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Molecular diagnostics of hepatitis C virus infection: a systematic review.

机译:丙型肝炎病毒感染的分子诊断:系统评价。

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CONTEXT: Hepatitis C virus (HCV) is a common blood-borne pathogen that relies heavily on nucleic acid testing for confirmation of infection. Nucleic acid tests are invaluable for the diagnosis of HCV infection and provide critical prognostic information for guiding treatment and measuring the response to antiviral therapy. OBJECTIVE: To review the currently available molecular diagnostic tests for HCV, their clinical applications, and how these tests shed light on the natural history of HCV. EVIDENCE ACQUISITION: Search of MEDLINE (1966 to July 2006), article reference lists, and national meeting abstracts for the diagnosis and applications of molecular diagnostic tests for HCV. Studies were selected on the basis of clinical relevance. EVIDENCE SYNTHESIS: Qualitative nucleic acid tests have low limits of detection (<50 IU HCV RNA/mL) and are used for confirmation of HCV infection and for screening blood donations. Hepatitis C virus genotype test results provide important prognostic information related to therapeutic response and are routinely used for selecting treatment regimens. Quantitative HCV RNA testing provides prognostic information regarding likelihood of treatment response and plays an important role in monitoring the antiviral response to treatment. Sustained virological response is defined as testing negative for HCV RNA 6 months after cessation of therapy. Recent studies suggest that the rate of response to therapy is also important. For example, conversion to an HCV RNA negative test result after 4 weeks of therapy constitutes a rapid virological response and is a strong predictor of treatment success. Patients who have not had an early virological response, defined as at least a 2-log decline in HCV RNA after 12 weeks of therapy, are unlikely to respond with an additional 36 weeks of therapy, and should stop therapy. CONCLUSIONS: A sensitive nucleic acid test should be used to confirm all cases of acute or chronic HCV infection. A genotype test and quantitative HCV RNA test should be performed on all patients prior to therapy to best assess probability of response and to aid in selection of appropriate therapeutic regimen. Monitoring HCV RNA during treatment provides important information on likelihood of sustained virological response. The same type of quantitative HCV RNA test should be used throughout a patient's treatment course.
机译:背景:丙型肝炎病毒(HCV)是一种常见的血源性病原体,在很大程度上依赖于核酸测试来确认感染。核酸测试对于HCV感染的诊断非常重要,并且可以提供重要的预后信息,以指导治疗和衡量对抗病毒治疗的反应。目的:回顾目前可用的HCV分子诊断测试,其临床应用以及这些测试如何阐明HCV的自然史。证据获取:检索MEDLINE(1966年至2006年7月),文章参考清单和全国会议摘要,以诊断和应用HCV分子诊断检测。根据临床相关性选择研究。证据综合:定性核酸检测的检测限低(<50 IU HCV RNA / mL),可用于确认HCV感染和筛查献血。丙型肝炎病毒基因型测试结果提供了与治疗反应有关的重要预后信息,通常用于选择治疗方案。 HCV RNA定量检测可提供有关治疗反应可能性的预后信息,并在监测对治疗的抗病毒反应中起重要作用。持续的病毒学应答定义为停止治疗后6个月HCV RNA阴性。最近的研究表明,对治疗的反应率也很重要。例如,在治疗4周后转换为HCV RNA阴性测试结果构成了快速的病毒学应答,并且是治疗成功的有力指标。尚无早期病毒学应答(定义为治疗12周后HCV RNA至少下降2个对数)的患者不太可能再接受36周治疗即可缓解,应停止治疗。结论:应该使用敏感的核酸测试来确认所有急性或慢性HCV感染病例。治疗前应对所有患者进行基因型检测和定量HCV RNA检测,以最好地评估反应的可能性并帮助选择合适的治疗方案。在治疗期间监测HCV RNA可提供有关持续病毒学应答可能性的重要信息。在患者的整个治疗过程中,应使用相同类型的定量HCV RNA定量检测。

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