TY - JOUR
T1 - Gastrointestinal bleeding from oral anticoagulant therapy among Japanese patients with atrial fibrillation identified from the Sakura atrial fibrillation registry
AU - SAKURA AF Registry Investigators
AU - Murata, Nobuhiro
AU - Okumura, Yasuo
AU - Nagashima, Koichi
AU - Fukamachi, Daisuke
AU - Yokoyama, Katsuaki
AU - Matsumoto, Naoya
AU - Tachibana, Eizo
AU - Kuronuma, Keiichiro
AU - Oiwa, Koji
AU - Matsumoto, Michiaki
AU - Kojima, Toshiaki
AU - Hanada, Shoji
AU - Nomoto, Kazumiki
AU - Arima, Ken
AU - Takahashi, Fumiyuki
AU - Kotani, Tomobumi
AU - Ikeya, Yukitoshi
AU - Fukushima, Seiji
AU - Itou, Satoru
AU - Kondo, Kunio
AU - Chiku, Masaaki
AU - Ohno, Yasumi
AU - Onikura, Motoyuki
AU - Hirayama, Atsushi
N1 - Publisher Copyright:
© All rights are reserved to the Japanese Circulation Society.
PY - 2020
Y1 - 2020
N2 - Background: In the Japanese clinical setting, the prevalence, potential cofounders of gastrointestinal (GI) bleeding from anticoagulant therapy, including direct oral anticoagulants (DOACs) and warfarin, and prognosis after GI bleeding are unclear. Methods and Results: We examined about GI bleeding from anticoagulant therapy using data from the SAKURA AF Registry, a prospective multicenter registry in Japan. Among 3,237 enrollees, 48.8% (n=1,561) were warfarin users and 51.2% (n=1,676) DOAC users. GI bleeding was identified in 68 patients (2.1%). No incidental differences in GI bleeding were observed between the DOAC and warfarin users (32 [1.9%] patients [0.67 events per 100 person-years] vs. 36 [2.3%] patients [0.75 events per 100 person-years], respectively; P=0.43). Multivariate Cox proportional hazard model analysis revealed that creatinine (hazard ratio [HR] 1.379, 95% confidence interval [CI] 1.091-1.743 P=0.007) and hemoglobin (HR 0.814, 95% CI 0.705-0.941, P=0.005) remained independent determinants of GI bleeding. Patients experiencing GI bleeding events had a higher risk of all-cause death (18%) than those without GI bleeding (6%) (P=0.045). Conclusions: GI bleeding was strongly associated with anemia and renal impairment. Patients experiencing GI bleeding had higher risk for all-cause death than those without GI bleeding.
AB - Background: In the Japanese clinical setting, the prevalence, potential cofounders of gastrointestinal (GI) bleeding from anticoagulant therapy, including direct oral anticoagulants (DOACs) and warfarin, and prognosis after GI bleeding are unclear. Methods and Results: We examined about GI bleeding from anticoagulant therapy using data from the SAKURA AF Registry, a prospective multicenter registry in Japan. Among 3,237 enrollees, 48.8% (n=1,561) were warfarin users and 51.2% (n=1,676) DOAC users. GI bleeding was identified in 68 patients (2.1%). No incidental differences in GI bleeding were observed between the DOAC and warfarin users (32 [1.9%] patients [0.67 events per 100 person-years] vs. 36 [2.3%] patients [0.75 events per 100 person-years], respectively; P=0.43). Multivariate Cox proportional hazard model analysis revealed that creatinine (hazard ratio [HR] 1.379, 95% confidence interval [CI] 1.091-1.743 P=0.007) and hemoglobin (HR 0.814, 95% CI 0.705-0.941, P=0.005) remained independent determinants of GI bleeding. Patients experiencing GI bleeding events had a higher risk of all-cause death (18%) than those without GI bleeding (6%) (P=0.045). Conclusions: GI bleeding was strongly associated with anemia and renal impairment. Patients experiencing GI bleeding had higher risk for all-cause death than those without GI bleeding.
KW - Atrial fibrillation
KW - Direct oral anticoagulants
KW - Gastrointestinal bleeding
UR - http://www.scopus.com/inward/record.url?scp=85090076485&partnerID=8YFLogxK
U2 - 10.1253/circj.CJ-20-0090
DO - 10.1253/circj.CJ-20-0090
M3 - Article
C2 - 32713873
AN - SCOPUS:85090076485
SN - 1346-9843
VL - 84
SP - 1475
EP - 1482
JO - Circulation Journal
JF - Circulation Journal
IS - 9
ER -