Risk Factors and Outcomes of Sudden Cardiac Arrest in Pediatric Heart Transplant Recipients

Background: Sudden cardiac arrest (SCA) is a prevailing cause of mortality after pediatric heart transplant (HT) but remains understudied. We analyzed the incidence, outcomes, and risk factors for SCA at our center. Methods: Retrospective review of all pediatric HT patients at our center from 1/1/20...

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Veröffentlicht in:The American heart journal 2022-10, Vol.252, p.31-38
Hauptverfasser: Hollander, Seth A, Barkoff, Lynsey, Giacone, Heather, Adamson, Greg T, Kaufman, Beth D, Motonaga, Kara S, Dubin, Anne M., Chubb, Henry
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container_end_page 38
container_issue
container_start_page 31
container_title The American heart journal
container_volume 252
creator Hollander, Seth A
Barkoff, Lynsey
Giacone, Heather
Adamson, Greg T
Kaufman, Beth D
Motonaga, Kara S
Dubin, Anne M.
Chubb, Henry
description Background: Sudden cardiac arrest (SCA) is a prevailing cause of mortality after pediatric heart transplant (HT) but remains understudied. We analyzed the incidence, outcomes, and risk factors for SCA at our center. Methods: Retrospective review of all pediatric HT patients at our center from 1/1/2009-9/1/2021. SCA was defined as an abrupt loss of cardiac function requiring cardiopulmonary resuscitation and/or mechanical circulatory support (MCS). Events that occurred in the setting of limited resuscitative wishes, or while on MCS were excluded. Patient characteristics and risk factors were analyzed. Results: Fourteen of 254 (6%) experienced SCA at a median of 3 (1, 4) years post-HT. Seven (50%) events occurred out-of-hospital. Eleven (79%) died from their initial event, 2 (18%) after failure to separate from extracorporeal membrane (ECMO). In univariate analysis, black race, younger donor age, prior acute cellular rejection (ACR) episode, pacemaker and/or ICD in place, and pre-mortem diagnosis of allograft vasculopathy were associated with SCA (P=0.003-0.02). In multivariable analysis, history of ACR, younger donor age, and black race retained significance. [OR=6.3, 95% CI: 1.6-25.4, P=0.01], [OR=0.9, 95% CI: 0.8-1, P=0.04], and [OR=7.3, 95% CI: 1.1-49.9, P=0.04], respectively. SCA occurred in 3 patients with a functioning ICD or pacemaker, which failed to restore a perfusing rhythm. Conclusions: SCA occurs relatively early after pediatric HT and is usually fatal. Half of events happen at home. Those who received younger donors, have a history of ACR, or are of black race are at increased risk. ICDs/pacemakers may offer limited protection.
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We analyzed the incidence, outcomes, and risk factors for SCA at our center. Methods: Retrospective review of all pediatric HT patients at our center from 1/1/2009-9/1/2021. SCA was defined as an abrupt loss of cardiac function requiring cardiopulmonary resuscitation and/or mechanical circulatory support (MCS). Events that occurred in the setting of limited resuscitative wishes, or while on MCS were excluded. Patient characteristics and risk factors were analyzed. Results: Fourteen of 254 (6%) experienced SCA at a median of 3 (1, 4) years post-HT. Seven (50%) events occurred out-of-hospital. Eleven (79%) died from their initial event, 2 (18%) after failure to separate from extracorporeal membrane (ECMO). In univariate analysis, black race, younger donor age, prior acute cellular rejection (ACR) episode, pacemaker and/or ICD in place, and pre-mortem diagnosis of allograft vasculopathy were associated with SCA (P=0.003-0.02). In multivariable analysis, history of ACR, younger donor age, and black race retained significance. [OR=6.3, 95% CI: 1.6-25.4, P=0.01], [OR=0.9, 95% CI: 0.8-1, P=0.04], and [OR=7.3, 95% CI: 1.1-49.9, P=0.04], respectively. SCA occurred in 3 patients with a functioning ICD or pacemaker, which failed to restore a perfusing rhythm. Conclusions: SCA occurs relatively early after pediatric HT and is usually fatal. Half of events happen at home. Those who received younger donors, have a history of ACR, or are of black race are at increased risk. ICDs/pacemakers may offer limited protection.