Harley Carolyn R, Gandhi Sanjay, Blasetto James, Heien Herbert, Sasane Rahul, Nelson Stephanie P
Health Economics and Outcomes, i3 Innovus, Palo Alto, California 94303, USA.
Am J Geriatr Pharmacother. 2007 Sep;5(3):185-94. doi: 10.1016/j.amjopharm.2007.10.002.
Reducing low-density lipoprotein cholesterol (LDL-C) levels lowers the risk of consequences of cardiovascular disease. Research has confirmed these benefits in elderly patients. The 3-hydroxy-3-methylglutaryl coenzyme A inhibitors (ie, statins) have long-standing proven efficacy in reducing levels of LDL-C and total cholesterol.
The goal of this study was to compare change in LDL-C from baseline and National Cholesterol Education Program (NCEP) Adult Treatment Panel (ATP) III LDL-C goal attainment in a population of elderly patients (aged > or =65 years) treated with rosuvastatin versus other statins in routine clinical practice.
This was a retrospective cohort analysis using medical and pharmacy claims data linked to clinical laboratory results from a large managed care health plan of commercial and Medicare Advantage members in the United States. Included were members aged > or =65 years who were newly treated with statins (index date) from August 1, 2003, through February 28, 2005. All subjects were continuously enrolled for 12 months preindex and > or =30 days postindex, with variable follow-up until therapy discontinuation or end of health plan eligibility. Based on NCEP ATP III guidelines, patients were grouped into risk categories with associated LDL-C goals. The primary outcomes were change in LDL-C from baseline and attainment of NCEP ATP III LDL-C goal among patients not at goal before starting therapy. Generalized linear modeling was used to assess percent change in LDL-C from baseline, controlling for covariates (including age, sex, NCEP risk level, medication possession ratio, preindex LDL-C value, days from index date to postindex LDL-C value, and number of preindex office visits for dyslipidemia). In the subset of patients not at goal before starting therapy, logistic regression was used to estimate the odds of individual patients on other statins reaching goal as compared with rosuvastatin and to produce predicted percent attaining LDL-C goal on individual statins.
Of the 2227 elderly new users of statin therapy, 8.0% started on rosuvastatin, 38.9% started on atorvastatin, 3.0% on fluvastatin, 31.0% on lovastatin, 5.5% on pravastatin, and 13.6% on simvastatin. Females comprised 57.7% of the population, and the mean (SD) age was 73 (5.8) years (range, 65-94 years). The mean (SD) doses of rosuvastatin, atorvastatin, fluvastatin, lovastatin, pravastatin, and simvastatin were 10.65 (4.59), 16.0 (12.78), 66.31 (23.56), 27.38 (14.07), 32.86 (16.46), and 28.1 (26.2) mg, respectively. After controlling for covariates, rosuvastatin-treated patients had a 35.8% decrease in LDL-C from baseline, which was significantly greater compared with patients in the atorvastatin, fluvastatin, lovastatin, pravastatin, and simvastatin (29.3%, 21.9%, 22.5%, 22.0%, and 24.9%, respectively; P < 0.05) groups. Atorvastatin (odds ratio [OR], 0.25; 95% CI, 0.12-0.52), fluvastatin (OR, 0.05; 95% CI, 0.02-0.14), lovastatin (OR, 0.10; 95% CI, 0.05-0.20), pravastatin (OR, 0.08; 95% CI, 0.03-0.20), and simvastatin (OR, 0.14; 95% CI, 0.06-0.30) were less likely to attain LDL-C goal compared with rosuvastatin (all, P < 0.001). Predicted percent attaining goal was 93.6% among rosuvastatin users, significantly greater than users of atorvastatin, fluvastatin, lovastatin, pravastatin, and simvastatin (81.2%, 55.8%, 66.8%, 64.1%, and 72.8%, respectively; P < 0.05).
