Madhavan T, Yaremchuk K, Levin N, Fisher E, Cox F, Burch K, Haas E, Pohlod D, Quinn E L
Antimicrob Agents Chemother. 1975 Jul;8(1):63-6. doi: 10.1128/AAC.8.1.63.
Serum and urinary levels of cefazolin were determined after a 500-mg parenteral dose in eight azotemic volunteers. The mean peak serum concentration was 1.5 to 5 times the levels obtained in nonazotemic patients. The serum half-life of cefazolin was increased significantly. In patients on dialysis, the mean serum half-life of cefazolin was 4.05 h during (or after) hemodialysis, and 32.1 h during (or after) peritoneal dialysis. There was a significant decrease in cefazolin removal when dialysate flow or membrane surface area of the dialyzer were decreased. It was also shown that one circuit through the dialysis unit caused measurable decrease in cefazolin concentration. These data and previously published reports suggest: (i) the maintenance dose of cefazolin can be decreased in azotemic patients; (ii) patients on hemodialysis will require an additional half dose after dialysis because of efficient removal during hemodialysis; and (iii) patients on peritoneal dialysis do not require an extra dose.
在8名氮血症志愿者接受500毫克胃肠外给药剂量后,测定了头孢唑林的血清和尿液水平。平均血清峰值浓度是非氮血症患者所获水平的1.5至5倍。头孢唑林的血清半衰期显著延长。在接受透析的患者中,血液透析期间(或之后)头孢唑林的平均血清半衰期为4.05小时,腹膜透析期间(或之后)为32.1小时。当透析液流量或透析器膜表面积减小时,头孢唑林的清除率显著降低。还表明,通过透析装置的一个回路会导致头孢唑林浓度出现可测量的下降。这些数据和先前发表的报告表明:(i)氮血症患者中头孢唑林的维持剂量可以降低;(ii)血液透析患者在透析后需要额外补充半剂,因为血液透析期间清除效率较高;(iii)腹膜透析患者不需要额外剂量。