Improving clinical and epidemiological predictors of Buruli ulcer

PLoS Negl Trop Dis. 2018 Aug 6;12(8):e0006713. doi: 10.1371/journal.pntd.0006713. eCollection 2018 Aug.

Abstract

Background: Buruli ulcer (BU) is a chronic necrotizing infectious skin disease caused by Mycobacterium ulcerans. The treatment with BU-specific antibiotics is initiated after clinical suspicion based on the WHO clinical and epidemiological criteria. This study aimed to estimate the predictive values of these criteria and how they could be improved.

Methodology/principal findings: A total of 224 consecutive patients presenting with skin and soft tissue lesions that could be compatible with BU, including those recognized as unlikely BU by experienced clinicians, were recruited in two BU treatment centers in southern Benin between March 2012 and March 2015. For each participant, the WHO and four additional epidemiological and clinical diagnostic criteria were recorded. For microbiological confirmation, direct smear examination and IS2404 PCR were performed. We fitted a logistic regression model with PCR positivity for BU confirmation as outcome variable. On univariate analysis, most of the clinical and epidemiological WHO criteria were associated with a positive PCR result. However, lesions on the lower limbs and WHO category 3 lesions were rather associated with a negative PCR result (respectively OR: 0.4, 95%CI: 0.3-0.8; OR: 0.5, 95%IC: 0.3-0.9). Among the additional characteristics studied, the characteristic smell of BU was strongest associated with a positive PCR result (OR = 16.4; 95%CI = 7.5-35.6).

Conclusion/significance: The WHO diagnostic criteria could be improved upon by differentiating between lesions on the upper and lower limbs and by including lesion size and the characteristic smell recognized by experienced clinicians.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Buruli Ulcer / microbiology*
  • Child
  • Female
  • Humans
  • Logistic Models
  • Male
  • Mycobacterium ulcerans*
  • Odds Ratio
  • Polymerase Chain Reaction / methods
  • Prospective Studies
  • Risk Factors
  • Skin / microbiology
  • Skin / pathology
  • World Health Organization
  • Young Adult

Grants and funding

This work was supported by the Medicor Foundation (www.medicor.li) and UBS Optimus Foundation (www.ubs.com/microsites/optimus-foundation) through the BU differential diagnosis project in Benin. Fondation Follereau Luxembourg (www.ffl.lu/) gives core support to the CDTUB in Allada. M. E was supported by the Department of Economy, Science and Innovation (www.ewi-vlaanderen.be/) of the Flemish government (Belgium). B. d. J. was supported by the European Research Council-INTERRUPTB (starting grant number 311725). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.