Institut de Recerca Sant Joan de Deu, Hospital Sant Joan de Deu, Barcelona, Spain; CIBER of Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain; Faculty of Medicine and Health Sciences, Universitat Internacional de Catalunya, Barcelona, Spain.
Pharmacy Department. Hospital Sant Joan de Deu, Barcelona, Spain.
Enferm Infecc Microbiol Clin (Engl Ed). 2022 Feb;40(2):53-58. doi: 10.1016/j.eimce.2020.08.010.
We aimed to determine the impact of utilizing a rapid panel test of respiratory viral and atypical bacteria (FilmArray® Respiratory Panel, FA RP) on etiological diagnosis of acute lower respiratory infection (ALRI) and antimicrobial stewardship in critical care pediatric patients.
Prospective cohort study of patients aged<18 years with clinical diagnosis of ALRI that were admitted to the Pediatric Intensive Care Unit (PICU) of Hospital Sant Joan de Deu (Barcelona, Spain) during December 2015-February 2017. Patients were diagnosed by FA RP and by a bundle of routine microbiological assays.
ALRI viral and bacterial etiology was confirmed by a composite reference standard of routine microbiological assays in 72 (55.4%) and 15 (11.5%) respiratory samples, respectively, that were collected from 130 children (median age, 3.5 months, IQR 1.1-14.8 months; 54.6% male). Comparatively, FA RP use increased etiological confirmation of ALRI in up to 123 (94.6%) samples (p<0.001) but only determined a bacterial origin in 2 (1.5%). Availability of diagnostic results before patient discharge from the PICU rose from 65.4 to 38.5% (p<0.001). Use of the new panel test directly influenced antimicrobial stewardship in 11 (8.4%) episodes, leading to discontinuation of antiviral drugs (n=5), administration of targeted antibiotics (n=3), antiviral therapy start (n=2) and both targeted antibiotic administration and discontinuation of antiviral drugs (n=1).
FA RP contributed to improve etiological diagnosis of ALRI in a timely manner while enhancing a more rational use of antimicrobial drugs in critical care pediatric patients.
我们旨在确定使用呼吸道病毒和非典型细菌快速检测试剂盒(FilmArray® Respiratory Panel,FA RP)对急性下呼吸道感染(ALRI)的病因诊断以及重症监护儿科患者的抗菌药物管理的影响。
这是一项前瞻性队列研究,纳入了 2015 年 12 月至 2017 年 2 月期间在西班牙巴塞罗那 Sant Joan de Deu 医院儿科重症监护病房(PICU)就诊的临床诊断为 ALRI 的<18 岁患者。通过 FA RP 和一系列常规微生物检测方法对患者进行诊断。
根据常规微生物检测的综合参考标准,在 130 名儿童(中位年龄为 3.5 个月,IQR 为 1.1-14.8 个月;54.6%为男性)的 15 份(11.5%)和 72 份(55.4%)呼吸道样本中证实了 ALRI 的病毒和细菌病因。相比之下,FA RP 的使用使 ALRI 的病因学确诊率增加到 123 份(94.6%)(p<0.001),但仅确定了 2 份(1.5%)为细菌来源。从 PICU 出院前获得诊断结果的患者比例从 65.4%上升到 38.5%(p<0.001)。新检测试剂盒的使用直接影响了 11 例(8.4%)患者的抗菌药物管理,导致停用抗病毒药物(n=5)、使用靶向抗生素(n=3)、开始抗病毒治疗(n=2)以及同时停用抗病毒药物和靶向抗生素(n=1)。
FA RP 有助于及时改善 ALRI 的病因诊断,并促进重症监护儿科患者更合理地使用抗菌药物。