Therapeutic practice patterns related to statin potency and ezetimibe/simvastatin combination therapies in lowering LDL-C in patients with high-risk cardiovascular disease

被引:33
作者
Toth, Peter P. [1 ,2 ]
Foody, JoAnne M. [3 ]
Tomassini, Joanne E. [4 ]
Sajjan, Shiva G. [4 ]
Ramey, Dena R. [4 ]
Neff, David R. [4 ]
Tershakovec, Andrew M. [4 ]
Hu, Henry [4 ]
Tunceli, Kaan [4 ]
机构
[1] CGH Med Ctr, Sterling, IL 61081 USA
[2] Univ Illinois, Coll Med, Peoria, IL 61656 USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Merck & Co Inc, Whitehouse Stn, NJ USA
关键词
Statins; Goal attainment; Low-density lipoprotein; cholesterol; Ezetimibe; Switch; COST-EFFECTIVENESS; GOAL ATTAINMENT; CHOLESTEROL; SIMVASTATIN; EZETIMIBE; ATORVASTATIN; CORONARY; HEART; EFFICACY; BENEFIT;
D O I
10.1016/j.jacl.2013.09.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Statin combination therapy and statin uptitration have been shown to be efficacious in low-density lipoprotein cholesterol (LDL-C) lowering and are recommended for patients with highrisk coronary heart disease (CHD) who do not reach guideline-endorsed LDL-C goals on statin monotherapy. OBJECTIVE: This analysis evaluated treatment practice patterns and LDL-C lowering for patients with CHD/CHD risk equivalent on statin monotherapy in a real-world practice setting in the United States. METHODS: In this retrospective, observational study, patients with CHD/CHD risk equivalent on statin therapy were identified during 2004 to 2008 in a US managed care database. Prescribing patterns and effect of switching from statin monotherapy to combination ezetimibe/simvastatin therapy vs uptitration to higher statin dose/potency level and no change from initial statin potency on LDL-C lowering were assessed. Percentage of change from baseline in LDL-C levels and odds ratios for LDL-C goal attainment were estimated with analyses of covariance and logistic regression. RESULTS: Of 27,919 eligible patients on statin therapy, 2671 (9.6%) switched to ezetimibe/ simvastatin therapy, 11,035 (39.5%) uptitrated statins, and 14,213 (50.9%) remained on the same statin monotherapy. LDL-C reduction from baseline and attainment of LDL-C <100 and <70 mg/dL were substantially greater for patients who switched to ezetimibe/simvastatin therapy (-24.0%, 81.2%, and 35.2%, respectively) than for patients who titrated (-9.6%, 68.0%, and 18.4%, respectively) or remained on initial statin therapy (4.9%, 72.2%, and 23.7%, respectively). The odds ratios for attainment of LDL-C <100 and <70 mg/dL were also higher for patients who switched than for patients who uptitrated and had no therapy change than for patients who titrated vs no therapy change. Similarly, among a subgroup of patients not at LDL-C <100 mg/dL on baseline therapy, attainment of LDL-C <100 and <70 mg/dL was greater for patients who switched than for statin uptitration vs no change, as well as for patients who uptritrated statins vs no therapy change. CONCLUSION: In this study, LDL-C lowering and goal attainment rates improved substantially for patients with high-risk CHD on statin monotherapy who switched to combination ezetimibe/statin or uptitrated their statin therapies; however, approximately one-third of these patients still did not attain the optional recommended LDL-C goal of <70 mg/dL. Moreover, these higher efficacy lipid-lowering therapies were infrequently prescribed, indicating the need for further assessment of barriers to LDL-C goal attainment in actual practice settings. (c) 2014 National Lipid Association. All rights reserved.
引用
收藏
页码:107 / 116
页数:10
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