Cost-effectiveness of screening and treating alcohol use and depression among people living with HIV in Zimbabwe: a mathematical modeling study.

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Jasmine I-Shin Su, Yao-Rui Yeo, Mellesia Jeetoo, Neo K Morojele, Joel M Francis, Sheela Shenoi, R Scott Braithwaite
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引用次数: 0

Abstract

Background: Alcohol use disorder (AUD) and major depressive disorder (MDD) drive HIV transmission in many sub-Saharan African settings. The impact of screening and treating AUD and MDD on HIV outcomes is unknown. We aimed to identify the cost-effectiveness of AUD and MDD interventions in Zimbabwe, and their potential contribution to reaching Zimbabwe's Ending the HIV Epidemic 2030 goal.

Methods: Using a validated HIV compartmental transmission model in Zimbabwe, we compared four policy scenarios: prevention as usual (baseline); implement AUD screening (using AUDIT) and treatment (motivational interviewing and cognitive-behavioral therapy); implement MDD screening (using PHQ-9) and treatment (cognitive-behavioral therapy); and implement screening and treatment for both. Outcomes were HIV incidence projections, infections averted through 2030, quality-adjusted life-years gained, cost per infection averted, and cost per QALY gained. Analyses considered "spillover," when treatment for AUD also results in an improvement in MDD and the converse. Sensitivity analyses identified cost reductions necessary for AUD and MDD interventions to be as cost-effective as other HIV interventions, particularly the scale-up of long-acting PrEP.

Results: AUD and MDD combined will be responsible for 21.1% of new HIV infections in Zimbabwe by 2030. Without considering spillover, compared to the baseline, MDD intervention can reduce new infections by 5.4% at $2039/infection averted and $3186/QALY. AUD intervention can reduce new infections by 5.8%, but at $2,968/infection averted and $4753/QALY, compared to baseline. Both MDD and AUD interventions can reduce new infections by 11.1% at $2810/infection averted and $4229/QALY, compared to baseline. Considering spillover, compared to the baseline, MDD intervention can reduce new infections by 6.4% at $1714/infection averted and $2630/QALY. AUD intervention can reduce new infections by 7.4%, but at $2299/infection averted and $3560/QALY compared to baseline. Both MDD and AUD interventions can reduce new infections by 11.9% at $2247/infection averted and $3382/QALY compared to baseline. For MDD intervention to match the cost-effectiveness of scaling long-acting PrEP, the cost of MDD intervention would need to be reduced from $16.64 to $12.88 per person.

Conclusions: Implementing AUD and MDD interventions can play an important role in HIV reduction in Zimbabwe, particularly if intervention cost can be decreased while preserving effectiveness.

津巴布韦艾滋病毒感染者中酗酒和抑郁症筛查与治疗的成本效益:数学建模研究。
背景:在撒哈拉以南非洲的许多环境中,酒精使用障碍(AUD)和重度抑郁障碍(MDD)导致了艾滋病毒的传播。筛查和治疗 AUD 和 MDD 对艾滋病结果的影响尚不清楚。我们旨在确定津巴布韦 AUD 和 MDD 干预措施的成本效益,以及它们对实现津巴布韦 2030 年终结 HIV 流行目标的潜在贡献:我们在津巴布韦使用了一个经过验证的 HIV 分区传播模型,比较了四种政策方案:预防如常(基线);实施 AUD 筛查(使用 AUDIT)和治疗(动机访谈和认知行为疗法);实施 MDD 筛查(使用 PHQ-9)和治疗(认知行为疗法);以及实施这两种筛查和治疗。结果包括艾滋病发病率预测、2030 年前避免的感染、获得的质量调整生命年、避免每次感染的成本以及获得每个质量调整生命年的成本。分析考虑了 "溢出效应",即治疗 AUD 也会改善 MDD,反之亦然。敏感性分析确定了为使 AUD 和 MDD 干预措施与其他 HIV 干预措施(尤其是扩大长效 PrEP 的规模)一样具有成本效益而必须降低的成本:到 2030 年,AUD 和 MDD 将占津巴布韦新增 HIV 感染病例的 21.1%。在不考虑溢出效应的情况下,与基线相比,MDD 干预措施可减少 5.4% 的新感染病例,避免的感染病例为 2039 美元/例,QALY 为 3186 美元/QALY。AUD 干预措施可减少 5.8%的新发感染,但与基线相比,每避免一次感染需花费 2968 美元,每 QALY 需花费 4753 美元。MDD 和 AUD 干预措施可减少 11.1%的新感染,与基线相比,每避免一次感染需花费 2810 美元,每 QALY 需花费 4229 美元。考虑到溢出效应,与基线相比,MDD 干预可减少 6.4%的新发感染,每例感染可避免 1714 美元,每 QALY 可减少 2630 美元。AUD 干预可减少 7.4% 的新感染,但与基线相比,每避免一次感染需花费 2299 美元,每 QALY 需花费 3560 美元。MDD 和 AUD 干预措施可减少 11.9%的新感染,与基线相比,每避免一次感染的成本为 2247 美元,每 QALY 为 3382 美元。要使 MDD 干预与推广长效 PrEP 的成本效益相匹配,MDD 干预的成本需要从每人 16.64 美元降至 12.88 美元:在津巴布韦,实施 AUD 和 MDD 干预措施可在减少 HIV 感染方面发挥重要作用,尤其是如果能在保持有效性的同时降低干预成本的话。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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