s)
| | - Rudi Coetzer
- Department of Psychology, Bangor University, Bangor, United Kingdom
- The Disabilities Trust, Wakefield, United Kingdom
- Faculty of Medical, Life and Health Science, Swansea University, Swansea, United Kingdom
| | - Leanne Rowlands
- School of Psychology, Arden University, Coventry, United Kingdom
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14
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Schmidt LM, Klingner C, Petersen I, Volkmer A, Schreiber M, Schmidt A, Reuken P, Besteher B, Geis C, Ullsperger M, Finke K, Martin EM, Rupprecht S, Brodoehl S, Wagner F. Cognitive impairment and associated neurobehavioral dysfunction in post-COVID syndrome. Psychiatry Res 2025; 349:116522. [PMID: 40319610 DOI: 10.1016/j.psychres.2025.116522] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/18/2024] [Revised: 04/23/2025] [Accepted: 04/25/2025] [Indexed: 05/07/2025]
Abstract
There is a high prevalence of neuropsychiatric sequelae in post-COVID syndrome, most commonly chronic fatigue, the mechanisms of which remain poorly understood. As altered function of the reward system has been suggested as a causal factor, we aimed to distinguish whether reward processing or task-unspecific cognitive operations are impaired in post-COVID syndrome. Our cohort study included 24 patients diagnosed with post-COVID syndrome and 24 demographically matched healthy controls. Questionnaire assessment of neuropsychiatric symptoms and socio-demographic variables, the Monetary Incentive Delay Task during an fMRI scan, and pupillary measurements were performed. In addition to clinical neuropsychiatric symptoms, participants in the post-COVID group demonstrated significantly slower task performance compared to healthy controls, although the function of behavioral reward circuits appeared unimpaired. However, the influence of rewarding cues on post-COVID patients increased significantly over time during task performance, correlating with temporally delayed activation of the left frontal gyrus and increased activity in task-unspecific brain regions in post-COVID patients. Furthermore, slower reaction times on the task were associated with a lower pupil diameter and a higher pupillary unrest index. This study proposes that post-COVID syndrome is a process that may not affect reward processing, but leads to neural hypoarousal and temporally altered brain activity in frontal and task-unspecific brain regions.
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Affiliation(s)
- Laura Marie Schmidt
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Friedrich Schiller University Jena, Jena, Germany
| | - Carsten Klingner
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Department of Neurology, Jena University Hospital, Jena, Germany
| | - Insa Petersen
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Friedrich Schiller University Jena, Jena, Germany
| | - Annika Volkmer
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Friedrich Schiller University Jena, Jena, Germany
| | - Minne Schreiber
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Friedrich Schiller University Jena, Jena, Germany
| | | | - Philipp Reuken
- Department of Internal Medicine IV (Gastroenterology, Hepatology and Infectious Diseases), Jena University Hospital, Jena, Germany
| | - Bianca Besteher
- Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany
| | - Christian Geis
- Department of Neurology, Jena University Hospital, Jena, Germany
| | - Markus Ullsperger
- Faculty of Natural Sciences, Institute of Psychology, Magdeburg, Germany; Center for Behavioral Brain Sciences, Magdeburg, Otto-von-Guericke University Magdeburg, Germany; German Center for Mental Health (DZPG), partner site Halle-Jena-Magdeburg, Germany
| | - Kathrin Finke
- Department of Neurology, Jena University Hospital, Jena, Germany
| | - Eva Maria Martin
- Department of Neurology, Jena University Hospital, Jena, Germany
| | - Sven Rupprecht
- Department of Neurology, Jena University Hospital, Jena, Germany
| | - Stefan Brodoehl
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Department of Neurology, Jena University Hospital, Jena, Germany
| | - Franziska Wagner
- Biomagnetic Center, Jena University Hospital, Jena, Germany; Department of Neurology, Jena University Hospital, Jena, Germany.
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Pickard A, Edwards KL, Farrow C, Haycraft E, Herle M, Llewellyn C, Croker H, Blissett J. Daily manifestations of Children's avid eating behaviour and associations with temperament, parental feeding practices and wellbeing. Appetite 2025; 211:107982. [PMID: 40187567 DOI: 10.1016/j.appet.2025.107982] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/12/2024] [Revised: 03/25/2025] [Accepted: 03/26/2025] [Indexed: 04/07/2025]
Abstract
Recent evidence has identified four distinct eating profiles in 3-5-year-old children in the UK: avid, happy, typical, and avoidant. Among these profiles, children with avid eating behaviour exhibit high responsiveness to food cues, emotional eating, fast eating speed, and low responsiveness to fullness, posing risks for overeating and higher adiposity. Despite the implications, there is limited research on how avid eating manifests and impacts parents' behaviour and wellbeing. This study aimed to report the frequency of children's avid eating behaviour and explore its associations with child demographics, child temperament, home environment, parental feeding practices, and parental wellbeing. This study collected data via Ecological Momentary Assessment from 109 parents of a 3-5-year-old child identified as having an avid eating profile through a latent profile analysis of parents' reports of their children's eating behaviour. Using baseline and momentary data, the novel findings revealed that children with avid eating frequently requested food, especially snacks, with higher occurrences during weekends. Older children and boys showed higher probabilities of avid eating. High surgency in children correlated with more frequent food requests, while greater effortful control in children related to fewer eating occasions. Parents of children with higher probability of avid eating reported higher stress, depression, and anxiety, as well as frequent food requests from their child. Additionally, food insecurity was linked to increased food requests, suggesting a complex interplay between food availability and eating behaviour. The study underscores the need for targeted interventions to support parents in managing children's avid eating behaviour and improving overall family wellbeing.
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Affiliation(s)
- Abigail Pickard
- School of Psychology and Institute of Health and Neurodevelopment, Aston University, Birmingham, UK; Department of Clinical Psychology, School of Health in Social Science, University of Edinburgh, Edinburgh, UK.
| | - Katie L Edwards
- School of Psychology and Institute of Health and Neurodevelopment, Aston University, Birmingham, UK; School of Psychology, University of Birmingham, Birmingham, UK
| | - Claire Farrow
- School of Psychology and Institute of Health and Neurodevelopment, Aston University, Birmingham, UK
| | - Emma Haycraft
- School of Sport, Exercise and Health Sciences, Loughborough University, UK
| | - Moritz Herle
- Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK
| | - Clare Llewellyn
- Research Department of Behavioural Science and Health, Institute of Epidemiology and Health Care, University College London, London, UK
| | - Helen Croker
- World Cancer Research Fund International, London, UK
| | - Jacqueline Blissett
- School of Psychology and Institute of Health and Neurodevelopment, Aston University, Birmingham, UK
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16
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Williams SE, Fergus TA, Ginty AT. Development and Validation of the Ease of Imagery Questionnaire. Assessment 2025; 32:759-777. [PMID: 39054848 PMCID: PMC12089667 DOI: 10.1177/10731911241260233] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 07/27/2024]
Abstract
The present series of studies aimed to develop and provide initial validation of the Ease of Imagery Questionnaire (EIQ)-a measure assessing ease of imaging different positive and negative imagery content reflective of valence and engaging or disengaging in adverse situations. Five studies were conducted to collectively examine the questionnaire's factor structure and concurrent validity. Study 1 (N = 336) and Study 2 (N = 207) informed the development of 16 items of the EIQ, with a four-factor structure supported in Studies 3 (N = 219), 4 (N = 135), and 5 (N = 184) using confirmatory factor analysis. Study 3 also supported concurrent validity with significant bivariate correlations (p < .05) with the similar Sport Imagery Ability Questionnaire subscales, while studies 4 and 5 demonstrated criterion validity in the EIQ's prediction of challenge and threat appraisal tendencies, perceived stress, stress mindset, and anxiety and depressive symptoms. Overall, the EIQ demonstrates a replicable four-factor structure and appears to assess ability to image content associated with positive and negative emotions as well as demanding stress-evoking situations.
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17
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Lin SM, Han Y, Hu JY, Wang XY, Zeng YM, Wei H, Shao Y, Yu Y. Resting-state functional brain networks in hypertensive retinopathy. Brain Res Bull 2025; 226:111350. [PMID: 40250734 DOI: 10.1016/j.brainresbull.2025.111350] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/11/2024] [Revised: 04/13/2025] [Accepted: 04/15/2025] [Indexed: 04/20/2025]
Abstract
OBJECTIVE Hypertensive retinopathy (HR) is known to have effects on the brain's function. This neuroimaging investigation aimed to evaluate alterations in functional network connectivity and the topological properties of brain networks in in patients with HR. METHODS The study involved twenty patients with HR and forty-one healthy controls (HC), all of whom underwent resting-state functional MRI scans. Independent component analysis and graph theory analysis were calculated to identify functional connectivity and topological property abnormalities between the two groups. RESULTS Compared to HC, patients with HR demonstrated increased internetwork functional connectivity. Furthermore, these patients showed increased intranetwork functional connectivity within the right precuneus of the default mode network. Graph theory analysis revealed that both groups demonstrated a small-world topology. However, significant differences were observed in global and regional network metrics in HR patients compared to HC. CONCLUSION These findings highlight the alterations in functional connectivity and topological properties of brain networks in patients with HR, offering valuable insights into the potential neural mechanisms underlying their condition.
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Affiliation(s)
- Si-Min Lin
- Department of Radiology, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Fujian Branch of National Clinical Research Center for Cardiovascular Diseases, Xiamen, Fujian, China
| | - Yi Han
- Department of Ophthalmology, The First Affiliated Hospital of University of South China, Hengyang Medical School, University of South China, Hengyang, Hunan, China
| | - Jin-Yu Hu
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Xiao-Yu Wang
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Yan-Mei Zeng
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Hong Wei
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Yi Shao
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China; Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
| | - Yao Yu
- Department of Endocrine and Metabolic, The First Affiliated Hospital, Jiangxi, Medical College, Nanchang University, Jiangxi Clinical Research Center for Endocrine and Metabolic Disease, Jiangxi Branch of National Clinical Research Center for Metabolic Disease, Nanchang, Jiangxi, China.
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18
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Cao X, Zhang Y, Wu H, Da H, Xiao Q, Shi H. Decoding depression: How DLPFC and SMA mediate stress perception's role in mental health? J Affect Disord 2025; 379:323-331. [PMID: 40086480 DOI: 10.1016/j.jad.2025.03.036] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/02/2024] [Revised: 03/04/2025] [Accepted: 03/10/2025] [Indexed: 03/16/2025]
Abstract
BACKGROUND Depression is a common mental disorder that significantly impacts global well-being. Although stress is a major contributor to depression, not all stress leads to depressive outcomes due to differences in stress perception. Understanding the neural mechanisms of stress perception may help identify biomarkers for targeted interventions to alleviate stress-related depression. METHODS This study included 113 participants. Each participant completed a Verbal Fluency Task (VFT) while undergoing functional near-infrared spectroscopy (fNIRS) to monitor brain activity. Oxyhemoglobin (Oxy-Hb) concentration data were analyzed using Matlab, and PROCESS v4.1 to examine neural mechanisms connecting stress perception and depression. RESULTS Correlation analysis showed a significant negative association between depression severity and Oxy-Hb concentration in several brain regions, including the bilateral dorsolateral prefrontal cortex (DLPFC), bilateral Broca's area (BA), right frontal pole (FP), and right orbitofrontal cortex (OFC). Mediation and moderation analyses revealed that the bilateral DLPFC serves as a key mediator in the relationship between stress perception and depression, with the supplementary motor area (SMA) acts as a moderator. Functional differentiation was observed, with the left DLPFC and left SMA influencing the effect of nervous on depression, and the right DLPFC and right SMA influencing the effect of uncontrolled on depression. CONCLUSION The bilateral DLPFC and SMA play critical roles in mediating and moderating stress perception's impact on depression, suggesting these regions as potential targets for interventions in stress-related depressive disorders.
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Affiliation(s)
- Xiaochen Cao
- School of Education, Huazhong University of Science and Technology, Wuhan 430074, China
| | - Yan Zhang
- School of Education, Huazhong University of Science and Technology, Wuhan 430074, China.
| | - Huifen Wu
- School of Education, Hubei Engineering University, Xiaogan 432000, China
| | - Hui Da
- School of Education, Huazhong University of Science and Technology, Wuhan 430074, China
| | - Qiang Xiao
- Department of Neurology, Hospital of Huazhong University of Science and Technology, Wuhan 430074, China
| | - Hui Shi
- The Department of Cardio-Psychiatry Liaison Consultation, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China.
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Modzelewski S, Stankiewicz A, Waszkiewicz N, Łukasiewicz K. Side effects of microdosing lysergic acid diethylamide and psilocybin: A systematic review of potential physiological and psychiatric outcomes. Neuropharmacology 2025; 271:110402. [PMID: 40058407 DOI: 10.1016/j.neuropharm.2025.110402] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/07/2024] [Revised: 02/25/2025] [Accepted: 03/02/2025] [Indexed: 03/15/2025]
Abstract
OBJECTIVE Psychedelics are gaining renewed attention, especially through the practice of microdosing, where low doses are taken regularly. Microdosing lysergic acid diethylamide (LSD) and psilocybin is used by both healthy individuals and those with mental health conditions to improve daily functioning, reduce anxiety, and enhance mood and cognition. However, there is limited information about the side effects of this practice. This review aimed to collect and characterize the side effects of psychedelic microdosing. METHODS We conducted a systematic review of original papers from PubMed, Web of Science, and Scopus (accessed August 03, 2024) that reported side effects of microdosing LSD and psilocybin. Non-English papers, non-original studies, studies without typical microdosing doses, or those lacking descriptions of side effects were excluded. Our methodology has been developed in accordance with PRISMA guidelines. Because side effects were assessed heterogeneously in these papers, we did not perform a bias evaluation. RESULTS We included 31 studies, 15 of which we classified as laboratory studies with higher quality evidence, and 14 studies with lower quality evidence, as well as 2 clinical cases. Side effects were typically dose-dependent, mild, and short-lived. Common adverse effects included increased blood pressure, anxiety, and cognitive impairment. DISCUSSION This review is limited by the heterogeneity in reporting side effects and the short duration of many studies. Future studies should transparently and systematically present a description of side effects.
