Real-world experience with continuous subcutaneous foslevodopa/foscarbidopa infusion: insights and recommendations

Traditional advanced therapies in Parkinson's disease (PD) with motor fluctuations and dyskinesias like continuous apomorphine infusion (CSAI), levodopa-carbidopa intestinal gel (LCIG), levodopa-carbidopa entacapone intestinal gel (LECIG), or deep brain stimulation (DBS) have played a central role in managing therapy-related complications. Recently, continuous subcutaneous foslevodopa/foscarbidopa infusion (CSFLI) has emerged as a novel therapeutic option. This manuscript provides insights from one year of real-world experience with CSFLI, addressing critical questions that clinicians face when selecting the most appropriate therapy for advanced PD. Our discussion centers on key considerations for patient selection, exploring which individuals may benefit more from CSFLI compared to other device-aided therapies. We highlight CSFLI's advantages in flexibility and ease of use but also consider limitations, particularly its side effects, such as skin-related issues. Recommendations are presented on how to prevent and manage these adverse effects to maximize patient compliance and therapeutic success. Additionally, the paper examines strategies for optimizing concurrent oral medications when combined with CSFLI, providing guidance on balancing pump infusion with necessary adjunctive oral treatments.

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Publication Details

Journal
Journal of Neural Transmission
Published
2025-03-22
DOI
https://doi.org/10.1007/s00702-025-02911-5
Citations
8
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
11.11
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article

Real-world experience with continuous subcutaneous foslevodopa/foscarbidopa infusion: insights and recommendations

Sebastian Paus, Sebastian Haferkamp, Christian Dresel, Péter Urbán et al.
8 citations
Journal of Neural Transmission
Parkinson's Disease Mechanisms and Treatments
11.11
article

Real-world experience with continuous subcutaneous foslevodopa/foscarbidopa infusion: insights and recommendations

Sebastian Paus, Sebastian Haferkamp, Christian Dresel, Péter Urbán, Christian Oehlwein, Thomas Koeglsperger, Rahel Müller, Jan Kassubek, Emir Berberovic
article en
8 citations

Abstract

Traditional advanced therapies in Parkinson's disease (PD) with motor fluctuations and dyskinesias like continuous apomorphine infusion (CSAI), levodopa-carbidopa intestinal gel (LCIG), levodopa-carbidopa entacapone intestinal gel (LECIG), or deep brain stimulation (DBS) have played a central role in managing therapy-related complications. Recently, continuous subcutaneous foslevodopa/foscarbidopa infusion (CSFLI) has emerged as a novel therapeutic option. This manuscript provides insights from one year of real-world experience with CSFLI, addressing critical questions that clinicians face when selecting the most appropriate therapy for advanced PD. Our discussion centers on key considerations for patient selection, exploring which individuals may benefit more from CSFLI compared to other device-aided therapies. We highlight CSFLI's advantages in flexibility and ease of use but also consider limitations, particularly its side effects, such as skin-related issues. Recommendations are presented on how to prevent and manage these adverse effects to maximize patient compliance and therapeutic success. Additionally, the paper examines strategies for optimizing concurrent oral medications when combined with CSFLI, providing guidance on balancing pump infusion with necessary adjunctive oral treatments.

Journal of Neural TransmissionVol. 133(2)
Johannes Gutenberg University Mainz (DE), German Center for Neurodegenerative Diseases (DE), University Hospital Augsburg (DE), LMU Klinikum (DE), University Hospital Regensburg (DE), University Medical Center of the Johannes Gutenberg University Mainz (DE), SRH Wald-Klinikum Gera (DE), Asklepios Klinik Barmbek (DE), University Hospital Ulm (DE), Parkinson-Klinik Ortenau (DE), Ludwig-Maximilians-Universität München (DE)
Good health and well-being
Openalex Percentile: Top 1%
Parkinson's Disease Mechanisms and Treatments
11.11
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