Droppa Michal, Borst Oliver, Rath Dominik, Müller Karin, Gawaz Meinrad, Bhatt Deepak L, Geisler Tobia
Department of Cardiology and Cardiovascular Medicine, University Hospital of Tuebingen, Tuebingen, Germany.
Brigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, Massachusetts, USA.
Cell Physiol Biochem. 2017;42(4):1336-1341. doi: 10.1159/000478962. Epub 2017 Jul 13.
BACKGROUND/AIMS: Patients with acute coronary syndromes (ACS) presenting with cardiogenic shock (CS) are at particular risk for death and adverse cardiac events. Impaired effects and absorption of oral P2Y12-receptor inhibitors due to decreased organ hypoperfusion or hypothermia and challenges regarding oral administration contribute to this risk. We report a single center experience regarding the use of intravenous P2Y12-receptor inhibitor cangrelor in patients with CS treated with percutaneous coronary intervention (PCI).
Twelve patients with ACS and CS undergoing PCI, not pretreated with oral P2Y12-receptor inhibitors, were treated with cangrelor. Platelet inhibition was assessed by multiple electrode aggregometry (MEA) before and after PCI, immediately and 2 hours after stopping the cangrelor infusion.
Nine patients recovered from their cardiogenic shock, 3 patients died. Platelet reactivity decreased from 65.9 (SD 41.0) U before PCI to 15.8 (SD 10.8) U after PCI, 13.4 (SD 7.7) U at the end of infusion and 33.8 (SD 19.9) 2 hours after stopping the cangrelor infusion. There was no non-responder under cangrelor infusion (MEA < 46 U).
Due to its favorable PK/PD profile, cangrelor overcomes problems with reduced absorption and effects of oral P2Y12-receptor inhibitors and should be considered for periprocedural treatment of patients with CS.
背景/目的:急性冠状动脉综合征(ACS)合并心源性休克(CS)的患者死亡及发生不良心脏事件的风险尤其高。因器官灌注不足或体温过低导致口服P2Y12受体抑制剂的效果及吸收受损,以及口服给药方面的难题,都促成了这一风险。我们报告了在接受经皮冠状动脉介入治疗(PCI)的CS患者中使用静脉P2Y12受体抑制剂坎格雷洛的单中心经验。
12例接受PCI的ACS合并CS患者,未预先接受口服P2Y12受体抑制剂治疗,接受了坎格雷洛治疗。在PCI前后、停止坎格雷洛输注后即刻及2小时,通过多电极聚集测定法(MEA)评估血小板抑制情况。
9例患者的心源性休克得到恢复,3例患者死亡。血小板反应性从PCI前的65.9(标准差41.0)U降至PCI后的15.8(标准差10.8)U、输注结束时的13.4(标准差7.7)U以及停止坎格雷洛输注2小时后的33.8(标准差19.9)U。在坎格雷洛输注期间无无反应者(MEA<46 U)。
由于其良好的药代动力学/药效学特性,坎格雷洛克服了口服P2Y12受体抑制剂吸收及效果降低的问题,对于CS患者的围手术期治疗应考虑使用。