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dc.contributor.authorBrandão, L. R.en
dc.contributor.authorTartakovsky, I.en
dc.contributor.authorAlbisetti, M.en
dc.contributor.authorHalton, J.en
dc.contributor.authorBomgaars, L.en
dc.contributor.authorChalmers, E.en
dc.contributor.authorLuciani, M.en
dc.contributor.authorSaracco, P.en
dc.contributor.authorFelgenhauer, J.en
dc.contributor.authorLvova, O.en
dc.contributor.authorSimetzberger, M.en
dc.contributor.authorSun, Z.en
dc.contributor.authorMitchell, L. G.en
dc.date.accessioned2024-04-08T11:07:20Z-
dc.date.available2024-04-08T11:07:20Z-
dc.date.issued2022-
dc.identifier.citationBrandão, LR, Tartakovsky, I, Albisetti, M, Halton, J, Bomgaars, L, Chalmers, E, Luciani, M, Saracco, P, Felgenhauer, J, Lvova, O, Simetzberger, M, Sun, Z & Mitchell, LG 2022, 'Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia', Blood Advances, Том. 6, № 22, стр. 5908-5923. https://doi.org/10.1182/bloodadvances.2021005681harvard_pure
dc.identifier.citationBrandão, L. R., Tartakovsky, I., Albisetti, M., Halton, J., Bomgaars, L., Chalmers, E., Luciani, M., Saracco, P., Felgenhauer, J., Lvova, O., Simetzberger, M., Sun, Z., & Mitchell, L. G. (2022). Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia. Blood Advances, 6(22), 5908-5923. https://doi.org/10.1182/bloodadvances.2021005681apa_pure
dc.identifier.issn2473-9529-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access; Gold Open Access; Green Open Access3
dc.identifier.otherhttps://ashpublications.org/bloodadvances/article-pdf/6/22/5908/1929545/blooda_adv-2021-005681-main.pdf1
dc.identifier.otherhttps://ashpublications.org/bloodadvances/article-pdf/6/22/5908/1929545/blooda_adv-2021-005681-main.pdfpdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/131435-
dc.description.abstractIn the phase 2b/3 DIVERSITY trial, 3 months treatment with dabigatran was noninferior to standard of care (SOC) for acute venous thromboembolism (VTE) in children. In a single-arm, phase 3, secondary VTE prevention study, up to 12 months dabigatran use was associated with favorable safety. Dabigatran is approved by the European Medicines Agency and US Food and Drug Administration for pediatric indications. We assessed primary composite efficacy (complete thrombus resolution and freedom from VTE recurrence/VTE-related death) in subgroups with thrombophilia vs those with negative/unknown thrombophilia status in the DIVERSITY trial and safety in both studies. Thrombophilia types were similar between the DIVERSITY trial (total population) and secondary prevention studies: factor V Leiden, 42% vs 33%; prothrombin mutation (G20210A), 19% vs 17%; antithrombin deficiency, 15% vs 20%; protein C/S deficiency, 23% vs 25%; and antiphospholipid antibodies, 18% vs 20% of patients, respectively. In DIVERSITY, 36% and 22% of thrombophilia subgroup patients treated with dabigatran and SOC, respectively, met the primary end point (Mantel-Haenszel–weighted rate difference, -0.135; 95% confidence interval, -0.36 to 0.08; noninferiority P = .0014); comparable to the total DIVERSITY trial population (46% vs 42%) showing dabigatran noninferiority to SOC. Within this subgroup, numerically fewer patients experienced VTE recurrence or progression of index thrombus in the dabigatran treatment group vs SOC. In the secondary prevention study, VTE recurrence at 12 months occurred in 2.8% of patients with thrombophilia vs 0% with negative/unknown thrombophilia. Safety profiles were consistent with those reported previously. Although they should be interpreted with caution, these exploratory findings suggest dabigatran could be an appropriate long-term anticoagulant for children with thrombophilia. © 2022 by The American Society of Hematology.en
dc.description.sponsorshipBoehringer Ingelheimen
dc.description.sponsorshipThe study was supported financially by Boehringer Ingelheim International GmbH.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherAmerican Society of Hematologyen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-by-nc-ndother
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/unpaywall
dc.sourceBlood Advances2
dc.sourceBlood Advancesen
dc.subjectBLOOD CLOTTING FACTOR 5 LEIDENen
dc.subjectDABIGATRANen
dc.subjectPHOSPHOLIPID ANTIBODYen
dc.subjectPROTHROMBINen
dc.subjectPROTHROMBIN ANTIBODYen
dc.subjectADVERSE OUTCOMEen
dc.subjectALOPECIAen
dc.subjectARTICLEen
dc.subjectCHILDen
dc.subjectCLINICAL EFFECTIVENESSen
dc.subjectCLINICAL FEATUREen
dc.subjectDISEASE EXACERBATIONen
dc.subjectDRUG EFFECTen
dc.subjectDRUG EFFICACYen
dc.subjectDRUG RESPONSEen
dc.subjectDRUG SAFETYen
dc.subjectEPISTAXISen
dc.subjectFEMALEen
dc.subjectHEADACHEen
dc.subjectHUMANen
dc.subjectMAJOR CLINICAL STUDYen
