Yang Chen-Chang, Jick Susan S, Testa Marcia A
Department of Internal Medicine, Faculty of Medicine, School of Medicine, National Yang-Ming University, 155 Li-Nong Street, Section 2, Taipei, Taiwan 11217.
Br J Clin Pharmacol. 2003 Jul;56(1):84-91. doi: 10.1046/j.1365-2125.2003.01818.x.
To evaluate the effects of comorbidities and patient characteristics on treatment continuation among patients starting their first course of lipid-lowering drug (LLD) therapy.
Within the UK General Practice Research Database (GPRD), we identified 22 408 patients who started LLD therapy due to coronary heart disease, hyperlipidaemia, or other atherosclerotic diseases, and who received > or = two prescriptions for LLD between January 1 1990 and December 31 1997. Differences in potential predictors of treatment continuation between patients who continued, and patients who discontinued/switched lipid-lowering therapy within 1 year after treatment initiation were compared by fitting multivariate logistic regression models. The effects of baseline characteristics on treatment continuation after switching of LLDs were also analysed.
Discontinuation/switching of lipid-lowering therapy was common during the study period, especially among patients who received nonstatin, nonfibrate LLDs (log-rank test P = 0.0001). Statin use, more frequent physician visits, more concurrent cardiovascular medications, diabetes, and fewer noncardiovascular medications were associated with treatment continuation of LLDs. Among patients who switched therapy, prescribing of a statin as the substituted LLD, more concurrent cardiovascular medications, and later treatment switching were related to a higher probability of treatment continuation after switching LLDs.
Treatment continuation after initiation or switching of lipid-lowering therapy largely increased with concomitant cardiovascular comorbidities, and more health care utilization, and is more common for statins than for other LLDs. Practice guidelines, patient education, and quality of care assessment for lipid-lowering therapy should emphasize factors that predispose patients to discontinuation/switching, in an effort to optimize the choice of therapeutic regimens and to improve patient adherence.
评估合并症及患者特征对开始首次降脂药物(LLD)治疗的患者持续治疗的影响。
在英国全科医学研究数据库(GPRD)中,我们确定了22408例因冠心病、高脂血症或其他动脉粥样硬化疾病开始LLD治疗且在1990年1月1日至1997年12月31日期间接受≥2次LLD处方的患者。通过拟合多变量逻辑回归模型,比较了治疗开始后1年内持续治疗的患者与停止/更换降脂治疗的患者之间治疗持续潜在预测因素的差异。还分析了基线特征对更换LLD后治疗持续的影响。
在研究期间,降脂治疗的停药/换药很常见,尤其是在接受非他汀类、非贝特类LLD的患者中(对数秩检验P = 0.0001)。使用他汀类药物、更频繁的医生就诊、更多的心血管合并用药、糖尿病以及较少的非心血管用药与LLD的治疗持续相关。在更换治疗的患者中,开具他汀类药物作为替代LLD、更多的心血管合并用药以及更晚的治疗更换与更换LLD后更高的治疗持续概率相关。
降脂治疗开始或更换后的治疗持续在很大程度上随着心血管合并症的存在、更多的医疗保健利用而增加,并且他汀类药物比其他LLD更常见。降脂治疗的实践指南、患者教育和护理质量评估应强调使患者易于停药/换药的因素,以优化治疗方案的选择并提高患者依从性。