坦桑尼亚达累斯萨拉姆地区痰涂片镜检诊断肺结核的质量。

G S Mfinanga, E Ngadaya, R Mtandu, B Mutayoba, D Basra, G Kimaro, T M Chonde, P Ngowi, S Mfaume, A M Kilale, S Egwaga, A Y Kitua
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引用次数: 35

摘要

本研究旨在确定周边结核病诊断中心(PDCs)和中央参考结核病实验室(CTRL)涂片阳性和阴性标本的镜检读数和培养阳性率的一致性或不一致性。这项研究涉及坦桑尼亚达累斯萨拉姆的13个发展中国家。采用批量质量保证抽样(LQAS)法采集222张痰涂片。选取有相应载玻片的晨痰标本190份进行培养。第一次读数由PDCs的技术人员完成,随后选择的载玻片和标本送至CTRL进行复查和培养。培养结果作为金标准。在222张切片中,214张适合复查。在阳性和阴性玻片上,PDCs和CTRL的涂片读数一致性百分比分别为42.9%和100%。一致性测量(Kappa统计量)为0.5,表示中度一致。在培养的190个样本中,在涂片阳性和阴性玻片上,PDCs和CTRL涂片读数的一致性百分比分别为37%和88.9%。Kappa统计数据为0.3,表明协议不公平。PDCs涂片读数与培养相比较,敏感性为36.9%,特异性为88.9%。CTRL涂片读数与培养结果比较,灵敏度为95.6%,特异性为98.6%。总之,达累斯萨拉姆周边诊断中心在使用涂片显微镜诊断结核病方面表现不佳。这就要求立即采取严格的措施来提高涂片镜检的质量。因此,通过支持性监督和培训加强实验室人员在涂片显微镜技术方面的能力是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The quality of sputum smear microscopy diagnosis of pulmonary tuberculosis in Dar es Salaam, Tanzania.

This study was carried out to determine the rate of agreement or disagreement of microscopy reading and culture positivity rate among smear positixe and negative specimens between peripheral tuberculosis diagnostic centres (PDCs) and Central Reference luberculosis laboratory (CTRL). In this study 13 PDCs in Dar es Salaam, Tanzania were involved. Lot Quality Assurance Sampling (LQAS) method was used to collect 222 sputum smear slides. A total of 190 morning sputum specimens with corresponding slides were selected for culture. First readings were done by technicians at PDCs and thereafter selected slides and specimens were sent to CTRL for re-examination and culture. Culture results were used as a gold standard. Of 222 slides selected, 214 were suitable for re-examination. Percentage of agreement of smear reading between PDCs and CTRL was 42.9% and 100% for positive and negative slides, respectively. Measure of agreement (Kappa statistic) was 0.5, indicating moderate agreement. Of 190 samples cultured, percentage of agreement between smear reading from PDCs and CTRL was 37% and 88.9% for smear positive and negative slides, respectively. Kappa statistic was 0.3 indicating poor-fair agreements. Comparison of smear reading from PDCs with culture showed sensitivity of 36.9% and specificity of 88.9%. Comparison of smear readings from CTRL with culture results showed sensitivity of 95.6% and specificity of 98.6%. In conclusion there was inadequate performance in diagnosis of TB using smear microscopy among peripheral diagnostic centres in Dar es Salaam. This calls for immediate and rigorous measures to improve the quality of smear microscopy. It is therefore important to strengthen the capacity of laboratory personnel in smear microscopy techniques through supportive supervision and training.

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