AI Article Synopsis

  • A 52-year-old male developed severe weakness and was hospitalized due to hypokalemia and rhabdomyolysis after increasing his chlorthalidone dosage from 25 mg to 50 mg daily.
  • Extensive testing eliminated other potential causes of his hypokalemia, indicating it was likely due to the medication.
  • The patient's condition improved significantly with potassium supplementation and stopping the chlorthalidone, highlighting the need for awareness about serious side effects of diuretics even with minor dose adjustments.

Article Abstract

Purpose: A case of hypokalemic rhabdomyolysis related to chlorthalidone use is reported CASE SUMMARY: A 52-year-old male was admitted to the hospital for acute onset generalized weakness and was found to have severe hypokalemia and rhabdomyolysis. The patient had been on chlorthalidone therapy with a dose increase from 25 mg daily to 50 mg daily 2 months prior to admission. Extensive workup ruled out neurologic, rheumatologic, and endocrinologic causes of hypokalemia. In the absence of other causes, it was determined that the patient was experiencing a severe presentation of chlorthalidone-induced hypokalemia resulting in rhabdomyolysis. The patient's rhabdomyolysis and weakness improved with aggressive potassium correction, and potassium wasting eventually resolved with discontinuation of chlorthalidone.

Conclusion: Although mild hypokalemia is a known side effect of thiazide and thiazide-like diuretics, health care providers should be aware of the possibility of severe manifestations of this adverse reaction, even at relatively small dose increases.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.japh.2024.102249DOI Listing

Publication Analysis

Top Keywords

hypokalemic rhabdomyolysis
8
hypokalemia rhabdomyolysis
8
rhabdomyolysis
5
probable chlorthalidone-induced
4
chlorthalidone-induced hypokalemic
4
rhabdomyolysis purpose
4
purpose case
4
case hypokalemic
4
rhabdomyolysis chlorthalidone
4
chlorthalidone reported
4

Similar Publications

A woman with a history of chronic idiopathic constipation and remote eating disorders presented to our hospital with generalised weakness and confusion due to severe hypokalaemic rhabdomyolysis. Her initial ECG showed down-sloping ST segment elevations consistent with the 'shark fin' sign, and initial echocardiography was consistent with Takotsubo cardiomyopathy (TCM). She later developed hypotension, hypoxaemia and low central venous oxygen saturation consistent with cardiogenic shock.

View Article and Find Full Text PDF
Article Synopsis
  • A 52-year-old male developed severe weakness and was hospitalized due to hypokalemia and rhabdomyolysis after increasing his chlorthalidone dosage from 25 mg to 50 mg daily.
  • Extensive testing eliminated other potential causes of his hypokalemia, indicating it was likely due to the medication.
  • The patient's condition improved significantly with potassium supplementation and stopping the chlorthalidone, highlighting the need for awareness about serious side effects of diuretics even with minor dose adjustments.
View Article and Find Full Text PDF

Primary aldosteronism with hypokalemic rhabdomyolysis: a case report and review of the literature.

J Med Case Rep

August 2024

Department of Endocrinology, Tianjin Hospital, 406 Jiefang South Road, Tianjin, 300210, China.

Article Synopsis
  • Hypokalemic rhabdomyolysis is a rare complication of primary aldosteronism, which can complicate its diagnosis, especially if it's the main symptom.
  • A case study of a 54-year-old male presented with limb paralysis and was ultimately diagnosed with primary aldosteronism and hypokalemic rhabdomyolysis, highlighting the need to consider this link in similar cases.
  • A review of the literature revealed only 43 relevant cases since 1978, all showing good recovery with treatment, underscoring the importance of early detection and management for better outcomes.
View Article and Find Full Text PDF

Licorice-induced severe hypokalemic rhabdomyolysis.

Arch Med Sci

June 2024

Department of Ambulatory Surgical Center, Zhuzhou Hospital Affiliated to Xiangya Medical College, Central South University, Hunan, China.

View Article and Find Full Text PDF

Gitelman syndrome (GS) is a rare renal tubulopathy, classically characterized by renal salt wasting and metabolic alkalosis. It is usually an incidental diagnosis, being asymptomatic or with mild symptoms. GS manifesting with acute flaccid paralysis is extremely uncommon.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!