- Klausner, Jeffrey D;
- Bristow, Claire C;
- Soge, Olusegun O;
- Shahkolahi, Akbar;
- Waymer, Toni;
- Bolan, Robert K;
- Philip, Susan S;
- Asbel, Lenore E;
- Taylor, Stephanie N;
- Mena, Leandro A;
- Goldstein, Deborah A;
- Powell, Jonathan A;
- Wierzbicki, Michael R;
- Morris, Sheldon R
Background
Novel treatment strategies to slow the continued emergence and spread of antimicrobial resistance in Neisseria gonorrhoeae are urgently needed. A molecular assay that predicts in vitro ciprofloxacin susceptibility is now available but has not been systematically studied in human infections.Methods
Using a genotypic polymerase chain reaction assay to determine the status of the N. gonorrhoeae gyrase subunit A serine 91 codon, we conducted a multisite prospective clinical study of the efficacy of a single oral dose of ciprofloxacin 500 mg in patients with culture-positive gonorrhea. Follow-up specimens for culture were collected to determine microbiological cure 5-10 days post-treatment.Results
Of the 106 subjects possessing culture-positive infections with wild-type gyrA serine N. gonorrhoeae genotype, the efficacy of single-dose oral ciprofloxacin treatment in the per-protocol population was 100% (95% 1-sided confidence interval, 97.5-100%).Conclusions
Resistance-guided treatment of N. gonorrhoeae infections with single-dose oral ciprofloxacin was highly efficacious. The widespread introduction and scale-up of gyrA serine 91 genotyping in N. gonorrhoeae infections could have substantial medical and public health benefits in settings where the majority of gonococcal infections are ciprofloxacin susceptible.Clinical trials registration
NCT02961751.