A Case of Reversible Atrioventricular Block Potentially Associated with Atenolol-Induced Hyperkalemia

Kay Thi Oo1, Hnin Wut Yee1

  • 1Internal Medicine, Interfaith Medical Center, Brooklyn, USA.

Cureus
|March 11, 2021
PubMed

Insights

Drug-induced hyperkalemia, a serious condition, can cause heart rhythm problems. This case highlights how atenolol can trigger hyperkalemia and heart block in kidney disease patients, resolving upon drug withdrawal.

Area of Science:

  • Cardiology
  • Nephrology
  • Clinical Pharmacology

Background:

  • Potassium is crucial for cardiac electrophysiology; abnormal levels, particularly hyperkalemia, can cause life-threatening arrhythmias.
  • Drug-induced hyperkalemia is a significant clinical concern, often precipitated by medications in patients with underlying conditions.
  • End-stage renal disease (ESRD) patients are particularly vulnerable to electrolyte imbalances due to impaired kidney function.

Observation:

  • A case report details an ESRD patient experiencing hyperkalemia and type II second-degree atrioventricular (AV) block.
  • The patient's condition emerged upon initiation of atenolol therapy.
  • Hyperkalemia and AV block resolved after discontinuing atenolol and treating the electrolyte imbalance.

Findings:

  • Atenolol, a beta-blocker, was identified as the likely cause of drug-induced hyperkalemia and subsequent AV block in this ESRD patient.
  • The resolution of both hyperkalemia and heart block upon atenolol withdrawal strongly suggests a causal relationship.
  • This case underscores the importance of monitoring potassium levels and cardiac function in patients with ESRD initiating beta-blocker therapy.

Implications:

  • Clinicians should be vigilant for hyperkalemia and associated cardiac conduction abnormalities in ESRD patients prescribed atenolol.
  • Discontinuation of the offending drug (atenolol) can effectively manage drug-induced hyperkalemia and related cardiac complications.
  • This case emphasizes the need for careful medication review and monitoring in vulnerable patient populations to prevent adverse drug events.

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