Nauffal Victor, Zhang Yiyi, Tanawuttiwat Tanyanan, Blasco-Colmenares Elena, Rickard John, Marine Joseph E, Butcher Barbara, Norgard Sanaz, Dickfeld Timm-Michael, Ellenbogen Kenneth A, Guallar Eliseo, Tomaselli Gordon F, Cheng Alan
Department of Medicine, Division of Cardiology, Johns Hopkins Medical Institutes, Baltimore, Maryland, United States of America.
Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
PLoS One. 2017 Apr 7;12(4):e0175205. doi: 10.1371/journal.pone.0175205. eCollection 2017.
Cardiac resynchronization therapy (CRT) devices reduce mortality through pacing-induced cardiac resynchronization and implantable cardioverter defibrillator (ICD) therapy for ventricular arrhythmias (VAs). Whether certain factors can predict if patients will benefit more from implantation of CRT pacemakers (CRT-P) or CRT defibrillators (CRT-D) remains unclear.
We followed 305 primary prevention CRT-D recipients for the two primary outcomes of HF hospitalization and ICD therapy for VAs. Serum biomarkers, electrocardiographic and clinical variables were collected prior to implant. Multivariable analysis using Cox-proportional hazards model was used to fit the final models. Among 282 patients with follow-up outcome data, 75 (26.6%) were hospitalized for HF and 31 (11%) received appropriate ICD therapy. Independent predictors of HF hospitalization were atrial fibrillation (HR = 1.8 (1.1,2.9)), NYHA class III/IV (HR = 2.2 (1.3,3.6)), ejection fraction <20% (HR = 1.7 (1.1,2.7)), HS-IL6 >4.03pg/ml (HR = 1.7 (1.1,2.9)) and hemoglobin (<12g/dl) (HR = 2.2 (1.3,3.6)). Independent predictors of appropriate therapy included BUN >20mg/dL (HR = 3.0 (1.3,7.1)), HS-CRP >9.42mg/L (HR = 2.3 (1.1,4.7)), no beta blocker therapy (HR = 3.2 (1.4,7.1)) and hematocrit ≥38% (HR = 2.7 (1.03,7.0)). Patients with 0-1 risk factors for appropriate therapy (IR 1 per 100 person-years) and ≥3 risk factors for HF hospitalization (IR 23 per 100-person-years) were more likely to die prior to receiving an appropriate ICD therapy.
Clinical and biomarker data can risk stratify CRT patients for HF progression and VAs. These findings may help characterize subgroups of patients that may benefit more from the use of CRT-P vs. CRT-D systems.
ClinicalTrials.gov NCT00733590.
心脏再同步治疗(CRT)设备通过起搏诱导的心脏再同步和用于室性心律失常(VA)的植入式心脏复律除颤器(ICD)治疗降低死亡率。某些因素是否能预测患者从植入CRT起搏器(CRT-P)还是CRT除颤器(CRT-D)中获益更多仍不清楚。
我们对305例接受一级预防的CRT-D患者进行随访,观察其心力衰竭住院和VA的ICD治疗这两个主要结局。在植入前收集血清生物标志物、心电图和临床变量。使用Cox比例风险模型进行多变量分析以拟合最终模型。在282例有随访结局数据的患者中,75例(26.6%)因心力衰竭住院,31例(11%)接受了适当的ICD治疗。心力衰竭住院的独立预测因素为心房颤动(HR = 1.8(1.1,2.9))、纽约心脏协会(NYHA)III/IV级(HR = 2.2(1.3,3.6))、射血分数<20%(HR = 1.7(1.1,2.7))、高敏白细胞介素-6(HS-IL6)>4.03pg/ml(HR = 1.7(1.1,2.9))和血红蛋白(<12g/dl)(HR = 2.2(1.3,3.6))。适当治疗的独立预测因素包括血尿素氮(BUN)>20mg/dL(HR = 3.0(1.3,7.1))、高敏C反应蛋白(HS-CRP)>9.42mg/L(HR = 2.3(1.1,4.7))、未接受β受体阻滞剂治疗(HR = 3.2(1.4,7.1))和血细胞比容≥38%(HR = 2.7(1.03,7.0))。适当治疗的危险因素为0 - 1个(发生率为每100人年1次)且心力衰竭住院的危险因素≥3个(发生率为每100人年23次)的患者在接受适当的ICD治疗前死亡的可能性更大。
临床和生物标志物数据可对CRT患者的心力衰竭进展和VA进行风险分层。这些发现可能有助于明确哪些亚组患者可能从使用CRT-P与CRT-D系统中获益更多。
ClinicalTrials.gov NCT00733590。