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一项关于布拉氏酵母菌联合标准抗生素治疗艰难梭菌病的随机安慰剂对照试验。

A randomized placebo-controlled trial of Saccharomyces boulardii in combination with standard antibiotics for Clostridium difficile disease.

作者信息

McFarland L V, Surawicz C M, Greenberg R N, Fekety R, Elmer G W, Moyer K A, Melcher S A, Bowen K E, Cox J L, Noorani Z

机构信息

Department of Medicinal Chemistry, School of Pharmacy, University of Washington, Seattle 98195.

出版信息

JAMA. 1994;271(24):1913-8.

PMID:8201735
Abstract

OBJECTIVE--To determine the safety and efficacy of a new combination treatment for patients with Clostridium difficile-associated disease (CDD). The treatment combines the yeast Saccharomyces boulardii with an antibiotic (vancomycin hydrochloride or metronidazole). DESIGN--A double-blind, randomized, placebo-controlled, parallel-group intervention study in patients with active CDD. Patients received standard antibiotics and S boulardii or placebo for 4 weeks, and were followed up for an additional 4 weeks after therapy. Effectiveness was determined by comparing the recurrence of CDD in the two groups using multivariate analysis to control for other risk factors for CDD. SETTING--National referral study of ambulatory or hospitalized patients from three main study coordinating centers. PATIENTS--A total of 124 eligible consenting adult patients, including 64 who were enrolled with an initial episode of CDD, and 60 who had a history of at least one prior CDD episode. Patients who were immunosuppressed due to acquired immunodeficiency syndrome or cancer chemotherapy within 3 months were not eligible. INTERVENTION--Treatment with oral S boulardii (1 g/d for 4 weeks) or placebo in combination with a standard antibiotic. MAIN OUTCOME MEASURE--Recurrence of active CDD. RESULTS--A history of CDD episodes dramatically increased the likelihood of further recurrences. Multivariate analysis revealed that patients treated with S boulardii and standard antibiotics had a significantly lower relative risk (RR) of CDD recurrence (RR, 0.43; 95% confidence interval, 0.20 to 0.97) compared with placebo and standard antibiotics. The efficacy of S boulardii was significant (recurrence rate 34.6%, compared with 64.7% on placebo; P = .04) in patients with recurrent CDD, but not in patients with initial CDD (recurrence rate 19.3% compared with 24.2% on placebo; P = .86). There were no serious adverse reactions associated with S boulardii. CONCLUSIONS--The combination of standard antibiotics and S boulardii was shown to be an effective and safe therapy for these patients with recurrent CDD; no benefit of S boulardii was demonstrated for those with an initial episode of CDD.

摘要

目的——确定一种针对艰难梭菌相关性疾病(CDD)患者的新联合治疗方法的安全性和有效性。该治疗方法将布拉氏酵母菌与一种抗生素(盐酸万古霉素或甲硝唑)联合使用。

设计——一项针对活动性CDD患者的双盲、随机、安慰剂对照、平行组干预研究。患者接受标准抗生素和布拉氏酵母菌或安慰剂治疗4周,并在治疗后再随访4周。通过多变量分析比较两组CDD的复发情况来确定有效性,以控制CDD的其他风险因素。

地点——来自三个主要研究协调中心的门诊或住院患者的全国转诊研究。

患者——共有124名符合条件并同意参与的成年患者,其中64名是首次发作CDD的患者,60名有至少一次CDD发作史。在3个月内因获得性免疫缺陷综合征或癌症化疗而免疫抑制的患者不符合条件。

干预——口服布拉氏酵母菌(1克/天,共4周)或安慰剂与标准抗生素联合治疗。

主要观察指标——活动性CDD的复发情况。

结果——CDD发作史显著增加了进一步复发的可能性。多变量分析显示,与安慰剂和标准抗生素相比,接受布拉氏酵母菌和标准抗生素治疗的患者CDD复发的相对风险(RR)显著降低(RR为0.43;95%置信区间为0.20至0.97)。布拉氏酵母菌对复发性CDD患者有效(复发率34.6%,而安慰剂组为64.7%;P = 0.04),但对首次发作CDD的患者无效(复发率19.3%,而安慰剂组为24.2%;P = 0.86)。未发现与布拉氏酵母菌相关的严重不良反应。

结论——标准抗生素与布拉氏酵母菌联合使用被证明是这些复发性CDD患者的一种有效且安全的治疗方法;对于首次发作CDD的患者,未证明布拉氏酵母菌有任何益处。

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