Department of Medicine, A. Manzoni Hospital, Lecco, Italy.
Am J Gastroenterol. 2012 Jun;107(6):922-31. doi: 10.1038/ajg.2012.56. Epub 2012 Apr 3.
Antibiotic-associated diarrhea (AAD) and Clostridium difficile-associated diarrhea (CDAD) are common complications of antibiotic use. Probiotics were effective in preventing AAD and CDAD in several randomized controlled trials. This study was aimed at testing the effect of Saccharomyces boulardii on the occurrence of AAD and CDAD in hospitalized patients.
A single-center, randomized, double-blind, placebo-controlled, parallel-group trial was performed. Patients being prescribed antibiotics or on antibiotic therapy for <48 h were eligible. Exclusion criteria were ongoing diarrhea, recent assumption of probiotics, lack of informed consent, inability to ingest capsules, and severe pancreatitis. Patients received a capsule containing S. boulardii or an indistinguishable placebo twice daily within 48 h of beginning antibiotic therapy, continued treatment for 7 days after antibiotic withdrawal, and were followed for 12 weeks after ending antibiotic treatment.
Of 562 consecutive eligible patients, 275 patients aged 79.2 ± 9.8 years (134 on placebo) were randomized and 204 aged 78.4 ± 10.0 years (98 on placebo) completed the follow-up. AAD developed in 13.3% (13/98) of the patients receiving placebo and in 15.1% (16/106) of those receiving S. boulardii (odds ratio for S. boulardii vs. placebo, 1.16; 95% confidence interval (CI), 0.53-2.56). Five cases of CDAD occurred, 2 in the placebo group (2.0%) and 3 in the probiotic group (2.8%; odds ratio for S. boulardii vs. placebo, 1.40; 95% CI, 0.23-8.55). There was no difference in mortality rates (12.7% vs. 15.6%, P=0.60).
In elderly hospitalized patients, S. boulardii was not effective in preventing the development of AAD.
抗生素相关性腹泻(AAD)和艰难梭状芽孢杆菌相关性腹泻(CDAD)是抗生素使用的常见并发症。益生菌在几项随机对照试验中被证明能有效预防 AAD 和 CDAD。本研究旨在检验布拉氏酵母菌对住院患者 AAD 和 CDAD 发生的影响。
进行了一项单中心、随机、双盲、安慰剂对照、平行组试验。正在接受抗生素治疗或抗生素治疗时间<48 h 的患者符合条件。排除标准为持续腹泻、近期使用益生菌、缺乏知情同意、无法摄入胶囊和严重胰腺炎。患者在开始抗生素治疗的 48 小时内每天接受两次含有布拉氏酵母菌的胶囊或无差别的安慰剂,在停止抗生素治疗后继续治疗 7 天,并在停止抗生素治疗后 12 周内进行随访。
在连续的 562 名符合条件的患者中,有 275 名年龄为 79.2±9.8 岁(134 名服用安慰剂)的患者被随机分组,204 名年龄为 78.4±10.0 岁(98 名服用安慰剂)的患者完成了随访。服用安慰剂的患者中有 13.3%(13/98)发生 AAD,服用布拉氏酵母菌的患者中有 15.1%(16/106)发生 AAD(布拉氏酵母菌与安慰剂相比的优势比,1.16;95%置信区间(CI),0.53-2.56)。发生了 5 例 CDAD,安慰剂组 2 例(2.0%),益生菌组 3 例(2.8%;布拉氏酵母菌与安慰剂相比的优势比,1.40;95%CI,0.23-8.55)。死亡率无差异(12.7%比 15.6%,P=0.60)。
在老年住院患者中,布拉氏酵母菌不能有效预防 AAD 的发生。