TY - JOUR
T1 - Use of a wearable automated defibrillator in children compared to young adults
AU - Collins, Kathryn K.
AU - Silva, Jennifer N.A.
AU - Rhee, Edward K.
AU - Schaffer, Michael S.
PY - 2010/9/1
Y1 - 2010/9/1
N2 - Background: A wearable automated external defibrillator has been shown to be efficacious in the prevention of sudden death in adults who had a history of cardiac arrest but who did not have a permanent internal cardioverter/ defibrillator (ICD) placed. The use of a wearable defibrillator has not been established in the pediatric population. Methods: We retrospectively reviewed the clinical database for the wearable external defibrillator from ZOLL Lifecor Corporation (Pittsburgh, PA, USA). We compared the use of the wearable defibrillator in patients ≤18 years of age to those aged 19-21 years. Results: There were 81 patients ≤18 years of age (median age = 16.5 years [9-18] and 52% male). There were 103 patients aged 19-21 years (median age = 20 years [19-21] and 47% male). There was no difference between groups in average hours/day or in total number of days the patients wore the defibrillator. In patients ≤18 years of age, there was one inappropriate therapy and one withholding of therapy due to a device-device interaction. In patients aged 19-21 years, there were five appropriate discharges in two patients and one inappropriate discharge in a single patient. Conclusion: It is reasonable to consider the wearable automated external defibrillator as a therapy for pediatric patients who are at high risk of sudden cardiac arrest but who have contraindications to or would like to defer placement of a permanent ICD. As there were no appropriate shocks in our patients ≤18 years of age, this study cannot address efficacy of the therapy.
AB - Background: A wearable automated external defibrillator has been shown to be efficacious in the prevention of sudden death in adults who had a history of cardiac arrest but who did not have a permanent internal cardioverter/ defibrillator (ICD) placed. The use of a wearable defibrillator has not been established in the pediatric population. Methods: We retrospectively reviewed the clinical database for the wearable external defibrillator from ZOLL Lifecor Corporation (Pittsburgh, PA, USA). We compared the use of the wearable defibrillator in patients ≤18 years of age to those aged 19-21 years. Results: There were 81 patients ≤18 years of age (median age = 16.5 years [9-18] and 52% male). There were 103 patients aged 19-21 years (median age = 20 years [19-21] and 47% male). There was no difference between groups in average hours/day or in total number of days the patients wore the defibrillator. In patients ≤18 years of age, there was one inappropriate therapy and one withholding of therapy due to a device-device interaction. In patients aged 19-21 years, there were five appropriate discharges in two patients and one inappropriate discharge in a single patient. Conclusion: It is reasonable to consider the wearable automated external defibrillator as a therapy for pediatric patients who are at high risk of sudden cardiac arrest but who have contraindications to or would like to defer placement of a permanent ICD. As there were no appropriate shocks in our patients ≤18 years of age, this study cannot address efficacy of the therapy.
KW - cardioverter/defibrillator
KW - pediatrics
KW - sudden death
KW - ventricular arrhythmias
UR - http://www.scopus.com/inward/record.url?scp=77956330940&partnerID=8YFLogxK
U2 - 10.1111/j.1540-8159.2010.02819.x
DO - 10.1111/j.1540-8159.2010.02819.x
M3 - Article
C2 - 20561227
AN - SCOPUS:77956330940
SN - 0147-8389
VL - 33
SP - 1119
EP - 1124
JO - PACE - Pacing and Clinical Electrophysiology
JF - PACE - Pacing and Clinical Electrophysiology
IS - 9
ER -