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2
Everolimus delayed and suppressed cytomegalovirus DNA synthesis, spread of the infection, and alleviated cytomegalovirus infection.依维莫司可延迟和抑制巨细胞病毒 DNA 的合成,阻止感染扩散,并缓解巨细胞病毒感染。
Antiviral Res. 2019 Feb;162:30-38. doi: 10.1016/j.antiviral.2018.12.004. Epub 2018 Dec 10.
3
2018 Annual Report of the European Liver Transplant Registry (ELTR) - 50-year evolution of liver transplantation.2018 年欧洲肝移植注册处(ELTR)年度报告——肝移植 50 年的发展历程。
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The Third International Consensus Guidelines on the Management of Cytomegalovirus in Solid-organ Transplantation.《实体器官移植中巨细胞病毒管理的第三次国际共识指南》。
Transplantation. 2018 Jun;102(6):900-931. doi: 10.1097/TP.0000000000002191.
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The Role of mTOR Inhibitors in the Management of Viral Infections: A Review of Current Literature.mTOR 抑制剂在病毒感染管理中的作用:文献复习。
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6
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Transplant Proc. 2014 Nov;46(9):3097-9. doi: 10.1016/j.transproceed.2014.09.173.
10
D-MELD does not predict post-liver transplantation survival: a single-center experience from Brazil.D-MELD评分不能预测肝移植术后生存率:来自巴西的单中心经验。
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无动脉并发症情况下肝移植术后胆道并发症的危险因素

RISK FACTORS FOR POST-LIVER TRANSPLANT BILIARY COMPLICATIONS IN THE ABSENCE OF ARTERIAL COMPLICATIONS.

作者信息

Lima Agnaldo Soares, Pereira Bárbara Buitrago, Jungmann Sven, Machado Carla Jorge, Correia Maria Isabel Toulson Davison

机构信息

Alfa Institute of Gastroenterology, Hospital das Clínicas, Federal University of Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.

Department of Surgery, Faculty of Medicine, UFMG, Belo Horizonte, MG, Brazil.

出版信息

Arq Bras Cir Dig. 2020 Dec 18;33(3):e1541. doi: 10.1590/0102-672020200003e1541. eCollection 2020.

DOI:10.1590/0102-672020200003e1541
PMID:33331436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7747483/
Abstract

BACKGROUND

  • Biliary complications (BC) represent the most frequent complication after liver transplantation, up to 34% of cases.

AIM

To identify modifiable risk factors to biliary complications after liver transplantation, essential to decrease morbidity.

METHOD

Clinical data, anatomical characteristics of recipient and donors, and transplant operation features of 306 transplants with full arterial patency were collected to identify risk factors associated with BC.

RESULTS

BC occurred in 22.9% after 126 days (median) post-transplantation. In univariate analyses group 1 (without BC, n=236) and group 2 patients (with BC, n=70) did not differ on their general characteristics. BC were related to recipient age under 40y (p=0.029), CMV infection (p=0.021), biliary disease as transplant indication (p=0.018), lower pre-transplant INR (p=0.009), and bile duct diameter <3 mm (p=0.033). CMV infections occurred sooner in patients with postoperative biliary complications vs. control (p=0.07). In a multivariate analysis, only CMV infection, lower INR, and shorter bile duct diameter correlated with BC. Positive CMV antigenemia correlated with biliary complications, even when titers lied below the treatment threshold.

CONCLUSIONS

Biliary complications after liver transplantation correlated with low recipient INR before operation, bile duct diameter <3 mm, and positive antigenemia for CMV or disease manifestation. As the only modifiable risk factor, routine preemptive CMV inhibition is suggested to diminish biliary morbidity after liver transplant.

摘要

背景

胆系并发症(BC)是肝移植后最常见的并发症,发生率高达34%。

目的

确定肝移植后胆系并发症的可改变危险因素,这对于降低发病率至关重要。

方法

收集306例动脉完全通畅的肝移植患者的临床资料、受者和供者的解剖特征以及移植手术特点,以确定与胆系并发症相关的危险因素。

结果

移植后126天(中位数)时,胆系并发症发生率为22.9%。单因素分析显示,第1组(无胆系并发症,n = 236)和第2组患者(有胆系并发症,n = 70)的一般特征无差异。胆系并发症与40岁以下受者年龄(p = 0.029)、巨细胞病毒(CMV)感染(p = 0.021)、作为移植指征的胆系疾病(p = 0.018)、移植前较低的国际标准化比值(INR)(p = 0.009)以及胆管直径<3 mm(p = 0.033)有关。术后发生胆系并发症的患者与对照组相比,CMV感染出现得更早(p = 0.07)。多因素分析显示,只有CMV感染、较低的INR和较短的胆管直径与胆系并发症相关。即使滴度低于治疗阈值,CMV抗原血症阳性也与胆系并发症相关。

结论

肝移植后胆系并发症与术前受者INR低、胆管直径<3 mm以及CMV抗原血症阳性或疾病表现相关。作为唯一可改变的危险因素,建议常规进行抢先性CMV抑制以降低肝移植后胆系疾病的发生率。