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Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme

INTRODUCTION: Percutaneous transluminal angioplasty (PTA), with or without stent placement, has become the treatment of choice for portal vein complications (PVC) following liver transplantation. We aimed to assess long-term outcomes of intervention in paediatric transplant recipients, in a single i...

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Autores principales: Patel, Ravi, Mahaveer, Jeevan, Tahir, Nasim, Rajwal, Sanjay, McClean, Patricia, Patel, Jai V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735201/
https://www.ncbi.nlm.nih.gov/pubmed/28913651
http://dx.doi.org/10.1007/s00270-017-1792-0
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author Patel, Ravi
Mahaveer, Jeevan
Tahir, Nasim
Rajwal, Sanjay
McClean, Patricia
Patel, Jai V.
author_facet Patel, Ravi
Mahaveer, Jeevan
Tahir, Nasim
Rajwal, Sanjay
McClean, Patricia
Patel, Jai V.
author_sort Patel, Ravi
collection PubMed
description INTRODUCTION: Percutaneous transluminal angioplasty (PTA), with or without stent placement, has become the treatment of choice for portal vein complications (PVC) following liver transplantation. We aimed to assess long-term outcomes of intervention in paediatric transplant recipients, in a single institution. MATERIALS AND METHODS: 227 children received 255 transplants between November 2000 and September 2016. 30 patients developed PVC of whom 21 had percutaneous intervention. Retrospective clinical and procedural outcome data on these 21 patients were collected. RESULTS: 21 patients, with median age 1.7 years (range 0.4–16.2), underwent 42 procedures with PTA with or without stenting. 36 procedures were for PV stenosis and 6 for PV thrombosis. Treatment was with primary PTA, with stenting reserved for suboptimal PTA result or restenosis within 3 months. 28 procedures were performed with PTA and 13 with stenting. Technical success (>50% reduction in mean pressure gradient, absolute pressure gradient ≤4 mmHg or venographic stenosis <30%) was achieved in 41 procedures. Failure to recanalise a thrombosed PV occurred in 1 procedure. There were no major procedural complications. Patients were followed-up with serial Doppler ultrasound surveillance. Kaplan–Meier estimated median primary patency was 9.9 months, with primary-assisted patency of 95% after median follow-up of 45.5 months (range 11.1–171.6). CONCLUSION: With regular surveillance, excellent patency rates can be achieved following percutaneous intervention for PVC post-paediatric liver transplantation.
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spelling pubmed-57352012017-12-26 Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme Patel, Ravi Mahaveer, Jeevan Tahir, Nasim Rajwal, Sanjay McClean, Patricia Patel, Jai V. Cardiovasc Intervent Radiol Clinical Investigation INTRODUCTION: Percutaneous transluminal angioplasty (PTA), with or without stent placement, has become the treatment of choice for portal vein complications (PVC) following liver transplantation. We aimed to assess long-term outcomes of intervention in paediatric transplant recipients, in a single institution. MATERIALS AND METHODS: 227 children received 255 transplants between November 2000 and September 2016. 30 patients developed PVC of whom 21 had percutaneous intervention. Retrospective clinical and procedural outcome data on these 21 patients were collected. RESULTS: 21 patients, with median age 1.7 years (range 0.4–16.2), underwent 42 procedures with PTA with or without stenting. 36 procedures were for PV stenosis and 6 for PV thrombosis. Treatment was with primary PTA, with stenting reserved for suboptimal PTA result or restenosis within 3 months. 28 procedures were performed with PTA and 13 with stenting. Technical success (>50% reduction in mean pressure gradient, absolute pressure gradient ≤4 mmHg or venographic stenosis <30%) was achieved in 41 procedures. Failure to recanalise a thrombosed PV occurred in 1 procedure. There were no major procedural complications. Patients were followed-up with serial Doppler ultrasound surveillance. Kaplan–Meier estimated median primary patency was 9.9 months, with primary-assisted patency of 95% after median follow-up of 45.5 months (range 11.1–171.6). CONCLUSION: With regular surveillance, excellent patency rates can be achieved following percutaneous intervention for PVC post-paediatric liver transplantation. Springer US 2017-09-14 2018 /pmc/articles/PMC5735201/ /pubmed/28913651 http://dx.doi.org/10.1007/s00270-017-1792-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Clinical Investigation
Patel, Ravi
Mahaveer, Jeevan
Tahir, Nasim
Rajwal, Sanjay
McClean, Patricia
Patel, Jai V.
Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title_full Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title_fullStr Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title_full_unstemmed Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title_short Outcomes of Percutaneous Portal Vein Intervention in a Single UK Paediatric Liver Transplantation Programme
title_sort outcomes of percutaneous portal vein intervention in a single uk paediatric liver transplantation programme
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735201/
https://www.ncbi.nlm.nih.gov/pubmed/28913651
http://dx.doi.org/10.1007/s00270-017-1792-0
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