Langlass T M, Mickle T R
Owen Healthcare, Inc., McAllen Medical Center, TX 78503, USA.
Am J Health Syst Pharm. 1999 Mar 1;56(5):440-3. doi: 10.1093/ajhp/56.5.440.
A standard gentamicin dosage regimen intended to result in fewer trough concentrations of >2 microg/mL was studied. At a neonatal intensive care unit, gentamicin dosage guidelines of 2.5 mg/kg (as the sulfate) administered i.v. over 30 minutes every 12, 18, or 24 hours to neonates with a gestational age (GA) of > or =30 weeks were resulting in some relatively high trough serum concentrations (>2 microg/mL). Pharmacokinetic values derived for this baseline group were used to predict the gentamicin concentrations that would result from a standard regimen of gentamicin 3.5 mg/kg i.v. over 30 minutes every 24 hours. No patient in the baseline group was predicted to have a trough of >2 microg/mL with the new regimen, which was then approved for routine use. The new regimen was used for every neonate with a GA of > or =30 weeks who was admitted and treated with gentamicin (the protocol group). One set of concentrations was collected for each infant. Compared with the baseline group, the protocol group had significantly lower trough and significantly higher peak gentamicin concentrations. The total frequency of high troughs in the baseline group (23 [33%] of 69 patients) differed significantly from that in the protocol group (3 [4%] of 74 patients). No patient had or developed renal impairment. A gentamicin dosage protocol of 3.5 mg/kg every 24 hours for neonates with a GA of > or =30 weeks resulted in higher gentamicin peaks, lower troughs, and a lower frequency of troughs of >2 microg/mL, compared with previous dosage practice.
对一种旨在减少谷浓度>2微克/毫升情况的标准庆大霉素给药方案进行了研究。在一家新生儿重症监护病房,对于胎龄(GA)≥30周的新生儿,每12、18或24小时静脉注射2.5毫克/千克(以硫酸盐计)的庆大霉素给药指南,导致了一些相对较高的血清谷浓度(>2微克/毫升)。从该基线组得出的药代动力学值被用于预测每24小时静脉注射3.5毫克/千克庆大霉素的标准方案所产生的庆大霉素浓度。预测基线组中没有患者采用新方案时谷浓度会>2微克/毫升,随后该新方案被批准用于常规治疗。新方案用于每一位胎龄≥30周且入院接受庆大霉素治疗的新生儿(方案组)。为每个婴儿收集一组浓度数据。与基线组相比,方案组的庆大霉素谷浓度显著更低,峰浓度显著更高。基线组高谷浓度的总发生率(69例患者中的23例[33%])与方案组(74例患者中的3例[4%])有显著差异。没有患者出现或发生肾功能损害。与之前的给药实践相比,对于胎龄≥30周的新生儿,每24小时3.5毫克/千克的庆大霉素给药方案导致更高的庆大霉素峰浓度、更低的谷浓度以及更低的谷浓度>2微克/毫升的发生率。