Gastrostomy and Tracheostomy After Complete Repair of Tetralogy of Fallot in Children With 22q11.2 Deletion Syndrome.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 14 3 2020
medline: 7 1 2021
entrez: 14 3 2020
Statut: ppublish

Résumé

Caring for a child with gastrostomy and/or tracheostomy can cause measurable parental stress. It is generally known that children with 22q11.2 deletion syndrome are at greater risk of requiring gastrostomy or tracheostomy after heart surgery, although the magnitude of that risk after complete repair of tetralogy of Fallot has not been described. We sought to determine the degree to which 22q11.2 deletion is associated with postoperative gastrostomy and/or tracheostomy after repair of tetralogy of Fallot. Retrospective cohort study. Pediatric Health Information System. Children undergoing complete repair of tetralogy of Fallot (ventricular septal defect closure and relief of right ventricular outflow tract obstruction) from 2003 to 2016. Patients were excluded if they had pulmonary atresia, other congenital heart defects, and/or genetic diagnoses other than 22q11.2 deletion. Two groups were formed on the basis of 22q11.2 deletion status. Outcomes were postoperative tracheostomy and postoperative gastrostomy. Bivariate analysis and Kaplan-Meier analysis at 150 days postoperatively were performed. There were 4,800 patients, of which 317 (7%) had a code for 22q11.2 deletion. There were no significant differences between groups for age at surgery or sex. Patients with 22q11.2 deletion had significantly higher rates of gastrostomy (18% vs 5%; p < 0.001) and higher rates of tracheostomy (7% vs 1%; p < 0.001); there was no difference for mortality. Kaplan-Meier analyses also showed higher rates of gastrostomy (p = 0.024) and tracheostomy (p = 0.037). The present study establishes rates of postoperative gastrostomy and tracheostomy in children with 22q11.2 deletion after complete repair of tetralogy of Fallot. These data are useful to clinicians for providing families with preoperative counseling.

Identifiants

pubmed: 32168301
doi: 10.1097/PCC.0000000000002339
pii: 00130478-202009000-00046
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e776-e781

Références

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Auteurs

Danielle M Herington (DM)

Department of Pediatrics, Division of General Pediatrics, Rainbow Babies and Children's Hospital, Cleveland, OH.

Xinyu Tang (X)

Department of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, AR.

Beverly J Spray (BJ)

Biostatistics Core, Arkansas Children's Research Institute, Little Rock, AR.

Brian L Reemtsen (BL)

Department of Surgery, Division of Pediatric Cardiovascular Surgery, University of Arkansas for Medical Sciences and Arkansas Children's Research Institute, Little Rock, AR.

Parthak Prodhan (P)

Department of Pediatrics, Division of Intensive Care, University of Arkansas for Medical Sciences and Arkansas Children's Research Institute, Little Rock, AR.

Gresham T Richter (GT)

Department of Otolaryngology, Division of Pediatric Otolaryngology, University of Arkansas for Medical Sciences and Arkansas Children's Research Institute, Little Rock, AR.

William B Kyle (WB)

Department of Pediatrics, Division of Cardiology, Baylor College of Medicine and Texas Children's Hospital, Houston, TX.

Elijah H Bolin (EH)

Department of Pediatrics, Division of Cardiology, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR.

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