Evaluation of antigen-positive toxin-negative enzyme immunoassay results for the diagnosis of toxigenic Clostridium difficile infection.

Clostridium difficile (C. difficile)-associated diarrhea (CDAD) is a challenging nosocomial infectious disease. C. DIFF Quik Chek Complete assay is widely used to detect glutamate dehydrogenase (GDH) antigen and toxin A/B of C. difficile simultaneously. However, the interpretation of GDH positive/toxin negative results is problematic. We performed a retrospective study of patients with GDH positive/toxin negative results to determine the probability of detecting toxigenic C. difficile and its risk factors. Between April 2012 and March 2017, we investigated cultures of fecal specimens followed by toxin detection tests. The clinical histories of patients with and without toxigenic C. difficile were compared using univariate- and multivariate-analyses. In total, 2675 patients were examined using C. Diff Quik Chek Complete assay. Among 356 GDH positive/toxin negative patients, cultures were performed in 220 cases and toxigenic C. difficile was recovered from 139 (63.2%) specimens. Patients with toxigenic C. difficile had significantly lower body mass index than those without. Over half the GDH positive/toxin negative patients were infected with toxigenic C. difficile. Lower BMI was a CDAD risk factor in this patient population. These data can be utilized to initiate isolation and clinical interventions before confirmatory test results are available. J. Med. Invest. 65:131-135, February, 2018.

[1]  J. Dobner,et al.  Body mass index and the risk of infection - from underweight to obesity. , 2018, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[2]  Y. Seo,et al.  Laboratory diagnosis of Clostridium difficile infection: Comparison of Techlab C. diff Quik Chek Complete, Xpert C. difficile, and multistep algorithmic approach , 2017, Journal of clinical laboratory analysis.

[3]  K. Yanagihara,et al.  Performance evaluation of the Verigene®Clostridium difficile nucleic acid test, an automated multiplex molecular testing system for detection of C. difficile toxin. , 2017, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

[4]  T. Riley,et al.  Prevalence and molecular epidemiology of Clostridium difficile infection in Indonesia , 2017, New microbes and new infections.

[5]  L. Villarreal-Treviño,et al.  Current knowledge on the laboratory diagnosis of Clostridium difficile infection , 2017, World journal of gastroenterology.

[6]  T. Norén,et al.  Clostridium difficile infection diagnostics – evaluation of the C. DIFF Quik Chek Complete assay, a rapid enzyme immunoassay for detection of toxigenic C. difficile in clinical stool samples , 2016, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[7]  M. Marín-Arriaza,et al.  [Laboratory diagnosis of Clostridium difficile infection]. , 2016, Enfermedades infecciosas y microbiologia clinica.

[8]  C. Kelly,et al.  Weight Gain After Fecal Microbiota Transplantation , 2015, Open forum infectious diseases.

[9]  E. Bouza,et al.  Comparison of GenomEra C. difficile and Xpert C. difficile as Confirmatory Tests in a Multistep Algorithm for Diagnosis of Clostridium difficile Infection , 2014, Journal of Clinical Microbiology.

[10]  S. Jeong,et al.  Evaluation of a Rapid Membrane Enzyme Immunoassay for the Simultaneous Detection of Glutamate Dehydrogenase and Toxin for the Diagnosis of Clostridium difficile Infection , 2014, Annals of laboratory medicine.

[11]  J. Stevens,et al.  Cost-effectiveness of a modified two-step algorithm using a combined glutamate dehydrogenase/toxin enzyme immunoassay and real-time PCR for the diagnosis of Clostridium difficile infection. , 2014, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi.

[12]  A. Berrington,et al.  Two-stage algorithm for Clostridium difficile: glutamate-dehydrogenase-positive toxin-negative enzyme immunoassay results may require further testing. , 2013, The Journal of hospital infection.

[13]  J. Rodriguez-Otero,et al.  Algorithm proposal based on the C. Diff Quik Chek Complete ICT device for detecting Clostridium difficile infection. , 2013, Enfermedades infecciosas y microbiologia clinica.

[14]  P. Gilligan,et al.  Evolution of Testing Algorithms at a University Hospital for Detection of Clostridium difficile Infections , 2012, Journal of Clinical Microbiology.

[15]  I. Brukner,et al.  Host and pathogen factors for Clostridium difficile infection and colonization. , 2011, The New England journal of medicine.

[16]  Susan E. Sefers,et al.  C. Diff Quik Chek Complete Enzyme Immunoassay Provides a Reliable First-Line Method for Detection of Clostridium difficile in Stool Specimens , 2011 .

[17]  M. Kawada,et al.  Evaluation of a simultaneous detection kit for the glutamate dehydrogenase antigen and toxin A/B in feces for diagnosis of Clostridium difficile infection , 2011, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

[18]  S. Sharp,et al.  Evaluation of the C.Diff Quik Chek Complete Assay, a New Glutamate Dehydrogenase and A/B Toxin Combination Lateral Flow Assay for Use in Rapid, Simple Diagnosis of Clostridium difficile Disease , 2010, Journal of Clinical Microbiology.

[19]  B. Oppenheim,et al.  Evaluation of Diagnostic Tests for Clostridium difficile Infection , 2009, Journal of Clinical Microbiology.

[20]  Susan E. Sefers,et al.  C. Diff Quik Chek Complete Enzyme Immunoassay Provides a Reliable First-Line Method for Detection of Clostridium difficile in Stool Specimens , 2009, Journal of Clinical Microbiology.

[21]  O. Dekkers,et al.  European Society of Clinical Microbiology and Infectious Diseases (ESCMID): data review and recommendations for diagnosing Clostridium difficile-infection (CDI). , 2009, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[22]  S. Sharp,et al.  A simple 3-step algorithm for improved laboratory detection of Clostridium difficile toxin without the need for tissue culture cytotoxicity neutralization assays. , 2009, Diagnostic microbiology and infectious disease.

[23]  J. Bartlett,et al.  Clinical recognition and diagnosis of Clostridium difficile infection. , 2008, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[24]  J Ignacio de Ulíbarri,et al.  CONUT: a tool for controlling nutritional status. First validation in a hospital population. , 2005, Nutricion hospitalaria.

[25]  A. Huang,et al.  Risk of Clostridium difficile diarrhea among hospital inpatients prescribed proton pump inhibitors: cohort and case–control studies , 2004, Canadian Medical Association Journal.

[26]  M. Stevenson,et al.  Antibiotics and hospital-acquired Clostridium difficile-associated diarrhoea: a systematic review. , 2003, The Journal of antimicrobial chemotherapy.

[27]  C. Kelly,et al.  Underlying Disease Severity as a Major Risk Factor for Nosocomial Clostridium difficile Diarrhea , 2002, Infection Control & Hospital Epidemiology.

[28]  D. Gerding,et al.  Acquisition of Clostridium difficile and Clostridium difficile-Associated Diarrhea in Hospitalized Patients Receiving Tube Feeding , 1998, Annals of Internal Medicine.

[29]  S. Hirschman,et al.  Clostridium difficile diarrhea induced by cancer chemotherapy. , 1992, Archives of internal medicine.