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Disease and treatment burden of patients with haemophilia entering the explorer6 non-interventional study

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dc.contributor.author유철주-
dc.date.accessioned2025-07-09T08:27:15Z-
dc.date.available2025-07-09T08:27:15Z-
dc.date.issued2024-11-
dc.identifier.issn0902-4441-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/206355-
dc.description.abstractObjectives: We aimed to characterise baseline disease and treatment burden in a large population with haemophilia A/B, both with (HAwI/HBwI) and without (HA/HB) inhibitors. Methods: The prospective, non-interventional explorer6 study included patients ≥12 years old with severe HA, severe/moderate HB or HAwI/HBwI of any severity, treated according to local standard of care (excluding previous/current exposure to concizumab or emicizumab). Baseline characteristics and historical clinical data were collected and patient-reported outcomes, including treatment burden, were assessed. Results: The explorer6 study enrolled 231 patients with haemophilia (84 HAwI/HBwI) from 33 countries. At baseline, patients with HA/HB treated with prophylaxis had the lowest median annualised bleeding rates (ABRs; 2.0), irrespective of haemophilia type; of these patients, 27.5% (HA) and 31.4% (HB) had target joints. Patients with HAwI/HBwI treated episodically reported the highest treatment burden. Of these patients, 28.5% (HAwI) and 25.1% (HBwI) performed sports activities in the month before screening. Conclusion: Despite receiving routine clinical care, historical and baseline information from patients enrolled in explorer6 showed that patients with HA/HB treated episodically and patients with HAwI/HBwI had higher ABRs, higher treatment burden and participated in sports less than those with HA/HB treated with prophylaxis. Emerging treatments could be beneficial in addressing these unmet medical needs.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherBlackwell-
dc.relation.isPartOfEUROPEAN JOURNAL OF HAEMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHChild-
dc.subject.MESHCost of Illness-
dc.subject.MESHDisease Management-
dc.subject.MESHFactor VIII / therapeutic use-
dc.subject.MESHFemale-
dc.subject.MESHHemophilia A* / diagnosis-
dc.subject.MESHHemophilia A* / drug therapy-
dc.subject.MESHHemophilia A* / epidemiology-
dc.subject.MESHHemophilia A* / therapy-
dc.subject.MESHHemophilia B / complications-
dc.subject.MESHHemophilia B / diagnosis-
dc.subject.MESHHemophilia B / drug therapy-
dc.subject.MESHHemophilia B / epidemiology-
dc.subject.MESHHemophilia B / therapy-
dc.subject.MESHHemorrhage / epidemiology-
dc.subject.MESHHemorrhage / etiology-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHProspective Studies-
dc.subject.MESHSeverity of Illness Index-
dc.subject.MESHYoung Adult-
dc.titleDisease and treatment burden of patients with haemophilia entering the explorer6 non-interventional study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pediatrics (소아과학교실)-
dc.contributor.googleauthorJerzy Windyga-
dc.contributor.googleauthorShashikant Apte-
dc.contributor.googleauthorMelissa Frei-Jones-
dc.contributor.googleauthorTeruhisa Fujii-
dc.contributor.googleauthorChuhl Joo Lyu-
dc.contributor.googleauthorLaura Villarreal Martinez-
dc.contributor.googleauthorJameela Sathar-
dc.contributor.googleauthorOleksandra Stasyshyn-
dc.contributor.googleauthorHuyen Tran-
dc.contributor.googleauthorNadezhda Zozulya-
dc.contributor.googleauthorRenée Brown Frandsen-
dc.contributor.googleauthorJesper Skov Neergaard-
dc.contributor.googleauthorJay Jay Thaung Zaw-
dc.contributor.googleauthorJohnny Mahlangu-
dc.identifier.doi10.1111/ejh.14277-
dc.contributor.localIdA02524-
dc.relation.journalcodeJ00822-
dc.identifier.eissn1600-0609-
dc.identifier.pmid39030946-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/ejh.14277-
dc.subject.keywordhaemophilia A-
dc.subject.keywordhaemophilia B-
dc.subject.keywordhealth‐related quality of life-
dc.subject.keywordphysical activity-
dc.subject.keywordsymptom burden-
dc.contributor.alternativeNameLyu, Chuhl Joo-
dc.contributor.affiliatedAuthor유철주-
dc.citation.volume113-
dc.citation.number5-
dc.citation.startPage631-
dc.citation.endPage640-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF HAEMATOLOGY, Vol.113(5) : 631-640, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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