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一种用于变时功能不全且反复阵发性心房颤动的窦房结疾病患者从DDDR起搏模式自动切换至DDIR起搏模式的新算法的可靠性

Reliability of a new algorithm for automatic mode switching from DDDR to DDIR pacing mode in sinus node disease patients with chronotropic incompetence and recurrent paroxysmal atrial fibrillation.

作者信息

Ricci R, Puglisi A, Azzolini P, Spampinato A, Pignalberi C, Bellocci F, Adinolfi E, Dini P, Cavaglià S, De Seta F

机构信息

Fatebenefratelli Hospital, Rome, Italy.

出版信息

Pacing Clin Electrophysiol. 1996 Nov;19(11 Pt 2):1719-23. doi: 10.1111/j.1540-8159.1996.tb03213.x.

Abstract

To evaluate the safety and efficacy of a new algorithm for automatic mode switching (AMS) from DDD-DDDR to DDIR, 26 patients, 16 females and 10 males, mean age 73 +/- 6 years of age, affected by sinus node disease, chronotropic incompetence, and recurrent paroxysmal atrial fibrillation (PAF) received the Medtronic Thera DR pacemaker. The device continuously calculates, in ms, the running average of the intrinsic atrial rate (MAR) and compares the current atrial interval (CAI) with the stored MAR. When the CAI is greater than the MAR it increases by 8 ms, and when the CAI is less than the MAR, it decreases by 23 ms. When MAR < or = 330 ms (182 beats/min), tachycardia is detected and AMS is activated. All patients had clinical evaluation, 12-lead ECG, Holter monitoring, and exercise testing after implantation and every 3 months for 1 year. The results were compared with the data stored in the pacemaker memory: AMS episodes number; the histogram of the last 14 episodes; and atrial electrogram recording. Twenty-two Holter recordings in 13 patients showed PAF and in all of them AMS occurred simultaneously. AMS lasted between 10 seconds and 20 hours, and MAR ranged from 195-400 beats/min. No episode of PAF and no AMS were recorded in 39 Holter recordings in 22 patients. Appropriate AMS was confirmed in five patients by stored atrial electrogram and in nine by 12-lead ECG and pacemaker event markers. Mean atrial sensing was 2.13 +/- 1.04 mV during PAF and 3.18 +/- 1.46 mV during sinus rhythm. No PAF episode and no AMS were recorded during exercise testing. In conclusion, this new algorithm was very reliable, sensitive, and specific.

摘要

为评估一种从DDD-DDDR自动转换为DDIR模式的新算法(自动模式转换,AMS)的安全性和有效性,26例患者(16例女性,10例男性,平均年龄73±6岁),患有窦房结疾病、变时性功能不全和复发性阵发性心房颤动(PAF),植入了美敦力Thera DR起搏器。该设备持续以毫秒为单位计算固有心房率(MAR)的移动平均值,并将当前心房间期(CAI)与存储的MAR进行比较。当CAI大于MAR时增加8毫秒,当CAI小于MAR时减少23毫秒。当MAR≤330毫秒(182次/分钟)时,检测到心动过速并激活AMS。所有患者在植入后以及之后的1年中每3个月进行临床评估、12导联心电图、动态心电图监测和运动试验。将结果与起搏器内存中存储的数据进行比较:AMS发作次数;最后14次发作的直方图;以及心房电图记录。13例患者的22份动态心电图记录显示有PAF,并且在所有这些记录中AMS同时发生。AMS持续时间为10秒至20小时,MAR范围为195 - 400次/分钟。22例患者的39份动态心电图记录中未记录到PAF发作和AMS。通过存储的心房电图在5例患者中证实了适当的AMS,通过12导联心电图和起搏器事件标记在9例患者中证实了适当的AMS。PAF期间平均心房感知为2.13±1.04毫伏,窦性心律期间为3.18±1.46毫伏。运动试验期间未记录到PAF发作和AMS。总之,这种新算法非常可靠、敏感且特异。

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