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利用催化模型估计低流行地区甲型肝炎发病率:对免疫政策建模的启示。

Use of a catalytic model to estimate hepatitis A incidence in a low-endemicity country: implications for modeling immunization policies.

机构信息

Toronto Health Economics and Technology Assessment Collaborative, University of Toronto, Toronto, Ontario, Canada (BP, MK)

Department of Health Policy, Management and Evaluation, University of Toronto (BP, MK)

出版信息

Med Decis Making. 2012 Jan-Feb;32(1):167-75. doi: 10.1177/0272989X11398489. Epub 2011 Mar 10.

Abstract

BACKGROUND

Evaluating the cost-effectiveness of vaccine programs with dynamic modeling requires accurate estimates of incidence over time. Because infectious diseases are often underreported, supplementary data and statistical analyses are required to estimate true incidence. This study estimates the true incidence of hepatitis A virus (HAV) infection in Canada using a catalytic model.

METHODS

A catalytic model was used to reconcile HAV seroprevalence data with the corresponding true cumulative risk of infection estimated from incidence data.

RESULTS

The average annual reported incidence was 6.2 cases per 100,000 from 1980 to 1989 and 7.7/100,000 from 1990 to 1999, indicating that Canada is a low-incidence country. The seroprevalence in Canadian-born individuals (n = 7 studies) was approximately 1%-8% in ages <20, 1%-11% in ages 20-29, 7%-29% in ages 30-39, and higher in older age groups. Between 1980 and 1995, the catalytic model estimated an average annual incidence of 60/100,000 (95% confidence interval, 33-524); approximately 7.73 (4.21-67.33) times the average annual reported incidence of 7.78/100,000. For a typical birth cohort of 403 434 Canadians born in 1990, the model predicted 32 750 HAV cases by age 39, with a corresponding seroprevalence of approximately 8.12% by the year 2029.

IMPLICATIONS

Reliable estimates of true incidence of infectious disease are required for cost-effectiveness analysis of infectious disease programs. Catalytic models enable the synthesis of dispersed data, quantification of data limitations, and reconciliation of these limitations to estimate true incidence for economic evaluations.

摘要

背景

使用动态模型评估疫苗项目的成本效益需要对随时间推移的发病率进行准确估计。由于传染病常常报告不足,因此需要补充数据和统计分析来估计真实的发病率。本研究使用催化模型来估计加拿大甲型肝炎病毒(HAV)感染的真实发病率。

方法

使用催化模型来协调 HAV 血清流行率数据与从发病率数据估计的相应真实累计感染风险。

结果

1980 年至 1989 年期间,报告的年平均发病率为每 10 万人 6.2 例,1990 年至 1999 年期间为每 10 万人 7.7 例,表明加拿大是一个发病率较低的国家。在加拿大出生的个体中(n = 7 项研究),<20 岁的人群血清阳性率约为 1%-8%,20-29 岁的人群为 1%-11%,30-39 岁的人群为 7%-29%,年龄较大的人群血清阳性率更高。1980 年至 1995 年期间,催化模型估计每年的平均发病率为 60/100,000(95%置信区间,33-524);大约是每年报告的 7.78/100,000 发病率的 7.73(4.21-67.33)倍。对于 1990 年出生的 403434 名加拿大典型出生队列,该模型预测到 39 岁时将有 32750 例 HAV 病例,到 2029 年时,相应的血清阳性率约为 8.12%。

意义

需要可靠的传染病真实发病率估计值来进行传染病计划的成本效益分析。催化模型可用于综合分散的数据、量化数据限制,并协调这些限制以估计经济评估的真实发病率。

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