Evidence map›Paper›PMID 42382134›Full record

ArticleEClinicalMedicine2026

Inter-centre heterogeneity, temporal evolution, and factors associated with treatment selection and outcomes in chronic inflammatory demyelinating polyradiculoneuropathy: a multicentre, combined prospective and retrospective observational study.

Alberto De Lorenzo, Maria Margherita Sechi, Fiore Manganelli, Dario Cocito, Chiara Briani, Yuri Falzone, Anna Mazzeo, Angelo Schenone, Vincenzo Di Stefano, Giuseppe Cosentino and 21 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 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

31 authors.

Alberto De LorenzoNeuromuscular and Neuroimmunology Unit, IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Maria Margherita SechiChild Neurology and Neuropsychiatry Unit, Department of Medicine, Surgery and Pharmacy, University Hospital of Sassari, Sassari, Italy.
Fiore ManganelliDepartment of Neuroscience, Reproductive Sciences and Odontostomatology, University of Naples 'Federico II', Napoli, Italy.
Dario CocitoDepartment of Clinical and Biological Sciences, University of Turin, Torino, Italy.
Chiara BrianiNeurology Unit, Department of Neuroscience, University of Padua, Padova, Italy.
Yuri FalzoneDivision of Neuroscience, Department of Neurology, Institute of Experimental Neurology (INSPE), San Raffaele Scientific Institute, Milano, Italy.
Anna MazzeoDepartment of Clinical and Experimental Medicine, Unit of Neurology, University of Messina, Messina, Italy.
Angelo SchenoneNeurology Clinic, IRCCS Ospedale Policlinico San Martino Genova, Genova, Italy.
Vincenzo Di StefanoDepartment of Biomedicine, Neuroscience, and advanced Diagnostic (BiND), University of Palermo, Palermo, Italy.
Giuseppe CosentinoDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Girolama Alessandra MarfiaDysimmune Neuropathies Unit, Department of Systems Medicine, Tor Vergata University of Rome, Roma, Italy.
Luana BenedettiNeurology Clinic, IRCCS Ospedale Policlinico San Martino Genova, Genova, Italy.
Marinella CarpoDepartment of Neurology, ASST Bergamo Ovest-Ospedale Treviglio, Treviglio, Italy.
Massimiliano FilostoDepartment of Clinical and Experimental Sciences, University of Brescia; NeMO-Brescia Clinical Center for Neuromuscular Diseases, Brescia, Italy.
Luca LeonardiNeuromuscular and Rare Disease Centre, Neurology Unit, Sant'Andrea Hospital, Rome, Italy.
Marco LuigettiNeurology Department, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Università Cattolica del Sacro Cuore, Roma, Italy.
Sabrina MatàDipartimento Neuromuscoloscheletrico e degli organi di Senso, Neurology Unit, University Hospital Careggi, Firenze, Italy.
Giuseppe PiscosquitoDepartment of Neurology, Azienda Ospedaliera Universitaria San Giovanni di Dio e Ruggi d'Aragona, Salerno, Italy.
Tiziana RossoUOC di Neurologia, Ospedale San Bassano, Vicenza, Italy.
Marta LucchettaUOC Neurologia, Ospedale Santa Maria della Misericordia, Rovigo, Italy.
Gabriele SicilianoNeurology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Giuseppe Lauria PinterUnit of Neuroalgology, IRCCS Foundation 'Carlo Besta' Neurological Institute, Milano, Italy.
Maurizio InghilleriDepartment of Human Neurosciences, Rare Neuromuscular Diseases Centre, Sapienza University of Rome, Rome, Italy.
Teresa CantisaniServizio di Neurofisiopatologia, Azienda Ospedaliera di Perugia, Perugia, Italy.
Francesca NotturnoNeurofisiopatologia, Ospedale SS Pescara, Pescara, Italy.
Dario RicciardiClinical Neurophysiology Unit, Cardarelli Hospital, Naples, Italy.
Francesco HabetswallnerClinical Neurophysiology Unit, Cardarelli Hospital, Naples, Italy.
Elisa VegezziIRCCS Mondino Foundation, Pavia, Italy.
Elisa BianchiIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Via Mario Negri 2, Milano, Italy.
Pietro Emiliano DonedduNeuromuscular and Neuroimmunology Unit, IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Eduardo Nobile-OrazioNeuromuscular and Neuroimmunology Unit, IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a treatable immune-mediated neuropathy, yet real-world evidence on therapeutic strategies and their evolution over time remains limited. This study aimed to characterise prescription patterns across Italian centres, assess adherence to international guidelines, and identify clinical, structural, and temporal determinants of therapeutic decision-making. Methods: This multicentre, combined prospective and retrospective observational study used data from the Italian CIDP registry, including 653 patients from 24 tertiary centres from 2015 to 2025. Detailed treatment histories were collected for induction and maintenance regimens, including intravenous immunoglobulin (IVIg), corticosteroids, plasma exchange (PE), subcutaneous immunoglobulin (SCIg), and immunosuppressants. A structured questionnaire assessed centre-level factors influencing treatment choices. Findings: Marked inter-centre heterogeneity across all treatment options was observed (p < 0.001). Over time, IVIg and SCIg use increased, while corticosteroids, PE, and traditional immunosuppressants declined. Independent determinants of induction therapy included patient characteristics, treatment period, and treating centre. Lower IVIg induction doses and oral corticosteroids were associated with worse long-term outcomes. Over time, induction response rates, residual disability, and therapy suspension rates improved. Questionnaire data revealed that although guideline recommendations strongly influenced decisions, organisational constraints, local prescribing culture, and patient preferences independently shaped treatment allocation. Interpretation: CIDP management in routine clinical practice is highly heterogeneous and influenced by both clinical and structural factors. These findings underscore the need for standardised, evidence-based, and sustainable treatment pathways to reduce unwarranted variability and ensure equitable access to optimal care as therapeutic options continue to expand. Funding: Grant from Regione Lombardia, Italy; Grant from Ministero della Salute, Ricerca Finalizzata; Kedrion Biopharma (Italy); CSL Behring (Italy); Humanitas Research Institute (Milan, Italy); GBS-CIDP Foundation International (USA).

Indexed as

Chronic inflammatory demyelinating polyradiculoneuropathyCIDPGuidelinesReal worldTreatment

Identifiers

PMID42382134
PMCPMC13316210

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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.