Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Science, Wayne State University, Detroit, Michigan, USA.
Pharmacotherapy. 2010 Feb;30(2):119-26. doi: 10.1592/phco.30.2.119.
To evaluate the efficacy of a Lactobacillus probiotic single-agent regimen in preventing antibiotic-associated diarrhea (AAD).
Meta-analysis of 10 randomized, blinded, placebo-controlled trials. Patients. A total of 1862 pediatric and adult patients who received a Lactobacillus single-agent regimen or placebo for the prevention of AAD.
The MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials databases were searched from inception through May 2008 by two investigators independently using the following key words: probiotic, Lactobacillus, antibiotic-associated diarrhea. Full reports published in English were included if the studies were randomized, blinded, and placebo-controlled trials that evaluated the efficacy of Lactobacillus single-agent regimens versus placebo in the prevention of AAD. Bibliographies of recent review articles and systematic reviews were hand searched. Quality of the studies was assessed by using the Jadad scoring system. Number of subjects, age, Lactobacillus regimen, follow-up period, and occurrence of AAD were extracted into a standardized data collection form. Overall impact of Lactobacillus on AAD was compared with placebo by using a random-effects model. Ten studies with a total of 1862 patients (50.4% male) met all criteria. Six studies included patients aged 18 years or older, whereas four included patients younger than 18 years (range 2 wks-14 yrs). Jadad scores ranged from 2-5 (out of 5). The total daily dose of Lactobacillus ranged from 2 x 10(9)-4 x 10(10) colony-forming units and was administered throughout the entire antibiotic treatment (5-14 days) for all patients. The follow-up period varied from 2 days-3 months after the end of the probiotic regimen. The combined risk ratio (RR) of developing AAD was significantly lower with Lactobacillus compared with placebo (RR 0.35, 95% confidence interval [CI] 0.19-0.67). In a subgroup analysis, this held true for adults but not pediatric patients (RR 0.24, 95% CI 0.08-0.75 and RR 0.44, 95% CI 0.18-1.08, respectively).
Administration of a Lactobacillus single-agent regimen as a prophylactic agent during antibiotic treatment reduced the risk of developing AAD compared with placebo in adults but not pediatric patients.
评估单剂量乳酸杆菌制剂预防抗生素相关性腹泻(AAD)的疗效。
对 10 项随机、双盲、安慰剂对照试验进行的荟萃分析。患者:共纳入 1862 例接受乳酸杆菌单剂量方案或安慰剂预防 AAD 的儿科和成年患者。
两名研究者独立通过以下关键词在 MEDLINE、EMBASE 和 Cochrane 对照试验中心注册数据库进行了从开始到 2008 年 5 月的搜索:益生菌、乳酸杆菌、抗生素相关性腹泻。如果研究是评估乳酸杆菌单剂量方案与安慰剂在预防 AAD 中的疗效的随机、双盲、安慰剂对照试验,且报告为英文全文,则纳入研究。检索近期综述文章和系统综述的参考文献。使用 Jadad 评分系统评估研究质量。提取受试者数量、年龄、乳酸杆菌方案、随访时间和 AAD 发生情况到标准化数据采集表中。使用随机效应模型比较乳酸杆菌与安慰剂对 AAD 的总体影响。10 项研究共纳入 1862 例患者(50.4%为男性),均符合所有标准。6 项研究纳入 18 岁或以上的患者,4 项研究纳入 18 岁以下的患者(2 周至 14 岁)。Jadad 评分范围为 2-5(满分 5 分)。乳酸杆菌的总日剂量范围为 2×10(9)-4×10(10)个菌落形成单位,所有患者在整个抗生素治疗期间(5-14 天)使用。随访时间在益生菌方案结束后 2 天至 3 个月不等。与安慰剂相比,乳酸杆菌治疗 AAD 的风险比(RR)显著降低(RR 0.35,95%置信区间[CI]0.19-0.67)。亚组分析显示,该结果对成人成立,但对儿科患者不成立(RR 0.24,95%CI 0.08-0.75 和 RR 0.44,95%CI 0.18-1.08)。
与安慰剂相比,抗生素治疗期间给予单剂量乳酸杆菌制剂作为预防剂可降低成人而非儿科患者发生 AAD 的风险。