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Authors
Cornille, Chloé https://orcid.org/0009-0001-6161-5477
Beuscart, Jean-Baptiste
Décaudin, Bertrand
Puisieux, François
Girault, Roxane
Mondet, Lisa
Toulemonde, Anne
Gautier, Sophie
Tempremant, Grégory
Kornobis, Jean-Paul
Dambrine, Mathilde
Bloch, Frédéric
Lenglet, Aurélie
,
Bouras, Syriane
Bullot, Charles
Charpentier, Anne
Degorre, Alexandra
Delabriere, Isabelle
Deschasse, Guillaume
Drieux, Pauline
Dupont, Corinne
Fabre, Anne-Marie
Farés, Farida
Feraux, Valentin
Gerard, Erwin
Guillier, Alban
Henry, Héloïse
Mailliez, Aurélie
Marcilly, Romaric
Marquant, Bénédicte
Meaux, Florine
Morgenroth, Thomas
Patinnier, Fanny
Pelayo, Sylvia
Quindroit, Paul
Renaudin, Pierre
Renoncourt, Thomas
Rognon, Carole
Roucout, Maya
Todessayi, Pietro
Truong-Minh, Julie
Verchin, Marine
Wimel, Marion
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Article History
Received: 18 July 2025
Revised: 7 December 2025
Accepted: 9 December 2025
First Online: 16 December 2025
Declarations
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: The authors have no financial or non-financial interests related to this work to disclose. The authors confirm that the principal investigators for this study are Professor Jean-Baptiste Beuscart and Professor Frédéric Bloch and that both had direct clinical responsibility for patients.
: This study was conducted in accordance with ethical standards and applicable national regulations. The project was carried out within the framework of a French government program (“Article 51”) aimed at improving healthcare pathway coordination and access to care. Given the nature of the study and the use of routinely collected clinical data, specific ethics committee approval was not required under French regulations. Data were handled in compliance with applicable data protection and privacy laws. Due to ethical and privacy restrictions, the data supporting the findings of this study are not publicly available.
: Informed consent was obtained from all patients involved in the study, in accordance with national legal and ethical requirements. Patients were informed about the use of their clinical data for research purposes and their right to object. All principal investigators, Professor Jean-Baptiste Beuscart and Professor Frédéric Bloch, had direct clinical responsibility for the patients included in the study.
