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.

Downloads

Download data is not yet available.
Abstract
50
PDF
30

Downloads

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

Issue

Section

Original Research Articles