晚发性炎症标志物在预测胰腺移植术后并发症和移植物存活中的作用

Q4 Medicine
Sandro Hügli, P. Müller, M. Pfister, F. Rössler
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引用次数: 0

摘要

背景:尽管移植物存活率和并发症发生率有了很大的进步,但胰腺移植(PT)后明显的炎症反应是常见的。在第一次术后炎症标志物升高之后,我们经常观察到c反应蛋白(CRP)和白细胞(wbc)在PT后出现第二次高峰。本分析旨在评估PT后晚发型炎症标志物升高的发生率和临床相关性。材料和方法:我们分析了20年期间所有连续的PT。CRP (SCP)和wbc (SWP)的第二个峰值被定义为在PT后相应的初始降低后3天的升高。结果:116例患者中,60例(51.7%)发生SCP。SCP与胰腺移植丢失或出院时或术后90天血栓形成无关(6.7% vs. 0.0%, p = 0.1;8.3% vs. 1.8%, p = 0.2;15.0% vs. 3.6%, p = 0.06)。SCP患者在出院时和90天的并发症总体上更多(85.0%比50.0%,p < 0.001, 93.3%比76.8%,p = 0.02)。在多变量分析中,SCP与移植前HbA1c显著相关(OR 2.1 (95% CI: 1.3-3.8);p = 0.005)和女性(OR 0.03 (95% CI: 0.004-0.14);P≤0.001)。SCP与胰腺冷缺血时间无显著相关性(OR 1.0 (95% CI: 1.0 - 1.0);p = 0.1),供体年龄(OR 1.01 (95% CI: 0.96-1.06);p = 0.7),接受者年龄(OR = 0.9 (95% CI: 0.9 - 1.0);p = 0.1),或受体BMI (or 0.9 (95% CI: 0.9 - 1.4);P = 0.3)。SWP在患有或未患有SCP的患者中无差异(p = 0.07),与胰腺移植丢失或再开腹手术无关(p = 0.3和p = 0.6)。SCP患者与非SCP患者在1、5和10年后无胰岛素移植物生存率无差异(分别为95.0%、90.2%、90.2% vs. 96.1%、91.2%、88.7%;P = 0.964)。结论:迟发性炎症反应在PT中较为常见,并与较高的总并发症发生率相关。然而,它们与移植物特异性并发症或无胰岛素移植物存活无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Late-Onset Inflammatory Markers in the Prediction of Complications and Graft Survival after Pancreas Transplantation
Background: Despite great progress in graft survival and complication rates, pronounced inflammatory responses are common after pancreas transplantation (PT). Subsequent to the first postoperative increase in inflammatory markers, we have frequently observed a second peak of C-reactive protein (CRP) and white blood cells (WBCs) following PT. This analysis is to assess the incidence and clinical relevance of late-onset increases in inflammatory markers following PT. Materials and methods: We analyzed all consecutive PTs over a 20-year period. The second peak of CRP (SCP) and WBCs (SWP) was defined as an increase >3 days after PT subsequent to a relevant initial decrease. Results: Of 116 patients, 60 (51.7%) developed SCP. SCP was not associated with pancreas graft loss or with thrombosis at discharge or at 90 days after PT (6.7% vs. 0.0%, p = 0.1; 8.3% vs. 1.8%, p = 0.2; and 15.0% vs. 3.6%, p = 0.06, respectively). Patients with SCP had more complications overall at discharge and at 90 days (85.0% vs. 50.0%, p < 0.001 and 93.3% vs. 76.8%, p = 0.02). In multivariable analysis, SCP was significantly associated with pre-transplant HbA1c (OR 2.1 (95% CI: 1.3–3.8); p = 0.005) and female gender (OR 0.03 (95% CI: 0.004–0.14); p ≤ 0.001). No significant association was found between SCP and pancreas cold ischemia time (OR 1.0 (95% CI: 1.0–1.0); p = 0.1), donor age (OR 1.01 (95% CI: 0.96–1.06); p = 0.7), recipient age (OR 0.9 (95% CI: 0.9–1.0); p = 0.1), or recipient BMI (OR 0.9 (95% CI: 0.9–1.4); p = 0.3). SWP did not differ in patients with or without SCP (p = 0.07) and there was no correlation with pancreas graft loss or relaparotomy (p = 0.3 and p = 0.6, respectively). Insulin-free graft survival after 1, 5, and 10 years did not differ between patients with SCP and those without SCP (95.0%, 90.2%, 90.2% vs. 96.1%, 91.2%, 88.7%, respectively; p = 0.964). Conclusion: Late-onset inflammatory reactions are frequently seen in PT and are correlated with higher overall complication rates. They are not correlated, however, with graft-specific complications or insulin-free graft survival.
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来源期刊
Cell and Organ Transplantology
Cell and Organ Transplantology Medicine-Transplantation
CiteScore
0.40
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