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dc.contributor.authorBlenkiron, Tom
dc.contributor.authorFerri Grazzi, Enrico
dc.contributor.authorBurke, Tom
dc.contributor.authorWatt, Maureen
dc.contributor.authorDavis, Kimberly H.
dc.date.accessioned2025-08-26T10:28:45Z
dc.date.available2025-08-26T10:28:45Z
dc.date.issued2025-08-06
dc.date.submitted2025-02-10
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/629593/Burke%20-%20Exploring-the-relationship-between-personalization.pdf?sequence=2
dc.identifier.citationBlenkiron, T., Ferri Grazzi, E., Burke, T., Watt, M., & Davis, K. H. (2025). Exploring the relationship between personalization of care and participation in sport activities among people with severe Hemophilia A across Europe: Post hoc analysis of the CHESS II study. Journal of Blood Medicine, 16, 359-372. https://doi.org/10.2147/JBM.S521079en_US
dc.identifier.doi10.2147/JBM.S521079en_US
dc.identifier.urihttp://hdl.handle.net/10034/629593
dc.description© 2025 The Takeda Pharmaceutical Company Limited (Takeda). This work is published and licensed by Dove Medical Press Limited.en_US
dc.description.abstractTo describe the demographic and clinical characteristics of patients with hemophilia A receiving different levels of treatment personalization (TP), and to assess the relationship between TP and sport active time (SAT). This post hoc analysis of the CHESS II study used data from physician-completed patient record forms and patient self-completion forms for adult males receiving prophylaxis for severe hemophilia A in Europe between November 2018 and October 2020. SAT was assessed using propensity score matching (PSM) across levels of TP, including pharmacokinetic (PK)-guided and non-PK-guided. Of 54 patients, 32 (59.3%) received TP. Of these, 22 (68.8%) and 10 (31.3%) received non-PK-guided and PK-guided treatment, respectively. Median age varied between the TP and no-TP groups (29.5 and 34.0 years, respectively). Median (IQR) annual bleeding incidence was higher with non-PK-guided vs PK-guided TP (4.0 [3.0-8.0] vs 3.5 [2.0-4.0]). Median (IQR) problem joints were similar with non-PK-guided and PK-guided TP (1.0 [0.0-1.0] and 1.0 [0.0-2.0]). Patients in the TP vs no-TP group had higher median (IQR) SAT per month (3.3 [1.8-6.2] vs 1.8 [0.7-5.0] hours). Median (IQR) SAT per month was higher with PK-guided vs non-PK-guided TP (4.0 [3.0-20.0] vs 3.0 [1.3-5.3] hours). After controlling for confounding in the PSM model, SAT remained higher with TP vs no-TP and with PK-guided vs non-PK-guided TP. In both PSM models, P values were <0.05 for the average treatment effect and <0.01 for the average treatment effect on the treated. Sensitivity analyses confirmed the robustness of the PSM. Patients receiving TP vs no-TP had higher median SAT. Of those with TP, those receiving PK-guided vs non-PK-guided TP experienced lower bleeding rates and higher SAT. PK-guided TP may help patients to be more active, potentially gaining the clinical and psychosocial benefits of exercise. [Abstract copyright: © 2025 The Takeda Pharmaceutical Company Limited (Takeda).]en_US
dc.description.sponsorshipThis study was funded by Takeda Development Center Americas, Inc., Lexington, MA, USA. The wider CHESS II study was supported by unrestricted research grants from BioMarin, Sanofi, and Takeda.en_US
dc.languageeng
dc.publisherDove Pressen_US
dc.publisherTaylor & Francis
dc.relation.urlhttps://www.dovepress.com/exploring-the-relationship-between-personalization-of-care-and-partici-peer-reviewed-fulltext-article-JBMen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.subjectHemophilia Aen_US
dc.subjectPersonalization of careen_US
dc.subjectExerciseen_US
dc.subjectSporten_US
dc.titleExploring the relationship between personalization of care and participation in sport activities among people with severe Hemophilia A across Europe: Post hoc analysis of the CHESS II studyen_US
dc.typeArticleen_US
dc.identifier.eissn1179-2736en_US
dc.contributor.departmentHCD Economics; University of Chester; Takeda Development Center Americasen_US
dc.identifier.journalJournal of Blood Medicineen_US
dc.date.updated2025-08-25T00:24:53Z
dc.date.accepted2025-07-07
rioxxterms.identifier.projectn/aen_US
rioxxterms.versionVoRen_US
rioxxterms.licenseref.startdate2025-08-06
dc.date.deposited2025-08-26en_US


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