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Cost-effectiveness analysis of emtricitabine/tenofovir versus lamivudine/zidovudine, in combination with efavirenz, in antiretroviral-naive, HIV-1-infected patients

Abstract Objective: The aim of this study was to compare the cost per unit of effectiveness (successful treatment episode) of 2 highly active antiretroviral therapy combinations–emtricitabine/tenofovir DF + efavirenz (TVD + EFV) and lamivudine/zidovudine + efavirenz (COMB + EFV)–in antiretroviral-na...

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Published in:Clinical therapeutics 2008-02, Vol.30 (2), p.372-381
Main Authors: Sánchez-de la Rosa, Rainel, MD, PhD, Herrera, Luis, MD, Moreno, Santiago, MD, PhD
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cited_by cdi_FETCH-LOGICAL-c397t-d2cbdf0aa97002ce55c88b8464c224f3892f97ffdcab1a4b2d5a7bf81bd604da3
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creator Sánchez-de la Rosa, Rainel, MD, PhD
Herrera, Luis, MD
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description Abstract Objective: The aim of this study was to compare the cost per unit of effectiveness (successful treatment episode) of 2 highly active antiretroviral therapy combinations–emtricitabine/tenofovir DF + efavirenz (TVD + EFV) and lamivudine/zidovudine + efavirenz (COMB + EFV)–in antiretroviral-naive, HIV-1-infected patients from the perspective of costs to society. Methods: This cost-effectiveness analysis was modeled using a decision tree that considered the therapeutic response (successful treatment episode, ie, HIV-1 RNA
doi_str_mv 10.1016/j.clinthera.2008.02.009
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Methods: This cost-effectiveness analysis was modeled using a decision tree that considered the therapeutic response (successful treatment episode, ie, HIV-1 RNA &lt;400 copies/mL using data obtained directly from a clinical trial) and the switch to rescue therapy in nonresponders. The time horizon was 24 months of treatment. Cost was defined as direct medical costs (drugs, diagnostic and/or laboratory tests, treatment of adverse effects) and indirect medical costs (productivity losses). All data are presented as €(2005). Sensitivity analysis was 1-factor threshold, adjustment of ex-factory cost, only direct costs, and applying discount rate in the study. The results are presented as incremental costs, success rates, and cost per patient with undetectable viral load or additional success. Results: The expected 48-week cost of the regimen that includes TVD + EFV was €46,464, and for the regimen that included COMB + EFV, €56,198. Therefore, savings of €9734 were achieved for each patient treated with TVD + EFV, as well as a gain of 13% of patients with undetectable viral load after 24 months of treatment. Consequently, treatment with TVD + EFV combination would be dominant in therapy for antiretroviral-naive, HIV-1-infected patients. Sensitivity tests supported the stability of the base-case analysis. The cost-effectiveness ratios were €619.52 for the TVD + EFV regimen versus €906.41 for the COMB + EFV regimen. Conclusion: Based on the results of this analysis, patients who started treatment of HIV-1 infection with combination TVD + EFV had significantly lower health care resource utilization and overall treatment costs compared with the COMB + EFV combination.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2008.02.009</identifier><identifier>PMID: 18343275</identifier><language>eng</language><publisher>Bridgewater, NJ: EM Inc USA</publisher><subject>Adenine - analogs &amp; derivatives ; Adenine - economics ; Adenine - therapeutic use ; Anti-HIV Agents - economics ; Anti-HIV Agents - therapeutic use ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiretroviral Therapy, Highly Active ; Antiviral agents ; Benzoxazines - economics ; Benzoxazines - therapeutic use ; Biological and medical sciences ; cost analysis ; Cost-Benefit Analysis ; Decision Trees ; Deoxycytidine - analogs &amp; derivatives ; Deoxycytidine - economics ; Deoxycytidine - therapeutic use ; Drug Costs ; Emtricitabine ; HAART ; Health Care Costs ; Health Resources - economics ; Health Resources - utilization ; HIV Infections - drug therapy ; HIV Infections - economics ; HIV Infections - virology ; HIV-1 ; Human viral diseases ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Infectious diseases ; Internal Medicine ; Lamivudine - economics ; Lamivudine - therapeutic use ; Medical Education ; Medical sciences ; Models, Economic ; nucleoside-analogue reverse transcriptase inhibitors ; Organophosphonates - economics ; Organophosphonates - therapeutic use ; Pharmacology. Drug treatments ; Reverse Transcriptase Inhibitors - economics ; Reverse Transcriptase Inhibitors - therapeutic use ; Tenofovir ; Time Factors ; Treatment Outcome ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Zidovudine - economics ; Zidovudine - therapeutic use</subject><ispartof>Clinical therapeutics, 2008-02, Vol.30 (2), p.372-381</ispartof><rights>Excerpta Medica Inc. All rights reserved.</rights><rights>2008 Excerpta Medica Inc. 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Methods: This cost-effectiveness analysis was modeled using a decision tree that considered the therapeutic response (successful treatment episode, ie, HIV-1 RNA &lt;400 copies/mL using data obtained directly from a clinical trial) and the switch to rescue therapy in nonresponders. The time horizon was 24 months of treatment. Cost was defined as direct medical costs (drugs, diagnostic and/or laboratory tests, treatment of adverse effects) and indirect medical costs (productivity losses). All data are presented as €(2005). Sensitivity analysis was 1-factor threshold, adjustment of ex-factory cost, only direct costs, and applying discount rate in the study. The results are presented as incremental costs, success rates, and cost per patient with undetectable viral load or additional success. Results: The expected 48-week cost of the regimen that includes TVD + EFV was €46,464, and for the regimen that included COMB + EFV, €56,198. Therefore, savings of €9734 were achieved for each patient treated with TVD + EFV, as well as a gain of 13% of patients with undetectable viral load after 24 months of treatment. Consequently, treatment with TVD + EFV combination would be dominant in therapy for antiretroviral-naive, HIV-1-infected patients. Sensitivity tests supported the stability of the base-case analysis. The cost-effectiveness ratios were €619.52 for the TVD + EFV regimen versus €906.41 for the COMB + EFV regimen. 