TY - JOUR
T1 - Cardiovascular Rehabilitation With a WCD-Data From the CR3 Study (Cardiac Rehab Retrospective Review)
AU - Rohrer, Ursula
AU - Reischl, Anja
AU - Manninger, Martin
AU - Binder, Ronald K
AU - Fiedler, Lukas
AU - Gruska, Michael
AU - Altenberger, Johann
AU - Dorr, Andreas
AU - Steinwender, Clemens
AU - Stuehlinger, Markus
AU - Wonisch, Manfred
AU - Zirngast, Birgit
AU - Zweiker, David
AU - Zirlik, Andreas
AU - Scherr, Daniel
AU - Austrian WCD Study Group
N1 - Lehr-KH Rehabilitation Center Großgmain
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Purpose: Patients at risk for sudden cardiac death may temporarily need a wearable cardioverter-defibrillator (WCD). Exercise-based cardiac rehabilitation (CR) has a class I recommendation in patients with cardiac disease. The aim of this study was to evaluate the safety and feasibility of undergoing CR with a WCD. Methods: We performed a retrospective analysis of all patients with a WCD who completed a CR in Austria (2010-2020). Results: Patients (n = 55, 60 +/- 11 yr, 16% female) with a median baseline left ventricular ejection fraction (LVEF) of 36 (30, 41)% at the start of CR showed a daily WCD wearing duration of 23.4 (22, 24) hr. There were 2848 (8 [1, 26]/patient) automatic alarms and 340 (3 [1, 7]/patient) manual alarms generated. No shocks were delivered by the WCD during the CR period. One patient had recurrent hemodynamically tolerated ventricular tachycardias that were controlled with antiarrhythmic drugs. No severe WCD-associated adverse events occurred during the CR stay of a median 28 (28, 28) d. The fabric garment and the device setting needed to be adjusted in two patients to diminish inappropriate automatic alarms. Left ventricular ejection fraction after CR increased significantly to 42 (30, 44)% (P < .001). Wearable cardioverter-defibrillator therapy was stopped due to LVEF restitution in 53% of patients. In 36% of patients an implantable cardioverter-defibrillator was implanted, 6% had LVEF improvement after coronary revascularization, one patient received a heart transplantation (2%), two patients discontinued WCD treatment at their own request (4%). Conclusion: Completing CR is feasible and safe for WCD patients and may contribute positively to the restitution of cardiac function.
AB - Purpose: Patients at risk for sudden cardiac death may temporarily need a wearable cardioverter-defibrillator (WCD). Exercise-based cardiac rehabilitation (CR) has a class I recommendation in patients with cardiac disease. The aim of this study was to evaluate the safety and feasibility of undergoing CR with a WCD. Methods: We performed a retrospective analysis of all patients with a WCD who completed a CR in Austria (2010-2020). Results: Patients (n = 55, 60 +/- 11 yr, 16% female) with a median baseline left ventricular ejection fraction (LVEF) of 36 (30, 41)% at the start of CR showed a daily WCD wearing duration of 23.4 (22, 24) hr. There were 2848 (8 [1, 26]/patient) automatic alarms and 340 (3 [1, 7]/patient) manual alarms generated. No shocks were delivered by the WCD during the CR period. One patient had recurrent hemodynamically tolerated ventricular tachycardias that were controlled with antiarrhythmic drugs. No severe WCD-associated adverse events occurred during the CR stay of a median 28 (28, 28) d. The fabric garment and the device setting needed to be adjusted in two patients to diminish inappropriate automatic alarms. Left ventricular ejection fraction after CR increased significantly to 42 (30, 44)% (P < .001). Wearable cardioverter-defibrillator therapy was stopped due to LVEF restitution in 53% of patients. In 36% of patients an implantable cardioverter-defibrillator was implanted, 6% had LVEF improvement after coronary revascularization, one patient received a heart transplantation (2%), two patients discontinued WCD treatment at their own request (4%). Conclusion: Completing CR is feasible and safe for WCD patients and may contribute positively to the restitution of cardiac function.
KW - Humans
KW - Female
KW - Male
KW - Retrospective Studies
KW - Cardiac Rehabilitation
KW - Stroke Volume
KW - Ventricular Function, Left
KW - Electric Countershock
KW - Defibrillators, Implantable
U2 - 10.1097/HCR.0000000000000832
DO - 10.1097/HCR.0000000000000832
M3 - Review article
C2 - 38032261
SN - 1932-7501
VL - 44
SP - 115
EP - 120
JO - JOURNAL OF CARDIOPULMONARY REHABILITATION AND PREVENTION
JF - JOURNAL OF CARDIOPULMONARY REHABILITATION AND PREVENTION
IS - 2
ER -