Published online Aug 27, 2026. doi: 10.4240/wjgs.121902
Revised: June 16, 2026
Accepted: July 14, 2026
Published online: August 27, 2026
Processing time: 96 Days and 16.9 Hours
Sphincter-preserving surgery is a common procedure for rectal cancer, but ante
To evaluate the efficacy of combined magnetic-electrical biofeedback therapy in patients with ARS after sphincter-preserving surgery for low rectal cancer.
Sixty patients with ARS following sphincter-preserving surgery for low rectal cancer admitted to our hospital between August 2024 to March 2026, were se
Baseline bowel function indicators, LARS scores, and MSKCC-BFI scores (P > 0.05) did not differ significantly between groups. After treatment, the study group showed fewer daily bowel movements, lower fecal incontinence frequency scores, lower LARS scores, and higher MSKCC-BFI scores than the control group (all P < 0.05). No significant differences were observed in anal pressure or anorectal function indicators before the intervention (P > 0.05). Anal resting pressure, maximum squeeze pressure, as first rectal sensation volume, maximum tolerated volume, and rectal compliance were also signifi
Combined intervention using magnetic-electrical biofeedback demonstrated significant efficacy in patients with ARS after sphincter-preserving surgery for low rectal cancer. It facilitates the synergistic recovery of rectal and anal canal functions, plays a positive role in improving patients’ bowel movements and anorectal function, and pro
Core Tip: Anterior resection syndrome remains one of the most challenging functional complications after sphincter-preserving surgery for low rectal cancer, substantially affecting patients' quality of life. This study demonstrates that combined magnetic-electrical biofeedback therapy significantly improves bowel function, anal sphincter function, anorectal physiological parameters, and patient-reported bowel function compared with conventional rehabilitation alone. The com
- Citation: Weng XH, Huang Y. Non-surgical magnetic-electrical biofeedback improves anterior resection syndrome after sphincter-preserving surgery for low rectal cancer. World J Gastrointest Surg 2026; 18(8): 121902
- URL: https://www.wjgnet.com/1948-9366/full/v18/i8/121902.htm
- DOI: https://dx.doi.org/10.4240/wjgs.121902
Lower rectal cancer is a common malignancy of the digestive tract. Sphincter-preserving surgery has become a widely adopted treatment because it retains the patient’s anal defecation function and improves postoperative quality of life[1]. Multiple clinical reports indicate that anterior resection syndrome (ARS) tends to occur after sphincter-preserving surgery for rectal cancer. The core manifestations in patients include increased defecation frequency, fecal incontinence, and fecal urgency. Some patients also experience abnormal rectal sensation and decreased anal sphincter function, which severely reduces their quality of life, making it a current clinical challenge in rehabilitation following sphincter-preserving surgery for low rectal cancer[2,3]. The current conventional clinical interventions for ARS primarily include dietary guidance[4], regular bowel habit training[5], and Kegel exercises[6]. Although these approaches can alleviate symptoms to some extent, they rely heavily on patients’ autonomous perception and motor control, and are prone to issues such as com
Magnetic-electrical biofeedback is a rehabilitation approach that combines physical stimulation with functional training. By integrating the dual intervention advantages of magnetic stimulation and electrical biofeedback, overcoming the limitations of traditional single-rehabilitation methods[8]. Magnetoelectric biofeedback technology has multiple functions such as nerve repair and muscle strength regulation. This is in line with the core pathogenesis of ARS and has the advantages of noninvasive safety and strong repeatability. This demonstrated good application prospects in the field of pelvic floor function rehabilitation.
Magnetic-electrical biofeedback technology, as a rehabilitation approach that combines physical stimulation with functional training, integrates the dual intervention advantages of magnetic stimulation and electrical biofeedback, breaking through the limitations of traditional single rehabilitation methods. Magnetoelectric biofeedback technology has multiple functions such as nerve repair and muscle strength regulation. It is in line with the core pathogenesis of ARS and has the advantages of non-invasive safety and strong repeatability. It shows a good application prospect in the field of pelvic floor function rehabilitation. However, relatively little research has been conducted on the application of this technology in patients with ARS after sphincter-preserving surgery for lower rectal cancer, and its effects on the core symptoms of ARS, rectoanal function, and patient quality of life have not yet been systematically validated. Therefore, this study considered patients with ARS after sphincter-preserving surgery for lower rectal cancer as research subjects to explore the intervention effects of combined magnetic-electrical biofeedback therapy.
