瑞舒伐他汀、阿托伐他汀和普伐他汀治疗血脂异常糖尿病的疗效和安全性比较。

ISRN Pharmacology Pub Date : 2013-01-01 Epub Date: 2013-02-10 DOI:10.1155/2013/146579
Lolwa Barakat, Amin Jayyousi, Abdulbari Bener, Bilal Zuby, Mahmoud Zirie
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引用次数: 43

摘要

目标。研究三种最常用的他汀类药物(瑞舒伐他汀、阿托伐他汀和普伐他汀)治疗卡塔尔糖尿病患者血脂异常的有效性和安全性。研究对象和方法。这项基于人群的回顾性观察性研究纳入了350名连续的糖尿病患者,这些患者在2005年9月至2009年9月期间被诊断为血脂异常并服用了他汀类药物。数据是通过审查药房数据库、电子病历数据库(EMR查看器)和患者病历收集的。比较基线、第一年和第二年的血脂测量值。结果。瑞舒伐他汀(10 mg)在降低LDL-C方面最有效(29.03%)。阿托伐他汀在40mg剂量时降低LDL-C最多(22.8%),普伐他汀在20mg剂量时降低LDL-C最多(20.3%)。这三种他汀类药物对肌肉和肝功能都是安全的。在肾功能方面,阿托伐他汀是最安全的他汀类药物,因为在2年治疗结束时,新发微量白蛋白尿的患者人数最少(10.9%),其次是瑞舒伐他汀(14.3%),然后是普伐他汀(26.6%)。结论。在卡塔尔,降低LDL-C最有效的他汀类药物是瑞舒伐他汀10mg。阿托伐他汀是对肾功能最安全的他汀类药物。需要进一步的大规模前瞻性研究来证实这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of Efficacy and Safety of Rosuvastatin, Atorvastatin and Pravastatin among Dyslipidemic Diabetic Patients.

Comparison of Efficacy and Safety of Rosuvastatin, Atorvastatin and Pravastatin among Dyslipidemic Diabetic Patients.

Comparison of Efficacy and Safety of Rosuvastatin, Atorvastatin and Pravastatin among Dyslipidemic Diabetic Patients.

Comparison of Efficacy and Safety of Rosuvastatin, Atorvastatin and Pravastatin among Dyslipidemic Diabetic Patients.

Objectives. To investigate the efficacy and the safety of the three most commonly prescribed statins (rosuvastatin, atorvastatin, and pravastatin) for managing dyslipidemia among diabetic patients in Qatar. Subjects and Methods. This retrospective observational population-based study included 350 consecutive diabetes patients who were diagnosed with dyslipidemia and prescribed any of the indicated statins between September 2005 and September 2009. Data was collected by review of the Pharmacy Database, the Electronic Medical Records Database (EMR viewer), and the Patient's Medical Records. Comparisons of lipid profile measurements at baseline and at first- and second-year intervals were taken. Results. Rosuvastatin (10 mg) was the most effective at reducing LDL-C (29.03%). Atorvastatin reduced LDL-C the most at a dose of 40 mg (22.8%), and pravastatin reduced LDL-C the most at a dose of 20 mg (20.3%). All three statins were safe in relation to muscular and hepatic functions. In relation to renal function, atorvastatin was the safest statin as it resulted in the least number of patients at the end of 2 years of treatment with the new onset of microalbuminuria (10.9%) followed by rosuvastatin (14.3%) and then pravastatin (26.6%). Conclusion. In the Qatari context, the most effective statin at reducing LDL-C was rosuvastatin 10 mg. Atorvastatin was the safest statin in relation to renal function. Future large-scale prospective studies are needed to confirm these results.

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