Open Access
Open access
volume 10 issue 2 pages 687-697

Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis

Publication typeJournal Article
Publication date2021-03-26
scimago Q1
wos Q1
SJR1.526
CiteScore9.7
Impact factor5.3
ISSN21938229, 21936382
Microbiology (medical)
Infectious Diseases
Abstract
Clostridium difficile infection (CDI) is a leading cause of healthcare-associated infections, accounting for significant disease burden and mortality. The clinical spectrum of C. difficile ranges from asymptomatic colonization to toxic megacolon and fulminant colitis. CDI is characterized by new onset of ≥ 3 unformed stools in 24 h and is confirmed by laboratory test for the presence of toxigenic C. difficile. Currently, laboratory tests to diagnose CDI include toxigenic culture, glutamate dehydrogenase (GDH), nucleic acid amplification test (NAAT), and toxins A/B enzyme immunoassay (EIA). The sensitivities of these tests are variable with toxin EIA ranging from 53 to 60% and with NAAT at about 95%. Overall, the specificity is > 90% for these methods. However, the positive predictive value (PPV) depends on the disease prevalence with lower CDI rates associated with lower PPVs. Notably, the widespread use of the highly sensitive NAAT and its relatively lower clinical specificity have led to overdiagnosis of C. difficile by identifying carriers when NAAT is used as the sole diagnostic method. Overdiagnosis of C. difficile has resulted in unwarranted treatment, possibly attributing to resistance to metronidazole and vancomycin, increased risk for overgrowth of vancomycin-resistant enterococci strains in stool specimens, and increased hospitalization thereby impacting patient safety and healthcare costs. Strategies to optimize the clinical sensitivity and specificity of current laboratory tests are critical to differentiate the clinical CDI from colonization. To achieve high diagnostic yield, if preagreed institutional criteria for stool submission are not used, a multistep approach to CDI diagnosis is recommended, such as either GDH or NAAT followed by toxins A/B EIA in conjunction with laboratory stewardship by evaluating C. difficile test orders for appropriateness and providing feedback. Furthermore, antimicrobial stewardship, along with provider education on appropriate testing for C. difficile, is vital to differentiate CDI from colonization.
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GOST |
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GOST Copy
Lee H. S. et al. Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis // Infectious Diseases and Therapy. 2021. Vol. 10. No. 2. pp. 687-697.
GOST all authors (up to 50) Copy
Lee H. S., Plechot K., Gohil S., Le J. Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis // Infectious Diseases and Therapy. 2021. Vol. 10. No. 2. pp. 687-697.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1007/s40121-021-00417-7
UR - https://doi.org/10.1007/s40121-021-00417-7
TI - Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis
T2 - Infectious Diseases and Therapy
AU - Lee, Helen S
AU - Plechot, Kamryn
AU - Gohil, Shruti
AU - Le, Jennifer
PY - 2021
DA - 2021/03/26
PB - Springer Nature
SP - 687-697
IS - 2
VL - 10
PMID - 33770398
SN - 2193-8229
SN - 2193-6382
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2021_Lee,
author = {Helen S Lee and Kamryn Plechot and Shruti Gohil and Jennifer Le},
title = {Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis},
journal = {Infectious Diseases and Therapy},
year = {2021},
volume = {10},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1007/s40121-021-00417-7},
number = {2},
pages = {687--697},
doi = {10.1007/s40121-021-00417-7}
}
MLA
Cite this
MLA Copy
Lee, Helen S., et al. “Clostridium difficile: Diagnosis and the Consequence of Over Diagnosis.” Infectious Diseases and Therapy, vol. 10, no. 2, Mar. 2021, pp. 687-697. https://doi.org/10.1007/s40121-021-00417-7.