Ferguson Neil M, Mallett Susan, Jackson Helen, Roberts Noel, Ward Penelope
Department of Infectious Disease Epidemiology, Imperial College London, St Mary's Campus, Norfolk Place, London W2 1PG, UK.
J Antimicrob Chemother. 2003 Apr;51(4):977-90. doi: 10.1093/jac/dkg136. Epub 2003 Mar 13.
A mathematical model of influenza transmission dynamics is used to simulate the impact of neuraminidase inhibitor therapy on infection rates and transmission of drug-resistant viral strains. The model incorporates population age structure, seasonal transmission, immunity and inclusion of elderly nursing home residents or non-residents. Key parameter values are estimated from epidemiological, clinical and experimental data. The analysis examines the factors determining the population spread of antiviral resistance, and predicts no significant transmission of neuraminidase inhibitor resistant virus. This conclusion is robust even at high therapy levels and under conservative assumptions regarding the likely frequency of transmission of resistant virus. The predicted incidence of resistance following protracted usage reflects primary drug resistance, currently estimated as approximately 2% for neuraminidase inhibitor therapy. It is also shown that until high levels of therapy are attained, early treatment of symptomatic cases is more efficient (per unit of drug) at preventing infections than prophylactic therapy.
流感传播动力学的数学模型用于模拟神经氨酸酶抑制剂疗法对感染率和耐药病毒株传播的影响。该模型纳入了人群年龄结构、季节性传播、免疫力以及老年疗养院居民或非居民的情况。关键参数值是根据流行病学、临床和实验数据估算得出的。分析考察了决定抗病毒耐药性在人群中传播的因素,并预测神经氨酸酶抑制剂耐药病毒不会有显著传播。即使在高治疗水平以及关于耐药病毒可能传播频率的保守假设下,这一结论依然可靠。长期使用后预测的耐药发生率反映了原发性耐药,目前估计神经氨酸酶抑制剂疗法的原发性耐药率约为2%。研究还表明,在达到高治疗水平之前,对有症状病例进行早期治疗(按单位药物计算)在预防感染方面比预防性治疗更有效。