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Percutaneous endoscopic gastrostomy in children
Jye Hae Park1, Seonkyeong Rhie, Su Jin Jeong
1Department of Pediatrics, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
Insights
Percutaneous endoscopic gastrostomy (PEG) provides safe and effective long-term enteral nutrition for neurologically impaired children. This feeding tube placement improved weight and reduced complications like vomiting and aspiration.
Area of Science:
- Pediatric Gastroenterology
- Surgical Nutrition
- Neurology
Background:
- Neurologically impaired children often require nutritional support.
- Percutaneous endoscopic gastrostomy (PEG) is a common method for enteral feeding.
- PEG can improve nutritional status and reduce feeding time in this population.
Purpose of the Study:
- To evaluate the characteristics, complications, and outcomes of PEG in neurologically impaired children.
- To assess the safety and efficacy of PEG for long-term nutritional support.
Main Methods:
- Retrospective review of 32 neurologically impaired children undergoing 42 PEG procedures (insertions and exchanges).
- Mean follow-up of 12.2 months.
- Analysis of indications, complications, and post-procedure outcomes.
Main Results:
- Main indications included swallowing difficulties, GI bleeding, and GERD.
- Overall complication rate was 47% (25% early, 22% late).
- Late complications included fistula, aggravated GERD, and wound infections. 87% of patients with pre-existing GERD showed improvement.
Conclusions:
- PEG is a safe, effective, and simple technique for long-term enteral nutrition in neurologically impaired children.
- PEG treatment led to increased body weight and reduced vomiting, GI bleeding, and aspiration.
- PEG with post-procedural observation is recommended for nutritional support in this patient group.
Purpose:
Percutaneous endoscopic gastrostomy (PEG) can improve nutritional status and reduce the amount of time needed to feed neurologically impaired children. We evaluated the characteristics, complications, and outcomes of neurologically impaired children treated with PEG.
Methods:
We retrospectively reviewed the records of 32 neurologically impaired children who underwent PEG between March 2002 and August 2008 at our medical center. Forty-two PEG procedures comprising 32 PEG insertions and 10 PEG exchanges, were performed. The mean follow-up time was 12.2 (6.6) months.
Results:
Mean patient age was 9.4 (4.5) years. The main indications for PEG insertion were swallowing difficulty with GI bleeding due to nasogastric tube placement and/or the presence of gastroesophageal reflux disease (GERD). The overall rate of complications was 47%, with early complications evident in 25% of patients and late complications in 22%. The late complications included one gastro-colic fistula, two cases of aggravated GERD, and four instances of wound infection. Among the 15 patients with histological evidence of GERD before PEG, 13 (87%) had less severe GERD, experienced no new aspiration events, and showed increased body weight after PEG treatment.
Conclusion:
PEG is a safe, effective, and relatively simple technique affording long-term enteral nutritional support in neurologically impaired children. Following PEG treatment, the body weight of most patients increased and the levels of vomiting, GI bleeding, and aspiration fell. We suggest that PEG with post-procedural observation be considered for enteral nutritional support of neurologically impaired children.
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