摘要
目的:分析诺唯赞量子点荧光分析仪对检验小儿感染性肺炎的应用价值。方法:纳入2023年4月1日~2023年8月31日医院临床收治的小儿感染性肺炎患者93例为研究对象,采用诺唯赞全自动量子点荧光免疫分析仪QD-S1200、迈瑞BC-6000plus全自动血液细胞分析仪以及普门特定蛋白分析仪PA-900检测93例患儿白细胞、超敏-C反应蛋白(hs-CRP)、白细胞介素-6 (IL-6)、降钙素原(PCT)、血清淀粉样蛋白A(SAA),探究不同检测仪器在小儿感染性肺炎诊断中的应用价值。结果:利用诺唯赞全自动量子点荧光免疫分析仪QDS1200、迈瑞BC-6000plus全自动血液细胞分析仪以及普门特定蛋白分析仪PA-900检测检出93例患儿白细胞(10.12±0.23)×10~9/L、hs-CRP (21.01±7.85) mg/L、PCT (0.44±0.06) ng/mL、IL-6 (39.24±6.32) pg/mL、SAA(101.28±29.63) mg/L;诺唯赞全自动量子点荧光免疫分析仪QD-S1200阳性检出率为100.00%,迈瑞BC-6000plus全自动血液细胞分析仪阳性检出率为97.85%,普门特定蛋白分析仪PA-900阳性检出率为96.77%,三组间差异无统计学意义(P>0.05);采用诺唯赞全自动量子点荧光免疫分析仪QD-S1200在感染性肺炎患儿不同指标检验中检出时间更短,差异有统计学意义(P<0.05);诺唯赞全自动量子点荧光免疫分析仪QD-S1200对hs-CRP、PCT、IL-6、SAA2个不同浓度质控品测定中,批内精密度<10%,批间精密度<15%,5项指标检测精密度较高。结论:诺唯赞全自动量子点荧光免疫分析仪QD-S1200检测小儿感染性肺炎相关实验室指标水平阳性率高,且检测等待时间更短,临床检测综合应用价值高。
Objective:To analyze the application value of the Vazyme quantum dot fluorescence analyzer in detecting infectious pneumonia in children.Methods:A study included 93 pediatric infectious pneumonia patients from April 1,2023 to August 31,2023,white blood cells of QD-S1200,Mindray BC-6000plus and PA-900(white blood cell,WBC),hypersensitivity-C-reactive protein(hypersensitivity-C-reactive protein;hs-CRP),interleukin-6(interleukin-6,IL-6),procalcitonin(PCT),and serum amyloid A(serum amyloid protein A,SAA),explore the application value of different monitoring instruments in the diagnosis of pediatric infectious pneumonia.Results:93 pediatric patients were detected to have white blood cells(10.12±0.23)×109/L,hs CRP(21.01±7.85)mg/L,PCT(0.44±0.06)ng/mL,IL-6(39.24±6.32)pg/mL,and SAA(101.28±29.63)mg/L using the Vazyme fully automated quantum dot fluorescence immunoassay analyzer QDS120,Mindray BC-6000plus fully automated hematology analyzer,and Pumen specific protein analyzer PA-900;The positive detection rate of the Vazyme fully automatic quantum dot fluorescence immunoassay analyzer QD-S1200 was 100.00%,the positive detection rate of the Mindray BC-6000plus fully automatic blood cell analyzer was 97.85%,and the positive detection rate of the Pumen specific protein analyzer PA-900 was 96.77%.There was no statistically significant difference among the three groups(P>0.05);The detection time of different indicators in children with infectious pneumonia was shorter and the difference was statistically significant(P<0.05)using the Vazyme fully automatic quantum dot fluorescence immunoassay analyzer QD-S1200;In the determination of two different concentration quality control samples,hs CRP,PCT,IL-6,and SAA,using the Vazyme fully automatic quantum dot fluorescence immunoassay analyzer QD-S1200,the intra batch precision was less than 10%,the inter batch precision was less than 15%,and the detection precision of five indicators was relatively high.Conclusion:QD immunoanalyzer QD-S1200 for pediatric infectious pneumonia is high,and the waiting time is shorter,and the comprehensive application value of clinical testing is high.
作者
邢双
裴彧
XING Shuang;PEI Yu(Department of Laboratory,Tianjin Binhai New Area Tanggu Obstetrics and Gynecology Hospital,Tianjin 300451)
出处
《中国医疗器械信息》
2024年第21期119-121,共3页
China Medical Device Information
基金
2019年度天津市滨海新区卫生健康委科技项目(项目名称:天津市滨海新区不同年龄段儿童肺炎支原体感染特征流行病学调查研究,项目编号:2019BWKY013)。