Lamarche Caroline, Pichette Maude, Ouimet Denis, Vallée Michel, Bell Robert, Ouellet Georges, Stewart John, Pichette Vincent
Department of nephrology, Maisonneuve-Rosemont Hospital, Montreal, Canada.
Sanofi Canada, Laval, Quebec.
Perit Dial Int. 2016 Jan-Feb;36(1):107-8. doi: 10.3747/pdi.2014.00328.
The aim of our study was to evaluate the efficacy and bioavailibility of a commonly used oral furosemide dose (500 mg) compared to a 250 mg intravenous (IV) dose in PD patients with significant residual renal function (urine volume > 100 mL). We also evaluated the immediate blood pressure effect in these patients. The data were obtained from a study we performed for the homologation of a 500-mg dose of furosemide by Health Canada.
我们研究的目的是评估常用口服呋塞米剂量(500毫克)与250毫克静脉注射剂量相比,在有显著残余肾功能(尿量>100毫升)的腹膜透析(PD)患者中的疗效和生物利用度。我们还评估了这些患者的即时血压效应。数据来自我们为加拿大卫生部对500毫克剂量呋塞米进行 homologation 而开展的一项研究。