Evidence map›Paper›PMID 40826893›Full record

ArticleJournal of the peripheral nervous system : JPNS2025

Real-World Multinational Survey of Chronic Inflammatory Demyelinating Polyneuropathy: Disease Characteristics and Therapeutic Landscape.

Luis Querol, Simon Rinaldi, Andras Borsi, Giorgio Maria Boggia, Jonathan de Courcy, Yasmin Taylor, Jack Wright, Wisam Karmous, Wim Noel, Charlotte Gary and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the peripheral nervous system : JPNS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

11 authors.

Luis QuerolHospital de la Santa Creu i Sant Pau, Barcelona, Spain.ORCID 0000-0002-4289-8264
Simon RinaldiNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Andras BorsiJanssen-Cilag Ltd, A Johnson & Johnson Company, High Wycombe, UK.
Giorgio Maria BoggiaJanssen-Cilag SpA, A Johnson & Johnson Company, Milan, Italy.
Jonathan de CourcyAdelphi Real World, Bollington, UK.
Yasmin TaylorAdelphi Real World, Bollington, UK.
Jack WrightAdelphi Real World, Bollington, UK.
Wisam KarmousJanssen-Cilag, A Johnson & Johnson Company, Strasbourg, France.
Wim NoelJanssen Pharmaceutica NV, A Johnson & Johnson Company, Beerse, Belgium.
Charlotte GaryJanssen-Cilag, A Johnson & Johnson Company, Strasbourg, France.
Gerd Meyer Zu HörsteUniversity Hospital Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsChronic inflammatory demyelinating polyneuropathy (CIDP) is an immune-mediated syndrome characterized by progressive muscle weakness and sensory impairment. Clinical similarities with other neuropathies can cause misdiagnoses and delayed diagnoses. Additionally, a large proportion of patients appropriately treated according to current guidelines still show residual disability. This real-world study aimed to characterize a global cohort of patients with CIDP.

methodsData were drawn from the Adelphi CIDP Disease Specific Programme, a cross-sectional survey with retrospective data collection, conducted in China, France, Germany, Italy, Japan, Spain, the United Kingdom, and the United States between September 2022 and April 2023. Neurologists and neuromuscular specialists reported on patient demographic and clinical characteristics at the time of the survey. Patients self-reported treatment satisfaction, disease control, and health-related outcome measures.

resultsOverall, 164 physicians provided data for 1056 patients, with 428 (40.5%) providing self-reported data. Patients were diagnosed with typical CIDP (69.2%) and variant CIDP (30.8%). Overall, initial misdiagnosis occurred in 37.2% of patients, with a median (interquartile range) diagnostic delay of 6.0 (3.0-12.0) months. Maintenance therapy was prescribed for 81.6% of patients, with corticosteroid use ranging from 25.7% in the United States to 80.0% in China. Some patients were dissatisfied by treatment outcomes (11.0%) and symptom control (12.2%). Overall, mean (SD) patient-reported scores were 62.1 (20.4) for I-RODS, 35.0 (11.1) for FACIT fatigue, and 0.662 (0.253) for EQ-5D-5L.

interpretationDiagnostic delay and misdiagnoses were common occurrences across typical CIDP and variant CIDP. Despite the use of guideline treatments, there were unmet needs and a continued disease burden for patients.

Indexed as

Diagnostic ErrorsPolyradiculoneuropathy, Chronic Inflammatory DemyelinatingAdultAgedCross-Sectional StudiesDelayed DiagnosisFemaleHumansMaleMiddle AgedRetrospective StudiesUnited Stateschronic inflammatory demyelinating polyneuropathydisease burdenhealthcare resource utilizationpatient reported outcomestreatment patterns

Identifiers

PMID40826893
PMCPMC12361836

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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.