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http://elar.urfu.ru/handle/10995/131435
Полная запись метаданных
Поле DC | Значение | Язык |
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dc.contributor.author | Brandão, L. R. | en |
dc.contributor.author | Tartakovsky, I. | en |
dc.contributor.author | Albisetti, M. | en |
dc.contributor.author | Halton, J. | en |
dc.contributor.author | Bomgaars, L. | en |
dc.contributor.author | Chalmers, E. | en |
dc.contributor.author | Luciani, M. | en |
dc.contributor.author | Saracco, P. | en |
dc.contributor.author | Felgenhauer, J. | en |
dc.contributor.author | Lvova, O. | en |
dc.contributor.author | Simetzberger, M. | en |
dc.contributor.author | Sun, Z. | en |
dc.contributor.author | Mitchell, L. G. | en |
dc.date.accessioned | 2024-04-08T11:07:20Z | - |
dc.date.available | 2024-04-08T11:07:20Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Brandão, 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.2021005681 | harvard_pure |
dc.identifier.citation | Brandão, 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.2021005681 | apa_pure |
dc.identifier.issn | 2473-9529 | - |
dc.identifier.other | Final | 2 |
dc.identifier.other | All Open Access; Gold Open Access; Green Open Access | 3 |
dc.identifier.other | https://ashpublications.org/bloodadvances/article-pdf/6/22/5908/1929545/blooda_adv-2021-005681-main.pdf | 1 |
dc.identifier.other | https://ashpublications.org/bloodadvances/article-pdf/6/22/5908/1929545/blooda_adv-2021-005681-main.pdf | |
dc.identifier.uri | http://elar.urfu.ru/handle/10995/131435 | - |
dc.description.abstract | In 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.sponsorship | Boehringer Ingelheim | en |
dc.description.sponsorship | The study was supported financially by Boehringer Ingelheim International GmbH. | en |
dc.format.mimetype | application/pdf | en |
dc.language.iso | en | en |
dc.publisher | American Society of Hematology | en |
dc.rights | info:eu-repo/semantics/openAccess | en |
dc.rights | cc-by-nc-nd | other |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | unpaywall |
dc.source | Blood Advances | 2 |
dc.source | Blood Advances | en |
dc.subject | BLOOD CLOTTING FACTOR 5 LEIDEN | en |
dc.subject | DABIGATRAN | en |
dc.subject | PHOSPHOLIPID ANTIBODY | en |
dc.subject | PROTHROMBIN | en |
dc.subject | PROTHROMBIN ANTIBODY | en |
dc.subject | ADVERSE OUTCOME | en |
dc.subject | ALOPECIA | en |
dc.subject | ARTICLE | en |
dc.subject | CHILD | en |
dc.subject | CLINICAL EFFECTIVENESS | en |
dc.subject | CLINICAL FEATURE | en |
dc.subject | DISEASE EXACERBATION | en |
dc.subject | DRUG EFFECT | en |
dc.subject | DRUG EFFICACY | en |
dc.subject | DRUG RESPONSE | en |
dc.subject | DRUG SAFETY | en |
dc.subject | EPISTAXIS | en |
dc.subject | FEMALE | en |
dc.subject | HEADACHE | en |
dc.subject | HUMAN | en |
dc.subject | MAJOR CLINICAL STUDY | en |
dc.subject | MALE | en |
dc.subject | PHASE 3 CLINICAL TRIAL | en |
dc.subject | RECURRENT DISEASE | en |
dc.subject | RHINOPHARYNGITIS | en |
dc.subject | RISK FACTOR | en |
dc.subject | THROMBOPHILIA | en |
dc.subject | THROMBOSIS PREVENTION | en |
dc.subject | TREATMENT OUTCOME | en |
dc.subject | VENOUS THROMBOEMBOLISM | en |
dc.title | Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia | en |
dc.type | Article | en |
dc.type | info:eu-repo/semantics/article | en |
dc.type | info:eu-repo/semantics/publishedVersion | en |
dc.identifier.doi | 10.1182/bloodadvances.2021005681 | - |
dc.identifier.scopus | 85143118299 | - |
local.contributor.employee | Brandão 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, Canada | en |
local.contributor.employee | Tartakovsky I., Therapeutic Area Cardiovascular Medicine, Boehringer Ingelheim International GmbH, Ingelheim, Germany | en |
local.contributor.employee | Albisetti M., Hematology Department, University Children’s Hospital, Zürich, Switzerland | en |
local.contributor.employee | Halton J., Division of Hematology/Oncology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada | en |
