Nowak Bernd, McMeekin James, Knops Marie, Wille Bernd, Schröder Eberhard, Moro Concepcion, Oelher Matthias, Castellanos Eduardo, Coutu Benoit, Petersen Ben, Pfeil Wolfgang, Kreuzer Joachim
Cardiovascular Center Bethanien, CCB, Frankfurt/Main, Germany.
Pacing Clin Electrophysiol. 2005 Jul;28(7):620-9. doi: 10.1111/j.1540-8159.2005.00159.x.
Pacemaker diagnostic counters are used to guide device programming and patient management. However, these data are susceptible to inappropriate classification of events. The aim of this multicenter study was to evaluate pacemaker diagnostic data using stored intracardiac electrograms (EGMs).
The study included 351 patients (191 males, aged 71 +/- 10 years) with standard indications for dual-chamber pacemaker implantation. EGM triggers were atrial tachycardia (AT), ventricular tachycardia (VT), sudden bradycardia response (SBR), and pacemaker-mediated tachycardia (PMT). For this study, the devices could store up to 5 EGMs of 8s each (with marker annotation and onset recording). After 3 months, the EGMs were analyzed and classified as "confirmed" if the EGM validated the trigger and as "false positive" if the EGM showed an event different from the trigger.
Of the 1,003 EGMs available, the triggers were AT in 640 EGMs, VT in 76, SBR in 105, and PMT in 178 EGMs. Four EGMs were triggered by magnet application. The trigger was confirmed in 614 EGMs (62%): 62% of AT episodes, 18% of VT episodes, 100% of SBR episodes, and 54% of PMT episodes. In 385 cases (45%), the EGMs revealed false-positive events due to far-field sensing (39%), noise and myopotential sensing (26%), sinus tachycardias (21%), double counting (9%), exit block (4%), and undersensing (1%).
This large-scale study of stored EGMs revealed their value in validating diagnostic counter data. Therapeutic decisions should not be based on diagnostic counters alone; they should be validated by sophisticated tools like stored EGMs.
起搏器诊断计数器用于指导设备编程和患者管理。然而,这些数据容易出现事件分类不当的情况。这项多中心研究的目的是使用存储的心内心电图(EGM)评估起搏器诊断数据。
该研究纳入了351例患者(191例男性,年龄71±10岁),这些患者具有双腔起搏器植入的标准适应症。EGM触发事件包括房性心动过速(AT)、室性心动过速(VT)、突然心动过缓反应(SBR)和起搏器介导的心动过速(PMT)。在本研究中,设备最多可存储5个时长为8秒的EGM(带有标记注释和起始记录)。3个月后,对EGM进行分析,若EGM证实了触发事件,则分类为“确诊”;若EGM显示的事件与触发事件不同,则分类为“假阳性”。
在1003份可用的EGM中,触发事件为AT的有640份,VT的有76份,SBR的有105份,PMT的有178份。4份EGM由磁铁应用触发。614份EGM(62%)的触发事件得到确诊:AT发作的确诊率为62%,VT发作的确诊率为18%,SBR发作的确诊率为100%,PMT发作的确诊率为54%。在385例(45%)病例中,EGM显示由于远场感知(39%)、噪声和肌电位感知(26%)、窦性心动过速(21%)、重复计数(9%)、出口阻滞(4%)和感知不足(1%)导致假阳性事件。
这项对存储EGM的大规模研究揭示了其在验证诊断计数器数据方面的价值。治疗决策不应仅基于诊断计数器;应通过存储EGM等精密工具进行验证。