Auranen K
Rolf Nevanlinna Institute, P.O. Box 4, FIN-00014 University of Helsinki, Finland.
Stat Med. 2000 Feb 15;19(3):281-96. doi: 10.1002/(sici)1097-0258(20000215)19:3<281::aid-sim344>3.0.co;2-d.
We consider the estimation of an age-specific incidence rate of a subclinical Haemophilus influenzae type b (Hib) infection from data recording the ages of children with a clinical Hib infection (Hib disease). The model is based on the assumption that the probability of being immune to clinical infection is determined by the time of the previous immunization caused by a subclinical infection, and by the distribution of the duration of immunity. We use a non-parametric Bayesian intensity model to arrive at smooth estimates of incidence rates. The estimated age-specific incidence rate of subclinical Hib infection is almost constant which indicates that the observed age-specific pattern of clinical Hib infection incidence is mainly due to immunity by either maternally derived antibodies or by immunizing subclinical infections. The estimated rate is relatively high, corresponding to one immunizing subclinical infection in less than two years.
我们考虑根据记录临床b型流感嗜血杆菌(Hib)感染(Hib病)患儿年龄的数据,来估计亚临床b型流感嗜血杆菌感染的年龄特异性发病率。该模型基于这样的假设:对临床感染产生免疫的概率由先前亚临床感染引起的免疫时间以及免疫持续时间的分布所决定。我们使用非参数贝叶斯强度模型来得出发病率的平滑估计值。亚临床Hib感染的估计年龄特异性发病率几乎是恒定的,这表明观察到的临床Hib感染发病率的年龄特异性模式主要是由于母体来源的抗体或亚临床感染免疫所致。估计的发病率相对较高,相当于不到两年就有一次亚临床感染免疫。