Debonnaire Philippe, Katsanos Spyridon, Joyce Emer, VAN DEN Brink Olivier V W, Atsma Douwe E, Schalij Martin J, Bax Jeroen J, Delgado Victoria, Marsan Nina Ajmone
Leiden University Medical Centre, Department of Cardiology, Leiden, the Netherlands.
Sint-Jan Hospital Bruges, Department of Cardiology, Bruges, Belgium.
J Cardiovasc Electrophysiol. 2015 May;26(5):547-55. doi: 10.1111/jce.12629. Epub 2015 Mar 27.
QRS fragmentation (fQRS) and prolonged QTc interval on surface ECG are prognostic in various cardiomyopathies other than hypertrophic cardiomyopathy (HCM). The association between fQRS and prolonged QTc duration with occurrence of ventricular tachyarrhythmias or sudden cardiac death (VTA/SCD) in patients with HCM was explored.
One hundred and ninety-five clinical HCM patients were studied. QTc duration was derived applying Bazett's formula; fQRS was defined as presence of various RSR' patterns, R or S notching and/or >1 additional R wave in any non-aVR lead in patients without pacing or (in)complete bundle branch block. The endpoints comprised SCD, ECG documented sustained VTA (tachycardia or fibrillation) or appropriate implantable cardioverter defibrillator (ICD) therapies (antitachycardia pacing [ATP] or shock) for VTA in ICD recipients (n = 58 [30%]). QT prolonging drugs recipients were excluded. After a median follow-up of 5.7 years (IQR 2.7-9.1), 26 (13%) patients experienced VTA or SCD. Patients with fQRS in ≥3 territories (inferior, lateral, septal, and/or anterior) (p = 0.004) or QTc ≥460 ms (p = 0.009) had worse cumulative survival free of VTA/SCD than patients with fQRS in <3 territories or QTc <460 ms. fQRS in ≥3 territories (ß 4.5, p = 0.020, 95%CI 1.41-14.1) and QTc ≥460 ms (ß 2.7, p = 0.037, 95%CI 1.12-6.33) were independently associated with VTA/SCD. Likelihood ratio test indicated assessment of fQRS and QTc on top of conventional SCD risk factors provides incremental predictive value for VTA/SCD (p = 0.035).
Both fQRS in ≥3 territories and QTc duration are associated with VTA/SCD in HCM patients, independently of and incremental to conventional SCD risk factors.
在肥厚型心肌病(HCM)以外的各种心肌病中,体表心电图上的QRS波碎裂(fQRS)和QTc间期延长具有预后价值。本研究探讨了HCM患者中fQRS和QTc间期延长与室性快速心律失常或心源性猝死(VTA/SCD)发生之间的关联。
对195例临床HCM患者进行了研究。应用Bazett公式计算QTc间期;fQRS定义为在无起搏或(不完全性)束支传导阻滞的患者中,任何非aVR导联出现各种RSR′型、R或S波切迹和/或多于1个额外R波。终点包括心源性猝死、心电图记录的持续性VTA(心动过速或颤动)或植入式心律转复除颤器(ICD)植入者(n = 58 [30%])针对VTA的适当治疗(抗心动过速起搏[ATP]或电击)。排除使用延长QT间期药物的患者。中位随访5.7年(四分位间距2.7 - 9.1年)后,26例(13%)患者发生VTA或心源性猝死。≥3个区域(下壁、侧壁、间隔和/或前壁)出现fQRS的患者(p = 0.004)或QTc≥460 ms的患者(p = 0.009),其无VTA/SCD的累积生存率低于<3个区域出现fQRS或QTc<460 ms的患者。≥3个区域出现fQRS(β 4.5,p = 0.020,95%CI 1.41 - 14.1)和QTc≥460 ms(β 2.7,p = 0.037,95%CI 1.12 - 6.33)与VTA/SCD独立相关。似然比检验表明,在传统心源性猝死危险因素基础上评估fQRS和QTc可为VTA/SCD提供额外的预测价值(p = 0.035)。
≥3个区域出现fQRS和QTc间期均与HCM患者的VTA/SCD相关,独立于传统心源性猝死危险因素且为其提供额外信息。