Stephenson Iain, Democratis Jane, Lackenby Angie, McNally Teresa, Smith James, Pareek Manish, Ellis Joanna, Bermingham Alison, Nicholson Karl, Zambon Maria
Infectious Diseases Unit, Leicester Royal Infirmary, Leicester, UK.
Clin Infect Dis. 2009 Feb 15;48(4):389-96. doi: 10.1086/596311.
Oseltamivir, a specific influenza neuraminidase inhibitor, is an effective treatment for seasonal influenza. Emergence of drug-resistant influenza viruses after treatment has been reported, particularly in children in Japan, where the dosing schedule is different from that used throughout the rest of the world. We investigated the emergence of drug-resistant infection in children treated with a tiered weight-based dosing regimen.
We analyzed sequential clinical nasopharyngeal samples, obtained before and after tiered weight-based oseltamivir therapy, from children with acute influenza during 2005-2007. We isolated viruses, tested for drug resistance with use of a fluorescence-based neuraminidase inhibition assay, performed neuraminidase gene sequencing, and determined quantitative viral loads.
Sixty-four children (34 with influenza A subtype H3N2, 11 with influenza A subtype H1N1, and 19 with influenza B virus) aged 1-12 years (median age, 3 years, 1 month) were enrolled. By days 4-7 after initiation of treatment, of 64 samples tested, 47 (73.4%) and 26 (40.6%) had virus detectable by reverse-transcriptase polymerase chain reaction and culture, respectively. By days 8-12 after initiation of treatment, of 53 samples tested, 18 (33.9%) and 1 (1.8%) had virus detectable by reverse-transcriptase polymerase chain reaction and culture, respectively. We found no statistically significant differences in the reduction of viral shedding or time to clearance of virus between viral subtypes. Antiviral-resistant viruses were recovered from 3 (27.3%) of 11 children with influenza A subtype H1N1, 1 (2.9%) of 34 children with influenza A subtype H3N2, and 0 (0%) of 19 children with influenza B virus, all of whom were treated with oseltamivir (P = .004). There was no evidence of prolonged illness in children infected with drug-resistant virus.
Drug resistance emerges at a higher rate in influenza A subtype H1N1 virus than in influenza A subtype H3N2 or influenza B virus after tiered weight-based oseltamivir therapy. Virological surveillance for patterns of drug resistance is essential for determination of antiviral treatment strategies and for composition of pandemic preparedness stockpiles.
奥司他韦是一种特异性流感神经氨酸酶抑制剂,是治疗季节性流感的有效药物。已有报道称治疗后出现耐药流感病毒,尤其是在日本儿童中,该国的给药方案与世界其他地区不同。我们调查了采用基于体重分层给药方案治疗的儿童中耐药感染的出现情况。
我们分析了2005年至2007年期间急性流感儿童在基于体重分层的奥司他韦治疗前后采集的连续临床鼻咽样本。我们分离病毒,使用基于荧光的神经氨酸酶抑制试验检测耐药性,进行神经氨酸酶基因测序,并测定病毒载量。
纳入了64名1至12岁(中位年龄3岁1个月)的儿童(34例甲型H3N2流感、11例甲型H1N1流感和19例乙型流感病毒感染)。治疗开始后第4至7天,在检测的64份样本中,分别有47份(73.4%)和26份(40.6%)通过逆转录聚合酶链反应和培养检测到病毒。治疗开始后第8至12天,在检测的53份样本中,分别有18份(33.9%)和1份(1.8%)通过逆转录聚合酶链反应和培养检测到病毒。我们发现不同病毒亚型在病毒脱落减少或病毒清除时间方面无统计学显著差异。在11例甲型H1N1流感儿童中有3例(27.3%)、34例甲型H3N2流感儿童中有1例(2.9%)以及19例乙型流感病毒感染儿童中有0例(0%)分离出抗病毒耐药病毒,所有这些儿童均接受了奥司他韦治疗(P = 0.004)。没有证据表明感染耐药病毒的儿童病程延长。
在基于体重分层的奥司他韦治疗后,甲型H1N1流感病毒的耐药发生率高于甲型H3N2流感或乙型流感病毒。对耐药模式进行病毒学监测对于确定抗病毒治疗策略和大流行储备药物的组成至关重要。