Enterostomy tube placement in children with spinal muscular atrophy type 1

K Sy1, S Mahant, N Taback

  • 1Division of Paediatric Medicine and Paediatric Outcomes Research Team, the Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Ontario, Canada.

The Journal of Pediatrics
|December 2, 2006
PubMed

Insights

Infants with spinal muscular atrophy (SMA) type 1 experienced significant complications, including death, within 30 days of enterostomy tube insertion. Aspiration pneumonia was the most frequent major complication in this vulnerable population.

Area of Science:

  • Pediatric Gastroenterology
  • Neuromuscular Disorders
  • Interventional Radiology

Background:

  • Spinal muscular atrophy (SMA) type 1 is a severe neuromuscular disorder affecting infants.
  • Enterostomy tube insertion is often necessary for nutritional support in infants with SMA type 1.
  • The safety and complication rates of enterostomy tube placement in this specific population require detailed investigation.

Purpose of the Study:

  • To evaluate the incidence of major complications within 30 days following enterostomy tube insertion in infants diagnosed with SMA type 1.
  • To identify specific types of major complications encountered post-procedure.

Main Methods:

  • Retrospective case review of pediatric patients with SMA type 1 who underwent image-guided gastrostomy or gastrojejunostomy tube placement.
  • Data collected from 1994-2004 at a single pediatric tertiary care center.
  • Major complications defined as peritonitis, aspiration pneumonia, respiratory failure, nonelective PICU admission, and mortality.

Main Results:

  • Twelve infants with SMA type 1 met the inclusion criteria.
  • Aspiration pneumonia occurred in 41.6% of patients, respiratory failure in 33%, and mortality in 16.7% within 30 days.
  • Older age at tube insertion was significantly associated with the development of aspiration pneumonia (P < .05).

Conclusions:

  • Enterostomy tube insertion in infants with SMA type 1 is associated with a substantial rate of major complications, including life-threatening events.
  • Close monitoring and consideration of patient age are crucial in the peri-procedural management of these infants.
  • These findings highlight the risks inherent in providing enteral access for infants with severe neuromuscular disease.
Abstract

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