Ye Sheng, Zhang Chenmei, Lin Shupeng
Pediatric Intensive Care Unit, Children's Hospital Zhejiang University School of Medicine, No. 3333, Binsheng Road, Hangzhou, 310052, China.
Division of Hematology-Oncology, Children's Hospital Zhejiang University School of Medicine, No. 57, Zhugan Road, Hangzhou, 310003, China.
Eur J Pediatr. 2018 Oct;177(10):1489-1496. doi: 10.1007/s00431-018-3208-9. Epub 2018 Jul 14.
Severe infection is a primary cause of mortality in children facing challenges from multidrug-resistant (MDR) pathogens, particularly MDR Acinetobacter baumannii. Tigecycline has an expanded spectrum of antibacterial activity, and some successful instances of its use in children have been reported. We conducted a retrospective chart review of children treated at a tertiary hospital between May 1, 2012 and May 1, 2017 to examine the efficacy and safety of tigecycline in children with severe infection. A total of 110 patients (69 males) were enrolled in this study, including 46 MDR A. baumannii infection patients, encompassing 51 A. baumannii strains. Totally, the median duration of tigecycline therapy was 10 days (range, 2-47 days), with a clinical improvement rate of 47.27% (52/110). In A. baumannii infection group, the clinical improvement rate was 50% (23/46) and the microbiology eradication rate was 50.98% (26/51). No adverse events were reported during therapy; however, in one case, a 9-year-old boy with hematologic disease developed tooth discoloration.Conclusion: Although some patients benefited from tigecycline, the efficacy and safety of tigecycline should not be overvalued. Additional data from randomized controlled trials are required to assess the administration of tigecycline. What is Known: • Severe infection is a primary cause of mortality in pediatric patients and its treatment is facing challenges from an increasing number of multidrug-resistant (MDR) pathogens. • Tigecycline has an expanded spectrum of antibacterial activity. • Several case reports have indicated that tigecycline could be used as a salvage therapy in children when options are limited or non-existent. What is New: • We found that rate of clinical improvement was different in various groups of different infection. The efficacy of tigecycline should not be overvalued. • Six dosage models and different infection types were observed in our series, with different improvement and eradication rate, indicating that more data are required to identify a proper tigecycline dosage.
严重感染是面临多重耐药(MDR)病原体挑战的儿童死亡的主要原因,尤其是多重耐药鲍曼不动杆菌。替加环素具有更广泛的抗菌活性谱,并且已有一些其在儿童中使用成功的实例报道。我们对2012年5月1日至2017年5月1日在一家三级医院接受治疗的儿童进行了一项回顾性病历审查,以研究替加环素在重症感染儿童中的疗效和安全性。本研究共纳入110例患者(69例男性),其中包括46例多重耐药鲍曼不动杆菌感染患者,涉及51株鲍曼不动杆菌菌株。总体而言,替加环素治疗的中位持续时间为10天(范围2 - 47天),临床改善率为47.27%(52/110)。在鲍曼不动杆菌感染组中,临床改善率为50%(23/46),微生物清除率为50.98%(26/51)。治疗期间未报告不良事件;然而,有1例患有血液系统疾病的9岁男孩出现牙齿变色。结论:虽然一些患者从替加环素中获益,但不应高估替加环素的疗效和安全性。需要来自随机对照试验的更多数据来评估替加环素的给药情况。已知信息:• 严重感染是儿科患者死亡的主要原因,其治疗正面临来自越来越多多重耐药(MDR)病原体的挑战。• 替加环素具有更广泛的抗菌活性谱。• 几例病例报告表明,当选择有限或不存在时,替加环素可作为儿童的挽救疗法。新发现:• 我们发现不同感染组的临床改善率不同。不应高估替加环素的疗效。• 在我们的系列研究中观察到六种剂量模式和不同的感染类型,具有不同的改善和清除率,表明需要更多数据来确定合适的替加环素剂量。