在野外环境中直接检测结核分枝杆菌的 "TBDetect 痰显微镜套件 "的操作可行性和多中心评估。

Infectious diseases (London, England) Pub Date : 2024-12-01 Epub Date: 2024-08-16 DOI:10.1080/23744235.2024.2375599
Keerti Chauhan, Rakesh Kumar Gupta, Divya Anthwal, Nikita Panwalkar, Prabha Desikan, Manpreet Bhalla, Ritu Singhal, Vithal Prasad Myneedu, Khalid Umar Khayyam, Siva Kumar Shanmugam, K Silambu Chelvi, A Radhakrishnan, Padmapriyadarsini Chandrasekaran, Sidhartha Giri, Jyotirmayee Turuk, Dasarathi Das, Sanghamitra Pati, Abhinav Goyal, Ashawant Gupta, Nalini Kant Gupta, Manjula Singh, Jaya Sivaswami Tyagi, Sagarika Haldar
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引用次数: 0

摘要

背景:印度主要依靠直接涂片显微镜诊断结核病(TB)。然而,涂片显微镜的灵敏度较低,因此需要提高其性能。我们最近介绍了 "TBDetect "试剂盒的开发情况,该试剂盒在印度国家参考实验室(NRLs)的使用情况显示,其性能优于直接涂片显微镜检查:本研究旨在评估 "TBDetect "显微镜在现场环境中的操作可行性。方法:本研究旨在评估 "TBDetect "显微镜在野外环境中的操作可行性。在布巴内斯瓦尔、博帕尔、钦奈和新德里的 4 个 NRL 下的指定显微镜检查中心(DMCs,n = 13)就诊的连续推定肺结核患者(n = 5300 人)进行 "TBDetect "显微镜检查与 LED 荧光显微镜检查(LED-FM)的性能评估,以及(ii)使用半结构式问卷调查从科学家(n = 10 人)和实验室技术人员(n = 42 人)处获得以下参数的反馈意见:在 DMC 启动 "TBDetect "显微镜检查的可行性、样本制备和检测、培训、出结果所需的时间、后勤和故障排除。此外,还使用了一份评分问卷来评估 "TBDetect "显微镜与 LED-FM 显微镜的对比,并使用配对 t 检验来计算得分的统计学意义:结果:在所有地点,"TBDetect "显微镜检查的总体阳性率为 10.32%(547/5300),而 LED-FM 检查的阳性率为 8.96%(475/5300),两者的阳性率差异显著(p = 0.019)。此外,与 LED-FM 相比,"TBDetect "显微镜检查可提高涂片等级状态(p = 0.043)。研究负责人和试剂盒使用者的反馈表明,"TBDetect "显微镜检查很容易在护理点环境中使用。对评分反馈的分析表明,与 LED-FM 相比,'TBDetect'显微镜检查更易于操作和观察(p 结论:'TBDetect'显微镜检查在临床上是可行的:这项研究证实了 "TBDetect "显微镜在野外环境中的可行性。
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Operational feasibility and multi-centric evaluation of 'TBDetect sputum microscopy kit' for the direct detection of Mycobacterium tuberculosis in field settings.

Background: India relies primarily on direct smear microscopy for tuberculosis (TB) diagnosis. However, the low sensitivity of smear microscopy emphasizes the need to improve its performance. We recently described the development of 'TBDetect' kit which showed improved performance over direct smear microscopy at National Reference Laboratories (NRLs) in India.

Methods: The present study was aimed to assess the operational feasibility of 'TBDetect' microscopy in field settings. This was evaluated by (i) assessing the performance of 'TBDetect' microscopy vs. LED-fluorescence microscopy (LED-FM) on consecutive presumptive pulmonary TB patients (n = 5300) who attended Designated Microscopy Centres (DMCs, n = 13) under 4 NRLs at Bhubaneswar, Bhopal, Chennai, and New Delhi, and (ii) obtaining feedback from Scientists (n = 10) and laboratory technicians (n = 42) using semi-structured questionnaires under the following parameters: feasibility of initiation of 'TBDetect' microscopy in DMCs, sample preparation and testing, training, time-to-result, logistics, and troubleshooting. A scoring questionnaire was also used to assess 'TBDetect' microscopy vs. LED-FM and statistical significance of the scores was calculated using paired t-test.

Results: The overall positivity of 'TBDetect' microscopy was 10.32% (547/5300) vs. 8.96% (475/5300) of LED-FM at all sites and the increment in positivity was significant (p = 0.019). In addition, 'TBDetect' microscopy yielded an increment in smear grade status over LED-FM (p = 0.043). The feedback from the study-in-charge and kit users indicated that 'TBDetect' microscopy was easily adapted in point-of-care settings. An analysis of scoring feedback suggested that it was easy to perform and observe in comparison to LED-FM (p < 0.005).

Conclusions: This study established the feasibility of 'TBDetect' microscopy in field settings.

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