Comparison of Cardiopulmonary Resuscitation Quality Between Standard Versus Telephone-Basic Life Support Training Program in Middle-Aged and Elderly Housewives: A Randomized Simulation Study.

Simul Healthc

From the Department of Emergency Medicine (T.H.K.), Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine, Seoul; Department of Emergency Medicine (Y.J.L.), Inha University Hospital, Incheon; Department of Emergency Medicine (E.J.L.), Korea University Anam Hospital; Laboratory of Emergency Medical Services (Y.S.R., H.L., D.B.J.), Seoul National University Hospital Biomedical Research Institute; Department of Emergency Medicine (K.W.L.), Inje University College of Medicine and Seoul Paik Hospital; Department of Emergency Medicine (K.J.S., S.D.S.), Seoul National University College of Medicine, Seoul, Korea; and Laerdal Medical (H.M., T.S.B.), Stavanger, Norway.

Published: February 2018

Introduction: For cardiac arrests witnessed at home, the witness is usually a middle-aged or older housewife. We compared the quality of cardiopulmonary resuscitation (CPR) performance of bystanders trained with the newly developed telephone-basic life support (T-BLS) program and those trained with standard BLS (S-BLS) training programs.

Methods: Twenty-four middle-aged and older housewives without previous CPR education were enrolled and randomized into two groups of BLS training programs. The T-BLS training program included concepts and current instruction protocols for telephone-assisted CPR, whereas the S-BLS training program provided training for BLS. After each training course, the participants simulated CPR and were assisted by a dispatcher via telephone. Cardiopulmonary resuscitation quality was measured and recorded using a mannequin simulator. The primary outcome was total no-flow time (>1.5 seconds without chest compression) during simulation.

Results: Among 24 participants, two (8.3%) who experienced mechanical failure of simulation mannequin and one (4.2%) who violated simulation protocols were excluded at initial simulation, and two (8.3%) refused follow-up after 6 months. The median (interquartile range) total no-flow time during initial simulation was 79.6 (66.4-96.9) seconds for the T-BLS training group and 147.6 (122.5-184.0) seconds for the S-BLS training group (P < 0.01). Median cumulative interruption time and median number of interruption events during BLS at initial simulation and 6-month follow-up simulation were significantly shorter in the T-BLS than in the S-BLS group (1.0 vs. 9.5, P < 0.01, and 1.0 vs. 10.5, P = 0.02, respectively).

Conclusions: Participants trained with the T-BLS training program showed shorter no-flow time and fewer interruptions during bystander CPR simulation assisted by a dispatcher.

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Source
http://dx.doi.org/10.1097/SIH.0000000000000286DOI Listing

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