Procedural Outcomes of Pulmonary Atresia With Intact Ventricular Septum in Neonates: A Multicenter Study.


Journal

The Annals of thoracic surgery
ISSN: 1552-6259
Titre abrégé: Ann Thorac Surg
Pays: Netherlands
ID NLM: 15030100R

Informations de publication

Date de publication:
06 2023
Historique:
received: 04 01 2022
revised: 10 06 2022
accepted: 19 07 2022
medline: 26 5 2023
pubmed: 8 9 2022
entrez: 7 9 2022
Statut: ppublish

Résumé

Multicenter contemporary data describing short-term outcomes after initial interventions of neonates with pulmonary atresia with intact ventricular septum (PA-IVS) are limited. This multicenter study describes characteristics and outcomes of PA-IVS neonates after their initial catheter or surgical intervention and identifies factors associated with major adverse cardiac events (MACE). Neonates with PA-IVS who underwent surgical or catheter intervention between 2009 and 2019 in 19 centers were reviewed. Risk factors for MACE, defined as cardiopulmonary resuscitation, mechanical circulatory support, stroke, or in-hospital mortality, were analyzed using multivariable logistic regression models. We reviewed 279 neonates: 79 (28%) underwent right ventricular decompression, 151 (54%) underwent systemic-to-pulmonary shunt or ductal stent placement only, 36 (13%) underwent right ventricular decompression with shunt or ductal stent placement, and 11 (4%) underwent transplantation. MACE occurred in 57 patients (20%): 26 (9%) received mechanical circulatory support, 37 (13%) received cardiopulmonary resuscitation, stroke occurred in 16 (6%), and 23 (8%) died. The presence of 2 major coronary artery stenoses (adjusted odds ratio, 4.99; 95% CI, 1.16-21.39) and lower weight at first intervention (adjusted odds ratio, 1.52; 95% CI, 1.01-2.27) were significantly associated with MACE. Coronary ischemia was the most frequent presumed mechanism of death (n = 10). In a multicenter cohort, 1 in 5 neonates with PA-IVS experienced MACE after their initial intervention. Patients with 2 major coronary artery stenoses or lower weight at the time of the initial procedure were most likely to experience MACE and warrant vigilance during preintervention planning and postintervention management.

Sections du résumé

BACKGROUND
Multicenter contemporary data describing short-term outcomes after initial interventions of neonates with pulmonary atresia with intact ventricular septum (PA-IVS) are limited. This multicenter study describes characteristics and outcomes of PA-IVS neonates after their initial catheter or surgical intervention and identifies factors associated with major adverse cardiac events (MACE).
METHODS
Neonates with PA-IVS who underwent surgical or catheter intervention between 2009 and 2019 in 19 centers were reviewed. Risk factors for MACE, defined as cardiopulmonary resuscitation, mechanical circulatory support, stroke, or in-hospital mortality, were analyzed using multivariable logistic regression models.
RESULTS
We reviewed 279 neonates: 79 (28%) underwent right ventricular decompression, 151 (54%) underwent systemic-to-pulmonary shunt or ductal stent placement only, 36 (13%) underwent right ventricular decompression with shunt or ductal stent placement, and 11 (4%) underwent transplantation. MACE occurred in 57 patients (20%): 26 (9%) received mechanical circulatory support, 37 (13%) received cardiopulmonary resuscitation, stroke occurred in 16 (6%), and 23 (8%) died. The presence of 2 major coronary artery stenoses (adjusted odds ratio, 4.99; 95% CI, 1.16-21.39) and lower weight at first intervention (adjusted odds ratio, 1.52; 95% CI, 1.01-2.27) were significantly associated with MACE. Coronary ischemia was the most frequent presumed mechanism of death (n = 10).
CONCLUSIONS
In a multicenter cohort, 1 in 5 neonates with PA-IVS experienced MACE after their initial intervention. Patients with 2 major coronary artery stenoses or lower weight at the time of the initial procedure were most likely to experience MACE and warrant vigilance during preintervention planning and postintervention management.

Identifiants

pubmed: 36070807
pii: S0003-4975(22)01185-7
doi: 10.1016/j.athoracsur.2022.07.055
pii:
doi:

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1470-1477

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Eva W Cheung (EW)

Division of Pediatric Critical Care & Hospital Medicine, Columbia University Irving Medical Center, New York, New York. Electronic address: ec2335@cumc.columbia.edu.

Christopher W Mastropietro (CW)

Division of Pediatric Critical Care, Indiana University School of Medicine, Riley Hospital for Children, Indianapolis, Indiana.

Saul Flores (S)

Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas.

Venugopal Amula (V)

Division of Pediatric Critical Care, University of Utah Health, Salt Lake City, Utah.

Monique Radman (M)

Division of Pediatric Critical Care, University of Washington, Seattle Children's Hospital, Seattle, Washington.

David Kwiatkowski (D)

Division of Pediatric Cardiology, Stanford University School of Medicine, Lucille Packard Children's Hospital, Palo Alto, California.

Bao Nguyen Puente (BN)

Division of Cardiac Critical Care, Children's National Health System, Washington, DC.

Jason R Buckley (JR)

Division of Pediatric Cardiology, Medical University of South Carolina, Charleston, South Carolina.

Kiona Allen (K)

Division of Pediatric Cardiology, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Rohit Loomba (R)

Department of Pediatrics, Chicago Medical School, Advocate Children's Hospital, Chicago, Illinois.

Karan Karki (K)

Division of Pediatric Cardiology, University of Tennessee Health Science Center, Le Bonheur Children's Hospital, Memphis, Tennessee.

Saurabh Chiwane (S)

Division of Pediatric Critical Care, Saint Louis University, Cardinal Glennon Children's Hospital, Saint Louis, Missouri.

Katherine Cashen (K)

Division of Critical Care Medicine, Duke University, Duke Children's Hospital, Durham, North Carolina.

Kurt Piggott (K)

Department of Pediatrics, LSU School of Medicine Children's Hospital, New Orleans, Louisiana.

Yamini Kapileshwarkar (Y)

Department of Pediatrics, Children's Hospital of Illinois, Peoria, Illinois.

Keshava Murthy Narayana Gowda (KMN)

Department of Pediatrics, Cleveland Clinic, Cleveland, Ohio.

Aditya Badheka (A)

Department of Pediatrics, University of Iowa Stead Family Children's Hospital, Iowa City, Iowa.

Rahul Raman (R)

Department of Pediatrics, Mercy Medical Center, Des Moines, Iowa.

John M Costello (JM)

Division of Pediatric Cardiology, Medical University of South Carolina, Charleston, South Carolina.

Huaiyu Zang (H)

The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Ilias Iliopoulos (I)

The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

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