首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Changes in peritoneal coagulation and fibrinolysis after discontinuation of chronic peritoneal dialysis.
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Changes in peritoneal coagulation and fibrinolysis after discontinuation of chronic peritoneal dialysis.

机译:停止慢性腹膜透析后腹膜凝血和纤维蛋白溶解的变化。

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OBJECTIVES: To study changes in peritoneal function after transfer from chronic peritoneal dialysis (CPD) to hemodialysis (HD), especially the effects on peritoneal coagulation, fibrinolytic markers, and mesothelium. DESIGN: Prospective observational study. SETTING: A tertiary-care university hospital. PATIENTS: Nine patients who transferred from CPD to HD were enrolled in the study after giving fully informed consent. METHODS: After transfer to HD, the peritoneal cavity was lavaged with low glucose PD solution once per day through PD catheters left in place. Thrombin-antithrombin III complex (TAT) was measured serially as a marker of peritoneal coagulation. As fibrinolytic markers, fibrinogen/fibrin degradation products (FDP) and plasmin-alpha2-antiplasmin complex (PIC) were assessed. Cancer antigen 125 (CA125) was measured as a marker of mesothelial cell mass. RESULTS: Levels of peritoneal TAT and FDP were much higher than plasma levels, indicating high local fibrin turnover. Transfer to HD induced a significant fall in mean peritoneal TAT, from 115.8 +/- 52.1 to 60.7 +/- 21.8 ng/mL, p < 0.05. Except for 1 patient with a 20-fold increase, mean peritoneal FDP decreased significantly, from 43.6 +/- 11.1 to 19.6 +/- 3.5 microg/mL, p < 0.05. Mean peritoneal PIC increased significantly, from 1.9 +/- 0.4 to 3.9 +/- 0.6 microg/mL, p < 0.05. Peritoneal CA125 increased from 156.4 +/- 57.3 to 1426.2 +/- 389.4 U/mL, p < 0.05. CONCLUSIONS: Peritoneal fibrin turnover was accelerated on CPD and stabilized after transfer to HD. Transfer to HD also induced mesothelial regeneration.
机译:目的:研究从慢性腹膜透析(CPD)转移到血液透析(HD)后腹膜功能的变化,特别是对腹膜凝血,纤溶标记物和间皮的影响。设计:前瞻性观察研究。地点:三级保健大学医院。患者:在完全知情同意后,将9名从CPD转移至HD的患者纳入研究。方法:转移至HD后,每天通过留置的PD导管用低葡萄糖PD溶液冲洗腹腔。连续测量凝血酶-抗凝血酶III复合物(TAT)作为腹膜凝血的标志物。作为纤维蛋白溶解标记,评估了纤维蛋白原/纤维蛋白降解产物(FDP)和纤溶酶-α2-抗纤溶酶复合物(PIC)。测量癌症抗原125(CA125)作为间皮细胞质量的标志。结果:腹膜TAT和FDP水平远高于血浆水平,表明局部纤维蛋白更新率很高。转移至HD会导致平均腹膜TAT显着下降,从115.8 +/- 52.1降至60.7 +/- 21.8 ng / mL,p <0.05。除1名患者增加20倍外,平均腹膜FDP明显降低,从43.6 +/- 11.1降至19.6 +/- 3.5 microg / mL,p <0.05。腹膜平均PIC显着增加,从1.9 +/- 0.4微克/毫升增加到3.9 +/- 0.6微克/毫升,p <0.05。腹膜CA125从156.4 +/- 57.3增加到1426.2 +/- 389.4 U / mL,p <0.05。结论:CPD促进了腹膜纤维蛋白的更新,转移至HD后稳定。转移到高清还诱导间皮再生。

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