Jacob Sony, Kommuri Naga V A, Zalawadiya Sandip K, Meissner Marc D, Lieberman Randy A
Division of Cardiology/Electrophysiology, Harper University Hospital, Wayne State University, Detroit, Michigan 48201, USA.
Pacing Clin Electrophysiol. 2010 Jul;33(7):834-40. doi: 10.1111/j.1540-8159.2009.02682.x. Epub 2010 Jan 28.
The implantable loop recorder (ILR) is a cost-effective tool with a high diagnostic yield in the evaluation of unexplained recurrent syncope. The Sleuth ILR (Transoma Medical, St. Paul MN, USA) is a new-generation ILR with wireless transmission capability approved by the Food and Drug Administration. We report the feasibility of achieving appropriate sensing over 1-year follow-up at the traditional midclavicular and alternative inframammary implantation sites without preimplant electrocardiogram (ECG) mapping.
We studied 32 patients with unexplained syncope, aged 58.4+/-18.44 years, with an ILR implanted at the left midclavicular location (n = 17) or the left inframammary site (n = 15) over 1-year post implant. No preimplant electrocardiogram (ECG) mapping was performed. The highest R-wave amplitudes were observed at the inframammary site, but over the entire follow-up period, amplitudes were not significantly different from those at the midclavicular site. At both sites, R-wave amplitudes at the 6-month follow-up were significantly higher than those measured at 1 week. P-waves were visible in 80-90% of the patients. There was no discernible difference in P-waves (amplitude) relative to implant location. Body mass index, left ventricular ejection fraction, and age did not significantly influence the R-wave amplitude or the ability to discern P-waves.
Our findings show that the Sleuth ILR implanted at both the midclavicular and inframammary locations without preimplant ECG mapping achieves acceptable "R" waves. This may simplify implantation procedures and improve patient satisfaction.
植入式循环记录仪(ILR)是一种经济高效的工具,在不明原因的反复晕厥评估中具有较高的诊断率。Sleuth ILR(美国明尼苏达州圣保罗市的Transoma Medical公司生产)是一种经美国食品药品监督管理局批准的具有无线传输功能的新一代ILR。我们报告了在不进行植入前心电图(ECG)标测的情况下,在传统的锁骨中线和替代的乳房下植入部位进行1年随访时实现适当感知的可行性。
我们研究了32例不明原因晕厥患者,年龄58.4±18.44岁,在植入后1年内在左锁骨中线位置(n = 17)或左乳房下部位(n = 15)植入ILR。未进行植入前心电图(ECG)标测。在乳房下部位观察到最高的R波振幅,但在整个随访期间,振幅与锁骨中线部位无显著差异。在两个部位,6个月随访时的R波振幅均显著高于1周时测量的振幅。80%-90%的患者可见P波。相对于植入位置,P波(振幅)没有明显差异。体重指数、左心室射血分数和年龄对R波振幅或辨别P波的能力没有显著影响。
我们的研究结果表明,在不进行植入前ECG标测的情况下,将Sleuth ILR植入锁骨中线和乳房下位置均可获得可接受的“R”波。这可能会简化植入程序并提高患者满意度。