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Pre-analytical and post-analytical evaluation in the era of molecular diagnosis of sexually transmitted diseases: cellularity control and internal control

机译:性传播疾病分子诊断时代的分析前和分析后评估:细胞控制和内部控制

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Background. A national project on Clostridium difficile infection (CDI), funded by the Center for Prevention and Control of Diseases of Italian Ministry of Health, was performed in 2012-2013. Microbiological laboratories of the National Public Heath System were invited by the Istituto Superiore di Sanita? to provide information on CDI diagnostics through a closed answer questionnaire. Materials and Methods. In total, 14 regions and the independent province of Trento participated in and 278 filled questionnaires were sent back. The data obtained indicate that 87% of the laboratories routinely perform diagnostic assays for C. difficile . GDH detection is used as the first screening test by 33% of these laboratories. Most of them declared to use toxins enzyme immunoassays (88%), whereas a minority performs C. difficile culture (26%) or molecular assays (19%). Only 37% of the laboratories stated to adopt a diagnostic algorithm. The algorithms adopted are different and high heterogeneity in the combination of the assays used was observed. Results . Fifty eight percent of laboratories declared to type C. difficil e strains, the majority (82%) sending faecal samples or strains to a reference laboratory. Sixty-two laboratories, routinely performing C. difficile culture, were invited by ISS to send five isolates for molecular typing. In total, 103 isolates from 22 hospitals were collected and 31 different PCR-ribotypes were identified. PCR-ribotype 356/607 was the most frequent (27%), followed by 018 (12%) and 027 (8%). The latter is a worldwide spread hypervirulent type only recently emerged in our country. A molecular characterization of the different PCR-ribotypes detected was also performed by Xpert? C . difficile . Conclusions . The study highlights the need for a more careful selection of diagnostic algorithms to improve CDI diagnosis and the urgency to implement a National Surveillance of CDI in Italy.
机译:背景。由意大利卫生部疾病预防和控制中心资助的国家难辨梭状芽胞杆菌感染国家项目于2012-2013年进行。 Istituto Superiore di Sanita?邀请了国家公共卫生系统的微生物实验室。通过封闭答案问卷提供有关CDI诊断的信息。材料和方法。总共有14个地区和独立的特伦托省参加了会议,并寄回了278份已填写的问卷。获得的数据表明,有87%的实验室常规进行艰难梭菌的诊断测定。其中33%的实验室将GDH检测用作首次筛选测试。他们中的大多数宣称使用毒素酶免疫测定(88%),而少数人进行艰难梭菌培养(26%)或分子测定(19%)。只有37%的实验室表示采用诊断算法。所采用的算法是不同的,并且在所用检测方法的组合中观察到高度异质性。结果。 58%的实验室宣布为艰难梭菌菌株,大多数实验室(82%)将粪便样品或菌株送到参考实验室。国际空间站邀请了62个常规进行艰难梭菌培养的实验室,将5个分离株进行分子分型。总共收集了来自22家医院的103个分离株,并鉴定了31种不同的PCR核型。 PCR核型356/607最常见(27%),其次是018(12%)和027(8%)。后者是最近才在我国出现的在世界范围传播的高毒力类型。 Xpert?还对检测到的不同PCR核型进行了分子表征。 C 。困难的。结论。这项研究强调了需要更仔细地选择诊断算法以改善CDI诊断的必要性,以及在意大利实施CDI国家监控的紧迫性。

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