Key result
Intracerebroventricular anaerobic dopamine completely controls PD motor symptoms without dyskinesia in a case report.
Why the study?
Continuous intracerebroventricular administration of anaerobic dopamine represents a potential new device-aided therapy option for Parkinson's disease with severe L-dopa-related complications.
Does continuous intracerebroventricular administration of anaerobic dopamine improve motor symptoms in a patient with Parkinson's disease with severe L-dopa-related complications?
Case Report (n=1)
Does continuous intracerebroventricular administration of anaerobic dopamine improve motor symptoms in a patient with Parkinson's disease with severe L-dopa-related complications?
Intracerebroventricular anaerobic dopamine monotherapy may provide complete control of motor symptoms without dyskinesia in patients with Parkinson's disease and severe L-dopa-related complications.
Should not yet change PD management; leaves open intracerebroventricular anaerobic dopamine monotherapy for controlled trials.
Plain language summary Continuous intracerebroventricular administration of anaerobic dopamine represents a potential new device-aided therapy option for Parkinson's disease with L-dopa-related complications. A-dopamine is administered via a telemetry-controlled subcutaneous abdominal pump connected to a catheter implanted in the ventricle, near the striatum. We present the case of one patient with A-dopamine as monotherapy. Continuous intracerebroventricular administration of anaerobic dopamine (A-dopamine) represents a potential new device-aided therapy option for Parkinson's disease in the stage of severe L-dopa-related complications. A-dopamine is administered via a telemetry-controlled subcutaneous abdominal pump connected to a catheter implanted in the ventricle, near the striatum. We previously demonstrated its value as an add-on therapy in a Phase I/II trial, which showed a 4.4-hour increase in the duration of perfect control without “off” episodes or dyskinesia, and a 6.2-hour increase in the duration of good autonomy, compared to the best oral treatment with a 60% reduction in oral L-dopa. We present here the case of one such patient who benefited from long-term administration of A-dopamine as monotherapy, as the sole treatment. A dose of 240 mg of A-dopamine during the day and 40 mg at night allowed for complete control of motor symptoms without any dyskinesia, painful dystonia, fluctuations, or mental agitation, and without any oral medication. Monotherapy with A-dopamine produced greater benefits than those of adjunctive therapy added to optimized oral treatment. It is interesting to note that A-dopamine and L-dopa had a different clinical effect, since no dyskinesia or psychic excitation was observed with A-dopamine, unlike with L-dopa.
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Moreau et al. (2026) conducted a case report in Parkinson's disease with L-dopa-related complications (n=1). Intracerebroventricular anaerobic dopamine (A-dopamine) was evaluated on Control of motor symptoms without dyskinesia, painful dystonia, fluctuations, or mental agitation. Intracerebroventricular anaerobic dopamine monotherapy allowed for complete control of Parkinson's disease motor symptoms without dyskinesia, fluctuations, or mental agitation.
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