Optimizing prevalence estimates for a novel pathogen by reducing uncertainty in test characteristics

被引:1
|
作者
Larremore, Daniel B. [1 ,2 ]
Fosdick, Bailey K. [3 ]
Zhang, Sam [4 ]
Grad, Yonatan H. [5 ]
机构
[1] Univ Colorado Boulder, Dept Comp Sci, Boulder, CO 80309 USA
[2] Univ Colorado, BioFrontiers Inst, Boulder, CO 80303 USA
[3] Colorado State Univ, Dept Stat, Ft Collins, CO 80523 USA
[4] Univ Colorado Boulder, Dept Appl Math, Boulder, CO 80309 USA
[5] Harvard TH Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
关键词
Bayesian inference; Prevalence; Sample size calculation; Sensitivity; Specificity; DIAGNOSTIC-TESTS; SPECIFICITY; SENSITIVITY; ABSENCE; DISEASE;
D O I
10.1016/j.epidem.2022.100634
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Emergence of a novel pathogen drives the urgent need for diagnostic tests that can aid in defining disease prevalence. The limitations associated with rapid development and deployment of these tests result in a dilemma: In efforts to optimize prevalence estimates, would tests be better used in the lab to reduce uncertainty in test characteristics or to increase sample size in field studies? Here, we provide a framework to address this question through a joint Bayesian model that simultaneously analyzes lab validation and field survey data, and we define the impact of test allocation on inferences of sensitivity, specificity, and prevalence. In many scenarios, prevalence estimates can be most improved by apportioning additional effort towards validation rather than to the field. The joint model provides superior estimation of prevalence, sensitivity, and specificity, compared with typical analyses that model lab and field data separately, and it can be used to inform sample allocation when testing is limited.
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页数:4
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