Document Detail


Motility of the oesophagus and small bowel in adults treated for Hirschsprung's disease during early childhood.
MedLine Citation:
PMID:  19735477     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Dysmotility of the upper gastrointestinal (GI) tract has been reported in children with Hirschsprung's disease (HD). In the present study, motility of the oesophagus and the small bowel was studied in adults treated for HD during early childhood to elucidate whether there are alterations in motility of the upper GI tract in this patient group. [Correction added after online publication 15 Sep: The preceding sentence has been rephrased for better clarity.] METHODS: Ambulatory small bowel manometry with recording sites in duodenum/jejunum was performed in 16 adult patients with surgically treated HD and 17 healthy controls. In addition, oesophageal manometry was performed with station pull-through technique. Key RESULTS: The essential patterns of small bowel motility were recognized in all patients and controls. During fasting, phase III of the migrating motor complex (MMC) was more prominent in patients with HD than in controls when accounting for duration and propagation velocity (P = 0.006). Phase I of the MMC was of shorter duration (P = 0.008), and phase II tended to be of longer duration (P = 0.05) in the patients. During daytime fasting, propagated clustered contractions (PCCs) were more frequent in the patients (P = 0.01). Postprandially, the patients demonstrated a higher contractile frequency (P = 0.02), a shorter duration of contractions (P = 0.008) and more frequent PCCs (P < 0.001). The patients had normal oesophageal motility. CONCLUSIONS & INFERENCES: This study demonstrates that adult patients with HD have preserved essential patterns of oesophageal and small bowel motility. However, abnormalities mainly characterized by increased contractile activity of the small bowel during fasting and postprandially are evident. These findings indicate alterations in neuronal control of motility and persistent involvement of the upper GI tract in this disease.
Authors:
A W Medhus; K Bj?rnland; R Emblem; E Husebye
Related Documents :
6714787 - Microvascular studies in human radiation bowel disease.
20431947 - Small intestinal clustered contractions and bacterial overgrowth: a frequent finding in...
21203597 - Ultrasonography contribution in detection of reno-urinary anomalies: a cohort study.
12425547 - Initial experience of wireless-capsule endoscopy for evaluating occult gastrointestinal...
3813197 - Acute upper airway injury in burn patients. serial changes of flow-volume curves and na...
9412967 - Fecal incontinence in scleroderma. clinical features, anorectal manometric findings, an...
Publication Detail:
Type:  In Vitro; Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-09-07
Journal Detail:
Title:  Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society     Volume:  22     ISSN:  1365-2982     ISO Abbreviation:  Neurogastroenterol. Motil.     Publication Date:  2010 Feb 
Date Detail:
Created Date:  2010-01-13     Completed Date:  2010-03-31     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9432572     Medline TA:  Neurogastroenterol Motil     Country:  England    
Other Details:
Languages:  eng     Pagination:  154-60, e49     Citation Subset:  IM    
Affiliation:
Department of Gastroenterology, Oslo University Hospital, Ullev?l, Oslo, Norway. a.w.medhus@medisin.uio.no
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Chi-Square Distribution
Child
Esophagus / physiopathology*
Gastrointestinal Motility / physiology*
Hirschsprung Disease / physiopathology*,  surgery
Humans
Intestine, Small / physiopathology*
Male
Manometry
Myoelectric Complex, Migrating / physiology
Statistics, Nonparametric

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  CaM kinase II in colonic smooth muscle contributes to dysmotility in murine DSS-colitis.
Next Document:  Persistent gut motor dysfunction in a murine model of T-cell-induced enteropathy.