TY - JOUR
T1 - Accuracy of genotype MTBDRplus line probe assay in patients with tuberculous pleural effusion
T2 - comparison with clinical and culture based diagnosis
AU - Irfan, Muhammad
AU - Idrees, Farah
AU - Jabeen, Kauser
AU - Zubairi, Ali Bin Sarwar
AU - Butt, Sehrish
AU - Hasan, Rumina
N1 - Funding Information:
This study was funded by University Research Council (URC) grant of Aga Khan University, Karachi, Pakistan [131007MED]. The funding source had no role in study design, collection, data analysis and interpretation, in manuscript writing and in the decision to submit the article for publication. The authors acknowledge the hard work of their research associate Dr Hira Shahzad in data and sample collection. This study has presented as poster in European Respiratory Society Annual Congress 2017, Milan –Italy and published as abstract in European Respiratory Journal supplement. (Irfan M, Jabeen K, Butt S, Zubairi ABS, Awan S, Hasan R. Sensitivity and specificity of Genotype MTBDRplus line probe assay in rapid diagnosis of tuberculous pleural effusion. Eur Respir J. 2017;50(Suppl. 61):PA2699. DOI:10.1183/1393003). Initial preliminary data of 22 patients was presented in 1st Asian African congress of Mycobacteriology 2015, Iran and published as abstract in International Journal of Mycobacteriology. (Irfan M, Jabeen K, Ali HS, Zubairi AB, Hasnan R. Evaluation of sensitivity and specificity of GenoType MTBDRplus line probe assay in rapid diagnosis of tuberculous pleural effusion. Int J Mycobacteriol. 2015;4(1):111. DOI:10.1016/j.ijmyco.2014.11.003).
Publisher Copyright:
© 2019, © 2019 Society for Scandinavian Journal of Infectious Diseases.
PY - 2020/4/2
Y1 - 2020/4/2
N2 - Background: Pleural tuberculosis (TB) diagnosis is challenging due to paucibacillary disease. Diagnostic accuracy of GenoType MTBDRplus Line Probe Assay (MTBDRplus) has been evaluated in this study for pleural TB diagnosis. Objective: To evaluate diagnostic accuracy of MTBDRplus for pleural TB diagnosis compared to clinical and microbiological diagnosis. Methods: This prospective study was conducted at the Aga Khan University, Pakistan. Pleural fluid from 203 suspected pleural TB patients was collected and tested for smear, culture and MTBDRplus. Diagnostic accuracy of MTBDRplus was determined using clinical diagnosis and culture as the gold standard. Results: Out of 203 TB suspect patients, MTBDRplus, culture and smear were positive in 14 (6. 9%), 27 (13.3%) and 4 (1.9%) cases, respectively. A total of 106/203 patients (27 culture positive and 79 culture negative) successfully completed TB treatment. Considering clinical diagnosis as gold standard, sensitivity of MTBDRplus was 13.2%; 95% CI (7.4–21.2%) and specificity was 100%; 95% CI (96.1–100%). The sensitivity and specificity of MTBDRplus in culture positive samples were 44.4%; 95% CI (25.5–64.7%) and 98.9%; 95% CI (95.9–99.9%), respectively. Excluding indeterminate results, MTBDRplus accurately detected isoniazid sensitivity in 5/6 and rifampicin sensitivity in 6/6 cases. Conclusion: MTBDRplus had a low sensitivity of 13.2% in clinically diagnosed and 44% in culture-confirmed pleural TB patients and therefore could not be included in most diagnostic algorithms. Due to a higher sensitivity than smear, MTBDRplus may have a role in tuberculous pleural effusion diagnosis if it is positive pending culture results and pleural biopsy.
AB - Background: Pleural tuberculosis (TB) diagnosis is challenging due to paucibacillary disease. Diagnostic accuracy of GenoType MTBDRplus Line Probe Assay (MTBDRplus) has been evaluated in this study for pleural TB diagnosis. Objective: To evaluate diagnostic accuracy of MTBDRplus for pleural TB diagnosis compared to clinical and microbiological diagnosis. Methods: This prospective study was conducted at the Aga Khan University, Pakistan. Pleural fluid from 203 suspected pleural TB patients was collected and tested for smear, culture and MTBDRplus. Diagnostic accuracy of MTBDRplus was determined using clinical diagnosis and culture as the gold standard. Results: Out of 203 TB suspect patients, MTBDRplus, culture and smear were positive in 14 (6. 9%), 27 (13.3%) and 4 (1.9%) cases, respectively. A total of 106/203 patients (27 culture positive and 79 culture negative) successfully completed TB treatment. Considering clinical diagnosis as gold standard, sensitivity of MTBDRplus was 13.2%; 95% CI (7.4–21.2%) and specificity was 100%; 95% CI (96.1–100%). The sensitivity and specificity of MTBDRplus in culture positive samples were 44.4%; 95% CI (25.5–64.7%) and 98.9%; 95% CI (95.9–99.9%), respectively. Excluding indeterminate results, MTBDRplus accurately detected isoniazid sensitivity in 5/6 and rifampicin sensitivity in 6/6 cases. Conclusion: MTBDRplus had a low sensitivity of 13.2% in clinically diagnosed and 44% in culture-confirmed pleural TB patients and therefore could not be included in most diagnostic algorithms. Due to a higher sensitivity than smear, MTBDRplus may have a role in tuberculous pleural effusion diagnosis if it is positive pending culture results and pleural biopsy.
KW - Diagnosis
KW - line probe assay
KW - nucleic acid amplification
KW - pleural effusion
KW - tuberculosis
UR - http://www.scopus.com/inward/record.url?scp=85075985387&partnerID=8YFLogxK
U2 - 10.1080/23744235.2019.1697462
DO - 10.1080/23744235.2019.1697462
M3 - Article
C2 - 31797723
AN - SCOPUS:85075985387
SN - 2374-4235
VL - 52
SP - 235
EP - 241
JO - Infectious Diseases
JF - Infectious Diseases
IS - 4
ER -