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High‐resolution colonic manometry accurately predicts colonic neuromuscular pathological phenotype in pediatric slow transit constipation

Background  Severe pediatric slow transit constipation (STC) is commonly due to intrinsic colonic neuromuscular disease. We sought to correlate neuromuscular histological phenotypes in pediatric STC with colonic manometric phenotypes using high‐resolution manometry (HRM). We tested the hypothesis th...

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Bibliographic Details
Published in:Neurogastroenterology and motility 2013-01, Vol.25 (1), p.70-e9
Main Authors: Giorgio, V., Borrelli, O., Smith, V. V., Rampling, D., Köglmeier, J., Shah, N., Thapar, N., Curry, J., Lindley, K. J.
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Language:English
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Summary:Background  Severe pediatric slow transit constipation (STC) is commonly due to intrinsic colonic neuromuscular disease. We sought to correlate neuromuscular histological phenotypes in pediatric STC with colonic manometric phenotypes using high‐resolution manometry (HRM). We tested the hypothesis that failure of motor quiescence (FQ) between bisacodyl‐induced high amplitude propagating sequences (HAPSs) might predict neuromuscular pathology. Methods  Eighteen children (10 males, median age: 7.5 years) with refractory STC underwent stationary colonic HRM before segmental colonic resection. Six age‐matched constipated children with normal colonic transit served as controls. Colonic resection specimens underwent histopathological analysis. Conventional manometric parameters and area under the curve (AUC) during a 1‐min period following bisacodyl‐induced HAPSs [PBAUC1], as measure of FQ, were calculated. Key Results  Numbers of postbisacodyl HAPSs in descending and sigmoid segments were lower in patients than controls (P 
ISSN:1350-1925
1365-2982
DOI:10.1111/nmo.12016