...
首页> 外文期刊>Scandinavian journal of clinical and laboratory investigation. >Platelet depletion, platelet activation and coagulation during treatment with hemodialysis.
【24h】

Platelet depletion, platelet activation and coagulation during treatment with hemodialysis.

机译:血液透析治疗期间的血小板耗竭,血小板活化和凝血。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Bioincompatibility is the total of side effects during hemodialysis (HD) including, amongst others, changes in platelet (PLT) level. Deviations in PLT count, immature PLT count, PLT morphology, CD62p expression, Platelet Factor 4 (PF4), beta-Thromboglobulin (beta-TG), serotonin, Thrombin-Antithrombin III (TAT) and Prothrombin Fragment 1+2 (F1+2) are monitored before and during treatment with HD in order to elucidate the interaction between modifications in PLT morphology, PLT activation and markers concerning activation of coagulation. Different patterns with time indicate that there is no correlation between an increased amount of depleted PLTs and increased amounts of PLT activation markers such as CD62p, PF4, beta-TG and serotonin. A statistically significant correlation between increased PLT activation markers and markers for increased activation of coagulation such as TAT and F1+2 has not been established. Only a weak correlation is demonstrated between the increase of markers for activation of coagulation and the decrease in PLT counts, immature PLT counts and depleted PLTs during HD treatment. The change in the extracorporeal circuit during HD is probably a more critical factor in the mechanism leading to activation of the coagulation pathway than the modifications in PLT morphology.
机译:生物相容性是血液透析(HD)期间副作用的总和,其中包括血小板(PLT)水平的变化。 PLT计数,未成熟PLT计数,PLT形态,CD62p表达,血小板因子4(PF4),β-血栓球蛋白(beta-TG),5-羟色胺,凝血酶-抗凝血酶III(TAT)和凝血酶原片段1 + 2(F1 + 2)的差异在用HD进行治疗之前和期间进行监测,以阐明PLT形态学修饰,PLT激活和有关凝血激活的标志物之间的相互作用。随时间变化的不同模式表明,增加的耗尽PLT数量与增加的PLT激活标记(例如CD62p,PF4,β-TG和5-羟色胺)之间没有相关性。尚未建立增加的PLT激活标记与增加的凝血激活标记(例如TAT和F1 + 2)之间的统计显着相关性。在HD治疗期间,仅在凝血激活标志物的增加与PLT计数,PLT计数未成熟和PLT减少之间存在弱相关性。在HD期间,体外回路的变化可能是导致凝血途径激活的机制中比PLT形态学改变更重要的因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号