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Affiliation(s)
| | - Anna Stankiewicz
- Department of Psychiatry, Medical University of Białystok, Poland
| | | | - Kacper Łukasiewicz
- Department of Psychiatry, Medical University of Białystok, Poland; Experimental Medicine Centre, Medical University of Białystok, Poland; School of Human Sciences, University of Economics and Human Sciences in Warsaw, Poland.
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Cho CY, Jeon JH, Kang HJ, Kim JW, Jhon M, Lee JY, Kim SW, Shin IS, Kim JM. Exploring the prospective association of serum interleukin-1β and brain-derived neurotrophic factor with antidepressant treatment response. Eur Neuropsychopharmacol 2025; 95:33-39. [PMID: 40222150 DOI: 10.1016/j.euroneuro.2025.03.004] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 12/30/2024] [Revised: 03/06/2025] [Accepted: 03/10/2025] [Indexed: 04/15/2025]
Abstract
This study investigated the prospective association of serum interleukin-1 beta (sIL-1β) and brain-derived neurotrophic factor (sBDNF) with 12-week antidepressant treatment outcomes in patients with depressive disorders. We analyzed baseline levels of sIL-1β and sBDNF in 1,086 patients participating in a naturalistic, stepwise antidepressant treatment study. Remission was defined by a Hamilton Depression Rating Scale score of ≤7 at 12 weeks. Logistic regression, adjusted for sociodemographic and clinical covariates, was used to assess the relationships between biomarker levels and treatment outcomes. Higher sIL-1β levels were significantly associated with non-remission at 12 weeks in patients with lower sBDNF levels, while in patients with higher sBDNF levels, sIL-1β did not significantly impact remission outcomes. The interaction between sIL-1β and sBDNF significantly associated with remission status, even after adjusting for confounders. The study suggests the significant role of the interplay between inflammatory and neuroplastic systems in influencing antidepressant treatment outcomes. These findings underscore the potential of integrating biomarker profiles to enhance personalized antidepressant strategies, advancing treatment precision in depressive disorders. Future research should focus on elucidating the dynamic mechanisms behind these biomarker interactions to further refine models that assess treatment responsiveness and develop targeted therapeutic interventions.
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Affiliation(s)
- Chan-Yeong Cho
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Ji Hyeon Jeon
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Hee-Ju Kang
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Ju-Wan Kim
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Min Jhon
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea; Mental Health Clinic, Chonnam National University Hwasun Hospital, Hwasun, South Korea
| | - Ju-Yeon Lee
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Sung-Wan Kim
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Il-Seon Shin
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea
| | - Jae-Min Kim
- Department of Psychiatry, Chonnam National University Medical School, Gwangju, South Korea.
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Ranta K. Psychological interventions for parents of children with intellectual disabilities to enhance child behavioral outcomes or parental well-being: A systematic review, content analysis and effects. JOURNAL OF INTELLECTUAL DISABILITIES : JOID 2025; 29:500-535. [PMID: 39603255 PMCID: PMC12084672 DOI: 10.1177/17446295241302857] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Accepted: 11/04/2024] [Indexed: 11/29/2024]
Abstract
The aim of this review was to identify the type, content, and effectiveness of psychological parenting interventions for parents of children with intellectual disabilities to enhance child behavior and/or parental well-being. A systematic search yielded 21 studies involving 1825 participants. Studies were evaluated according to intervention content, pre- and post-treatment and follow-up effect sizes, and risk of bias. We categorized the interventions into those targeting 'Child or interaction' (child behavior, interaction and learning, understanding disability), and those targeting 'Parent' (parental well-being) or both themes. All these interventions had positive effects on parental well-being or child behavior. Parental outcomes were improved by interventions targeting 'Parental well-being', as well as 'Child or interaction'. Child behavior showed improvements in programs focusing on 'Child or interaction', and in a mindfulness-based parental well-being program. During follow-up, most effects were sustained or further increased, but some studies showed no improvements over the control group.
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Affiliation(s)
- Kati Ranta
- Doctoral Program in Psychology and Logopaedics, Faculty of Social Sciences, Tampere University, Finland
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Mao YJ, Lai HJ, Liu YM, Liao MN, Tung TH, Lin YC, Beaton RD, Jane SW, Huang HP. Unmet Care Needs of Colorectal Cancer Survivors in Taiwan and Related Predictors. J Nurs Res 2025; 33:e391. [PMID: 40358116 DOI: 10.1097/jnr.0000000000000676] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/15/2025] Open
Abstract
BACKGROUND Despite advancements in medical technology and early cancer detection, many colorectal cancer (CRC) survivors report unmet care needs after completion of their cancer treatment that compromise their quality of life (QoL). Previous studies on the care needs of cancer survivors have yielded inconsistent results, and few studies have been conducted on survivors of CRC in Taiwan or on predictors of their unmet care needs. PURPOSE The purpose of this study was to examine the unmet care needs, psychological distress, and QoL of Taiwanese CRC survivors ( n = 100) as well as to assess the mean differences by sociodemographic characteristics in their unmet care needs and other related predictors after treatment completion. METHODS This cross-sectional study using a purposive sampling method was conducted at a regional hospital in northern Taiwan between October 2019 and February 2020. The measurements used in this study included Chinese Cancer Survivors' Unmet Needs, Hospital Anxiety and Depression Scale, and European Organization for Research and Treatment Quality of Life Questionnaire-Core 30 and Quality of Life Questionnaire-Colorectal Cancer Module 29. The independent t test and one-way analysis of variance were employed to assess sociodemographic differences in unmet care needs, and multivariate linear regression was used to identify significant predictors. RESULTS More than half of the participants (63.2%) reported at least one unmet care need, with the highest categories including information needs ("signs and symptoms of cancer recurrence" 31.7% and "information related to health promotion" 31.7%), "medical care needs" ("managing health with the medical team" 13.9%), and "physical/psychological effect needs ("concerns about cancer recurrence" 23.8%). Also, 7%-57% of the participants experienced differing degrees of distress symptoms including fatigue, intestinal and urogenital dysfunctions, and anxiety or depression. The results of the univariate analyses showed unmet needs to differ significantly by age ( p = .021), employment status ( p = .007), and chronic disease status ( p = .025). The findings revealed being of older age (β = 0.23, p = .049), being employed (β = 0.26, p = .014), and having a lower functional level (β = -0.31, p = .012) to be associated with significantly higher levels of unmet care needs, collectively accounting for nearly 27.3% of the variance (adjusted R2 = .273). CONCLUSIONS/IMPLICATIONS FOR PRACTICE CRC survivors continue to experience unmet care needs and various forms of physical-psychological distress for an average of almost 2 years after their completion of CRC treatment. The findings of this study may assist healthcare providers in identifying the major risk factors that interfere with survivor care needs following treatment, thus facilitating the development of timely interventions to mitigate the impact of cancer on this vulnerable population.
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Affiliation(s)
- Yu-Ju Mao
- Department of Nursing, Landseed International Hospital, Taoyuan, Taiwan
| | - Huang-Jen Lai
- Division of Colorectal Surgery, Department of Surgery, Landseed International Hospital, Taoyuan, Taiwan
| | | | - Mei-Nan Liao
- Executive Office, Chang Gung Medical Foundation Administration Center, Taoyuan, Taiwan
| | - Tao-Hsin Tung
- Evidence-Based Medicine Center, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Linhai, Zhejiang, China
| | - Yung-Chang Lin
- Division of Hematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Lin-Kou, Taiwan
| | - Randal D Beaton
- Child, Family and Population Health Nursing and Health Services, Schools of Nursing and Public Health, University of Washington, Seattle, USA
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Zeng S, Yang T, Tian R, Jin X, Zhang L, Li F, Fu L, Cai J, Liao J, Song G, Luo X, Wang Y, Yang M, Zhang W, Liu Y, Yu C, Xiao C, Liu Z. The association between greenspace exposure and sperm quality: A retrospective cohort study focusing on sperm kinematics and the influence of buffer settings. ENVIRONMENTAL RESEARCH 2025; 274:121243. [PMID: 40020854 DOI: 10.1016/j.envres.2025.121243] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/28/2024] [Revised: 01/25/2025] [Accepted: 02/25/2025] [Indexed: 03/03/2025]
Abstract
BACKGROUND While previous studies have suggested a potential link between greenspace and semen quality, the effect of greenspace exposure on sperm kinematics, as well as the impact of greenspace estimation scales, remains underexplored. OBJECTIVES This study aimed to examine the association between greenspace exposure and sperm kinematics, and to determine whether this relationship varies across different greenspace estimation scales. METHODS We conducted a retrospective longitudinal study of 5025 semen measurements from 1674 sperm donors recruited by the Sichuan Provincial Human Sperm Bank (SHSB) between June 2019 and December 2021. Greenspace exposure was estimated using the Normalized Difference Vegetation Index (NDVI) for four buffer zones (250 m, 500 m, 1,000 m, and 2000 m) centred on the geocoded residential addresses. Linear mixed-effects models and restricted cubic spline models (knots = 4) were used to assess the associations between greenspace exposure and both conventional semen parameters and sperm kinematic parameters across all buffer zones. RESULTS A non-linear association between NDVI-500m and progressive motility was observed for conventional semen parameters (P non-linear = 0.018). For sperm kinematics, NDVI-500m could be associated with multiple kinematic measures (VCL: % change = 1.81, 95% CI: 0.72, 2.91; VAP: % change = 2.57, 95% CI: 1.46, 3.70; VSL: % change = 3.37, 95% CI: 2.11, 4.66; LIN: % change = 1.51, 95% CI: 0.82, 2.21; STR: % change = 0.83, 95% CI: 0.44, 1.23; WOB: % change = 0.69, 95% CI: 0.35, 1.04; BCF: % change = 1.82, 95% CI: 0.97, 2.68), and significant non-linear associations were found between NDVI-500m and LIN (P non-linear = 0.011), STR (P non-linear = 0.015), WOB (P non-linear = 0.012), and ALH (P non-linear <0.001). Regarding the impact of greenspace estimation scales, smaller buffer zones exhibited stronger non-linear relationships for conventional semen parameters, whereas larger buffer zones revealed more pronounced non-linear relationships for sperm kinematics. There was a stable and significant linear association between greenspace exposure and sperm kinematics during the 70-90 days before ejaculation (spermatocytogenesis). PM2.5 and PM10 attenuated the negative effect of greenspace exposure on IM at a buffer scale of 250 m, while enhanced the positive effect of greenspace on kinematics at all scales. CONCLUSIONS Greenspace exposure were significantly associated with sperm kinematics, with the strength and nature of these associations varying by buffer scale. 70-90 days before ejaculation (spermatocytogenesis) was the window of susceptibility for greenspace exposures at all buffer scales. As PM2.5 and PM10 increased, increasing levels of greenspace can improve sperm kinematics more significantly. These findings support the beneficial effect of greenspace on male fertility, and underscore the importance of considering greenspace buffer zones in urban planning to optimize health benefits effectively.
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Affiliation(s)
- Sixuan Zeng
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Tingting Yang
- Department of Andrology/Sichuan Human Sperm Bank, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Key Laboratory of Birth Defects and Related Diseases of Women and Children, (Sichuan University), Ministry of Education, Chengdu, Sichuan, 610041, China
| | - Run Tian
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Xin Jin
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Lu Zhang
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Fuping Li
- Department of Andrology/Sichuan Human Sperm Bank, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Key Laboratory of Birth Defects and Related Diseases of Women and Children, (Sichuan University), Ministry of Education, Chengdu, Sichuan, 610041, China
| | - Leyao Fu
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Jiarui Cai
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Junhao Liao
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Guishuang Song
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Xiaoli Luo
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Yujue Wang
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Menghan Yang
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Weidong Zhang
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Yuqing Liu
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Chuan Yu
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
| | - Chenghan Xiao
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
| | - Zhenmi Liu
- Department of Maternal and Child Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China; Institute of Systems Epidemiology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
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Fausto DY, Martins JBB, Dominski FH, de Azevedo Guimarães AC. Effects of jazz dance and concurrent training on psychological variables in menopausal women: A randomized controlled trial. Arch Womens Ment Health 2025; 28:525-540. [PMID: 39190115 DOI: 10.1007/s00737-024-01509-2] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/29/2023] [Accepted: 08/20/2024] [Indexed: 08/28/2024]
Abstract
PURPOSE To analyze the effect of two 16-week interventions with jazz dance and concurrent training compared to a control group on anxiety, depression, stress, mood, and the perspective of aging in menopausal women, after 1-month, post-intervention, and at the 6-month follow-up. METHODS 70 post-menopausal women (53.19 ± 3.39 years) randomized into 3 groups:intervention group with Jazz Dance (JD); intervention group with Concurrent Training (CT), and Control Group (CG). Both interventions lasted 16 weeks, with 60-min classes, JD with a frequency of two weekly classes, and CT three times a week. The intensity of the JD was progressive and according to the frequency of beats per minute of the songs. In CT, the aerobic an initial intensity of 60% of HRmax, reaching 90%, and resistance the volume of sets and loads increased progressively throughout the intervention. Questionnaires related to symptoms of anxiety and depression (Hospital Anxiety and Depression Scale); stress (Perceived Stress Scale); mood (Brunel Mood Scale); and aging perspective (Sheppard Inventory) were applied. Intention-to-treat (ITT) and protocol adherence analysis were performed. RESULTS In the protocol analysis, the JD showed improvements in anxiety and depressive symptoms after 1-month, which remained at the follow-up. The TC presented reduced anxiety and depressive symptoms after 16 weeks, which also remained at the follow-up. Considering stress, the CT showed improvements at all times and the JD post-intervention. As for mood, the CT presented reduced anger, mental confusion, and fatigue only after 1-month, and both exercise groups presented increased vigor at all times. CONCLUSION Both interventions were beneficial, however dance showed immediate results for anxiety and depression, and concurrent training for stress. Considering mood, concurrent training was more effective for anger, mental confusion, and fatigue, while both interventions were effective for vigor. REGISTRATION Brazilian Clinical Trials Registry (REBEC) RBR - 87ndrv.
