Piccini Jonathan P, Stromberg Kurt, Jackson Kevin P, Laager Verla, Duray Gabor Z, El-Chami Mikhael, Ellis Christopher R, Hummel John, Jones D Randy, Kowal Robert C, Narasimhan Calambur, Omar Razali, Ritter Philippe, Roberts Paul R, Soejima Kyoko, Zhang Shu, Reynolds Dwight
Duke University Medical Center, Durham, North Carolina.
Medtronic plc, Mounds View, Minnesota.
Heart Rhythm. 2017 May;14(5):685-691. doi: 10.1016/j.hrthm.2017.01.026. Epub 2017 Jan 19.
Device repositioning during Micra leadless pacemaker implantation may be required to achieve optimal pacing thresholds.
The purpose of this study was to describe the natural history of acute elevated Micra vs traditional transvenous lead thresholds.
Micra study VVI patients with threshold data (at 0.24 ms) at implant (n = 711) were compared with Capture study patients with de novo transvenous leads at 0.4 ms (n = 538). In both cohorts, high thresholds were defined as >1.0 V and very high as >1.5 V. Change in pacing threshold (0-6 months) with high (1.0 to ≤1.5 V) or very high (>1.5 V) thresholds were compared using the Wilcoxon signed-rank test.
Of the 711 Micra patients, 83 (11.7%) had an implant threshold of >1.0 V at 0.24 ms. Of the 538 Capture patients, 50 (9.3%) had an implant threshold of >1.0 V at 0.40 ms. There were no significant differences in patient characteristics between those with and without an implant threshold of >1.0 V, with the exception of left ventricular ejection fraction in the Capture cohort (high vs low thresholds, 53% vs 58%; P = .011). Patients with an implant threshold of >1.0 V decreased significantly (P < .001) in both cohorts. Micra patients with high and very high thresholds decreased significantly (P < .01) by 1 month, with 87% and 85% having 6-month thresholds lower than the implant value. However, when the capture threshold at implant was >2 V, only 18.2% had a threshold of ≤1 V at 6 months and 45.5% had a capture threshold of >2 V.
Pacing thresholds in most Micra patients with elevated thresholds decrease after implant. Micra device repositioning may not be necessary if the pacing threshold is ≤2 V.
在Micra无导线起搏器植入过程中,可能需要重新调整装置位置以达到最佳起搏阈值。
本研究的目的是描述急性升高的Micra与传统经静脉导线阈值的自然病程。
将植入时具有阈值数据(0.24毫秒时)的Micra研究VVI患者(n = 711)与在0.4毫秒时植入全新经静脉导线的Capture研究患者(n = 538)进行比较。在两个队列中,高阈值定义为>1.0 V,非常高阈值定义为>1.5 V。使用Wilcoxon符号秩检验比较高(1.0至≤1.5 V)或非常高(>1.5 V)阈值下起搏阈值(0至6个月)的变化。
在711例Micra患者中,83例(11.7%)在0.24毫秒时植入阈值>1.0 V。在538例Capture患者中,50例(9.3%)在0.40毫秒时植入阈值>1.0 V。植入阈值>1.0 V和未>1.0 V的患者之间,除Capture队列中的左心室射血分数外(高阈值与低阈值,53%对58%;P = 0.011),患者特征无显著差异。两个队列中植入阈值>1.0 V的患者均显著下降(P < 0.001)。Micra高阈值和非常高阈值患者在1个月时显著下降(P < 0.01),87%和85%的患者6个月时的阈值低于植入值。然而,当植入时的捕捉阈值>2 V时,6个月时只有18.2%的患者阈值≤1 V,45.5%的患者捕捉阈值>2 V。
大多数阈值升高的Micra患者植入后起搏阈值下降。如果起搏阈值≤2 V,可能无需重新调整Micra装置位置。