Relationship between the Renal Function and Adverse Clinical Events in Patients with Atrial Fibrillation: A Japanese Multicenter Registry Substudy.

Japanese adverse clinical events atrial fibrillation direct oral anticoagulant renal function

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
08 Jan 2020
Historique:
received: 08 12 2019
revised: 30 12 2019
accepted: 07 01 2020
entrez: 16 1 2020
pubmed: 16 1 2020
medline: 16 1 2020
Statut: epublish

Résumé

Atrial fibrillation (AF) and chronic kidney disease (CKD) often coexist, but the real-world data after approval of direct oral anticoagulants (DOACs) are still lacking in Japan. We investigated the association of the baseline renal function and adverse clinical events and risk of adverse clinical events with DOACs compared to warfarin for each renal functional level in Japanese AF patients. The present substudy was based on the SAKURA AF Registry, a Japanese multicenter observational registry (median follow-up period: 39 months). The creatinine clearance (CrCl) values were estimated by the Cockcroft-Gault formula, and divided into normal renal function, and mild and moderate-severe CKD (CrCl ≥ 80, 50-79, <50 mL/min). In the SAKURA AF Registry, the baseline CrCl data were available for 3242 patients (52% for DOAC and 48% for warfarin user). The relative risk of adverse clinical events was significantly higher in the patients with a CrCl < 50 mL/min as compared to those with a CrCl ≥ 80 mL/min (adjusted HRs: 2.53 for death, 2.53 for cardiovascular [CV] events, 2.13 for strokes, and 1.83 for major bleeding). Risks of all adverse clinical events were statistically even between DOAC and warfarin users for each renal function level. Moderate-severe CKD was associated with a higher mortality, CV events, strokes, and major bleeding than normal renal function. The safety and effectiveness of DOACs over warfarin were similar for each renal function level. By a worsening renal function, the incidence of adverse clinical events increased, especially deaths and CV events as compared to strokes and major bleeding.

Sections du résumé

BACKGROUND BACKGROUND
Atrial fibrillation (AF) and chronic kidney disease (CKD) often coexist, but the real-world data after approval of direct oral anticoagulants (DOACs) are still lacking in Japan. We investigated the association of the baseline renal function and adverse clinical events and risk of adverse clinical events with DOACs compared to warfarin for each renal functional level in Japanese AF patients.
METHODS METHODS
The present substudy was based on the SAKURA AF Registry, a Japanese multicenter observational registry (median follow-up period: 39 months). The creatinine clearance (CrCl) values were estimated by the Cockcroft-Gault formula, and divided into normal renal function, and mild and moderate-severe CKD (CrCl ≥ 80, 50-79, <50 mL/min).
RESULTS RESULTS
In the SAKURA AF Registry, the baseline CrCl data were available for 3242 patients (52% for DOAC and 48% for warfarin user). The relative risk of adverse clinical events was significantly higher in the patients with a CrCl < 50 mL/min as compared to those with a CrCl ≥ 80 mL/min (adjusted HRs: 2.53 for death, 2.53 for cardiovascular [CV] events, 2.13 for strokes, and 1.83 for major bleeding). Risks of all adverse clinical events were statistically even between DOAC and warfarin users for each renal function level.
CONCLUSION CONCLUSIONS
Moderate-severe CKD was associated with a higher mortality, CV events, strokes, and major bleeding than normal renal function. The safety and effectiveness of DOACs over warfarin were similar for each renal function level. By a worsening renal function, the incidence of adverse clinical events increased, especially deaths and CV events as compared to strokes and major bleeding.

Identifiants

pubmed: 31936260
pii: jcm9010167
doi: 10.3390/jcm9010167
pmc: PMC7019418
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Yasuhumi Yuzawa (Y)

Department of Cardiology, Nihon University Hospital, Tokyo 101-8309, Japan.

Keiichiro Kuronuma (K)

Kawaguchi Municipal Medical Center, Kawaguchi 333-0833, Japan.

Yasuo Okumura (Y)

Division of Cardiology, Nihon University Itabashi Hospital, Tokyo 173-8610, Japan.

Katsuaki Yokoyama (K)

Department of Cardiology, Nihon University Hospital, Tokyo 101-8309, Japan.

Naoya Matsumoto (N)

Department of Cardiology, Nihon University Hospital, Tokyo 101-8309, Japan.

Eizo Tachibana (E)

Kawaguchi Municipal Medical Center, Kawaguchi 333-0833, Japan.

Koji Oiwa (K)

Yokohama Chuo Hospital, Yokohama 231-0023, Japan.

Michiaki Matsumoto (M)

Yokohama Chuo Hospital, Yokohama 231-0023, Japan.

Toshiaki Kojima (T)

Sekishindo Hospital, Kawagoe 350-1123, Japan.

Hironori Haruta (H)

Asaka Medical Center, Asaka 351-0023, Japan.

Kazumiki Nomoto (K)

Tokyo Rinkai Hospital, Tokyo 134-0086, Japan.

Kazumasa Sonoda (K)

Tokyo Rinkai Hospital, Tokyo 134-0086, Japan.

Ken Arima (K)

Kasukabe Municipal Hospital, Kasukabe 344-8588, Japan.

Rikitake Kogawa (R)

Kasukabe Municipal Hospital, Kasukabe 344-8588, Japan.

Fumiyuki Takahashi (F)

Yasuda Hospital, Tokyo 175-0094, Japan.

Tomobumi Kotani (T)

Makita General Hospital, Tokyo 143-0016, Japan.

Kimie Okubo (K)

Itabashi Medical Association Hospital, Tokyo 175-0082, Japan.

Seiji Fukushima (S)

Ukima Central Hospital, Tokyo 115-0052, Japan.

Satoru Itou (S)

Itou Cardiovascular Clinic, Tokorozawa 359-1124, Japan.

Kunio Kondo (K)

Kondo Clinic, Tokyo 167-0022, Japan.

Masaaki Chiku (M)

Keiai Clinic, Tokyo 173-0036, Japan.

Yasumi Ohno (Y)

Ohno Medical Clinic, Tokyo 173-0004, Japan.

Motoyuki Onikura (M)

Onikura Clinic, Yachiyo 276-0023, Japan.

Atsushi Hirayama (A)

Division of Cardiology, Nihon University Itabashi Hospital, Tokyo 173-8610, Japan.

Classifications MeSH