Citation Information :
JH HR, R MK, Sundarsingh V, Misquith LA, K F. A Rare Case of BRASH Syndrome: Diagnostic and Therapeutic Challenges. 2025; 4 (2):50-53.
Aim and background: BRASH syndrome (bradycardia, renal failure, AV-nodal blockade, shock, and hyperkalemia) is a rare and underrecognized clinical entity that poses significant diagnostic and therapeutic challenges.
Case description: We report the case of a 75-year-old female with multiple comorbidities presenting with symptomatic bradycardia and shock due to BRASH syndrome, triggered by AV nodal-blocking medications and sepsis-induced hypovolemia. Early recognition, prompt discontinuation of precipitating drugs, correction of hyperkalemia, and hemodynamic stabilization resulted in a favorable outcome.
Conclusion: This case underscores the importance of timely diagnosis and comprehensive management to prevent complications, reduce the need for invasive interventions, and improve overall patient outcomes in BRASH syndrome.
Clinical significance: In elderly patients with multiple comorbidities, combining calcium channel blockers (CCBs) and beta-blockers should be done with caution. Vigilant monitoring for BRASH features is essential, and even mild hyperkalemia must be treated promptly. Early recognition and tailored management can improve outcomes in BRASH syndrome.
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