Skip to main content
Erschienen in: Digestive Diseases and Sciences 10/2012

01.10.2012 | Original Article

Superiority of the DNA Amplification Assay for the Diagnosis of C. difficile Infection: A Clinical Comparison of Fecal Tests

verfasst von: Jodie A. Barkin, Neilanjan Nandi, Nancimae Miller, Alexandra Grace, Jamie S. Barkin, Daniel A. Sussman

Erschienen in: Digestive Diseases and Sciences | Ausgabe 10/2012

Einloggen, um Zugang zu erhalten

Abstract

Background

Clostridium difficile infection (CDI) is a major infectious concern, accounting for substantial morbidity and resource utilization. Advances in microbiological and molecular techniques have resulted in an increasing number of testing options for CDI. A glutamate dehydrogenase (GDH) enzyme immunoassay (EIA) and a DNA amplification (DNA-A) test for the diagnosis of CDI have recently become commercially available.

Aims

The aim of this prospective study was to compare the test performance characteristics of the traditional diagnostic modality for CDI diagnosis, the toxin A/B (TOX) EIA, with those of the GDH EIA and DNA-A test, utilizing enriched toxigenic culture (TGC) as the gold standard. Clinical variables predictive of CDI were also studied.

Methods

Participants fulfilled one or more criteria placing them at increased risk for CDI. Each stool sample was tested by each of the methods mentioned above. Clinical data parameters were collected via a 12-month review of the electronic medical record prior to the index date of the first stool test.

Results

A total of 272 stool samples from 144 admissions of 139 patients were evaluated for CDI. The sensitivity and positive predictive value (PPV) of the TOX EIA were 86.1 and 58.4 %, respectively, whereas the sensitivity and PPV of the GDH EIA and DNA-A test were 100 %. 1.8 % of the GDH tests yielded inconclusive results. Using TGC as the gold standard, nosocomial exposure with emphasis on nursing home residence, history of previous CDI, and female gender were predictive of CDI.

