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临床实践中瑞舒伐他汀与其他他汀类药物的滴定模式:一项使用电子病历数据库的回顾性观察队列研究。

Titration patterns with rosuvastatin as compared with other statins in clinical practice: a retrospective observational cohort study using an electronic medical record database.

作者信息

Fox Kathleen M, Gandhi Sanjay K, Ohsfeldt Robert L, Blasetto James W, Davidson Michael H

机构信息

Department of Epidemiology & Preventive Medicine, School of Medicine, University of Maryland, Baltimore, MD, USA.

出版信息

Clin Ther. 2007 Nov;29(11):2385-94. doi: 10.1016/j.clinthera.2007.11.010.

Abstract

BACKGROUND

Lipid management in clinical practice has been suboptimal with a significant proportion of patients not achieving recommended cholesterol levels. A reason for low goal attainment may be the limited use of upward dose titration.

OBJECTIVE

The aim of this study was to determine if, in routine clinical practice, a lower rate of titration is observed among rosuvastatin patients who achieved the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) target low-density lipoprotein cholesterol (LDL-C) goals as compared with patients achieving the target LDL-C goals on other statins.

METHODS

This retrospective database study included the patients, aged > or =18 years, of approximately 3000 physicians across the United States, who were newly prescribed statin treatment from August 2003 to May 2005. Patients were excluded if they started on a maximum dose of statin, were at LDL-C goal at baseline (no clinical reason for titrating), or on fluvastatin (<70 patients). Titration rate with rosuvastatin was compared with other statins. Multivariate logistic regression models adjusted for baseline LDL-C, coronary heart disease risk, treatment duration, and target LDL-C goal attainment.

RESULTS

This study assessed 12,041 patients for upward titration. Of the 5955 eligible patients (mean age, 63 years; male, 47%), 7.2% were prescribed rosuvastatin, 63.5% atorvastatin, 15.3% simvastatin, 7.2% pravastatin, and 6.9% lovastatin. Overall, 4337 patients (72.8%) attained the NCEP ATP III target LDL-C goal. Mean duration of statin treatment was 188 days for rosuvastatin compared with 238 to 260 days for the other statins (all, P < 0.05). Among patients attaining the target LDL-C goal, significantly fewer rosuvastatin patients (8.3%) had titration compared with atorvastatin (17.0%), simvastatin (20.0%), pravastatin (20.7%), and lovastatin (23.5%) (all, P < 0.05). After adjusting for baseline characteristics, patients attaining the target LDL-C goal on other statins were significantly more likely to be titrated as compared with rosuvastatin (odds ratios, 2.0-3.3; P < 0.05). Lower titration rates for rosuvastatin patients were also observed in the total population (P < 0.05).

CONCLUSION

Our study found that rosuvastatin patients who attained the NCEP ATP III target LDL-C goal had significantly lower titration rates than patients receiving other statins.

摘要

背景

临床实践中的血脂管理并不理想,相当一部分患者未达到推荐的胆固醇水平。目标达成率低的一个原因可能是向上剂量滴定的使用有限。

目的

本研究的目的是确定在常规临床实践中,与使用其他他汀类药物达到美国国家胆固醇教育计划成人治疗小组第三次报告(NCEP ATP III)目标低密度脂蛋白胆固醇(LDL-C)水平的患者相比,瑞舒伐他汀治疗的患者滴定率是否更低。

方法

这项回顾性数据库研究纳入了美国约3000名医生的年龄≥18岁的患者,这些患者于2003年8月至2005年5月开始新的他汀类药物治疗。如果患者开始使用他汀类药物的最大剂量、基线时已达到LDL-C目标(无滴定的临床理由)或使用氟伐他汀(<70例患者),则将其排除。将瑞舒伐他汀的滴定率与其他他汀类药物进行比较。多因素逻辑回归模型对基线LDL-C、冠心病风险、治疗持续时间和目标LDL-C目标达成情况进行了校正。

结果

本研究评估了12041例患者的向上滴定情况。在5955例符合条件的患者中(平均年龄63岁;男性占47%),7.2%的患者使用瑞舒伐他汀,63.5%使用阿托伐他汀,15.3%使用辛伐他汀,7.2%使用普伐他汀,6.9%使用洛伐他汀。总体而言,4337例患者(72.8%)达到了NCEP ATP III目标LDL-C水平。瑞舒伐他汀治疗的平均持续时间为188天,而其他他汀类药物为238至260天(均P<0.05)。在达到目标LDL-C水平的患者中,与阿托伐他汀(17.0%)、辛伐他汀(20.0%)、普伐他汀(20.7%)和洛伐他汀(23.5%)相比,使用瑞舒伐他汀的患者进行滴定的显著较少(8.3%)(均P<0.05)。在校正基线特征后,与瑞舒伐他汀相比,使用其他他汀类药物达到目标LDL-C水平的患者更有可能进行滴定(优势比为2.0 - 3.3;P<0.05)。在总体人群中也观察到瑞舒伐他汀治疗患者的滴定率较低(P<0.05)。

结论

我们的研究发现,达到NCEP ATP III目标LDL-C水平的瑞舒伐他汀治疗患者的滴定率显著低于使用其他他汀类药物的患者。

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