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辛伐他汀/依折麦布联合治疗对高胆固醇血症患者的持续疗效:临床实践中的观察性队列研究

Sustained effects in hypercholesterolaemic patients on combined simvastatin/ezetimibe treatment: observational cohort study in clinical practice.

作者信息

Hildemann Steven K, Barho Christian, Karmann Barbara, Darius Harald, Bode Christoph

机构信息

essex pharma, Medical Department, Munich, Germany.

出版信息

Curr Med Res Opin. 2008 Oct;24(10):2777-84. doi: 10.1185/03007990802381406. Epub 2008 Aug 21.

Abstract

BACKGROUND

In order to reduce individual cardiovascular risk, many patients require life-long lipid-lowering therapy, often as a drug combination approach. We aimed to describe the usage pattern, effectiveness and tolerability of long-term treatment with lipid-lowering agents, with particular focus on an oral combination of simvastatin (SIM 10, 20, 40 or 80 mg) plus ezetimibe (EZ 10 mg).

METHODS

A prospective, observational study in 512 general practices throughout Germany. From a sample of patients at moderate or high cardiovascular risk who had previously taken part in a half-year study of an SIM/EZ combination, 5485 patients were documented after 1 year of treatment (mean 58 +/- 16 weeks) with regard to lipid parameters, adverse drug reactions (ADRs) and adverse events.

RESULTS

At the start of follow-up, 78.6% of patients were still on the SIM/EZ combination. At the end of follow-up, mean low density lipoprotein cholesterol (LDL-C) in patients on the combination versus those on other lipid-lowering therapy was reduced by 29.3 vs. 17.6% compared with baseline, total cholesterol by 23.1 vs. 14.5%, mean high density lipoprotein cholesterol (HDL-C) was increased by 15.9 vs. 13.4%, and mean triglycerides were reduced by 16.1 vs. 7.9%. Individual LDL-C targets were achieved by 56.6% on the SIM/EZ combination versus 35.9% on other therapy. In the long term (but not the short term), low acceptance of nutrition counselling as rated by the physician was associated with poor lipid levels. ADRs during follow-up occurred in 18 patients (0.3%; all cases non-serious), with seven cases of myalgia, and three cases each of nausea or arthralgia.

CONCLUSIONS

This observational study showed that long-term therapy with the SIM/EZ combination resulted in sustained beneficial effects on serum lipids and was well-tolerated. Compared to patients with therapy discontinuations or switches, those remaining on the combination had better outcomes regarding lipid status.

摘要

背景

为降低个体心血管疾病风险,许多患者需要长期进行降脂治疗,通常采用联合用药的方法。我们旨在描述降脂药物长期治疗的使用模式、有效性和耐受性,特别关注辛伐他汀(10、20、40或80毫克)加依折麦布(10毫克)的口服联合用药。

方法

在德国全国512家普通诊所进行的一项前瞻性观察性研究。从之前参加过半年辛伐他汀/依折麦布联合用药研究的中度或高度心血管疾病风险患者样本中,记录了5485例患者在接受1年治疗(平均58±16周)后的血脂参数、药物不良反应(ADR)和不良事件。

结果

随访开始时,78.6%的患者仍在使用辛伐他汀/依折麦布联合用药。随访结束时,与接受其他降脂治疗的患者相比,联合用药患者的平均低密度脂蛋白胆固醇(LDL-C)较基线水平降低了29.3%,而其他降脂治疗患者降低了17.6%;总胆固醇降低了23.1%和14.5%;平均高密度脂蛋白胆固醇(HDL-C)升高了15.9%和13.4%;平均甘油三酯降低了16.1%和7.9%。辛伐他汀/依折麦布联合用药组有56.6%的患者达到了个体LDL-C目标,而其他治疗组为35.9%。从长期来看(而非短期),医生评估的营养咨询接受度较低与血脂水平不佳有关。随访期间有18例患者发生药物不良反应(0.3%;所有病例均不严重),其中7例为肌痛,3例为恶心,3例为关节痛。

结论

这项观察性研究表明,辛伐他汀/依折麦布联合用药的长期治疗对血脂有持续的有益影响,且耐受性良好。与停药或换药的患者相比,继续使用联合用药的患者在血脂状况方面有更好的结果。

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