-
Je něco špatně v tomto záznamu ?
Warfarin loading dose guided by pharmacogenetics is effective and safe in cardioembolic stroke patients - a randomized, prospective study
T. Ruzickova, M. Sramek, V. Kaplan, S. Kumstyrova, Z. Lacinova, P. Jansky, H. Magerova, I. Sarbochova, JP. Schwabova, V. Matoska, A. Tomek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
NLK
ProQuest Central
od 2001-01-01 do Před 1 rokem
Open Access Digital Library
od 2001-01-01
Health & Medicine (ProQuest)
od 2001-01-01 do Před 1 rokem
- MeSH
- antikoagulancia aplikace a dávkování MeSH
- cévní mozková příhoda farmakoterapie MeSH
- farmakogenetika MeSH
- INR MeSH
- ischemie mozku farmakoterapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- prospektivní studie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- warfarin aplikace a dávkování škodlivé účinky MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
Warfarin treatment is commonly started with a fixed loading dose that might be associated with an increased risk of bleeding. An individual maintenance dose can then be estimated based on a pharmacogenetic algorithm. Starting treatment with the estimated dose implies a longer time to reach the therapeutic range. Our goal was to compare the safety and efficacy of initiating warfarin treatment with a loading dose guided by pharmacogenetics versus a maintenance dose. The primary endpoint was time in the therapeutic range (TTR) in the first 10 days of treatment. Secondary endpoints were time to the first international normalized ratio (INR) in therapeutic range (2.0-3.0) and occurrence of serious adverse events. Consenting cardioembolic stroke patients were genotyped for CYP2C9 (cytochrome P450 2C9 gene) and VKORC1 (vitamin K epoxide reductase complex, subunit 1 gene) polymorphisms and a maintenance warfarin dose was estimated. Patients were randomized into two groups. The loading dose group (LDG) patients received twice the estimated dose in the first 2 days of treatment. The maintenance dose group (MDG) patients received the estimated dose directly from day one. The TTR in the first 10 days was significantly higher in the LDG than in the MDG (50.5% vs. 38.3%, p = 0.003). The time to the first INR in this range was significantly shorter in the LDG (5.24 vs. 7.3 days). There were no significant differences in the INR above this range or serious adverse events. Warfarin loading dose guided by pharmacogenetics after recent cardioembolic stroke improved the efficacy of warfarin initiation without increasing the risk of adverse events.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20025638
- 003
- CZ-PrNML
- 005
- 20201222155323.0
- 007
- ta
- 008
- 201125s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1038/s41397-019-0066-4 $2 doi
- 035 __
- $a (PubMed)30647445
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Ruzickova, Tereza $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic. terez.ruzickova@gmail.com.
- 245 10
- $a Warfarin loading dose guided by pharmacogenetics is effective and safe in cardioembolic stroke patients - a randomized, prospective study / $c T. Ruzickova, M. Sramek, V. Kaplan, S. Kumstyrova, Z. Lacinova, P. Jansky, H. Magerova, I. Sarbochova, JP. Schwabova, V. Matoska, A. Tomek,
- 520 9_
- $a Warfarin treatment is commonly started with a fixed loading dose that might be associated with an increased risk of bleeding. An individual maintenance dose can then be estimated based on a pharmacogenetic algorithm. Starting treatment with the estimated dose implies a longer time to reach the therapeutic range. Our goal was to compare the safety and efficacy of initiating warfarin treatment with a loading dose guided by pharmacogenetics versus a maintenance dose. The primary endpoint was time in the therapeutic range (TTR) in the first 10 days of treatment. Secondary endpoints were time to the first international normalized ratio (INR) in therapeutic range (2.0-3.0) and occurrence of serious adverse events. Consenting cardioembolic stroke patients were genotyped for CYP2C9 (cytochrome P450 2C9 gene) and VKORC1 (vitamin K epoxide reductase complex, subunit 1 gene) polymorphisms and a maintenance warfarin dose was estimated. Patients were randomized into two groups. The loading dose group (LDG) patients received twice the estimated dose in the first 2 days of treatment. The maintenance dose group (MDG) patients received the estimated dose directly from day one. The TTR in the first 10 days was significantly higher in the LDG than in the MDG (50.5% vs. 38.3%, p = 0.003). The time to the first INR in this range was significantly shorter in the LDG (5.24 vs. 7.3 days). There were no significant differences in the INR above this range or serious adverse events. Warfarin loading dose guided by pharmacogenetics after recent cardioembolic stroke improved the efficacy of warfarin initiation without increasing the risk of adverse events.
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a antikoagulancia $x aplikace a dávkování $7 D000925
- 650 _2
- $a ischemie mozku $x farmakoterapie $7 D002545
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a INR $7 D019934
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a farmakogenetika $7 D010597
- 650 _2
- $a prospektivní studie $7 D011446
- 650 _2
- $a cévní mozková příhoda $x farmakoterapie $7 D020521
- 650 _2
- $a warfarin $x aplikace a dávkování $x škodlivé účinky $7 D014859
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a randomizované kontrolované studie $7 D016449
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Sramek, Martin $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic. Department of Neurology, Central Military University Hospital, Prague, Czech Republic.
- 700 1_
- $a Kaplan, Vojtech $u Hospital Na Homolce, Department of Clinical Biochemistry, Haematology and Immunology, Laboratory of Molecular Genetics, Prague, Czech Republic.
- 700 1_
- $a Kumstyrova, Simona $u Hospital Na Homolce, Department of Clinical Biochemistry, Haematology and Immunology, Laboratory of Molecular Genetics, Prague, Czech Republic.
- 700 1_
- $a Lacinova, Zuzana $u Hospital Na Homolce, Department of Clinical Biochemistry, Haematology and Immunology, Laboratory of Molecular Genetics, Prague, Czech Republic.
- 700 1_
- $a Jansky, Petr $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic.
- 700 1_
- $a Magerova, Hana $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic.
- 700 1_
- $a Sarbochova, Ivana $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic.
- 700 1_
- $a Schwabova, Jaroslava Paulasova $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic.
- 700 1_
- $a Matoska, Vaclav $u Hospital Na Homolce, Department of Clinical Biochemistry, Haematology and Immunology, Laboratory of Molecular Genetics, Prague, Czech Republic.
- 700 1_
- $a Tomek, Ales $u Department of Neurology, 2nd Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic. Hospital Na Homolce, Department of Clinical Biochemistry, Haematology and Immunology, Laboratory of Molecular Genetics, Prague, Czech Republic.
- 773 0_
- $w MED00008068 $t The pharmacogenomics journal $x 1473-1150 $g Roč. 19, č. 5 (2019), s. 446-454
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30647445 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201222155318 $b ABA008
- 999 __
- $a ok $b bmc $g 1599783 $s 1116324
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 19 $c 5 $d 446-454 $e 20190116 $i 1473-1150 $m Pharmacogenomics journal $n Pharmacogenomics J $x MED00008068
- LZP __
- $a Pubmed-20201125