40 research outputs found
Regional gastrointestinal transit times in patients with chronic pancreatitis
The mechanisms behind disrupted gastrointestinal (GI) motor function in patients with chronic pancreatitis (CP) have not been fully elucidated. We compared regional transit times in patients with CP to those in healthy controls, and investigated whether they were associated with diabetes mellitus, exocrine dysfunction, opioid treatment or quality of life. Twenty-eight patients with CP and 28 age- and gender-matched healthy controls were included. Regional GI transit times were determined using the 3D-Transit system, which consists of an ingestible electromagnetic capsule and a detector worn in an abdominal belt for 5 days. Exocrine function was assessed using the fecal elastase-1 test, and quality of life was assessed using the European Organization for Research and Treatment of Cancer questionnaire. Transit times were analyzed for associations with diabetes mellitus, exocrine pancreatic insufficiency (EPI), opioid treatment and quality of life. Compared with healthy controls, patients with CP had prolonged transit times in the small intestine (6.6â
Âąâ
1.8 vs 4.8â
Âąâ
2.2 hours, Pâ
=â
.006), colon (40â
Âąâ
23 vs 28â
Âąâ
26 hours, Pâ
=â
.02), and total GI tract (52â
Âąâ
26 vs 36â
Âąâ
26 hours, Pâ
=â
.02). There was no difference in gastric emptying time (4.8â
Âąâ
5.2 vs 3.1â
Âąâ
1.3 hours, Pâ
=â
.9). No associations between transit times and diabetes, EPI, or opioid consumption were found (all Pâ
>â
.05). Quality of life and associated functional and symptom subscales were not associated with transit times, except for diarrhea (Pâ
=â
.03). Patients with CP have prolonged small intestinal and colonic transit times. However, these alterations do not seem to be mediated by diabetes, EPI, or opioid consumption
Colonic volume in patients with functional constipation or irritable bowel syndrome determined by magnetic resonance imaging
BACKGROUND: Functional constipation (FC) and irritable bowel syndrome constipation type (IBSâC) share many similarities, and it remains unknown whether they are distinct entities or part of the same spectrum of disease. Magnetic resonance imaging (MRI) allows quantification of intraluminal fecal volume. We hypothesized that colonic volumes of patients with FC would be larger than those of patients with IBSâC, and that both patient groups would have larger colonic volumes than healthy controls (HC). METHODS: Based on validated questionnaires, three groups of participants were classified into FC (n = 13), IBSâC (n = 10), and HC (n = 19). The colonic volume of each subject was determined by MRI. Stool consistency was described by the Bristol stool scale and colonic transit times were assessed with radiopaque makers. KEY RESULTS: Overall, total colonic volumes were different in the three groups, HC (median 629 ml, interquartile range (IQR)(562â868)), FC (864 ml, IQR(742â940)), and IBSâC (520 ml IQR(489â593)) (p = 0.001). Patients with IBSâC had lower colonic volumes than patients with FC (p = 0.001) and HC (p = 0.019), but there was no difference between FC and HC (p = 0.10). Stool consistency was similar in the two patient groups, but patients with FC had longer colonic transit time than those with IBSâC (117.6 h versus 43.2 h, p = 0.019). CONCLUSION: Patients with IBSâC have lower total colonic volumes and shorter colonic transit times than patients with FC. Future studies are needed to confirm that colonic volume allows objective distinction between the two conditions