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Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult
PURPOSE: The purpose of this study is to describe a case report of a patient experiencing hyponatremia from trimethoprim–sulfamethoxazole (TMP–SMX) upon initial use and subsequent rechallenge. SUMMARY: An 82-year-old woman presented to the emergency department with altered mental status thought to b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494188/ https://www.ncbi.nlm.nih.gov/pubmed/26170649 http://dx.doi.org/10.2147/CIA.S82823 |
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author | Huntsberry, Ashley M Linnebur, Sunny A Vejar, Maria |
author_facet | Huntsberry, Ashley M Linnebur, Sunny A Vejar, Maria |
author_sort | Huntsberry, Ashley M |
collection | PubMed |
description | PURPOSE: The purpose of this study is to describe a case report of a patient experiencing hyponatremia from trimethoprim–sulfamethoxazole (TMP–SMX) upon initial use and subsequent rechallenge. SUMMARY: An 82-year-old woman presented to the emergency department with altered mental status thought to be due to complicated cystitis and was treated with TMP–SMX 160 mg/800 mg orally twice daily for 7 days. Her basic metabolic panel prior to initiation of TMP–SMX was within normal limits, with the exception of her serum sodium of 132 mmol/L (range 133–145 mmol/L). The day after completing her 7-day course of TMP–SMX therapy the patient was evaluated by her primary care provider and another basic metabolic panel revealed a reduction in the serum sodium to 121 mmol/L. The patient’s serum sodium concentrations increased to baseline 7 days after completion of the TMP–SMX therapy, and remained normal until she was treated in the emergency department several months later for another presumed urinary tract infection. She was again started on TMP–SMX therapy empirically, and within several days her serum sodium concentrations decreased from 138 mmol/L to a low of 129 mmol/L. The TMP–SMX therapy was discontinued upon negative urine culture results and her serum sodium increased to 134 mmol/L upon discharge. Based upon the Naranjo probability scale score of 9, TMP–SMX was the probable cause of the patient’s hyponatremia. CONCLUSION: Our patient developed hyponatremia from TMP–SMX therapy upon initial use and rechallenge. Although hyponatremia appears to be rare with TMP–SMX therapy, providers should be aware of this potentially life-threatening adverse event. |
format | Online Article Text |
id | pubmed-4494188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44941882015-07-13 Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult Huntsberry, Ashley M Linnebur, Sunny A Vejar, Maria Clin Interv Aging Case Report PURPOSE: The purpose of this study is to describe a case report of a patient experiencing hyponatremia from trimethoprim–sulfamethoxazole (TMP–SMX) upon initial use and subsequent rechallenge. SUMMARY: An 82-year-old woman presented to the emergency department with altered mental status thought to be due to complicated cystitis and was treated with TMP–SMX 160 mg/800 mg orally twice daily for 7 days. Her basic metabolic panel prior to initiation of TMP–SMX was within normal limits, with the exception of her serum sodium of 132 mmol/L (range 133–145 mmol/L). The day after completing her 7-day course of TMP–SMX therapy the patient was evaluated by her primary care provider and another basic metabolic panel revealed a reduction in the serum sodium to 121 mmol/L. The patient’s serum sodium concentrations increased to baseline 7 days after completion of the TMP–SMX therapy, and remained normal until she was treated in the emergency department several months later for another presumed urinary tract infection. She was again started on TMP–SMX therapy empirically, and within several days her serum sodium concentrations decreased from 138 mmol/L to a low of 129 mmol/L. The TMP–SMX therapy was discontinued upon negative urine culture results and her serum sodium increased to 134 mmol/L upon discharge. Based upon the Naranjo probability scale score of 9, TMP–SMX was the probable cause of the patient’s hyponatremia. CONCLUSION: Our patient developed hyponatremia from TMP–SMX therapy upon initial use and rechallenge. Although hyponatremia appears to be rare with TMP–SMX therapy, providers should be aware of this potentially life-threatening adverse event. Dove Medical Press 2015-07-01 /pmc/articles/PMC4494188/ /pubmed/26170649 http://dx.doi.org/10.2147/CIA.S82823 Text en © 2015 Huntsberry et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Huntsberry, Ashley M Linnebur, Sunny A Vejar, Maria Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title | Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title_full | Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title_fullStr | Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title_full_unstemmed | Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title_short | Hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
title_sort | hyponatremia after initiation and rechallenge with trimethoprim–sulfamethoxazole in an older adult |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494188/ https://www.ncbi.nlm.nih.gov/pubmed/26170649 http://dx.doi.org/10.2147/CIA.S82823 |
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