A Randomized Controlled Study of Mesalamine After Acute Diverticulitis: Results of the DIVA Trial

BACKGROUND/AIMS:We evaluated the efficacy of mesalamine (Asacol) in reducing gastrointestinal symptoms after an acute attack of diverticulitis. METHODS:This was a 1-year double-blind, randomized, placebo-controlled study in which patients with computed tomography scan confirmed acute diverticulitis...

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Veröffentlicht in:Journal of clinical gastroenterology 2013-08, Vol.47 (7), p.621-629
Hauptverfasser: Stollman, Neil, Magowan, Simon, Shanahan, Fergus, Quigley, Eamonn M.M
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Sprache:eng
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Zusammenfassung:BACKGROUND/AIMS:We evaluated the efficacy of mesalamine (Asacol) in reducing gastrointestinal symptoms after an acute attack of diverticulitis. METHODS:This was a 1-year double-blind, randomized, placebo-controlled study in which patients with computed tomography scan confirmed acute diverticulitis received placebo, mesalamine, or mesalamine+Bifidobacterium infantis 35624 (Align) for 12 weeks and followed for 9 additional months. Efficacy was assessed using a global symptom score (GSS) of 10 symptoms (abdominal pain, abdominal tenderness, nausea/vomiting, bloating, constipation, diarrhea, mucus, urgency, painful straining, and dysuria). Patients were required to have a GSS≥12 at baseline, including an abdominal pain score >2. RESULTS:One hundred seventeen patients (placebo, 41; mesalamine, 40; mesalamine+probiotic, 36) were randomized and treated. GSS decreased in all groups during treatment without a statistically significant difference between mesalamine and placebo, however; scores were consistently lower for mesalamine at all time points. The rate of complete response (GSS=0) was significantly higher with mesalamine than placebo at weeks 6 and 52 (P
ISSN:0192-0790
1539-2031
DOI:10.1097/MCG.0b013e31828003f6