Department of Respiratory Diseases, Children's Hospital of Chongqing Medical University/Ministry of Education Key Laboratory of Child Development and Disorders/National Clinical Research Center for Child Health and Disorders/China International Science and Technology Cooperation Base of Child Development and Critical Disorders/Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China com).
Zhongguo Dang Dai Er Ke Za Zhi. 2021 Nov 15;23(11):1127-1131. doi: 10.7499/j.issn.1008-8830.2108154.
To study the consistency between nasopharyngeal aspirates (NPA) and bronchoalveolar lavage fluid (BALF) in pathogen detection in children with pneumonia
A retrospective analysis was performed on the data of pathogens detected in 533 children with pneumonia from February 2017 to March 2020. The paired McNemar's test was used to compare the difference in pathogen detection between NPA and BALF groups. The coefficient was used to analyze the consistency in pathogen detection between the two groups.
NPA had a sensitivity of 28%, a specificity of 74%, a positive predictive value of 14%, and a negative predictive value of 91% in detecting bacteria, and a coefficient of 0.013 suggested poor consistency between NPA and BALF. NPA had a sensitivity of 52%, a specificity of 81%, a positive predictive value of 24%, and a negative predictive value of 94% in detecting viruses, and a coefficient of 0.213 suggested poor consistency between NPA and BALF. NPA had a sensitivity of 78%, a specificity of 71%, a positive predictive value of 49%, and a negative predictive value of 90% in detecting , and a coefficient of 0.407 suggested moderate consistency between NPA and BALF.
There is poor consistency between NPA and BALF in the detection of bacteria and viruses, and clinicians should be cautious in diagnosing lower respiratory tract infection based on bacteria or viruses detected in NPA. There is moderate consistency between NPA and BALF in the detection of , suggesting that it may be reliable to diagnose lower respiratory tract infection based on detected in NPA, while comprehensive judgment in combination with clinical conditions is needed.
研究鼻咽抽吸物(NPA)和支气管肺泡灌洗液(BALF)在儿童肺炎病原体检测中的一致性。
对 2017 年 2 月至 2020 年 3 月间 533 例肺炎患儿的病原体检测数据进行回顾性分析。采用配对 McNemar 检验比较 NPA 组和 BALF 组病原体检测的差异,采用 系数分析两组病原体检测的一致性。
NPA 检测细菌的灵敏度为 28%,特异度为 74%,阳性预测值为 14%,阴性预测值为 91%, 系数为 0.013,提示 NPA 与 BALF 之间一致性差。NPA 检测病毒的灵敏度为 52%,特异度为 81%,阳性预测值为 24%,阴性预测值为 94%, 系数为 0.213,提示 NPA 与 BALF 之间一致性差。NPA 检测 的灵敏度为 78%,特异度为 71%,阳性预测值为 49%,阴性预测值为 90%, 系数为 0.407,提示 NPA 与 BALF 之间一致性中等。
NPA 与 BALF 在细菌和病毒检测方面一致性差,临床医生应谨慎根据 NPA 中检测到的细菌或病毒来诊断下呼吸道感染。NPA 与 BALF 在 检测方面具有中等一致性,提示根据 NPA 中检测到的 来诊断下呼吸道感染可能是可靠的,但需要结合临床情况进行综合判断。