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Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report
Bartter syndrome is a rare disorder that is characterized by weakness and fatigue with laboratory findings of hypokalemia and metabolic alkalosis with increased aldosterone and angiotensin. It specifically acts on the ascending loop of Henle, characterized by miscoded proteins affecting NaCl transpo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758653/ https://www.ncbi.nlm.nih.gov/pubmed/33349065 http://dx.doi.org/10.1177/2324709620982440 |
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author | Sobash, Philip T. Vedala, Krishna McClain, Charles M. Oster, Caleb |
author_facet | Sobash, Philip T. Vedala, Krishna McClain, Charles M. Oster, Caleb |
author_sort | Sobash, Philip T. |
collection | PubMed |
description | Bartter syndrome is a rare disorder that is characterized by weakness and fatigue with laboratory findings of hypokalemia and metabolic alkalosis with increased aldosterone and angiotensin. It specifically acts on the ascending loop of Henle, characterized by miscoded proteins affecting NaCl transports and channels. Patients will require replacement of potassium and sometimes magnesium due to the kidneys’ inability to reabsorb these ions. So what happens when the body’s other primary mechanism of absorption of these elements are taken out? In this article, we present the case of a 47-year-old woman with Bartter syndrome on oral potassium 40 mg BID (twice a day) and magnesium oxide 800 TID (thrice a day), who recently had a small bowel resection that required intravenous potassium and magnesium throughout her hospital admission. Significant questions arose as to how her electrolytes should be managed, given her unusual presentation with rare underlying disorder. We discuss the implications of her bowel resection in the context of Bartter syndrome and our views on her future course based on available literature. |
format | Online Article Text |
id | pubmed-7758653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77586532021-01-08 Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report Sobash, Philip T. Vedala, Krishna McClain, Charles M. Oster, Caleb J Investig Med High Impact Case Rep Case Report Bartter syndrome is a rare disorder that is characterized by weakness and fatigue with laboratory findings of hypokalemia and metabolic alkalosis with increased aldosterone and angiotensin. It specifically acts on the ascending loop of Henle, characterized by miscoded proteins affecting NaCl transports and channels. Patients will require replacement of potassium and sometimes magnesium due to the kidneys’ inability to reabsorb these ions. So what happens when the body’s other primary mechanism of absorption of these elements are taken out? In this article, we present the case of a 47-year-old woman with Bartter syndrome on oral potassium 40 mg BID (twice a day) and magnesium oxide 800 TID (thrice a day), who recently had a small bowel resection that required intravenous potassium and magnesium throughout her hospital admission. Significant questions arose as to how her electrolytes should be managed, given her unusual presentation with rare underlying disorder. We discuss the implications of her bowel resection in the context of Bartter syndrome and our views on her future course based on available literature. SAGE Publications 2020-12-21 /pmc/articles/PMC7758653/ /pubmed/33349065 http://dx.doi.org/10.1177/2324709620982440 Text en © 2020 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Sobash, Philip T. Vedala, Krishna McClain, Charles M. Oster, Caleb Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title | Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title_full | Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title_fullStr | Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title_full_unstemmed | Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title_short | Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report |
title_sort | electrolyte replacement in bartter syndrome with abnormal small bowel: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758653/ https://www.ncbi.nlm.nih.gov/pubmed/33349065 http://dx.doi.org/10.1177/2324709620982440 |
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