Hartley Christopher, Morrisette Taylor, Malloy Katherine, Steed Lisa L, Dixon Terry, Garner Sandra S
From the Department of Pharmacy Services, Medical University of South Carolina Shawn Jenkins Children's Hospital, Charleston, South Carolina.
Department of Clinical Pharmacy & Outcomes Sciences, Medical University of South Carolina College of Pharmacy, Charleston, South Carolina.
Pediatr Infect Dis J. 2023 Dec 1;42(12):e461-e465. doi: 10.1097/INF.0000000000004132. Epub 2023 Oct 16.
Elizabethkingia anophelis is a Gram-negative bacillus that can exhibit highly resistant phenotypes against most antibiotics with evidence of efficacy and safety in the neonatal population. Given the limited antimicrobial options, clinicians may be forced into challenging treatment scenarios when faced with central nervous system infections in premature neonates caused by E. anophelis . We report a case of successful treatment of hospital-acquired meningitis and bacteremia caused by E. anophelis at 11 days of life in a male infant born at 29 weeks, 1 day gestation and birth weight of 1.41 kg. Therapy consisted of vancomycin, dose adjusted to maintain goal troughs of 15-20 mg/L, and rifampin 10 mg/kg/dose every 12 hours, with ciprofloxacin 15 mg/kg/dose every 12 hours and trimethoprim/sulfamethoxazole 5 mg/kg/dose every 12 hours added due to antimicrobial susceptibilities and unsatisfactory response, for a total of 21 days. Following initiation of this multidrug regimen, repeat cultures were negative, laboratory parameters improved [with exception of elevated cerebrospinal fluid (CSF) white blood cell count], the patient remained otherwise stable, and there were no adverse effects noted from therapy. Complications after treatment included the requirement of bilateral hearing aids and the development of hydrocephalus necessitating ventriculoperitoneal shunt placement. To our knowledge, we report the first case of meningitis in a premature neonate initially identified as E. anophelis in the United States treated with this regimen which led to successful microbiologic eradication with no antimicrobial safety concerns.
嗜蚊伊氏放线菌是一种革兰氏阴性杆菌,对大多数抗生素可表现出高度耐药表型,在新生儿群体中有疗效和安全性证据。鉴于抗菌选择有限,临床医生在面对由嗜蚊伊氏放线菌引起的早产儿中枢神经系统感染时,可能会被迫陷入具有挑战性的治疗场景。我们报告了一例在一名孕29周加1天出生、出生体重1.41千克的男婴出生11天时,成功治疗由嗜蚊伊氏放线菌引起的医院获得性脑膜炎和菌血症的病例。治疗方案包括万古霉素,剂量调整以维持目标谷浓度为15 - 20毫克/升,利福平每12小时10毫克/千克/剂量,由于抗菌药敏情况和反应不佳,加用环丙沙星每12小时15毫克/千克/剂量和甲氧苄啶/磺胺甲恶唑每12小时5毫克/千克/剂量,共治疗21天。开始这种多药联合治疗方案后,重复培养结果为阴性,实验室参数改善[脑脊液白细胞计数升高除外],患者其他方面保持稳定,且治疗未观察到不良反应。治疗后的并发症包括需要双侧助听器以及发生脑积水需要进行脑室腹腔分流术。据我们所知,我们报告了美国首例最初鉴定为嗜蚊伊氏放线菌的早产儿脑膜炎病例,采用该治疗方案成功根除微生物,且无抗菌药物安全性问题。