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Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review

BACKGROUND: Encapsulating Peritoneal Sclerosis (EPS) is a rare phenomenon in paediatric patients with kidney failure treated with peritoneal dialysis (PD). This study highlights clinical challenges in the management of EPS, with particular emphasis on peri-operative considerations and surgical techn...

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Autores principales: Sharma, Videha, Moinuddin, Zia, Summers, Angela, Shenoy, Mohan, Plant, Nicholas, Vranic, Semir, Prytula, Agnieszka, Zvizdic, Zlatan, Karava, Vasiliki, Printza, Nikoleta, Vlot, John, van Dellen, David, Augustine, Titus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921033/
https://www.ncbi.nlm.nih.gov/pubmed/34448023
http://dx.doi.org/10.1007/s00467-021-05243-0
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author Sharma, Videha
Moinuddin, Zia
Summers, Angela
Shenoy, Mohan
Plant, Nicholas
Vranic, Semir
Prytula, Agnieszka
Zvizdic, Zlatan
Karava, Vasiliki
Printza, Nikoleta
Vlot, John
van Dellen, David
Augustine, Titus
author_facet Sharma, Videha
Moinuddin, Zia
Summers, Angela
Shenoy, Mohan
Plant, Nicholas
Vranic, Semir
Prytula, Agnieszka
Zvizdic, Zlatan
Karava, Vasiliki
Printza, Nikoleta
Vlot, John
van Dellen, David
Augustine, Titus
author_sort Sharma, Videha
collection PubMed
description BACKGROUND: Encapsulating Peritoneal Sclerosis (EPS) is a rare phenomenon in paediatric patients with kidney failure treated with peritoneal dialysis (PD). This study highlights clinical challenges in the management of EPS, with particular emphasis on peri-operative considerations and surgical technique. METHODS: Retrospective analysis of all paediatric patients with EPS treated at the Manchester Centre for Transplantation. RESULTS: Four patients were included with a median duration of 78 months on PD. All patients had recurrent peritonitis (> 3 episodes), and all had symptoms within three months of a change of dialysis modality from PD to haemodialysis or transplant. In Manchester, care was delivered by a multi-disciplinary team, including surgeons delivering the adult EPS surgical service with a particular focus on nutritional optimisation, sepsis control, and wound management. The surgery involved laparotomy, lavage, and enterolysis of the small bowel + / − stoma formation, depending on intra-abdominal contamination. Two patients had a formal stoma, which were reversed at three and six months, respectively. Two patients underwent primary closure of the abdomen, whereas two patients had re-look procedures at 48 h with secondary closure. One patient had a post-operative wound infection, which was managed medically. One patient’s stoma became detached, leading to an intra-abdominal collection requiring re-laparotomy. The median length of stay was 25 days, and patients were discharged once enteral feeding was established. All patients remained free of recurrence with normal gut function and currently two out of four have functioning transplants. CONCLUSIONS: This series demonstrates 100% survival and parenteral feed independence following EPS surgery. Post-operative morbidity was common; however, with individualised experience-based decision-making and relevant additional interventions, patients made full recoveries. Health and development post-surgery continued, allowing the potential for transplantation. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-021-05243-0.
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spelling pubmed-89210332022-03-17 Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review Sharma, Videha Moinuddin, Zia Summers, Angela Shenoy, Mohan Plant, Nicholas Vranic, Semir Prytula, Agnieszka Zvizdic, Zlatan Karava, Vasiliki Printza, Nikoleta Vlot, John van Dellen, David Augustine, Titus Pediatr Nephrol Original Article BACKGROUND: Encapsulating Peritoneal Sclerosis (EPS) is a rare phenomenon in paediatric patients with kidney failure treated with peritoneal dialysis (PD). This study highlights clinical challenges in the management of EPS, with particular emphasis on peri-operative considerations and surgical technique. METHODS: Retrospective analysis of all paediatric patients with EPS treated at the Manchester Centre for Transplantation. RESULTS: Four patients were included with a median duration of 78 months on PD. All patients had recurrent peritonitis (> 3 episodes), and all had symptoms within three months of a change of dialysis modality from PD to haemodialysis or transplant. In Manchester, care was delivered by a multi-disciplinary team, including surgeons delivering the adult EPS surgical service with a particular focus on nutritional optimisation, sepsis control, and wound management. The surgery involved laparotomy, lavage, and enterolysis of the small bowel + / − stoma formation, depending on intra-abdominal contamination. Two patients had a formal stoma, which were reversed at three and six months, respectively. Two patients underwent primary closure of the abdomen, whereas two patients had re-look procedures at 48 h with secondary closure. One patient had a post-operative wound infection, which was managed medically. One patient’s stoma became detached, leading to an intra-abdominal collection requiring re-laparotomy. The median length of stay was 25 days, and patients were discharged once enteral feeding was established. All patients remained free of recurrence with normal gut function and currently two out of four have functioning transplants. CONCLUSIONS: This series demonstrates 100% survival and parenteral feed independence following EPS surgery. Post-operative morbidity was common; however, with individualised experience-based decision-making and relevant additional interventions, patients made full recoveries. Health and development post-surgery continued, allowing the potential for transplantation. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-021-05243-0. Springer Berlin Heidelberg 2021-08-26 2022 /pmc/articles/PMC8921033/ /pubmed/34448023 http://dx.doi.org/10.1007/s00467-021-05243-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Sharma, Videha
Moinuddin, Zia
Summers, Angela
Shenoy, Mohan
Plant, Nicholas
Vranic, Semir
Prytula, Agnieszka
Zvizdic, Zlatan
Karava, Vasiliki
Printza, Nikoleta
Vlot, John
van Dellen, David
Augustine, Titus
Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title_full Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title_fullStr Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title_full_unstemmed Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title_short Surgical management of Encapsulating Peritoneal Sclerosis (EPS) in children: international case series and literature review
title_sort surgical management of encapsulating peritoneal sclerosis (eps) in children: international case series and literature review
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921033/
https://www.ncbi.nlm.nih.gov/pubmed/34448023
http://dx.doi.org/10.1007/s00467-021-05243-0
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