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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Myocardial microvascular disease and major adverse cardiovascular events in patients with end-stage renal disease: Rationale and design of the MICROCARD study
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Myocardial microvascular disease and major adverse cardiovascular events in patients with end-stage renal disease: Rationale and design of the MICROCARD study

机译:终末期肾脏疾病患者的心肌微血管疾病和主要不良心血管事件:MICROCARD研究的原理和设计

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Background Myocardial ischaemia, a consequence of coronary artery disease, is a major cause of death in patients with end-stage renal disease (ESRD). The pathophysiology and clinical presentation of coronary artery disease in ESRD patients seem to differ from non-ESRD patients with higher implication of myocardial microvascular disease (MMD), higher mortality, fewer myocardial infarctions, less significant coronary stenosis and low efficacy of well-established drugs such as statin and angiotensin-converting enzyme inhibitors. No study has investigated the presence of MMD and its clinical impact in ESRD patients. Methods We designed an observational prospective cohort study to investigate the prevalence of MMD and its association with major adverse cardiovascular events (MACE) in ESRD patients with a positive non-invasive test for myocardial ischaemia. Patients eligible for inclusion are those >18 years old receiving dialysis and/or undergoing investigation for kidney transplantation, who are referred to our renal clinic and meet all the inclusion criteria but none of the exclusion criteria. Patients with a positive test for myocardial ischaemia will be enrolled in the 'invasive group'. They will be further examined to detect simultaneously epicardial coronary stenosis by coronary angiography and MMD using pressure wire measurement of fractional flow reserve and coronary flow reserve followed by calculation of the index of microcirculatory resistance. Patients with a negative test for myocardial ischaemia will be enrolled in a 'control group' designed to verify whether the invasive group is indeed at high risk for MACE. Both groups will be followed up for 2 years to compare the incidence of MACE. Conclusion The MICROCARD study will phenotype MMD and will investigate its relation with the incidence of MACE in ESRD patients with myocardial ischaemia. Clinicaltrial.gov NCT01291771.
机译:背景技术心肌缺血是冠心病的结果,是终末期肾病(ESRD)患者的主要死亡原因。 ESRD患者中冠状动脉疾病的病理生理学和临床表现似乎与非ESRD患者不同,后者具有更高的心肌微血管疾病(MMD)影响,更高的死亡率,更少的心肌梗塞,更少的冠状动脉狭窄和公认的药物疗效低如他汀类药物和血管紧张素转化酶抑制剂。尚无研究调查MMD在ESRD患者中的存在及其临床影响。方法我们设计了一项观察性前瞻性队列研究,以通过无创性心肌缺血检查对ESRD患者进行MMD患病率及其与主要不良心血管事件(MACE)的关系。符合纳入条件的患者是接受透析和/或接受肾脏移植检查的18岁以上的患者,这些患者被转介到我们的肾脏诊所,并且符合所有纳入标准,但没有一个排除标准。心肌缺血检测阳性的患者将被纳入“侵入性治疗组”。他们将进一步检查以通过冠状动脉造影和MMD同时检测心外膜冠状动脉狭窄,方法是使用压力线测量分数血流储备量和冠状动脉血流储备量,然后计算微循环阻力指数。心肌缺血测试阴性的患者将被纳入“对照组”,旨在验证侵入性组是否确实存在发生MACE的高风险。两组将随访2年,以比较MACE的发生率。结论MICROCARD研究将表型MMD,并将调查其与ESRD心肌缺血患者MACE发生率的关系。 Clinicaltrial.gov NCT01291771。

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