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1.
Gastroenterology ; 82(6): 1369-73, 1982 Jun.
Article in English | MEDLINE | ID: mdl-7040158

ABSTRACT

To determine the value of bethanechol in the treatment of erosive esophagitis, a double-blind study was undertaken in which 28 patients were randomized to either bethanechol and antacid, or placebo and antacid. Patients were evaluated clinically, endoscopically, and by esophageal manometry before and after 8 wk of therapy. After treatment both groups showed significant improvement in heartburn and in healing of esophageal lesions. Patients who received bethanechol plus antacids did not show a greater improvement than patients who received placebo plus antacids in any category, nor did patients in the bethanechol-treated group have a greater incidence of complete healing. In addition, pretreatment mean lower esophageal sphincter pressure was normal in approximately 30% of patients with erosive esophagitis and this finding was associated with a greater chance for complete healing of esophageal lesions. These results fail to show that the addition of bethanechol to an intensive antacid regimen is more effective than the antacid regimen alone in the treatment of erosive esophagitis and that patients with esophagitis and normal lower esophageal sphincter pressures respond more favorably to medical treatment.


Subject(s)
Antacids/administration & dosage , Bethanechol Compounds/administration & dosage , Esophagitis, Peptic/drug therapy , Antacids/adverse effects , Bethanechol Compounds/adverse effects , Clinical Trials as Topic , Double-Blind Method , Drug Therapy, Combination , Esophagitis, Peptic/diagnosis , Female , Humans , Male , Middle Aged
2.
J Am Acad Dermatol ; 4(5): 619-29, 1981 May.
Article in English | MEDLINE | ID: mdl-7016935

ABSTRACT

We have come to understand the cause of antibiotic-associated pseudomembranous colitis (PMC) only in the last decade. Clostridium difficile produces the intestinal dysfunction and the characteristic finding of exudative plaques on the mucosa by elaborating a toxin in the colon. This report reviews the development of our knowledge of this disease and the rapid adoption of a rational therapy once the cause was specified. C. difficile or its toxin can be cultured or isolated from the stools of 90% of the patients with PMC. This organism is almost never found in healthy people or in any other conditions except inflammatory bowel disease, where its significance is not yet known. The detection of pseudomembranes by sigmoidoscopy establishes the diagnosis. The laboratory technics that confirm the presence of C. difficile and its toxin are being incorporated into many laboratories around the country. Treatment of diagnosed PMC is relatively simple and usually completely effective. The offending antibiotic is stopped, a proper fluid and electrolyte balance maintained, and oral vancomycin begun, 125 to 500 mg four times a day. Cholestyramine can also be used as an adjunct to this regimen. Relapse can occur in patients treated with oral vancomycin, necessitating a repeat course of therapy.


Subject(s)
Enterocolitis, Pseudomembranous/diagnosis , Anti-Bacterial Agents/adverse effects , Bacterial Toxins/adverse effects , Cholestyramine Resin/therapeutic use , Clostridium , Colestipol/therapeutic use , Colon/pathology , Enterocolitis, Pseudomembranous/etiology , Enterocolitis, Pseudomembranous/therapy , Humans , Prognosis , Vancomycin/therapeutic use
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