Outcomes and characteristics of cardiac arrest in children with pulmonary hypertension: A secondary analysis of the ICU-RESUS clinical trial.
Blood pressure
Cardiac arrest
Cardiopulmonary resuscitation
Pediatrics
Pulmonary hypertension
Journal
Resuscitation
ISSN: 1873-1570
Titre abrégé: Resuscitation
Pays: Ireland
ID NLM: 0332173
Informations de publication
Date de publication:
09 2023
09 2023
Historique:
received:
26
04
2023
revised:
09
06
2023
accepted:
27
06
2023
pmc-release:
01
09
2024
medline:
28
8
2023
pubmed:
6
7
2023
entrez:
5
7
2023
Statut:
ppublish
Résumé
Previous studies have identified pulmonary hypertension (PH) as a relatively common diagnosis in children with in-hospital cardiac arrest (IHCA), and preclinical laboratory studies have found poor outcomes and low systemic blood pressures during CPR for PH-associated cardiac arrest. The objective of this study was to determine the prevalence of PH among children with IHCA and the association between PH diagnosis and intra-arrest physiology and survival outcomes. This was a prospectively designed secondary analysis of patients enrolled in the ICU-RESUS clinical trial (NCT02837497). The primary exposure was a pre-arrest diagnosis of PH. The primary survival outcome was survival to hospital discharge with favorable neurologic outcome (Pediatric Cerebral Performance Category score 1-3 or unchanged from baseline). The primary physiologic outcome was event-level average diastolic blood pressure (DBP) during CPR. Of 1276 patients with IHCAs during the study period, 1129 index IHCAs were enrolled; 184 (16.3%) had PH and 101/184 (54.9%) were receiving inhaled nitric oxide at the time of IHCA. Survival with favorable neurologic outcome was similar between patients with and without PH on univariate (48.9% vs. 54.4%; p = 0.17) and multivariate analyses (aOR 0.82 [95%CI: 0.56, 1.20]; p = 0.32). There were no significant differences in CPR event outcome or survival to hospital discharge. Average DBP, systolic BP, and end-tidal carbon dioxide during CPR were similar between groups. In this prospective study of pediatric IHCA, pre-existing PH was present in 16% of children. Pre-arrest PH diagnosis was not associated with statistically significant differences in survival outcomes or intra-arrest physiologic measures.
Sections du résumé
BACKGROUND
Previous studies have identified pulmonary hypertension (PH) as a relatively common diagnosis in children with in-hospital cardiac arrest (IHCA), and preclinical laboratory studies have found poor outcomes and low systemic blood pressures during CPR for PH-associated cardiac arrest. The objective of this study was to determine the prevalence of PH among children with IHCA and the association between PH diagnosis and intra-arrest physiology and survival outcomes.
METHODS
This was a prospectively designed secondary analysis of patients enrolled in the ICU-RESUS clinical trial (NCT02837497). The primary exposure was a pre-arrest diagnosis of PH. The primary survival outcome was survival to hospital discharge with favorable neurologic outcome (Pediatric Cerebral Performance Category score 1-3 or unchanged from baseline). The primary physiologic outcome was event-level average diastolic blood pressure (DBP) during CPR.
RESULTS
Of 1276 patients with IHCAs during the study period, 1129 index IHCAs were enrolled; 184 (16.3%) had PH and 101/184 (54.9%) were receiving inhaled nitric oxide at the time of IHCA. Survival with favorable neurologic outcome was similar between patients with and without PH on univariate (48.9% vs. 54.4%; p = 0.17) and multivariate analyses (aOR 0.82 [95%CI: 0.56, 1.20]; p = 0.32). There were no significant differences in CPR event outcome or survival to hospital discharge. Average DBP, systolic BP, and end-tidal carbon dioxide during CPR were similar between groups.
CONCLUSIONS
In this prospective study of pediatric IHCA, pre-existing PH was present in 16% of children. Pre-arrest PH diagnosis was not associated with statistically significant differences in survival outcomes or intra-arrest physiologic measures.
Identifiants
pubmed: 37406760
pii: S0300-9572(23)00210-1
doi: 10.1016/j.resuscitation.2023.109897
pmc: PMC10530491
mid: NIHMS1915950
pii:
doi:
Banques de données
ClinicalTrials.gov
['NCT02837497']
Types de publication
Clinical Trial
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
109897Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL131544
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL147616
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL153759
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD049983
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD050096
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL148541
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD063108
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD083171
Pays : United States
Organisme : NICHD NIH HHS
ID : U01 HD049934
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD049981
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD083170
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD083166
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2023 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Financial support for this project was provided through the National Institutes of Health Eunice Kennedy Shriver National Institute of Child Health and Human Development (U01HD049934, UG1HD049981, UG1HD049983, UG1HD050096, UG1HD063108, UG1HD083166, UG1HD083170, and UG1HD083171) and National Heart, Lung, and Blood Institute (R01HL131544, R01HL147616, K23HL148541, and K23HL153759) and by the Children’s Hospital of Philadelphia Resuscitation Science Center and Department of Anesthesiology and Critical Care Medicine.
Références
Crit Care. 2015 Sep 15;19:328
pubmed: 26369409
Resuscitation. 2021 May;162:351-364
pubmed: 33515637
Pediatr Crit Care Med. 2020 Apr;21(4):305-313
pubmed: 31688674
Pediatr Crit Care Med. 2017 Oct;18(10):935-943
pubmed: 28737598
JAMA. 2022 Mar 8;327(10):934-945
pubmed: 35258533
Resuscitation. 2004 Dec;63(3):233-49
pubmed: 15582757
Pediatrics. 2006 Dec;118(6):2424-33
pubmed: 17142528
Crit Care. 2023 Mar 13;27(1):105
pubmed: 36915182
Circulation. 2019 Oct 29;140(18):e746-e757
pubmed: 31522544
Crit Care. 2015 Nov 17;19:408
pubmed: 26577797
JAMA Pediatr. 2017 Jan 1;171(1):39-45
pubmed: 27820606
Am J Respir Crit Care Med. 2018 Apr 1;197(7):905-912
pubmed: 29244522
Crit Care Med. 2023 Jan 1;51(1):91-102
pubmed: 36519983
Trials. 2018 Apr 3;19(1):213
pubmed: 29615134
Circulation. 2018 Apr 24;137(17):1784-1795
pubmed: 29279413
Eur Respir J. 2019 Jan 24;53(1):
pubmed: 30545978
J Pediatr. 1992 Jul;121(1):68-74
pubmed: 1625096
Am J Respir Crit Care Med. 2021 Aug 15;204(4):454-461
pubmed: 33798036
Crit Care Med. 2013 Oct;41(10):2292-7
pubmed: 23921270
N Engl J Med. 2006 Jun 1;354(22):2328-39
pubmed: 16738269
Resuscitation. 2021 May;162:274-283
pubmed: 33766668
Pediatr Crit Care Med. 2020 Aug;21(8):708-719
pubmed: 32195895
Am J Respir Crit Care Med. 2016 Oct 1;194(7):898-906
pubmed: 27689707
Resuscitation. 2021 Nov;168:52-57
pubmed: 34536558
Crit Care Med. 2020 Jun;48(6):881-889
pubmed: 32301844
J Pediatr. 2019 Aug;211:63-71.e6
pubmed: 31176455
Circ Cardiovasc Qual Outcomes. 2019 Jul 09;12(7):e005580
pubmed: 31545574
Circulation. 2013 Jan 29;127(4):442-51
pubmed: 23339874