Estimation of the cost-effectiveness of HIV prevention portfolios for people who inject drugs in the United States: A model-based analysis

The risks of HIV transmission associated with the opioid epidemic make cost-effective programs for people who inject drugs (PWID) a public health priority. Some of these programs have benefits beyond prevention of HIV-a critical consideration given that injection drug use is increasing across most U...

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Veröffentlicht in:PLoS medicine 2017-05, Vol.14 (5), p.e1002312
Hauptverfasser: Bernard, Cora L, Owens, Douglas K, Goldhaber-Fiebert, Jeremy D, Brandeau, Margaret L
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Owens, Douglas K
Goldhaber-Fiebert, Jeremy D
Brandeau, Margaret L
description The risks of HIV transmission associated with the opioid epidemic make cost-effective programs for people who inject drugs (PWID) a public health priority. Some of these programs have benefits beyond prevention of HIV-a critical consideration given that injection drug use is increasing across most United States demographic groups. To identify high-value HIV prevention program portfolios for US PWID, we consider combinations of four interventions with demonstrated efficacy: opioid agonist therapy (OAT), needle and syringe programs (NSPs), HIV testing and treatment (Test & Treat), and oral HIV pre-exposure prophylaxis (PrEP). We adapted an empirically calibrated dynamic compartmental model and used it to assess the discounted costs (in 2015 US dollars), health outcomes (HIV infections averted, change in HIV prevalence, and discounted quality-adjusted life years [QALYs]), and incremental cost-effectiveness ratios (ICERs) of the four prevention programs, considered singly and in combination over a 20-y time horizon. We obtained epidemiologic, economic, and health utility parameter estimates from the literature, previously published models, and expert opinion. We estimate that expansions of OAT, NSPs, and Test & Treat implemented singly up to 50% coverage levels can be cost-effective relative to the next highest coverage level (low, medium, and high at 40%, 45%, and 50%, respectively) and that OAT, which we assume to have immediate and direct health benefits for the individual, has the potential to be the highest value investment, even under scenarios where it prevents fewer infections than other programs. Although a model-based analysis can provide only estimates of health outcomes, we project that, over 20 y, 50% coverage with OAT could avert up to 22,000 (95% CI: 5,200, 46,000) infections and cost US$18,000 (95% CI: US$14,000, US$24,000) per QALY gained, 50% NSP coverage could avert up to 35,000 (95% CI: 8,900, 43,000) infections and cost US$25,000 (95% CI: US$7,000, US$76,000) per QALY gained, 50% Test & Treat coverage could avert up to 6,700 (95% CI: 1,200, 16,000) infections and cost US$27,000 (95% CI: US$15,000, US$48,000) per QALY gained, and 50% PrEP coverage could avert up to 37,000 (22,000, 58,000) infections and cost US$300,000 (95% CI: US$162,000, US$667,000) per QALY gained. When coverage expansions are allowed to include combined investment with other programs and are compared to the next best intervention, the model projects that scaling OAT cov
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Some of these programs have benefits beyond prevention of HIV-a critical consideration given that injection drug use is increasing across most United States demographic groups. To identify high-value HIV prevention program portfolios for US PWID, we consider combinations of four interventions with demonstrated efficacy: opioid agonist therapy (OAT), needle and syringe programs (NSPs), HIV testing and treatment (Test &amp; Treat), and oral HIV pre-exposure prophylaxis (PrEP). We adapted an empirically calibrated dynamic compartmental model and used it to assess the discounted costs (in 2015 US dollars), health outcomes (HIV infections averted, change in HIV prevalence, and discounted quality-adjusted life years [QALYs]), and incremental cost-effectiveness ratios (ICERs) of the four prevention programs, considered singly and in combination over a 20-y time horizon. We obtained epidemiologic, economic, and health utility parameter estimates from the literature, previously published models, and expert opinion. We estimate that expansions of OAT, NSPs, and Test &amp; Treat implemented singly up to 