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首页> 外文期刊>European journal of clinical microbiology and infectious diseases: Official publication of the European Society of Clinical Microbiology >Variability in testing policies and impact on reported Clostridium difficile infection rates: results from the pilot Longitudinal European Clostridium difficile Infection Diagnosis surveillance study (LuCID)
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Variability in testing policies and impact on reported Clostridium difficile infection rates: results from the pilot Longitudinal European Clostridium difficile Infection Diagnosis surveillance study (LuCID)

机译:测试政策的差异及其对报告的难辨梭状芽胞杆菌感染率的影响:欧洲纵向难辨梭状芽胞杆菌感染诊断监测研究(LuCID)的初步结果

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摘要

Lack of standardised Clostridium difficile testing is a potential confounder when comparing infection rates. We used an observational, systematic, prospective large-scale sampling approach to investigate variability in C. difficile sampling to understand C. difficile infection (CDI) incidence rates. In-patient and institutional data were gathered from 60 European hospitals (across three countries). Testing methodology, testing/CDI rates and case profiles were compared between countries and institution types. The mean annual CDI rate per hospital was lowest in the UK and highest in Italy (1.5 vs. 4.7 cases/10,000 patient bed days [pbds], p < 0.001). The testing rate was highest in the UK compared with Italy and France (50.7/10,000 pbds vs. 31.5 and 30.3, respectively, p < 0.001). Only 58.4 % of diarrhoeal samples were tested for CDI across all countries. Overall, only 64 % of hospitals used recommended testing algorithms for laboratory testing. Small hospitals were significantly more likely to use standalone toxin tests (SATTs). There was an inverse correlation between hospital size and CDI testing rate. Hospitals using SATT or assays not detecting toxin reported significantly higher CDI rates than those using recommended methods, despite testing similar testing frequencies. These data are consistent with higher false-positive rates in such (non-recommended) testing scenarios. Cases in Italy and those diagnosed by SATT or methods NOT detecting toxin were significantly older. Testing occurred significantly earlier in the UK. Assessment of testing practice is paramount to the accurate interpretation and comparison of CDI rates.
机译:在比较感染率时,缺乏标准化的艰难梭菌检测可能是一个混杂因素。我们使用观察性,系统性,前瞻性的大规模采样方法来研究艰难梭菌采样的变异性,以了解艰难梭菌感染(CDI)的发生率。住院和机构数据来自60个欧洲医院(横跨三个国家)。在国家和机构类型之间比较了测试方法,测试/ CDI率和案例资料。每家医院的年平均CDI率在英国最低,在意大利最高(1.5比4.7例/ 10,000病人就诊天[pbds],p <0.001)。与意大利和法国相比,英国的测试率最高(分别为50.7 / 10,000 pbds与31.5和30.3,p <0.001)。在所有国家/地区,仅58.4%的腹泻样品进行了CDI测试。总体而言,只有64%的医院使用推荐的测试算法进行实验室测试。小型医院使用独立毒素检测(SATT)的可能性明显更高。医院规模和CDI检测率之间呈负相关。尽管使用相似的测试频率,但使用SATT或未检测到毒素的检测方法的医院报告的CDI率明显高于使用推荐方法的医院。这些数据与此类(非推荐)测试方案中较高的假阳性率相一致。意大利的病例以及通过SATT确诊或未检测到毒素的方法的病例明显更年长。测试在英国进行得很早。评估测试实践对准确解释和比较CDI率至关重要。

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