首页> 外文期刊>The annals of pharmacotherapy >An Observational Study of Ezetimibe in Cardiac Transplant Recipients Receiving Calcineurin Inhibitors
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An Observational Study of Ezetimibe in Cardiac Transplant Recipients Receiving Calcineurin Inhibitors

机译:依西替米贝在接受钙调神经磷酸酶抑制剂的心脏移植受者中的观察研究

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Background: Cardiac transplant patients are at risk for developing cardiac allograft vasculopathy, and dyslipidemia in this patient population has been associated with increased risk. Data evaluating the efficacy and safety of ezetimibe in this population are minimal. Objectives: The purpose of this study was to assess the effects of ezetimibe, alone or in combination with other lipid-lowering agents, in cardiac transplant recipients receiving calcineurin inhibitors (CNIs). Methods: This study was a single-center retrospective chart review. Data on demographics, medications prescribed for dyslipidemia and prevention of transplant rejection, results of lipid panels, CNI blood concentrations, and adverse effects were extracted from medical records of cardiac transplant recipients who were prescribed ezetimibe, either alone or in combination with other lipid-lowering agents, and seen at least once in a 12-month period at a cardiac transplantation clinic of an 800-bed teaching hospital. Results: There were 71 patients prescribed ezetimibe in whom a safety analysis was performed. Approximately 49% (n = 35) were included in the analysis for lipid lowering. Ezetimibe significantly decreased low-density lipoprotein cholesterol (LDL-C; 129 mg/dL vs 94 mg/dL, P<.0001), non-high-density lipoprotein cholesterol (non-HDL-C; 170 mg/dL vs 127.5 mg/dL, P =.0058), and total cholesterol (236 mg/dL vs 200 mg/dL, P<.0001). There was no significant change in HDL-C and triglycerides as compared with baseline. The proportion of patients achieving goal LDL-C < 100 mg/dL significantly increased from 11.5% at baseline to 60.5% after the addition of ezetimibe (P<.0001). Ezetimibe had no measurable effect on blood CNI concentrations or doses. Adverse effects were reported by 15.5% of patients (n = 11), with 4% (n = 3) of patients discontinuing therapy. The most common complaints were gastrointestinal intolerance and myalgia. Conclusions: Ezetimibe was associated with lower LDL-C in cardiac transplant recipients either as combination therapy in patients with elevated LDL-C or as monotherapy, with a low frequency of adverse effects.
机译:背景:心脏移植患者有发展为同种异体移植血管病的风险,并且该患者人群中的血脂异常与危险性增加有关。评估依泽替米贝在该人群中的疗效和安全性的数据很少。目的:本研究的目的是评估依泽替米贝单独或与其他降脂药联合使用对接受钙调神经磷酸酶抑制剂(CNI)的心脏移植受者的影响。方法:本研究为单中心回顾性图表审查。从单独或与其他降脂药合用的依泽替米贝处方的心脏移植接受者的病历中提取有关人口统计学,血脂异常和预防移植排斥的药物,脂质检测结果,CNI血药浓度和不良反应的数据代理商,并且在800张床位教学医院的心脏移植诊所中至少每12个月见过一次。结果:71例接受依泽替米贝处方的患者进行了安全性分析。降脂分析中包括约49%(n = 35)。依泽替米贝显着降低低密度脂蛋白胆固醇(LDL-C; 129 mg / dL vs 94 mg / dL,P <.0001),非高密度脂蛋白胆固醇(非HDL-C; 170 mg / dL vs 127.5 mg / dL,P = .0058)和总胆固醇(236 mg / dL vs 200 mg / dL,P <.0001)。与基线相比,HDL-C和甘油三酸酯没有显着变化。添加依折麦布后,达到目标LDL-C <100 mg / dL的患者比例从基线的11.5%显着增加到60.5%(P <.0001)。依泽替米贝对血液CNI浓度或剂量没有可测量的影响。据报道,有15.5%的患者(n = 11)出现不良反应,其中4%(n = 3)的患者停止治疗。最常见的主诉是肠胃不适和肌痛。结论:依泽替米贝与心脏移植受者中低密度脂蛋白胆固醇降低有关,可作为低密度脂蛋白胆固醇升高患者的联合治疗或单一疗法,不良反应发生率较低。

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