50% coverage levels can be cost-effective relative to the next highest coverage level (low, medium, and high at 40%, 45%, and 50%, respectively) and that OAT, which we assume to have immediate and direct health benefits for the individual, has the potential to be the highest value investment, even under scenarios where it prevents fewer infections than other programs. Although a model-based analysis can provide only estimates of health outcomes, we project that, over 20 y, 50% coverage with OAT could avert up to 22,000 (95% CI: 5,200, 46,000) infections and cost US$18,000 (95% CI: US$14,000, US$24,000) per QALY gained, 50% NSP coverage could avert up to 35,000 (95% CI: 8,900, 43,000) infections and cost US$25,000 (95% CI: US$7,000, US$76,000) per QALY gained, 50% Test &amp; Treat coverage could avert up to 6,700 (95% CI: 1,200, 16,000) infections and cost US$27,000 (95% CI: US$15,000, US$48,000) per QALY gained, and 50% PrEP coverage could avert up to 37,000 (22,000, 58,000) infections and cost US$300,000 (95% CI: US$162,000, US$667,000) per QALY gained. When coverage expansions are allowed to include combined investment with other programs and are compared to the next best intervention, the model projects that scaling OAT coverage up to 50%, then scaling NSP coverage to 50%, then scaling Test &amp; Treat coverage to 50% can be cost-effective, with each coverage expansion having the potential to cost less than US$50,000 per QALY gained relative to the next best portfolio. In probabilistic sensitivity analyses, 59% of portfolios prioritized the addition of OAT and 41% prioritized the addition of NSPs, while PrEP was not likely to be a priority nor a cost-effective addition. Our findings are intended to be illustrative, as data on achievable coverage are limited and, in practice, the expansion scenarios considered may exceed feasible levels. We assumed independence of interventions and constant returns to scale. Extensive sensitivity analyses allowed us to assess parameter sensitivity, but the use of a dynamic compartmental model limited the exploration of structural sensitivities. We estimate that OAT, NSPs, and Test &amp; Treat, implemented singly or in combination, have the potential to effectively and cost-effectively prevent HIV in US PWID. PrEP is not likely to be cost-effective in this population, based on the scenarios we evaluated. While local budgets or policy may constrain feasible coverage levels for the various interventions, our findings suggest that investments in combined prevention programs can substantially reduce HIV transmission and improve health outcomes among PWID.</description><identifier>ISSN: 1549-1676</identifier><identifier>ISSN: 1549-1277</identifier><identifier>EISSN: 1549-1676</identifier><identifier>DOI: 10.1371/journal.pmed.1002312</identifier><identifier>PMID: 28542184</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antiretroviral drugs ; Biology and Life Sciences ; Budgeting ; Cost-Benefit Analysis ; Demographics ; Disease transmission ; Drug abuse ; Drug Users ; Effectiveness ; Epidemics ; Feasibility studies ; Health care costs ; Health risk assessment ; Health risks ; HIV ; HIV infections ; HIV Infections - epidemiology ; HIV Infections - prevention &amp; control ; Human immunodeficiency virus ; Humans ; Injectable drugs ; Injection ; Management ; Medicine and Health Sciences ; Methadone ; Models, Theoretical ; Needle exchange programs ; Opioids ; Oral cavity ; Portfolios ; Prevalence ; Prevention ; Prevention programs ; Primary Prevention - economics ; Probabilistic methods ; Probability theory ; Prophylaxis ; Public health ; Scaling ; Sensitivity ; Sensitivity analysis ; Social Sciences ; Substance Abuse, Intravenous - epidemiology ; Substance Abuse, Intravenous - prevention &amp; control ; United States - epidemiology</subject><ispartof>PLoS medicine, 2017-05, Vol.14 (5), p.e1002312</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Bernard CL, Owens DK, Goldhaber-Fiebert JD, Brandeau ML (2017) Estimation of the cost-effectiveness of HIV prevention portfolios for people who inject drugs in the United States: A model-based analysis. PLoS Med 14(5): e1002312. https://doi.org/10.1371/journal.pmed.1002312</rights><rights>2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Bernard CL, Owens DK, Goldhaber-Fiebert JD, Brandeau ML (2017) Estimation of the cost-effectiveness of HIV prevention portfolios for people who inject drugs in the United States: A model-based analysis. PLoS Med 14(5): e1002312. https://doi.org/10.1371/journal.pmed.1002312</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c764t-c1bcd5b9b24f9fd4c35c7f7c6bf81f28c07f30bb7347fad42045fd45b4ab5f543</citedby><cites>FETCH-LOGICAL-c764t-c1bcd5b9b24f9fd4c35c7f7c6bf81f28c07f30bb7347fad42045fd45b4ab5f543</cites><orcidid>0000-0002-1967-6356</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443477/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443477/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28542184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Tsai, Alexander C.