Rorsman Cecilia, Farouq Maiwand, Marinko Sofia, Platonov Pyotr G, Borgquist Rasmus
Cardiology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Internal Medicine Department, Varberg Hospital, Varberg, Sweden.
Cardiology. 2024;149(5):474-483. doi: 10.1159/000538529. Epub 2024 Mar 30.
Patients with heart failure (HF) and bradycardia may be eligible for different types of cardiac implantable electronic devices (CIED), depending on the presence of atrioventricular conduction disease, age, and comorbidities. We aimed to assess the prognosis for these patients, after CIED implantation, stratified for the type of CIED device.
All patients with preexisting HF diagnosis who received a CIED with a right ventricular lead during the period 2005-2018 in Sweden were identified via the pacemaker registry. Data were crossmatched with the population registry and national disease registries. The outcome was 5-year risk of HF hospitalization and mortality.
A total of 37,745 patients were included in the study. Comparing demographics for implantable cardioverter defibrillator versus pacemaker implants, median age was 66 years versus 83 years, 20% versus 41% were female, 64% versus 50% had ischemic heart disease, and 35% versus 67% had atrial fibrillation (all p < 0.001). Five-year mortality was highest in single-chamber pacemaker recipients (61% compared to average 40%, p < 0.001), but the proportion of cardiovascular mortality was highest for cardiac resynchronization therapy (CRT) recipients (68% vs. 63% p < 0.001). Adjusted mortality was higher for pacemaker patients in all age decile groups (ranging from <60 to >90 years old, all p < 0.001), HF hospitalization occurred in 28% (dual-chamber pacemaker) to 39% (CRT-P) of patients, and cause of death was HF in 15% (dual-chamber pacemaker) to 25% (CRT-D), all p < 0.001.
In this large real-world cohort of CIED-treated patients with prior HF, demography and mortality data indicate that clinicians chose devices according to the overall status of the patient. HF-related events occurred in all groups but were more common in CRT-treated patients.
心力衰竭(HF)合并心动过缓的患者可能适合不同类型的心脏植入式电子设备(CIED),这取决于房室传导疾病的存在、年龄和合并症情况。我们旨在评估这些患者在植入CIED后的预后,并根据CIED设备类型进行分层。
通过起搏器登记处识别出2005年至2018年期间在瑞典接受带有右心室导线的CIED且先前已诊断为HF的所有患者。数据与人口登记处和国家疾病登记处进行交叉匹配。结局指标为HF住院和死亡的5年风险。
共有37745名患者纳入研究。比较植入式心律转复除颤器与起搏器植入患者的人口统计学特征,中位年龄分别为66岁和83岁,女性比例分别为20%和41%,缺血性心脏病患者比例分别为64%和50%,房颤患者比例分别为35%和67%(所有p<0.001)。单腔起搏器接受者的5年死亡率最高(61%,而平均为40%,p<0.001),但心脏再同步治疗(CRT)接受者的心血管死亡率比例最高(68%对63%,p<0.001)。所有年龄十分位组的起搏器患者调整后死亡率均较高(年龄范围从<60岁至>90岁,所有p<0.001),28%(双腔起搏器)至39%(CRT-P)的患者发生HF住院,死亡原因是HF的比例为15%(双腔起搏器)至25%(CRT-D),所有p<0.001。
在这个接受CIED治疗的既往有HF的大型真实世界队列中,人口统计学和死亡率数据表明临床医生根据患者的总体状况选择设备。所有组均发生了与HF相关的事件,但在接受CRT治疗的患者中更为常见。