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Emicizumab prophylaxis in current haemophilia A care in the Czech Republic - data from the Czech National Haemophilia Programme Registry

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F25%3AE0112022" target="_blank" >RIV/00843989:_____/25:E0112022 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/25:00143362 RIV/00216208:11130/25:10505319 RIV/00216208:11140/25:10505319 RIV/61989592:15110/25:73632872 and 2 more

  • Result on the web

    <a href="https://doi.org/10.1016/j.rpth.2025.103215" target="_blank" >https://doi.org/10.1016/j.rpth.2025.103215</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.rpth.2025.103215" target="_blank" >10.1016/j.rpth.2025.103215</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Emicizumab prophylaxis in current haemophilia A care in the Czech Republic - data from the Czech National Haemophilia Programme Registry

  • Original language description

    Background: Nonfactor therapy with emicizumab has become an important part of the haemophilia A treatment landscape recently. Objectives: We aimed to analyze data on the transition from previous treatment regimens to emicizumab in routine clinical practice in the Czech Republic. Methods: Retrospective analysis of data from the Czech National Haemophilia Programme (CNHP) registry of all consecutive pediatric and adult persons treated with emicizumab prophylaxis. We evaluated bleeding control, injection frequency, and drug consumption in the period before and after emicizumab initiation. Results: Seventy-three persons with severe haemophilia A, median (IQR) age 4 (1-18) years, treated with emicizumab were reported in the CNHP registry up to the end of 2023. Two age categories were used for further stratification, 0-11 (n = 45) and 12+ (n = 28) years. For the whole group, we observed a significant reduction in total annualized bleeding rate (ABR) from a mean of 3.44 to 0.46 (P < .001), in joint ABR from 0.70 to 0.27 (P = .004), and in spontaneous ABR from 1.18 to 0.19 (P = .002) after starting emicizumab. The proportion of persons with no reported bleeding increased from 26.0% to 60.3% (P < .001). A sub-analysis, focused on inhibitors presence (present in 27 cases) and age, showed a more significant effect of emicizumab switch in observed parameters in persons with inhibitors and in the younger age group. Conclusion: The retrospective analysis of nation-wide data from the CNHP registry supports the fact that emicizumab has the potential to reduce bleeding and to provide an opportunity for a significant proportion of patients, with and without factor VIII inhibitors, to achieve zero bleeds.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Research and Practice in Thrombosis and Haemostasis

  • ISSN

    2475-0379

  • e-ISSN

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    1-8

  • UT code for WoS article

    001620334300002

  • EID of the result in the Scopus database

    2-s2.0-105020926250