Division of Pediatric Hematology/Oncology, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Kinderaerzte Kurwerk, Burgdorf, Switzerland.
PLoS One. 2021 Feb 12;16(2):e0246654. doi: 10.1371/journal.pone.0246654. eCollection 2021.
Fever in neutropenia (FN) is a potentially life-threatening complication of chemotherapy in pediatric cancer patients. The current standard of care at most institutions is emergency hospitalization and empirical initiation of broad-spectrum antibiotic therapy.
We analyzed in retrospect FN episodes with bacteremia in pediatric cancer patients in a single center cohort from 1993 to 2012. We assessed the distribution of pathogens, the in vitro antibiotic susceptibility patterns, and their trends over time.
From a total of 703 FN episodes reported, we assessed 134 FN episodes with bacteremia with 195 pathogens isolated in 102 patients. Gram-positive pathogens (124, 64%) were more common than Gram-negative (71, 36%). This proportion did not change over time (p = 0.26). Coagulase-negative staphylococci (64, 32%), viridans group streptococci (42, 22%), Escherichia coli (33, 17%), Klebsiella spp. (10, 5%) and Pseudomonas aeruginosa (nine, 5%) were the most common pathogens. Comparing the in vitro antibiotic susceptibility patterns, the antimicrobial activity of ceftriaxone plus amikacin (64%; 95%CI: 56%-72%), cefepime (64%; 95%CI 56%-72%), meropenem (64%; 95%CI 56%-72), and piperacillin/tazobactam (62%; 95%CI 54%-70%), respectively, did not differ significantly. The addition of vancomycin to those regimens would have increased significantly in vitro activity to 99% for ceftriaxone plus amikacin, cefepime, meropenem, and 96% for piperacillin/tazobactam (p < 0.001).
Over two decades, we detected a relative stable pathogen distribution and found no relevant trend in the antibiotic susceptibility patterns. Different recommended antibiotic regimens showed comparable in vitro antimicrobial activity.
中性粒细胞减少症(FN)发热是儿科癌症患者化疗中潜在的危及生命的并发症。目前,大多数机构的标准治疗方法是紧急住院并经验性地开始广谱抗生素治疗。
我们回顾性分析了 1993 年至 2012 年期间在单中心队列中发生的儿科癌症患者 FN 合并菌血症的 FN 发作。我们评估了病原体的分布、体外抗生素药敏模式及其随时间的变化趋势。
在报告的总共 703 例 FN 发作中,我们评估了 134 例 FN 合并菌血症发作,其中 102 例患者分离出 195 种病原体。革兰阳性病原体(124 种,64%)比革兰阴性病原体(71 种,36%)更为常见。这一比例在不同时间没有变化(p = 0.26)。凝固酶阴性葡萄球菌(64 株,32%)、草绿色链球菌(42 株,22%)、大肠埃希菌(33 株,17%)、克雷伯菌属(10 株,5%)和铜绿假单胞菌(9 株,5%)是最常见的病原体。比较体外抗生素药敏模式,头孢曲松联合阿米卡星(64%;95%CI:56%-72%)、头孢吡肟(64%;95%CI 56%-72%)、美罗培南(64%;95%CI 56%-72%)和哌拉西林/他唑巴坦(62%;95%CI 54%-70%)的抗菌活性无显著差异。在这些方案中加入万古霉素可使头孢曲松联合阿米卡星、头孢吡肟、美罗培南的体外活性显著增加至 99%,哌拉西林/他唑巴坦的体外活性增加至 96%(p < 0.001)。
在过去二十年中,我们发现病原体的分布相对稳定,抗生素药敏模式也没有发现明显的趋势。不同推荐的抗生素方案显示出相当的体外抗菌活性。