Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3548
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dc.contributor.authorJain, N.en
dc.contributor.authorKerlin, B.en
dc.contributor.authorKulkarni, R.en
dc.contributor.authorNolan, B.en
dc.contributor.authorLiesner, R.en
dc.contributor.authorBrown, S.en
dc.contributor.authorTsao, E.en
dc.contributor.authorWinding, B.en
dc.contributor.authorLethagen, S.en
dc.contributor.authorPasi, K. J.en
dc.contributor.authorPabinger, I.en
dc.contributor.authorWang, M.en
dc.date.accessioned2022-11-07T23:43:35Z-
dc.date.available2022-11-07T23:43:35Z-
dc.date.issued2017en
dc.identifier.citation1 , 2017, p. 658en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/3548-
dc.description.abstractBackground: Long-term safety and efficacy of rFVIIIFc are being evaluated in the ongoing ASPIRE extension study of subjects with severe haemophilia A who completed A-LONG or Kids A-LONG. Aims: To present data on re-bleeds and target joint resolution from subjects with target joints at entry into the parent study through the third ASPIRE interim data cut. Methods: Subjects with ≥1 target joint (major joint with ≥3 bleeding episodes in a 6-mo period) at parent study entry with available pre-parent study data and on-study data were evaluated. ASPIRE treatment groups (≥12 y) were: individualised prophylaxis (IP), weekly prophylaxis (WP), modified prophylaxis (MP) or episodic treatment (ET); or (< 12 y) IP or MP. Outcomes were analysed over the duration of the parent study through the third ASPIRE interim data cut (11 Jan 2016). Results: 113 A-LONG subjects had target joints at baseline; 111 with evaluable data had 287 target joints at baseline and a cumulative median (IQR) 4.0 (2.8, 4.1) y on rFVIIIFc. 13 Kids A-LONG subjects had 15 target joints at baseline and 3.0 (0.5, 3.1) y on rFVIIIFc. Target joint annualised bleeding rates were low for subjects on rFVIIIFc prophylaxis (Table 1). 43.9% of IP, 42.3% of WP and 6.3% of MP A-LONG subjects and 53.8% of Kids A-LONG subjects (all IP) had no target joint bleeding episodes. Among prophylaxis subjects with target joints at baseline and 12 mo follow-up, 100% of A-LONG and Kids A-LONG subjects had ≥1 target joint resolved (≤2 spontaneous bleeding episodes in 12 consecutive mo); 99.6% and 100% of evaluable target joints in A-LONG and Kids A-LONG subjects were resolved, respectively. Table 2 shows prophylactic dose and dosing intervals. In adults/ adolescents, 96.4% of target joint bleeding episodes were controlled with ≤2 rFVIIIFc injections; patients rated 82.0% of injections to control a bleeding episode as excellent or good. Conclusions: Low target joint ABRs and effective target joint resolution occurred in children, adolescents, and adults on long-term rFVIIIFc prophylaxis.L6241557302018-10-09 <br />en
dc.language.isoenen
dc.relation.ispartofResearch and Practice in Thrombosis and Haemostasisen
dc.titleLong-term impact of RFVIIIFC prophylaxis in paediatric, adolescent, and adult subjects with target joints and severe haemophilia aen
dc.typeArticleen
dc.identifier.doi10.1002/rth2.12012en
dc.subject.keywordsfollow upen
dc.subject.keywordshemarthrosisen
dc.subject.keywordshemophilia Aen
dc.subject.keywordshumanen
dc.subject.keywordsinjectionen
dc.subject.keywordsmajor clinical studyen
dc.subject.keywordschilden
dc.subject.keywordsprophylaxisen
dc.subject.keywordsadolescentadulten
dc.subject.keywordsmaleen
dc.subject.keywordsconference abstracten
dc.subject.keywordscontrolled studyen
dc.subject.keywordsfemaleen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L624155730&from=exporthttp://dx.doi.org/10.1002/rth2.12012 |en
dc.identifier.risid1202en
dc.description.pages658en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
Appears in Sites:Children's Health Queensland Publications
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