Key result
Switching to lurasidone shortens prolonged QTc intervals induced by other antipsychotics or antidepressants.
Why the study?
The effect of switching to lurasidone after antipsychotic- or antidepressant-induced QTc prolongation remains underexplored.
Does switching to lurasidone reduce prolonged QTc intervals in inpatients treated with other antipsychotics or antidepressants?
Does switching to lurasidone reduce prolonged QTc intervals in inpatients treated with other antipsychotics or antidepressants?
Switching to lurasidone may effectively reverse QTc prolongation induced by other psychiatric medications, potentially lowering the risk of sudden cardiac death.
Supports lurasidone for psychotropic-induced QTc prolongation; hypothesis-generating and should not yet change practice.
Background: QTc prolongation is a known side effect of antipsychotics and antidepressants and can lead to torsade de pointes, a potentially fatal tachycardia that may result in sudden death. Lurasidone is an atypical antipsychotic associated with a low incidence of QTc prolongation. However, the effect of switching to lurasidone after antipsychotic- or antidepressant-induced QTc prolongation remains underexplored. Procedures: Nine inpatients with prolonged QTc intervals following treatment with various antipsychotics or antidepressants were included. QTc intervals were compared before and after switching to lurasidone. Findings: Most patients exhibited shorter QTc intervals after switching to lurasidone. Implications/Conclusions: This case series demonstrated that switching to lurasidone reduced QTc prolongation induced by other antipsychotics or antidepressants. Lurasidone may lower the risk of sudden cardiac death in patients with psychiatric disorders by shortening QTc intervals.
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Takeuchi et al. (2026) studied this question. Switching to lurasidone shortened prolonged QTc intervals induced by other antipsychotics or antidepressants in most patients, suggesting reduced cardiac risk.
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