TY - JOUR
T1 - Acute kidney injury and edaravone in acute ischemic stroke
T2 - The fukuoka stroke registry
AU - Kamouchi, Masahiro
AU - Sakai, Hironori
AU - Kiyohara, Yutaka
AU - Minematsu, Kazuo
AU - Hayashi, Kunihiko
AU - Kitazono, Takanari
N1 - Funding Information:
We thank Dr Fumie Tokuda and Dr Chizuko Wakabayashi (Basic Sciences, Department of Basic Sciences, Faculty of Medicine, Gunma University) for their skillful help in data analysis and Ms Ikumi Fukuyama, Mr Katsuhiko Murakami, and Mr Satoshi Toriyama (Mitsubishi Tanabe Pharma Corporation) for their assistance in developing the study concept. We also thank Associate Professor Hitoshi Inoue (Research Institute for Information Technology, Kyushu University) for his technical support for the secure FSR Data Collection System. We are grateful to all the clinical research co-ordinators (Hisayama Research Institute For Lifestyle Diseases) for their help in collecting clinical data. This study was supported by the Mitsubishi Tanabe Pharma Corporation .
PY - 2013/11
Y1 - 2013/11
N2 - Background: A free radical scavenger, edaravone, which has been used for the treatment of ischemic stroke, was reported to cause acute kidney injury (AKI) as a fatal adverse event. The aim of the present study was to clarify whether edaravone is associated with AKI in patients with acute ischemic stroke. Methods: From the Fukuoka Stroke Registry database, 5689 consecutive patients with acute ischemic stroke who were hospitalized within 24 hours of the onset of symptoms were included in this study. A logistic regression analysis for the Fukuoka Stroke Registry cohort was done to identify the predictors for AKI. A propensity score-matched nested case-control study was also performed to elucidate any association between AKI and edaravone. Results: Acute kidney injury occurred in 128 of 5689 patients (2.2%) with acute ischemic stroke. A multivariate analysis revealed that the stroke subtype, the basal serum creatinine level, and the presence of infectious complications on admission were each predictors of developing AKI. In contrast, a free radical scavenger, edaravone, reduced the risk of developing AKI (multivariate-adjusted odds ratio [OR].45, 95% confidence interval [CI].30-.67). Propensity score-matched case-control study confirmed that edaravone use was negatively associated with AKI (propensity score-adjusted OR.46, 95% CI.29-.74). Conclusions: Although AKI has a significant impact on the clinical outcome of hospital inpatients, edaravone has a protective effect against the development of AKI in patients with acute ischemic stroke.
AB - Background: A free radical scavenger, edaravone, which has been used for the treatment of ischemic stroke, was reported to cause acute kidney injury (AKI) as a fatal adverse event. The aim of the present study was to clarify whether edaravone is associated with AKI in patients with acute ischemic stroke. Methods: From the Fukuoka Stroke Registry database, 5689 consecutive patients with acute ischemic stroke who were hospitalized within 24 hours of the onset of symptoms were included in this study. A logistic regression analysis for the Fukuoka Stroke Registry cohort was done to identify the predictors for AKI. A propensity score-matched nested case-control study was also performed to elucidate any association between AKI and edaravone. Results: Acute kidney injury occurred in 128 of 5689 patients (2.2%) with acute ischemic stroke. A multivariate analysis revealed that the stroke subtype, the basal serum creatinine level, and the presence of infectious complications on admission were each predictors of developing AKI. In contrast, a free radical scavenger, edaravone, reduced the risk of developing AKI (multivariate-adjusted odds ratio [OR].45, 95% confidence interval [CI].30-.67). Propensity score-matched case-control study confirmed that edaravone use was negatively associated with AKI (propensity score-adjusted OR.46, 95% CI.29-.74). Conclusions: Although AKI has a significant impact on the clinical outcome of hospital inpatients, edaravone has a protective effect against the development of AKI in patients with acute ischemic stroke.
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U2 - 10.1016/j.jstrokecerebrovasdis.2013.05.018
DO - 10.1016/j.jstrokecerebrovasdis.2013.05.018
M3 - Article
C2 - 23800495
AN - SCOPUS:84889057404
SN - 1052-3057
VL - 22
SP - e470-e476
JO - Journal of Stroke and Cerebrovascular Diseases
JF - Journal of Stroke and Cerebrovascular Diseases
IS - 8
ER -