Amiodarone-Induced Hyponatremia in An Elderly Patient: A Rare Case Report.

J Pharm Pract

Department of Geriatric Medicine, JSS Medical College & Hospital, JSS Academy of Higher Education and Research, Mysore, India.

Published: June 2023

AI Article Synopsis

  • - Amiodarone is a Class III antiarrhythmic drug that can have serious side effects, leading to therapy discontinuation in around 20% of patients due to issues like liver damage and thyroid dysfunction.
  • - A case study highlighted a 73-year-old woman with severe hyponatremia linked to her amiodarone treatment for hypertension and ischemic heart disease, resulting in multiple hospital visits.
  • - The report emphasizes the need for healthcare providers to consider hyponatremia as a potential side effect of amiodarone, as it is not widely recognized in existing literature.

Article Abstract

Amiodarone is an antiarrhythmic drug belonging to Vaughan-Williams Class III with additional Class IV effects, which is known to cause many adverse drug reactions (ADRs) necessitating close monitoring. In about 20% of patients, their therapy is discontinued due to adverse effects such as hepatic impairment, thyroid dysfunction, and several pulmonary complications. Although dyselectrolytemia is a common adverse reaction reported with many cardiac medications, the incidence of hyponatremia associated with amiodarone intake is not reported widely in the literature. We are reporting a case of a 73-year-old female patient, with hypertension and ischemic heart disease (IHD) receiving oral amiodarone, presenting with severe hyponatremia, requiring recurrent hospitalization. Amiodarone was found to be responsible after evaluating for the possible causes of hyponatremia. As the incidence of amiodarone-associated hyponatremia is unknown, and not many cases are reported, this case report serves to sensitize the clinician to consider amiodarone-induced hyponatremia as one of the differential diagnoses in cases of unexplained hyponatremia.

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Source
http://dx.doi.org/10.1177/08971900211054199DOI Listing

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