Garcia I, Fainstein V, Smith R G, Bodey G P
Antimicrob Agents Chemother. 1983 Aug;24(2):141-4. doi: 10.1128/AAC.24.2.141.
The pharmacokinetic parameters of ceftazidime were determined in 25 patients with neoplastic diseases. A group of 13 patients each received 1 g of ceftazidime over 15 min as a single intravenous dose. The mean peak drug concentration in serum was 77.4 micrograms/ml, and the serum half-life was 144 min. Urinary excretion at 12 h was 64.5%. These 13 patients also received 2 g of ceftazidime over 15 min at 8-h intervals for 7 or 8 days. The mean peak drug concentrations in serum were 103.6 micrograms/ml on day 1 and 87 micrograms/ml on day 7 or 8. A second group of 12 patients received 1 g of ceftazidime over 30 min, followed by 1 g over 2 h and every 4 h thereafter. The mean peak drug concentration in serum at 30 min was 57.5 micrograms/ml. Average peak and trough levels obtained on day 2 or 3 were 65 and 34.8 micrograms/ml, respectively, and remained in this range thereafter. The above-mentioned dose schedules produced high and adequate ceftazidime concentrations in serum.
对25例肿瘤疾病患者测定了头孢他啶的药代动力学参数。一组13例患者,每例均在15分钟内静脉注射1克头孢他啶作为单次剂量。血清中药物平均峰值浓度为77.4微克/毫升,血清半衰期为144分钟。12小时的尿排泄率为64.5%。这13例患者还每隔8小时在15分钟内静脉注射2克头孢他啶,共注射7或8天。第1天血清中药物平均峰值浓度为103.6微克/毫升,第7或8天为87微克/毫升。另一组12例患者,先在30分钟内静脉注射1克头孢他啶,随后在2小时内静脉注射1克,此后每4小时注射1克。30分钟时血清中药物平均峰值浓度为57.5微克/毫升。第2或3天测得的平均峰值和谷值水平分别为65和34.8微克/毫升,此后一直保持在此范围内。上述给药方案在血清中产生了高且合适的头孢他啶浓度。