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针对患有冠心病和慢性肾脏病的管理式医疗患者的阿托伐他汀聚焦治疗。

Focused atorvastatin therapy in managed-care patients with coronary heart disease and CKD.

作者信息

Koren Michael J, Davidson Michael H, Wilson Daniel J, Fayyad Rana S, Zuckerman Andrea, Reed David P

机构信息

Jacksonville Center for Clinical Research, Jacksonville, FL 32216, USA.

出版信息

Am J Kidney Dis. 2009 May;53(5):741-50. doi: 10.1053/j.ajkd.2008.11.025. Epub 2009 Feb 11.

Abstract

BACKGROUND

This post hoc analysis of the Aggressive Lipid-Lowering Initiation Abates New Cardiac Events (ALLIANCE) Study investigates the effect of focused atorvastatin therapy versus usual care on cardiovascular outcomes in patients with coronary heart disease (CHD) with and without chronic kidney disease (CKD).

STUDY DESIGN

Prospective randomized open-label; median follow-up, 54.3 months.

SETTING & PARTICIPANTS: Managed care or Veterans Affairs facilities; 2,442 patients with CHD with dyslipidemia; mean age, 61.6 years.

INTERVENTION

Focused atorvastatin therapy to a low-density lipoprotein cholesterol goal of less than 80 mg/dL or maximum dose of 80 mg/d versus usual care as deemed appropriate by patients' regular physicians.

PREDICTOR

Baseline estimated glomerular filtration rate (eGFR) calculated using the Modification of Diet in Renal Disease Study equation of less than 60 mL/min/1.73 m(2) (patients with CKD) and 60 mL/min/1.73 m(2) or greater (patients without CKD).

OUTCOMES & MEASUREMENTS: The primary end point was time to first cardiovascular event. Change from baseline eGFR was assessed in 1,768 patients with follow-up renal data.

RESULTS

At baseline, 579 patients (23.7%) had CKD: 31.6% of these patients experienced a primary cardiovascular event during the study versus 23.6% of patients without CKD (hazard ratio [HR], 1.41; 95% confidence interval [CI], 1.18 to 1.68; P < 0.001). Compared with usual care, atorvastatin therapy reduced the relative risk of a primary outcome by 28% in patients with CKD (HR, 0.72; 95% CI, 0.54 to 0.97; P = 0.02) and 11% in patients without CKD (HR, 0.89; 95% CI, 0.74 to 1.07; P = 0.3) (P for treatment by CKD interaction = 0.2). There was no decrease in eGFR in atorvastatin-treated patients during the course of the study.

LIMITATIONS

Follow-up of atorvastatin patients was restricted to every 6 months; interim data were unavailable for usual-care patients.

CONCLUSIONS

Patients with CHD and CKD are at increased risk of cardiovascular events. Compared with usual care, focused atorvastatin treatment decreased cardiovascular risk for established patients in real-world settings, with no significant difference in treatment effects observed between patients with and without CKD.

摘要

背景

本项对积极降脂起始预防新的心脏事件(ALLIANCE)研究的事后分析,旨在调查针对合并或不合并慢性肾脏病(CKD)的冠心病(CHD)患者,使用阿托伐他汀强化治疗与常规治疗相比对心血管结局的影响。

研究设计

前瞻性随机开放标签研究;中位随访时间为54.3个月。

研究地点与参与者

管理式医疗或退伍军人事务机构;2442例患有血脂异常的冠心病患者;平均年龄61.6岁。

干预措施

将阿托伐他汀强化治疗至低密度脂蛋白胆固醇目标值低于80mg/dL或最大剂量80mg/d,而常规治疗则由患者的常规医生酌情决定。

预测指标

使用肾脏病饮食改良研究方程计算的基线估计肾小球滤过率(eGFR)低于60mL/min/1.73m²(CKD患者)以及60mL/min/1.73m²或更高(无CKD患者)。

结局与测量指标

主要终点为首次发生心血管事件的时间。对1768例有随访肾脏数据的患者评估了eGFR相对于基线的变化。

结果

基线时,579例患者(23.7%)患有CKD:这些患者中有31.6%在研究期间发生了主要心血管事件,而无CKD患者为23.6%(风险比[HR]为1.41;95%置信区间[CI]为1.18至1.68;P<0.001)。与常规治疗相比,阿托伐他汀治疗使CKD患者主要结局的相对风险降低了28%(HR为0.72;95%CI为0.54至0.97;P=0.02),使无CKD患者降低了11%(HR为0.89;95%CI为0.74至1.07;P=0.3)(CKD交互作用的治疗P值=0.2)。在研究过程中,接受阿托伐他汀治疗的患者eGFR没有下降。

局限性

对阿托伐他汀治疗患者的随访限于每6个月一次;常规治疗患者的中期数据不可用。

结论

患有CHD和CKD的患者发生心血管事件的风险增加。与常规治疗相比,在实际临床环境中,阿托伐他汀强化治疗降低了确诊患者的心血管风险,在有或无CKD的患者之间未观察到治疗效果的显著差异。

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