TY - JOUR
T1 - Patient Factors against Stable Control of Warfarin Therapy for Japanese Non-valvular Atrial Fibrillation Patients
AU - Tomita, Hideharu
AU - Kadokami, Toshiaki
AU - Momii, Hidetoshi
AU - Kawamura, Natsumi
AU - Yoshida, Masayoshi
AU - Inou, Tetsuji
AU - Fukuizumi, Yutaka
AU - Usui, Makoto
AU - Funakoshi, Kouta
AU - Yamada, Satoshi
AU - Aomori, Tohru
AU - Yamamoto, Koujiro
AU - Uno, Tsukasa
AU - Ando, Shin Ichi
N1 - Funding Information:
This study was partially funded by Eisai Corporation.
PY - 2013/11
Y1 - 2013/11
N2 - Introduction Effectiveness and safety of warfarin therapy for non-valvular atrial fibrillation (NVAF) patients are strongly associated with its stability presented such as time in therapeutic range (TTR) of PT-INR. However, the factors that affect TTR have not been fully elucidated in Japan where majority of patients are controlled within the range of 1.6-2.6 of PT-INR irrespective of the age. Methods We retrospectively analyzed 163 NVAF patients taking warfarin to determine the factors that affect TTR including metabolic enzymes polymorphisms after TTR calculation with both the standard PT-INR range and the actual control range of 1.6-2.6. Results Overall TTR calculated using Japanese Guideline was 69.7 ± 25.1% (< 70 and ≥ 70 years; 49.6 ± 24.8% and 77.8 ± 20.3%, respectively). After confirming that PT-INR values in patients < 70 years distributed in the same range as in those ≥ 70 years, as in a Japanese large cohort, we recalculated TTR of those < 70 years with 1.6-2.6 of PT-INR and found that it was 79.5 ± 20.1%. Poor control of this new TTR were significantly associated with the lower height, the higher serum creatinine, the lower creatinine clearance, female gender, and presence of congestive heart failure, (p < 0.05 respectively). Multivariate analysis revealed female gender and presence of congestive heart failure as independent predictor of the lower TTR (p < 0.05, p < 0.01, respectively). Polymorphism of CYP2C9 and VKORC1 were related to the dosage of warfarin but not determinant of TTR. Conclusions When evaluated using a range of PT-INR actually used in Japan, TTR is generally well controlled and female gender and presence of congestive heart failure significantly affected the poorer TTR control.
AB - Introduction Effectiveness and safety of warfarin therapy for non-valvular atrial fibrillation (NVAF) patients are strongly associated with its stability presented such as time in therapeutic range (TTR) of PT-INR. However, the factors that affect TTR have not been fully elucidated in Japan where majority of patients are controlled within the range of 1.6-2.6 of PT-INR irrespective of the age. Methods We retrospectively analyzed 163 NVAF patients taking warfarin to determine the factors that affect TTR including metabolic enzymes polymorphisms after TTR calculation with both the standard PT-INR range and the actual control range of 1.6-2.6. Results Overall TTR calculated using Japanese Guideline was 69.7 ± 25.1% (< 70 and ≥ 70 years; 49.6 ± 24.8% and 77.8 ± 20.3%, respectively). After confirming that PT-INR values in patients < 70 years distributed in the same range as in those ≥ 70 years, as in a Japanese large cohort, we recalculated TTR of those < 70 years with 1.6-2.6 of PT-INR and found that it was 79.5 ± 20.1%. Poor control of this new TTR were significantly associated with the lower height, the higher serum creatinine, the lower creatinine clearance, female gender, and presence of congestive heart failure, (p < 0.05 respectively). Multivariate analysis revealed female gender and presence of congestive heart failure as independent predictor of the lower TTR (p < 0.05, p < 0.01, respectively). Polymorphism of CYP2C9 and VKORC1 were related to the dosage of warfarin but not determinant of TTR. Conclusions When evaluated using a range of PT-INR actually used in Japan, TTR is generally well controlled and female gender and presence of congestive heart failure significantly affected the poorer TTR control.
KW - Non-valvular Atrial Fibrillation
KW - Time in therapeutic range
KW - Warfarin
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U2 - 10.1016/j.thromres.2013.09.003
DO - 10.1016/j.thromres.2013.09.003
M3 - Article
C2 - 24071466
AN - SCOPUS:84886099035
SN - 0049-3848
VL - 132
SP - 537
EP - 542
JO - Thrombosis Research
JF - Thrombosis Research
IS - 5
ER -