热带病与寄生虫学 ›› 2024, Vol. 22 ›› Issue (5): 301-305.doi: 10.20199/j.issn.1672-2302.2024.05.009

• 临床研究 • 上一篇    下一篇

不同实验室检测技术在非结核病定点医院诊断肺结核的效果评价

王甜甜(), 王晓君, 吴刚, 周美兰, 张正斌, 鲁周琴, 李月华()   

  1. 武汉市肺科医院(武汉市结核病防治所),湖北武汉430030
  • 收稿日期:2024-03-05 出版日期:2024-10-20 发布日期:2024-11-15
  • 通信作者: 李月华, E-mail: 664748060@qq.com
  • 作者简介:王甜甜,女,硕士,医师,研究方向:结核病预防控制。E-mail: 1178443298@qq.com
  • 基金资助:
    湖北省自然科学基金项目(2022CFB176);武汉市医学科学研究项目(WX23Q46)

Evaluation of the effectiveness of different laboratory testing technologies in diagnosing pulmonary tuberculosis at non-tuberculosis designated hospitals

WANG Tiantian(), WANG Xiaojun, WU Gang, ZHOU Meilan, ZHANG Zhengbin, LU Zhouqin, LI Yuehua()   

  1. Wuhan Pulmonary Hospital (Wuhan Tuberculosis Prevention and Control Institute), Wuhan 430030, Hubei Province, China
  • Received:2024-03-05 Online:2024-10-20 Published:2024-11-15
  • Contact: LI Yuehua, E-mail: 664748060@qq.com

摘要:

目的 分析不同实验室检测技术在非结核病定点医院(简称非定点医院)首次就诊肺结核患者中的使用情况和效果,为非定点医院优化结核病检测流程提供参考。方法 在中国疾病预防控制信息系统传染病报告管理信息系统(简称传染病报告系统)中选择2021年1月—2022年6月由武汉市6家非定点医院报告的初次建档收治、并经结核病定点医院确诊的肺结核患者为研究对象。在传染病报告系统中搜集患者个案资料,在非定点医院信息系统中搜集患者就诊期间的结核病相关检查结果、诊断信息等资料。比较不同实验室检测技术在非定点医院单独或联合使用对结核病患者的检出率,并比较开展与未开展GeneXpert MTB/RIF(简称GeneXpert)检测患者的诊断天数、诊断费用、利福平耐药检出情况等指标。结果 研究共纳入确诊肺结核患者386例,其中8例为利福平耐药患者。非定点医院采用单一实验室检测技术时,GeneXpert、分枝杆菌培养、结核分枝杆菌DNA(TB-DNA)检测、涂片抗酸染色的检出率分别为86.79%(138/159)、79.37%(50/63)、75.00%(45/60)、48.25%(138/286);采用两种实验室检测技术时,GeneXpert+分枝杆菌培养、GeneXpert+涂片抗酸染色、涂片抗酸染色+分枝杆菌培养的检出率分别为90.00%(45/50)、84.75%(100/118)、79.66%(47/59)。开展GeneXpert检测的患者结核病平均诊断天数和诊断费用分别为1(1,1)d和(2 039±2 075)元,未开展的患者则分别为4(2,9)d和(3 140±4 557)元,差异均有统计学意义(H=110.975,t=-3.198;P均<0.01)。GeneXpert组和非GeneXpert组均有4例利福平耐药患者,GeneXpert组检出3例,非GeneXpert组未能检出。结论 非定点医院利用GeneXpert检测诊断肺结核患者的平均成本相对较低,若联合开展GeneXpert检测和常规痰检将有利于普通肺结核和利福平耐药肺结核的诊断,对早期快速发现传染源、控制肺结核流行传播具有重要意义。

关键词: 肺结核, 非结核病定点医院, 实验室检测技术, 效果评价

Abstract:

Objective To investigate the application and effectiveness of different laboratory testing technologies in the tuberculosis patients at first visit in the non-designated tuberculosis hospitals for evidences in optimizing the testing procedures for diagnosis of tuberculosis in these hospitals. Methods The pulmonary tuberculosis patients who were initially registered and admitted in six non-designated hospitals in Wuhan City and subsequently confirmed as tuberculosis in the designated hospital, reported in the Infectious Disease Reporting and Management System under the China Information System for Disease Control and Prevention from January 2021 to June 2022, were included as study subjects. Individual patient data were collected from the Infectious Disease Reporting System, and tuberculosis-related test results, diagnostic information, and other data during the patients′ visits were gathered from the information systems of the non-designated hospitals. Then the detection rate was compared among the patients underwent single or combined tests in the non-designated hospitals by different laboratory testing technologies. Finally, the days of diagnosis, cost of diagnosis, and detection of rifampicin resistance were analyzed between patients who received GeneXpert MTB/RIF (GeneXpert) system test and those who did not. Results A total of 386 confirmed tuberculosis patients were finally included, in whom 8 were rifampicin resistant. When a single laboratory testing technology was used in non-designated hospitals, the detection rate by GeneXpert system, mycobacterial culture, tuberculosis deoxyribonucleic acid test (TB-DNA) and smear acid-fast staining was 86.79% (138/159), 79.37% (50/63), 75.00% (45/60) and 48.25% (138/286), respectively. When two laboratory testing technologies were applied in combination, the detection rate by GeneXpert system + mycobacterial culture, GeneXpert + smear acid-fast staining, and smear acid-fast staining + mycobacterial culture arrived at 90.00% (45/50), 84.75% (100/118) and 79.66% (47/59), respectively. The average days to tuberculosis diagnosis and the average diagnostic cost for patients who underwent GeneXpert system testing were 1 (1, 1) day and (2 039 ± 2 075) yuan, respectively, compared to 4 (2, 9) days and (3 140 ± 4 557) yuan for those who did not undergo GeneXpert system testing. The difference was significant (H=110.975, t=-3.198, both P<0.01). In both the GeneXpert group and the non-GeneXpert group, there were 4 patients resistant to rifampin. The GeneXpert group detected 3 cases, while the non-GeneXpert group did not detect any. Conclusion The average cost of diagnosis is relatively lower by application of GeneXpert test for detection of tuberculosis in non-tuberculosis designated hospitals, and combined GeneXpert system with other detection technology and routine sputum examination can be conductive to diagnosis of common tuberculosis and rifampicin-resistant tuberculosis, which is of great significance for rapid sourcing of the infection and control of tuberculosis spreading.

Key words: Pulmonary tuberculosis, Non-tuberculosis designated hospital, Laboratory testing technology, Effect evaluation

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