Buckingham Steven C, McCullers Jonathan A, Luján-Zilbermann Jorge, Knapp Katherine M, Orman Karen L, English B Keith
Department of Pediatrics, University of Tennessee Health Science Center, Le Bonheur Children's Medical Center, Memphis, Tennessee, USA.
Pediatrics. 2006 May;117(5):1688-94. doi: 10.1542/peds.2005-2282.
Experts recommend that children with suspected pneumococcal meningitis should empirically receive combination therapy with vancomycin plus either ceftriaxone or cefotaxime. The relationship between timing of the first dose of vancomycin relative to other antibiotics and outcome in these children, however, has not been addressed.
Medical records of children with pneumococcal meningitis at a single institution from 1991-2001 were retrospectively reviewed. Vancomycin start time was defined as the number of hours from initiation of cefotaxime or ceftriaxone therapy until the administration of vancomycin therapy. Outcome variables were death, sensorineural hearing loss, and other neurologic deficits at discharge. Associations between independent variables and outcome variables were assessed in univariate and multiple logistic regression analyses.
Of 114 subjects, 109 received empiric vancomycin therapy in combination with cefotaxime or ceftriaxone. Ten subjects (9%) died, whereas 37 (55%) of 67 survivors who underwent audiometry had documented hearing loss, and 14 (13%) of 104 survivors were discharged with other neurologic deficits. Subjects with hearing loss had a significantly shorter median vancomycin start time than did those with normal hearing (<1 vs 4 hours). Vancomycin start time was not significantly associated with death or other neurologic deficits in univariate or multivariate analyses. Multiple logistic regression revealed that hearing loss was independently associated with vancomycin start time <2 hours, blood leukocyte count <15000/microL, and cerebrospinal fluid glucose concentration <30 mg/dL.
Early empiric vancomycin therapy was not clinically beneficial in children with pneumococcal meningitis but was associated with a substantially increased risk of hearing loss. It may be prudent to consider delaying the first dose of vancomycin therapy until > or =2 hours after the first dose of parenteral cephalosporin in children beginning therapy for suspected or confirmed pneumococcal meningitis.
专家建议,疑似肺炎球菌性脑膜炎的儿童应经验性地接受万古霉素联合头孢曲松或头孢噻肟的联合治疗。然而,在这些儿童中,万古霉素首剂给药时间相对于其他抗生素的时间与治疗结果之间的关系尚未得到探讨。
回顾性分析了1991年至2001年在一家机构中患肺炎球菌性脑膜炎儿童的病历。万古霉素开始时间定义为从头孢噻肟或头孢曲松治疗开始至万古霉素治疗给药的小时数。结局变量为出院时的死亡、感音神经性听力损失和其他神经功能缺损。在单因素和多因素逻辑回归分析中评估自变量与结局变量之间的关联。
114名受试者中,109名接受了万古霉素经验性治疗联合头孢噻肟或头孢曲松。10名受试者(9%)死亡,而67名接受听力测定的幸存者中有37名(55%)记录有听力损失,104名幸存者中有14名(13%)出院时伴有其他神经功能缺损。听力损失的受试者万古霉素开始时间的中位数明显短于听力正常的受试者(<1小时对4小时)。在单因素或多因素分析中,万古霉素开始时间与死亡或其他神经功能缺损无显著关联。多因素逻辑回归显示,听力损失与万古霉素开始时间<2小时、血白细胞计数<15000/μL和脑脊液葡萄糖浓度<30mg/dL独立相关。
早期经验性万古霉素治疗对肺炎球菌性脑膜炎儿童在临床上并无益处,但与听力损失风险大幅增加相关。对于开始治疗疑似或确诊肺炎球菌性脑膜炎的儿童,考虑将万古霉素治疗的首剂推迟至静脉注射头孢菌素首剂后≥2小时可能是谨慎的做法。