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dc.contributor.authorHughes, Derralynn A.
dc.contributor.authorAguiar, Patricio
dc.contributor.authorDeegan, Patrick B
dc.contributor.authorEzgu, Fatih
dc.contributor.authorFrustaci, Andrea
dc.contributor.authorLidove, Olivier
dc.contributor.authorLinhart, Aleš
dc.contributor.authorLubanda, Jean-Claude
dc.contributor.authorMoon, James C
dc.contributor.authorNicholls, Kathleen
dc.contributor.authorNiu, Dau-Ming
dc.contributor.authorNowak, Albina
dc.contributor.authorRamaswami, Uma
dc.contributor.authorReisin, Ricardo
dc.contributor.authorRozenfeld, Paula
dc.contributor.authorSchiffmann, Raphael
dc.contributor.authorSvarstad, Einar
dc.contributor.authorThomas, Mark
dc.contributor.authorTorra, Roser
dc.contributor.authorVujkovac, Bojan
dc.contributor.authorWarnock, David G.
dc.contributor.authorWest, Michael L
dc.contributor.authorJohnson, Jack
dc.contributor.authorRolfe, Mark J
dc.contributor.authorFeriozzi, Sandro
dc.date.accessioned2021-04-29T11:24:34Z
dc.date.available2021-04-29T11:24:34Z
dc.date.created2020-11-11T13:03:59Z
dc.date.issued2020
dc.PublishedBMJ Open. 2020, 10:e035182 (10), 1-12.
dc.identifier.issn2044-6055
dc.identifier.urihttps://hdl.handle.net/11250/2740367
dc.description.abstractObjectives The PRoposing Early Disease Indicators for Clinical Tracking in Fabry Disease (PREDICT-FD) initiative aimed to reach consensus among a panel of global experts on early indicators of disease progression that may justify FD-specific treatment initiation. Design and setting Anonymous feedback from panellists via online questionnaires was analysed using a modified Delphi consensus technique. Questionnaires and data were managed by an independent administrator directed by two non-voting cochairs. First, possible early indicators of renal, cardiac and central/peripheral nervous system (CNS/PNS) damage, and other disease and patient-reported indicators assessable in routine clinical practice were compiled by the cochairs and administrator from panellists’ free-text responses. Second, the panel scored indicators for importance (5-point scale: 1=not important; 5=extremely important); indicators scoring ≥3 among >75% of panellists were then rated for agreement (5-point scale: 1=strongly disagree; 5=strongly agree). Indicators awarded an agreement score ≥4 by >67% of panellists achieved consensus. Finally, any panel-proposed refinements to consensus indicator definitions were adopted if >75% of panellists agreed. Results A panel of 21 expert clinicians from 15 countries provided information from which 83 possible current indicators of damage (kidney, 15; cardiac, 15; CNS/PNS, 13; other, 16; patient reported, 24) were compiled. Of 45 indicators meeting the importance criteria, consensus was reached for 29 and consolidated as 27 indicators (kidney, 6; cardiac, 10; CNS/PNS, 2; other, 6; patient reported, 3) including: (kidney) elevated albumin:creatinine ratio, histological damage, microalbuminuria; (cardiac) markers of early systolic/diastolic dysfunction, elevated serum cardiac troponin; (CNS/PNS) neuropathic pain, gastrointestinal symptoms suggestive of gastrointestinal neuropathy; (other) pain in extremities/neuropathy, angiokeratoma; (patient-reported) febrile crises, progression of symptoms/signs. Panellists revised and approved proposed chronologies of when the consensus indicators manifest. The panel response rate was >95% at all stages. Conclusions PREDICT-FD captured global opinion regarding current clinical indicators that could prompt FD-specific treatment initiation earlier than is currently practised.en_US
dc.language.isoengen_US
dc.publisherBMJen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleEarly indicators of disease progression in Fabry disease that may indicate the need for disease-specific treatment initiation: Findings from the opinion-based PREDICT-FD modified Delphi consensus initiativeen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2020 The Authorsen_US
dc.source.articlenumbere035182en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1136/bmjopen-2019-035182
dc.identifier.cristin1846944
dc.source.journalBMJ Openen_US
dc.source.4010:e035182
dc.source.1410
dc.identifier.citationBMJ Open. 2020, 10:e035182en_US
dc.source.volume10en_US


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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