Predictors of portal vein complications after pediatric liver transplantation: A German center experience.


Journal

Pediatric transplantation
ISSN: 1399-3046
Titre abrégé: Pediatr Transplant
Pays: Denmark
ID NLM: 9802574

Informations de publication

Date de publication:
08 2022
Historique:
revised: 03 03 2022
received: 10 02 2022
accepted: 09 04 2022
pubmed: 24 4 2022
medline: 14 7 2022
entrez: 23 4 2022
Statut: ppublish

Résumé

Portal vein complications (PVCs) after pediatric liver transplantation (LT) are sometimes asymptomatic, especially in the early phase, and can threaten both the graft and patient's survival. Therefore, the purpose of this study is to analyze the risk factors for portal vein thrombosis (PVT) and portal vein stenosis (PVS) after pediatric LT. All pediatric patients (n = 115) who underwent primary LT at Regensburg University Hospital between January 2010 and April 2017 were included in this study. The pre-, intra-, and postoperative parameters of all patients were retrospectively reviewed and risk factors for both PVT and PVS were analyzed. Of the 115 patients, living donor LT was performed on 57 (49.5%) patients, and biliary atresia was the primary diagnosis in 65 patients (56%). After pediatric LT, 9% of patients developed PVT, and 16.5% developed PVS. Patient weight ≤7 kg [odds ratio (OR) 9.35, 95% confidence interval (CI) 1.03-84.9, p = .04] and GRWR >3% (OR 15.4, 95% CI 1.98-129.5, p = .01) were the independent risk factors for the development of PVT and PVS, respectively upon multivariate analysis. The overall patient survival rates at 1, 3, and 5 years were 91%, 90%, and 89%, respectively, and there was no difference in patient survival among those with and without PVCs. Pediatric patients with body weight <7 kg and/or receiving a graft with GRWR >3% may develop PVCs and so require certain surgical modifications, close follow-up, and prophylactic anticoagulant therapy following transplant.

Sections du résumé

BACKGROUND
Portal vein complications (PVCs) after pediatric liver transplantation (LT) are sometimes asymptomatic, especially in the early phase, and can threaten both the graft and patient's survival. Therefore, the purpose of this study is to analyze the risk factors for portal vein thrombosis (PVT) and portal vein stenosis (PVS) after pediatric LT.
METHODS
All pediatric patients (n = 115) who underwent primary LT at Regensburg University Hospital between January 2010 and April 2017 were included in this study. The pre-, intra-, and postoperative parameters of all patients were retrospectively reviewed and risk factors for both PVT and PVS were analyzed.
RESULTS
Of the 115 patients, living donor LT was performed on 57 (49.5%) patients, and biliary atresia was the primary diagnosis in 65 patients (56%). After pediatric LT, 9% of patients developed PVT, and 16.5% developed PVS. Patient weight ≤7 kg [odds ratio (OR) 9.35, 95% confidence interval (CI) 1.03-84.9, p = .04] and GRWR >3% (OR 15.4, 95% CI 1.98-129.5, p = .01) were the independent risk factors for the development of PVT and PVS, respectively upon multivariate analysis. The overall patient survival rates at 1, 3, and 5 years were 91%, 90%, and 89%, respectively, and there was no difference in patient survival among those with and without PVCs.
CONCLUSIONS
Pediatric patients with body weight <7 kg and/or receiving a graft with GRWR >3% may develop PVCs and so require certain surgical modifications, close follow-up, and prophylactic anticoagulant therapy following transplant.

Identifiants

pubmed: 35460136
doi: 10.1111/petr.14298
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14298

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Amr Badawy (A)

Department of Surgery, University Hospital Regensburg, Regensburg, Germany.
General Surgery Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.

Stefan M Brunner (SM)

Department of Surgery, University Hospital Regensburg, Regensburg, Germany.

Birgit Knoppke (B)

University Children's Hospital of Regensburg (KUNO), Regensburg, Germany.

Melanie Völkl (M)

University Children's Hospital of Regensburg (KUNO), Regensburg, Germany.

Henrik Junger (H)

Department of Surgery, University Hospital Regensburg, Regensburg, Germany.

Martin Loss (M)

Department of Surgery, University Hospital Regensburg, Regensburg, Germany.

Barbara Sinner (B)

Department of Anesthesiology, University Hospital Regensburg, Regensburg, Germany.

Veronika Huf (V)

Department of Anesthesiology, University Hospital Regensburg, Regensburg, Germany.
Institute of Radiology, University Hospital Regensburg, Regensburg, Germany.

Dirk Grothues (D)

University Children's Hospital of Regensburg (KUNO), Regensburg, Germany.

Michael Melter (M)

University Children's Hospital of Regensburg (KUNO), Regensburg, Germany.

Hans J Schlitt (HJ)

Department of Surgery, University Hospital Regensburg, Regensburg, Germany.

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