Al Taii Haider, Saxena Ritika, Morcos Ramez, Al-Shammari Ali Saad, Farhat Kassem, Al Sakini Ahmed Sermed, Al-Wssawi Ameer, Gaalema Diann, Naraynan Arun, Sabayon Dean, Albani Aiham, Jneid Hani
Cardiovascular Department, University of Texas Medical Branch, Galveston, TX, USA.
Geisinger Heart Institute, Wilkes Barre, PA, USA.
J Interv Card Electrophysiol. 2025 Jan 9. doi: 10.1007/s10840-025-01986-0.
Ventricular tachycardia (VT) in patients with cardiac sarcoidosis (CS) can lead to sudden cardiac death. The role of ventricular tachycardia ablation (VTA) in CS has been investigated in a few small, single-center, and larger observational studies, but the evidence still needs to be provided. This study aimed to investigate the clinical outcomes of VTA in patients with CS admitted with a diagnosis of VT.
A retrospective analysis was conducted using the TriNetX database: US collaborative network from 2010 to 2024. Patients undergoing ablation for VT with and without CS were identified. Two groups were created for propensity score analysis matching a history of hypertension, diabetes, obesity, peripheral vascular diseases, heart failure, ischemic heart diseases, atrial fibrillation, and chronic kidney disease. The primary outcome was the incidence of death, cardiogenic shock, heart failure, acute myocardial infarction, hemorrhagic stroke, ischemic stroke, and ventricular tachycardia within 1 year from the date of the index procedure.
Out of 15,958 patients who underwent catheter ablation for VT, 778 patients had CS. After propensity matching, the mean age of patients with VT and CS who underwent ablation was 58.6 (SD = 11.3), compared to 59.5 (SD = 13) in patients with VT without CS (p-value = 0.07). The propensity-matched analysis showed no significant differences in procedure-related complications between those with cardiac sarcoidosis (CS) and those without. Both cohorts had 10 events each for cardiac tamponade (p = 0.195), groin hematoma requiring transfusion (p = 0.102), pneumothorax (p = 0.317), and sepsis (p = 0.654). Cardiogenic shock occurred in 13 patients in the non-CS group versus 12 in the CS group (p = 0.840). At the 1-year follow-up, there was no significant difference in the mortality rate between the two groups (HR = 1.228, 95% CI 0.834-1.809, p = 0.298). Cardiogenic shock was also similar, with 13 events in the non-CS group and 12 in the CS group (HR = 0.879, 95% CI 0.636-1.213, p = 0.430). However, CS was associated with a higher risk of acute exacerbation of heart failure (314 in non-CS vs. 378 in CS, HR = 0.823, 95% CI 0.709-0.956, p = 0.010) and a lower risk of acute myocardial infarction (96 in non-CS vs. 74 in CS, HR = 1.389, 95% CI 1.026-1.881, p = 0.033). There was no significant difference in ICD shock (147 in non-CS vs. 185 in CS, HR = 0.817, 95% CI 0.658-1.014, p = 0.066), ischemic stroke (10 cases each, HR = 0.941, 95% CI 0.382-2.316, p = 0.895), or hemorrhagic stroke (10 cases each, HR = 1.455, 95% CI 0.326-6.501, p = 0.620). However, CS was associated with a higher risk of pericarditis (91 in non-CS vs. 151 in CS, HR = 0.593, 95% CI 0.457-0.769, p < 0.05). At the 5-year follow-up, CS was associated with a lower risk of mortality (123 deaths in non-CS vs. 104 in CS, HR = 1.341, 95% CI 1.033-1.741, p = 0.027) and a lower risk of acute myocardial infarction (134 in non-CS vs. 109 in CS, HR = 1.381, 95% CI 1.072-1.778, p = 0.012). CS patients had a higher risk of acute exacerbation of heart failure (366 in non-CS vs. 467 in CS, HR = 0.780, 95% CI 0.680-0.894, p < 0.05) and ICD shock (182 in non-CS vs. 242 in CS, HR = 0.789, 95% CI 0.651-0.956, p = 0.015). There were no significant differences in the incidence of cardiogenic shock (98 in non-CS vs. 129 in CS, HR = 0.825, 95% CI 0.635-1.074, p = 0.150), ischemic stroke (11 in non-CS vs. 12 in CS, HR = 0.981, 95% CI 0.433-2.224, p = 0.963), or hemorrhagic stroke (10 cases each, HR = 1.320, 95% CI 0.509-3.424, p = 0.570). The risk of pericarditis was higher in CS patients (122 in non-CS vs. 187 in CS, HR = 0.655, 95% CI 0.522-0.823, p < 0.05).
