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起搏器患者心房颤动的发生及其与睡眠呼吸暂停和心率变异性的关系。

Occurrence of atrial fibrillation in pacemaker patients and its association with sleep apnea and heart rate variability.

机构信息

Cardiology Division, S. Maria della Stella Hospital, Orvieto, Italy.

Boston Scientific, Milan, Italy.

出版信息

Eur J Intern Med. 2019 Oct;68:13-17. doi: 10.1016/j.ejim.2019.07.020. Epub 2019 Jul 26.

Abstract

AIMS

Sleep apnea (SA) is a risk factor for atrial fibrillation (AF) occurrence. Sympathovagal imbalance is a mechanism that predisposes to the development of AF and that occurs in SA. Some pacemakers can detect SA events and continuously measure a time domain measure of heart rate variability (HRV), i.e. the standard deviation of 5-min median atrial-atrial sensed intervals (SDANN). We evaluated the association between the occurrence of AF and device-detected SA and SDANN in patients who received pacemakers.

METHODS

We enrolled 150 consecutive patients undergoing implantation of a dual-chamber pacemaker, capable of SA and SDANN estimation. The SA was defined as severe if the Respiratory Disturbance Index was ≥30 episodes/h for at least one night during the first week after implantation.

RESULTS

Sixteen patients in permanent AF were excluded from our analysis. During follow-up, AF (cumulative device-detected AF duration > 6 h/day) occurred in 24(18%) patients out of the remaining 134 patients. Severe SA was detected in 84 patients. SDANN values were available in 74 patients and the median value was 76 ms [25°-75°percentile:58-77]. The risk of AF was higher in patients with severe SA (log-rank test; p = .033). The presence of either or both conditions (severe SA and SDANN < 76 ms) was associated with shorter time to AF event (p = .042) and was an independent predictor of AF (hazard ratio: 2.37; 95%CI:1.08 to 5.21; p = .033).

CONCLUSION

In pacemaker patients, device-diagnosed severe SA and reduced SDANN are associated with a higher risk of AF.

摘要

目的

睡眠呼吸暂停(SA)是心房颤动(AF)发生的一个危险因素。交感神经迷走神经失衡是导致 AF 发生的一种机制,并且在 SA 中发生。一些起搏器可以检测到 SA 事件,并连续测量心率变异性(HRV)的时域测量值,即 5 分钟中位数心房感知间期的标准差(SDANN)。我们评估了在接受起搏器治疗的患者中,AF 的发生与设备检测到的 SA 和 SDANN 之间的关联。

方法

我们招募了 150 例连续接受双腔起搏器植入的患者,该起搏器能够估计 SA 和 SDANN。如果在植入后第一周的至少一个晚上,呼吸干扰指数≥30 次/小时,则将 SA 定义为严重。

结果

在我们的分析中,有 16 例永久性 AF 患者被排除在外。在随访期间,剩余的 134 例患者中有 24 例(18%)发生了 AF(设备检测到的 AF 持续时间累积>6 小时/天)。在 84 例患者中检测到严重的 SA。在 74 例患者中可获得 SDANN 值,中位数为 76 ms[25°-75°百分位:58-77]。严重 SA 患者发生 AF 的风险更高(对数秩检验;p=0.033)。存在严重的 SA 或 SDANN<76 ms 或两者兼有与 AF 事件发生时间较短相关(p=0.042),并且是 AF 的独立预测因素(风险比:2.37;95%CI:1.08 至 5.21;p=0.033)。

结论

在起搏器患者中,设备诊断的严重 SA 和降低的 SDANN 与 AF 风险增加相关。

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