Accuracy of cholera rapid diagnostic tests: a systematic review and meta-analysis

Clin Microbiol Infect. 2022 Feb;28(2):155-162. doi: 10.1016/j.cmi.2021.08.027. Epub 2021 Sep 15.

Abstract

Background: Cholera is an acute diarrheal disease caused by Vibrio cholerae O1 or O139. Cholera rapid diagnostic tests (RDTs) are widely used to screen for cholera cases. However, their accuracy has not been systematically reviewed.

Objectives: To evaluate the diagnostic accuracy of cholera RDTs.

Methods: Systematic review and meta-analysis.

Data sources: Medline, EMBASE and Web of science through to November 2020; references of included studies and a technical guidance on cholera RDTs. This review is registered with PROSPERO (CRD42021233124).

Study eligibility criteria: Cross-sectional studies comparing the performance of cholera RDTs either to stool culture or PCR.

Participants: Individuals with clinically suspected cholera.

Data extraction: Two authors independently extracted data and assessed the quality using Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) criteria.

Results: Eighteen studies were included in the systematic review of which 17 were used for meta-analysis. Crystal VC was the most frequently used RDT (13 studies), followed by Cholkit and Institut Pasteur cholera dipstick (three studies each), SD Bioline (two studies), Artron (one study) and Smart (one study). Using direct testing (n = 12 627 specimens), the bivariate random-effects model yielded a pooled sensitivity and specificity of 91% (95% CI 87%-94%) and 80% (95% CI 74%-84%), respectively. However, through alkaline peptone water (APW) enrichment (n = 3403 specimens), the pooled sensitivity and specificity were 89% (95% CI 79%-95%) and 98% (95% CI 95%-99%), respectively.

Conclusion: Cholera RDTs, especially when enriched with APW, have moderate sensitivity and specificity. Although less useful for clinical management, the current generation of RDTs have clear utility for surveillance efforts if used in a principled manner. Enrichment of stool specimens in APW before using cholera RDTs reduces the possibility of obtaining false-positive results, despite the few cholera cases that go undetected. It is noteworthy that APW-enriched cholera RDTs are not necessarily rapid tests, and are not listed in the Global Task Force on Cholera Control/WHO target product profile.

Keywords: Accuracy; Cholera; Rapid test; Sensitivity; Specificity.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Cholera* / diagnosis
  • Cross-Sectional Studies
  • Humans
  • Reagent Kits, Diagnostic
  • Sensitivity and Specificity
  • Vibrio cholerae O1*

Substances

  • Reagent Kits, Diagnostic