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Clinical and virologic outcomes in patients with oseltamivir‐resistant seasonal influenza A (H1N1) infections: results from a clinical trial

机译:耐奥司他韦的季节性甲型流感(H1N1)感染患者的临床和病毒学结果:一项临床试验的结果

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摘要

Please cite this paper as: Dharan et al. (2011) Clinical and virologic outcomes in patients with oseltamivir‐resistant seasonal influenza A (H1N1) infections: results from a clinical trial. Influenza and Other Respiratory Viruses 6(3), 153–158.Nineteen patients with oseltamivir‐resistant seasonal influenza A (H1N1) infections were randomized to receive oseltamivir or placebo. Nasopharyngeal swabs were obtained, and clinical and virologic outcomes were compared, stratified by early or late treatment. Neuraminidase inhibition assay and pyrosequencing for H275Y confirmed resistance. Twelve (63%) patients received oseltamivir; 8 (67%) received late treatment. Seven (37%) patients received placebo; 6 (86%) presented >48 hours after onset. Time to 50% decrease in symptom severity, complete symptom resolution, and first negative culture were shortest among the early treatment group. While sample size prohibits a strong conclusion, future studies should evaluate for similar trends.
机译:请将此论文引用为:Dharan等。 (2011)对奥司他韦耐药的季节性甲型流感(H1N1)感染患者的临床和病毒学结果:一项临床试验的结果。流感和其他呼吸道病毒6(3),153–158。19例耐奥司他韦耐药的季节性A型流感(H1N1)感染的患者被随机分配接受奥司他韦或安慰剂。获得鼻咽拭子,并比较临床和病毒学结果,按早期或晚期治疗分层。神经氨酸酶抑制测定和H275Y的焦磷酸测序证实了耐药性。十二名(63%)患者接受了奥司他韦治疗; 8(67%)人接受了后期治疗。七名(37%)患者接受了安慰剂;发病后48小时以上有6例(86%)出现。在早期治疗组中,症状严重程度降低,症状完全缓解和首次阴性培养的时间最短为50%。尽管样本量无法得出有力的结论,但未来的研究应评估类似趋势。

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