Hildemann Steven K, Barho Christian, Karmann Barbara, Darius Harald, Bode Christoph
essex pharma, Medical Department, Munich, Germany.
Curr Med Res Opin. 2008 Oct;24(10):2777-84. doi: 10.1185/03007990802381406. Epub 2008 Aug 21.
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).
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.
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.
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.
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。
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。
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。
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。