</contributor><creatorcontrib>Bernard, Cora L</creatorcontrib><creatorcontrib>Owens, Douglas K</creatorcontrib><creatorcontrib>Goldhaber-Fiebert, Jeremy D</creatorcontrib><creatorcontrib>Brandeau, Margaret L</creatorcontrib><title>Estimation of the cost-effectiveness of HIV prevention portfolios for people who inject drugs in the United States: A model-based analysis</title><title>PLoS medicine</title><addtitle>PLoS Med</addtitle><description>The risks of HIV transmission associated with the opioid epidemic make cost-effective programs for people who inject drugs (PWID) a public health priority. Some of these programs have benefits beyond prevention of HIV-a critical consideration given that injection drug use is increasing across most United States demographic groups. To identify high-value HIV prevention program portfolios for US PWID, we consider combinations of four interventions with demonstrated efficacy: opioid agonist therapy (OAT), needle and syringe programs (NSPs), HIV testing and treatment (Test &amp; Treat), and oral HIV pre-exposure prophylaxis (PrEP). We adapted an empirically calibrated dynamic compartmental model and used it to assess the discounted costs (in 2015 US dollars), health outcomes (HIV infections averted, change in HIV prevalence, and discounted quality-adjusted life years [QALYs]), and incremental cost-effectiveness ratios (ICERs) of the four prevention programs, considered singly and in combination over a 20-y time horizon. We obtained epidemiologic, economic, and health utility parameter estimates from the literature, previously published models, and expert opinion. We estimate that expansions of OAT, NSPs, and Test &amp; Treat implemented singly up to 50% coverage levels can be cost-effective relative to the next highest coverage level (low, medium, and high at 40%, 45%, and 50%, respectively) and that OAT, which we assume to have immediate and direct health benefits for the individual, has the potential to be the highest value investment, even under scenarios where it prevents fewer infections than other programs. Although a model-based analysis can provide only estimates of health outcomes, we project that, over 20 y, 50% coverage with OAT could avert up to 22,000 (95% CI: 5,200, 46,000) infections and cost US$18,000 (95% CI: US$14,000, US$24,000) per QALY gained, 50% NSP coverage could avert up to 35,000 (95% CI: 8,900, 43,000) infections and cost US$25,000 (95% CI: US$7,000, US$76,000) per QALY gained, 50% Test &amp; Treat coverage could avert up to 6,700 (95% CI: 1,200, 16,000) infections and cost US$27,000 (95% CI: US$15,000, US$48,000) per QALY gained, and 50% PrEP coverage could avert up to 37,000 (22,000, 58,000) infections and cost US$300,000 (95% CI: US$162,000, US$667,000) per QALY gained. When coverage expansions are allowed to include combined investment with other programs and are compared to the next best intervention, the model projects that scaling OAT coverage up to 50%, then scaling NSP coverage to 50%, then scaling Test &amp; Treat coverage to 50% can be cost-effective, with each coverage expansion having the potential to cost less than US$50,000 per QALY gained relative to the next best portfolio. In probabilistic sensitivity analyses, 59% of portfolios prioritized the addition of OAT and 41% prioritized the addition of NSPs, while PrEP was not likely to be a priority nor a cost-effective addition. Our findings are intended to be illustrative, as data on achievable coverage are limited and, in practice, the expansion scenarios considered may exceed feasible levels. We assumed independence of interventions and constant returns to scale. Extensive sensitivity analyses allowed us to assess parameter sensitivity, but the use of a dynamic compartmental model limited the exploration of structural sensitivities. We estimate that OAT, NSPs, and Test &amp; Treat, implemented singly or in combination, have the potential to effectively and cost-effectively prevent HIV in US PWID. PrEP is not likely to be cost-effective in this population, based on the scenarios we evaluated. While local budgets or policy may constrain feasible coverage levels for the various interventions, our findings suggest that investments in combined prevention programs can substantially reduce HIV transmission and improve health outcomes among PWID.