Sixty patients with ARS after sphincter-preserving surgery for low rectal cancer, admitted to our hospital between August 2024 to March 2026. The inclusion criteria include: (1) Low rectal adenocarcinoma confirmed by histopathological examination[9]; (2) Lower tumor margin ≤ 10 cm from the anal verge; (3) Laparoscopic or open low anterior resection or other sphincter-preserving surgeries, with negative surgical margins and no abdominal stoma; and (4) normal cognitive and communication abilities, allowing participation in magnetic-electrical biofeedback training and outcome assessments. The exclusion criteria include: (1) Primary malignant tumors in other sites; (2) Previous anorectal surgery or organic injury to the anal sphincter; (3) inflammatory bowel disease, irritable bowel syndrome, chronic diarrhea, constipation, or intestinal infection; (4) inability to tolerate biofeedback training; and (5) Contraindications to magnetic-electrical biofeed
| Group | Gender | Age (years) | Distance (cm) from the tumor to the anal margin | Clinical staging | ||
| Male | Female | Phase II | Phase III | |||
| Control group (n = 30) | 19 (63.33) | 11 (36.67) | 61.17 ± 3.05 | 7.15 ± 0.63 | 23 (76.67) | 7 (23.33) |
| Study group (n = 30) | 18 (60.00) | 12 (40.00) | 60.47 ± 3.36 | 7.21 ± 0.59 | 22 (73.33) | 8 (26.67) |
| χ2/t | 0.071 | 0.845 | 0.381 | 0.089 | ||
| P value | 0.791 | 0.402 | 0.705 | 0.765 | ||
The control group received conventional interventions focused on intestinal function regulation and health guidance. Postoperatively, the patients were informed about the pathogenesis of ARS and the patterns of postoperative intestinal function recovery using one-on-one explanations combined with video demonstrations. A personalized diet plan was developed to guide the patients to consume high-fiber, easily digestible foods, with daily water intake controlled at 1500-2000 mL, avoiding spiky, greasy, and gas-producing foods. Regular bowel habit training was implemented as follows: Attempting defecation upon waking or 30 minutes after meals daily and maintaining a seated posture during defecation, with each session not exceeding 10 minutes. Abdominal clockwise massage can be used for assistance, if necessary. Patients were guided daily to perform Kegel exercises, simulating the actions of holding back stool or gas to contract the anal sphincter, holding the contraction for 5-10 seconds, and relaxing for 5-10 seconds, with 10-15 repetitions per set, three sets per day. The contraction duration and number of sets were gradually increased based on patient tolerance, avoiding excessive training and muscle fatigue.
The study group received a combined magnetic-electrical biofeedback intervention in addition to the control group’s regimen.
Biostimulation feedback intervention: The instrument used was a bioelectric feedback stimulator (model: SA9805; Nanjing Weisi Medical Technology Co., Ltd., Jiangsu Province, China). Patients were assisted in a semi-recumbent position and exposed to the treatment and monitoring areas (abdomen and anus). Appropriate sizes of rectal electrodes and electrode patches were selected based on the treatment area. The surface of the rectal electrode was evenly coated with a lubricating conductive gel and gently inserted into the anus (the electrode head was completely inside the anal opening). The electrode patches were adhered to the abdomen. The initial parameters were set at low intensity, with electrical stimulation frequency (10-20 Hz) gradually adjusted based on tolerance, aiming for a level at which the patient consciously felt anal sphincter contraction without pain. During treatment, the patients’ facial expressions, physical reactions, and device data (such as electromyography values and stimulation intensity) were monitored, with attention paid to inquiring about their sensations. Parameters and electrode positions were adjusted to prevent burning or stinging. Electrical stimulation can enhance pelvic floor function, promote local tissue blood circulation, and repair damaged or abnormal floor muscles.
