Literature DB >> 21496527

Costs of congenital diaphragmatic hernia repair in the United States-extracorporeal membrane oxygenation foots the bill.

Mehul V Raval1, Xue Wang2, Marleta Reynolds3, Anne C Fischer4.   

Abstract

BACKGROUND: Congenital diaphragmatic hernia (CDH) is the costliest noncardiac congenital defect. Extracorporeal membrane oxygenation (ECMO) is a treatment strategy offered to those babies with CDH who would not otherwise survive on conventional therapy. The primary objective of our study was to identify the leading source of expenditures in CDH care.
METHODS: All patients surviving CDH repair were identified in the Kids' Inpatient Database (KID) from 1997 to 2006, with costs converted to 2006 US dollars. Patients were categorized into groups based on severity of disease for comparison including CDH repair only, prolonged ventilator dependence, and ECMO use. Factors associated with greater expenditures in CDH management were analyzed using a regression model.
RESULTS: Eight hundred thirty-nine patients from 213 hospitals were studied. Extracorporeal membrane oxygenation use decreased from 18.2% in 1997 to 11.4% in 2006 (P = .002). Congenital diaphragmatic hernia survivors managed with ECMO cost more than 2.4 times as much as CDH survivors requiring only prolonged ventilation postrepair and 3.5 times as much as those with CDH repair only (both P < .001). Age, multiplicity of diagnoses, patient transfer, inhaled nitric oxide use, prolonged ventilation, and ECMO use were all associated with higher costs. Extracorporeal membrane oxygenation use was the single most important factor associated with higher costs, increasing expenditures 2.4-fold (95% confidence interval, 2.1-2.8). Though the CDH repair with ECMO group constituted 12.2% of patients, this group has the highest median costs ($156,499.90/patient) and constitutes 28.5% of national costs based on CDH survivors in the KID. Annual national cost for CDH survivors is $158 million based on the KID, and projected burden for all CDH patients exceeds $250 million/year.
CONCLUSIONS: Extracorporeal membrane oxygenation use is the largest contributing factor to the economic burden in CDH. With limited health care resources, judicious resource utilization in CDH care merits further study.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21496527     DOI: 10.1016/j.jpedsurg.2010.09.047

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  14 in total

1.  Population-Based Validation of a Clinical Prediction Model for Congenital Diaphragmatic Hernias.

Authors:  Daniel P Bent; Jason Nelson; David M Kent; Howard C Jen
Journal:  J Pediatr       Date:  2018-06-25       Impact factor: 4.406

2.  Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia.

Authors:  Lan Yu; Ashley D Sawle; Julia Wynn; Gudrun Aspelund; Charles J Stolar; Marc S Arkovitz; Douglas Potoka; Kenneth S Azarow; George B Mychaliska; Yufeng Shen; Wendy K Chung
Journal:  Hum Mol Genet       Date:  2015-06-01       Impact factor: 6.150

3.  Vascular Endothelial Growth Factor Enhances Compensatory Lung Growth in Piglets.

Authors:  Duy T Dao; Lorenzo Anez-Bustillos; Amy Pan; Alison A O'Loughlin; Paul D Mitchell; Gillian L Fell; Meredith A Baker; Bennet S Cho; Prathima Nandivada; Arthur P Nedder; Charles J Smithers; Nancy Chen; Robert Comeau; Kevin Holmes; Susan Kalled; Angela Norton; Bohong Zhang; Mark Puder
Journal:  Surgery       Date:  2018-09-05       Impact factor: 3.982

4.  Pulmonary support on day of life 30 is a strong predictor of increased 1 and 5-year morbidity in survivors of congenital diaphragmatic hernia.

Authors:  Ryan P Cauley; Kristina Potanos; Nora Fullington; Sigrid Bairdain; Catherine A Sheils; Jonathan A Finkelstein; Dionne A Graham; Jay M Wilson
Journal:  J Pediatr Surg       Date:  2014-12-17       Impact factor: 2.545

Review 5.  Congenital diaphragmatic hernia.

Authors:  Augusto Zani; Wendy K Chung; Jan Deprest; Matthew T Harting; Tim Jancelewicz; Shaun M Kunisaki; Neil Patel; Lina Antounians; Pramod S Puligandla; Richard Keijzer
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6.  Fibroblast-derived Hgf controls recruitment and expansion of muscle during morphogenesis of the mammalian diaphragm.

Authors:  Elizabeth M Sefton; Mirialys Gallardo; Claire E Tobin; Brittany C Collins; Mary P Colasanto; Allyson J Merrell; Gabrielle Kardon
Journal:  Elife       Date:  2022-09-26       Impact factor: 8.713

7.  The Canadian Pediatric Surgery Network Congenital Diaphragmatic Hernia Evidence Review Project: Developing national guidelines for care.

Authors:  Pramod S Puligandla; Erik D Skarsgard
Journal:  Paediatr Child Health       Date:  2016-05       Impact factor: 2.253

8.  Pulmonary support on day 30 as a predictor of morbidity and mortality in congenital diaphragmatic hernia.

Authors:  Ryan P Cauley; Alexander Stoffan; Kristina Potanos; Nora Fullington; Dionne A Graham; Jonathan A Finkelstein; Heung Bae Kim; Jay M Wilson
Journal:  J Pediatr Surg       Date:  2013-06       Impact factor: 2.545

9.  Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias.

Authors:  Allyson J Merrell; Benjamin J Ellis; Zachary D Fox; Jennifer A Lawson; Jeffrey A Weiss; Gabrielle Kardon
Journal:  Nat Genet       Date:  2015-03-25       Impact factor: 38.330

10.  The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin-Siris syndrome in an infant with left congenital diaphragmatic hernia, congenital heart disease, and recurrent infections.

Authors:  Nathaly M Sweeney; Shareef A Nahas; Shimul Chowdhury; Miguel Del Campo; Marilyn C Jones; David P Dimmock; Stephen F Kingsmore
Journal:  Cold Spring Harb Mol Case Stud       Date:  2018-06-01
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