P1672: OCCUPATIONAL INTEGRATION OF ADULTS WITH SEVERE HAEMOPHILIA (INTHEMO): A STUDY BASED ON THE FRANCECOAG REGISTRY

Autor: Ngoc Anh Thu Nguyen, Pascal Auquier, Any Beltran Anzola, Roseline D’oiron, Thierry Lambert, Céline Falaise, Christine Biron, Anne Lienhart, Jenny Goudemand, Antoine Rauch, Bénédicte Wibaut, Sabine Marie Castet, Dominique Desprez, Annie Harroche, Natalie Stieltjes, Annie Borel-Derlon, Marc Trossaërt, Amandine Celli, Benoît Guillet, Sophie Bayart, Marie-Anne Bertrand, Alexandra Fournel, Guillaume Mourey, Valérie Gay, Pierre Chamouni, Emmanuelle DE Raucourt, Birgit Frotscher, Michèle Martin, Mathieu Puyade, Brigitte Tardy, Stéphane Vanderbecken, Fabienne Genre-Volot, Philippe Nguyen, Benoît Polack, Caroline Oudot-Challard, Stéphane Girault, Annelise Voyer, Aurélien Lebreton, Abel Hassoun, Philippe Moreau, Pierre-Simon Rohrlich, Karine Baumstarck, Mohamed Boucekine, Vanessa Milien, Natacha Rosso, Clemence Tabele, Marie Viprey, Nicolas Giraud, Thomas Sannie, Hervé Chambost, Noémie Resseguier

Publikováno v: HemaSphere, Vol 7, p e623777c (2023)

Externí odkaz: https://doaj.org/article/35f0ccb00974432f92e9847dd92e5503

A French Real-World Evidence Study Evaluating the Efficacy, Safety, and Pharmacokinetic Parameters of rVIII-SingleChain in Patients with Hemophilia A Receiving Prophylaxis

Autor: Benoit Guillet, Abel Hassoun, Bénédicte Wibaut, Annie Harroche, Christine Biron-Andréani, Yohan Repesse, Roseline d'Oiron, Brigitte Tardy, Brigitte Pan Petesch, Pierre Chamouni, Valérie Gay, Marc Fouassier, Claire Pouplard, Cédric Martin, Hasan Catovic, Xavier Delavenne

Publikováno v: Thrombosis and Haemostasis. 123:490-500

Background rVIII-SingleChain is a recombinant factor VIII (FVIII) with increased binding affinity to von Willebrand factor compared with other FVIII products. rVIII-SingleChain is indicated for the treatment and prevention of bleeding episodes in pat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::92834625bd9f2c3538b8fe6462a38270
https://doi.org/10.1055/s-0043-1761449

Prostate biopsy and prostate cancer management in patients with haemophilia: The experience of French Haemophilia Treatment Centres

Autor: Philippe Gautier, Benoit Guillet, Marianne Sigaud, Ségolène Claeyssens, Fabienne Genre Volot, Pierre Chamouni, Anne Lienahrt, Birgit Frotscher, Alexandra Fournel, Sabine Castet, Catherine Poumayou, Valérie Gay, Rodolphe Thuret, Bénédicte Wibaut, Christine Biron‐Andreani

Publikováno v: Haemophilia. 28:437-444

Data are limited on prostate cancer (PC) management in patients with haemophilia (PWH).To describe PC screening and diagnosis, treatment modalities and bleeding complications in a group of unselected PWH followed at French Haemophilia Treatment Centr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9709f5ed31a98eebeca8734b030f9757
https://doi.org/10.1111/hae.14507

Haemophilia in France: Modelisation of the Clinical Pathway for Patients

Autor: Karen Beny, Benjamin du Sartz de Vigneulles, Florence Carrouel, Denis Bourgeois, Valérie Gay, Claude Negrier, Claude Dussart

Publikováno v: International Journal of Environmental Research and Public Health, Vol 19, Iss 646, p 646 (2022)
International Journal of Environmental Research and Public Health; Volume 19; Issue 2; Pages: 646
International Journal of Environmental Research and Public Health

Process-of-care studies participate in improving the efficiency of the care pathway for patient with haemophilia (CPPH) and rationalize the multidisciplinary management of patients. Our objective is to establish a current overview of the different ac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef86728789c7f06422c1e2f1b1821b0a
https://www.mdpi.com/1660-4601/19/2/646

Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls

Autor: Rita Marchi, Marguerite Neerman-Arbez, Valérie Gay, Guillaume Mourey, Mathieu Fiore, Christine Mouton, Philippe Gautier, Philippe De Moerloose, Alessandro Casini

Publikováno v: Blood Coagulation and Fibrinolysis, Vol. 32, No 2 (2021) pp. 108-114

Turbidity analysis is widely used as a quantitative technique in hereditary dysfibrinogenemia. We aimed to compare several coagulation triggers in hereditary dysfibrinogenemia and control plasmas. We included 20 patients with hereditary dysfibrinogen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03aa743358c6375ad676ef8f8d93bf9a
https://pubmed.ncbi.nlm.nih.gov/33443927