Biofeedback Training Intervention: Visual (screen waveforms) or auditory (verbal prompts) feedback was provided. Patients control feedback signals by contracting and relaxing their muscles. Targeted active training (relaxation, coordination, and strength training) was conducted, maintaining contraction for 10 seconds and relaxation for 10 seconds. Based on feedback signals, patients were guided to precisely contract and relax the anal sphincter, correct improper contraction actions, and avoid compensatory contractions of the abdominal or thigh muscles. This study aimed to ree
Magnetic Stimulation Intervention: A magnetic stimulator was used (model: Magneuro60F; Nanjing Weisi Medical Technology Co., Ltd., Jiangsu Province, China). The patients were assisted in a sitting or prone position according to the treatment plan, and the magnetic field intensity was adjusted. In the sitting position, the intensity was adjusted until the patient felt a bellows-like sensation of movement in the buttocks. The coil was positioned over the sacral nerve with the patient in the prone position. The magnetic induction intensity ranged from 0.5-1 T, gradually adjusted based on tolerance. The magnetic stimulation intensity should not be too high and should be adjusted to a level where the sti
The combined magnetic-electrical biofeedback intervention was conducted three to five times per week. Each session lasted 50 minutes (30 minutes for biostimulation feedback therapy and 20 minutes for magnetic stimulation therapy). Patients were instructed to simultaneously perform biofeedback reinforcement training at home to consolidate the intervention effects. The combined magnetic-electrical biofeedback therapy for anorectal and pelvic floor diseases aims to help patients achieve better therapeutic outcomes and improve quality of life through the combination of multiple technologies. Both groups were followed up for 3 months via online and outpatient review methods.
Indicators related to bowel movement: The frequency of bowel movements was recorded in both groups before and after the intervention (three months). Simultaneously, the fecal incontinence frequency scores were assessed before and after the intervention. This score includes evaluations across five dimensions: Incontinence to liquid stool, incontinence to solid stool, incontinence to gas, lifestyle alterations, and the need to wear pads. Each dimension is scored from 0 to 4 based on severity and frequency, with a total possible score of 20 points. Higher scores indicated a higher frequency of incontinence.
Low ARS score: The severity of bowel dysfunction in both groups was assessed using the LARS score before the intervention and 1 month and 3 months after the intervention. This scale assesses fecal urgency, incontinence, frequency, evacuation difficulties, and painful defecation. Each item is rated using a Likert 4-point scale (0 to 3) based on symptom frequency or severity. Symptom frequency scoring criteria: Never counted as 0 points, 1 point for < 1 occurrence per week, 2 points for ≥ 1 occurrence per week but < 1 occurrence per day, and 3 points for ≥ 1 occurrence per day; A higher score indicates more severe bowel dysfunction.
Memorial Sloan Kettering Cancer Center Bowel Function Instrument score: Quality of life related to bowel function was assessed in both groups using the Memorial Sloan Kettering Cancer Center Bowel Function Instrument (MSKCC-BFI)[10] score before and 1 month and 3 months after the intervention. The instrument comprises three dimensions (diet-related symptoms, fecal urgency/soiling of undergarments, and stool frequency) and four independent questions, with a total of 18 items. The total score ranged from 0 to 90, with a higher score indicating a better quality of life related to bowel function.
Anal pressure indicators: Before including anal resting pressure (ARP) and maximum squeeze pressure (MSP), were measured before and after the intervention (3 months) using anorectal manometry equipment (model IGJ-D3; Hefei Aoyuan Technology Development Co., Ltd., Anhui Province, China) in both groups, including ARP and MSP.
Anal function: Rectal sensory function was measured using an anorectal pressure detector and matching balloon. The patient was placed in the left lateral position, and a catheter was placed in the ampulla of the rectum. The balloon is filled with air at a constant rate of 1 mL/second. The volume of inflation when the patient first experiences defecation is the rectal sensation volume, and the total inflation volume when the patient reaches the limit of intolerance to defecation is the maximum tolerable rectal volume. The pressure difference in the rectal cavity corresponding to the maximum tole
Efficacy evaluation: After 3-month follow-up, the therapeutic efficacy in both groups was statistically analyzed. The criteria were: “Markedly effective” if the LARS score decreased by > 70%, and ARP and squeeze pressure increased by > 30%; “effective” if the LARS score decreased by 50%, and anal canal pressure showed improvement compared to before intervention; “ineffective” if the above criteria were not met or if the LARS score continued to increase.
