Ferraz M B, Tugwell P, Goldsmith C H, Atra E
Division of Rheumatology, Escola Paulista de Medicina, Sao Paulo, Brazil.
J Rheumatol. 1990 Nov;17(11):1482-6.
At present there is no widely accepted therapy for ankylosing spondylitis (AS), a progressive debilitating disease. The effectiveness of sulfasalazine in AS still lacks strong evidence, as well, the magnitude of its benefit is unknown. A meta-analysis was carried out to assess the effectiveness of sulfasalazine in AS. A search of the literature was done using Medline, Index Medicus, the reference lists of articles located and contacting content experts to reveal unpublished studies. Five randomized controlled trials (RCT) comparing sulfasalazine to placebo were located and assessed methodologically. The methodologic quality of all 5 RCT was considered satisfactory and consequently these studies were included in the meta-analysis. The pooled estimate of clinical benefit (and its 95% confidence interval) favoring sulfasalazine, over and above that observed in the placebo group was as follows: Duration of morning stiffness -28.2% (-54.6 to -1.8%); severity of morning stiffness -30.6% (-52.5 to -8.7%); severity of pain -26.7% (-44.3 to -9.1%); general well being -7.1% (-24.3 to 10.0%); erythrocyte sedimentation rate -9.2% (-24.8 to 6.4%); and IgA -11.7% (-18.8 to -4.7%). Adverse effects, mostly mild, were more frequently observed in the sulfasalazine group (odds ratio [OR] = 1.5746, p = 0.1082). The occurrence of dropouts (OR = 1.1554, p = 0.6119) was similar in both groups. Sulfasalazine is a safe and effective drug in the short term treatment of AS.
目前,对于强直性脊柱炎(AS)这一进行性致残疾病,尚无广泛认可的治疗方法。柳氮磺胺吡啶治疗AS的有效性仍缺乏有力证据,其益处的程度也未知。进行了一项荟萃分析以评估柳氮磺胺吡啶治疗AS的有效性。通过使用医学文献数据库(Medline)、医学索引(Index Medicus)、所检索文章的参考文献列表以及联系内容专家以揭示未发表的研究来进行文献检索。找到了五项比较柳氮磺胺吡啶与安慰剂的随机对照试验(RCT),并对其进行了方法学评估。所有五项RCT的方法学质量被认为是令人满意的,因此这些研究被纳入荟萃分析。与安慰剂组相比,柳氮磺胺吡啶在临床益处方面的合并估计值(及其95%置信区间)如下:晨僵持续时间-28.2%(-54.6至-1.8%);晨僵严重程度-30.6%(-52.5至-8.7%);疼痛严重程度-26.7%(-44.3至-9.1%);总体健康状况-7.1%(-24.3至10.0%);红细胞沉降率-9.2%(-24.8至6.4%);以及免疫球蛋白A(IgA)-11.7%(-18.8至-4.7%)。不良反应大多为轻度,在柳氮磺胺吡啶组中更频繁出现(优势比[OR]=1.5746,p=0.1082)。两组的退出率(OR=1.1554,p=0.6119)相似。柳氮磺胺吡啶在AS的短期治疗中是一种安全有效的药物。