Key result
Olanzapine discontinuation is linked to ~41% LVEF recovery in severe drug-associated dilated cardiomyopathy.
Case Report (n=1)
Long-term olanzapine use may be associated with reversible nonischemic dilated cardiomyopathy, highlighting the need for clinical vigilance in patients on chronic antipsychotic therapy.
May warrant LVEF monitoring on chronic olanzapine; hypothesis-generating case report leaves causality and generalizability open.
Olanzapine is a widely prescribed second-generation antipsychotic. We report the case of an 81-year-old woman with hypertension, type 2 diabetes mellitus, osteoporosis, and long-term olanzapine use who presented with progressive dyspnea, orthopnea, paroxysmal nocturnal dyspnea, lower extremity edema, and palpitations. Transthoracic echocardiography demonstrated four-chamber dilation, global left ventricular hypokinesis, and a reduced left ventricular ejection fraction (LVEF) of 30-35%. Coronary angiography revealed normal coronary arteries. After initiation of guideline-directed medical therapy for heart failure and discontinuation of olanzapine because of suspected drug-associated cardiomyopathy, the patient clinically stabilized. At outpatient follow-up, transthoracic echocardiography demonstrated partial recovery of left ventricular systolic function, with the LVEF improving to 40.77%. This case emphasizes the necessity of considering medication-associated cardiomyopathy in the differential diagnosis of new-onset nonischemic heart failure, particularly in patients receiving long-term antipsychotic therapy. Early recognition of cardiotoxicity and withdrawal of the offending agent may improve clinical outcomes.
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Abdelmoneim et al. (2026) conducted a case report in Nonischemic dilated cardiomyopathy (n=1). Olanzapine was evaluated. Long-term olanzapine exposure was associated with severe nonischemic dilated cardiomyopathy, with partial recovery of left ventricular ejection fraction from 30-35% to 40.77% following drug withdrawal.
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