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Updated: Jul 26, 2025
A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
Published on: June 15, 2018
Does this patient have Clostridioides difficile infection? A systematic review and meta-analysis
Fizza Manzoor1, Saba Manzoor1, Ruxandra Pinto2
1Department of Medicine, University of Toronto, Toronto, ON, Canada.
Background:
The clinical features and predictors of Clostridioides difficile infection overlap with many conditions.
Objectives:
We performed a systematic review to evaluate the diagnostic utility of clinical features (clinical examination, risk factors, laboratory tests, and radiographic findings) associated with C. difficile.
Methods:
Systematic review and meta-analysis of diagnostic features for C. difficile.
Data Sources:
MEDLINE, EMBASE, CINAHL, and Cochrane databases were searched up to September 2021.
Study Eligibility Criteria:
Studies that reported clinical features of C. difficile, a valid reference standard test for confirming diagnosis of C. difficile, and a comparison among patients with a positive and negative test result.
Participants:
Adult and paediatric patients across diverse clinical settings.
Outcomes:
Sensitivity, specificity, likelihood ratios.
Reference Standard:
Stool nucleic acid amplification tests, enzyme immunoassays, cell cytotoxicity assay, and stool toxigenic culture.
Assessment Of Risk Of Bias:
Rational Clinical Examination Series and Quality Assessment of Diagnostic Accuracy Studies-2.
Methods Of Data Synthesis:
Univariate and bivariate analyses.
Results:
We screened 11 231 articles of which 40 were included, enabling the evaluation of 66 features for their diagnostic utility for C. difficile (10 clinical examination findings, 4 laboratory tests, 10 radiographic findings, prior exposure to 13 antibiotic types, and 29 clinical risk factors). Of the ten features identified on clinical examination, none were significantly clinically associated with increased likelihood of C. difficile infection. Some features that increased likelihood of C. difficile infection were stool leukocytes (LR+ 5.31, 95% CI 3.29-8.56) and hospital admission in the prior 3 months (LR+ 2.14, 95% CI 1.48-3.11). Several radiographic findings also strongly increased the likelihood of C. difficile infection like ascites (LR+ 2.91, 95% CI 1.89-4.49).
Discussion:
There is limited utility of bedside clinical examination alone in detecting C. difficile infection. Accurate diagnosis of C. difficile infection requires thoughtful clinical assessment for interpretation of microbiologic testing in all suspected cases.