Statistical analysis was performed using SPSS software (version 23.0). Categorical data are presented as n (%) and analyzed using the χ2 test. Measurement data are presented as mean ± SD and analyzed using the t-test. Statistical signi
There were no significant differences in bowel movement frequency or fecal incontinence frequency scores between the two groups before the intervention (P > 0.05). After intervention, the number of bowel movements in the study group was (2.64 ± 0.59) times, which was less than that in the control group (3.35 ± 0.72) times. The fecal incontinence frequency score in the study group after intervention was (2.47 ± 0.52) points, which was lower than that in the control group (4.61 ± 1.13) points, and the difference was significant (P < 0.05), as shown in Table 2.
| Group | Number of bowel movements (times/day) | Frequency of fecal incontinence (points) | ||
| Before | After | Before | After | |
| Control group (n = 30) | 5.17 ± 1.36 | 3.35 ± 0.72 | 7.12 ± 1.46 | 4.61 ± 1.13 |
| Study group (n = 30) | 5.28 ± 1.41 | 2.64 ± 0.59 | 7.35 ± 1.54 | 2.47 ± 0.52 |
| t | 0.308 | 4.178 | 0.594 | 9.423 |
| P value | 0.760 | < 0.001 | 0.555 | < 0.001 |
There was no significant difference in the LARS scores between the two groups before the intervention (P > 0.05). One and three months after the intervention, the LARS scores for both groups significantly decreased compared to their respective scores before the intervention. At the same follow-up time points, the intervention group exhibited signifi
Intra-group comparison: One and three months after the intervention, the MSKCC-BFI scores of both groups were significantly higher than those before the intervention (P < 0.05), and at the same time points between groups, the MSKCC-BFI scores of the study group at one month and three months after intervention were both higher than those of the control group (P < 0.05), as shown in Table 4.
There were no significant differences in the ARP and MSP levels between the two groups before the intervention (P > 0.05). After the intervention, both ARP and MSP levels were significantly higher in the intervention group than in the control group (P < 0.05). See Table 5.
There were no significant differences in any anorectal function indicators between the two groups before the intervention (P > 0.05). After the intervention, parameters including rectal first sensation volume, rectal maximum tolerated volume, and rectal compliance were significantly higher in the intervention group than in the control group (P < 0.05). See Table 6.
| Group | Rectal sensation of stool volume (mL) | Maximum rectal tolerance (mL) | Rectal compliance (mL/kPa) | |||
| Before | After | Before | After | Before | After | |
| Control group (n = 30) | 61.27 ± 4.95 | 67.53 ± 5.81a | 137.25 ± 11.61 | 164.17 ± 12.85a | 3.56 ± 0.61 | 4.83 ± 0.54a |
| Study group (n = 30) | 60.79 ± 5.13 | 71.39 ± 5.72a | 136.84 ± 12.15 | 171.78 ± 12.61a | 3.68 ± 0.57 | 5.36 ± 0.62a |
| t | 0.369 | 2.593 | 0.134 | 2.315 | 0.787 | 3.531 |
| P value | 0.714 | 0.012 | 0.894 | 0.024 | 0.434 | 0.001 |
The total efficacy rate in the study group was 96.67%, which was significantly higher than that in the control group (73.33%; P < 0.05). See Table 7.
