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J Neurosurg Pediatr. 2014 Sep;14(3):255-8. doi: 10.3171/2014.6.PEDS13636. Epub 2014 Jul 18.

Ogilvie's syndrome after pediatric spinal deformity surgery: successful treatment with neostigmine.

Author information

1
Department of Neurological Surgery and.

Abstract

Ogilvie's syndrome is a rare and potentially fatal disease that can easily be mistaken for postoperative ileus. Also known as acute colonic pseudo-obstruction, early recognition and diagnosis of the syndrome allows for treatment prior to bowel perforation and requisite abdominal surgery. The authors report a case of Ogilvie's syndrome following spinal deformity correction and tethered cord release in an adolescent who presented with acute abdominal distension, nausea, and vomiting on postoperative Day 0. The patient was initially diagnosed with adynamic ileus and treated conservatively with bowel rest, reduction in narcotic dosage, and a regimen of stool softeners, laxatives, and enemas. Despite this treatment, her clinical course failed to improve, and she demonstrated significant colonic distension radiographically. Intravenous neostigmine was administered as a bolus with a rapid and dramatic response. This case is the first reported instance of neostigmine use for Ogilvie's syndrome treatment following a pediatric neurosurgical operation.

KEYWORDS:

Ogilvie's syndrome; adolescent spinal deformity; neostigmine; neurosurgery; pediatric; spine

PMID:
25036854
DOI:
10.3171/2014.6.PEDS13636
[Indexed for MEDLINE]

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