Results of a Markov Model Analysis to Assess the Cost-Effectiveness of a Single Tablet of Fixed-Dose Amlodipine and Atorvastatin for the Primary Prevention of Cardiovascular Disease in Korea

被引:18
作者
Liew, Danny [1 ]
Park, Hye-Jin [2 ]
Ko, Su-Kyoung [2 ]
机构
[1] Univ Melbourne, St Vincents Hosp, Dept Med, Fitzroy, Vic 3065, Australia
[2] Pfizer Pharmaceut Korea Ltd, Outcomes Res Dept, Seoul, South Korea
关键词
atorvastatin; amlodipine; single-pill combination; cardiovascular disease; cost-effectiveness; CORONARY-ARTERY-DISEASE; LONG-TERM PERSISTENCE; PHARMACOECONOMIC EVALUATION; ECONOMIC-EVALUATION; STATIN THERAPY; MEDICATION ADHERENCE; UNITED-KINGDOM; HEART-DISEASE; EVENTS; HYPERTENSION;
D O I
10.1016/j.clinthera.2009.10.015
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Background: In Korea, the treatment of hypertension and dyslipidemia constitutes an important strategy for the prevention of cardiovascular disease (CVD). Objective: This study sought to investigate the cost-effectiveness (from the Korean health care system perspective) of prescribing a proprietary formulation single-tablet fixed-dose combination of amlodipine and atorvastatin (at weighted mean doses of 5 mg and 10.25 mg, respectively) to all eligible patients aged >= 45 years for the primary prevention of CVD (ie, coronary heart disease and ischemic stroke) in Korea, compared with currently observed patterns of blood-pressure and lipid-lowering medication prescription and use. Methods: A Markov model was developed with 4 health states: alive without CVD, alive with CVD, dead from CVD, and dead from non-CVD causes. The model population comprised 244 Koreans aged > 45 years from the 2005 Korean National Health and Nutrition Examination Survey (KNHNES) without a history of myocardial infarction (MI) or stroke who met current criteria for both blood-pressure and lipid-lowering treatment. From a 2008 baseline, follow-up was simulated for 40 years. Cardiovascular risk was estimated for each subject individually using a multivariate, Asian population-specific equation, and updated with ongoing cycles. Decision analysis compared the effects of prescribing the fixed-dose combination to all subjects versus currently observed patterns of treatment. Data regarding the blood-pressure and lipid-lowering efficacies of combination therapy were drawn from the Respond trial. Costs of the fixed-dose combination tablet and CVD were sourced from pharmaceutical pricing lists and Korean Health Insurance Review and Assessment Services estimates, respectively. Utility values for CVD were obtained from a large Korean utility study. Results: In the model, of the 244 treatment-eligible subjects, 126 (51.6%) and 13 (5.3%) were taking blood-pressure and lipid-lowering therapy, respectively. Use of single-tablet fixed-dose combination amlodipine and atorvastatin by all subjects was associated with estimated incremental cost-effectiveness ratios of 7,773,063 Korean won (KRW) per quality-adjusted life-year gained and 10,378,230 KRW per overall life-year gained (1300 KRW approximate to US $1). Sensitivity and uncertainty analyses indicated these results to be robust. Conclusions: In this model, based on data from the 2005 KNHNES, hypertension and dyslipidemia were undertreated among Koreans aged >= 45 years without a history of MI or stroke. The administration of single-tablet fixed-dose combination amlodipine and atorvastatin to all such individuals was likely to represent a cost-effective means of preventing first-onset CVD (ie, coronary heart disease and ischemic stroke) in this subgroup, compared with current patterns of treatment. (Clin Ther 2009;31:2189-2203) (C) 2009 Excerpta Medica Inc.
引用
收藏
页码:2189 / 2203
页数:15
相关论文
共 67 条
[1]
CARDIOVASCULAR-DISEASE RISK PROFILES [J].
ANDERSON, KM ;
ODELL, PM ;
WILSON, PWF ;
KANNEL, WB .
AMERICAN HEART JOURNAL, 1991, 121 (01) :293-298
[2]
An Asian regional analysis of cost-effectiveness of early irbesartan treatment versus conventional antihypertensive, late amlodipine, and late irbesartan treatments in patients with type 2 diabetes, hypertension, and nephropathy [J].
Annemans, Lieven ;
Demarteau, Nadia ;
Hu, Shanlian ;
Lee, Tae-Jin ;
Morad, Zaher ;
Supaporn, Thanom ;
Yang, Wu-Chang ;
Palmer, Andrew J. .
VALUE IN HEALTH, 2008, 11 (03) :354-364
[3]
[Anonymous], HEALTH TECHNOL ASSES
[4]
Cost effectiveness of statin therapy for primary prevention of major coronary events in individuals with type 2 diabetes [J].
Brandle, M ;
Davidson, MB ;
Schriger, DL ;
Lorber, B ;
Herman, WH .
DIABETES CARE, 2003, 26 (06) :1796-1801
[5]
Handling uncertainty in cost-effectiveness models [J].
Briggs, AH .
PHARMACOECONOMICS, 2000, 17 (05) :479-500
[6]
Survival and cause of death after myocardial infarction: The Danish MONICA study [J].
Bronnum-Hansen, H ;
Jorgensen, T ;
Davidsen, M ;
Madsen, M ;
Osler, M ;
Gerdes, LU ;
Schroll, M .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2001, 54 (12) :1244-1250
[7]
Long-term survival and causes of death after stroke [J].
Bronnum-Hansen, H ;
Davidsen, M ;
Thorvaldsen, P .
STROKE, 2001, 32 (09) :2131-2136
[8]
A pharmacoeconomic evaluation of the Myocardial Ischaemia Reduction with Aggressive Cholesterol Lowering (MIRACL) study in the United Kingdom [J].
Buller, N ;
Gillen, D ;
Casciano, R ;
Doyle, J ;
Wilson, K .
PHARMACOECONOMICS, 2003, 21 (Suppl 1) :25-32
[9]
Casciano Roman, 2004, Can J Clin Pharmacol, V11, pe179
[10]
The economic efficiency of amlodipine in the treatment of coronary atherosclerosis - An analysis based on the PREVENT study [J].
Cathomas, G ;
Erne, P ;
Schwenkglenks, M ;
Szucs, TD .
CARDIOVASCULAR DRUGS AND THERAPY, 2002, 16 (01) :61-66