Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism.


Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
07 2022
Historique:
received: 30 08 2021
revised: 24 02 2022
accepted: 24 03 2022
pubmed: 1 4 2022
medline: 29 6 2022
entrez: 31 3 2022
Statut: ppublish

Résumé

To assess the outcomes of neonates in a contemporary multi-institutional cohort who receive renal replacement therapy (RRT) for hyperammonemia. We performed a retrospective analysis of 51 neonatal patients with confirmed inborn errors of metabolism that were treated at 9 different children's hospitals in the US between 2000 and 2015. Twenty-nine patients received hemodialysis (57%), 21 patients received continuous renal replacement therapy (41%), and 1 patient received peritoneal dialysis (2%). The median age at admission of both survivors (n = 33 [65%]) and nonsurvivors (n = 18) was 3 days. Peak ammonia and ammonia at admission were not significantly different between survivors and nonsurvivors. Hemodialysis, having more than 1 indication for RRT in addition to hyperammonemia, and complications during RRT were all risk factors for mortality. After accounting for multiple patient factors by multivariable analyses, hemodialysis was associated with a higher risk of death compared with continuous renal replacement therapy. When clinical factors including evidence of renal dysfunction, number of complications, concurrent extracorporeal membrane oxygenation, vasopressor requirement, and degree of hyperammonemia were held constant in a single Cox regression model, the hazard ratio for death with hemodialysis was 4.07 (95% CI 0.908-18.2, P value = .067). To help providers caring for neonates with hyperammonemia understand their patient's likelihood of survival, we created a predictive model with input variables known at the start of RRT. Our large, multicenter retrospective review supports the use of continuous renal replacement therapy for neonatal hyperammonemia.

Identifiants

pubmed: 35358588
pii: S0022-3476(22)00293-1
doi: 10.1016/j.jpeds.2022.03.043
pmc: PMC9233075
mid: NIHMS1808145
pii:
doi:

Substances chimiques

Ammonia 7664-41-7

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

116-122.e1

Subventions

Organisme : NIDDK NIH HHS
ID : L40 DK130155
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

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Auteurs

Elizabeth G Ames (EG)

Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, University of Michigan Health System, Ann Arbor, MI. Electronic address: amese@med.umich.edu.

Corey Powell (C)

Consulting for Statistics, Computing and Analytics Research, University of Michigan, Ann Arbor, MI.

Rachel M Engen (RM)

Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL.

Donald J Weaver (DJ)

Division of Nephrology and Hypertension, Department of Pediatrics, Atrium Health Levine Children's, Charlotte, NC.

Asif Mansuri (A)

Children's Hospital of Georgia, Augusta University, Augusta, GA.

Michelle N Rheault (MN)

University of Minnesota Masonic Children's Hospital, Minneapolis, MN.

Keia Sanderson (K)

University of North Carolina Department of Medicine-Nephrology, Chapel Hill, NC.

Uta Lichter-Konecki (U)

Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA.

Ankana Daga (A)

Division of Nephrology, Boston Children's Hospital, Boston, MA.

Lindsay C Burrage (LC)

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

Ayesha Ahmad (A)

Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, University of Michigan Health System, Ann Arbor, MI.

Scott E Wenderfer (SE)

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

Kera E Luckritz (KE)

Division of Pediatric Nephrology, Department of Pediatrics, University of Michigan Health System, Ann Arbor, MI.

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