TY - JOUR
T1 - Cholestyramine - A useful adjunct for the treatment of patients with fecal incontinence
AU - Remes-Troche, Jose M.
AU - Ozturk, Ramazan
AU - Philips, Carrie
AU - Stessman, Mary
AU - Rao, Satish S.C.
N1 - Funding Information:
Grant Support Dr. Remes-Troche was supported by the AGA, Jon I. Isenberg International Scholar Award; Dr Ozturk was supported by a grant from Department of Health, Turkish Air Force, Ankara; and Dr Rao was supported in part by grant R01DK57100-03 National Institutes of Health.
PY - 2008/2
Y1 - 2008/2
N2 - Aim/Background: Cholestyramine may improve fecal incontinence, but its use has not been assessed. We report our experience with the use of cholestyramine in the treatment of fecal incontinence. Materials and methods: Twenty-one patients (19 female, mean age 65 years) with fecal incontinence (≥1 episode/week) received cholestyramine along with biofeedback therapy (group A). Stool frequency, stool consistency (Bristol scale), number of incontinent episodes, satisfaction with bowel function (VAS), and anorectal physiology were assessed at 3 months and at 1 year after treatment. Data were compared with a matched group of 21 incontinent subjects (19 female, mean age 64 years) who received biofeedback alone (group B). Results: At 3 months and at 1 year, group A patients showed decreased stool frequency (p<0.01), stool consistency (p=0.001), and number of incontinent episodes (p<0.04). In contrast, stool frequency (p=0.8) and stool consistency (0.23) were not different from baseline in group B subjects. In both groups, there was improvement in the satisfaction with bowel function (p<0.05), anal sphincter pressures (p<0.05) and ability to retain saline infusion (p<0.05). Mean dose of cholestyramine used was 3.6 g; 13 subjects (62%) required dose titration, and 7 (33%) subjects reported minor side effects. Conclusion: Cholestyramine is safe and useful adjunct for the treatment of diarrhea and fecal incontinence. Most patients require small doses, and dose titration is important. The improvement in stool characteristics favors a drug effect, over and above the benefits of biofeedback therapy.
AB - Aim/Background: Cholestyramine may improve fecal incontinence, but its use has not been assessed. We report our experience with the use of cholestyramine in the treatment of fecal incontinence. Materials and methods: Twenty-one patients (19 female, mean age 65 years) with fecal incontinence (≥1 episode/week) received cholestyramine along with biofeedback therapy (group A). Stool frequency, stool consistency (Bristol scale), number of incontinent episodes, satisfaction with bowel function (VAS), and anorectal physiology were assessed at 3 months and at 1 year after treatment. Data were compared with a matched group of 21 incontinent subjects (19 female, mean age 64 years) who received biofeedback alone (group B). Results: At 3 months and at 1 year, group A patients showed decreased stool frequency (p<0.01), stool consistency (p=0.001), and number of incontinent episodes (p<0.04). In contrast, stool frequency (p=0.8) and stool consistency (0.23) were not different from baseline in group B subjects. In both groups, there was improvement in the satisfaction with bowel function (p<0.05), anal sphincter pressures (p<0.05) and ability to retain saline infusion (p<0.05). Mean dose of cholestyramine used was 3.6 g; 13 subjects (62%) required dose titration, and 7 (33%) subjects reported minor side effects. Conclusion: Cholestyramine is safe and useful adjunct for the treatment of diarrhea and fecal incontinence. Most patients require small doses, and dose titration is important. The improvement in stool characteristics favors a drug effect, over and above the benefits of biofeedback therapy.
KW - Cholestyramine
KW - Diarrhea
KW - Fecal incontinence
KW - Medical treatment
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U2 - 10.1007/s00384-007-0391-y
DO - 10.1007/s00384-007-0391-y
M3 - Article
C2 - 17938939
AN - SCOPUS:37349055139
SN - 0179-1958
VL - 23
SP - 189
EP - 194
JO - International Journal of Colorectal Disease
JF - International Journal of Colorectal Disease
IS - 2
ER -