Key result
Reducing Madopar from 0.25 g tid to 0.125 g tid led to significant resolution of both motor and respiratory symptoms within two weeks.
Why the study?
Diagnosing respiratory dyskinesia in Parkinson disease patients with long-term antipsychotic use is challenging due to the need to differentiate levodopa-induced dyskinesia from tardive dyskinesia.
Case Report (n=1)
Careful symptom-medication timing analysis and dose reduction can resolve levodopa-induced respiratory dyskinesia in patients with complex psychiatric and neurologic medication histories.
May support dose reduction for suspected levodopa-induced respiratory dyskinesia; leaves open confirmation via prospective studies.
Background Diagnosing respiratory dyskinesia (RD) in Parkinson's disease (PD) patients with long-term antipsychotic use is challenging, requiring differentiation between levodopa-induced dyskinesia (LID) and tardive dyskinesia (TD). Case description A 70-year-old female with PD and a 30-year history of schizophrenia on chlorpromazine presented with aggravated limb tremor and new-onset abnormal breathing. Following a switch to quetiapine and intensification of her PD medication (Madopar increased to 0.25 g tid), she developed perioral/shoulder chorea and irregular respirations. Symptoms occurred synchronously with peak Madopar doses. Reducing Madopar to 0.125 g tid led to significant resolution of both motor and respiratory symptoms within two weeks. Conclusion This case highlights the diagnostic challenge of dyskinesia in patients with complex medication histories. A detailed symptom-medication timing analysis and a cautious drug adjustment trial were crucial for diagnosis and management. The atypical respiratory phenotype may be influenced by long-term antipsychotic exposure.
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Shi et al. (2026) conducted a case report in Parkinson's disease and schizophrenia with respiratory dyskinesia (n=1). Madopar dose reduction vs. Madopar 0.25 g tid was evaluated on Resolution of motor and respiratory symptoms. Reducing Madopar from 0.25 g tid to 0.125 g tid led to significant resolution of both motor and respiratory symptoms within two weeks.
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