</description><identifier>ISSN: 0002-8703</identifier><identifier>EISSN: 1097-6744</identifier><identifier>DOI: 10.1016/j.ahj.2022.06.003</identifier><identifier>PMID: 35705134</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Age ; Autopsies ; Cardiac arrest ; Cardiac arrhythmia ; Data collection ; Death &amp; dying ; Defibrillator ; Defibrillators ; Extracorporeal membrane oxygenation ; Failure analysis ; Fatalities ; Graft rejection ; Heart failure ; Heart Transplantation ; Heart transplants ; Hemodynamics ; Medical prognosis ; Pacemaker ; Pacemakers ; Patients ; Pediatric ; Pediatrics ; Race ; Resuscitation ; Risk analysis ; Risk factors ; Sudden Cardiac Arrest ; Transplants &amp; implants ; Vascular diseases</subject><ispartof>The American heart journal, 2022-10, Vol.252, p.31-38</ispartof><rights>2022</rights><rights>Copyright © 2022. 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We analyzed the incidence, outcomes, and risk factors for SCA at our center. Methods: Retrospective review of all pediatric HT patients at our center from 1/1/2009-9/1/2021. SCA was defined as an abrupt loss of cardiac function requiring cardiopulmonary resuscitation and/or mechanical circulatory support (MCS). Events that occurred in the setting of limited resuscitative wishes, or while on MCS were excluded. Patient characteristics and risk factors were analyzed. Results: Fourteen of 254 (6%) experienced SCA at a median of 3 (1, 4) years post-HT. Seven (50%) events occurred out-of-hospital. Eleven (79%) died from their initial event, 2 (18%) after failure to separate from extracorporeal membrane (ECMO). In univariate analysis, black race, younger donor age, prior acute cellular rejection (ACR) episode, pacemaker and/or ICD in place, and pre-mortem diagnosis of allograft vasculopathy were associated with SCA (P=0.003-0.02). In multivariable analysis, history of ACR, younger donor age, and black race retained significance. [OR=6.3, 95% CI: 1.6-25.4, P=0.01], [OR=0.9, 95% CI: 0.8-1, P=0.04], and [OR=7.3, 95% CI: 1.1-49.9, P=0.04], respectively. SCA occurred in 3 patients with a functioning ICD or pacemaker, which failed to restore a perfusing rhythm. Conclusions: SCA occurs relatively early after pediatric HT and is usually fatal. Half of events happen at home. Those who received younger donors, have a history of ACR, or are of black race are at increased risk. 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We analyzed the incidence, outcomes, and risk factors for SCA at our center. Methods: Retrospective review of all pediatric HT patients at our center from 1/1/2009-9/1/2021. SCA was defined as an abrupt loss of cardiac function requiring cardiopulmonary resuscitation and/or mechanical circulatory support (MCS). Events that occurred in the setting of limited resuscitative wishes, or while on MCS were excluded. Patient characteristics and risk factors were analyzed. Results: Fourteen of 254 (6%) experienced SCA at a median of 3 (1, 4) years post-HT. Seven (50%) events occurred out-of-hospital. Eleven (79%) died from their initial event, 2 (18%) after failure to separate from extracorporeal membrane (ECMO). In univariate analysis, black race, younger donor age, prior acute cellular rejection (ACR) episode, pacemaker and/or ICD in place, and pre-mortem diagnosis of allograft vasculopathy were associated with SCA (P=0.003-0.02). In multivariable analysis, history of ACR, younger donor age, and black race retained significance. [OR=6.3, 95% CI: 1.6-25.4, P=0.01], [OR=0.9, 95% CI: 0.8-1, P=0.04], and [OR=7.3, 95% CI: 1.1-49.9, P=0.04], respectively. SCA occurred in 3 patients with a functioning ICD or pacemaker, which failed to restore a perfusing rhythm. Conclusions: SCA occurs relatively early after pediatric HT and is usually fatal. Half of events happen at home. Those who received younger donors, have a history of ACR, or are of black race are at increased risk. 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subjects Age
Autopsies
Cardiac arrest
Cardiac arrhythmia
Data collection
Death & dying
Defibrillator
Defibrillators
Extracorporeal membrane oxygenation
Failure analysis
Fatalities
Graft rejection
Heart failure
Heart Transplantation
Heart transplants
Hemodynamics
Medical prognosis
Pacemaker
Pacemakers
Patients
Pediatric
Pediatrics
Race
Resuscitation
Risk analysis
Risk factors
Sudden Cardiac Arrest
Transplants & implants
Vascular diseases
title Risk Factors and Outcomes of Sudden Cardiac Arrest in Pediatric Heart Transplant Recipients
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