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美国高危年轻女性衣原体检测主动退出模式的成本效益分析

Cost-Effectiveness of Opt-Out Chlamydia Testing for High-Risk Young Women in the U.S.

作者信息

Owusu-Edusei Kwame, Hoover Karen W, Gift Thomas L

机构信息

Division of STD Prevention, CDC, Atlanta, Georgia.

Division of STD Prevention, CDC, Atlanta, Georgia.

出版信息

Am J Prev Med. 2016 Aug;51(2):216-224. doi: 10.1016/j.amepre.2016.01.007. Epub 2016 Mar 4.

Abstract

INTRODUCTION

In spite of chlamydia screening recommendations, U.S. testing coverage continues to be low. This study explored the cost-effectiveness of a patient-directed, universal, opportunistic Opt-Out Testing strategy (based on insurance coverage, healthcare utilization, and test acceptance probabilities) for all women aged 15-24 years compared with current Risk-Based Screening (30% coverage) from a societal perspective.

METHODS

Based on insurance coverage (80%); healthcare utilization (83%); and test acceptance (75%), the proposed Opt-Out Testing strategy would have an expected annual testing coverage of approximately 50% for sexually active women aged 15-24 years. A basic compartmental heterosexual transmission model was developed to account for population-level transmission dynamics. Two groups were assumed based on self-reported sexual activity. All model parameters were obtained from the literature. Costs and benefits were tracked over a 50-year period. The relative sensitivity of the estimated incremental cost-effectiveness ratios to the variables/parameters was determined. This study was conducted in 2014-2015.

RESULTS

Based on the model, the Opt-Out Testing strategy decreased the overall chlamydia prevalence by >55% (2.7% to 1.2%). The Opt-Out Testing strategy was cost saving compared with the current Risk-Based Screening strategy. The estimated incremental cost-effectiveness ratio was most sensitive to the female pre-opt out prevalence, followed by the probability of female sequelae and discount rate.

CONCLUSIONS

The proposed Opt-Out Testing strategy was cost saving, improving health outcomes at a lower net cost than current testing. However, testing gaps would remain because many women might not have health insurance coverage, or not utilize health care.

摘要

引言

尽管有衣原体筛查建议,但美国的检测覆盖率仍然很低。本研究从社会角度探讨了一种针对所有15至24岁女性的患者导向型、普遍、机会性选择退出检测策略(基于保险覆盖范围、医疗保健利用率和检测接受概率)与当前基于风险的筛查(覆盖率30%)相比的成本效益。

方法

基于保险覆盖范围(80%)、医疗保健利用率(83%)和检测接受率(75%),拟议的选择退出检测策略预计15至24岁性活跃女性的年度检测覆盖率约为50%。开发了一个基本的分区异性传播模型来考虑人群水平的传播动态。根据自我报告的性活动假设分为两组。所有模型参数均从文献中获得。在50年期间跟踪成本和效益。确定了估计的增量成本效益比相对于变量/参数的相对敏感性。本研究于2014 - 2015年进行。

结果

基于该模型,选择退出检测策略使衣原体总体患病率降低了>55%(从2.7%降至1.2%)。与当前基于风险的筛查策略相比,选择退出检测策略节省了成本。估计的增量成本效益比最敏感于女性选择退出前的患病率,其次是女性后遗症概率和贴现率。

结论

拟议的选择退出检测策略节省了成本,以低于当前检测的净成本改善了健康结果。然而,检测差距仍将存在,因为许多女性可能没有医疗保险覆盖,或者不利用医疗保健。

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