Cardiac sarcoidosis's influence on immediate periprocedural complications was comparable to that of non-cardiac sarcoidosis in patients undergoing catheter ablation. However, it was associated with increased incidences of pericarditis, acute heart failure exacerbations at 1 and 5 years, and ICD shocks at 5 years of follow-up. These findings support VT ablation as a reasonable and safe therapeutic option for cardiac sarcoidosis patients. Operators should be prepared to address the unique challenges of this population, including potential follow-up complications and their management. Further prospective and multicenter studies are warranted to validate these findings and optimize clinical outcomes.
心脏结节病(CS)患者的室性心动过速(VT)可导致心源性猝死。室性心动过速消融术(VTA)在CS中的作用已在一些小型、单中心及大型观察性研究中进行了调查,但仍需提供相关证据。本研究旨在调查因VT入院的CS患者接受VTA后的临床结局。
使用TriNetX数据库进行回顾性分析,该数据库是2010年至2024年的美国合作网络。识别接受VT消融术的有或无CS的患者。创建两组进行倾向评分分析,匹配高血压、糖尿病、肥胖、外周血管疾病、心力衰竭、缺血性心脏病、心房颤动和慢性肾病病史。主要结局是自索引手术日期起1年内死亡、心源性休克、心力衰竭、急性心肌梗死、出血性卒中、缺血性卒中和室性心动过速的发生率。
在15958例接受VT导管消融术的患者中,778例患有CS。倾向匹配后,接受消融的VT合并CS患者的平均年龄为58.6岁(标准差=11.3),而无CS的VT患者平均年龄为59.5岁(标准差=13)(p值=0.07)。倾向匹配分析显示,心脏结节病(CS)患者和无CS患者在手术相关并发症方面无显著差异。两组心包填塞(p=0.195)、需要输血的腹股沟血肿(p=0.102)、气胸(p=0.317)和败血症(p=0.654)的事件均为10例。非CS组13例患者发生心源性休克,CS组12例(p=0.840)。在1年随访时,两组死亡率无显著差异(HR=1.228,95%CI 0.834-1.809,p=0.298)。心源性休克情况也相似,非CS组13例事件,CS组12例(HR=0.879,95%CI 0.636-1.213,p=0.430)。然而,CS与心力衰竭急性加重风险较高相关(非CS组314例,CS组378例,HR=0.823,95%CI 0.709-0.956,p=0.010),与急性心肌梗死风险较低相关(非CS组96例,CS组74例,HR=1.389,95%CI 1.026-1.881,p=0.033)。植入式心律转复除颤器(ICD)电击(非CS组147例,CS组185例,HR=0.817,95%CI 0.658-1.014,p=0.066)、缺血性卒中(每组10例,HR=0.941,95%CI 0.382-2.316,p=0.895)或出血性卒中(每组10例,HR=1.455,95%CI 0.326-6.501,p=0.620)无显著差异。然而,CS与心包炎风险较高相关(非CS组91例,CS组151例,HR=0.593,95%CI 0.457-0.769,p<0.05)。在5年随访时,CS与较低的死亡风险相关(非CS组123例死亡,CS组104例,HR=1.341,95%CI 1.033-1.741,p=0.027)和较低的急性心肌梗死风险相关(非CS组134例,CS组109例,HR=1.381,95%CI 1.072-1.778,p=0.012)。CS患者心力衰竭急性加重风险较高(非CS组366例,CS组467例,HR=0.780,95%CI 0.680-0.894,p<0.05)和ICD电击风险较高(非CS组182例,CS组242例,HR=0.789,95%CI 0.651-0.956,p=0.015)。心源性休克发生率(非CS组98例,CS组129例,HR=0.825,95%CI 0.635-1.074,p=0.150)、缺血性卒中(非CS组11例,CS组12例,HR=0.981,95%CI 0.433-2.224,p=0.963)或出血性卒中(每组10例,HR=1.320,95%CI 0.509-3.424,p=0.570)无显著差异。CS患者心包炎风险较高(非CS组122例,CS组187例,HR=0.655,95%CI