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Affiliation(s)
- Danielly Yani Fausto
- Physical Activity Leisure Research Laboratory, College of Health and Sport Science, Santa Catarina State University, Pascoal Simone, 358, Coqueiros, Florianopolis, Brazil.
| | - Julia Beatriz Bocchi Martins
- Physical Activity Leisure Research Laboratory, College of Health and Sport Science, Santa Catarina State University, Pascoal Simone, 358, Coqueiros, Florianopolis, Brazil
| | - Fábio Hech Dominski
- Laboratory of Sport and Exercise Psychology, College of Health and Sport Science, Santa Catarina State University, Florianopolis, Brazil
| | - Adriana Coutinho de Azevedo Guimarães
- Physical Activity Leisure Research Laboratory, College of Health and Sport Science, Santa Catarina State University, Pascoal Simone, 358, Coqueiros, Florianopolis, Brazil
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Câmara-Costa H, Dellatolas G, Jourdan C, Ruet A, Bayen E, Vallat-Azouvi C, Allain P, Chevignard M, Azouvi P. The 20-item dysexecutive questionnaire after severe traumatic brain injury: Distribution of the total score and its significance. Neuropsychol Rehabil 2025; 35:1059-1080. [PMID: 39106184 DOI: 10.1080/09602011.2024.2387065] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/20/2024] [Accepted: 07/26/2024] [Indexed: 08/09/2024]
Abstract
TRIAL REGISTRATION ClinicalTrials.gov identifier: NCT01437683..
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Affiliation(s)
- Hugo Câmara-Costa
- Rehabilitation Department for Children with Acquired Brain Injury; Saint Maurice Hospitals, Saint Maurice, France
- Sorbonne Université, CNRS, INSERM, Laboratoire d'Imagerie Biomédicale (LIB), F-75006, Paris, France
- Sorbonne Université, GRC 24 Handicap Moteur Cognitif et Réadaptation (HaMCRe), AP-HP, F-75013, Paris, France
| | - Georges Dellatolas
- Sorbonne Université, GRC 24 Handicap Moteur Cognitif et Réadaptation (HaMCRe), AP-HP, F-75013, Paris, France
| | - Claire Jourdan
- Physical Medicine and Rehabilitation Department, Lapeyronie Hospital, CHRU, Montpellier, France
| | - Alexis Ruet
- Physical Medicine and Rehabilitation Department, CHU Caen, INSERM U1077, Caen, France
| | - Eléonore Bayen
- Sorbonne Université, CNRS, INSERM, Laboratoire d'Imagerie Biomédicale (LIB), F-75006, Paris, France
- Sorbonne Université, GRC 24 Handicap Moteur Cognitif et Réadaptation (HaMCRe), AP-HP, F-75013, Paris, France
- Assistance Publique-Hôpitaux de Paris (APHP), Groupe Hospitalier Pitié-Salpêtrière, Service De Médecine Physique et Réadaptation, Paris, France
| | | | - Philippe Allain
- Laboratoire de Psychologie des Pays de la Loire, LPPL EA 4638, SFR Confluences, UNIV Angers, Nantes Université, Maison de la recherche Germaine Tillion, Angers, France
- Département de Neurologie, Centre Hospitalier Universitaire d'Angers, Angers, France
| | - Mathilde Chevignard
- Rehabilitation Department for Children with Acquired Brain Injury; Saint Maurice Hospitals, Saint Maurice, France
- Sorbonne Université, CNRS, INSERM, Laboratoire d'Imagerie Biomédicale (LIB), F-75006, Paris, France
- Sorbonne Université, GRC 24 Handicap Moteur Cognitif et Réadaptation (HaMCRe), AP-HP, F-75013, Paris, France
| | - Philippe Azouvi
- AP-HP, GH Paris Saclay, Hôpital Raymond Poincaré, Service de Médecine Physique et de Réadaptation, Garches, France
- Université Paris-Saclay, UVSQ, Inserm, CESP, 94807, Villejuif, France
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Bocchi Martins JB, Amaral da Rocha AR, Fausto DY, da Silva E, da Silva G, Pinheiro GP, de Azevedo Guimarães AC. Comparing urban dance and functional fitness for postmenopausal women: A randomized clinical trial protocol. Eur J Obstet Gynecol Reprod Biol 2025; 310:113936. [PMID: 40188682 DOI: 10.1016/j.ejogrb.2025.113936] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/14/2025] [Revised: 03/24/2025] [Accepted: 03/26/2025] [Indexed: 05/23/2025]
Abstract
INTRODUCTION Physical exercise is a non-pharmacological treatment that can bring positive changes to menopausal women experiencing physiological and hormonal changes leading to various physical and psychological symptoms. This study introduces the MenosPausa Mais Movimento Project protocol, aiming to compare the effects of Urban Dance and Functional Fitness with a control group on the physical and psychological well-being of postmenopausal women. METHODS This study outlines a protocol for a three-arm randomized clinical trial involving two interventions (Urban Dance and Functional Fitness) lasting 12 weeks. The participants will be women in early postmenopause, aged between 40 and 59 years, assigned to three groups: (1) Urban Dance Intervention Group, (2) Functional Fitness Intervention Group, and (3) Control Group. Both interventions will consist of two weekly sessions lasting 60 min each. The outcomes to be assessed include physical aspects (body mass index, fat percentage, waist circumference, muscle strength, cardiorespiratory fitness, bone densitometry, sleep quality, urinary incontinence, sexual function, and follicle-stimulating hormone) as well as psychological aspects (stress, cognition, mood state, depressive symptoms, and anxiety). Data collection and analysis will be conducted during pre- and post-intervention periods. DISCUSSION The study is proposed with the aim of expanding the evidence related to the effects of different types of physical exercise in reducing and/or stopping symptoms resulting from menopause. The hypothesis is that women who perform the types of physical exercise will significantly improve the symptoms investigated when compared to those in the control group, thus expanding the possibilities of non-pharmacological therapies to assist the work of health professionals, favoring the physical and psychological aspects of this population.
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Affiliation(s)
| | | | | | - Emily da Silva
- State University of Santa Catarina, Florianópolis, Santa Catarina, Brazil
| | - Giulian da Silva
- State University of Santa Catarina, Florianópolis, Santa Catarina, Brazil
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Hatakeyama J, Nakamura K, Kanda N, Kawauchi A, Fujitani S, Oshima T, Kato H, Ota K, Kamijo H, Asahi T, Muto Y, Hori M, Iba A, Hosozawa M, Iso H. Long-term functional prognosis with tocilizumab in severe COVID-19 infection: A multicenter prospective observational study on mechanically ventilated ICU patients in the COVID-19 recovery study II. J Infect Chemother 2025; 31:102708. [PMID: 40250803 DOI: 10.1016/j.jiac.2025.102708] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/07/2025] [Revised: 04/10/2025] [Accepted: 04/14/2025] [Indexed: 04/20/2025]
Abstract
BACKGROUND Tocilizumab, an IL-6 receptor antagonist, may prevent functional impairments in critically ill patients by attenuating the cytokine storm. This study investigated a potential effect of tocilizumab on preventing functional impairments in patients with severe coronavirus infection 2019 (COVID-19). METHODS In a multicenter prospective observational study, patients with COVID-19 ≥ 20 years requiring mechanical ventilation admitted to the intensive care unit between April 2021 and September 2021 and discharged alive were followed for one year. A self-administered questionnaire on sequelae and functional impairments was mailed in August 2022, and data were collected. A multivariate logistic regression was used to assess the impact of tocilizumab on physical function, mental health, and Long COVID. RESULTS Of 157 analyzed patients, 41 received tocilizumab. The tocilizumab group had more severe illness, but a lower prevalence of physical impairment (17.1 % vs. 23.3 %, p = 0.41) and mental disorders (19.5 % vs. 39.7 %, p = 0.009) than the non-tocilizumab group. The prevalence of Long COVID was higher in the tocilizumab group (92.7 % vs. 80.2 %, p = 0.06), whereas fatigue/malaise was significantly lower (19.5 % vs. 37.1 %, p = 0.039). Adjusted odds ratios (95 % confidence interval) for physical impairment, mental disorders, and Long COVID with tocilizumab were 0.70 (0.2-2.1), 0.40 (0.16-1.01), and 2.94 (0.7-12.3), respectively, with no significant difference. CONCLUSIONS Tocilizumab was associated with a lower prevalence of physical impairment and mental disorders at 1 year in patients with severe COVID-19. Furthermore, Long COVID had a weaker impact on physical and cognitive functions.
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Affiliation(s)
- Junji Hatakeyama
- Department of Emergency and Critical Care Medicine, Osaka Medical and Pharmaceutical University, Osaka, Japan
| | - Kensuke Nakamura
- Department of Critical Care Medicine, Yokohama City University Hospital, Kanagawa, Japan; Department of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan.
| | - Naoki Kanda
- Department of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan; Division of General Internal Medicine, Jichi Medical University Hospital, Tochigi, Japan
| | - Akira Kawauchi
- Department of Critical Care and Emergency Medicine, Japanese Red Cross Maebashi Hospital, Gunma, Japan
| | - Shigeki Fujitani
- Department of Emergency Medicine and Critical Care Medicine, St. Marianna University, Kanagawa, Japan
| | - Taku Oshima
- Department of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan
| | - Hideaki Kato
- Infection Prevention and Control Department, Yokohama City University Hospital, Kanagawa, Japan
| | - Kohei Ota
- Department of Emergency and Critical Care Medicine, Hiroshima University Hospital, Hiroshima, Japan
| | - Hiroshi Kamijo
- Department of Emergency and Critical Care Medicine, Shinshu University School of Medicine, Nagano, Japan
| | - Tomohiro Asahi
- Department of Cardiology, Naha City Hospital, Okinawa, Japan
| | - Yoko Muto
- Institute for Global Health Policy Research, Bureau of Global Health Cooperation, Japan Institute for Health Security, Tokyo, Japan
| | - Miyuki Hori
- Institute for Global Health Policy Research, Bureau of Global Health Cooperation, Japan Institute for Health Security, Tokyo, Japan
| | - Arisa Iba
- Institute for Global Health Policy Research, Bureau of Global Health Cooperation, Japan Institute for Health Security, Tokyo, Japan
| | - Mariko Hosozawa
- Institute for Global Health Policy Research, Bureau of Global Health Cooperation, Japan Institute for Health Security, Tokyo, Japan
| | - Hiroyasu Iso
- Institute for Global Health Policy Research, Bureau of Global Health Cooperation, Japan Institute for Health Security, Tokyo, Japan
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Gil-Ugidos A, Rubal-Otero L, González-Villar A, Carrillo-De-la-Peña MT. Conditioned Pain Modulation (CPM) Paradigms: Reliability and Relationship With Individual Characteristics. Pain Manag Nurs 2025; 26:e293-e302. [PMID: 39743474 DOI: 10.1016/j.pmn.2024.12.001] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/30/2024] [Revised: 10/16/2024] [Accepted: 12/01/2024] [Indexed: 01/04/2025]
Abstract
PURPOSE Conditioned Pain Modulation (CPM) is a useful tool for testing the functionality of endogenous pain modulation. However, inconsistent results have been obtained in clinical populations, possibly due to the wide variety of CPM protocols used and the influence of demographic and psychological characteristics of the individuals assessed. METHODS We tested the sensitivity and reliability of four commonly used CPM paradigms in a sample of 58 healthy participants. We also checked how these measures were related to Temporal Summation of Second Pain (TSSP), sociodemographic (age and sex) and psychological variables (anxiety and stress). RESULTS CPM results were influenced by the test stimulus used, with tests using pain pressure threshold (PPT) obtaining a greater number of responders (over 65%) and being the most sensitive (higher size effect: Cohen's d > 0.5). However, all measures showed excellent intrasession reliability, with strong agreement between the CPM magnitudes. CPM indices were not correlated with TSSP, age or sex, and the psychological scales did not differentiate CPM responders and non-responders. CONCLUSIONS Although the CPM indices showed good reliability, construction of a large database with standardized values for healthy individuals seems necessary for the use of CPM in clinical settings.
