BLATNY, Jan, Vladimir KOMRSKA, Bohumir BLAZEK, Miroslav PENKA a Petra OVESNÁ. Inhibitors incidence rate in Czech previously untreated patients with haemophilia A has not increased since introduction of recombinant factor VIII treatment in 2003. Blood Coagulation and Fibrinolysis. Philadelphia: Lippincott Williams and Wilkins, 2015, roč. 26, č. 6, s. 673-678. ISSN 0957-5235. Dostupné z: https://dx.doi.org/10.1097/MBC.0000000000000298.
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Základní údaje
Originální název Inhibitors incidence rate in Czech previously untreated patients with haemophilia A has not increased since introduction of recombinant factor VIII treatment in 2003
Autoři BLATNY, Jan (203 Česká republika), Vladimir KOMRSKA (203 Česká republika), Bohumir BLAZEK (203 Česká republika), Miroslav PENKA (203 Česká republika) a Petra OVESNÁ (203 Česká republika, garant, domácí).
Vydání Blood Coagulation and Fibrinolysis, Philadelphia, Lippincott Williams and Wilkins, 2015, 0957-5235.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.242
Kód RIV RIV/00216224:14110/15:00085183
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1097/MBC.0000000000000298
UT WoS 000364400500013
Klíčová slova anglicky bleeding; factor; haemophilia; inhibitors; recombinant
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 10. 12. 2015 15:23.
Anotace
Our objective was to assess the incidence of inhibitors development in Czech Republic since the introduction of recombinant factor VIII (rFVIII) and to look for the factors potentially influencing this parameter. It is to be expected that inhibitors risk may be increased after the introduction of recombinant products. Data of Czech National Haemophilia Programme registry entered from 2003 till 2013 were analysed. Both annual and absolute incidences of newly developed inhibitors in previously untreated patients (PUPs) were calculated. Bleeding and treatment data were also extracted, and association to the treatment regimen and development of inhibitors were analysed. Within the given period, we commenced 45 PUPs with haemophilia A on rFVIII and treated them for 137 treatment-years. Twenty-two of the PUPs had severe haemophilia A, being treated for 88 treatment-years. Treatment strategy for them was prophylaxis. Other PUPs were treated on demand. Median annual bleeding rate was 5 for boys with severe haemophilia, 3 for moderate haemophilia and 1 for mild form of the disease. No inhibitors developed in PUPs with moderate/mild haemophilia A. Annual inhibitor incidence rate in PUPs with severe haemophilia A treated with rFVIII was 56.8 per 1000 treatment-years. Absolute incidence was 22.7% (5/22). All inhibitors appeared within the first 50 exposure days. Comparing rFVIII-treated group with the control group treated under same/similar conditions with plasma-derived FVIII during the same follow-up period, we were not able to find significant difference in inhibitor development between these two groups. Our results support the finding that use of rFVIII is not a proven risk factor for inhibitor development in patients with haemophilia A.
Návaznosti
EE2.4.12.0048, projekt VaVNázev: Vzdělávací síť hemofilických center
VytisknoutZobrazeno: 26. 4. 2024 03:07