Keelan E T, Krum D, Hare J, Mughal K, Li H, Akhtar M, Jazayeri M R
Electrophysiology Laboratories, University of Wisconsin Medical School-Milwaukee Clinical Campus, Sinai Samaritan and St Luke's Medical Centers, USA.
Circulation. 1997 Sep 16;96(6):2022-30. doi: 10.1161/01.cir.96.6.2022.
The potential ventricular proarrhythmic effect of atrial defibrillation shocks (ADS) remains a concern with automatic internal atrial defibrillation. Optimal R-wave synchronization alone may not be sufficient to prevent the induction of ventricular fibrillation (VF).
The proarrhythmic effect of ADS synchronized to normally conducted QRS complexes (NQRS) and to supraventricular complexes with left or right bundle-branch block (L/RBBB) was investigated in a canine atrial pacing study. Short-long-short, single premature, and burst pacing protocols from the high right atrium were performed at baseline, during isoproterenol infusion, and after intravenous procainamide. The ADS were delivered between decapolar catheters in the coronary sinus and lateral right atrium. They were initially delivered 20 milliseconds (ms) after the end of the last conducted QRS complex and then scanned decrementally through that complex until VF was induced. For NQRS complexes, VF occurred only when the ADS were delivered at or before the onset of the QRS complex and never during the complex itself. In the presence of LBBB or RBBB, VF was induced by ADS delivered at the onset of or within the first 45 ms of the QRS complex in 16 animals. The longest RR (VV) intervals preceding ADS-induced VF were 345 ms at baseline and 380 ms after procainamide.
In this study, ADS synchronized to NQRS complexes appeared to be safe regardless of the preceding RR interval. In the presence of LBBB or RBBB, RR intervals preceding the ADS of >345 ms at baseline and >380 ms in the presence of procainamide would have been required to avoid VF. Alternatively, ADS delivered 50 ms after the onset of the RV electrogram appeared to be safe in all circumstances regardless of the preceding RR interval.
心房除颤电击(ADS)潜在的心室促心律失常作用仍是自动体内心房除颤关注的问题。仅最佳R波同步可能不足以预防心室颤动(VF)的诱发。
在一项犬心房起搏研究中,研究了与正常传导的QRS波群(NQRS)以及伴有左或右束支传导阻滞(L/RBBB)的室上性复合波同步的ADS的促心律失常作用。在基线、异丙肾上腺素输注期间和静脉注射普鲁卡因酰胺后,从高位右心房进行短-长-短、单个早搏和短阵起搏方案。ADS在冠状窦和右心房外侧的十极导管之间传递。最初在最后一个传导的QRS波群结束后20毫秒(ms)传递,然后逐渐扫描该复合波直至诱发VF。对于NQRS复合波,仅当ADS在QRS复合波开始时或之前传递时才会发生VF,而在复合波本身期间从未发生。在存在LBBB或RBBB的情况下,16只动物中,在QRS复合波开始时或在其前45 ms内传递的ADS诱发了VF。ADS诱发VF之前的最长RR(VV)间期在基线时为345 ms,在使用普鲁卡因酰胺后为380 ms。
在本研究中,与NQRS复合波同步的ADS无论之前的RR间期如何似乎都是安全的。在存在LBBB或RBBB的情况下,为避免VF,基线时ADS之前的RR间期需>345 ms,使用普鲁卡因酰胺时需>380 ms。或者,无论之前的RR间期如何,在右心室电图开始后50 ms传递的ADS在所有情况下似乎都是安全的。