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Affiliation(s)
- Antonio Gil-Ugidos
- Brain and Pain lab, Institute of Psychology (IPsiUS), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.
| | - Lara Rubal-Otero
- Brain and Pain lab, Institute of Psychology (IPsiUS), Universidade de Santiago de Compostela, Santiago de Compostela, Spain; Foundation for Health Research Institute of Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.
| | - Alberto González-Villar
- Department of Basic Psychology, Psychological Neuroscience Lab, Research Center in Psychology, School of Psychology, University of Minho, Braga, Portugal.
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Zhang L, Mazor Y, Prott G, Jones M, Malcolm A. Characterization of Anal Slow Waves and Ultraslow Waves in Patients With Constipation and Healthy Subjects. Neurogastroenterol Motil 2025; 37:e70006. [PMID: 40032992 DOI: 10.1111/nmo.70006] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/30/2024] [Revised: 01/16/2025] [Accepted: 02/04/2025] [Indexed: 03/05/2025]
Abstract
BACKGROUND Anal slow waves (SW) and ultraslow waves (USW) have been documented previously, yet their significance remains uncertain. Our aims were to characterize the prevalence and features of SW and USW in healthy subjects and patients with constipation and to correlate them with clinical features and anorectal physiological testing. METHODS Forty-three healthy female subjects and 83 female tertiary referral patients with constipation were included. High-resolution water-perfused manometry was performed. Retrospective blinded descriptive and quantitative analyses of manometric tracings were completed with a focus on SW and USW. KEY RESULTS SW were present in 58% of healthy subjects and 62% of constipated patients (p = 0.72) yet USW were seen almost exclusively in constipated patients (27% vs. 2% health; p < 0.0001). Frequencies and mean amplitudes of SW and USW were similar in both groups. Anal resting and squeeze pressures were higher in patients with SW compared to those without (p < 0.001, p = 0.004, respectively). Patients with USW had higher anal resting pressure and shorter duration of sustained squeeze compared to those without (p < 0.001 for both). There was a trend for less obstetric injury in constipated patients with USW compared to those without (23% vs. 48%; p = 0.05). CONCLUSIONS AND INTERFERENCES While SW were common in both constipated and healthy subjects, USW were almost exclusively observed in constipated patients. Some correlations were observed with other anorectal physiology parameters such as high resting anal pressure with both SW and USW. Formal definitions for SW and USW are proposed. Further research into the clinical significance of these waves is warranted.
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Affiliation(s)
- Lulu Zhang
- Neurogastroenterology Unit, Royal North Shore Hospital, Sydney, New South Wales, Australia
| | - Yoav Mazor
- Neurogastroenterology Unit, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel
| | - Gillian Prott
- Neurogastroenterology Unit, Royal North Shore Hospital, Sydney, New South Wales, Australia
| | - Michael Jones
- School of Psychological Sciences, Macquarie University, Sydney, New South Wales, Australia
| | - Allison Malcolm
- Neurogastroenterology Unit, Royal North Shore Hospital, Sydney, New South Wales, Australia
- Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia
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Ellmers TJ, Ibitoye R, Castro P, Kal EC, Kaski D, Bronstein AM. Chronic dizziness in older adults: Disrupted sensorimotor EEG beta oscillations during postural instability. Clin Neurophysiol 2025; 174:31-36. [PMID: 40198974 DOI: 10.1016/j.clinph.2025.03.032] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/09/2024] [Revised: 02/13/2025] [Accepted: 03/09/2025] [Indexed: 04/10/2025]
Abstract
OBJECTIVE Chronic dizziness is common in older adults, yet frequently occurs without a clear cause ('idiopathic dizziness'). Patients experience subjective unsteadiness with minimal objective imbalance, potentially related to small vessel disease. Here we examine the hypothesis that this syndrome is associated with disrupted cortical processing of postural instability. METHODS EEG and postural sway were recorded in 33 older adults with chronic, idiopathic dizziness (Age, Mean = 77.3 years, SD = 6.4, 61 % female) and 25 matched controls (Age, Mean = 76.9 years, SD = 6.0, 56 % female). EEG was time-locked to spontaneous instances of postural instability and analysed via time-frequency decomposition. RESULTS Significant between-group differences in EEG were observed during the early phase of postural instability (p < 0.05, cluster-corrected). Whilst controls exhibited broadband increase in EEG power across sensorimotor areas, dizzy patients displayed suppressed beta activity (19-24 Hz). Contrary to predictions, these differences did not relate to small vessel disease markers (rs < 0.05, ps > 0.720) but to fear of falling (r = -0.44, p = 0.001). CONCLUSIONS Previous work implies that suppressing cortical beta enhances the relay of sensory information. We therefore propose that the modulation in beta EEG observed in patients reflects an anxious, top-down strategy to increase sensitivity to instability, which paradoxically causes persistent feelings of subjective imbalance. SIGNIFICANCE These results identify associations between idiopathic dizziness and disrupted sensorimotor beta activation during postural instability. Cortical beta during imbalance may be a possible biomarker of chronic, idiopathic dizziness in older adults and/or fear of falling.
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Affiliation(s)
- Toby J Ellmers
- Department of Brain Sciences, Imperial College London, Charing Cross Hospital, London, UK.
| | - Richard Ibitoye
- Department of Brain Sciences, Imperial College London, Charing Cross Hospital, London, UK; Department of Clinical and Movement Neurosciences, University College London, London, UK
| | - Patricia Castro
- Department of Brain Sciences, Imperial College London, Charing Cross Hospital, London, UK; Universidad del Desarrollo, Escuela de Fonoaudiología, Facultad de Medicina Clínica Alemana, Santiago, Chile
| | - Elmar C Kal
- Centre for Cognitive and Clinical Neuroscience, Department of Health Sciences, College of Health, Medicine, and Life Sciences, Brunel University London, Uxbridge, UK
| | - Diego Kaski
- Department of Clinical and Movement Neurosciences, University College London, London, UK
| | - Adolfo M Bronstein
- Department of Brain Sciences, Imperial College London, Charing Cross Hospital, London, UK
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Kamo T, Ogihara H, Tanaka R, Azami M, Kato T, Tsunoda R, Fushiki H. Effects of Customized Web Video-Based Vestibular Rehabilitation for Patients With Vestibular Hypofunction: A Randomized Controlled Study. Otol Neurotol 2025; 46:573-580. [PMID: 40164976 DOI: 10.1097/mao.0000000000004494] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/02/2025]
Abstract
OBJECTIVE To investigate the effects of customized web video-based vestibular rehabilitation in patients with chronic vestibular hypofunction. STUDY DESIGN This study is a randomized controlled trial. SETTING The dizziness specialty clinic. PATIENTS The participants were diagnosed with chronic vestibular hypofunction. INTERVENTIONS The study used a randomized controlled trial design, in which participants were randomly assigned to either the customized web video-based vestibular rehabilitation or booklet-based vestibular rehabilitation in a 1:1 ratio. MAIN OUTCOME MEASURES Patients were assessed at three time points: before-intervention (baseline), post-intervention completion (6 wk), and follow-up (12 wk). The primary outcome was the Dynamic Gait Index (DGI), the secondary outcome was the Dizziness Handicap Inventory (DHI), and tertiary outcomes included other functional and psychological assessments. RESULTS The baseline characteristics of the patients were comparable between the two groups. Statistical analysis revealed a significant time effect for the DGI score ( p < 0.0001). Comparing the post-intervention and follow-up assessments to the baseline assessment, the customized web video-based VR group showed a significant increase in the DGI score. Time × group interaction effects were observed ( F = 5.739, p < 0.01). Both groups showed decreased DHI_total scores when comparing the postintervention and follow-up assessments to the baseline assessment. No serious adverse events were reported during intervention period. CONCLUSIONS The present study demonstrated that customized web video-based VR improved DGI compared with booklet-based VR, and the intervention effect was maintained at 6-week follow-up. Additionally, the findings suggested that both interventions improve to a similar extent DHI. Therefore, vestibular rehabilitation with motion visualized by video may be more effective than that with still image by booklet.
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Affiliation(s)
| | | | | | | | - Takumi Kato
- Otolaryngology, Mejiro University Ear Institute Clinic, Saitama, Japan
| | - Reiko Tsunoda
- Otolaryngology, Mejiro University Ear Institute Clinic, Saitama, Japan
| | - Hiroaki Fushiki
- Otolaryngology, Mejiro University Ear Institute Clinic, Saitama, Japan
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Barillari MR, Giordano GM, Costa G, Caporusso E, Giumello F, Tolone S, Lechien JR, Maniaci A, Chiesa-Estomba CM, Yanez MM, Nacci A, Mucci A, Galderisi S, Bastiani L. Laryngopharyngeal reflux and psychological distress: a vicious cycle worth investigating. Eur Arch Otorhinolaryngol 2025; 282:3103-3113. [PMID: 40258993 PMCID: PMC12122629 DOI: 10.1007/s00405-025-09313-z] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/30/2024] [Accepted: 02/24/2025] [Indexed: 04/23/2025]
Abstract
OBJECTIVES To investigate the correlation between laryngopharyngeal reflux (LPR) and psychological distress in a sample of adult Italian patients. METHODS LPR was assessed using the Reflux Symptom Index (RSI), Reflux Finding Score (RFS), and 24-hour impedance-pH monitoring. Psychological distress was evaluated with the following clinical tools: the Hospital Anxiety and Depression Scale (HADS), the Hamilton Anxiety Rating Scale (HAM-A), the Hamilton Depression Rating Scale (HAM-D), the Impact of Event Scale-Revised (IES-R), the Insomnia Severity Index (ISI), and the Perceived Stress Scale-10 (PSS-10). Associations between RSI, RFS, and psychological scores were analyzed. RESULTS A total of 45 patients with LPR (Study Group, SG) and 29 healthy volunteers (Control Group, CG) were included in the study. Psychological assessments revealed significant differences between the CG and SG, except for the ISI. The HAM-A score was 6.79 ± 6.5 in the CG versus 9.53 ± 5.8 in the SG (p = 0.025), with similar results for the HADS (p = 0.029). For the HAM-D, mean scores in both groups were below the threshold for mild depressive symptoms, though SG scores were just below the cut-off (CG: 4.86 ± 5.1; SG: 6.89 ± 4.1; p = 0.010). The PSS-10 indicated mild to moderate perceived stress, with significantly higher scores in the SG (CG: 13.90 ± 5.5; SG: 21.62 ± 8.1; p = 0.000). RSI scores were positively correlated with HAM-D, HADS, and HAM-A scores. CONCLUSIONS Psychological distress is significantly higher in LPR patients compared to healthy controls. These preliminary findings suggest that psychological factors should be considered in the management of LPR.
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Affiliation(s)
- Maria Rosaria Barillari
- Department of Mental and Physical Health and Preventive Medicine, "L. Vanvitelli" University, Naples, Italy.
- Laryngology Study Group of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Marseille, France.
| | | | - Giuseppe Costa
- Department of Mental and Physical Health and Preventive Medicine, "L. Vanvitelli" University, Naples, Italy
| | | | - Federica Giumello
- Division of Phoniatrics and Audiology, "L. Vanvitelli" University Hospital, Nples, Italy
| | - Salvatore Tolone
- Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy
| | - Jerome R Lechien
- Laryngology Study Group of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Marseille, France
- Division of Laryngology and Bronchoesophagology, EpiCURA Hospital, University of Mons, Mons, Belgium
| | - Antonino Maniaci
- Laryngology Study Group of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Marseille, France
- Department of Medicine and Surgery, University of Enna "Kore", 94100, Enna, Italy
| | - Carlos Maria Chiesa-Estomba
- Laryngology Study Group of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Marseille, France
- Department of Otorhinolaryngology-Head and Neck Surgery, Hospital Universitario Donostia, San Sebastian, 20003, Spain
| | - Miguel Mayo Yanez
- Laryngology Study Group of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Marseille, France
- Department of Otorhinolaryngology-Head and Neck Surgery, Hospital San Rafael (HSR), Coruña, 15006 A, Spain
| | - Andrea Nacci
- ENT, Audiology and Phoniatrics Unit, University of Pisa, Pisa, Italy
| | - Armida Mucci
- Department of Psychiatry, "L. Vanvitelli" University, Naples, Italy
| | | | - Luca Bastiani
- Epidemiology Section, CNR Institute of Clinical Physiology, Pisa, Italy
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van der Meulen C, van de Stadt LA, Kroon FPB, Niesters M, Rosendaal FR, Kloppenburg M. In clinical hand osteoarthritis research, self-reported pain questionnaires do not reflect the patient experience. Rheumatology (Oxford) 2025; 64:3492-3499. [PMID: 39836613 DOI: 10.1093/rheumatology/keaf029] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/26/2024] [Revised: 12/28/2024] [Accepted: 01/04/2025] [Indexed: 01/23/2025] Open
Abstract
OBJECTIVE Pain in hand osteoarthritis (OA) is evaluated with repeated pain questionnaires. It is unclear whether these questionnaires adequately capture changes in pain recalled by patients. This study investigated whether changes on pain questionnaires (real-time evaluation) correspond to recalled pain. METHODS Data from hand OA patients from the HOSTAS cohort (four one-yearly) and HOPE trial (one six-week interval) were used. Pain was measured with the Australian/Canadian hand Osteoarthritis Index (AUSCAN, range 0-20) and a recall question (how is the pain compared with your last visit). Changes in AUSCAN pain were categorized into improved (≤-1), stable or worsened pain (≥1) and compared with the recall question using Cohen's kappa and percentage agreement. We determined concordance between measurement methods, and investigated associations of mental well-being and illness perceptions with concordance using generalized estimating equations (GEE). RESULTS Of 708 intervals from HOSTAS (307 patients, 82% women, mean age 61.0 years, mean AUSCAN 9.1), AUSCAN changes and recall were concordant in 42% (Cohen's kappa 0.13). There was concordance in 47% of 86 intervals (Cohen's kappa 0.14) from the HOPE trial (86 patients, 80% women, mean age 63.5, mean AUSCAN 10.7). The most frequent recall answer was worsened pain in the HOSTAS (60%), improved pain in the HOPE trial (76%). In both studies, AUSCAN pain most frequently improved. Depression and anxiety showed no association with concordance. CONCLUSION Changes in repeatedly measured AUSCAN pain often differ from the recalled course of pain over the same period. This has profound implications for evaluating patient-reported pain in clinical trials.