dc.subjectMALEen
dc.subjectPHASE 3 CLINICAL TRIALen
dc.subjectRECURRENT DISEASEen
dc.subjectRHINOPHARYNGITISen
dc.subjectRISK FACTORen
dc.subjectTHROMBOPHILIAen
dc.subjectTHROMBOSIS PREVENTIONen
dc.subjectTREATMENT OUTCOMEen
dc.subjectVENOUS THROMBOEMBOLISMen
dc.titleDabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophiliaen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1182/bloodadvances.2021005681-
dc.identifier.scopus85143118299-
local.contributor.employeeBrandão L.R., Division of Haematology/Oncology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada, Department of Pediatrics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canadaen
local.contributor.employeeTartakovsky I., Therapeutic Area Cardiovascular Medicine, Boehringer Ingelheim International GmbH, Ingelheim, Germanyen
local.contributor.employeeAlbisetti M., Hematology Department, University Children’s Hospital, Zürich, Switzerlanden
local.contributor.employeeHalton J., Division of Hematology/Oncology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canadaen
local.contributor.employeeBomgaars L., Department of Pediatrics, Texas Children’s Cancer Center, Baylor College of Medicine, Houston, TX, United Statesen
local.contributor.employeeChalmers E., Royal Hospital for Children, Glasgow, United Kingdomen
local.contributor.employeeLuciani M., Pediatric Hematology/Oncology Department, Pediatric Hospital Bambino Gesù, Rome, Italyen
local.contributor.employeeSaracco P., Pediatric Hematology, University Hospital, City of Health and Science of Turin, and Pediatric Hematology, Queen Margaret’s Children’s Hospital, Turin, Italyen
local.contributor.employeeFelgenhauer J., Pediatric Hematology & Oncology, Providence Sacred Heart Medical Center, Children’s Hospital, Spokane, WA, United Statesen
local.contributor.employeeLvova O., Laboratory for Brain and Neurocognitive Development, Department of Psychology, Ural Federal University, Yekaterinburg, Russian Federation, Children’s City Hospital No. 9, Yekaterinburg, Russian Federationen
local.contributor.employeeSimetzberger M., Clinical Development and Operations, Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austriaen
local.contributor.employeeSun Z., Biostatistics and Data Sciences, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, United Statesen
local.contributor.employeeMitchell L.G., Division of Pediatric Hematology/Oncology, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canadaen
local.description.firstpage5908-
local.description.lastpage5923-
local.issue22-
local.volume6-
dc.identifier.wos000913702900015-
local.contributor.departmentDivision of Haematology/Oncology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canadaen
local.contributor.departmentDepartment of Pediatrics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canadaen
local.contributor.departmentTherapeutic Area Cardiovascular Medicine, Boehringer Ingelheim International GmbH, Ingelheim, Germanyen
local.contributor.departmentHematology Department, University Children’s Hospital, Zürich, Switzerlanden
local.contributor.departmentDivision of Hematology/Oncology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canadaen
local.contributor.departmentDepartment of Pediatrics, Texas Children’s Cancer Center, Baylor College of Medicine, Houston, TX, United Statesen
local.contributor.departmentRoyal Hospital for Children, Glasgow, United Kingdomen
local.contributor.departmentPediatric Hematology/Oncology Department, Pediatric Hospital Bambino Gesù, Rome, Italyen
local.contributor.departmentPediatric Hematology, University Hospital, City of Health and Science of Turin, and Pediatric Hematology, Queen Margaret’s Children’s Hospital, Turin, Italyen
local.contributor.departmentPediatric Hematology & Oncology, Providence Sacred Heart Medical Center, Children’s Hospital, Spokane, WA, United Statesen
local.contributor.departmentLaboratory for Brain and Neurocognitive Development, Department of Psychology, Ural Federal University, Yekaterinburg, Russian Federationen
local.contributor.departmentChildren’s City Hospital No. 9, Yekaterinburg, Russian Federationen
local.contributor.departmentClinical Development and Operations, Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austriaen
local.contributor.departmentBiostatistics and Data Sciences, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, United Statesen
local.contributor.departmentDivision of Pediatric Hematology/Oncology, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canadaen
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local.identifier.eid2-s2.0-85143118299-
local.identifier.wosWOS:000913702900015-
local.identifier.pmid36150047-
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