跳至主要内容
临床试验/NCT03421834
NCT03421834已完成不适用

Impact of PREVENTIVE Substrate Catheter Ablation on Implantable cardioVerter-defibrillaTor Interventions in Patients With Ischaemic Cardiomyopathy and Infarct-related Coronary Chronic Total Occlusion

University Medical Centre Ljubljana5 个研究点 分布在 2 个国家目标入组 60 人开始时间: 2018年2月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
5
主要终点
Time to first event comprising appropriate ICD therapy and unplanned hospital admission for symptomatic ventricular tachycardia (VT)/ ventricular fibrillation (VF)

研究概览

简要总结

The aim of this study is to assess whether preventive substrate ablation of chronic total occlusion infarct-related artery (CTO-IRA) area in heart failure (HF) patients correlates with lower appropriate implantable cardiac defibrillator (ICD) therapies. In addition, the purpose of the study is to determine whether prophylactic substrate ablation at the time of primary ICD implantation in high-risk ischemic patients affects unplanned hospitalization, HF progression, and quality of life.

详细描述

Implantable cardioverter-defibrillators (ICDs) improve survival among patients with ischemic heart failure (HF) who have not previously had a sustained ventricular arrhythmia. However, ICD shocks that terminate ventricular tachycardia (VT) are associated with higher mortality, which may be a reflection of ICD shocks being a marker of more advanced disease versus shocks causing a worse prognosis. In addition, ICD shocks are associated with decreased functional status and quality of life. Antiarrhythmic medications (AAD) reduce ICD shocks but have high rates of side effects and lack of compliance within 1 year of initiation. Some randomized, controlled clinical trials have shown that catheter ablation (CA) of VT can decrease the number of episodes of VT and ICD shocks which could translate to an improvement in patient outcomes.

Regarding the approach to CA of VT, several controversies and gaps of knowledge can be found in the literature. Some authors target predominantly "clinical VTs" (activation and entrainment mapping), while others focus on the substrate causing VTs without focusing on VT morphologies (elimination of local abnormal ventricular activities and late potentials). In addition, data on timing of the CA procedure is inconsistent. However, early CA strategy seems feasible as end-stage cardiovascular disease increases procedural risk and is associated with arrhythmias that may be less amenable to successful treatment with ablation.

The current focus on risk stratifying patients with ischemic cardiomyopathy who could benefit from a primary prevention ICD solely on basis of ejection fraction and NYHA class is far from ideal. In patients with ischemic HF, the presence of the coronary chronic total occlusion (CTO) is related to worse long-term prognosis. Moreover, in a subgroup of ischemic patients, CTO associated with a previous infarction in its territory was an independent predictor of ventricular arrhythmias. Recent studies reported that primary prevention patients with CTO of an infarct-related artery (CTO-IRA) have a very high risk of appropriate ICD therapies due to fast VTs. As post-myocardial infarction scar is a well-recognized substrate of VTs, these patients might benefit from prophylactic substrate ablation at the time of primary ICD implantation.

Eligible and consenting patients on optimal medical HF treatment with confirmed CTO-IRA will be equally randomized to receive either a primary prevention ICD or a CA procedure and an ICD. Catheter ablation with a uniform procedural endpoint and definition of acute procedural success was to be performed before ICD implantation. ICD programming will be standardized for all subjects according to primary prevention settings.

Subjects will be seen at baseline randomization, then 1 month after ICD implantation and every 6 months thereafter until the end of the study. Subjects will be followed up for a minimum of 24 months. Quality of life questionnaires will be done at each visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ischemic cardiomyopathy with reduced ejection fraction (EF ≤ 40%) estimated by cardiac MRI or echocardiography within 30 days before enrollment
  • Coronary Chronic Total Occlusion (CTO) associated with a previous MI confirmed by coronary angiography and late gadolinium enhancement MRI or myocardial perfusion imaging within 30 days before enrollment
  • Implantable cardioverter-defibrillator (ICD) indication for primary prevention
  • Patient has provided written informed consent

排除标准

  • Age < 18 years or > 85 years
  • Documented sustained ventricular tachycardia before enrollment
  • Class IV New York Heart Association (NYHA) heart failure
  • CTOs not associated with a prior infarction in their territory
  • Acute myocardial infarction (MI) or acute coronary syndrome
  • Subjects with active ischemia that are eligible for revascularization
  • Documented history of MI less than 6 months before enrollment
  • Patients requiring chronic renal dialysis
  • Thrombocytopenia or coagulopathy
  • Pre-existing implantable cardioverter-defibrillator (ICD)
  • Pregnancy or breastfeeding women
  • Acute illness or active systemic infection
  • Life expectancy less than 12 months
  • Unwillingness to participate or lack of availability for follow-up
  • Valvular heart disease or mechanical heart valve precluding access to the left ventricle

研究组 & 干预措施

Prophylactic VT ablation prior to ICD implantation

Experimental

干预措施: Catheter ablation of ventricular tachycardia (Procedure)

Prophylactic VT ablation prior to ICD implantation

Experimental

干预措施: Optimal medical treatment (Drug)

ICD implantation and optimal medical treatment

Active Comparator

ICD implantation and optimal medical care until at least 2 appropriate ICD shock occurs or an arrhythmic storm and catheter ablation thereafter.

干预措施: Optimal medical treatment (Drug)

结局指标

主要结局

Time to first event comprising appropriate ICD therapy and unplanned hospital admission for symptomatic ventricular tachycardia (VT)/ ventricular fibrillation (VF)

时间窗: From randomization until official study end or drop-out, patients will be followed and assessed at least 24 months.

Appropriate ICD therapy defined as shock or ATP therapy.

次要结局

  • Incidence of appropriate ICD therapy(At least 24 months after enrolment)
  • Time to unplanned hospital admission for symptomatic ventricular tachycardia (VT)/ ventricular fibrillation (VF)(At least 24 months after enrolment)
  • Time to electrical storm(At least 24 months after enrolment)
  • Time to appropriate ICD therapy(At least 24 months after enrolment)
  • Time to unplanned cardiac hospital admission(At least 24 months after enrolment)
  • Cardio-vascular mortality(At least 24 months after enrolment)
  • Changes in quality of life using the EQ-5D questionnaire(At least 24 months after enrolment)
  • Psychometric evaluation of ICD shock-related anxiety using The Florida Shock Anxiety Scale (FSAS)(At least 24 months after enrolment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David Žižek, MD, PhD

Assistant Professor, Principal Investigator

University Medical Centre Ljubljana

研究点 (5)

Loading locations...

相似试验