Conclusions

Test performance characteristics of the DNA-A test and GDH EIA were superior to those of the traditional TOX EIA. The GDH test is limited by inconclusive test results and requires a multi-step diagnostic algorithm. Therefore, the DNA-A test should be implemented as the diagnostic method of choice for CDI. CDI clinical predictors are important for diagnostic decision-making.
Literatur
1.
Zurück zum Zitat Zilberberg MD, Shorr AF, Kollef MH. Increase in adult Clostridium difficile related hospitalizations and case-fatality rate, United States 2000–2005. Emerg Infect Dis. 2008;14:929–931.PubMedCrossRef Zilberberg MD, Shorr AF, Kollef MH. Increase in adult Clostridium difficile related hospitalizations and case-fatality rate, United States 2000–2005. Emerg Infect Dis. 2008;14:929–931.PubMedCrossRef
2.
Zurück zum Zitat Kyne L, Hamel MB, Plavaram R, et al. Healthcare costs and mortality associated with nosocomial diarrhea due to Clostridium difficile. Clin Infect Dis. 2002;34:346–353.PubMedCrossRef Kyne L, Hamel MB, Plavaram R, et al. Healthcare costs and mortality associated with nosocomial diarrhea due to Clostridium difficile. Clin Infect Dis. 2002;34:346–353.PubMedCrossRef
3.
Zurück zum Zitat Ananthakrishnan AN. Clostridium difficile infection: epidemiology, risk factors, and management. Nat Rev Gastroenterol Hepatol. 2011;8:17–26. Ananthakrishnan AN. Clostridium difficile infection: epidemiology, risk factors, and management. Nat Rev Gastroenterol Hepatol. 2011;8:17–26.
5.
Zurück zum Zitat Dubberke ER, Wertheimer AI. Review of current literature on the economic burden of Clostridium difficile and C. difficile infection. Infect Control Hosp Epidemiol. 2009;30:57–66.PubMedCrossRef Dubberke ER, Wertheimer AI. Review of current literature on the economic burden of Clostridium difficile and C. difficile infection. Infect Control Hosp Epidemiol. 2009;30:57–66.PubMedCrossRef
6.
Zurück zum Zitat Hookman P, Barkin JS. Clostridium difficile associated infection, diarrhea, and colitis. World J Gastroenterol. 2009;15:1554–1580. Hookman P, Barkin JS. Clostridium difficile associated infection, diarrhea, and colitis. World J Gastroenterol. 2009;15:1554–1580.
7.
Zurück zum Zitat Carroll KC, Bartlett JG. Biology of Clostridium difficile: implications for epidemiology and diagnosis. Ann Rev Microbiol. 2011;65:501–521. Carroll KC, Bartlett JG. Biology of Clostridium difficile: implications for epidemiology and diagnosis. Ann Rev Microbiol. 2011;65:501–521.
8.
Zurück zum Zitat Rupnik M. Heterogeneity of large clostridial toxins: importance of Clostridium difficile toxinotypes. FEMS Microbiol Rev. 2008;32:541–555.PubMedCrossRef Rupnik M. Heterogeneity of large clostridial toxins: importance of Clostridium difficile toxinotypes. FEMS Microbiol Rev. 2008;32:541–555.PubMedCrossRef
9.
Zurück zum Zitat Doing KM, Hintz MS, Keefe C, et al. Reevaluation of the Premier Clostridium difficile toxin A and B immunoassay with comparison to glutamate dehydrogenase common antigen testing evaluation Bartels cytotoxin and ProdeseProGastro Cd polymerase chain reaction as confirmatory procedures. Diagn Microbiol Infect Dis. 2010;66:129–134.PubMedCrossRef Doing KM, Hintz MS, Keefe C, et al. Reevaluation of the Premier Clostridium difficile toxin A and B immunoassay with comparison to glutamate dehydrogenase common antigen testing evaluation Bartels cytotoxin and ProdeseProGastro Cd polymerase chain reaction as confirmatory procedures. Diagn Microbiol Infect Dis. 2010;66:129–134.PubMedCrossRef
10.
Zurück zum Zitat Larson AM, Fung AM, Fang FC. Evaluation of the tcdB real-time PCR in a three-step diagnostic algorithm for detection of toxigenic Clostridium difficile. J Clin Microbiol. 2010;48:124–130.PubMedCrossRef Larson AM, Fung AM, Fang FC. Evaluation of the tcdB real-time PCR in a three-step diagnostic algorithm for detection of toxigenic Clostridium difficile. J Clin Microbiol. 2010;48:124–130.PubMedCrossRef
11.
Zurück zum Zitat Kvach EJ, Ferguson D, Riska PF, et al. Comparison of BD GeneOhmCdiff real-time PCR assay with a two-step algorithm and a toxin A/B enzyme-linked immunosorbent assay for diagnosis of toxigenic Clostridium difficile infection. J Clin Microbiol. 2010;48:109–114.PubMedCrossRef Kvach EJ, Ferguson D, Riska PF, et al. Comparison of BD GeneOhmCdiff real-time PCR assay with a two-step algorithm and a toxin A/B enzyme-linked immunosorbent assay for diagnosis of toxigenic Clostridium difficile infection. J Clin Microbiol. 2010;48:109–114.PubMedCrossRef
12.
Zurück zum Zitat Peterson LR, Manson RU, Paule SM, et al. Detection of toxigenic Clostridium difficile in stool samples by real-time polymerase chain reaction for the diagnosis of C. difficile-associated diarrhea. Clin Infect Dis. 2007;45:1152–1160.PubMedCrossRef Peterson LR, Manson RU, Paule SM, et al. Detection of toxigenic Clostridium difficile in stool samples by real-time polymerase chain reaction for the diagnosis of C. difficile-associated diarrhea. Clin Infect Dis. 2007;45:1152–1160.PubMedCrossRef
13.
Zurück zum Zitat Stamper PD, Alcabasa R, Aird D, et al. Comparison of a commercial real-time PCR assay for tcdB detection to a cell culture cytotoxicity assay and toxigenic culture for direct detection of toxin-producing Clostridium difficile in clinical samples. J Clin Microbiol. 2009;47:373–378.PubMedCrossRef Stamper PD, Alcabasa R, Aird D, et al. Comparison of a commercial real-time PCR assay for tcdB detection to a cell culture cytotoxicity assay and toxigenic culture for direct detection of toxin-producing Clostridium difficile in clinical samples. J Clin Microbiol. 2009;47:373–378.PubMedCrossRef
14.
Zurück zum Zitat Stamper PD, Babiker W, Alcabasa R, et al. Evaluation of a new commercial TaqMan PCR assay for direct detection of the Clostridium difficile toxin B gene in clinical stool specimens. J Clin Microbiol. 2009;47:3846–3850.PubMedCrossRef Stamper PD, Babiker W, Alcabasa R, et al. Evaluation of a new commercial TaqMan PCR assay for direct detection of the Clostridium difficile toxin B gene in clinical stool specimens. J Clin Microbiol. 2009;47:3846–3850.PubMedCrossRef
15.
Zurück zum Zitat Sloan LM, Duresko BJ, Gustafson DR, et al. Comparison of a real-time PCR for detection of the tcdC gene with four toxin immunoassays and culture in diagnosis of Clostridium difficile infection. J Clin Microbiol. 2008;46:1996–2001.PubMedCrossRef Sloan LM, Duresko BJ, Gustafson DR, et al. Comparison of a real-time PCR for detection of the tcdC gene with four toxin immunoassays and culture in diagnosis of Clostridium difficile infection. J Clin Microbiol. 2008;46:1996–2001.PubMedCrossRef
16.
Zurück zum Zitat Barbut F, Braun M, Burghoffer B, et al. Rapid detection of toxigenic strains of Clostridium difficile in diarrheal stools by real-time PCR. J Clin Microbiol. 2009;47:1276–1277.PubMedCrossRef Barbut F, Braun M, Burghoffer B, et al. Rapid detection of toxigenic strains of Clostridium difficile in diarrheal stools by real-time PCR. J Clin Microbiol. 2009;47:1276–1277.PubMedCrossRef
17.
Zurück zum Zitat Eastwood K, Else P, Charlett A, et al. Comparison of nine commercially available Clostridium difficile toxin detection assays, a real-time PCR assay for C. difficile tcdB, and a glutamate dehydrogenase detection assay to cytotoxin testing and cytotoxigenic culture methods. J Clin Microbiol. 2009;47:3211–3217.PubMedCrossRef Eastwood K, Else P, Charlett A, et al. Comparison of nine commercially available Clostridium difficile toxin detection assays, a real-time PCR assay for C. difficile tcdB, and a glutamate dehydrogenase detection assay to cytotoxin testing and cytotoxigenic culture methods. J Clin Microbiol. 2009;47:3211–3217.PubMedCrossRef
18.
Zurück zum Zitat Novak-Weekley SM, Marlowe EM, Miller JM, et al. Clostridium difficile testing in the clinical laboratory by use of multiple testing algorithms. J Clin Microbiol. 2010;48:889–893.PubMedCrossRef Novak-Weekley SM, Marlowe EM, Miller JM, et al. Clostridium difficile testing in the clinical laboratory by use of multiple testing algorithms. J Clin Microbiol. 2010;48:889–893.PubMedCrossRef
20.
Zurück zum Zitat Currie B. Real-time PCR testing for CDI improves outcomes and reduces costs. MLO Med Lab Obs. 2009;41:18–20.PubMed Currie B. Real-time PCR testing for CDI improves outcomes and reduces costs. MLO Med Lab Obs. 2009;41:18–20.PubMed
21.
Zurück zum Zitat Mellow M, Kanatzar A, Brandt L, et al. Long term follow-up of colonoscopic fecal microbiota transplant (FMT) for recurrent C. difficile infection (RCDI). Podium Presentation at American College of Gastroenterology 2011 National Meeting. Washington, DC. Mellow M, Kanatzar A, Brandt L, et al. Long term follow-up of colonoscopic fecal microbiota transplant (FMT) for recurrent C. difficile infection (RCDI). Podium Presentation at American College of Gastroenterology 2011 National Meeting. Washington, DC.
22.
Zurück zum Zitat Loo VG, Bourgault A, Poirier L, et al. Host and pathogen factors for Clostridium difficile infection and colonization. N Eng J Med. 2011;365:1693–1703.CrossRef Loo VG, Bourgault A, Poirier L, et al. Host and pathogen factors for Clostridium difficile infection and colonization. N Eng J Med. 2011;365:1693–1703.CrossRef
Metadaten
Titel
Superiority of the DNA Amplification Assay for the Diagnosis of C. difficile Infection: A Clinical Comparison of Fecal Tests
verfasst von
Jodie A. Barkin
Neilanjan Nandi
Nancimae Miller
Alexandra Grace
Jamie S. Barkin
Daniel A. Sussman
Publikationsdatum
01.10.2012
Verlag
Springer US
Erschienen in
Digestive Diseases and Sciences / Ausgabe 10/2012
Print ISSN: 0163-2116
Elektronische ISSN: 1573-2568
DOI
https://doi.org/10.1007/s10620-012-2200-x

