Evidence map›Paper›PMID 42675499›Full record

ReviewNeurological research and practice2026

Real-world experience with foslevodopa/foscarbidopa in Germany: therapeutic insights and lessons learned.

David Weise, Tobias Warnecke, Carsten Buhmann, Georg Ebersbach, Carsten Eggers, Björn Falkenburger, Günter Höglinger, Brit Mollenhauer, David Pedrosa, Martin Südmeyer and 3 more

Abstract readReview
In one paragraph

Review in Neurological research and practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

David Weise *Department of Neurology, Asklepios Fachklinikum Stadtroda, Stadtroda, Germany. da.weise@asklepios.com.ORCID http://orcid.org/0000-0002-5772-6609
Tobias Warnecke *Department of Neurology and Neurorehabilitation, Klinikum Osnabrück - Academic Teaching Hospital of the University of Münster, Osnabrück, Germany.
Carsten BuhmannDepartment of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Georg EbersbachMovement Disorders Hospital Beelitz, Beelitz-Heilstätten, Germany.
Carsten EggersDepartment of Neurology, Knappschaft Kliniken Bottrop, Bottrop, Germany.
Björn FalkenburgerDepartment of Neurology, Faculty of Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Günter HöglingerDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Brit MollenhauerDepartment of Neurology, Universitätsmedizin Göttingen, and Paracelsus-Elena- Klinik, Kassel, both, Germany.
David PedrosaPhilipps-University Marburg, Marburg, Germany.
Martin SüdmeyerDepartment of Neurology, Klinikum Ernst von Bergmann, Potsdam, Germany.
Daniel WeissCentre for Neurology, and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Jan Kassubek *Department of Neurology, University Hospital Ulm, Ulm, Germany.
Wolfgang H Jost *Parkinson-Klinik Ortenau, Wolfach, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with advanced Parkinson's disease (PD) often need to continue with device-aided therapies (DAT), such as intestinal and subcutaneous infusion therapies. Recently, continuous subcutaneous administration of foslevodopa/foscarbidopa (LDp/CDp) has emerged as a new therapeutic method. Two years after its approval in Germany, a large amount of real-world experience has been collected. Based on this, we present important practical recommendations to help clinicians optimise treatment. Key topics include identifying suitable patients, approaches to initiation and dose determination as well as strategies for balancing LDp/CDp with concomitant oral dopaminergic therapies. Practical challenges, particularly infusion site reactions and neuropsychiatric vulnerability in older or cognitively impaired patients, are discussed, and recommendations are presented on how to prevent and manage these adverse effects during routine management. The review also addresses reasons for discontinuation, organisational factors relevant to real-world implementation and future directions in pump technology. Overall, LDp/CDp is effective in managing motor fluctuations and provides sustained benefits with an overall favourable tolerability profile. Dermatological reactions are common but manageable, and careful adjustment of oral medication rather than rapid pursuit of monotherapy is advisable. The rate of early discontinuation has decreased with growing clinical experience.

Indexed as

Foslevodopa/FoscarbidopaParkinson’s diseaseReal-world experienceRecommendations, Device-aided therapy

Identifiers

PMID42675499
PMCPMC13531757

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.