首页> 外文期刊>Acta Cardiologica >Belgian Society of Cardiology. Belgian Heart Rhythm Association (BeHRA).The 5th Belgian Heart Rhythm Meeting, 6-7 October 2011, Brussels. Abstracts.
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Belgian Society of Cardiology. Belgian Heart Rhythm Association (BeHRA).The 5th Belgian Heart Rhythm Meeting, 6-7 October 2011, Brussels. Abstracts.

机译:比利时心脏病学会。比利时心律协会(BeHRA).2011年10月6日至7日在布鲁塞尔举行的第五届比利时心律会议。摘要。

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Data of the Belgian register on implantable loop recorder in unexplained syncope and stroke. - C. Bar-braud, J. Castro Rodriguez, T. Verbeet (on behalf of all participants to the ILR database, Department of Cardiology, CHUBrugmann, Belgium).-Syncope is common in the general population and in 23 to 50% an initial evaluation including a detailed clinical history and oriented examinations (orthostatic blood pressure measurements, electrocardiogram, carotid sinus massage, echocardiogram, tilt testing) leads to an etiological diagnosis (neuro-mediated syncope, syncope due to orthostatic hypotension or cardiac syncope). However, in some patients, syncope remains unexplained, and an arrhythmia is often strongly suspected. Implantable loop recorder, by making a correlation between syncope and heart rhythm, is thus indicated to demonstrate a cause of syncope with a specific treatment or to definitely exclude an arrhythmia in such patients. Implantable loop recorder may also be useful in stroke to identify a paroxysmal atrial fibrillation, especially in young people with unexplained ischemic attack after an initial neurologic evaluation (including transoesophagal echocardiography, holter monitoring, carotids Doppler ultrasound) .We describe here the data of the national Belgian register between 2008 and 2011, including 437 patients. 384 patients (87,8%) were implanted for unexplained syncope and 53 patients (12, 1%) were implanted for stroke of unknown origin. After a mean period of 7.7 months, the follow-up is closed in 49 patients; the device is still implanted in 353 patients. A recurrent episode appeared and allowed to make a diagnosis in 42/45 (93.3%) cases of syncope and in 1 case of stroke. In this diagnosed syncope population, 24/45 (53%) had an arrhythmia consisting in atrio-ventricular blocks, asystoles or severe bradycardia, leading to the implantation of a pacemaker; or ventricular arrhythmias, leading to a defi-brillator implantation. The other diagnosis were ...
机译:无法解释的晕厥和中风时,可植入式循环记录仪上比利时寄存器的数据。 -C. Bar-braud,J。Castro Rodriguez,T。Verbeet(代表ILR数据库的所有参与者,比利时CHUBrugmann心脏病学系)。晕厥在普通人群中很常见,在23%至50%的人中初步评估包括详细的临床病史和定向检查(体位血压测量,心电图,颈动脉窦按摩,超声心动图,倾斜测试)可导致病因诊断(神经介导的晕厥,因体位性低血压引起的晕厥或心脏晕厥)。但是,在某些患者中,晕厥仍无法解释,通常强烈怀疑心律不齐。因此,通过在晕厥和心律之间建立相关性,植入式记录仪被证明可通过某种特定疗法证明晕厥的原因,或明确排除此类患者的心律失常。植入式记录仪在卒中中也可能有用,以识别阵发性房颤,特别是在初步神经系统评估(包括经食道超声心动图,动态心电图监测,颈动脉多普勒超声检查)后患有无法解释的缺血性发作的年轻人中。比利时人在2008年至2011年之间登记,包括437名患者。 384例(87.8%)患者因无法解释的晕厥而被植入,53例(12%,1%)因原因不明的中风被植入。平均7.7个月后,对49例患者进行了随访。该设备仍被植入353名患者。复发发作出现并允许对42/45(93.3%)晕厥病例和1例中风进行诊断。在这个被诊断为晕厥的人群中,有24/45(53%)的心律失常包括房室传导阻滞,心搏停止或严重的心动过缓,导致了起搏器的植入。或室性心律不齐,导致除纤颤器植入。其他诊断是...

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