Department of Pediatric Pulmonology, CF-Clinic and Pediatric Infectious Diseases, niversitair Ziekenhuis Brussel (UZ Brussel), Brussels.
Clin Infect Dis. 2011 Jun 15;52(12):1437-44. doi: 10.1093/cid/cir235.
Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging.
We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute nonresponsive CAP (NR-CAP; n = 127) or recurrent CAP (Rec-CAP; n = 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture of BAL fluid (significance cutoff point, ≥ 10⁴ colony-forming units/mL) was used. Blood culture results, serological test results, nasopharyngeal secretion findings, and pleural fluid culture results were also assessed, where available.
An infectious agent was detected in 76.0% of cases. In 51.2% of infections, aerobic bacteria were isolated, of which 75.0%, 28.9%, and 13.3% were Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae, respectively. Most (97.9%) of the H. influenzae strains were nontypeable (NTHi). H. influenzae was detected in 26.0% of NR-CAP cases and 51.2% of Rec-CAP cases, whereas Mycoplasma pneumoniae was the predominant pathogen in the NR-CAP group (accounting for 34.9% of cases) but not in the Rec-CAP group (19.3%). Viruses were found in 30.4% of cases, with respiratory syncytial virus, parainfluenzaviruses, and influenzaviruses detected most frequently. Mixed infections were found in 18.9% of NR-CAP cases and 30.1% of Rec-CAP cases.
A variety of microorganisms were isolated with frequent mixed infection. NTHi was one of the major pathogens found, especially in association with recurrent CAP, possibly because of improved detection with the FOB with BAL procedure. This suggests that the burden of pediatric CAP could be reduced by addressing NTHi as a major causative pathogen.
小儿社区获得性肺炎(CAP)的精确病因诊断仍然具有挑战性。
我们对两组接受纤维支气管镜(FOB)下支气管肺泡灌洗(BAL)的小儿 CAP 病因进行了回顾性研究;一组为急性非应答性 CAP(NR-CAP;n=127)患儿,另一组为复发性 CAP(Rec-CAP;n=123)患儿。采取了程序措施以限制污染风险,并使用 BAL 液的定量细菌培养(意义截断点,≥10⁴菌落形成单位/mL)。还评估了血培养结果、血清学检测结果、鼻咽分泌物发现和胸腔液培养结果(如果有)。
76.0%的病例检测到感染病原体。在 51.2%的感染中,分离出需氧菌,其中 75.0%、28.9%和 13.3%分别为流感嗜血杆菌、卡他莫拉菌和肺炎链球菌。大多数(97.9%)流感嗜血杆菌菌株为不可分型(NTHi)。NTHi 见于 26.0%的 NR-CAP 病例和 51.2%的 Rec-CAP 病例,而肺炎支原体是 NR-CAP 组的主要病原体(占 34.9%的病例),但不是 Rec-CAP 组(19.3%)的主要病原体。30.4%的病例发现病毒,最常检测到呼吸道合胞病毒、副流感病毒和流感病毒。18.9%的 NR-CAP 病例和 30.1%的 Rec-CAP 病例存在混合感染。
分离出多种微生物,且常存在混合感染。NTHi 是主要病原体之一,特别是与复发性 CAP 有关,可能是由于 FOB 联合 BAL 程序提高了检测率。这表明,通过将 NTHi 作为主要致病病原体来解决,可以减轻小儿 CAP 的负担。