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5-氨基水杨酸在克罗恩病中的长期治疗:是否有效?我们的四年经验。

Long-term therapy with 5-aminosalicylic acid in Crohn's disease: is it useful? Our four years experience.

作者信息

Bresci G, Parisi G, Banti S

机构信息

Unità Operativa Gastroenterologia, Unità Sanitaria Locale 12, Pisa, Italy.

出版信息

Int J Clin Pharmacol Res. 1994;14(4):133-8.

PMID:7607786
Abstract

At present it is not clear if long-term therapy with 5-aminosalicylic acid (5-ASA) is useful in the prevention of relapses of Crohn's disease (CD) in remission. Long-lasting randomized studies are necessary to gauge the efficacy of a long-term therapy, but actually the trials are rarely longer than 12 months. The aim of our study was therefore to evaluate the efficacy of 5-ASA in maintaining the remission in inactive CDs followed up for 4 years. Sixty-six patients, 41 males, mean age 35 +/- 8, having a definitive diagnosis of CD made at least 2 years before, with ileum localization in 39 and ileocolic in 27, entered the study when Crohn's disease activity index (CDAI) and a laboratory index (LI) values were lower than 150 and 100 respectively for at least 6 weeks. Subjects with previous surgical treatment or with an endoscopic index severity (CDEIS) more than 4 were excluded. The patients were randomly divided into two groups: 33 received 5-ASA at 2.4 g/day in a delayed-release formulation (Eudragit-S-coated Mesaline) while another 33 as a control group received non-specific therapy. CDAI and LI were evaluated every 6 months, relapse being defined by a CDAI > or = 150 and LI > or = 100. To confirm the clinical and laboratory diagnosis of relapse, all the patients with CDAI > or = 150 and LI > or = 100 underwent X-ray and/or endoscopic examination. Statistical analysis was made at the end of the study.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

目前尚不清楚5-氨基水杨酸(5-ASA)长期治疗对预防缓解期克罗恩病(CD)复发是否有用。需要进行长期随机研究来评估长期治疗的疗效,但实际上试验很少超过12个月。因此,我们研究的目的是评估5-ASA对随访4年的非活动期CD患者维持缓解的疗效。66例患者,41例男性,平均年龄35±8岁,确诊CD至少2年,其中39例病变位于回肠,27例为回结肠型,当克罗恩病活动指数(CDAI)和实验室指标(LI)值分别低于150和100至少6周时进入研究。排除既往有手术治疗史或内镜指数严重程度(CDEIS)超过4的患者。患者被随机分为两组:33例接受2.4 g/天的缓释制剂(Eudragit-S包衣美沙拉嗪)5-ASA治疗,另外33例作为对照组接受非特异性治疗。每6个月评估CDAI和LI,CDAI≥150且LI≥100定义为复发。为了确认复发的临床和实验室诊断,所有CDAI≥150且LI≥100的患者均接受X线和/或内镜检查。研究结束时进行统计分析。(摘要截断于250字)

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