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Fluoroquinolones kill bacteria by inhibiting DNA gyrase. They also downregulate a gene involved in cardiac repolarization, which can cause prolongation of the QT interval. Some fluoroquinolones have been withdrawn from the market because of their cardiac toxicity, but the cardiac risks of those currently in clinical use remain controversial.
Scandinavian investigators probed national medical databases to quantitate risk for arrhythmia among adults (age range, 40–79) who were treated with fluoroquinolones in Denmark (1997–2001) and Sweden (2006–2013). Only 66 instances of arrhythmia were identified during or after more than 900,000 fluoroquinolone courses. This low rate was nearly identical to the rate of arrhythmia in an equally large control group that received penicillin V (a drug without cardiac toxicity that was standard treatment for respiratory infection in these countries). The patient cohorts were well matched for a long list of medical conditions and concomitant medications; in subgroup analyses, no characteristics were identified that conferred excess risk for fluoroquinolone-associated arrhythmia. The most commonly prescribed fluoroquinolones were ciprofloxacin (in 83% of courses) and norfloxacin (in 12% of courses).
Inghammar M et al. Oral fluoroquinolone use and serious arrhythmia: Bi-national cohort study. BMJ 2016 Feb 26; 352:i843. (http://dx.doi.org/10.1136/bmj.i843)
Comment
This study argues against the cardiac toxicity of ciprofloxacin and norfloxacin, with the caveat that investigators lacked access to such pertinent clinical information as treatment indications, treatment durations, and presence of concomitant electrolyte disorders. The study is somewhat less convincing in exonerating other fluoroquinolones, some of which have been implicated as cardiotoxic in similar, albeit smaller, studies (Clin Infect Dis 2015; 60:566).