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Antiparasitic agents</subject><subject>Antiretroviral Therapy, Highly Active</subject><subject>Antiviral agents</subject><subject>Benzoxazines - economics</subject><subject>Benzoxazines - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>cost analysis</subject><subject>Cost-Benefit Analysis</subject><subject>Decision Trees</subject><subject>Deoxycytidine - analogs &amp; derivatives</subject><subject>Deoxycytidine - economics</subject><subject>Deoxycytidine - therapeutic use</subject><subject>Drug Costs</subject><subject>Emtricitabine</subject><subject>HAART</subject><subject>Health Care Costs</subject><subject>Health Resources - economics</subject><subject>Health Resources - utilization</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - economics</subject><subject>HIV Infections - virology</subject><subject>HIV-1</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Infectious diseases</subject><subject>Internal Medicine</subject><subject>Lamivudine - economics</subject><subject>Lamivudine - therapeutic use</subject><subject>Medical Education</subject><subject>Medical sciences</subject><subject>Models, Economic</subject><subject>nucleoside-analogue reverse transcriptase inhibitors</subject><subject>Organophosphonates - economics</subject><subject>Organophosphonates - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Reverse Transcriptase Inhibitors - economics</subject><subject>Reverse Transcriptase Inhibitors - therapeutic use</subject><subject>Tenofovir</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Methods: This cost-effectiveness analysis was modeled using a decision tree that considered the therapeutic response (successful treatment episode, ie, HIV-1 RNA &lt;400 copies/mL using data obtained directly from a clinical trial) and the switch to rescue therapy in nonresponders. The time horizon was 24 months of treatment. Cost was defined as direct medical costs (drugs, diagnostic and/or laboratory tests, treatment of adverse effects) and indirect medical costs (productivity losses). All data are presented as €(2005). Sensitivity analysis was 1-factor threshold, adjustment of ex-factory cost, only direct costs, and applying discount rate in the study. The results are presented as incremental costs, success rates, and cost per patient with undetectable viral load or additional success. Results: The expected 48-week cost of the regimen that includes TVD + EFV was €46,464, and for the regimen that included COMB + EFV, €56,198. Therefore, savings of €9734 were achieved for each patient treated with TVD + EFV, as well as a gain of 13% of patients with undetectable viral load after 24 months of treatment. Consequently, treatment with TVD + EFV combination would be dominant in therapy for antiretroviral-naive, HIV-1-infected patients. Sensitivity tests supported the stability of the base-case analysis. The cost-effectiveness ratios were €619.52 for the TVD + EFV regimen versus €906.41 for the COMB + EFV regimen. Conclusion: Based on the results of this analysis, patients who started treatment of HIV-1 infection with combination TVD + EFV had significantly lower health care resource utilization and overall treatment costs compared with the COMB + EFV combination.</abstract><cop>Bridgewater, NJ</cop><pub>EM Inc USA</pub><pmid>18343275</pmid><doi>10.1016/j.clinthera.2008.02.009</doi><tpages>10</tpages></addata></record>
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ispartof Clinical therapeutics, 2008-02, Vol.30 (2), p.372-381
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source ScienceDirect Journals
subjects Adenine - analogs & derivatives
Adenine - economics
Adenine - therapeutic use
Anti-HIV Agents - economics
Anti-HIV Agents - therapeutic use
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiretroviral Therapy, Highly Active
Antiviral agents
Benzoxazines - economics
Benzoxazines - therapeutic use
Biological and medical sciences
cost analysis
Cost-Benefit Analysis
Decision Trees
Deoxycytidine - analogs & derivatives
Deoxycytidine - economics
Deoxycytidine - therapeutic use
Drug Costs
Emtricitabine
HAART
Health Care Costs
Health Resources - economics
Health Resources - utilization
HIV Infections - drug therapy
HIV Infections - economics
HIV Infections - virology
HIV-1
Human viral diseases
Humans
Immunodeficiencies
Immunodeficiencies. Immunoglobulinopathies
Immunopathology
Infectious diseases
Internal Medicine
Lamivudine - economics
Lamivudine - therapeutic use
Medical Education
Medical sciences
Models, Economic
nucleoside-analogue reverse transcriptase inhibitors
Organophosphonates - economics
Organophosphonates - therapeutic use
Pharmacology. Drug treatments
Reverse Transcriptase Inhibitors - economics
Reverse Transcriptase Inhibitors - therapeutic use
Tenofovir
Time Factors
Treatment Outcome
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Zidovudine - economics
Zidovudine - therapeutic use
title Cost-effectiveness analysis of emtricitabine/tenofovir versus lamivudine/zidovudine, in combination with efavirenz, in antiretroviral-naive, HIV-1-infected patients
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