| Group | Excellence | Effective | Invalid | Total effective rate |
| Control group (n = 30) | 9 (30.00) | 13 (43.33) | 8 (26.67) | 22 (73.33) |
| Study group (n = 30) | 15 (50.00) | 14 (46.67) | 1 (3.33) | 29 (96.67) |
| t | 4.706 | |||
| P value | 0.030 |
ARS following sphincter-preserving surgery for lower rectal cancer refers to a series of postoperative defecatory dysfunc
After intervention, the study group exhibited fewer daily bowel movements and a lower fecal incontinence frequency score than the control group (P < 0.05). Only two time points were set for defecation-related indicators: Before and three months after the intervention. The main consideration was that pelvic floor biofeedback could not reverse the entire chain of pathological changes in the short term, and that short-term values were easily affected by multiple confounding factors. In addition, one month after the anus-preserving surgery for lower rectal cancer, the patient was in the regression period of anastomotic edema and the acute compensatory disorder period of the intestinal tract. One month after the operation, there were still varying degrees of inflammatory edema in the anastomotic mucosa, and the rectal stump receptors were in a highly sensitive state. Moreover, the patient’s diet gradually transitioned from liquid to regular food postoperatively, and the intestinal flora had not yet been fully reconstructed. The frequency of defecation and incon
In addition to subjective symptom assessment, anal canal pressure was evaluated as an objective indicator for evalua
Anal canal pressure focuses on the ability of the anal sphincter to control defecation, whereas rectal defecation sensory capacity, maximum rectal tolerance capacity, and rectal compliance focus on rectal defecation storage and visceral sensory function. These two belong to the two key anatomical sites of the anal canal and rectum, respectively, and together, they form a complete physiological function chain of the anus and rectum. Previous studies have shown that, surgical trauma associated with sphincter-preserving surgery for low rectal cancer may alter rectal mucosal sensation and reduce rectal elasticity wall. This manifests as a decreased first sensation volume, directly contributing to frequent urges to defecate[25]. A reduced maximum tolerated volume suggests a weak fecal storage capacity in patients, whereas decreased compliance typically indicates poor rectal adaptability to internal distension. In the present study, after the intervention, the study group exhibited significantly higher rectal first sensation volume, maximum tolerated volume, and compliance compared to the control group (P < 0.05). The core reason lies in the different dimensions through which intervention protocols improve rectal function. Although the conventional intervention in the control group indirectly affected the rectal contents through dietary adjustments, it did not directly improve rectal mucosal sensation or com
The results also showed that the total efficacy rate (96.67%) was significantly higher in the study group than in the control group (73.33%), P < 0.05. From a physiological perspective, the combined magnetic-electrical biofeedback therapy enhanced both the “valve” function of the anal canal for defecation control and improved rectal first sensation volume, maximum tolerated volume, and compliance. At the symptom level, the restoration of physiological functions directly reduces the frequency of bowel movements and the incidence of fecal incontinence, achieving a progressive effect of physiological function repair, symptom alleviation, and quality of life improvement, which ultimately translates into a higher overall clinical efficacy rate. In contrast, conventional intervention primarily focused only on behavioral manage
In summary, combined magnetic-electrical biofeedback demonstrated significant efficacy in patients with ARS following sphincter-preserving surgery for low rectal cancer. It improved anorectal function and rectal status while enhancing overall therapeutic outcomes. It can be considered the preferred non-surgical intervention option for patients with ARS after sphincter-preserving surgery for low rectal cancer.
| 1. | Piozzi GN, Baek SJ, Kwak JM, Kim J, Kim SH. Anus-Preserving Surgery in Advanced Low-Lying Rectal Cancer: A Perspective on Oncological Safety of Intersphincteric Resection. Cancers (Basel). 2021;13:4793. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 44] [Cited by in RCA: 34] [Article Influence: 6.8] [Reference Citation Analysis (2)] |
