Forge B H, Briganti E M
West Gippsland Hospital, Warragul, VIC.
Med J Aust. 2001 Nov 5;175(9):471-5. doi: 10.5694/j.1326-5377.2001.tb143679.x.
To assess the effectiveness of current Australian guidelines for prescribing lipid-lowering drugs in identifying high-risk individuals in primary prevention of coronary heart disease.
Coronary heart disease risk profiles were obtained for 280 consecutive patients dispensed lipid-lowering drugs in rural Victoria. Their 10-year absolute risk of coronary heart disease was determined using the Framingham formula. PATIENTS were categorised according to their eligibility for lipid-lowering drugs as defined by current Pharmaceutical Benefits Scheme (PBS) and National Heart Foundation (NHF) guidelines.
Complete data were available for 230 patients dispensed lipid-lowering drugs. Of these, the 138 patients (60%) with no history of vascular disease are the subjects of our study.
Proportion of patients with various 10-year coronary heart disease thresholds (15%, 20% and 30%), compared with their eligibility for lipid-lowering drugs based on Australian PBS and NHF guidelines.
Twenty-six per cent of patients with no history of vascular disease who are currently dispensed lipid-lowering drugs do not fulfil PBS guidelines for treatment. Of patients conforming with PBS guidelines as suitable for lipid-lowering drugs, 39% (95% CI, 30%-49%) had a 10-year risk of coronary heart disease of less than 15%. A similar proportion (41% [95% CI, 32%-50%]) had a 10-year risk of coronary heart disease of less than 15%, but were eligible for lipid-lowering drugs according to NHF guidelines. Adherence to PBS and NHF guidelines in patients currently dispensed lipid-lowering drugs would result in as many as 14% (95% CI, 8%-21%) and 7% (95% CI, 3%-12%) of patients, respectively, not being eligible for treatment, despite having a 10-year risk of coronary heart disease greater than 15%.
Australian guidelines for prescribing of lipid-lowering drugs are poor discriminators of absolute risk of coronary heart disease in primary prevention. Strategies based on the continuous relationship between risk-factor intensity and absolute coronary heart disease risk, such as the Framingham risk estimates, provide a more rational basis for formulating treatment guidelines.
评估澳大利亚现行的降脂药物处方指南在识别冠心病一级预防中的高危个体方面的有效性。
获取了维多利亚州农村地区连续280例接受降脂药物治疗患者的冠心病风险概况。使用弗雷明汉公式确定他们患冠心病的10年绝对风险。根据现行的药品福利计划(PBS)和国家心脏基金会(NHF)指南中降脂药物的适用标准对患者进行分类。
有230例接受降脂药物治疗的患者可获得完整数据。其中,138例(60%)无血管疾病史的患者是我们的研究对象。
不同10年冠心病风险阈值(15%、20%和30%)的患者比例,与根据澳大利亚PBS和NHF指南其使用降脂药物的适宜性进行比较。
目前正在接受降脂药物治疗且无血管疾病史的患者中,26%不符合PBS治疗指南。在符合PBS指南适合使用降脂药物的患者中,39%(95%可信区间,30%-49%)患冠心病的10年风险低于15%。有相似比例(41%[95%可信区间,32%-50%])的患者患冠心病的10年风险低于15%,但根据NHF指南有资格使用降脂药物。目前接受降脂药物治疗的患者中,分别有多达14%(95%可信区间,8%-21%)和7%(95%可信区间,3%-12%)的患者尽管患冠心病的10年风险大于15%,但不符合PBS和NHF指南的治疗资格。
澳大利亚的降脂药物处方指南在冠心病一级预防中对绝对风险的鉴别能力较差。基于风险因素强度与绝对冠心病风险之间连续关系的策略,如弗雷明汉风险评估,为制定治疗指南提供了更合理的依据。