Outcomes and factors associated with early mortality in pediatric and neonatal patients requiring extracorporeal membrane oxygenation for heart and lung failure.

Pediatric and neonatal patients congenital cardiac surgery (CCS) extracorporeal membrane oxygenation (ECMO) neonatal and pediatric intensive care unit resuscitation

Journal

Journal of thoracic disease
ISSN: 2072-1439
Titre abrégé: J Thorac Dis
Pays: China
ID NLM: 101533916

Informations de publication

Date de publication:
Apr 2019
Historique:
entrez: 12 6 2019
pubmed: 12 6 2019
medline: 12 6 2019
Statut: ppublish

Résumé

Mortality and morbidity after surgical repair for complex congenital heart defects and severe cardiopulmonary failure on extracorporeal membrane oxygenation (ECMO) support remain high despite significant advances in medical management and technological improvements. We report on outcomes and factors after using ECMO in our surgical pediatric population including short- and long-term survival. A total of 45 neonatal and pediatric patients were identified who needed ECMO in our department between January 2008 and December 2016. In 41 cases (91%) a vaECMO (ECLS) was implemented, whereas 4 patients (9%) received vvECMO treatment for respiratory failure. In 33 cases vaECMO was implanted following cardiac surgery for congenital heart disease (CHD), whereas in 8 patients ECMO was utilized by means of extracorporeal cardiopulmonary resuscitation (eCPR) following refractory cardiac arrest. The primary endpoint of the present study was survival to discharge and long-term survival free from neurological impairments. Univariate and bivariate analysis was performed to address predictors for outcome. Kaplan-Meier survival analysis was used to address mid- and long-term survival. Median [IQR] duration of ECMO support was 3 [2, 5] days (range, 1-17 days). Median age at ECMO implantation was 128 [14, 1,813] days, median weight of patients was 5.4 [3.3, 12] kg. Totally 10 patients included in this study were diagnosed with concomitant genetic conditions. A total of 20 (44%) patients were successfully weaned off ECMO (survived >24 h after ECMO explantation), whereas 15 (33%) of them survived to discharge. Single ventricle (SV) repair was performed in 14, biventricular repair in 19 patients. Neonates (<30 days of age), female patients, patients with genetic conditions, SV repair patients, and eCPR patient cohort showed lower odds of survival on ECMO. Failed myocardial recovery (P=0.001), profound circulatory failure despite a high dose of catecholamines (P<0.001), neurological impairment pre-ECMO and post-ECMO (P=0.04 and P<0.001, respectively), and severe pulmonary failure despite high respiratory pressure settings were most common mortality reasons. ECMO provides efficient therapy opportunities for life-threatening conditions. Nevertheless, neonates and pediatric patients who underwent ECMO were at high risk for cerebrovascular events and poor survival. Appropriate patient selection using predictors of outcome reducing complications might improve outcomes of this patient cohort.

Sections du résumé

BACKGROUND BACKGROUND
Mortality and morbidity after surgical repair for complex congenital heart defects and severe cardiopulmonary failure on extracorporeal membrane oxygenation (ECMO) support remain high despite significant advances in medical management and technological improvements. We report on outcomes and factors after using ECMO in our surgical pediatric population including short- and long-term survival.
METHODS METHODS
A total of 45 neonatal and pediatric patients were identified who needed ECMO in our department between January 2008 and December 2016. In 41 cases (91%) a vaECMO (ECLS) was implemented, whereas 4 patients (9%) received vvECMO treatment for respiratory failure. In 33 cases vaECMO was implanted following cardiac surgery for congenital heart disease (CHD), whereas in 8 patients ECMO was utilized by means of extracorporeal cardiopulmonary resuscitation (eCPR) following refractory cardiac arrest. The primary endpoint of the present study was survival to discharge and long-term survival free from neurological impairments. Univariate and bivariate analysis was performed to address predictors for outcome. Kaplan-Meier survival analysis was used to address mid- and long-term survival.
RESULTS RESULTS
Median [IQR] duration of ECMO support was 3 [2, 5] days (range, 1-17 days). Median age at ECMO implantation was 128 [14, 1,813] days, median weight of patients was 5.4 [3.3, 12] kg. Totally 10 patients included in this study were diagnosed with concomitant genetic conditions. A total of 20 (44%) patients were successfully weaned off ECMO (survived >24 h after ECMO explantation), whereas 15 (33%) of them survived to discharge. Single ventricle (SV) repair was performed in 14, biventricular repair in 19 patients. Neonates (<30 days of age), female patients, patients with genetic conditions, SV repair patients, and eCPR patient cohort showed lower odds of survival on ECMO. Failed myocardial recovery (P=0.001), profound circulatory failure despite a high dose of catecholamines (P<0.001), neurological impairment pre-ECMO and post-ECMO (P=0.04 and P<0.001, respectively), and severe pulmonary failure despite high respiratory pressure settings were most common mortality reasons.
CONCLUSIONS CONCLUSIONS
ECMO provides efficient therapy opportunities for life-threatening conditions. Nevertheless, neonates and pediatric patients who underwent ECMO were at high risk for cerebrovascular events and poor survival. Appropriate patient selection using predictors of outcome reducing complications might improve outcomes of this patient cohort.

Identifiants

pubmed: 31183167
doi: 10.21037/jtd.2018.11.107
pii: jtd-11-S6-S871
pmc: PMC6535479
doi:

Types de publication

Journal Article

Langues

eng

Pagination

S871-S888

Déclaration de conflit d'intérêts

Conflict of Interest: The authors have no conflicts of interest to declare.

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Auteurs

Farid Azizov (F)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Julia Merkle (J)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Javid Fatullayev (J)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Kaveh Eghbalzadeh (K)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Ilija Djordjevic (I)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Carolyn Weber (C)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Sergey Saenko (S)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Axel Kroener (A)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Mohamed Zeriouh (M)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Anton Sabashnikov (A)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Gerardus Bennink (G)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Thorsten Wahlers (T)

Department of Cardiothoracic Surgery, University Hospital of Cologne, Cologne, Germany.

Classifications MeSH