| 2. | Zhang Q, Lin H, Wang F, Li Q, Song W. Factors Affecting Low Anterior Resection Syndrome following Anus-Preserving Surgery for Rectal Cancer and Assessing the Impact of Nursing Interventions in Rapid Rehabilitation Surgery. Altern Ther Health Med. 2024;AT10827. [PubMed] |
| 3. | Wang W, Cai Y, Peng J, Liu L, Feng X, Wan S. Research on preventing low anterior resection syndrome following sphincter-preserving surgery for rectal cancer through high-risk screening and pelvic floor biofeedback therapy. Support Care Cancer. 2025;33:291. [RCA] [PubMed] [DOI] [Full Text] [Reference Citation Analysis (0)] |
| 4. | Liu W, Xu JM, Zhu A. Remote precise diet management intervention of defecation dysfunction among patients with rectal cancer after the sphincter-saving surgery: a study protocol for a randomized controlled trial. Trials. 2025;26:428. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Reference Citation Analysis (0)] |
| 5. | Rosen H, Sebesta CG, Sebesta C. Management of Low Anterior Resection Syndrome (LARS) Following Resection for Rectal Cancer. Cancers (Basel). 2023;15:778. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 52] [Reference Citation Analysis (0)] |
| 6. | Zhang L, Wang F. Evaluation of Nursing Effects of Pelvic Floor Muscle Rehabilitation Exercise on Gastrointestinal Tract Rectal Cancer Patients Receiving Anus-preserving Operation by Intelligent Algorithm-based Magnetic Resonance Imaging. Contrast Media Mol Imaging. 2022;2022:1613632. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 7] [Cited by in RCA: 7] [Article Influence: 1.8] [Reference Citation Analysis (0)] |
| 7. | Asnong A, D'Hoore A, Van Kampen M, Wolthuis A, Van Molhem Y, Van Geluwe B, Devoogdt N, De Groef A, Guler Caamano Fajardo I, Geraerts I. The Role of Pelvic Floor Muscle Training on Low Anterior Resection Syndrome: A Multicenter Randomized Controlled Trial. Ann Surg. 2022;276:761-768. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 35] [Cited by in RCA: 48] [Article Influence: 12.0] [Reference Citation Analysis (1)] |
| 8. | Sacomori C, Lorca LA, Martinez-Mardones M, Salas-Ocaranza RI, Reyes-Reyes GP, Pizarro-Hinojosa MN, Plasser-Troncoso J. A randomized clinical trial to assess the effectiveness of pre- and post-surgical pelvic floor physiotherapy for bowel symptoms, pelvic floor function, and quality of life of patients with rectal cancer: CARRET protocol. Trials. 2021;22:448. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 23] [Cited by in RCA: 23] [Article Influence: 4.6] [Reference Citation Analysis (1)] |
| 9. | Benson AB, Venook AP, Al-Hawary MM, Azad N, Chen YJ, Ciombor KK, Cohen S, Cooper HS, Deming D, Garrido-Laguna I, Grem JL, Gunn A, Hecht JR, Hoffe S, Hubbard J, Hunt S, Jeck W, Johung KL, Kirilcuk N, Krishnamurthi S, Maratt JK, Messersmith WA, Meyerhardt J, Miller ED, Mulcahy MF, Nurkin S, Overman MJ, Parikh A, Patel H, Pedersen K, Saltz L, Schneider C, Shibata D, Skibber JM, Sofocleous CT, Stotsky-Himelfarb E, Tavakkoli A, Willett CG, Gregory K, Gurski L. Rectal Cancer, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2022;20:1139-1167. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 672] [Cited by in RCA: 568] [Article Influence: 142.0] [Reference Citation Analysis (3)] |
| 10. | Celasin H, Akyol C, Gecim IE, Halil Elhan A, Juul T, Sokmen S, Sungurtekin U, Akyuz S. Validation of the Turkish translation of the low anterior resection syndrome (LARS) score. Tech Coloproctol. 2023;27:465-474. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 2] [Cited by in RCA: 3] [Article Influence: 1.0] [Reference Citation Analysis (0)] |
| 11. | Xu LL, Cheng TC, Xiang NJ, Chen P, Jiang ZW, Liu XX. Risk factors for severe low anterior resection syndrome in patients with rectal cancer undergoing sphincterpreserving resection: A systematic review and metaanalysis. Oncol Lett. 2024;27:30. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in RCA: 8] [Reference Citation Analysis (0)] |
| 12. | Sorokin BV, Zlobenets SO, Yakovenko VO, Pyrogovsky VY, Milyanovska AO. Low anterior resection syndrome in distal rectal cancer patients and its correction methods. Wiad Lek. 2024;77:2252-2260. [RCA] [PubMed] [DOI] [Full Text] [Reference Citation Analysis (0)] |
