Cost-effectiveness of lipid lowering with statins and ezetimibe in chronic kidney disease.


Journal

Kidney international
ISSN: 1523-1755
Titre abrégé: Kidney Int
Pays: United States
ID NLM: 0323470

Informations de publication

Date de publication:
07 2019
Historique:
received: 22 04 2018
revised: 08 01 2019
accepted: 10 01 2019
pubmed: 22 4 2019
medline: 22 9 2020
entrez: 22 4 2019
Statut: ppublish

Résumé

Statin-based treatments reduce cardiovascular disease (CVD) risk in patients with non-dialysis chronic kidney disease (CKD), but it is unclear which regimen is the most cost-effective. We used the Study of Heart and Renal Protection (SHARP) CKD-CVD policy model to evaluate the effect of statins and ezetimibe on quality-adjusted life years (QALYs) and health care costs in the United States (US) and the United Kingdom (UK). Net costs below $100,000/QALY (US) or £20,000/QALY (UK) were considered cost-effective. We investigated statin regimens with or without ezetimibe 10 mg. Treatment effects on cardiovascular risk were estimated per 1-mmol/L reduction in low-density lipoprotein (LDL) cholesterol as reported in the Cholesterol Treatment Trialists' Collaboration meta-analysis, and reductions in LDL cholesterol were estimated for each statin/ezetimibe regimen. In the US, atorvastatin 40 mg ($0.103/day as of January 2019) increased life expectancy by 0.23 to 0.31 QALYs in non-dialysis patients with stages 3B to 5 CKD, at a net cost of $20,300 to $78,200/QALY. Adding ezetimibe 10 mg ($0.203/day) increased life expectancy by an additional 0.05 to 0.07 QALYs, at a net cost of $43,600 to $91,500/QALY. The cost-effectiveness findings and policy implications in the UK were similar. In summary, in patients with non-dialysis-dependent CKD, the evidence suggests that statin/ezetimibe combination therapy is a cost-effective treatment to reduce the risk of CVD.

Identifiants

pubmed: 31005271
pii: S0085-2538(19)30171-1
doi: 10.1016/j.kint.2019.01.028
pmc: PMC6595178
pii:
doi:

Substances chimiques

Cholesterol, LDL 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Ezetimibe EOR26LQQ24

Banques de données

ClinicalTrials.gov
['NCT00125593']

Types de publication

Clinical Trial, Phase IV Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

170-179

Subventions

Organisme : Medical Research Council
ID : MC_U137686855
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/1996001/9454
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R007764/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0701732
Pays : United Kingdom

Investigateurs

R Collins (R)
C Baigent (C)
M J Landray (MJ)
C Bray (C)
Y Chen (Y)
A Baxter (A)
A Young (A)
M Hill (M)
C Knott (C)
A Cass (A)
B Feldt-Rasmussen (B)
B Fellström (B)
D E Grobbee (DE)
C Grönhagen-Riska (C)
M Haas (M)
H Holdaas (H)
L S Hooi (LS)
L Jiang (L)
B Kasiske (B)
U Krairittichai (U)
A Levin (A)
Z A Massy (ZA)
V Tesar (V)
R Walker (R)
C Wanner (C)
D C Wheeler (DC)
A Wiecek (A)
T Dasgupta (T)
W Herrington (W)
D Lewis (D)
M Mafham (M)
W Majoni (W)
C Reith (C)
J Emberson (J)
S Parish (S)
D Simpson (D)
J Strony (J)
T Musliner (T)
L Agodoa (L)
J Armitage (J)
Z Chen (Z)
J Craig (J)
D de Zeeuw (D)
J M Gaziano (JM)
R Grimm (R)
V Krane (V)
B Neal (B)
V Ophascharoensuk (V)
T Pedersen (T)
P Sleight (P)
J Tobert (J)
C Tomson (C)

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Iryna Schlackow (I)

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, UK.

Seamus Kent (S)

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, UK.

William Herrington (W)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

Jonathan Emberson (J)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

Richard Haynes (R)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

Christina Reith (C)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK.

Rory Collins (R)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK.

Martin J Landray (MJ)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

Alastair Gray (A)

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, UK.

Colin Baigent (C)

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

Borislava Mihaylova (B)

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, UK; Centre for Primary Care and Public Health, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, UK. Electronic address: boby.mihaylova@dph.ox.ac.uk.

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