Assessment of Detection Efficacy of Mycobacterium Tuberculosis in Sputum Samples by Real-Time PCR-Based Method

Authors

  • S. K. Upadhyaya Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal
  • S. M. Dixit Center for Molecular Dynamics Nepal affiliated Intrepid Nepal, Kathmandu, Nepal
  • S. Shrestha Center for Molecular Dynamics Nepal affiliated Intrepid Nepal, Kathmandu, Nepal
  • S. D. Dangol Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal
  • D. Pokhrel Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal
  • S. Banjara Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal
  • K. S. Shrestha Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal
  • S. Hengoju Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal
  • B. K. Dahal Department of Biotechnology, Kathmandu University, Dhulikhel, Nepal

DOI:

https://doi.org/10.3126/kuset.v9i1.63859

Keywords:

Acid fast Bacilli test, Real time PCR, TB

Abstract

Tuberculosis (TB) is a major public health problem in Nepal and ranks as one of the most prevalent communicable diseases throughout the country. In Nepal, 45% of the total population is infected with TB, and 40,000 people get TB every year. Twenty thousand new sputum-positive cases are seen annually, with 5000-7000 people dying each year from TB. Thirty sputum samples were collected from Sukraraj Tropical and Infectious Disease Hospital, Teku, Kathmandu, Nepal, and a comparative study of Acid-fast Bacilli (AFB) test and Real-time PCR was conducted separately with the culture test, regarded as the gold standard by WHO. Detection of Mycobacterium tuberculosis through the use of Real-time PCR was found to be higher compared to AFB and culture. The Real-time PCR test showed higher sensitivity (100%) and specificity (94.11%) compared to the AFB test, with sensitivity of 84.61% and specificity of 88.24%. The positive predictive value was found to be 84.61% and 92.86% for AFB and Q-PCR, respectively. The negative predictive value was found to be 88.24% for AFB and 100% for Q-PCR. Our statistics clearly show that TB diagnosis by Q-PCR is highly efficient and reliable over conventional methods of diagnosis, and we recommend its use in the hospitals and clinics of Nepal.

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Published

2013-07-31

How to Cite

Upadhyaya, S. K., Dixit, S. M., Shrestha, S., Dangol, S. D., Pokhrel, D., Banjara, S., Shrestha, K. S., Hengoju, S., & Dahal, B. K. (2013). Assessment of Detection Efficacy of Mycobacterium Tuberculosis in Sputum Samples by Real-Time PCR-Based Method. Kathmandu University Journal of Science, Engineering and Technology, 9(1), 181–188. https://doi.org/10.3126/kuset.v9i1.63859

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Section

Original Research Articles