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Risk factors for development of Clostridium difficile infection due to BI/NAP1/027 strain: a meta-analysis

机译:BI / NAP1 / 027菌株导致艰难梭菌感染发展的危险因素:一项荟萃分析

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Objective: To identify risk factors for the development of Clostridium difficile infection (CDI) due to C. difficile BI/NAP1/027 strain. Methods: PubMed and Scopus databases were searched for studies that sought to identify risk factors for CDI due to the BI/NAP1/027 strain. The technique of meta-analysis was applied. Results: Five studies compared CDI BI/NAP1/027 patients to CDI patients infected with non-BI/NAP1/027 strains, one compared CDI BI/NAP1/027 patients to non-CDI patients, and one provided data for both comparisons. The meta-analysis showed that fluoroquinolones were associated with a higher risk of CDI due to BI/NAP1/027 when compared to non-BI/NAP1/027 CDI (odds ratio (OR) 1.96, 95% confidence interval (95% CI) 1.37-2.80). A trend towards a lower risk for CDI due to BI/NAP1/027 was observed with cephalosporins when compared to non-BI/NAP1/027 CDI (OR 0.70, 95% CI 0.46-1.07). Prior macrolides were not associated with a higher risk for CDI BI/NAP1/027 when compared with non-BI/NAP1/027 CDI controls (OR 0.88, 95% CI 0.44-1.78). Clindamycin administration was associated with a lower risk for CDI due to BI/NAP1/027 when compared to non-BI/NAP1/027 CDI (OR 0.24, 95% CI 0.12-0.48). Age over 65 years was associated with an increased risk of CDI BI/NAP1/027 compared to non-BI/NAP1/027 CDI (OR 1.77, 95% CI 1.31-2.38). Conclusions: Fluoroquinolones and age over 65 years were associated with a higher risk of CDI due to the BI/NAP1/027 strain. Clindamycin was associated with a lower risk of CDI due to BI/NAP1/027.
机译:目的:确定难辨梭状芽胞杆菌BI / NAP1 / 027菌株导致艰难梭菌感染(CDI)发展的危险因素。方法:在PubMed和Scopus数据库中进行搜索,以寻找鉴定BI / NAP1 / 027菌株引起的CDI危险因素的研究。应用荟萃分析技术。结果:五项研究将CDI BI / NAP1 / 027患者与感染非BI / NAP1 / 027菌株的CDI患者进行了比较,一项研究将CDI BI / NAP1 / 027患者与非CDI患者进行了比较,其中一项为这两个比较提供了数据。荟萃分析显示,与非BI / NAP1 / 027 CDI相比,BI / NAP1 / 027导致氟喹诺酮类药物与CDI风险更高(比值(OR)1.96,95%置信区间(95%CI)) 1.37-2.80)。与非BI / NAP1 / 027 CDI相比,头孢菌素有BI / NAP1 / 027导致CDI风险降低的趋势(OR 0.70,95%CI 0.46-1.07)。与非BI / NAP1 / 027 CDI对照相比,先前的大环内酯类药物与CDI BI / NAP1 / 027的较高风险无关(OR 0.88,95%CI 0.44-1.78)。与非BI / NAP1 / 027 CDI相比,克林霉素给药与BI / NAP1 / 027 CDI引起的CDI风险较低(OR 0.24,95%CI 0.12-0.48)。与非BI / NAP1 / 027 CDI相比,超过65岁的年龄与CDI BI / NAP1 / 027的患病风险增加相关(OR 1.77,95%CI 1.31-2.38)。结论:由于BI / NAP1 / 027菌株,氟喹诺酮类药物和65岁以上的年龄与更高的CDI风险相关。由于BI / NAP1 / 027,克林霉素与降低CDI的风险有关。

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