Department of Pediatrics, Massachusetts General Hospital, Boston, Massachusetts; Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington; Seattle Children's Hospital, Seattle, Washington.
Pediatr Pulmonol. 2011 Feb;46(2):184-92. doi: 10.1002/ppul.21350. Epub 2010 Oct 20.
In cystic fibrosis (CF), conventional antibiotic susceptibility results correlate poorly with clinical outcomes. We hypothesized that biofilm testing would more accurately reflect the susceptibilities of bacteria infecting CF airways.
A multicenter randomized pilot trial was conducted to assess the efficacy and safety of using biofilm susceptibility testing of Pseudomonas aeruginosa sputum isolates to guide antibiotic regimens for chronic airway infections in clinically stable adolescent and adult CF patients. Thirty-nine participants were randomized to biofilm or conventional treatment groups; 14-day courses of two antibiotics were selected according to an activity-based algorithm using the corresponding susceptibility results.
Of the agents tested, meropenem was most active against biofilm-grown bacteria, and was included in regimens for about half of each study group. For 19 of 39 randomized participants, randomization to the other study group would not have changed the antibiotic classes of the assigned regimen. Study groups were comparable at baseline, and had similar mean decreases in bacterial density, measured in log(10) colony forming units per gram of sputum (biofilm, -2.94 [SD 2.83] vs. conventional, -3.27 [SD 3.09]), and mean increases in forced expiratory volume in 1 sec, measured in liters (0.18 [SD 0.20] vs. 0.12 [SD 0.22]).
In this pilot study, antibiotic regimens based on biofilm testing did not differ significantly from regimens based on conventional testing in terms of microbiological and clinical responses. The predictive value of biofilm testing may nonetheless warrant evaluation in an adequately powered clinical trial in younger CF patients or those experiencing acute pulmonary exacerbation.
在囊性纤维化(CF)中,传统的抗生素药敏结果与临床结果相关性较差。我们假设生物膜检测将更准确地反映感染 CF 气道的细菌的敏感性。
进行了一项多中心随机试点试验,以评估使用铜绿假单胞菌痰液分离物的生物膜药敏试验来指导临床稳定的青少年和成年 CF 患者慢性气道感染的抗生素方案的疗效和安全性。39 名参与者随机分为生物膜或常规治疗组;根据基于活性的算法,根据相应的药敏结果选择为期 14 天的两种抗生素疗程。
在所测试的药物中,美罗培南对生物膜生长的细菌最具活性,并且包含在每个研究组的一半左右的方案中。对于 39 名随机参与者中的 19 名,随机分配到另一个研究组不会改变分配方案的抗生素类别。研究组在基线时具有可比性,并且在细菌密度方面具有相似的平均降低,以每克痰的对数(10)菌落形成单位(生物膜,-2.94[SD 2.83]与常规,-3.27[SD 3.09])和用力呼气量的平均增加测量,以升为单位(0.18[SD 0.20]与 0.12[SD 0.22])。
在这项试点研究中,基于生物膜检测的抗生素方案在微生物学和临床反应方面与基于常规检测的方案没有显著差异。生物膜检测的预测价值可能需要在年轻 CF 患者或经历急性肺部恶化的患者中进行充分功率的临床试验中进行评估。