Determinants for the prognosis of acute renal disorders that developed during or after treatment with edaravone

被引:26
作者
Hishida, Akira [1 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Med 1, Higashi Ku, Hamamatsu, Shizuoka 4313192, Japan
关键词
Edaravone; Renal disorder; Recovery rate of renal function; Mortality rate; Risk factor; Severe infection; RADICAL SCAVENGER; INJURY; PROTECTS; FAILURE; KIDNEY;
D O I
10.1007/s10157-008-0108-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Edaravone, a drug for treating acute ischemic stroke, has been reported to provoke acute renal disorders. In the previous study, the author evaluated the role of edaravone in the development of renal disorders in 207 patients reported as having developed them in the post-marketing survey of the drug. The overall recovery rate of renal function in the survey was 43%. Risk factors that affect the recovery rate of renal function and mortality remain to be clarified. The recovery rate of renal function and mortality rate were examined according to the extent of edaravone involvement in renal disorder onset, which was defined by the concurrence of other risk factors for renal disorders, in previously reported 207 patients. Risk factors for the nonrecovery of renal function and death were determined by using a stepwise logistic regression analysis. The recovery rate of renal function was low and mortality rate was high in the group where the above extent of edaravone involvement was slight. The above analysis showed that risk factors for the nonrecovery of renal function were the complication of severe infection and the implementation of blood purification, and that risk factors for death were advanced age (a parts per thousand yen80 years) and the complication of severe infection. The nonrecovery rate of renal function and mortality rate were high in the cases of patients that were complicated with factors that affected renal function other than edaravone. The complication of severe infection was a risk factor for the nonrecovery of renal function and for death.
引用
收藏
页码:118 / 122
页数:5
相关论文
共 9 条
[1]   A case report of acute renal failure and fulminant hepatitis associated with edaravone administration in a cerebral infarction patient [J].
Abe, Masanori ;
Kaizu, Kazo ;
Matsumoto, Koichi .
THERAPEUTIC APHERESIS AND DIALYSIS, 2007, 11 (03) :235-240
[2]   Radical scavenger edaravone developed for clinical use ameliorates ischemia/reperfusion injury in rat kidney [J].
Doi, K ;
Suzuki, Y ;
Nakao, A ;
Fujita, T ;
Noiri, E .
KIDNEY INTERNATIONAL, 2004, 65 (05) :1714-1723
[3]   Clinical analysis of 207 patients who developed renal disorders during or after treatment with edaravone reported during post-marketing surveillance [J].
Hishida A. .
Clinical and Experimental Nephrology, 2007, 11 (4) :292-296
[4]  
Lee VWS, 2007, DIS KIDNEY URINARY T, P986
[5]   The effect of acute renal failure on mortality - A cohort analysis [J].
Levy, EM ;
Viscoli, CM ;
Horwitz, RI .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (19) :1489-1494
[6]   Acute kidney injury in the intensive care unit according to RIFLE [J].
Ostermann, Marlies ;
Chang, Rene W. S. .
CRITICAL CARE MEDICINE, 2007, 35 (08) :1837-1843
[7]   A novel free radical scavenger, edarabone, protects against cisplatin-induced acute renal damage in vitro and in vivo [J].
Satoh, M ;
Kashihara, N ;
Fujimoto, S ;
Horike, H ;
Tokura, T ;
Namikoshi, T ;
Sasaki, T ;
Makino, H .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 305 (03) :1183-1190
[8]   A radical scavenger, edaravone, protects canine kidneys from ischemia-reperfusion injury after 72 hours of cold preservation and autotransplantation [J].
Tahara, M ;
Nakayama, M ;
Jin, MB ;
Fujita, M ;
Suzuki, T ;
Taniguchi, M ;
Shimamura, T ;
Furukawa, H ;
Todo, S .
TRANSPLANTATION, 2005, 80 (02) :213-221
[9]   The novel antioxidant edaravone: From bench to bedside [J].
Watanabe, Toshiaki ;
Tahara, Munenori ;
Todo, Satoru .
CARDIOVASCULAR THERAPEUTICS, 2008, 26 (02) :101-114