Abstract

BackgroundEuropean Gonococcal Antimicrobial Surveillance Programme (Euro-GASP) antimicrobial resistance (AMR) data are used to inform gonorrhoea treatment guidelines; therefore the data need to be robust and representative. We assessed the extent to which Euro-GASP reflects national measures of the AMR situation for Neisseria gonorrhoeae across the European Union/European Economic Area (EU/EEA).MethodsWe compared data from Euro-GASP with published national gonococcal AMR data from 15 countries for azithromycin, cefixime and ciprofloxacin for the period 2009 to 2013 and performed Poisson regression to identify differences (p < 0.05) between the proportions of resistant isolates. The 2014 Euro-GASP AMR data for each country (n = 19) were weighted to account for differences in the distribution of patient characteristics between Euro-GASP and EU/EEA epidemiological gonorrhoea surveillance data. Data were compared to determine whether estimates of resistance levels differed with regards to the 5% threshold used to assess the clinical utility of first-line gonorrhoea treatments. We assessed the quality of decentralised testing by comparing AMR data for isolates tested both centrally and in the participating laboratories, and by evaluating external quality assessment (EQA) performance.ResultsThere was no significant difference for azithromycin, cefixime and ciprofloxacin resistance when Euro-GASP country data were compared with data from national reports. Weighting slightly altered the Euro-GASP AMR estimates (by between − 4.7 and 4.7% from the unweighted estimates). Weighting resulted in greater changes in estimates of resistance to azithromycin (from − 9.5 to 2.7%) and ciprofloxacin (from − 14.8 to 17.9%) in countries with low isolate numbers and low completeness of reporting (n = 3). Weighting caused AMR levels to fall below or above the 5% threshold for cefixime or azithromycin, respectively in only two countries. Susceptibility category data submitted from the decentralised Euro-GASP laboratories were concordant with the Euro-GASP data (> 90%). EQA performance was also good; < 5% of the minimum inhibitory concentration (MIC) results differed by > 4-fold from the modal MIC of the EQA isolate.ConclusionsThe overall prevalence of AMR reported by Euro-GASP reflects closely the AMR situation for N. gonorrhoeae in the EU/EEA. Euro-GASP data can be used to provide robust AMR estimates to inform the European guideline for the management of gonorrhoea.

Highlights

  • European Gonococcal Antimicrobial Surveillance Programme (Euro-Gonococcal Antimicrobials Surveillance Programme (GASP)) antimicrobial resistance (AMR) data are used to inform gonorrhoea treatment guidelines; the data need to be robust and representative

  • The overall prevalence of AMR reported by Euro-GASP reflects closely the AMR situation for N. gonorrhoeae in the European Union (EU)/Economic Area (EEA)

  • Euro-GASP data can be used to provide robust AMR estimates to inform the European guideline for the management of gonorrhoea

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Summary

Introduction

European Gonococcal Antimicrobial Surveillance Programme (Euro-GASP) antimicrobial resistance (AMR) data are used to inform gonorrhoea treatment guidelines; the data need to be robust and representative. To ensure effective empirical therapy, surveillance of antimicrobial susceptibility in Neisseria gonorrhoeae, which informs revisions of gonorrhoea treatment guidelines, should be robust, reliable and quality-assured. Euro-GASP laboratories, usually one per country that frequently perform their own national or regional (sub-national) gonococcal antimicrobial susceptibility surveillance, have been invited to participate in decentralised testing by submitting their own gonococcal antimicrobial susceptibility data. Quality criteria have been agreed for countries to participate in decentralised testing using their own methods to test an agreed core antimicrobial panel: (i) a high concordance between the laboratories’ own antimicrobial susceptibility testing data and susceptibility data generated by Euro-GASP centralised susceptibility testing is required, and (ii) decentralised testing laboratories need to perform consistently well in the Euro-GASP external quality assessment (EQA) programme [7]

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