Evidence map›Paper›PMID 39902569›Full record

ArticleMovement disorders clinical practice2025

Localization Matters: Impacts of PEG-J Localization in Intestinal Levodopa Therapy for Parkinson's Disease.

Philipp Klocke, Moritz A Loeffler, Idil Cebi, Karl-Ernst Grund, Christine Daniels, Jens Volkmann, Jiri Koschel, Wolfgang H Jost, Kazimierz Logmin, Lars Wojtecki and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Movement disorders clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. Review
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

12 authors.

Philipp KlockeCentre for Neurology, Department for Neurodegenerative Diseases, and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0003-0868-5270
Moritz A LoefflerCentre for Neurology, Department for Neurodegenerative Diseases, and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Idil CebiCentre for Neurology, Department for Neurodegenerative Diseases, and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0002-1458-9173
Karl-Ernst GrundCentre for General Surgery, Department for Surgical Endoscopy, University Medical Centre Tübingen, Tübingen, Germany.
Christine DanielsDepartment of Neurology, University Hospital and Julius-Maximilians-University, Würzburg, Germany.
Jens VolkmannDepartment of Neurology, University Hospital and Julius-Maximilians-University, Würzburg, Germany.
Jiri KoschelParkinson-Klinik Ortenau, Wolfach, Germany.
Wolfgang H JostParkinson-Klinik Ortenau, Wolfach, Germany.ORCID https://orcid.org/0000-0002-8574-3297
Kazimierz LogminDepartment of Neurology and Neurorehabilitation, Hospital Zum Heiligen Geist, Academic Teaching Hospital of the Heinrich-Heine-University Düsseldorf, Kempen, Germany.
Lars WojteckiDepartment of Neurology and Neurorehabilitation, Hospital Zum Heiligen Geist, Academic Teaching Hospital of the Heinrich-Heine-University Düsseldorf, Kempen, Germany.
Christoph R WernerDepartment of Gastroenterology, Gastrointestinal Oncology, Hepatology, Infectiology, and Geriatrics, University Hospital of Tübingen, Tübingen, Germany.
Daniel WeissCentre for Neurology, Department for Neurodegenerative Diseases, and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0003-0447-7132

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReal-world clinical evidence is missing to understand the resorption characteristics of levodopa through duodenal and jejunal parts of the small intestine.

objectiveTo characterize how different application sites of intestinal levodopa gel would impact on levodopa dosing and clinical outcomes.

methodsThis multicentre retrospective analysis investigated Parkinson's disease patients (n = 111) and their change in levodopa equivalent dosage when switching from oral treatment to intestinal continuous infusion therapy while stratifying for differences in percutaneous gastrojejunostomy (PEG-J) tube localizations. We analyzed data from patients treated with both levodopa-carbidopa (LCIG) and levodopa-carbidopa-entacapone (LECIG) intestinal gel.

resultsIn dichotomic analysis, duodenal and jejunal tube positions showed similar levodopa equivalent dosages changes from baseline (P = 0.143). This was similar when subdividing patients for LCIG and LECIG treatment. In duodenal PEG-J positions, 44.4% of patients showed persistent motor fluctuations compared to 21.9% in jejunal placements (P = 0.026). In duodenal positions, fluctuations most often persisted when the PEG-J tube was placed proximally into the duodenum. In jejunal localizations, several patients displayed a satisfactory outcome from the primary intervention but experienced dislocation of the PEG-J tube to a duodenal position. This was associated with re-emergence of motor fluctuations in a majority of them.

conclusionsOur real-world data suggest that LCIG and LECIG are absorbed similarly in both duodenal and jejunal portions of the small intestine. However, clinical data suggest, that jejunal positioning is critical to the stabilization of dopaminergic motor fluctuations.

Indexed as

Antiparkinson AgentsCarbidopaCatecholsGastric BypassLevodopaParkinson DiseaseAgedDrug CombinationsDuodenumFemaleHumansJejunumMaleMiddle AgedNitrilesRetrospective StudiesAntiparkinson AgentsCarbidopacarbidopa, levodopa drug combinationCatecholsDrug CombinationsentacaponeLevodopaNitrilesduodenaljejunalLCIGLECIGParkinson's disease

Identifiers

PMID39902569
PMCPMC12070182

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.