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Updated: Apr 14, 2026

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Published on: March 5, 2018
Acute colonic pseudo-obstruction in a child taking trihexyphenidyl for drooling: Prescribers beware
F Begbie1, G Walker2, H Kubba1
1Department of Paediatric Otolaryngology, Yorkhill Children's Hospital, Glasgow, United Kingdom.
Insights
Colonic pseudo-obstruction, a rare condition in children, occurred in an 8-year-old treated with trihexyphenidyl. This case highlights a potential complication of anticholinergic medication in patients with motility issues.
Area of Science:
- Pediatric Gastroenterology
- Clinical Case Reports
- Pharmacology
Background:
- Colonic pseudo-obstruction (Ogilvie's Syndrome) is rare in pediatric populations.
- Anticholinergic medications, like trihexyphenidyl, are used for conditions such as drooling.
- Patients with pre-existing intestinal hypomotility are at higher risk for gastrointestinal complications.
Observation:
- An 8-year-old child with cerebral palsy and chronic hypomotility was treated with trihexyphenidyl for drooling.
- The child presented with acute abdominal distension, tenderness, and vomiting, indicative of an obstruction.
- Emergency laparotomy revealed significant colonic dilatation.
Findings:
- This case represents the first reported instance of colonic pseudo-obstruction potentially linked to trihexyphenidyl use.
- The anticholinergic effects of trihexyphenidyl may exacerbate underlying intestinal hypomotility, leading to pseudo-obstruction.
- Surgical intervention, including a defunctioning ileostomy, was necessary to manage the acute condition.
Implications:
- Healthcare providers should exercise caution when prescribing trihexyphenidyl to pediatric patients with pre-existing intestinal hypomotility.
- Awareness of this potential adverse drug reaction is crucial for early diagnosis and management of colonic pseudo-obstruction.
- Further research may be warranted to explore the specific mechanisms and incidence of trihexyphenidyl-induced colonic pseudo-obstruction in vulnerable pediatric populations.
Abstract:
Colonic pseudo-obstruction (Ogilvie's Syndrome) in children is relatively uncommon. We report an unusual case of colonic pseudo-obstruction in an 8-year-old child with cerebral palsy and long-term hypomotility issues being treated for drooling with the anticholinergic medication trihexyphenidyl. He presented as an emergency with severe abdominal distension, abdominal tenderness and vomiting. An emergency laparotomy revealed colonic dilatation and a defunctioning ileostomy was created. To our knowledge, this is the first case reporting colonic pseudo-obstruction as a possible complication of treatment with trihexyphenidyl. We suggest prescribers should exercise caution when prescribing trihexyphenidyl in patients with long-term intestinal hypomotility issues.
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