首页> 外文期刊>BMC Cardiovascular Disorders >Detection of occult paroxysmal atrial fibrilation by implantable long-term electrocardiographic monitoring in cryptogenic stroke and transient ischemic attack population: a study protocol for prospective matched cohort study
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Detection of occult paroxysmal atrial fibrilation by implantable long-term electrocardiographic monitoring in cryptogenic stroke and transient ischemic attack population: a study protocol for prospective matched cohort study

机译:通过植入性长期心电图监测隐源性卒中和短暂性脑缺血发作人群的隐匿性阵发性房颤:前瞻性配对研究的研究方案

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Cardio-embolic etiology is the most frequently predicted cause of cryptogenic stroke/TIA. Detection of occult paroxysmal atrial fibrillation is crucial for selection of appropriate medication. Enrolment of eligible cryptogenic stroke and TIA patients began in 2014 and will continue until 2018. The patients undergo long-term (12?months) ECG monitoring (implantable loop recorder) and testing for PITX2 (chromosome 4q25) and ZFHX3 (chromosome 16q22) gene mutations. There will be an appropriate control group of age- and sex-matched healthy volunteers. To analyse the results descriptive statistics, statistical tests for group differences, and correlation analyses will be used. In our study we are focusing on a possible correlation between detection of atrial fibrillation by an implantable ECG recorder, and PITX2 and/or ZFHX3 gene mutations in cryptogenic stroke/TIA patients. A correlation could lead to implementation of this genomic approach to cryptogenic stroke/TIA diagnostics and management. The results will be published in 2018. ClinicalTrials.gov: NCT02216370 .
机译:心脏栓塞病因是最常预测的隐源性卒中/ TIA病因。隐匿性阵发性心房颤动的检测对于选择合适的药物至关重要。合格的隐源性卒中和TIA患者的入组于2014年开始,并将持续到2018年。患者接受长期(12个月)ECG监测(植入式循环记录仪)并测试PITX2(染色体4q25)和ZFHX3(染色体16q22)基因。突变。将有一个年龄和性别相匹配的健康志愿者的适当对照组。为了分析结果的描述统计量,将使用组差异的统计检验和相关性分析。在我们的研究中,我们将重点放在可植入ECG记录仪对房颤的检测与隐源性卒中/ TIA患者中PITX2和/或ZFHX3基因突变之间的可能关联。相关性可能导致这种基因组学方法可用于隐源性卒中/ TIA诊断和管理。结果将在2018年发布。ClinicalTrials.gov:NCT02216370。

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