Electrolyte Replacement in Bartter Syndrome With Abnormal Small Bowel: A Case Report.
Bartter syndrome
hypokalemia
hypomagnesemia
short bowel syndrome
Journal
Journal of investigative medicine high impact case reports
ISSN: 2324-7096
Titre abrégé: J Investig Med High Impact Case Rep
Pays: United States
ID NLM: 101624758
Informations de publication
Date de publication:
Historique:
entrez:
22
12
2020
pubmed:
23
12
2020
medline:
16
10
2021
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 33349065
doi: 10.1177/2324709620982440
pmc: PMC7758653
doi:
Substances chimiques
Magnesium
I38ZP9992A
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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