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现有的口服降脂药物可使大多数高危患者达标:基于血脂异常国际研究 II-意大利的估计。

Available oral lipid-lowering agents could bring most high-risk patients to target: an estimate based on the Dyslipidemia International Study II-Italy.

机构信息

Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology, Fondazione IRCCS Policlinico San Matteo.

Dipartimento di Medicina Molecolare, Università degli Studi di Pavia, Pavia.

出版信息

J Cardiovasc Med (Hagerstown). 2018 Sep;19(9):485-490. doi: 10.2459/JCM.0000000000000680.

Abstract

AIMS

The analysis evaluated the contemporary percentage of patients with established coronary heart disease (CHD) reaching the European guidelines recommended LDL-cholesterol (LDL-C) levels of less than 70 mg/dl and the threshold required for proprotein convertase subtlisin/kexin type 9 reimbursement in Italy (100 mg/dl). It also assessed how these percentages would change in case of diffuse use of ezetimibe.

METHODS

The Dyslipidemia International Study II enrolled CHD patients aged at least 18 either on lipid-lowering therapy (LLT) for at least 3 months or not on LLT at the time of the lipid profile. Distribution of LLTs and LDL-C target attainment were assessed. Multivariate logistic regression evaluated predictors of LDL-C target attainment. A 24% LDL-C lowering was modeled in patients not taking ezetimibe to assess its potential effects.

RESULTS

Among 676 Italian CHD patients enrolled, LDL-C concentrations were lower among the 631 patients (93.3%) who were on LLT (82 versus 118 mg/dl; P < 0.001). The LDL-C target was attained by 35.4% of patients. Statin dose (median atorvastatin dose 40 mg/day) was the sole significant predictor of LDL-C target attainment. The simple addition of ezetimibe in the model reduced the percentage of patients more than 70 and 100 mg/dl from 64.6 to 37.9% and from 25.1 to 11.8%, respectively.

CONCLUSION

Despite treatment in more than 90%, only one-third of Italian stable CHD patients attained the recommended LDL-C target. Statin dose was the sole predictor of the target achievement. The addition of ezetimibe would almost double patients at target and halve the potential candidates for reimbursement of more expensive agents such as proprotein convertase subtlisin/kexin type 9 inhibitors.

摘要

目的

本分析评估了当前达到欧洲指南推荐的 LDL-胆固醇(LDL-C)水平低于 70mg/dl 的稳定型冠心病(CHD)患者比例,以及在意大利 proprotein convertase subtlisin/kexin type 9 报销的阈值(100mg/dl)。还评估了如果广泛使用依泽替米贝,这些百分比将如何变化。

方法

血脂异常国际研究 II 纳入了年龄至少 18 岁的 CHD 患者,这些患者或正在接受降脂治疗(LLT)至少 3 个月,或在进行血脂谱检查时未接受 LLT。评估了 LLT 的分布和 LDL-C 目标的实现情况。多变量逻辑回归评估了 LDL-C 目标实现的预测因素。对未服用依泽替米贝的患者进行了 24%的 LDL-C 降低建模,以评估其潜在影响。

结果

在纳入的 676 名意大利 CHD 患者中,631 名接受 LLT 的患者(93.3%)的 LDL-C 浓度较低(82 与 118mg/dl;P<0.001)。35.4%的患者达到 LDL-C 目标。他汀类药物剂量(阿托伐他汀中位数剂量为 40mg/天)是 LDL-C 目标实现的唯一显著预测因素。在模型中简单地添加依泽替米贝将 LDL-C 水平在 70mg/dl 以下的患者比例从 64.6%降低至 37.9%,将 LDL-C 水平在 100mg/dl 以下的患者比例从 25.1%降低至 11.8%。

结论

尽管超过 90%的患者接受了治疗,但只有三分之一的意大利稳定型 CHD 患者达到了推荐的 LDL-C 目标。他汀类药物剂量是目标实现的唯一预测因素。添加依泽替米贝将使达标患者增加近一倍,将 proprotein convertase subtlisin/kexin type 9 抑制剂等更昂贵药物的潜在报销候选人减半。

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