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Affiliation(s)
- Coen van der Meulen
- Department of Rheumatology, Leiden University Medical Centre, Leiden, The Netherlands
| | - Lotte A van de Stadt
- Department of Rheumatology, Leiden University Medical Centre, Leiden, The Netherlands
- Department of Rheumatology, Reade, Amsterdam Rheumatology and Immunology Center, The Netherlands, Amsterdam
| | - Féline P B Kroon
- Department of Rheumatology, Zuyderland Medical Centre, Heerlen, The Netherlands
| | - Marieke Niesters
- Department of Anesthesiology, Leiden University Medical Centre, Leiden, The Netherlands
| | - Frits R Rosendaal
- Department of Clinical Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands
| | - Margreet Kloppenburg
- Department of Rheumatology, Leiden University Medical Centre, Leiden, The Netherlands
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Aasdahl L, Gismervik SØ, Johnsen R, Vasseljen O, Bjørnelv GMW, Bjørngaard JH, Fimland MS. Effects of Inpatient Occupational Rehabilitation vs. Outpatient Acceptance and Commitment Therapy on Sick Leave and Cost of Lost Production: 7-Year Follow-Up of a Randomized Controlled Trial. JOURNAL OF OCCUPATIONAL REHABILITATION 2025; 35:288-293. [PMID: 38678497 PMCID: PMC12089147 DOI: 10.1007/s10926-024-10195-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Accepted: 03/30/2024] [Indexed: 05/01/2024]
Abstract
OBJECTIVES Previously, we reported that an inpatient multimodal occupational rehabilitation program (I-MORE) was more effective than outpatient Acceptance and Commitment Therapy (O-ACT) in reducing sickness absence and was cost-effective over a 24-month period. Here we present 7-years of follow-up on sick leave and the cost of lost production. METHODS We randomized individuals aged 18-60, sick-listed due to musculoskeletal or mental health disorders to I-MORE (n = 82) or O-ACT (n = 79). I-MORE, lasting 3.5 weeks, integrated ACT, physical training, and work-related problem-solving. In contrast, O-ACT mainly offered six weekly 2.5 h group sessions of ACT. We measured outcomes using registry data for days on medical benefits and calculated costs of lost production. Our analysis included regression analyses to examine differences in sickness absence days, logistic general estimating equations for repeated events, and generalized linear models to assess differences in costs of lost production. RESULTS Unadjusted regression analyses showed 80 fewer days of sickness absence in the 7-year follow-up for I-MORE compared to O-ACT (95% CI - 264 to 104), with an adjusted difference of 114 fewer days (95% CI - 298 to 71). The difference in costs of production loss in favour of I-MORE was 27,048 euros per participant (95% CI - 35,009 to 89,104). CONCLUSIONS I-MORE outperformed O-ACT in reducing sickness absence and production loss costs during seven years of follow-up, but due to a limited sample size the results were unprecise. Considering the potential for substantial societal cost savings from reduced sick leave, there is a need for larger, long-term studies to evaluate return-to-work interventions.
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Affiliation(s)
- Lene Aasdahl
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway.
- Unicare Helsefort Rehabilitation Centre, Rissa, Norway.
| | - Sigmund Østgård Gismervik
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway
- Clinic of Rehabilitation, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway
| | - Roar Johnsen
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway
| | - Ottar Vasseljen
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway
| | - Gudrun M W Bjørnelv
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway
- Department of Health Management and Health Economics, Faculty of Medicine, University of Oslo, Oslo, Norway
| | - Johan Håkon Bjørngaard
- Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Postboks 8905, 7491, Trondheim, Norway
- Faculty of Nursing and Health Sciences, Nord University, Levanger, Norway
| | - Marius Steiro Fimland
- Unicare Helsefort Rehabilitation Centre, Rissa, Norway
- Clinic of Rehabilitation, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway
- Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway
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Kifell J, Burns KEA, Duong J, Fiest K, Gagné C, Gélinas C, Krewulak K, Price C, Stephenson A, Wang HT, Goldfarb M. Measuring family engagement in intensive care: Validation of the FAME tool. J Crit Care 2025; 87:155046. [PMID: 40036994 DOI: 10.1016/j.jcrc.2025.155046] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/25/2024] [Revised: 01/30/2025] [Accepted: 02/20/2025] [Indexed: 03/06/2025]
Abstract
INTRODUCTION Engaging family members in patient care in the intensive care unit (ICU) is a recommended practice by critical care societies. However, there are currently no validated tools to measure family engagement in the ICU setting. The objective of this study was to validate the FAMily Engagement (FAME) tool in the ICU. METHODS The FAME study was a multicenter prospective cohort study of family members of ICU patients in 8 Canadian ICUs. Family members completed the FAME questionnaire during the ICU stay. The FAME questionnaire comprised 12 items that assessed various domains of family engagement behavior. FAME scores were reported in a 0-100 scoring system with higher scores indicating increased care engagement. Following hospital discharge, we assessed associations between the FAME score and family satisfaction with care and mental health (anxiety and depression). The internal consistency (reliability), convergent validity, and predictive validity of the FAME tool were evaluated. RESULTS There were 269 family members (age 56.8 ± 15.1; 68.4 % women) included in the analysis. The most common relationships to the patient were spouse/partner (40.5 %) and daughter/son (33.8 %). The overall mean FAME score was 77.7 ± 14.8. The FAME score had high internal consistency (Cronbach's α = 0.83) and the tool demonstrated convergent and predictive validity. The FAME score was associated with family satisfaction, but not with mental health outcomes. CONCLUSION The FAME tool demonstrated reliability, convergent, and predictive validity in this multicenter ICU cohort. The FAME tool could be used to evaluate the effectiveness of family engagement interventions.
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Affiliation(s)
- Jillian Kifell
- Division of Experimental Medicine, McGill University, Montreal, QC, Canada
| | - Karen E A Burns
- Interdepartmental Division of Critical Care, Department of Medicine, University of Toronto, Toronto, ON, Canada; Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada
| | - Julia Duong
- Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, Canada
| | - Kirsten Fiest
- Department of Critical Care Medicine, University of Calgary, Calgary, AB, Canada
| | | | - Céline Gélinas
- Lady Davis Institute, Montreal, QC, Canada; Ingram School of Nursing, McGill University, Montreal, QC, Canada
| | - Karla Krewulak
- Department of Critical Care Medicine, University of Calgary, Calgary, AB, Canada
| | | | | | - Han Ting Wang
- Division of Critical Care Medicine, Centre hospitalier de l'Université de Montréal, Montreal, QC, Canada
| | - Michael Goldfarb
- Division of Experimental Medicine, McGill University, Montreal, QC, Canada; Lady Davis Institute, Montreal, QC, Canada; Division of Cardiology, Jewish General Hospital, McGill University, Montreal, QC, Canada.
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Shahar G, Aslan C, Rüdiger Z, Elmar B, Globus O, Beutel M. Depressive Personality Vulnerability and Adaptation to Breast Cancer: A Matter of Self-Criticism? Stress Health 2025; 41:e70054. [PMID: 40448936 DOI: 10.1002/smi.70054] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/16/2023] [Revised: 04/08/2025] [Accepted: 05/15/2025] [Indexed: 06/02/2025]
Abstract
Dependency and self-criticism are two dimensions of personality vulnerability to depression, whereas efficacy is a dimension of personality resilience. The aim of this study was to examine the unique role of these personality dimensions in adaptation following a diagnosis of breast cancer, while controlling for the potentially confounding role of symptoms of depression and anxiety. Three adaptation outcomes were examined: Functioning, symptomatic load, and fatigue. Patients residing in Germany, diagnosed with breast cancer and comorbid depression, participated in a Randomized Clinical Trial (RCT) testing Supportive-Expressive Psychodynamic Psychotherapy (SEP; N = 78)) versus Treatment as Usual (TAU; N = 79). Assessments were made pre-treatment, at termination, and at 6-month follow-up. Analyses were conducted via General Linear Modelling (GLM). Pretreatment self-criticism prospectively predicted a rank-order decrease in functioning and a rank order increase in symptomatic load and fatigue. Dependency predicted an increase in breast symptoms. No effects were found for efficacy. Self-criticism may complicate adaptation to breast cancer. Implications for early detection and illness management are discussed.
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Affiliation(s)
- Golan Shahar
- Department of Psychology, Ben-Gurion University of the Negev, Beer-Sheva, Israel
| | - Chen Aslan
- Department of Psychology, Ben-Gurion University of the Negev, Beer-Sheva, Israel
| | - Zwerenz Rüdiger
- Department of Psychosomatic Medicine and Psychotherapy, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany
| | - Brähler Elmar
- Department of Psychosomatic Medicine and Psychotherapy, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany
- Department of Medical Psychology and Medical Sociology, University Medical Center, Leipzig, Germany
| | - Opher Globus
- Oncology Institute, Sheba Medical Center, Tel HaShomer, Israel
| | - Manfred Beutel
- Department of Psychosomatic Medicine and Psychotherapy, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany
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Adam BD, Monteza-Quiroz D, Hart TA, Skakoon-Sparling S, Moore DM, Zhang T, Gormezano A, Grace D. Inequitable access to PrEP among gay, bisexual, and other men who have sex with men in Canada: A network analysis of social indicators. SSM Popul Health 2025; 30:101771. [PMID: 40177026 PMCID: PMC11964654 DOI: 10.1016/j.ssmph.2025.101771] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/19/2024] [Revised: 02/27/2025] [Accepted: 03/01/2025] [Indexed: 04/05/2025] Open
Abstract
This paper examines demographic, structural, and syndemic variables to map facilitators and barriers to accessing pre-exposure prophylaxis (PrEP) among gay, bisexual, and other men who have sex with men (GBM) in the three largest cities in Canada, Vancouver, Toronto, and Montreal. Focusing on factors in the later stages of the PrEP cascade, this study first performed a logistic regression analysis and reports adjusted odds ratios, then entered statistically significant social indicators into a network analysis to profile the interrelated and sometimes mutually reinforcing social conditions that shape inequitable access to PrEP among Canadian GBM. Barriers to accessing a gay-friendly health care provider (HCP) and financial barriers remain primary nodes associated with inequitable PrEP access. These two nodes are, in turn, linked to other social indicators: experiencing stigma from an HCP, being less likely to be out to an HCP (most common among bisexual and queer men), and not being able to find an HCP accepting of their sexuality (most common among Indigenous, Black, and some other GBM of colour). The cost of PrEP was also a barrier, especially for less educated and un- or under-employed GBM, as well as newcomers to Canada, who more often lacked insurance for medications. These findings point toward the importance of having a primary HCP and finding an HCP who is culturally competent regarding the sexualities of gay and bisexual men, queer and trans people. These barriers may also explain other social inequities experienced by Black, Indigenous, and other GBM of colour, and by people who do not have health insurance that covers all or most of the cost of PrEP. This pattern of inequitable access to PrEP points toward the urgency of providing universal access without financial barriers (currently available in some Canadian provinces but not others) and supporting access points with a reputation for welcoming GBM in their full diversity.
