Rivers Shannon M, Kane Michael P, Busch Robert S, Bakst Gary, Hamilton Robert A
Department of Pharmacy Practice, Albany College of Pharmacy, Albany, NY 12208, USA.
Endocr Pract. 2007 Jan-Feb;13(1):11-6. doi: 10.4158/EP.13.1.11.
To determine the effectiveness and safety of colesevelam hydrochloride (HCl) and ezetimibe combination therapy in statin-intolerant patients with dyslipidemia and diabetes mellitus (DM) or metabolic syndrome (MS).
We identified potential study subjects through a computerized text search of patient electronic medical records using the terms colesevelam, WelChol, ezetimibe, and Zetia. Medical records were subsequently reviewed to identify all patients with DM or MS. Baseline total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, and triglyceride levels immediately before the initiation of therapy with colesevelam HCl (1.875 g twice a day) or ezetimibe (10 mg daily) were compared with those after a minimum of 3 months of single drug therapy and after a minimum of 3 months of combination therapy. Drug safety was evaluated by review of transaminase levels and reports of side effects or drug discontinuation.
The computerized search initially identified 91 electronic medical records; 16 patients fulfilled all study criteria. Baseline patient demographics included a mean age of 62.5 (+/-11.8) years and a mean body mass index of 31.4 (+/-5.2) kg/m2; 50% of patients were female, 75% had type 2 DM, and 25% had MS. In comparison with baseline, colesevelam HCl-ezetimibe combination therapy was associated with significant reductions in mean levels of total cholesterol (27.5%), LDL-C (42.2%), and non-HDL-C (37.1%). In addition, 50% of patients achieved the National Cholesterol Education Program Adult Treatment Panel III LDL-C target of less than 100 mg/dL. Therapy was well tolerated, with no significant changes in mean transaminase levels, no reports of myalgia, and no discontinuation of therapy.
Colesevelam HCl-ezetimibe combination therapy was associated with improved TC, LDL-C, and non-HDL-C lipid profiles and was well tolerated. Such therapy may be a reasonable consideration for statin-intolerant patients with DM or MS who have elevated cholesterol levels.
确定盐酸考来维仑与依折麦布联合治疗对他汀类药物不耐受的血脂异常合并糖尿病(DM)或代谢综合征(MS)患者的有效性和安全性。
我们通过使用考来维仑、WelChol、依折麦布和Zetia等术语对患者电子病历进行计算机文本搜索来确定潜在研究对象。随后对病历进行审查以识别所有患有DM或MS的患者。将开始使用盐酸考来维仑(1.875 g,每日两次)或依折麦布(10 mg,每日一次)治疗前即刻的基线总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、非HDL-C和甘油三酯水平与至少3个月单药治疗后以及至少3个月联合治疗后的水平进行比较。通过审查转氨酶水平以及副作用或停药报告来评估药物安全性。
计算机搜索最初识别出91份电子病历;16名患者符合所有研究标准。基线患者人口统计学特征包括平均年龄62.5(±11.8)岁,平均体重指数31.4(±5.2)kg/m²;50%的患者为女性,75%患有2型DM,25%患有MS。与基线相比,盐酸考来维仑 - 依折麦布联合治疗使总胆固醇、LDL-C和非HDL-C的平均水平显著降低,分别降低了27.5%、42.2%和37.1%。此外,50%的患者达到了美国国家胆固醇教育计划成人治疗小组第三次报告设定的LDL-C目标,即低于100 mg/dL。治疗耐受性良好,平均转氨酶水平无显著变化,无肌痛报告,也无停药情况。
盐酸考来维仑 - 依折麦布联合治疗可改善TC、LDL-C和非HDL-C血脂谱,且耐受性良好。对于胆固醇水平升高的他汀类药物不耐受的DM或MS患者,这种治疗可能是一个合理的选择。