荷兰心脏再同步治疗(CRT)人群中心室心律失常的风险:CRT除颤器与CRT起搏器的比较。

The risk of ventricular arrhythmias in a Dutch CRT population: CRT-defibrillator versus CRT-pacemaker.

作者信息

Ter Horst I A H, van 't Sant J, Wijers S C, Vos M A, Cramer M J, Meine M

机构信息

Department of Cardiology, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA, PO Box 85500, Utrecht, The Netherlands.

Department of Cardiology, St. Antonius Hospital Nieuwegein, Nieuwegein, The Netherlands.

出版信息

Neth Heart J. 2016 Mar;24(3):204-13. doi: 10.1007/s12471-015-0800-8.

Abstract

BACKGROUND

Patients eligible for cardiac resynchronisation therapy (CRT) have an indication for primary prophylactic implantable cardioverter defibrillator (ICD) therapy. However, response to CRT might influence processes involved in arrhythmogenesis and therefore change the necessity of ICD therapy in certain patients.

METHOD

In 202 CRT-defibrillator patients, the association between baseline variables, 6-month echocardiographic outcome (volume response: left ventricular end-systolic volume decrease < ≥15 % and left ventricular ejection fraction (LVEF) ≤ >35 %) and the risk of first appropriate ICD therapy was analysed retrospectively.

RESULTS

Fifty (25 %) patients received appropriate ICD therapy during a median follow-up of 37 (23-52) months. At baseline ischaemic cardiomyopathy (hazard ratio (HR) 2.0, p = 0.019) and a B-type natriuretic peptide level > 163 pmol/l (HR 3.8, p < 0.001) were significantly associated with the risk of appropriate ICD therapy. After 6 months, 105 (52 %) patients showed volume response and 51 (25 %) reached an LVEF > 35 %. Three (6 %) patients with an LVEF > 35 % received appropriate ICD therapy following echocardiography at ± 6 months compared with 43 patients (29 %) with an LVEF ≤ 35 % (p = 0.001). LVEF post-CRT was more strongly associated to the risk of ventricular arrhythmias than volume response (LVEF > 35 %, HR 0.23, p = 0.020).

CONCLUSION

Assessing the necessity of an ICD in patients eligible for CRT remains a challenge. Six months post-CRT an LVEF > 35 % identified patients at low risk of ventricular arrhythmias. LVEF might be used at the time of generator replacement to identify patients suitable for downgrading to a CRT-pacemaker.

摘要

背景

符合心脏再同步治疗(CRT)条件的患者有植入一级预防性植入式心律转复除颤器(ICD)治疗的指征。然而,对CRT的反应可能会影响心律失常发生过程,从而改变某些患者ICD治疗的必要性。

方法

对202例ICD患者进行回顾性分析,分析基线变量、6个月超声心动图结果(容积反应:左心室收缩末期容积减少<≥15%且左心室射血分数(LVEF)≤>35%)与首次适当ICD治疗风险之间的关联。

结果

在中位随访37(23 - 52)个月期间,50例(25%)患者接受了适当的ICD治疗。基线时,缺血性心肌病(风险比(HR)2.0,p = 0.019)和B型利钠肽水平>163 pmol/l(HR 3.8,p < 0.001)与适当ICD治疗风险显著相关。6个月后,105例(52%)患者显示容积反应,51例(25%)患者LVEF>35%。与43例(29%)LVEF≤35%的患者相比,3例(6%)LVEF>35%的患者在±6个月超声心动图检查后接受了适当的ICD治疗(p = 0.001)。CRT后LVEF与室性心律失常风险的相关性比容积反应更强(LVEF>35%,HR 0.23,p = 0.020)。

结论

评估符合CRT条件患者ICD的必要性仍然是一项挑战。CRT后6个月,LVEF>35%可识别出室性心律失常低风险患者。在更换发生器时,LVEF可用于识别适合降级为CRT起搏器的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b31/4771627/8424b93bd588/12471_2015_800_Fig1_HTML.jpg

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