Systematic Reviews
Copyright ©The Author(s) 2025.
World J Crit Care Med. Sep 9, 2025; 14(3): 103402
Published online Sep 9, 2025. doi: 10.5492/wjccm.v14.i3.103402
Table 2 Inclusion of a summary of the studies, n (%)
Ref.
Linderoth et al[22], 2021
Ofoma et al[26], 2022
Plata et al[18], 2021
Lee et al[27], 2021
Aranda-García et al[16], 2023
Pérez Alonso et al[14], 2017
Lee et al[28], 2020
Ecker et al 2021[35]
Yang et al[29], 2009
ComparatorsVideoTelemedicineNo telemedicineVideoV-DACPR with rapid transitionV-DACPR with delayed transitionC-DACPRVideoAudioGGControlVideoAudioAudio and video telephonyVideoAudio
CountryDenmarkUnited StatesGermanySouth KoreaSpainSpainSeoul, South KoreaGermanyTaiwan
Study period2019-2021July 1, 2017, and December 31, 2019September 2019 to February 2020October 2019 to July 20202021-2022November 2014 to July 20152017August to September 20182009
Study designRetrospective studyA prospective, voluntary, multi-site registry of IHCARandomised controlled simulation trialRandomised controlled simulation trialRandomised controlled simulation trialRandomised clinical simulationRetrospective cohortProspective randomized pilotRandomized controlled study
Sample size9014373302129343454314143636231148954 venues with realistic full-scale CPR mannequin4353
ParticipantsBystanderAdult patientsParamedics and emergency physiciansBystanderAdult volunteersNurseEmergency medical techniciansBystanderVolunteers (bystander)
Inclusion criteriaThe training included simulation-based scenarios with unconscious patients and cardiac arrest cases with a focus on high-quality CPR with simultaneously real-time guidance (video-instructed DA-CPR)We identified 70881 patients 18 years or older with an index pulseless IHCA between July 1, 2017, and December 31, 2019. We excluded arrests at hospitals that did not respond to the AHA surveys or had missing information on TCC availability; at hospitals with less than 10 cardiac arrests over the study period; that occurred outside of an ICU or hospital ward (e.g., emergency room and operating room); and in patients with an implantable cardioverterdefibrillator. Additionally, we excluded patients with missing information related to arrest time or survivalNo specefic criteriaVolunteers aged 18 years or older were recruited for the simulation trial from October 2019 to July 2020. Healthcare providers, and participants with chronic lung diseases, cardiovascular diseases, visual disabilities, or hearing disabilities were excluded during initial enrollment. Written consent was obtained from all participantsInclusion criteria were no theoretical or practical training on BLS in the previous 2 yearsTraining in BLS in the last 2 years and a minimum of 2 years of professional experience in emergency services as well as familiarity with the use of AED and the ALSOHCA patients with a presumed cardiacetiology who were more than 18 years of age between January and December 2017NRNinety-six adults without CPR training within 5 years were recruited
Age (years)21.25 (11.17)65.5 (15.4)65.6 (15.1)NR30.5 (12.0)29.1 (10.2)30.8 (12.1)232333 ± 832 ± 7NRNRNRNR50.1 ± 11.550.4 ± 12.7
BMI (kg/m2)NRNRNRNRNRNRNR22.522.1NRNRNRNRNRNRNRNR
Male508500 (59.1)17724 (58.7)NR10119141439%28%NRNRNRNRNRNR
Female405873 (40.9)12488 (41.3)NR3334340061%72%NRNRNRNRNRNR
Has provided CPR52NRNR93NRNRNRNRNRNRNRNRNRNRNR4 (70)1 (90)
Witnessed an emergency29NRNR93NRNRNRNRNRNRNRNRNRNRNR--
Had first aid course48NRNR93NRNRNRNRNRNRNRNRNRNRNR18 (60)18 (90)