法律程序的简要总结。

Emanuele Nicastri
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引用次数: 1

摘要

该小组于2002年4月在罗马举行,有100多名意大利传染病病房主任参加。该小组采用了一种系统的方法,审查任何具体使用基因型测定法检测抗逆转录病毒耐药性的证据。这些单一的建议是使用一种评级方案制定的,该方案基于对证据的考虑,在缺乏直接证据时,根据专家意见。本次会议讨论的另一个新问题是HIV-1逆转录酶和蛋白酶测序在临床环境中的可重复性。还报告了12个有经验的实验室的基因型测定的一致性程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brief summary of the legal proceeding.

The panel, held in Rome in April 2002 with the participation of more than 100 Italian directors of infectious diseases wards, followed a systematic approach to reviewing the evidence of any specific use of the genotypic assays to detect antiretroviral resistance. The single recommendations have been developed using a rating scheme based on consideration of the evidence and, when direct evidence was lacking, on expert opinion. Another emerging issue approached during this meeting is represented by the reproducibility of HIV-1 reverse transcriptase and protease sequencing in clinical settings. The degree of concordance of genotypic assays among 12 experienced laboratories is also reported.

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