Abstract

BackgroundAmong HIV+ patients, alcohol use is a highly prevalent risk factor for both HIV transmission and poor adherence to HIV treatment. The large-scale implementation of effective interventions for treating alcohol problems remains a challenge in low-income countries with generalized HIV epidemics. It is essential to consider an intervention’s cost-effectiveness in dollars-per-health-outcome, and the long-term economic impact —or “return on investment” in monetary terms.MethodsWe conducted a cost-benefit analysis, measuring economic return on investment, of a task-shifted cognitive-behavioral therapy (CBT) intervention delivered by paraprofessionals to reduce alcohol use in a modeled cohort of 13,440 outpatients in Kenya. In our base-case, we estimated the costs and economic benefits from a societal perspective across a six-year time horizon, with a 3% annual discount rate. Costs included all costs associated with training and administering task-shifted CBT therapy. Benefits included the economic impact of lowered HIV incidence as well as the improvements in household and labor-force productivity. We conducted univariate and multivariate probabilistic sensitivity analyses to test the robustness of our results.ResultsUnder the base case, total costs for CBT rollout was $554,000, the value of benefits were $628,000, and the benefit-to-cost ratio was 1.13. Sensitivity analyses showed that under most assumptions, the benefit-to-cost ratio remained above unity indicating that the intervention was cost-saving (i.e., had positive return on investment). The duration of the treatment effect most effected the results in sensitivity analyses.ConclusionsCBT can be effectively and economically task-shifted to paraprofessionals in Kenya. The intervention can generate not only reductions in morbidity and mortality, but also economic savings for the health system in the medium and long term. The findings have implications for other countries with generalized HIV epidemics, high prevalence of alcohol consumption, and shortages of mental health professionals.Trial registrationThis paper uses data derived from “Cognitive Behavioral Treatment to Reduce Alcohol Use Among HIV-Infected Kenyans (KHBS)” with ClinicalTrials.gov registration NCT00792519 on 11/17/2008; and preliminary data from “A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention” (NCT01503255, registered on 12/16/2011).

Highlights

  • Among Human immunodeficiency virus (HIV)+ patients, alcohol use is a highly prevalent risk factor for both HIV transmission and poor adherence to HIV treatment

  • Dramatic progress against HIV/Acquired immune deficiency syndrome (AIDS) has been made in sub-Saharan Africa [12] –with disease incidence decreasing by 25% in 22 countries from 1990 to 2009 and treatment access expanding from 50,000 to over 5 million persons from 2002 to 2012 [13] – the progress towards “zero new infections and zero AIDSrelated deaths” promoted by UNAIDS [14] is hampered by several challenges

  • High levels of alcohol use are associated with higher rates of AIDSrelated complications and higher health care costs, any level of alcohol use places a patient at higher risk for such complications and higher costs— suggesting that there is no “safe” level of alcohol consumption for HIV-infected patients

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Summary

Introduction

Among HIV+ patients, alcohol use is a highly prevalent risk factor for both HIV transmission and poor adherence to HIV treatment. Dramatic progress against HIV/AIDS has been made in sub-Saharan Africa [12] –with disease incidence decreasing by 25% in 22 countries from 1990 to 2009 and treatment access expanding from 50,000 to over 5 million persons from 2002 to 2012 [13] – the progress towards “zero new infections and zero AIDSrelated deaths” promoted by UNAIDS [14] is hampered by several challenges These include the growing HIV prevalence due to expanded lifespans, limited accessibility to antiretrovirals (ARVs), and continued suboptimal adherence to treatment [13, 14]. We consider alcohol use of all levels as harmful for HIV+ persons throughout this paper

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