Namtu Katie C, Crain Julianna C, Messina Allison F, Dumois Juan A, Berman David M
Department of Pharmacy, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.
Division of Pediatric Infectious Diseases, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.
Pharmacotherapy. 2017 Jan;37(1):105-108. doi: 10.1002/phar.1872. Epub 2017 Jan 6.
The management of gram-positive infections has been complicated in recent years by the emergence of antimicrobial resistance, leaving fewer options for therapy. Daptomycin is a lipopeptide antibiotic used for the systemic treatment of gram-positive infections. It has a distinct mechanism of action and a favorable side effect profile, and it requires once/day dosing. Unfortunately, there is a paucity of safety, efficacy, and pharmacokinetic data in neonatal and pediatric patients. The objective of this study was to review our experience with daptomycin use for the treatment of gram-positive infections in these patient populations.
We conducted a retrospective analysis of electronic medical records of hospitalized children who received daptomycin between October 2008 and June 2014 for the treatment of proven gram-positive infections.
Of the 146 patients who received at least 3 days of daptomycin therapy, 109 patients had a proven gram-positive infection and were included for further analysis. Of the 109 patients, 71 were males (65%) and the median age was 12 years (range: 2.5 mo to 24 yrs). The median duration of therapy was 12 days (range: 3-121 days; mean = 16 days). Catheter-related bloodstream infections were the most common type of infections (n=81 patients) in those receiving daptomycin treatment. One hundred seven patients (98%) had documented improvement and resolution at the time of hospital discharge. One hundred four patients (95%) had a baseline creatine phosphokinase (CPK) level obtained. Of these 104 patients, 48 (46%) had at least one follow-up CPK level after the start of therapy. Three patients' charts showed laboratory evidence of elevated CPK values.
The majority of patients demonstrated clinical improvement after receiving daptomycin as primary therapy for proven gram-positive infections. Larger randomized controlled trials focusing on safety and efficacy are necessary to assess these outcomes with daptomycin use in the pediatric population.
近年来,由于抗菌药物耐药性的出现,革兰氏阳性菌感染的治疗变得复杂,可供选择的治疗方案减少。达托霉素是一种用于全身治疗革兰氏阳性菌感染的脂肽类抗生素。它具有独特的作用机制和良好的副作用谱,且每日只需给药一次。遗憾的是,关于新生儿和儿科患者的安全性、疗效及药代动力学数据较少。本研究的目的是回顾我们使用达托霉素治疗这些患者群体革兰氏阳性菌感染的经验。
我们对2008年10月至2014年6月期间因确诊革兰氏阳性菌感染而接受达托霉素治疗的住院儿童的电子病历进行了回顾性分析。
在146例接受至少3天达托霉素治疗的患者中,109例确诊为革兰氏阳性菌感染并纳入进一步分析。在这109例患者中,71例为男性(65%),中位年龄为12岁(范围:2.5个月至24岁)。中位治疗持续时间为12天(范围:3 - 121天;平均 = 16天)。导管相关血流感染是接受达托霉素治疗患者中最常见的感染类型(n = 81例患者)。107例患者(98%)在出院时记录显示病情改善并得到缓解。104例患者(95%)获得了基线肌酸磷酸激酶(CPK)水平。在这104例患者中,48例(46%)在治疗开始后至少有一次随访CPK水平。3例患者的病历显示有CPK值升高的实验室证据。
大多数患者在接受达托霉素作为确诊革兰氏阳性菌感染的主要治疗后临床症状有所改善。有必要开展更大规模的关注安全性和疗效的随机对照试验,以评估在儿科人群中使用达托霉素的这些结果。