| Literature DB >> 33723693 |
Guolin Liu1,2, Xin Xu1,2, Qijian Yi1,2, Tiewei Lv3,4.
Abstract
PURPOSE: Although implantable cardioverter defibrillator (ICD) could prevent the sudden death of ventricular tachycardia (VT) in patients with ischemic heart disease, it could not effectively prevent the recurrence of ventricular tachycardia. Several studies have suggested that catheter ablation may effectively decrease the incidence of ICD events, but relevant dates from randomized controlled trials were limited.Entities:
Keywords: Catheter ablation; Implantable cardioverter defibrillator; Ischemic heart disease; Ventricular tachycardia
Mesh:
Year: 2021 PMID: 33723693 PMCID: PMC8376706 DOI: 10.1007/s10840-020-00848-1
Source DB: PubMed Journal: J Interv Card Electrophysiol ISSN: 1383-875X Impact factor: 1.900
Baseline characteristics of patients
| Study | Age | Male (%) | Size | Time from MI to enrollment (years) | LVEF (%) | HTN (%) | DM (%) |
|---|---|---|---|---|---|---|---|
| SMASH-VT | 67/66 | 92/81 | 64/64 | Ablation: 8.8 ± 8.5 | Ablation: 30.7 ± 9.5 | 73/67 | 38/50 |
| Control: 7.9 ± 7.8 | Control: 32.9 ± 8.5 | ||||||
| VTACH | 68/64 | 96/91 | 52/55 | Ablation: 12.6 ± 8 | Ablation: 34 ± 9.6 | NR | NR |
| Control: 13.3 ± 8.6 | Control: 34.1 ± 8.8 | ||||||
| VANISH | 68/70 | 93/93 | 132/127 | NR | Ablation: 31.1 ± 10.4 | 70/69 | 28/30 |
| Control: 31.2 ± 10.7 | |||||||
| SMS | 68/66 | 87/81 | 54/57 | Ablation: 11.1 ± 6.6 | Ablation: 32 ± 6.9 | NR | NR |
| Control: 8.6 ± 7.8 | Control: 30.4 ± 7.3 |
NR = not reported; HTN = hypertension; DM = diabetes mellitus; MI = myocardial infarction; LVEF = left ventricular ejection fraction
Study characteristics
| Study | SMASH-VT | VTACH | VANISH | SMS |
|---|---|---|---|---|
| Year | 2007 | 2010 | 2016 | 2017 |
| Sample size | 128 | 107 | 259 | 111 |
| Comparator | ICD alone | ICD alone | ICD + escalating AADs | ICD alone |
| Procedure design | Substrate modification in sinus rhythm | Ablation in stable VT, and substrate modification in case of non-inducible or unstable VT. | Standardized approach targeted all inducible VT. | Substrate modification |
| Included criteria | MI > 1 month; planned or recent (within 6 months) ICD for VF, unstable VF, or syncope with inducible VF | Indication for an ICD as secondary prevention for documented stable clinical VT without any reversible cause, CAD, MI, LVEF ≤ 50% | Myocardial infarction, an ICD, episode of ventricular tachycardia when using class I or class III AAD within the previous 6 months | CAD, LVEF ≤ 40%, unstable spontaneous VT, cardiac arrest or syncope with unstable VT inducible |
| Epicardial ablation | NR late potential | NR | NR | NR |
| Amiodarone | 0 | 35% ablation 35% control | 66.1% ablation 64.2% control | 30% ablation 35% control |
| BB (%) | 94/98 | 75/75 | 93.9/96.1 | 91/91 |
| Follow-up (months) | 22.5 ± 5.5 | 22.5 ± 9 | 27.9 ± 17.1 | 27.6 ± 13.2 |
| Cross-over to ablation | NR | 12 | 11 | 1 |
| Complication related to ablation | Pericardial effusion without tamponade (1), exacerbation of congestive heart failure (1), deep venous thrombosis (1) | None | Vascular injury (3), cardiac perforation (2), heart block (1) | Third-degree atrioventricular conduction block (2), tamponade requiring pericardiocentesis (2) |
ICD = implantable cardioverter defibrillator; BB = beta-blockers; AAD = antiarrhythmic drug; VT = ventricular tachycardia; VF = ventricular fibrillation; CAD = coronary artery disease; MI = myocardial infarction; IHD = ischemic heart disease; NR = not reported
Risk-of-bias assessment of included randomized controlled trials
| Citation: name and year | Random sequence generation | Allocation Concealment | Blinding of participants | Blinding of outcome assessment | Incomplete outcomes data | Selective reporting | Other bias | Risk of bias |
|---|---|---|---|---|---|---|---|---|
| SMASH-VT 2007 | Unclear | Low | High | Unclear | Low | Low | Low | Low |
| VTACH 2010 | Low | Low | High | Unclear | Unclear | Low | Unclear | Moderate |
| VANISH 2016 | Low | Low | High | Unclear | Low | Low | Unclear | Low |
| SMS 2017 | Low | Unclear | High | Unclear | Low | Low | Low | Low |
Risk of bias was assessed with use of the Cochrane risk of bias tool. The overall risk of bias of a study was considered “low” if > 4 items were rated as “low risk” and “moderate” if 2 or 3 items were rated as “low risk.” The overall risk of bias of a study was considered “high” if < 2 items were rated as “low risk” or if > 1 item was rated as “high risk”
Fig. 1The selection flowchart of literature screening for the meta-analysis
Fig. 2Summary forest plot of ICD therapy, ICD shock, VT storm, and all-cause mortality
Fig. 3Summary forest plot of cardiovascular mortality, cardiovascular-related hospitalization, and complication
Fig. 4Summary forest plot for sensitive analysis of ICD shock, VT storm, all-cause mortality, cardiovascular mortality, cardiovascular-related hospitalization, and complication