Department of Cardiothoracic Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Molecular and Clinical Medicine, Institute of medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Eur J Cardiothorac Surg. 2024 Oct 1;66(4). doi: 10.1093/ejcts/ezae365.
Previous reports suggest that betablockers appear non-beneficial after surgical aortic valve replacement (SAVR). This study aims to clarify the associations between betablockers and long-term outcome after SAVR.
All patients with isolated SAVR due to aortic stenosis in Sweden between 2006 and 2020, alive at 6 months after surgery, were included. Patients were identified in the SWEDEHEART registry, and records were merged with data from 3 other mandatory national registries. Association between dispensed betablockers and major adverse cardiovascular events (MACE) (all-cause mortality, myocardial infarction and stroke) was analyzed using Cox proportional hazards models, with time-updated data on medication and adjusted for age, sex and comorbidities at baseline.
In total, 11 849 patients were included [median follow-up 5.4 years (range 0-13.5)]. Betablockers were prescribed to 79.7% of patients at baseline, decreasing to 62.2% after 5 years. Continuing treatment was associated with higher risk of MACE [adjusted hazard ratio 1.14 (95% confidence interval, CI 1.05-1.23)]. The association was consistent over subgroups based on age, sex and comorbidities except atrial fibrillation [hazard ratio (HR) 1.05 (95% CI 0.93-1.19)]. A sensitivity analysis including time-updated data on comorbidites attenuated the difference between the groups [HR 1.04 (95% CI 0.95-1.14, P = 0.33)].
Treatment with betablockers did not appear to be associated with inferior long-term outcome after SAVR, when adjusting for new concomitant diseases. Thus, it is likely that it is the underlying cardiac diseases that are associated with MACE rather than betablocker treatment.
先前的报告表明,β受体阻滞剂在主动脉瓣置换术后(SAVR)似乎无益。本研究旨在阐明β受体阻滞剂与 SAVR 后长期预后之间的关系。
纳入 2006 年至 2020 年期间在瑞典因主动脉瓣狭窄接受单纯 SAVR 的所有患者,术后 6 个月存活。患者在 SWEDEHEART 登记处确定,并与另外 3 个强制性国家登记处的数据合并。使用 Cox 比例风险模型分析处方β受体阻滞剂与主要不良心血管事件(MACE)(全因死亡率、心肌梗死和中风)之间的关系,药物数据随时间更新,并根据基线时的年龄、性别和合并症进行调整。
共纳入 11 849 例患者[中位随访时间为 5.4 年(范围 0-13.5)]。基线时,79.7%的患者服用β受体阻滞剂,5 年后降至 62.2%。持续治疗与 MACE 风险增加相关[校正后的危险比 1.14(95%置信区间,CI 1.05-1.23)]。除房颤外,该关联在基于年龄、性别和合并症的亚组中一致[风险比(HR)1.05(95%CI 0.93-1.19)]。包括随时间更新的合并症数据的敏感性分析减弱了两组之间的差异[HR 1.04(95%CI 0.95-1.14,P=0.33)]。
在调整新发合并症后,β受体阻滞剂治疗似乎与 SAVR 后的长期预后不良无关。因此,可能是潜在的心脏疾病与 MACE 相关,而不是β受体阻滞剂治疗。