Continuous Subcutaneous Apomorphine as a Temporary Bridging Therapy for Dopamine Dysregulation Syndrome in Patients with Deep Brain Stimulation
BACKGROUND: Dopamine dysregulation syndrome (DDS) is a challenging complication of dopaminergic therapy in Parkinson's disease and can persist despite subthalamic deep brain stimulation (STN-DBS). We evaluated a temporary bridging concept in which oral dopaminergic medication was replaced by continuous subcutaneous apomorphine infusion while maintaining DBS. CASES: Six patients with STN-DBS and DDS were temporarily transitioned from oral dopaminergic medication to continuous subcutaneous apomorphine infusion. Treatment success was defined as reduction of DDS below a predefined threshold (<3 characteristic DDS features). Four of six patients (66.7%) no longer fulfilled the operational DDS criteria. Typical apomorphine-related adverse effects occurred in all patients; however, nausea and malaise limited the treatment in two non-responders. CONCLUSIONS: In this uncontrolled case series, continuous subcutaneous apomorphine may represent a useful temporary adjunct to STN-DBS for managing DDS in selected patients. Treatment tolerability appears to be a major determinant of success and requires careful patient selection and monitoring.
Authors
- Johannes Hartig (ORCID: https://orcid.org/0000-0001-6361-4374)
- Christine Daniels (ORCID: https://orcid.org/0000-0003-0368-0438)
- Florian Lange (ORCID: https://orcid.org/0000-0002-8336-5608)
- Martin M. Reich (ORCID: https://orcid.org/0000-0001-9115-5136)
- Jens Volkmann (ORCID: https://orcid.org/0000-0002-9570-593X)
- Chi Wang Ip (ORCID: https://orcid.org/0000-0003-0484-385X)
- Philipp Capetian (ORCID: https://orcid.org/0000-0003-1712-3659)
- Tobias Binder
- Lennart Sitzmann
Institutions
- Universitätsklinikum Würzburg (DE)
Publication Details
- Journal
- Movement Disorders Clinical Practice
- Published
- 2026-10-08
- DOI
- https://doi.org/10.1002/mdc3.70831
- Primary Topic
- Neurological disorders and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00