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Affiliation(s)
- Barry D. Adam
- Department of Sociology and Criminology, University of Windsor, Windsor, ON, Canada
| | - Diego Monteza-Quiroz
- Department of Agrarian Economics, Pontificia Universidad Católica de Chile, Santiago, Chile
| | - Trevor A. Hart
- Department of Psychology, Toronto Metropolitan University, Toronto, ON, Canada
- Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada
| | - Shayna Skakoon-Sparling
- Department of Psychology, Toronto Metropolitan University, Toronto, ON, Canada
- Department of Psychology, University of Guelph, Guelph, ON, Canada
| | - David M. Moore
- British Columbia Centre for Excellence in HIV/AIDS, Vancouver, BC, Canada
- University of British Columbia, Vancouver, BC, Canada
| | - Terri Zhang
- Department of Psychology, Toronto Metropolitan University, Toronto, ON, Canada
| | - Aki Gormezano
- School of Public Health and Social Policy, University of Victoria, Victoria, BC, Canada
| | - Daniel Grace
- Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada
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Briggs-Price S, Mills G, Houchen-Wolloff L, Daynes E, Gerlis C, Latimer LE, Esler C, Targett D, Singh SJ. The effects of combining electrical stimulation of the calf and thigh muscles on WOMAC pain in knee osteoarthritis: A double-blind, randomised, sham-controlled trial. OSTEOARTHRITIS AND CARTILAGE OPEN 2025; 7:100607. [PMID: 40255320 PMCID: PMC12008679 DOI: 10.1016/j.ocarto.2025.100607] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/19/2025] [Accepted: 03/25/2025] [Indexed: 04/22/2025] Open
Abstract
Objective To explore the effectiveness of a NMES device in improving pain and function for individuals with KOA. Method This was a randomised, sham-controlled, superiority trial recruiting individuals with symptomatic KOA, with both participants and outcome assessors blinded to the treatment allocation. Participants were randomised to receive either self-administered NMES, consisting of quadriceps (5 times a week) and footplate stimulation (7 times a week), or a sham device for 8 weeks. The primary outcome was the change in Western Ontario and McMaster Universities Arthritis Index (WOMAC) pain domain at week 8. Results 179 participants were randomised; 50.8 % female, mean (SD) age 66.9 (8.7) years. 164 attended the follow up visit. No difference in the WOMAC pain domain was seen between groups (-0.7; 95 % CI: -1.5, 0.1; P = 0.10), though within group improvements were reported in both groups (NMES: -1.5; 95 % CI: -2.0, 0.8; P < 0.01, sham: -0.8; 95 % CI: -1.4, 0.2; P < 0.01). There were no differences in strength, exercise and functional capacity, swelling, health related quality of life or anxiety and depression between groups. Sub-group analysis for NMES compliance or recruitment source did not change response in primary outcome. Conclusion Use of an NMES device on the quadriceps and plantar flexors did not enhance pain relief or improve function over the sham control in people with KOA.
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Affiliation(s)
- Samuel Briggs-Price
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
| | - George Mills
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
| | - Linzy Houchen-Wolloff
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
| | - Enya Daynes
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
| | - Charlotte Gerlis
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
| | - Lorna E. Latimer
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
| | - Colin Esler
- Orthopaedics, Leicester General Hospital, University Hospitals of Leicester, Gwendolen Road, Leicester, LE5 4PW, United Kingdom
| | - Darren Targett
- Primoris Contract Solutions Ltd, Ascot, Berkshire, United Kingdom
| | - Sally J. Singh
- Centre for Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, United Kingdom
- Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom
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Xu H, Li H, Fan Y, Wang Y, Li Z, Zhou L, Hao X. Analysis of factors influencing chemotherapy-induced peripheral neuropathy in breast cancer patients using a random forest model. Breast 2025; 81:104457. [PMID: 40245641 DOI: 10.1016/j.breast.2025.104457] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/09/2024] [Revised: 03/03/2025] [Accepted: 03/19/2025] [Indexed: 04/19/2025] Open
Abstract
OBJECTIVE This study aimed to analyze the factors influencing chemotherapy-induced peripheral neuropathy (CIPN) in breast cancer patients, identify modifiable factors, and provide a theoretical basis for targeted interventions. METHODS A total of 542 patients with breast cancer who were hospitalized for chemotherapy in multiple hospitals from September 2022 to September 2023 were selected as the study objects. Data were collected using questionnaires covering demographic characteristics, disease-related information, lifestyle, and psychological status. Lasso-logistic regression was employed to identify influencing factors, and a random forest model was used to rank the importance of variables. RESULTS Lasso-logistic regression analysis identified age, BMI, cumulative chemotherapy dose, hypertension, physical activity level, and depression as significant factors associated with CIPN (P < 0.05). The variable importance ranking from the random forest model was as follows: age, BMI, cumulative chemotherapy dose, physical activity, hypertension, and depression. CONCLUSION Early identification of high-risk CIPN patients is crucial for guiding clinical nursing practices. These findings provide a foundation for the management and intervention of CIPN in breast cancer patients.
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Affiliation(s)
- Huiqian Xu
- North China University of Science and Technology, Tangshan, 063210, China
| | - Hong Li
- North China University of Science and Technology, Tangshan, 063210, China
| | - Yijing Fan
- North China University of Science and Technology, Tangshan, 063210, China
| | - Yaqi Wang
- Tangshan People's Hospital, Tangshan, 063000, China
| | - Zeyuan Li
- North China University of Science and Technology, Tangshan, 063210, China
| | - Lizhi Zhou
- Tangshan People's Hospital, Tangshan, 063000, China.
| | - Xijun Hao
- North China University of Science and Technology, Tangshan, 063210, China.
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Leung JL, Deeble N, Yang V, Liew DFL, Buchanan RRC, Owen CE. Higher Rates of Depression in Polymyalgia Rheumatica Are Strongly Associated With Poor Physical Function. J Clin Rheumatol 2025; 31:170-174. [PMID: 40036143 DOI: 10.1097/rhu.0000000000002219] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/06/2025]
Abstract
OBJECTIVE To assess the prevalence of and risk factors for depression in a cohort of patients with polymyalgia rheumatica (PMR) compared with a cohort of participants without PMR (control group). METHODS In a longitudinal cohort study, patients with recently diagnosed PMR (within 3 months of starting treatment) were recruited together with matched control subjects. Assessments were undertaken 3 and 21 months after initiation of steroid therapy. Mood was assessed using the Hospital Anxiety and Depression Scale (HADS) and the 36-item Short-Form Survey (SF-36) Mental Health (MH) scale, with scores ≥8 on the HADS and ≤56 on the SF-36 MH Scale indicating depression. Other data collected included current prednisolone dose, PMR-Activity Score, pain visual analog scale, SF-36, and Health Assessment Questionnaire Disability Index. RESULTS Thirty-six subjects with PMR and 32 control subjects were recruited. At baseline, depression rates were significantly higher in PMR cases than in control subjects (22.2% vs. 3.1% and 25.0% vs. 0.0% as determined by HADS and SF-36 MH Scale, respectively). After adjusting for a previous diagnosis of depression, poor physical function (Health Assessment Questionnaire Disability Index) had the strongest association with depression determined by SF-36 MH Scale, with odds ratios of 8.19 (95% confidence interval, 1.06-63.46; p = 0.04) and 13.25 (95% confidence interval, 1.15-152.31; p = 0.04) at baseline and follow-up, respectively. Other significant associations with depression were identified with current prednisolone dose, disease activity (PMR-Activity Score), pain (pain visual analog scale and SF-36 Bodily Pain Scale), and fatigue (SF-36 Vitality Scale). CONCLUSION Depression affects up to 1 in 4 patients with PMR. The strongest association is with poor physical function, highlighting the psychological impact of physical limitations in PMR and the need to address comorbid depression to optimize patient outcomes.
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Affiliation(s)
| | | | - Victor Yang
- From the Department of Rheumatology, Austin Health
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Devita S, Deforges C, Bickle-Graz M, Tolsa JF, Sandoz V, Horsch A. Maternal childbirth-related posttraumatic stress symptoms, bonding, and infant development: a prospective study. J Reprod Infant Psychol 2025; 43:718-732. [PMID: 37740725 DOI: 10.1080/02646838.2023.2261057] [Citation(s) in RCA: 3] [Impact Index Per Article: 3.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/09/2023] [Accepted: 09/15/2023] [Indexed: 09/25/2023]
Abstract
BACKGROUND Childbirth-related posttraumatic stress symptoms (CB-PTSS) including general symptoms (GS, i.e., mainly negative cognitions and mood and hyperarousal symptoms) and birth-related symptoms (BRS, i.e., mostly re-experiencing and avoidance symptoms) may disrupt mother-infant bonding and infant development. This study investigated prospective and cross-sectional associations between maternal CB-PTSS and mother-infant bonding or infant development (language, motor, and cognitive). METHOD We analysed secondary data of the control group of a randomised control trial (NCT03576586) with full-term French-speaking mother-infant dyads (n = 55). Maternal CB-PTSS and mother-infant bonding were assessed via questionnaires at six weeks (T1) and six months (T2) postpartum: PTSD Checklist for DSM-5 (PCL-5) and Mother-Infant Bonding Scale (MIBS). Infant development was assessed with the Bayley Scales of Infant Development at T2. Sociodemographic and medical data were collected from questionnaires and medical records. Bivariate and multivariate regression were used. RESULTS Maternal total CB-PTSS score at T1 was associated with poorer bonding at T2 in the unadjusted model (B = 0.064, p = 0.043). In the adjusted model, cross-sectional associations were found at T1 between a higher total CB-PTSS score and poorer bonding (B = 0.134, p = 0.017) and between higher GS and poorer bonding (B = 0.306, p = 0.002). Higher BRS at T1 was associated with better infant cognitive development at T2 in the unadjusted model (B = 0.748, p = 0.026). CONCLUSIONS Results suggest that CB-PTSS were associated with mother-infant bonding difficulties, while CB-PTSS were not significantly associated with infant development. Additional studies are needed to increase our understanding of the intergenerational consequences of perinatal trauma.
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Affiliation(s)
- Sella Devita
- Institute of Higher Education and Research in Healthcare (IUFRS), University of Lausanne and Lausanne University Hospital, Lausanne, Switzerland
| | - Camille Deforges
- Institute of Higher Education and Research in Healthcare (IUFRS), University of Lausanne and Lausanne University Hospital, Lausanne, Switzerland
| | - Myriam Bickle-Graz
- Department Woman-Mother-Child, Clinic of Neonatology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland
| | - Jean-François Tolsa
- Department Woman-Mother-Child, Clinic of Neonatology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland
| | - Vania Sandoz
- Institute of Higher Education and Research in Healthcare (IUFRS), University of Lausanne and Lausanne University Hospital, Lausanne, Switzerland
- Department Woman-Mother-Child, Child Abuse and Neglect Team, Lausanne University Hospital, Lausanne, Switzerland
| | - Antje Horsch
- Institute of Higher Education and Research in Healthcare (IUFRS), University of Lausanne and Lausanne University Hospital, Lausanne, Switzerland
- Department Woman-Mother-Child, Clinic of Neonatology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland
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Volpato E, Poletti V, Banfi P, Bonanomi A, Pagnini F. Illness Expectations and Asthma Symptoms: A 6-Month Longitudinal Study. Health Expect 2025; 28:e70285. [PMID: 40325877 PMCID: PMC12053105 DOI: 10.1111/hex.70285] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/26/2024] [Revised: 03/06/2025] [Accepted: 04/10/2025] [Indexed: 05/07/2025] Open
Abstract
BACKGROUND After receiving a diagnosis, individuals often develop expectations about how their condition will evolve. This cognitive framework, known as 'Illness Expectations' (IEs), encompasses future-oriented beliefs regarding the course of the illness and its symptoms. In chronic conditions such as asthma, IEs may play a critical role in shaping patient-reported outcomes and clinical markers of disease progression. This study aims to empirically evaluate the impact of IEs on asthma symptoms and respiratory function. METHODS A cohort of 310 individuals diagnosed with asthma was followed over a 6-month period, with three assessment points. Asthma control was measured using the Asthma Control Test (ACT), while respiratory function was evaluated through forced expiratory volume in 1 s (FEV1) using spirometry. IEs were assessed using the validated 'Illness Expectation Test' (IET), which captures both explicit (conscious) and implicit (unconscious) expectations. Predictive analyses were conducted using latent growth modelling and linear regression to examine the influence of IEs on asthma symptoms and respiratory function over time. RESULTS People with more negative explicit IEs about their asthma reported worse symptoms over time (β = -0.50, SE = 0.21, p = 0.01). Implicit IEs were not statistically significant (β = -0.014, SE = 0.008, p = 0.09). Explicit IEs about symptom progression were also associated with changes in lung function, with more negative expectations predicting greater declines in respiratory performance (β = 0.51, SE = 0.11, p = 0.001). CONCLUSIONS These findings suggest that IEs may be meaningfully associated with asthma outcomes, highlighting their potential relevance in understanding patient experiences and symptom perception. These results support further research into interventions targeting cognitive frameworks, with the aim of informing more personalised, patient-centred approaches to asthma management. PATIENT OR PUBLIC CONTRIBUTION This study was developed in response to patient-reported challenges in asthma management, particularly around understanding and managing IEs. Patients contributed to identifying key areas of concern, and their perspectives informed the choice of outcomes and tools. While direct involvement in recruitment and dissemination was limited due to the pandemic, the study's design and focus were guided by patient priorities, with potential applications in clinical consultations and future co-designed interventions.