Weitere Artikel der Ausgabe 10/2012

Digestive Diseases and Sciences 10/2012 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Positiver FIT: Die Ursache liegt nicht immer im Dickdarm

27.05.2024 Blut im Stuhl Nachrichten

Immunchemischer Stuhltest positiv, Koloskopie negativ – in solchen Fällen kann die Blutungsquelle auch weiter proximal sitzen. Ein Forschungsteam hat nachgesehen, wie häufig und in welchen Lokalisationen das der Fall ist.

GLP-1-Agonisten können Fortschreiten diabetischer Retinopathie begünstigen

24.05.2024 Diabetische Retinopathie Nachrichten

Möglicherweise hängt es von der Art der Diabetesmedikamente ab, wie hoch das Risiko der Betroffenen ist, dass sich sehkraftgefährdende Komplikationen verschlimmern.

Mehr Lebenszeit mit Abemaciclib bei fortgeschrittenem Brustkrebs?

24.05.2024 Mammakarzinom Nachrichten

In der MONARCHE-3-Studie lebten Frauen mit fortgeschrittenem Hormonrezeptor-positivem, HER2-negativem Brustkrebs länger, wenn sie zusätzlich zu einem nicht steroidalen Aromatasehemmer mit Abemaciclib behandelt wurden; allerdings verfehlte der numerische Zugewinn die statistische Signifikanz.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.