1 Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Clinical Research, Innovation and Education Center, Tohoku University Hospital, Sendai, Japan.
2 Department of Cardiology, Gentofte University Hospital, Copenhagen, Denmark.
Eur Heart J Acute Cardiovasc Care. 2017 Dec;6(8):778-786. doi: 10.1177/2048872616649860. Epub 2016 May 10.
Rheumatologic disorders are characterised by inflammation and an increased risk of coronary artery disease (CAD). However, the association between rheumatologic disorders and long-term prognosis in CAD patients undergoing percutaneous coronary intervention (PCI) is unknown. Thus, we aimed to examine the association between rheumatologic disorders and long-term prognosis in CAD patients undergoing PCI.
A post-hoc analysis was performed in 4605 patients (age: 63.3 ± 11.0 years; male: 76.6%) with ST-segment elevation myocardial infarction (STEMI; n = 1396), non-STEMI ( n = 1541), and stable CAD ( n = 1668) from the all-comer stent trials, the BAsel Stent Kosten-Effektivitäts Trial-PROspective Validation Examination (BASKET-PROVE) I and II trials. We evaluated the association between rheumatologic disorders and 2-year major adverse cardiac events (MACEs; cardiac death, nonfatal myocardial infarction (MI), and target vessel revascularisation (TVR)) by Cox regression analysis. Patients with rheumatologic disorders ( n = 197) were older, more often female, had a higher prevalence of renal disease, multi-vessel coronary disease, and bifurcation lesions, and had longer total stent lengths. During the 2-year follow-up, the MACE rate was 8.6% in the total cohort. After adjustment for potential confounders, rheumatologic disorders were associated with MACEs in the total cohort (adjusted hazard ratio: 1.55; 95% confidence interval (CI): 1.04-2.31) driven by the STEMI subgroup (adjusted hazard ratio: 2.38; 95% CI: 1.26-4.51). In all patients, rheumatologic disorders were associated with all-cause death (adjusted hazard ratio: 2.05; 95% CI: 1.14-3.70), cardiac death (adjusted hazard ratio: 2.63; 95% CI: 1.27-5.43), and non-fatal MI (adjusted hazard ratio: 2.64; 95% CI: 1.36-5.13), but not with TVR (adjusted hazard ratio: 0.81; 95% CI: 0.41-1.58).
The presence of rheumatologic disorders appears to be independently associated with worse outcome in CAD patients undergoing PCI. This calls for further studies and focus on this high-risk group of patients following PCI.
风湿性疾病的特征是炎症和冠状动脉疾病(CAD)风险增加。然而,风湿性疾病与接受经皮冠状动脉介入治疗(PCI)的 CAD 患者的长期预后之间的关系尚不清楚。因此,我们旨在研究风湿性疾病与接受 PCI 的 CAD 患者的长期预后之间的关系。
对来自所有患者支架试验(BASKET-PROVE I 和 II 试验)的 4605 例患者(年龄:63.3±11.0 岁;男性:76.6%)进行了一项基于队列的事后分析,包括 ST 段抬高型心肌梗死(STEMI;n=1396)、非 ST 段抬高型心肌梗死(n=1541)和稳定型 CAD(n=1668)。我们通过 Cox 回归分析评估了风湿性疾病与 2 年主要不良心脏事件(MACE;心脏死亡、非致死性心肌梗死(MI)和靶血管血运重建(TVR))之间的关系。风湿性疾病患者(n=197)年龄较大,女性较多,患有肾脏疾病、多支血管冠状动脉疾病和分叉病变的比例较高,总支架长度较长。在 2 年的随访期间,总队列的 MACE 发生率为 8.6%。调整潜在混杂因素后,风湿性疾病与总队列的 MACE 相关(调整后的危险比:1.55;95%置信区间(CI):1.04-2.31),主要由 STEMI 亚组驱动(调整后的危险比:2.38;95% CI:1.26-4.51)。在所有患者中,风湿性疾病与全因死亡(调整后的危险比:2.05;95% CI:1.14-3.70)、心脏死亡(调整后的危险比:2.63;95% CI:1.27-5.43)和非致死性 MI(调整后的危险比:2.64;95% CI:1.36-5.13)相关,但与 TVR 无关(调整后的危险比:0.81;95% CI:0.41-1.58)。
风湿性疾病的存在似乎与接受 PCI 的 CAD 患者的预后较差独立相关。这需要进一步的研究和关注 PCI 后这一高危患者群体。