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Anesthetic management of child with Gitelman Syndrome: case report
Gitelman syndrome is a rare autosomal recessive inherited disease that affects the thiazidesensitive sodium-chloride cotransport channels and the magnesium channels in the distal convoluted tubule, leading to hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. There is no cure for thi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373332/ https://www.ncbi.nlm.nih.gov/pubmed/34090920 http://dx.doi.org/10.1016/j.bjane.2021.05.003 |
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author | Ferreira, Sara Antunes, Cláudia Pereira, Marta Rodrigues, Susana |
author_facet | Ferreira, Sara Antunes, Cláudia Pereira, Marta Rodrigues, Susana |
author_sort | Ferreira, Sara |
collection | PubMed |
description | Gitelman syndrome is a rare autosomal recessive inherited disease that affects the thiazidesensitive sodium-chloride cotransport channels and the magnesium channels in the distal convoluted tubule, leading to hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. There is no cure for this condition and supportive treatment relies on ionic supplementation and symptom management. Literature regarding the anesthetic approach is scarce. This case report presents the anesthetic management of a child with Gitelman syndrome and its difficult electrolyte optimization. |
format | Online Article Text |
id | pubmed-9373332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-93733322022-08-15 Anesthetic management of child with Gitelman Syndrome: case report Ferreira, Sara Antunes, Cláudia Pereira, Marta Rodrigues, Susana Braz J Anesthesiol Case Report Gitelman syndrome is a rare autosomal recessive inherited disease that affects the thiazidesensitive sodium-chloride cotransport channels and the magnesium channels in the distal convoluted tubule, leading to hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. There is no cure for this condition and supportive treatment relies on ionic supplementation and symptom management. Literature regarding the anesthetic approach is scarce. This case report presents the anesthetic management of a child with Gitelman syndrome and its difficult electrolyte optimization. Elsevier 2021-06-06 /pmc/articles/PMC9373332/ /pubmed/34090920 http://dx.doi.org/10.1016/j.bjane.2021.05.003 Text en © 2021 Sociedade Brasileira de Anestesiologia. Published by Elsevier Editora Ltda. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Ferreira, Sara Antunes, Cláudia Pereira, Marta Rodrigues, Susana Anesthetic management of child with Gitelman Syndrome: case report |
title | Anesthetic management of child with Gitelman Syndrome: case report |
title_full | Anesthetic management of child with Gitelman Syndrome: case report |
title_fullStr | Anesthetic management of child with Gitelman Syndrome: case report |
title_full_unstemmed | Anesthetic management of child with Gitelman Syndrome: case report |
title_short | Anesthetic management of child with Gitelman Syndrome: case report |
title_sort | anesthetic management of child with gitelman syndrome: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373332/ https://www.ncbi.nlm.nih.gov/pubmed/34090920 http://dx.doi.org/10.1016/j.bjane.2021.05.003 |
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