Department of Clinical and Surgical Sciences, University of Edinburgh, Edinburgh, United Kingdom.
J Vasc Surg. 2010 Sep;52(3):697-703. doi: 10.1016/j.jvs.2010.04.024.
Patients with critical limb ischemia (CLI) have a high rate of adverse cardiovascular events, particularly when undergoing surgery. We sought to determine the effect of surgery and vascular disease on platelet and monocyte activation in vivo in patients with CLI.
An observational, cross-sectional study was performed at a tertiary referral hospital in the southeast of Scotland. Platelet and monocyte activation were measured in whole blood in patients with CLI scheduled for infrainguinal bypass and compared with matched healthy controls, patients with chronic intermittent claudication, patients with acute myocardial infarction, and those undergoing arthroplasty (n = 30 per group). Platelet and monocyte activation were quantified using flow cytometric assessment of platelet-monocyte aggregation, platelet P-selectin expression, platelet-derived microparticles, and monocyte CD40 and CD11b expression.
Compared with those with intermittent claudication, subjects with CLI had increased platelet-monocyte aggregates (41.7% +/- 12.2% vs 32.6% +/- 8.5%, respectively), platelet microparticles (178.7 +/- 106.9 vs 116.9 +/- 53.4), and monocyte CD40 expression (70.0% +/- 12.2% vs 52.4% +/- 15.2%; P < .001 for all). Indeed, these levels were equivalent (P-selectin, 4.4% +/- 2.0% vs 4.9% +/- 2.2%; P > .05) or higher (platelet-monocyte aggregation, 41.7% +/- 12.2% vs 33.6% +/- 7.0%; P < .05; platelet microparticles, 178.7 +/- 106.9 vs 114.4 +/- 55.0/microL; P < .05) than in patients with acute myocardial infarction. All platelet and monocyte activation markers remained elevated throughout the perioperative period in patients with CLI (P < .01) but not those undergoing arthroplasty.
Patients undergoing surgery for CLI have the highest level of in vivo platelet and monocyte activation, and these persist throughout the perioperative period. Additional antiplatelet therapy may be of benefit in protecting vascular patients with more severe disease during this period of increased risk.
患有严重肢体缺血(CLI)的患者心血管不良事件发生率较高,尤其是在接受手术治疗时。我们旨在确定 CLI 患者手术和血管疾病对体内血小板和单核细胞激活的影响。
在苏格兰东南部的一家三级转诊医院进行了一项观察性、横断面研究。对计划进行下肢旁路手术的 CLI 患者的全血中的血小板和单核细胞激活进行了测量,并与匹配的健康对照组、慢性间歇性跛行患者、急性心肌梗死患者和接受关节置换术的患者(每组 30 例)进行了比较。使用流式细胞术评估血小板-单核细胞聚集、血小板 P-选择素表达、血小板衍生的微颗粒和单核细胞 CD40 和 CD11b 表达来量化血小板和单核细胞激活。
与间歇性跛行患者相比,CLI 患者的血小板-单核细胞聚集物(分别为 41.7%+/-12.2%和 32.6%+/-8.5%)、血小板微颗粒(178.7+/-106.9 和 116.9+/-53.4)和单核细胞 CD40 表达(70.0%+/-12.2%和 52.4%+/-15.2%;均<.001)更高。事实上,这些水平相当(P-选择素,4.4%+/-2.0%和 4.9%+/-2.2%;>.05)或更高(血小板-单核细胞聚集物,41.7%+/-12.2%和 33.6%+/-7.0%;<.05;血小板微颗粒,178.7+/-106.9 和 114.4+/-55.0/微升;<.05)比急性心肌梗死患者更高。CLI 患者围手术期所有血小板和单核细胞激活标志物均升高(<.01),但接受关节置换术的患者则不然。
接受 CLI 手术治疗的患者体内血小板和单核细胞激活程度最高,并且在围手术期持续存在。在这段风险增加的时期,对血管疾病更严重的患者给予额外的抗血小板治疗可能有助于保护。