Literature DB >> 2066156

Treatment of the irritable bowel syndrome.

G Friedman1.   

Abstract

Individualization of treatment for patients with IBS is predicated on a thorough analysis of the patient's symptoms, consideration of the reasons for seeking health care, evaluation of symptom-precipitating factors, elimination of confounding features, and the absolute knowledge of the absence of organic illness. Collecting and codifying appropriate historical data allow the physician to educate the patient with respect to the origin of his symptoms, and to enlist the patient as a partner in his future health care. There is no single, universally accepted therapeutic agent available for the treatment of the IBS patient. As a result, treatment is directed at reducing the frequency and intensity of triggering factors as well as ameliorating the symptoms when they arise. Symptoms evoked by psychologic factors may be effectively reduced by psychotherapy or hypnotherapy. Situational anxiety may be treated for brief periods by using antianxiety agents such as diazepam, chlordiazepoxide, buspirone, or similar agents. Depressive reactions may be reduced with suitable doses of antidepressant agents such as amitriptyline. Smooth muscle hyperreactivity may be dulled with small amounts of selected anticholinergics, which are usually most effective in reducing meal-induced discomfort. Peppermint oil may be of additional benefit. Gas-related symptoms require elimination of contributory dietary factors, such as lactose-containing foods, sorbitol, or fructose, as well as certain oligosaccharides. Simethecone, charcoal, or beanase may be helpful. Functional constipation is best treated with graded doses of insoluble or soluble fiber. Diarrheal episodes may be reduced with either loperamide or diphenoxylate. Careful, continued follow-up assessment of therapeutic endeavors, a sincere interest in the patient's concerns, and surveillance for intercurrent organic illness are the cornerstones of complete ongoing care.

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Year:  1991        PMID: 2066156

Source DB:  PubMed          Journal:  Gastroenterol Clin North Am        ISSN: 0889-8553            Impact factor:   3.806


  3 in total

1.  Effect of modulation of serotonergic, cholinergic, and nitrergic pathways on murine fundic size and compliance measured by ultrasonomicrometry.

Authors:  Lin Xue; G Richard Locke; Michael Camilleri; Jan A J Schuurkes; Ann Meulemans; Bernard J Coulie; Joseph H Szurszewski; Gianrico Farrugia
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2005-09-15       Impact factor: 4.052

2.  Intestinal Acid Sphingomyelinase Protects From Severe Pathogen-Driven Colitis.

Authors:  Jana Meiners; Vittoria Palmieri; Robert Klopfleisch; Jana-Fabienne Ebel; Lukasz Japtok; Fabian Schumacher; Ayan Mohamud Yusuf; Katrin A Becker; Julia Zöller; Matthias Hose; Burkhard Kleuser; Dirk M Hermann; Richard N Kolesnick; Jan Buer; Wiebke Hansen; Astrid M Westendorf
Journal:  Front Immunol       Date:  2019-06-19       Impact factor: 7.561

Review 3.  Inhibition of acid sphingomyelinase by tricyclic antidepressants and analogons.

Authors:  Nadine Beckmann; Deepa Sharma; Erich Gulbins; Katrin Anne Becker; Bärbel Edelmann
Journal:  Front Physiol       Date:  2014-09-02       Impact factor: 4.566

  3 in total

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