local.contributor.employee | Bomgaars L., Department of Pediatrics, Texas Children’s Cancer Center, Baylor College of Medicine, Houston, TX, United States | en |
local.contributor.employee | Chalmers E., Royal Hospital for Children, Glasgow, United Kingdom | en |
local.contributor.employee | Luciani M., Pediatric Hematology/Oncology Department, Pediatric Hospital Bambino Gesù, Rome, Italy | en |
local.contributor.employee | Saracco P., Pediatric Hematology, University Hospital, City of Health and Science of Turin, and Pediatric Hematology, Queen Margaret’s Children’s Hospital, Turin, Italy | en |
local.contributor.employee | Felgenhauer J., Pediatric Hematology & Oncology, Providence Sacred Heart Medical Center, Children’s Hospital, Spokane, WA, United States | en |
local.contributor.employee | Lvova O., Laboratory for Brain and Neurocognitive Development, Department of Psychology, Ural Federal University, Yekaterinburg, Russian Federation, Children’s City Hospital No. 9, Yekaterinburg, Russian Federation | en |
local.contributor.employee | Simetzberger M., Clinical Development and Operations, Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria | en |
local.contributor.employee | Sun Z., Biostatistics and Data Sciences, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, United States | en |
local.contributor.employee | Mitchell L.G., Division of Pediatric Hematology/Oncology, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada | en |
local.description.firstpage | 5908 | - |
local.description.lastpage | 5923 | - |
local.issue | 22 | - |
local.volume | 6 | - |
dc.identifier.wos | 000913702900015 | - |
local.contributor.department | Division of Haematology/Oncology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada | en |
local.contributor.department | Department of Pediatrics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada | en |
local.contributor.department | Therapeutic Area Cardiovascular Medicine, Boehringer Ingelheim International GmbH, Ingelheim, Germany | en |
local.contributor.department | Hematology Department, University Children’s Hospital, Zürich, Switzerland | en |
local.contributor.department | Division of Hematology/Oncology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada | en |
local.contributor.department | Department of Pediatrics, Texas Children’s Cancer Center, Baylor College of Medicine, Houston, TX, United States | en |
local.contributor.department | Royal Hospital for Children, Glasgow, United Kingdom | en |
local.contributor.department | Pediatric Hematology/Oncology Department, Pediatric Hospital Bambino Gesù, Rome, Italy | en |
local.contributor.department | Pediatric Hematology, University Hospital, City of Health and Science of Turin, and Pediatric Hematology, Queen Margaret’s Children’s Hospital, Turin, Italy | en |
local.contributor.department | Pediatric Hematology & Oncology, Providence Sacred Heart Medical Center, Children’s Hospital, Spokane, WA, United States | en |
local.contributor.department | Laboratory for Brain and Neurocognitive Development, Department of Psychology, Ural Federal University, Yekaterinburg, Russian Federation | en |
local.contributor.department | Children’s City Hospital No. 9, Yekaterinburg, Russian Federation | en |
local.contributor.department | Clinical Development and Operations, Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria | en |
local.contributor.department | Biostatistics and Data Sciences, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, United States | en |
local.contributor.department | Division of Pediatric Hematology/Oncology, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada | en |
local.identifier.pure | 32801602 | - |
local.identifier.pure | f16b190c-a372-42f1-bd92-889793178d35 | uuid |
local.identifier.eid | 2-s2.0-85143118299 | - |
local.identifier.wos | WOS:000913702900015 | - |
local.identifier.pmid | 36150047 | - |
Располагается в коллекциях: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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2-s2.0-85143118299.pdf | 609,65 kB | Adobe PDF | Просмотреть/Открыть |
Лицензия на ресурс: Лицензия Creative Commons