</description><subject>Antiretroviral drugs</subject><subject>Biology and Life Sciences</subject><subject>Budgeting</subject><subject>Cost-Benefit Analysis</subject><subject>Demographics</subject><subject>Disease transmission</subject><subject>Drug abuse</subject><subject>Drug Users</subject><subject>Effectiveness</subject><subject>Epidemics</subject><subject>Feasibility studies</subject><subject>Health care costs</subject><subject>Health risk assessment</subject><subject>Health risks</subject><subject>HIV</subject><subject>HIV infections</subject><subject>HIV Infections - epidemiology</subject><subject>HIV Infections - prevention &amp; control</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Injectable drugs</subject><subject>Injection</subject><subject>Management</subject><subject>Medicine and Health Sciences</subject><subject>Methadone</subject><subject>Models, Theoretical</subject><subject>Needle exchange programs</subject><subject>Opioids</subject><subject>Oral cavity</subject><subject>Portfolios</subject><subject>Prevalence</subject><subject>Prevention</subject><subject>Prevention programs</subject><subject>Primary Prevention - economics</subject><subject>Probabilistic methods</subject><subject>Probability theory</subject><subject>Prophylaxis</subject><subject>Public health</subject><subject>Scaling</subject><subject>Sensitivity</subject><subject>Sensitivity analysis</subject><subject>Social Sciences</subject><subject>Substance Abuse, Intravenous - epidemiology</subject><subject>Substance Abuse, Intravenous - prevention &amp; 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Owens, Douglas K ; Goldhaber-Fiebert, Jeremy D ; Brandeau, Margaret L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c764t-c1bcd5b9b24f9fd4c35c7f7c6bf81f28c07f30bb7347fad42045fd45b4ab5f543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antiretroviral drugs</topic><topic>Biology and Life Sciences</topic><topic>Budgeting</topic><topic>Cost-Benefit Analysis</topic><topic>Demographics</topic><topic>Disease transmission</topic><topic>Drug abuse</topic><topic>Drug Users</topic><topic>Effectiveness</topic><topic>Epidemics</topic><topic>Feasibility studies</topic><topic>Health care costs</topic><topic>Health risk assessment</topic><topic>Health risks</topic><topic>HIV</topic><topic>HIV infections</topic><topic>HIV Infections - epidemiology</topic><topic>HIV Infections - prevention &amp; control</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Injectable drugs</topic><topic>Injection</topic><topic>Management</topic><topic>Medicine and Health Sciences</topic><topic>Methadone</topic><topic>Models, Theoretical</topic><topic>Needle exchange programs</topic><topic>Opioids</topic><topic>Oral cavity</topic><topic>Portfolios</topic><topic>Prevalence</topic><topic>Prevention</topic><topic>Prevention programs</topic><topic>Primary Prevention - economics</topic><topic>Probabilistic methods</topic><topic>Probability theory</topic><topic>Prophylaxis</topic><topic>Public health</topic><topic>Scaling</topic><topic>Sensitivity</topic><topic>Sensitivity analysis</topic><topic>Social Sciences</topic><topic>Substance Abuse, Intravenous - epidemiology</topic><topic>Substance Abuse, Intravenous - prevention &amp; 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Some of these programs have benefits beyond prevention of HIV-a critical consideration given that injection drug use is increasing across most United States demographic groups. To identify high-value HIV prevention program portfolios for US PWID, we consider combinations of four interventions with demonstrated efficacy: opioid agonist therapy (OAT), needle and syringe programs (NSPs), HIV testing and treatment (Test &amp; Treat), and oral HIV pre-exposure prophylaxis (PrEP). We adapted an empirically calibrated dynamic compartmental model and used it to assess the discounted costs (in 2015 US dollars), health outcomes (HIV infections