首页> 外文期刊>PACE: Pacing and clinical electrophysiology >Noise detection during bradycardia pacing with a hybrid nonthoracotomy implantable cardioverter defibrillator system: incidence and clinical significance.
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Noise detection during bradycardia pacing with a hybrid nonthoracotomy implantable cardioverter defibrillator system: incidence and clinical significance.

机译:混合式非开胸植入式心脏复律除颤器系统在心动过缓起搏中的噪声检测:发生率和临床意义。

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The purpose of this study was to prospectively evaluate the incidence of noise detection during bradycardia pacing by an FDA approved hybrid nonthoracotomy ICD system. An illustrative case report which prompted this investigation is provided. Backup bradycardia pacing by tiered therapy cardioverter defibrillators has been useful in preventing postshock bradycardia and occasionally for chronic rate support in bradycardic patients. Unexplained "noise" detected by real-time telemetry has been previously described during bradycardia pacing by a device utilizing automatic gain control for sensing. Eighteen patients were prospectively evaluated for noise detection during ventricular pacing by the ICD. Real-time telemetry was analyzed with each patient: (1) supine, (2) supine with deep inspiration/expiration, (3) supine during Valsalva, and (4) during a change in position from supine to sitting. Analysis of pacing threshold and lead impedance was made in each patient. Eleven of 18 patients had noise detected on real-time telemetry during bradycardia pacing. In 10 patients this was noted during deep inspiration/expiration, in 2 during Valsalva maneuver, and in 5 with position change. There was no evidence in any patient of lead malfunction nor any difference in pacing threshold or lead impedance between patients with noise detected versus those without it. Noise detection by an approved hybrid ICD system is common and may be due to the automatic gain control which maximizes sensitivity during bradycardia pacing. This may lead to clinically significant events, with both suppression of bradycardia pacing and triggering of tachycardia therapy in the absence of ventricular tachyarrhythmias in pacemaker-dependent patients.
机译:这项研究的目的是前瞻性评估通过FDA批准的混合非开胸ICD系统进行的心动过缓起搏过程中噪音检测的发生率。提供了示例性案例报告,该报告提示了此调查。通过分级治疗心脏复律除颤器进行后备心动过缓起搏可用于预防休克后心动过缓,有时还可用于心动过缓患者的长期心律失常支持。先前已经描述了通过使用自动增益控制进行感应的设备在心动过缓起搏期间通过实时遥测检测到的无法解释的“噪声”。前瞻性评估了18名患者在ICD起搏期间的噪声检测。对每位患者进行了实时遥测:(1)仰卧,(2)具有深层吸气/呼气的仰卧,(3)瓦尔萨尔瓦(Valsalva)期间仰卧,以及(4)从仰卧到坐姿改变时的仰卧。对每个患者的起搏阈值和导线阻抗进行分析。 18例患者中有11例在心动过缓起搏期间通过实时遥测检测到噪音。在深吸气/呼气期间,有10例患者,在瓦尔萨尔瓦(Valsalva)操纵期间有2例,随着位置变化在5例中注意到。没有证据表明有噪音的患者与没有噪音的患者之间没有导线故障,也没有起搏阈值或导线阻抗的差异。由认可的混合ICD系统进行噪声检测很常见,这可能是由于自动增益控制使心动过缓起搏过程中的灵敏度最大化所致。这可能会导致临床上的重大事件,在不依赖起搏器的患者中,如果不存在心室性心律失常,则会抑制心动过缓起搏并触发心动过速疗法。

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