PLACEBO-CONTROLLED TRIAL OF ORAL 5-ASA IN RELAPSE PREVENTION OF CROHNS-DISEASE

被引:70
作者
BRIGNOLA, C
IANNONE, P
PASQUALI, S
CAMPIERI, M
GIONCHETTI, P
BELLUZZI, A
BASSO, O
MIGLIOLI, M
BARBARA, L
机构
[1] Istituto di Clinica Medica e Gastroenterologia, Policlinico S. Orsola, University of Bologna, Bologna, 40138
关键词
CROHNS DISEASE; 5-AMINOSALICYLIC ACID; THERAPY;
D O I
10.1007/BF01308338
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Treatment of Crohn's disease (CD) in clinical remission is still a debated issue. Previous studies have shown a high risk of relapse for patients with CD in clinical remission (CDAI < 150) but with some abnormally high laboratory parameters as well as a possible beneficial role of low-dosage steroid treatment in this group of patients. Furthermore, good results have been reported on the efficacy of 5-aminosalicyclic acid (5-ASA) in moderately active CD. In our study we verified the efficacy of a slow-release oral 5-ASA preparation in preventing relapses in a group of patients in clinical remission but with raised laboratory parameters. Forty-four patients were randomized in a double-blind manner to receive either 5-ASA (2 g/day) or placebo for four months. Location of disease and previous steroid treatment were similar in both groups. One patient in the 5-ASA group discontinued the drug because of uterine bleeding. During the study period, 13 of 22 placebo-treated patients and 11 of 21 5-ASA-treated patients relapsed (corrected chi square = NS). Considering the location of disease, three of 10 patients in the 5-ASA group and six of nine patients in the placebo group with ileal CD relapsed (therapeutic gain with 5-ASA: 36.6%; 95% allowance for error from -6% to 79.2%). Moreover, in seven patients with ileal CD who remained in remission, we found a statistically significant decrease in alpha(1) acid glycoprotein and C-reactive protein from the second month of the study. In conclusion, although results with 5-ASA in CD seem disappointing, the possible benefit of higher dosages of 5-ASA in selected subgroups of CD patients is discussed.
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页码:29 / 32
页数:4
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