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比利时降脂药物首次授权情况分析。

An analysis of first authorizations for lipid-lowering drugs in Belgium.

作者信息

Devroey D, Betz W

机构信息

Department of General Practice, University of Brussels, Laarbeeklaan 103, 1090 Brussels, Belgium.

出版信息

Acta Clin Belg. 2003 May-Jun;58(3):152-8. doi: 10.1179/acb.2003.58.3.002.

DOI:10.1179/acb.2003.58.3.002
PMID:12945474
Abstract

INTRODUCTION

In Belgium lipid-lowering drugs are reimbursed in primary and secondary prevention when after a non-specified diet of at least three months total cholesterol (TC) remains higher than 250 mg/dl or triglycerides (TG) remain higher than 200 mg/dl. Low-density lipoprotein cholesterol (LDL-C) is only taken into account for the reimbursement of fibrates when it remains higher than 160 mg/dl in secondary prevention. The aim of this study was to evaluate the changes in fasting lipoproteins levels among patients who wait for the reimbursement of a lipid-lowering drug. Additionally, the parameters influencing the physicians' choice to prescribe a statin or a fibrate were analysed.

METHODS

In total 286 first authorizations for the reimbursement of lipid-lowering drugs were recorded during February and March of 2002 at two regional health insurance offices. We studied a mixed primary and secondary prevention population.

RESULTS

The mean age at the initiation of the treatment was 61 years (SD = 12). Mean fasting TC was 285 mg/dl before the diet and 286 mg/dl after the diet. Fasting TC and TG did not decrease with the diet for respectively 51% and 54% of the patients. High TC and an improvement of TG during the diet were the only two factors correlated with the prescription of a statin instead of a fibrate.

CONCLUSIONS

Half of the patients receiving lipid-lowering drugs in Belgium were not able to decrease their TC with diet before the initiation of the treatment. Cardiovascular risk factors were not taken into account for the reimbursement of statins. Belgian reimbursement criteria should be adapted.

摘要

引言

在比利时,当经过至少三个月未明确规定的饮食后,总胆固醇(TC)仍高于250毫克/分升或甘油三酯(TG)仍高于200毫克/分升时,降脂药物在一级和二级预防中可获得报销。在二级预防中,只有当低密度脂蛋白胆固醇(LDL-C)仍高于160毫克/分升时,贝特类药物的报销才会考虑该指标。本研究的目的是评估等待降脂药物报销的患者空腹脂蛋白水平的变化。此外,还分析了影响医生选择开具他汀类药物或贝特类药物的参数。

方法

2002年2月和3月期间,在两个地区医疗保险办公室共记录了286份降脂药物报销的首次申请。我们研究了一级和二级预防的混合人群。

结果

开始治疗时的平均年龄为61岁(标准差=12)。饮食前平均空腹TC为285毫克/分升,饮食后为286毫克/分升。分别有51%和54%的患者饮食后空腹TC和TG没有下降。高TC和饮食期间TG的改善是与开具他汀类药物而非贝特类药物相关的仅有的两个因素。

结论

在比利时,接受降脂药物治疗的患者中有一半在开始治疗前通过饮食无法降低其TC。他汀类药物报销未考虑心血管危险因素。比利时的报销标准应予以调整。

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BMC Fam Pract. 2008 Jun 30;9:39. doi: 10.1186/1471-2296-9-39.