averted, change in HIV prevalence, and discounted quality-adjusted life years [QALYs]), and incremental cost-effectiveness ratios (ICERs) of the four prevention programs, considered singly and in combination over a 20-y time horizon. We obtained epidemiologic, economic, and health utility parameter estimates from the literature, previously published models, and expert opinion. We estimate that expansions of OAT, NSPs, and Test &amp; Treat implemented singly up to 50% coverage levels can be cost-effective relative to the next highest coverage level (low, medium, and high at 40%, 45%, and 50%, respectively) and that OAT, which we assume to have immediate and direct health benefits for the individual, has the potential to be the highest value investment, even under scenarios where it prevents fewer infections than other programs. Although a model-based analysis can provide only estimates of health outcomes, we project that, over 20 y, 50% coverage with OAT could avert up to 22,000 (95% CI: 5,200, 46,000) infections and cost US$18,000 (95% CI: US$14,000, US$24,000) per QALY gained, 50% NSP coverage could avert up to 35,000 (95% CI: 8,900, 43,000) infections and cost US$25,000 (95% CI: US$7,000, US$76,000) per QALY gained, 50% Test &amp; Treat coverage could avert up to 6,700 (95% CI: 1,200, 16,000) infections and cost US$27,000 (95% CI: US$15,000, US$48,000) per QALY gained, and 50% PrEP coverage could avert up to 37,000 (22,000, 58,000) infections and cost US$300,000 (95% CI: US$162,000, US$667,000) per QALY gained. When coverage expansions are allowed to include combined investment with other programs and are compared to the next best intervention, the model projects that scaling OAT coverage up to 50%, then scaling NSP coverage to 50%, then scaling Test &amp; Treat coverage to 50% can be cost-effective, with each coverage expansion having the potential to cost less than US$50,000 per QALY gained relative to the next best portfolio. In probabilistic sensitivity analyses, 59% of portfolios prioritized the addition of OAT and 41% prioritized the addition of NSPs, while PrEP was not likely to be a priority nor a cost-effective addition. Our findings are intended to be illustrative, as data on achievable coverage are limited and, in practice, the expansion scenarios considered may exceed feasible levels. We assumed independence of interventions and constant returns to scale. Extensive sensitivity analyses allowed us to assess parameter sensitivity, but the use of a dynamic compartmental model limited the exploration of structural sensitivities. We estimate that OAT, NSPs, and Test &amp; Treat, implemented singly or in combination, have the potential to effectively and cost-effectively prevent HIV in US PWID. PrEP is not likely to be cost-effective in this population, based on the scenarios we evaluated. While local budgets or policy may constrain feasible coverage levels for the various interventions, our findings suggest that investments in combined prevention programs can substantially reduce HIV transmission and improve health outcomes among PWID.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28542184</pmid><doi>10.1371/journal.pmed.1002312</doi><orcidid>https://orcid.org/0000-0002-1967-6356</orcidid><oa>free_for_read</oa></addata></record>
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1549-1676
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subjects Antiretroviral drugs
Biology and Life Sciences
Budgeting
Cost-Benefit Analysis
Demographics
Disease transmission
Drug abuse
Drug Users
Effectiveness
Epidemics
Feasibility studies
Health care costs
Health risk assessment
Health risks
HIV
HIV infections
HIV Infections - epidemiology
HIV Infections - prevention & control
Human immunodeficiency virus
Humans
Injectable drugs
Injection
Management
Medicine and Health Sciences
Methadone
Models, Theoretical
Needle exchange programs
Opioids
Oral cavity
Portfolios
Prevalence
Prevention
Prevention programs
Primary Prevention - economics
Probabilistic methods
Probability theory
Prophylaxis
Public health
Scaling
Sensitivity
Sensitivity analysis
Social Sciences
Substance Abuse, Intravenous - epidemiology
Substance Abuse, Intravenous - prevention & control
United States - epidemiology
title Estimation of the cost-effectiveness of HIV prevention portfolios for people who inject drugs in the United States: A model-based analysis
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