Kinnaird Tim, Butt Mehmood, Abdul Fairoz, Yazji Khaled, Hailan Ahmed, Gallagher Sean, Ossei-Gerning Nicholas, Chase Alexander, Choudhury Anirban, Smith David, Anderson Richard
Department of Cardiology, University Hospital of Wales, Cardiff, United Kingdom.
Department of Cardiology Morriston Cardiac Centre, Swansea, United Kingdom.
PLoS One. 2016 Jun 30;11(6):e0157812. doi: 10.1371/journal.pone.0157812. eCollection 2016.
Prolonged dual anti-platelet therapy (DAPT) may cause excess bleeding in certain patients. The biolimus-A9 drug-coated stent (BA9-DCS) has a rapid drug-elution profile allowing shortened DAPT. Data were gathered on the early experience implanting this stent in drug-eluting stent eligible patients deemed to be at high risk of bleeding.
The demographics, procedural data and clinical outcomes were gathered prospectively for 249 patients treated with a BA9-DCS stent at 2 UK centres, and compared to a cohort of patients treated in the same period with drug-eluting stents (PCI-DES).
Operator-defined BA9-DCS indications included warfarin therapy, age, and anaemia. Patients receiving a BA9-DCS were older (71.6±11.8 vs. 64.8±11.6yrs, p<0.001), more often female (38.2 vs. 26.8%, P<0.001), and more likely to have comorbidity including chronic kidney disease or poor LV function than PCI-DES patients. The baseline Mehran bleed risk score was also significantly higher in the BA9-DCS group (19.4±8.7 vs. 13.1±5.8, p<0.001). Of the BA9-DCS cohort, 95.5% of patients demonstrated disease fitting NICE criteria for DES placement. The number of lesions treated (1.81±1.1 vs. 1.58±0.92, p = 0.003), total lesion length (32.1±21.7 vs. 26.1±17.6mm, p<0.001), number of stents used (1.93±1.11 vs. 1.65±1.4, p = 0.007) and total stent length (37.5±20.8 vs. 32.4±20.3, p<0.01) were greater for BA9-DCS patients. DAPT was prescribed for 3.3±3.9 months for BA9-DCS patients and 11.3±2.4 months for PCI-DES patients (p<0.001). At follow up of 392±124 days despite the abbreviated DAPT course stent related event were infrequent with ischemia-driven restenosis PCI (2.8 vs. 3.4%, p = 0.838), and stent thrombosis (1.6 vs. 2.1%, p = 0.265) rates similar between the BA9-DCS ad PCI-DES groups. After propensity scoring all clinical end-points were similar between both cohorts.
This early experience using polymer-free BA9 drug-coated stents in drug-eluting stent type patients at risk of bleeding are encouraging. Further studies are warranted.
长期双重抗血小板治疗(DAPT)可能会导致某些患者出现过度出血。生物雷帕霉素-A9药物涂层支架(BA9-DCS)具有快速药物洗脱特性,可缩短DAPT疗程。我们收集了在有出血高风险的符合药物洗脱支架植入条件的患者中植入该支架的早期经验数据。
前瞻性收集了英国2个中心接受BA9-DCS支架治疗的249例患者的人口统计学、手术数据和临床结局,并与同期接受药物洗脱支架(PCI-DES)治疗的一组患者进行比较。
术者确定的BA9-DCS适应症包括华法林治疗、年龄和贫血。接受BA9-DCS治疗的患者年龄更大(71.6±11.8岁 vs. 64.8±11.6岁,p<0.001),女性比例更高(38.2% vs. 26.8%,P<0.001),与PCI-DES患者相比,合并症(包括慢性肾病或左心室功能不佳)的可能性更大。BA9-DCS组的基线梅兰出血风险评分也显著更高(19.4±8.7 vs. 13.1±5.8,p<0.001)。在BA9-DCS队列中,95.5%的患者病变符合NICE关于DES植入的标准。BA9-DCS患者治疗的病变数量(1.81±1.1 vs. 1.58±0.92,p = 0.003)、总病变长度(32.1±21.7 vs. 26.1±17.6mm,p<0.001)、使用的支架数量(1.93±1.11 vs. 1.65±1.4,p = 0.007)和总支架长度(37.5±20.8 vs. 32.4±20.3,p<0.01)均更多。BA9-DCS患者的DAPT疗程为3.3±3.9个月,PCI-DES患者为11.3±2.4个月(p<0.001)。在392±124天的随访中,尽管DAPT疗程缩短,但BA9-DCS组与PCI-DES组之间的支架相关事件并不常见,缺血驱动的再狭窄PCI发生率(2.8% vs. 3.4%,p = 0.838)和支架血栓形成率(1.6% vs. 2.1%,p = 0.265)相似。经过倾向评分后,两个队列的所有临床终点均相似。
在有出血风险的药物洗脱支架类型患者中使用无聚合物的BA9药物涂层支架的这一早期经验令人鼓舞。有必要进行进一步研究。