| 13. | Sun V, Crane TE, Arnold KB, Guthrie K, Freylersythe S, Braun-Inglis C, Jones L, Cohen SA, Al-Kasspooles M, Krouse RS, Thomson CA. SWOG S1820: Altering Intake, Managing Symptoms for bowel dysfunction in survivors of Rectal Cancer (The AIMS-RC intervention trial). Contemp Clin Trials Commun. 2021;22:100768. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 2] [Cited by in RCA: 6] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 14. | Popeskou SG, Roesel R, Faes S, Vanoni A, Galafassi J, di Tor Vajana AF, Piotet LM, Christoforidis D. Ondansetron for Low Anterior Resection Syndrome (LARS): A Double-Blind, Placebo-Controlled, Cross-Over, Randomized Study. Ann Surg. 2024;279:196-202. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 6] [Reference Citation Analysis (0)] |
| 15. | Hong M, Yu W, Gao Y, Pei B, Chen J, Lou Y. Pelvic floor muscle training for the prevention and management of low anterior resection syndrome in patients with rectal cancer: An evidence-based summary. Asia Pac J Oncol Nurs. 2025;12:100620. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in RCA: 1] [Reference Citation Analysis (0)] |
| 16. | Pires M, Severo M, Lopes A, Neves S, Matzel K, Povo A. Sacral neuromodulation for low anterior resection syndrome: current status-a systematic review and meta-analysis. Int J Colorectal Dis. 2023;38:189. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 18] [Cited by in RCA: 23] [Article Influence: 7.7] [Reference Citation Analysis (0)] |
| 17. | Xu LL, Xiang NJ, Cheng TC, Li YX, Chen P, Jiang ZW, Liu XX. Application of electroacupuncture in the prevention of low anterior resection syndrome after rectal cancer surgery. World J Gastrointest Surg. 2023;15:2765-2773. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in CrossRef: 9] [Cited by in RCA: 6] [Article Influence: 2.0] [Reference Citation Analysis (0)] |
| 18. | Liu T, Jiao X, Hu C, Su R, Dong J, Niu Q. Therapeutic strategies for low anterior resection syndrome: an umbrella review of systematic reviews. Int J Colorectal Dis. 2025;40:171. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in RCA: 1] [Reference Citation Analysis (0)] |
| 19. | Cao G, Zhang X, Wang F, Man D, Wu L, Pan X, Chen S. Biofeedback combined with percutaneous electrical pudendal nerve stimulation for the treatment of low anterior rectal resection syndrome: a study protocol for a randomized controlled trial. Trials. 2024;25:440. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 3] [Reference Citation Analysis (0)] |
| 20. | Zhou P, Li H, Pang X, Wang T, Wang Y, He H, Zhuang D, Zhu F, Zhu R, Hu S. Effect of a Mobile Health-Based Remote Interaction Management Intervention on the Quality of Life and Self-Management Behavior of Patients With Low Anterior Resection Syndrome: Randomized Controlled Trial. J Med Internet Res. 2024;26:e53909. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 3] [Reference Citation Analysis (0)] |
| 21. | Ansar M, Boddeti S, Noor K, Malireddi A, Abera M, Suresh SB, Malasevskaia I. A Systematic Review of Comparative Effectiveness of Interventions for Low Anterior Resection Syndrome: Impacts on Bowel Function and Quality of Life. Cureus. 2024;16:e72772. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 4] [Reference Citation Analysis (0)] |
| 22. | Koneru S, Cornish J, Chapuis PH, Keshava A, Rickard MJFX, Ng KS. Low anterior resection syndrome phenotypes-Different symptom profiles for different patients. Colorectal Dis. 2024;26:1214-1222. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 10] [Cited by in RCA: 7] [Article Influence: 3.5] [Reference Citation Analysis (0)] |
| 23. | Chen SC, Futaba K, Leung WW, Wong C, Mak T, Ng S, Gregersen H. Functional anorectal studies in patients with low anterior resection syndrome. Neurogastroenterol Motil. 2022;34:e14208. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 6] [Cited by in RCA: 15] [Article Influence: 3.8] [Reference Citation Analysis (0)] |
| 24. | Korai T, Akizuki E, Okita K, Nishidate T, Okuya K, Sato Y, Hamabe A, Ishii M, Nobuoka T, Takemasa I. Defecation disorder and anal function after surgery for lower rectal cancer in elderly patients. Ann Gastroenterol Surg. 2022;6:101-108. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 1] [Reference Citation Analysis (0)] |
| 25. | Koifman E, Armoni M, Gorelik Y, Harbi A, Streltsin Y, Duek SD, Brun R, Mazor Y. Long term persistence and risk factors for anorectal symptoms following low anterior resection for rectal cancer. BMC Gastroenterol. 2024;24:31. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 5] [Reference Citation Analysis (0)] |