Mansour Ibrahim Alrasheed, Reem Khalid Almanea, Bashayr Mohammed Hijaz, Muhammad Riazuddin
{"title":"Severe hyponatremia due to trimethoprim-sulfamethoxazole: a case report.","authors":"Mansour Ibrahim Alrasheed, Reem Khalid Almanea, Bashayr Mohammed Hijaz, Muhammad Riazuddin","doi":"10.21037/acr-24-175","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hyponatremia, a prevalent electrolyte imbalance with varying degrees of severity, can lead to mild to severe complications. Trimethoprim-sulfamethoxazole (TMP-SMX) and spironolactone are two frequently administered medications; regrettably, most healthcare professionals are not aware that these medications might cause hyponatremia. Concurrently, the two drugs have a high chance of medication interactions that raise the risk of hyponatremia, hyperkalemia, and death overall. TMP-SMX is implicated in causing hyponatremia through diverse mechanisms, such as inhibiting the renal tubular epithelial enzyme carbonic anhydrase. Structurally akin to the potassium-sparing diuretic amiloride, TMP-SMX is linked to hyperkalemia and hyponatremia by obstructing epithelial sodium channels in the distal nephron. Moreover, TMP-SMX may enhance antidiuretic hormone (ADH) release, exacerbating the imbalance.</p><p><strong>Case description: </strong>This is a case of a 76-year-old man with a medical history including hypertension, type II diabetes, coronary artery disease, and dyslipidemia. This case highlights an elderly patient treated with TMP-SMX for a soft tissue wound infection, which resulted in severe hyponatremia.</p><p><strong>Conclusions: </strong>Timely identification and careful monitoring of TMP-SMX-induced hyponatremia enabled the correction of sodium levels without severe complications. Thus, this report underscores the importance of vigilant monitoring and prompt identification of hyponatremia in patients undergoing TMP-SMX treatment. Further research is warranted due to limited data on the precise mechanisms of TMP-SMX-induced hyponatremia.</p>","PeriodicalId":29752,"journal":{"name":"AME Case Reports","volume":"9 ","pages":"43"},"PeriodicalIF":0.7000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12053988/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AME Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/acr-24-175","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Hyponatremia, a prevalent electrolyte imbalance with varying degrees of severity, can lead to mild to severe complications. Trimethoprim-sulfamethoxazole (TMP-SMX) and spironolactone are two frequently administered medications; regrettably, most healthcare professionals are not aware that these medications might cause hyponatremia. Concurrently, the two drugs have a high chance of medication interactions that raise the risk of hyponatremia, hyperkalemia, and death overall. TMP-SMX is implicated in causing hyponatremia through diverse mechanisms, such as inhibiting the renal tubular epithelial enzyme carbonic anhydrase. Structurally akin to the potassium-sparing diuretic amiloride, TMP-SMX is linked to hyperkalemia and hyponatremia by obstructing epithelial sodium channels in the distal nephron. Moreover, TMP-SMX may enhance antidiuretic hormone (ADH) release, exacerbating the imbalance.
Case description: This is a case of a 76-year-old man with a medical history including hypertension, type II diabetes, coronary artery disease, and dyslipidemia. This case highlights an elderly patient treated with TMP-SMX for a soft tissue wound infection, which resulted in severe hyponatremia.
Conclusions: Timely identification and careful monitoring of TMP-SMX-induced hyponatremia enabled the correction of sodium levels without severe complications. Thus, this report underscores the importance of vigilant monitoring and prompt identification of hyponatremia in patients undergoing TMP-SMX treatment. Further research is warranted due to limited data on the precise mechanisms of TMP-SMX-induced hyponatremia.