Bell M J, Shackelford P, Smith R, Schroeder K
J Pediatr. 1984 Sep;105(3):482-6. doi: 10.1016/s0022-3476(84)80033-5.
The pharmacokinetics of intravenously administered clindamycin phosphate was studied in 40 children less than 1 year of age. Mean peak serum concentrations were 10.92 micrograms/ml in premature infants less than 4 weeks of age, 10.45 micrograms/ml in term infants greater than 4 weeks, and 12.69 micrograms/ml in term infants less than 4 weeks of age. Mean trough concentrations were 5.52, 2.8, and 3.03 micrograms/ml, respectively, in the same groups. Serum half-life was significantly longer (8.68 vs 3.60 hours) in premature compared with term infants less than 4 weeks of age. Both premature and term infants less than 4 weeks had significantly decreased clearance when compared with infants greater than 4 weeks (0.294 and 0.678, respectively, vs 1.58 L/hr). Clearance was significantly greater (1.919 vs 0.310 L/hr) and serum half-life less (1.75 vs 7.57 hours) in infants with body weight greater than 3.5 kg. On the basis of these data it is recommended that in infants greater than 4 weeks or greater than 3.5 kg, intravenous clindamycin dosage be 20 mg/kg/day in four divided doses. In premature neonates less than 4 weeks, the dose should be reduced to 15 mg/kg/day in three divided doses. Term infants greater than 1 week of age may also receive 20 mg/kg/day in four doses.
对40名1岁以下儿童静脉注射磷酸克林霉素的药代动力学进行了研究。小于4周的早产儿平均血清峰浓度为10.92微克/毫升,大于4周的足月儿为10.45微克/毫升,小于4周的足月儿为12.69微克/毫升。相同组别的平均谷浓度分别为5.52、2.8和3.03微克/毫升。与小于4周的足月儿相比,早产儿的血清半衰期明显更长(8.68小时对3.60小时)。与大于4周的婴儿相比,小于4周的早产儿和足月儿的清除率均显著降低(分别为0.294和0.678对1.58升/小时)。体重超过3.5千克的婴儿清除率明显更高(1.919对0.310升/小时),血清半衰期更短(1.75小时对7.57小时)。基于这些数据,建议4周以上或体重超过3.5千克的婴儿,静脉注射克林霉素剂量为每日20毫克/千克,分4次给药。对于小于4周的早产新生儿,剂量应减至每日15毫克/千克,分3次给药。大于1周龄的足月儿也可按每日20毫克/千克分4次给药。