Evaluation of Rapid Assay (Tox A/B Quik Chek) for the Detection of Clostridium difficile Toxins A and B
2
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
배경: Clostridium difficile 연관 설사의 빠른 진단을 위해 독소 면역시험이 널리 사용되고 있다. 본 연구에서는 Tox A/B Quik Chek (TECHLAB, Blacksburg, VA, USA)으로 시험한 결과를 독소생성 C. difficile 배양 결과와 비교하여 그 유용성을 평가하고자 하였다. 방법: 2006년 9월부터 2007년 8월까지 959개의 변 검체로 시행한 Tox A/B Quik Chek 시험과 독소생성 C. difficile 배양 (변 검체를 선택배지에 접종하고, 증식된 집락으로 tcdB PCR을 시행) 결과를 비교 분석하였다. 결과: 독소생성 C. difficile 배양 결과를 근거로 하였을 때, Tox A/B Quik Chek 시험의 민감도와 특이도는 각각 47.5%와 97.5%이었다. 결론: Tox A/B Quik Chek 시험은 민감도는 높지 않았으나 특이도는 높아서, 이를 단독으로 진단에 이용하기에는 충분하 지 않을 수 있으나, 세균 배양, 독소시험 등과 병행 사용하면 환자의 조기진단, 치료, 원내감염의 전파방지에 도움이 될 수 있을 것으로 생각된다.
Abstract
Background: Toxin immunoassay is widely used for rapid diagnosis of Clostridium difficile-associated diarrhea. The aim of this study was to evaluate the performance of Tox A/B Quik Chek test (TECHLAB, Blacksburg, VA, USA) compared to toxigenic culture. Methods: From September 2006 to August 2007, 959 stools were examined by Tox A/B Quik Chek test and toxigenic culture (C. difficile culture plus tcdB PCR using colonies obtained from culture). Results: Compared to the results of toxigenic culture, the sensitivity and specificity of Tox A/B Quik Chek test were 47.5% and 97.5%, respectively. Conclusion: The sensitivity of Tox A/B Quik Chek test was not high, but the specificity was high. Although Tox A/B Quik Chek test alone is not sufficient to diagnose Clostridium difficile-associated diarrhea, it may aid rapid diagnosis, early treatment and prevention of nosocomial spread of the infection, if supplemented by C. difficile culture or tissue culture cytotoxin assay.
참고문헌 (27)
- Moncrief JS, "Genetic characterization of toxin A-negative, toxin B-positive Clostridium difficile isolates by PCR", J Clin Microbiol, 38, pp.3072~3075 (2000)
- Voth DE, "Clostridium difficile toxins: mechanism of action and role in di", Clin Microbiol Rev, 18, pp.247~263 (2005)
- Johnson S, "Clostridium difficile-associated diarrhea", Clin Infect Dis, 26, pp.1027~1034 (1998)
- Snell H, "Performance of the TechLab C. DIFF CHEK-60 enzyme immunoassay (EIA) in combination with the C. difficile Tox A", B II EIA kit, the Triage C. difficile panel immunoassay, and a cytotoxin assay for diagnosis of Clostridium difficile-associated diarrhea, 2004, pp.42, 4863~4865
- De Girolami PC, "Multicenter evaluation of a new enzyme immunoassay for detection of Clostridium difficile enterotoxin A", J Clin Microbiol, 300, pp.1085~1088 (1992)
- Lee H, "Detection of toxin B gene of Clostridium difficile by polymerase chain reaction from clinical isolates", Korean J Clin Microbiol, 2, pp.77~81 (1999)
- Park HK, "Direct detection of Clostridium difficile toxin B gene by nested PCR in human stool specimens", Korean J Clin Microbiol, 6, pp.63~68 (2003)
- Kato H, "Identification of toxin A-negative, toxin B-positive Clostridium difficile by PCR", J Clin Microbiol, 36, pp.2178~2182 (1998)
- Novak-Weekley SM, "Comparison of the premier toxin A and B assay and the TOX A", B II assay for diagnosis of Clostridium difficile infection, 2008, pp.15, 575~578
- McDonald LC, "Clostridium difficile infection in patients discharged from US short-stay hospitals, 1996-2003", Emerg Infect Dis, 12, pp.409~415 (2006)
- Massey V, "Clinical usefulness of components of the Triage immunoassay, enzyme immunoassay for toxins A and B, and cytotoxin B tissue culture assay for the diagnosis of Clostridium difficile diarrhea", Am J Clin Pathol, 119, pp.45~49 (2003)
- Vanpoucke H, "Evaluation of six commercial assays for the rapid detection of Clostridium difficile toxin and", or antigen in stool specimens, 2001, pp.7, 55~64
- Reyes RC, "Performance of TechLab C. DIFF QUIK CHEK and TechLab C. DIFFICILE TOX A", B II for the detection of Clostridium difficile in stool samples, 2007, pp.59, 33~37
- Murray PR, "Manual of Clinical Microbiology. 9th ed", pp.897~901 (2007), ASM Press
- 신보문, "독소 A음성, 독소 B양성 Clostridium difficile 변이주에 관한 연구", 대한진단검사의학회지, 26(1), pp.27~31 (2006), 대한진단검사의학회
- Shin BM, "Emerging toxin A-B+ variant strain of Clostridium difficile responsible for pseudomembranous colitis at a tertiary care hospital in Korea", Diagn Microbiol Infect Dis, 60, pp.333~337 (2008)
- Gilligan PH, "Is a two-step glutamate dehyrogenase antigencytotoxicity neutralization assay algorithm superior to the Premier toxin A and B enzyme immunoassay for laboratory detection of Clostridium difficile?", J Clin Microbiol, 46, pp.1523~1525 (2008)
- Fenner L, "Rapid and reliable diagnostic algorithm for detection of Clostridium difficile", J Clin Microbiol, 46, pp.328~330 (2008)
- Sloan LM, "Comparison of real-time PCR for detection of the tcdC gene with four toxin immunoassays and culture in diagnosis of Clostridium difficile infection", J Clin Microbiol, 46, pp.1996~2001 (2008)
- 유수진, "Clostridium difficile 독소 A 검출을 위한 효소면역법의 비교", 대한진단검사의학회지, 26(6), pp.408~411 (2006), 대한진단검사의학회
- Shin BM, "Comparison of toxin A enzyme linked fluorescence assay and latex agglutination based on Clostridium difficile culture and toxin A and B PCR assay", Korean J Clin Microbiol, 8, pp.130~135 (2005)
- Brazier JS, "The diagnosis of Clostridium difficile-associated disease", J Antimicrob Chemother, 41(Suppl C), pp.29~40 (1998)
- Bartley SL, "Comparison of media for the isolation of Clostridium difficile from faecal specimens", Lab Med, 22, pp.335~338 (1991)
- Bowman RA, "Isolation of Clostridium difficile from stored specimens and comparative susceptibility of various tissue culture cell lines to cytotoxin", FEMS Microbiol Lett, 34, pp.31~35 (1986)
- Freeman J, "The effects of storage conditions on viability of Clostridium difficile vegetative cells and spores and toxin activity in human faeces", J Clin Pathol, 56, pp.126~128 (2003)
- Delmée M, "Laboratory diagnosis of Clostridium difficile-associated diarrhoea: a plea for culture", J Med Microbiol, 54, pp.187~191 (2005)
- Yong D, "Evaluation of quantitative culture of Clostridium difficile from fecal specimens for the diagnosis of C. difficile-associated disease", Korean J Clin Microbiol, 5, pp.124~128 (2002)
