Cost-effectiveness of statins for primary prevention of atherosclerotic cardiovascular disease among people living with HIV in the United States.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
03 2021
Historique:
revised: 04 02 2021
received: 04 09 2020
accepted: 23 02 2021
entrez: 22 3 2021
pubmed: 23 3 2021
medline: 18 9 2021
Statut: ppublish

Résumé

Expanding statin use may help to alleviate the excess burden of atherosclerotic cardiovascular disease in people living with HIV (PLHIV). Pravastatin and pitavastatin are preferred agents due to their lack of substantial interaction with antiretroviral therapy. We aimed to evaluate the cost-effectiveness of pravastatin and pitavastatin for the primary prevention of atherosclerotic cardiovascular disease among PLHIV in the United States. We developed a microsimulation model that randomly selected (with replacement) individuals from the Data-collection on Adverse Effects of Anti-HIV Drugs study with follow-up between 2013 and 2016. Our study population was PLHIV aged 40 to 75 years, stable on antiretroviral therapy, and not currently using lipid-lowering therapy. Direct medical costs and quality-adjusted life-years (QALYs) were assigned in annual cycles and discounted at 3% per year. We assumed a willingness-to-pay threshold of $100,000/QALY gained. The interventions assessed were as follows: (1) treating no one with statins; (2) treating everyone with generic pravastatin 40 mg/day (drug cost $236/year) and (3) treating everyone with branded pitavastatin 4 mg/day (drug cost $2,828/year). The model simulated each individual's probability of experiencing atherosclerotic cardiovascular disease over 20 years. Persons receiving pravastatin accrued 0.024 additional QALYs compared with those not receiving a statin, at an incremental cost of $1338, giving an incremental cost-effectiveness ratio of $56,000/QALY gained. Individuals receiving pitavastatin accumulated 0.013 additional QALYs compared with those using pravastatin, at an additional cost of $18,251, giving an incremental cost-effectiveness ratio of $1,444,000/QALY gained. These findings were most sensitive to the pill burden associated with daily statin administration, statin costs, statin efficacy and baseline atherosclerotic cardiovascular disease risk. In probabilistic sensitivity analysis, no statin was optimal in 5.2% of simulations, pravastatin was optimal in 94.8% of simulations and pitavastatin was never optimal. Pravastatin was projected to be cost-effective compared with no statin. With substantial price reduction, pitavastatin may be cost-effective compared with pravastatin. These findings bode well for the expanded use of statins among PLHIV in the United States. To gain greater confidence in our conclusions it is important to generate strong, HIV-specific estimates on the efficacy of statins and the quality-of-life burden associated with taking an additional daily pill.

Sections du résumé

BACKGROUND
Expanding statin use may help to alleviate the excess burden of atherosclerotic cardiovascular disease in people living with HIV (PLHIV). Pravastatin and pitavastatin are preferred agents due to their lack of substantial interaction with antiretroviral therapy. We aimed to evaluate the cost-effectiveness of pravastatin and pitavastatin for the primary prevention of atherosclerotic cardiovascular disease among PLHIV in the United States.
METHODS
We developed a microsimulation model that randomly selected (with replacement) individuals from the Data-collection on Adverse Effects of Anti-HIV Drugs study with follow-up between 2013 and 2016. Our study population was PLHIV aged 40 to 75 years, stable on antiretroviral therapy, and not currently using lipid-lowering therapy. Direct medical costs and quality-adjusted life-years (QALYs) were assigned in annual cycles and discounted at 3% per year. We assumed a willingness-to-pay threshold of $100,000/QALY gained. The interventions assessed were as follows: (1) treating no one with statins; (2) treating everyone with generic pravastatin 40 mg/day (drug cost $236/year) and (3) treating everyone with branded pitavastatin 4 mg/day (drug cost $2,828/year). The model simulated each individual's probability of experiencing atherosclerotic cardiovascular disease over 20 years.
RESULTS
Persons receiving pravastatin accrued 0.024 additional QALYs compared with those not receiving a statin, at an incremental cost of $1338, giving an incremental cost-effectiveness ratio of $56,000/QALY gained. Individuals receiving pitavastatin accumulated 0.013 additional QALYs compared with those using pravastatin, at an additional cost of $18,251, giving an incremental cost-effectiveness ratio of $1,444,000/QALY gained. These findings were most sensitive to the pill burden associated with daily statin administration, statin costs, statin efficacy and baseline atherosclerotic cardiovascular disease risk. In probabilistic sensitivity analysis, no statin was optimal in 5.2% of simulations, pravastatin was optimal in 94.8% of simulations and pitavastatin was never optimal.
CONCLUSIONS
Pravastatin was projected to be cost-effective compared with no statin. With substantial price reduction, pitavastatin may be cost-effective compared with pravastatin. These findings bode well for the expanded use of statins among PLHIV in the United States. To gain greater confidence in our conclusions it is important to generate strong, HIV-specific estimates on the efficacy of statins and the quality-of-life burden associated with taking an additional daily pill.

Identifiants

pubmed: 33749164
doi: 10.1002/jia2.25690
pmc: PMC7982504
doi:

Substances chimiques

Anti-HIV Agents 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25690

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI046362
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069907
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI042170
Pays : United States

Informations de copyright

© 2021 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

David C Boettiger (DC)

Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, CA, USA.
Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.

Anthony T Newall (AT)

The School of Public Health and Community Medicine, UNSW Sydney, Sydney, NSW, Australia.

Andrew Phillips (A)

Institute for Global Health, University College London, London, UK.

Eran Bendavid (E)

Center for Health Policy and the Center for Primary Care and Outcomes Research, Stanford University, Stanford, CA, USA.

Matthew G Law (MG)

Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.

Lene Ryom (L)

Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Peter Reiss (P)

Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
HIV Monitoring Foundation, Amsterdam, The Netherlands.

Amanda Mocroft (A)

Institute for Global Health, University College London, London, UK.

Fabrice Bonnet (F)

Université Bordeaux, CHU de Bordeaux, France.

Rainer Weber (R)

University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Wafaa El-Sadr (W)

ICAP-Columbia University and Harlem Hospital, New York, NY, USA.

Antonella d'Arminio Monforte (A)

Clinica di Malattie Infettive e Tropicali, Azienda Ospedaliera-Polo Universitario San Paolo, Milan, Italy.

Stephane de Wit (S)

Saint Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Christian Pradier (C)

Department of Public Health, Nice University Hospital, Nice, France.

Camilla I Hatleberg (CI)

Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Jens Lundgren (J)

Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Caroline Sabin (C)

Institute for Global Health, University College London, London, UK.

James G Kahn (JG)

Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, CA, USA.

Dhruv S Kazi (DS)

Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Harvard Medical School, Harvard University, Boston, MA, USA.

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