In this elderly patient population, rosuvastatin was a more effective treatment for reducing LDL-C levels and attaining NCEP ATP III LDL-C goals than the other statins.
降低低密度脂蛋白胆固醇(LDL-C)水平可降低心血管疾病后果的风险。研究已在老年患者中证实了这些益处。3-羟基-3-甲基戊二酰辅酶A抑制剂(即他汀类药物)在降低LDL-C和总胆固醇水平方面具有长期 proven 的疗效。
本研究的目的是比较在常规临床实践中,使用瑞舒伐他汀治疗的老年患者(年龄≥65岁)与其他他汀类药物治疗的患者相比,LDL-C从基线的变化以及达到美国国家胆固醇教育计划(NCEP)成人治疗小组(ATP)III LDL-C目标的情况。
这是一项回顾性队列分析,使用了与美国一家大型商业和医疗保险优势成员管理式医疗健康计划的临床实验室结果相关的医疗和药房索赔数据。纳入的是2003年8月1日至2005年2月28日开始新接受他汀类药物治疗(索引日期)的年龄≥65岁的成员。所有受试者在索引前连续登记12个月,索引后≥30天,随访时间不等,直至治疗中断或健康计划资格结束。根据NCEP ATP III指南,将患者分为具有相关LDL-C目标的风险类别。主要结局是开始治疗前未达目标的患者中LDL-C从基线的变化以及达到NCEP ATP III LDL-C目标的情况。使用广义线性模型评估LDL-C从基线的百分比变化,控制协变量(包括年龄、性别、NCEP风险水平、药物持有率、索引前LDL-C值、从索引日期到索引后LDL-C值的天数以及索引前血脂异常门诊就诊次数)。在开始治疗前未达目标的患者子集中,使用逻辑回归估计与瑞舒伐他汀相比,使用其他他汀类药物的个体患者达到目标的几率,并得出个体他汀类药物达到LDL-C目标的预测百分比。
在2227名他汀类药物治疗的老年新用户中,8.0%开始使用瑞舒伐他汀,38.9%开始使用阿托伐他汀,3.0%使用氟伐他汀,31.0%使用洛伐他汀,5.5%使用普伐他汀,13.6%使用辛伐他汀。女性占人群的57.7%,平均(标准差)年龄为73(5.8)岁(范围65-94岁)。瑞舒伐他汀、阿托伐他汀、氟伐他汀、洛伐他汀、普伐他汀和辛伐他汀的平均(标准差)剂量分别为10.65(4.59)、16.0(12.78)、66.31(23.56)、27.38(14.07)、32.86(16.46)和28.1(26.2)mg。在控制协变量后,与阿托伐他汀、氟伐他汀、洛伐他汀、普伐他汀和辛伐他汀组的患者相比,使用瑞舒伐他汀治疗的患者LDL-C从基线下降了35.8%,显著更大(分别为29.3%;21.9%;22.5%;!22.0%和24.9%;P<0.05)。与瑞舒伐他汀相比,阿托伐他汀(比值比[OR],0.25;95%置信区间,0.12-0.52)、氟伐他汀(OR,0.05;95%置信区间,0.02-0.14)、洛伐他汀(OR,0.10;95%置信区间,0.05-0.20)、普伐他汀(OR,0.!0;95%置信区间,0.03-0.20)和辛伐他汀(OR,0.14;95%置信区间,0.06-0.30)达到LDL-C目标的可能性较小(均P<0.001)。瑞舒伐他汀使用者达到目标的预测百分比为93.6%,显著高于阿托伐他汀、氟伐他汀、洛伐他汀、普伐他汀和辛伐他汀使用者(分别为81.2%、55.8%、66.8%、64.1%和72.8%;P<0.05)。
在这个老年患者群体中,与其他他汀类药物相比,瑞舒伐他汀在降低LDL-C水平和达到NCEP ATP III LDL-C目标方面是一种更有效的治疗方法。