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Affiliation(s)
- Eleonora Volpato
- Department of PsychologyUniversità Cattolica del Sacro CuoreMilanItaly
- IRCCS Fondazione Don Carlo GnocchiMilanItaly
- Research Group Health PsychologyUniversity of LeuvenLeuvenBelgium
| | - Valentina Poletti
- Department of PsychologyUniversità Cattolica del Sacro CuoreMilanItaly
- IRCCS Fondazione Don Carlo GnocchiMilanItaly
| | - Paolo Banfi
- IRCCS Fondazione Don Carlo GnocchiMilanItaly
| | - Andrea Bonanomi
- Department of Statistical ScienceUniversità Cattolica del Sacro CuoreMilanItaly
| | - Francesco Pagnini
- Department of PsychologyUniversità Cattolica del Sacro CuoreMilanItaly
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Hisaoka T, Suzuki J, Ikeda R, Hirano-Kawamoto A, Ohta J, Katori Y. Association between the Hospital Anxiety and Depression Scale and Swallowing Function in Dysphagic Patients in Japan. Auris Nasus Larynx 2025; 52:222-228. [PMID: 40120197 DOI: 10.1016/j.anl.2025.03.001] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/10/2025] [Revised: 02/19/2025] [Accepted: 03/06/2025] [Indexed: 03/25/2025]
Abstract
OBJECTIVE Dysphagia affects 2.3 %-16 % of the general population and increases with age. It can lead to malnutrition, weight loss, aspiration pneumonia, and emotional symptoms such as anxiety and depression. Mental health disorders impact appetite and muscle mass, further worsening dysphagia. Additionally, cultural and economic factors influence anxiety and depression, which can either result from or contribute to dysphagia. Studies on the relationship between anxiety, depression, and swallowing function using FEES are limited in Asian populations. The Hospital Anxiety and Depression Scale (HADS) is a useful tool for assessing mood disorders. Therefore, in this study, we aimed to investigate the associations among anxiety, depression, and swallowing function in Japanese patients with dysphagia using HADS. METHODS Data on age; sex; HADS; Eating Assessment Tool-10 (EAT-10); Functional Oral Intake Scale (FOIS); tongue pressure; Hyodo score, a scoring system for evaluating the swallowing function determined by flexible endoscopic evaluation of swallowing (FEES); and videofluoroscopic dysphagia scale (VDS), assessed by videofluoroscopic swallowing study, were collected and analyzed from medical records. Hyodo score consists of four parameters: (1) salivary pooling in the vallecula and piriform sinuses; (2) glottal closure reflex or cough reflex induced by touching the epiglottis or arytenoid; (3) swallowing reflex induced by colored water; and (4) extent of pharyngeal clearance after colored water is swallowed. The Mann-Whitney U test, Fisher's exact test, and multiple logistic regression analyses were used to estimate associations between HADS and swallowing function. RESULTS No significant relationships were observed between the EAT-10, FOIS, and VDS with HADS scores. Patients with depression were associated with a significantly higher percentage of anorexia complaints (p = 0.047). Lower tongue pressure was observed in patients with depression than in patients without depression (p = 0.002). Patients with anxiety had better swallowing function, as assessed by the Hyodo score (p = 0.047). Fluid clearance, a component of the Hyodo score, was significantly better in patients with anxiety (p = 0.03) even after propensity score matching adjusted for the effects of age, sex, and fluid clearance. CONCLUSION In patients with anxiety, swallowing function assessed by FEES was favorable, whereas a higher proportion of patients with depression reported decreased appetite, and lower tongue pressure. This discrepancy between subjective dysphagia and FEES findings suggests that patients with anxiety may underestimate their swallowing function.
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Affiliation(s)
- Takuma Hisaoka
- Department of Otolaryngology and Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan.
| | - Jun Suzuki
- Department of Otolaryngology and Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan
| | - Ryoukichi Ikeda
- Department of Otolaryngology and Head and Neck Surgery, Iwate Medical University, 1-1-1 Idaidori, Yahaba-cho, Shiwa-gun, Iwate Prefecture 028-3694, Japan
| | - Ai Hirano-Kawamoto
- Department of Otolaryngology and Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan
| | - Jun Ohta
- Department of Otolaryngology and Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan
| | - Yukio Katori
- Department of Otolaryngology and Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan
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Krijnen EA, Jelgerhuis J, Van Dam M, Bouman PM, Barkhof F, Klawiter EC, Hulst HE, Strijbis EMM, Schoonheim MM. Evolution of Cortical Lesions and Function-Specific Cognitive Decline in People With Multiple Sclerosis. Neurology 2025; 104:e213650. [PMID: 40354586 PMCID: PMC12067090 DOI: 10.1212/wnl.0000000000213650] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/10/2024] [Accepted: 03/20/2025] [Indexed: 05/14/2025] Open
Abstract
BACKGROUND AND OBJECTIVES Cortical lesions in multiple sclerosis (MS) severely affect cognition, but their longitudinal evolution and impact on specific cognitive functions remain understudied. This study investigates the evolution of function-specific cognitive functioning over 10 years in people with MS and assesses the influence of cortical lesion load and formation on these trajectories. METHODS In this prospectively collected study, people with MS underwent 3T MRI (T1 and fluid-attenuated inversion recovery) at 3 study visits between 2008 and 2022. Cognitive functioning was evaluated based on neuropsychological assessment reflecting 7 cognitive functions: attention; executive functioning (EF); information processing speed (IPS); verbal fluency; and verbal, visuospatial, and working memory. Cortical lesions were manually identified on artificial intelligence-generated double-inversion recovery images. Linear mixed models were constructed to assess the temporal evolution between cortical lesion load and function-specific cognitive decline. In addition, analyses were stratified by MS disease stage: early and late relapsing-remitting MS (cutoff disease duration at 15 years) and progressive MS. RESULTS The study included 223 people with MS (mean age, 47.8 ± 11.1 years; 153 women) and 62 healthy controls. All completed 5-year follow-up, and 37 healthy controls and 94 with MS completed 10-year follow-up. At baseline, people with MS exhibited worse functioning of IPS and working memory. Over 10 years, cognitive decline was most severe in attention, verbal memory, and EF. At baseline, people with MS had a median cortical lesion count of 7 (range 0-73), which was related to subsequent decline in attention (B[95% CI] = -0.22 [-0.40 to -0.03]) and verbal fluency (B[95% CI] = -0.23[-0.37 to -0.09]). Over time, cortical lesions increased by a median count of 4 (range -2 to 71), particularly in late and progressive disease, and was related to decline in verbal fluency (B [95% CI] = -0.33 [-0.51 to -0.15]). The associations between (change in) cortical lesion load and cognitive decline were not modified by MS disease stage. DISCUSSION Cognition worsened over 10 years, particularly affecting attention, verbal memory, and EF, while preexisting impairments were worst in other functions such as IPS. Worse baseline cognitive functioning was related to baseline cortical lesions, whereas baseline cortical lesions and cortical lesion formation were related to cognitive decline in functions less affected at baseline. Accumulating cortical damage leads to spreading of cognitive impairments toward additional functions.
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Affiliation(s)
- Eva A Krijnen
- MS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
- Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA
| | - Julia Jelgerhuis
- MS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
| | - Maureen Van Dam
- MS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
| | - Piet M Bouman
- MS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
| | - Frederik Barkhof
- MS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
- Queen Square Institute of Neurology and Centre for Medical Image Computing, University College London, United Kingdom
| | - Eric C Klawiter
- Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA
| | - Hanneke E Hulst
- Institute of Psychology, Health, Medical and Neuropsychology Unit, Leiden University, the Netherlands
- Leiden Institute for Brain and Cognition, Leiden University, the Netherlands; and
| | - Eva M M Strijbis
- MS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
| | - Menno M Schoonheim
- MS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands
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Silva RL, da Silva E Sousa FI, Ferreira da Silva GL, Almeida VDR, Silva SB, Mendes Santos Freire M, Loiola Ponte de Souza MH, Braga LLBC. The impact of anxiety and depression on quality of life in a cohort of inflammatory bowel disease patients from Northeastern of Brazil. GASTROENTEROLOGIA Y HEPATOLOGIA 2025; 48:502283. [PMID: 39477185 DOI: 10.1016/j.gastrohep.2024.502283] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/03/2024] [Revised: 10/21/2024] [Accepted: 10/23/2024] [Indexed: 11/24/2024]
Abstract
OBJECTIVE This study aims to assess whether the association between chronic pathologies and depressive and/or anxious disorders is high, resulting in a reduction in the patient's quality of life. PATIENTS AND METHODS This is a prospective cross-sectional study with a descriptive and analytical design. Sociodemographic data and lifestyle habits were collected. Subsequently, the Inflammatory Bowel Disease Questionnaire (IBDQ) and the Hospital Anxiety and Depression Scale (HADS) were applied. RESULTS A total of 141 patients participated in the study, with a mean age of 45.78 (SD 16.01) years, of which 60.3% were female (n=85) and 39.7% were male (n=56). 58.9% had ulcerative colitis (UC) (n=83), and 41.1% had Crohn's disease (CD) (n=58). 16.5% of patients had a previous diagnosis of generalized anxiety disorder (GAD) and/or major depression (MD) (n=23). Regarding IBDQ scores, participants with anxiety had significantly lower mean scores in all IBDQ items (p<0.001), while the depression diagnosis obtained significantly lower mean values for systemic (p=0.015), emotional (p=0.001), and intestinal symptoms (p=0.005). CONCLUSION The results indicate that anxiety and depression negatively impact the quality of life of patients with IBD independently of the disease activity.
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Affiliation(s)
- Raiza Lima Silva
- School of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil
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Budzisz A, Jung A, Luedtke K, Carvalho GF, Szikszay TM, Bąbel P, Wand BM, Adamczyk WM. The Fremantle Back Awareness Questionnaire: Cross-cultural adaptation, validity and reliability of the Polish version. Musculoskelet Sci Pract 2025; 77:103291. [PMID: 40048948 DOI: 10.1016/j.msksp.2025.103291] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/14/2024] [Revised: 02/13/2025] [Accepted: 02/19/2025] [Indexed: 05/12/2025]
Abstract
BACKGROUND Body image disturbance is observed in individuals with chronic low back pain (CLBP) and is a potential treatment target. The Fremantle Back Awareness Questionnaire (FreBAQ) is designed to identify disrupted body image specific to the low back. This study aimed to develop and assess the measurement properties of a Polish language version of this questionnaire (FreBAQ-PL). METHODS Following the translation process, cognitive interviews were carried out as a qualitative assessment of content validity. Subsequently a quantitative assessment of content validity was undertaken among in a study sample with CLBP and experts. Measurement properties were assessed in 114 participants with CLBP and 53 pain-free participants. The CLBP sample repeated the FreBAQ-PL assessment within 14-days. The measurement properties assessed in this study were content validity, internal consistency, frequency of responses, known-groups validity, convergent validity and test-retest reliability. RESULTS Content validity was supported, affirming relevance and comprehensiveness. Known-groups validity was confirmed by significant differences in FreBAQ-PL scores between participants with CLBP and pain-free participants (p < 0.05). Convergent validity was established through moderate associations between FreBAQ-PL scores and pain variables (intensity and duration) (ρ's = 0.24-0.27, p's < 0.01), disability (ρ = 0.34, p < 0.01), kinesiophobia (ρ = 0.37, p < 0.01), depression (ρ = 0.30, p < 0.01) and anxiety (ρ = 0.24, p < 0.01). The scale was internally consistent (Cronbach's alpha 0.81). Test-retest reliability was good (ICC 0.90). CONCLUSIONS The FreBAQ-PL is a reliable, internally consistent, and valid measure that can be used in clinical and research settings to assess the presence of body image disturbance in Polish-speaking individuals with CLBP.
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Affiliation(s)
- Aleksandra Budzisz
- Pain Research Group, Institute of Psychology, Jagiellonian University, Kraków, Poland; Laboratory of Pain Research, Institute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland.
| | - Andres Jung
- Department of Sport Science and Sport, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany
| | - Kerstin Luedtke
- Institute of Health Sciences, Department of Physiotherapy, Pain and Exercise Research Luebeck (P.E.R.L), Universität zu Lübeck, Luebeck, Germany
| | - Gabriela F Carvalho
- Department of Physiotherapy, Faculty of Health, Safety and Society, Furtwangen University, Furtwangen, Germany
| | - Tibor M Szikszay
- Institute of Health Sciences, Department of Physiotherapy, Pain and Exercise Research Luebeck (P.E.R.L), Universität zu Lübeck, Luebeck, Germany
| | - Przemysław Bąbel
- Pain Research Group, Institute of Psychology, Jagiellonian University, Kraków, Poland
| | - Benedict M Wand
- School of Health Sciences, The University of Notre Dame Australia, Fremantle, WA, Australia
| | - Wacław M Adamczyk
- Institute of Health Sciences, Department of Physiotherapy, Pain and Exercise Research Luebeck (P.E.R.L), Universität zu Lübeck, Luebeck, Germany; Laboratory of Pain Research, Institute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland
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Grégoire AM, Dricot L, Huart C, Decat M, Deggouj N, Kupers R. Preoperative MRI, audiovisual speech perception, and mood are associated with cochlear implant outcomes in adults with postlingual deafness. Hear Res 2025; 461:109272. [PMID: 40239263 DOI: 10.1016/j.heares.2025.109272] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/11/2025] [Revised: 03/25/2025] [Accepted: 04/05/2025] [Indexed: 04/18/2025]
Abstract
Acquired severe to profound hearing loss is an increasingly challenging problem of our aging population. Cochlear implantation (CI) is the gold standard treatment for this advanced form of sensory deprivation. Despite the overall satisfactory results of CI, a substantial number of patients show unsatisfactory outcomes. This study aims to improve current predictive models of CI outcome by integrating preoperative MRI with behavioral data. We acquired a 3D T1 MRI to measure cortical thickness (CT) and volume using surface-based analysis and parcellation from the Brainnetome atlas. CI success at 6 months post-implant, as measured by audiovisual speech perception, was correlated with preoperative speech and audiovisual perception with hearing aids, and residual hearing, especially at the side of the non-implanted ear. In addition, CI outcome correlated positively with CT of the left superior temporal gyrus and sulcus, left inferior frontal region, and bilateral superior frontal regions. The volume of the left middle frontal gyrus and regions of the parietal lobe, especially at the left side, also correlated with CI outcome. Linear regression models revealed that CI outcome was best predicted by the combination of preoperative measures of audiovisual speech perception, residual hearing, depression and CT. Our results highlight the importance of preserved brain areas implicated in hearing, language, audiovisual integration, and cognitive functions for CI success. Furthermore, brain MRI in conjunction with other predictors can help to identify patients who may need more time to adjust to the CI, allowing a more tailored rehabilitation, and potentially greater efficacy.
