Protocol liver biopsies in stable long-term pediatric liver transplant recipients: risk or benefit?

被引:5
|
作者
Ohlsson, Sinja [1 ]
Kathemann, Simone [1 ]
Pilic, Denisa [1 ]
Prusinskas, Benas [1 ]
Baba, Hideo Andreas
Theurer, Sarah [2 ]
Dechene, Alexander [3 ]
Paul, Andreas [4 ]
Heinold, Andreas [5 ]
Hoyer, Peter Friedrich [1 ]
Lainka, Elke [1 ]
机构
[1] Univ Hosp Essen, Dept Pediat Pediat Gastroenterol Hepatol & Liver, Hufelandstr 55, D-45147 Essen, Germany
[2] Univ Hosp Essen, Inst Pathol, Essen, Germany
[3] Paracelsus Med Univ, Dept Gastroenterol Hepatol & Endocrinol, Klinikum Nuernberg, Salzburg, Austria
[4] Univ Hosp Essen, Dept Gen Visceral & Transplantat Surg, Essen, Germany
[5] Univ Hosp Essen, Inst Transfus Med, Essen, Germany
关键词
donor-specific anti-human leukocyte antigen antibodies; pediatric liver transplantation; protocol liver biopsy; transient elastography; HUMAN-LEUKOCYTE ANTIGEN; 10-YEAR FOLLOW-UP; LATE GRAFT LOSS; ALLOGRAFT FIBROSIS; BILIARY ATRESIA; HLA ANTIBODIES; SURVIVAL; PATIENT; ASSOCIATION; HEPATITIS;
D O I
10.1097/MEG.0000000000002006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Follow-up after pediatric liver transplantation (LTX) is challenging and needs to be refined to extend graft survival as well as general functional health and patients' quality of life. Strategies towards individual immunosuppressive therapy seem to play a key role. Our aim was to evaluate protocol liver biopsies (PLB) as a tool in personalized follow up after pediatric LTX. Patients and methods Our retrospective analysis evaluates 92 PLB in clinically asymptomatic pediatric patients after LTX between 2009 and 2019. Histological findings were characterized using the Desmet scoring system. In addition to PLB, other follow-up tools like laboratory parameters, ultrasound imaging and transient elastography were evaluated. Risk factors for development of fibrosis or inflammation were analyzed. Results PLB revealed a high prevalence of graft fibrosis (67.4%) and graft inflammation (47.8%). Graft inflammation was significantly (P = 0.0353*) more frequent within the first 5 years after transplantation compared to later time points. Besides conventional ultrasound, the measurement of liver stiffness using transient elastography correlate with stage of fibrosis (r = 0.567, P = <0.0001***). Presence of donor-specific anti-human leukocyte antigen antibodies in blood correlates with grade of inflammation in PLB (r = 0.6040, P = 0.0018**). None of the patients who underwent PLB suffered from intervention-related complications. Histopathological results had an impact on clinical decision making in one-third of all patients after PLB. Conclusion PLB are a safe and useful tool to detect silent immune-mediated allograft injuries in the context of normal liver parameters. Copyright (C) 2021 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:E223 / E232
页数:10
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