Tuberc Respir Dis.  2010 Jun;68(6):345-349. 10.4046/trd.2010.68.6.345.

Significance of Repeated Polymerase Chain Reaction (PCR) Testing for Diagnosis of Pulmonary Tuberculosis

Affiliations
  • 1Department of Internal Medicine, Seonam University Medical School, Namwon, Korea.
  • 2Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea. droij@chonnam.ac.kr

Abstract

BACKGROUND
The polymerase chain reaction (PCR) test is important for the confirmatory diagnosis of tuberculosis (TB) caused by Mycobacterium tuberculosis. The aim of this study was to analyze the yield of repeated PCR testing in patients with confirmed pulmonary TB.
METHODS
The medical records of 130 patients, who had more than two consecutive PCR tests and a M. tuberculosis-positive sputum culture from August, 2006 to December, 2007, were retrospectively reviewed for the purposes of this study. A positive TB-PCR test was defined as at least one positive test result.
RESULTS
The cumulative positive PCR test rate was 80% (104/130), with gradually increasing rates of positive findings upon the first, second and third TB-PCR tests with 52.3%, 68.5% and 75.4%, respectively. However, further testing did not increase the positive rate further.
CONCLUSION
Repeated PCR testing at least three times for M. tuberculosis is helpful for diagnosis of pulmonary TB.

Keyword

Polymerase Chain Reaction; Tuberculosis; Sputum

MeSH Terms

Humans
Medical Records
Mycobacterium tuberculosis
Polymerase Chain Reaction
Retrospective Studies
Sputum
Tuberculosis
Tuberculosis, Pulmonary

Figure

  • Figure 1 Statistical analysis by binomial test. Trends of cumulative positive rate by number of tuberculosis-polymerase chain reaction (TB-PCR) trials. Difference with cumulative positive rate by trial times were verified by the binomial test. The difference in the rates between the first and second trials was significant (p<0.001), the difference between the second and third trials was borderline significant (p=0.055), whereas the difference between the third and fourth trials was statistically insignificant.


Reference

1. Diagnostic Standards and Classification of Tuberculosis in Adults and Children. This official statement of the American Thoracic Society and the Centers for Disease Control and Prevention was adopted by the ATS Board of Directors, July 1999. This statement was endorsed by the Council of the Infectious Disease Society of America, September 1999. Am J Respir Crit Care Med. 2000. 161:1376–1395.
2. Cheng VC, Yam WC, Hung IF, Woo PC, Lau SK, Tang BS, et al. Clinical evaluation of the polymerase chain reaction for the rapid diagnosis of tuberculosis. J Clin Pathol. 2004. 57:281–285.
3. Laifer G, Widmer AF, Frei R, Zimmerli W, Fluckiger U. Polymerase chain reaction for Mycobacterium tuberculosis: impact on clinical management of refugees with pulmonary infiltrates. Chest. 2004. 125:981–986.
4. Korea Centers for Disease Control and Prevention, Korean Institute of Tuberculosis. Guidelines for the control of tuberculosis 2008. 2008. Seoul: Korea Centers for Disease Control and Prevention, Korean Institute of Tuberculosis.
5. Mase SR, Ramsay A, Ng V, Henry M, Hopewell PC, Cunningham J, et al. Yield of serial sputum specimen examinations in the diagnosis of pulmonary tuberculosis: a systematic review. Int J Tuberc Lung Dis. 2007. 11:485–495.
6. Al Zahrani K, Al Jahdali H, Poirier L, Rene P, Menzies D. Yield of smear, culture and amplification tests from repeated sputum induction for the diagnosis of pulmonary tuberculosis. Int J Tuberc Lung Dis. 2001. 5:855–860.
7. Yam WC, Yuen KY, Seto WH. Direct detection of Mycobacterium tuberculosis in respiratory specimens using an automated DNA amplification assay and a single tube nested polymerase chain reaction (PCR). Clin Chem Lab Med. 1998. 36:597–599.
8. Suh SP, Huh Y, Kee SJ, Shin JH, Ryang DW. Detection of Mycobacterium tuberculosis in clinical samples by nested polymerase chain reaction. Korean J Clin Pathol. 1995. 15:61–73.
9. Kim HJ. Current situation of tuberculosis and its control in Korea. J Korean Med Assoc. 2006. 49:762–772.
10. Levy H, Feldman C, Sacho H, van der Meulen H, Kallenbach J, Koornhof H. A reevaluation of sputum microscopy and culture in the diagnosis of pulmonary tuberculosis. Chest. 1989. 95:1193–1197.
11. Behr MA, Warren SA, Salamon H, Hopewell PC, Ponce de Leon A, Daley CL, et al. Transmission of Mycobacterium tuberculosis from patients smear-negative for acid-fast bacilli. Lancet. 1999. 353:444–449.
12. Bartlett JM, Stirling D. A short history of the polymerase chain reaction. Methods Mol Biol. 2003. 226:3–6.
13. Brisson-Noel A, Gicquel B, Lecossier D, Levy-Frebault V, Nassif X, Hance AJ. Rapid diagnosis of tuberculosis by amplification of mycobacterial DNA in clinical samples. Lancet. 1989. 2:1069–1071.
14. Tueller C, Chhajed PN, Buitrago-Tellez C, Frei R, Frey M, Tamm M. Value of smear and PCR in bronchoalveolar lavage fluid in culture positive pulmonary tuberculosis. Eur Respir J. 2005. 26:767–772.
15. Kivihya-Ndugga L, van Cleeff M, Juma E, Kimwomi J, Githui W, Oskam L, et al. Comparison of PCR with the routine procedure for diagnosis of tuberculosis in a population with high prevalences of tuberculosis and human immunodeficiency virus. J Clin Microbiol. 2004. 42:1012–1015.
16. Ozkutuk A, Terek G, Coban H, Esen N. Is it valuable to examine more than one sputum smear per patient for the diagnosis of pulmonary tuberculosis? Jpn J Infect Dis. 2007. 60:73–75.
17. Park SS, Kwak KR, Hwang JY, Yun SM, Ryue CC, Chang CH, et al. Clinical utility of amplified mycobacterium tuberculosis direct test in the diagnosis of pulmonary tuberculosis. Tuberc Respir Dis. 1999. 47:747–756.
18. Carpentier E, Drouillard B, Dailloux M, Moinard D, Vallee E, Dutilh B, et al. Diagnosis of tuberculosis by Amplicor Mycobacterium tuberculosis test: a multicenter study. J Clin Microbiol. 1995. 33:3106–3110.
19. Beige J, Lokies J, Schaberg T, Finckh U, Fischer M, Mauch H, et al. Clinical evaluation of a Mycobacterium tuberculosis PCR assay. J Clin Microbiol. 1995. 33:90–95.
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