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Affiliation(s)
- Anaïs M Grégoire
- Institute of Neurosciences (IoNS), Catholic University of Louvain (UCLouvain), Brussels, Belgium; Department of ENT, Academic Hospital of Saint-Luc, Brussels, Belgium.
| | - Laurence Dricot
- Institute of Neurosciences (IoNS), Catholic University of Louvain (UCLouvain), Brussels, Belgium
| | - Caroline Huart
- Institute of Neurosciences (IoNS), Catholic University of Louvain (UCLouvain), Brussels, Belgium; Department of ENT, Academic Hospital of Saint-Luc, Brussels, Belgium
| | - Monique Decat
- Department of ENT, Academic Hospital of Saint-Luc, Brussels, Belgium
| | - Naïma Deggouj
- Institute of Neurosciences (IoNS), Catholic University of Louvain (UCLouvain), Brussels, Belgium; Department of ENT, Academic Hospital of Saint-Luc, Brussels, Belgium
| | - Ron Kupers
- Institute of Neurosciences (IoNS), Catholic University of Louvain (UCLouvain), Brussels, Belgium; Ecole d'optométrie, Montréal University, QC, Canada
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Burge ME, Espinoza D, Sjoquist KM, Siu DH, Mercieca-Bebber R, Chantrill LA, Karapetis CS, Steer CB, Yip S, Cuff J, Winata S, Tie J, Thaker DA, Srivastav R, Abdi E, Strickland A, Segelov E, Francesconi A, Price T, Ladwa R, Joubert W, Tebbutt NC. AGITG MONARCC: A Randomized Phase 2 Study of Panitumumab Monotherapy and Panitumumab Plus 5-Fluorouracil as First-Line Therapy for Older Patients With RAS and BRAF Wild Type Metastatic Colorectal Cancer. A Study by the Australasian Gastro-Intestinal Trials Group (AGITG). Clin Colorectal Cancer 2025; 24:120-128. [PMID: 39779412 DOI: 10.1016/j.clcc.2024.11.003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/14/2024] [Revised: 11/21/2024] [Accepted: 11/24/2024] [Indexed: 01/11/2025]
Abstract
BACKGROUND Panitumumab (pan) plus chemotherapy is a preferred first-line therapy for unresectable RAS and BRAF wild type metastatic colorectal cancer (mCRC). Older patients may not be suitable for combination regimens. We investigated 2 lower intensity pan-containing regimens. METHODS Prospective, noncomparative, randomized (1:1) phase 2 study of pan alone (Arm A) or pan plus FU (Arm B). Previously untreated mCRC were ≥70 years; RAS/BRAF wild type. PRIMARY ENDPOINT 6-month progression-free survival (PFS). Secondary endpoints included: overall survival (OS), response rate (RR), feasibility of geriatric assessments and overall treatment utility (OTU)-a composite measure based on radiological response, clinical progress, toxicity and patient-reported treatment worth. Planned sample size was 40 patients per arm. RESULTS 36 patients (Arm A n = 19, Arm B n = 17) were randomized between June 2018 and June 2021. Median age was 79 and 80 years respectively. 6-month PFS 63% (95% CI 38%-80%) arm A 82% (95%CI 55%-94%) Arm B. Median OS 21 months Arm A (95%CI 13-31) 28 (95%CI 14-39) months Arm B. RR 47% and 65% Arms A and B respectively. Baseline comprehensive geriatric assessments were completed in >80% of patients. At week 16, OTU was categorized as good in 92% (Arm A) and 90% (Arm B). No unexpected adverse events were seen. CONCLUSIONS Six-month PFS in both arms was consistent with that achieved with FU/bev, whilst the rate was numerically higher for Arm B. Baseline comprehensive geriatric assessments were feasible and OTU was high. Both treatment arms might be suitable in appropriately selected patients.
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Affiliation(s)
- Matthew E Burge
- Royal Brisbane and Women's Hospital, Brisbane, Australia; The University of Queensland, Brisbane, Australia.
| | - David Espinoza
- NHMRC Clinical Trials Centre, The University of Sydney, New South Wales, Australia
| | | | - Derrick Ho Siu
- NHMRC Clinical Trials Centre, The University of Sydney, New South Wales, Australia
| | | | | | | | - Christopher B Steer
- Border Medical Oncology, Albury Wodonga Regional Cancer Centre, Victoria, Australia
| | - Sonia Yip
- NHMRC Clinical Trials Centre, The University of Sydney, New South Wales, Australia
| | - Jeff Cuff
- Australasian Gastro-Intestinal Trials Group-Community Advisory Panel. Level 6, Camperdown, New South Wales, Australia
| | - Stephanie Winata
- NHMRC Clinical Trials Centre, The University of Sydney, New South Wales, Australia
| | | | | | | | - Ehtesham Abdi
- The Tweed Hospital, Tweed Heads, New South Wales, Australia; Griffith University, Southport, Queensland, Australia
| | - Andrew Strickland
- Department of Medical Oncology, Monash Health, Clayton, Victoria, Australia; Monash University, Clayton, Australia
| | - Eva Segelov
- Department of Medical Oncology, Monash Health, Clayton, Victoria, Australia
| | | | - Timothy Price
- The Queen Elizabeth Hospital, Woodville South, South Australia
| | - Rahul Ladwa
- Princess Alexandra Hospital, Woolloongabba, Queensland, Australia
| | - Warren Joubert
- Princess Alexandra Hospital, Woolloongabba, Queensland, Australia
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Mendes-Bastos P, Lazaridou E, Torres T, Aggelakopoulos C, Katsantonis I, Aronis P, Rigopoulos D, Azevedo F, Santiago F, Papakonstantis M, Varela P, Ribeiro VSG, Kollia A, Papadavid E. Multidimensional Burden of Moderate-to-Severe Atopic Dermatitis in Adolescent and Adult Patients from Portugal and Greece: Results from the Global Cross-Sectional Study MEASURE-AD. Dermatol Ther (Heidelb) 2025; 15:1487-1505. [PMID: 40285916 PMCID: PMC12092850 DOI: 10.1007/s13555-025-01414-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/13/2025] [Accepted: 04/08/2025] [Indexed: 04/29/2025] Open
Abstract
INTRODUCTION Despite significant progress observed in the treatment of atopic dermatitis (AD), a considerable number of patients with severe disease are undertreated and have inadequate symptom control. This may be due to several reasons, such as underestimation of the implications of the disease on patients, families, and society, as well as inconsistent access to effective treatment. The multidimensional disease burden of AD includes other atopic comorbidities, sleep disturbance, and functional impairment and secondary consequences, including neuropsychiatric issues (anxiety and depression) and reduced health-related quality of life. METHODS MEASURE-AD was a global, cross-sectional observational study in adolescents and adults with moderate-to-severe AD, conducted to describe disease burden, treatment patterns, and healthcare resource utilization. RESULTS The results concerning patients from Portugal and Greece indicate moderate-to-severe disease for most of the population with frequent disease flares. The quality of life of both adolescents and adults was greatly affected, mainly owing to itch. One out of five patients perceived that their treatment was not effectively controlling AD. Disease resulted in important out-of-pocket expenses and loss of productivity. CONCLUSIONS Understanding and recognizing the complex burden of moderate-to-severe AD is required to encourage and guide changes in public policy for the effective management of patients.
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Affiliation(s)
- Pedro Mendes-Bastos
- Dermatology Center, Hospital CUF Descobertas, R. Mário Botas, 1998-018, Lisboa, Portugal
| | - Elisavet Lazaridou
- 2nd Department of Dermatology-Venereology, Aristotle University School of Medicine, "Papageorgiou" General Hospital, Agiou Pavlou 76, Ag. Pavlos 564 29, Thessaloniki, Greece
| | - Tiago Torres
- Unidade Local de Saúde de Santo António, Largo do Prof. Abel Salazar, 4099-001, Porto, Portugal
| | | | - Ioannis Katsantonis
- Dermatology Department, Tzaneio General Hospital, Zanni & Afentouli, 185 36, Piraeus, Greece
| | - Pantelis Aronis
- Clinic of Dermatology, Hellenic Airforce 251 General Hospital, Panagioti Kanellopoulou 3, 115 25, Athens, Greece
| | - Dimitrios Rigopoulos
- 1st Department of Dermatology and Venereology, National and Kapodistrian University of Athens School of Medicine, "A. Syggros" Hospital for Skin and Venereal Diseases, Ionos Dragoumi 5, 161 21, Athens, Greece
| | - Filomena Azevedo
- Unidade Local de Saúde de São João, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal
| | - Felicidade Santiago
- Unidade Local de Saúde da Região de Leiria, Hospital de Santo André, R. de Santo André, 2410-197, Leiria, Portugal
| | - Markos Papakonstantis
- Clinic of Dermatology, 401 General Military Hospital of Athens, Panagioti Kanellopoulou, 115 25, Athens, Greece
| | - Paulo Varela
- Unidade Local de Saúde deGaia e Espinho, R. Conceição Fernandes, 4434-502, Vila Nova de Gaia, Portugal
| | - Vera S G Ribeiro
- AbbVie, Lda.; Estrada Alfragide 67 Alfrapark, Edifício D, 2610-008, Amadora, Portugal
| | - Aikaterini Kollia
- AbbVie Pharmaceuticals S.A, Marinou Antipa 41-45, 141 21, Iraklio, Athens, Greece
| | - Evaggelia Papadavid
- 2nd Department of Dermatology and Venereology, National and Kapodistrian University of Athens, "Attikon" University General Hospital, 1 Rimini Street, 124 62, Chaidari, Athens, Greece.
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50
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Francken L, Rood PJT, Peters MAA, Teerenstra S, Zegers M, van den Boogaard M. Exploring differences in reported mental health outcomes and quality of life between physically restrained and non-physically restrained ICU patients; a prospective cohort study. Intensive Crit Care Nurs 2025; 88:103928. [PMID: 39798478 DOI: 10.1016/j.iccn.2024.103928] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/25/2024] [Revised: 12/02/2024] [Accepted: 12/05/2024] [Indexed: 01/15/2025]
Abstract
BACKGROUND Physical restraints are frequently used in ICU patients, while their effects are unclear. OBJECTIVE To explore differences in patient reported mental health outcomes and quality of life between physical restrained and non-physical restrained ICU patients at 3- and 12-months post ICU admission, compared to pre-ICU health status. RESEARCH METHODOLOGY/DESIGN Prospective cohort study. Patients were included when 16 years or older, admitted for at least 12 h and provided informed consent. Differences between groups were analysed using linear mixed model analyses. SETTING Two ICUs, a 35 bed academic ICU and a 12 bed ICU in a teaching hospital in the Netherlands. MAIN OUTCOME MEASURES Symptoms of anxiety and depression were measured using the Hospital Anxiety and Depression Scale, post-traumatic stress disorder using the Impact of Event Scale-Revised, and Quality of life using the Short Form-36 scores. RESULTS 2,764 patients were included, of which 486 (17.6 %) were physically restrained for median 2 [IQR 1-6] days. Significantly worse outcomes were reported at 3-months by physically restrained patients (symptoms of depression 0.89, 95 %CI 0.37 to 1.41, p < 0.001; PCS -2.82, 95 %CI -4.47 to -1,17p < 0.001; MCS -2.67, 95 %CI -4.39 to -0.96, p < 0.01). At 12-months, only the PCS scores remained significantly lower (-1.71, 95 %CI -3.42 to -0.004, p < 0.05). CONCLUSION Use of physical restraints is associated with worse self-reported symptoms of depression and decreased quality of life 3-months post ICU, and lower physical quality of life after 12-months. IMPLICATIONS FOR CLINICAL PRACTICE Use of physical restraints is associated with statistical significant worse mental and physical outcomes.
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Affiliation(s)
- L Francken
- Radboud University Medical Center, Department of Intensive Care Medicine, PO Box 9101, 6500 HB Nijmegen, the Netherlands
| | - P J T Rood
- Radboud University Medical Center, Department of Intensive Care Medicine, PO Box 9101, 6500 HB Nijmegen, the Netherlands; Research Groups 'Technology for Health' and 'Emergency and Critical Care', School of Health Studies Nijmegen, HAN University of Applied Sciences, Nijmegen, the Netherlands; Department for Quality, Research and Development, Rijnstate Hospital, Arnhem, the Netherlands
| | - M A A Peters
- Department of Intensive Care Medicine, Canisius Wilhelmina Hospital, Nijmegen, the Netherlands
| | - S Teerenstra
- Department for Health Evidence, Section Biostatistics, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands
| | - M Zegers
- Radboud University Medical Center, Department of Intensive Care Medicine, PO Box 9101, 6500 HB Nijmegen, the Netherlands
| | - M van den Boogaard
- Radboud University Medical Center, Department of Intensive Care Medicine, PO Box 9101, 6500 HB Nijmegen, the Netherlands.
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