Lau C P, Leung S K, Lee I S
Department of Medicine, Queen Mary Hospital, Hong Kong.
Pacing Clin Electrophysiol. 1996 Nov;19(11 Pt 1):1574-81. doi: 10.1111/j.1540-8159.1996.tb03183.x.
Floating P wave sensing can be derived from bipolar atrial electrodes with different electrode configurations, although the relative clinical efficacy of these methods of atrial sensing has not been studied. We evaluated 32 sex and age matched patients with advanced AV block who received AV synchronous pacers using either a single lead with diagonally arranged bipole (Unity VDDR, Model 292, Intermedics Inc.) or closely spaced bipolar complete ring electrodes (Thera VDD, Model 8948, Medtronic Inc.). The total surface area of the atrial electrodes were 17.2 and 25 mm2, and the highest programmable atrial sensitivities were 0.1 and 0.25 mV, respectively. Atrial electrogram amplitude and sensing threshold were evaluated at implant and at each follow-up clinic visit (1, 3, and 6 months). Stability of atrial sensing was assessed during physical maneuvers, treadmill exercise test, and Holter recording. Atrial electrogram amplitude at implantation was higher in the Thera VVD (2.08 +/- 0.79 vs 1.45 +/- 0.59 mV in Unity VDDR; P < 0.05), but the value of atrial sensing threshold was lower during follow-up than Unity VDDR. P wave undersensing was additionally observed with both pacemakers during physical maneuvers and exercise testing (6%-19% of patients). Two and four patients had atrial undersensing on Holter in the Unity VDDR and Thera VDD, respectively, and the percentage P wave undersensing were 0.88% +/- 2.41% versus 3.63% +/- 8.16%, respectively. Reprogramming of the atrial sensitivity in the Unity VDDR and the use of investigational software allowing 0.18 mV atrial sensitivity to be programmed in the Thera VDD substantially reduced the percentage of P wave undersensing on Holter to 0.46% +/- 1.67% and 0.10% +/- 0.24%, respectively. Beginning at discharge with a programmed atrial sensitivity level at least twice the sensing margin, the mean atrial sensitivity level was reprogrammed from 0.29 to 0.26 mV for Unity VDDR and 0.33 to 0.24 mV for Thera VDD at 6 months. There was no incidence of atrial oversensing. Despite differences in atrial amplitudes at implantation between the diagonally arranged bipole and closely spaced full ring single lead systems, the clinical performances of atrial sensing were similar at an appropriately high atrial sensitivities. The absence of atrial oversensing suggests that single pass VDD pacemakers should probably be programmed at the highest available atrial sensitivity to ensure adequate P wave sensing as guided by physical maneuvers and Holter recording to minimize the need of subsequent reprogramming.
尽管尚未对这些心房感知方法的相对临床疗效进行研究,但漂浮P波感知可从具有不同电极配置的双极心房电极获得。我们评估了32例年龄和性别匹配的晚期房室传导阻滞患者,他们接受了房室同步起搏器治疗,其中一部分使用对角排列双极的单根导线(Unity VDDR,型号292,Intermedics公司),另一部分使用紧密间隔的双极完整环形电极(Thera VDD,型号8948,美敦力公司)。心房电极的总表面积分别为17.2和25平方毫米,最高可编程心房感知灵敏度分别为0.1和0.25毫伏。在植入时以及每次随访门诊(1、3和6个月)评估心房电图幅度和感知阈值。在体格检查、跑步机运动试验和动态心电图记录期间评估心房感知的稳定性。Thera VVD植入时的心房电图幅度较高(2.08±0.79毫伏,而Unity VDDR为1.45±0.59毫伏;P<0.05),但随访期间心房感知阈值低于Unity VDDR。在体格检查和运动试验期间,两种起搏器均额外观察到P波感知不足(6%-19%的患者)。在Unity VDDR和Thera VDD中,分别有2例和4例患者在动态心电图上出现心房感知不足,P波感知不足的百分比分别为0.88%±2.41%和3.63%±8.16%。在Unity VDDR中重新编程心房感知灵敏度,以及在Thera VDD中使用允许将心房感知灵敏度编程为0.18毫伏的研究性软件,可将动态心电图上P波感知不足的百分比分别大幅降低至0.46%±1.67%和0.10%±0.24%。从出院时将心房感知灵敏度编程为至少两倍于感知余量开始,6个月时Unity VDDR的平均心房感知灵敏度水平从0.29毫伏重新编程为0.26毫伏,Thera VDD从0.33毫伏重新编程为0.24毫伏。未发生心房感知过度事件。尽管对角排列双极和紧密间隔全环单根导线系统在植入时心房幅度存在差异,但在适当高的心房感知灵敏度下,心房感知的临床性能相似。心房感知过度的不存在表明,单通道VDD起搏器可能应编程为最高可用心房感知灵敏度,以确保在体格检查和动态心电图记录的指导下充分感知P波,从而尽量减少后续重新编程的需要。