Scolaris Content Display Scolaris Content Display

Fluoroquinolones for treating tuberculosis

Esta versión no es la más reciente

Abstract

disponible en

Background

Fluoroquinolones are sometimes used to treat multiple‐drug‐resistant and drug‐sensitive tuberculosis. The effects of fluoroquinolones in tuberculosis regimens need to be assessed.

Objectives

To assess fluoroquinolones as additional or substitute components to antituberculous drug regimens for drug‐sensitive and drug‐resistant tuberculosis.

Search methods

In July 2007, we searched the Cochrane Infectious Diseases Group Specialized Register, CENTRAL (The Cochrane Library 2007, Issue 3), MEDLINE, EMBASE, LILACS, Science Citation Index, Database of Russian Publications, and metaRegister of Controlled Trials. We also scanned reference lists of all identified studies and contacted researchers.

Selection criteria

Randomized controlled trials of antituberculous regimens containing fluoroquinolones in people diagnosed with bacteriologically positive (sputum smear or culture) pulmonary tuberculosis.

Data collection and analysis

Two authors independently applied inclusion criteria, assessed the risk of bias in the trials, and extracted data. We used risk ratio (RR) for dichotomous data, mean difference (MD) for continuous data (both with 95% confidence intervals (CI)), and the random‐effects model if we detected heterogeneity and it was appropriate to combine data.

Main results

Eleven trials (1514 participants) met the inclusion criteria. No statistically significant difference was found in trials substituting ciprofloxacin, ofloxacin or moxifloxacin for first‐line drugs in relation to cure (416 participants, 3 trials), treatment failure (388 participants, 3 trials), or clinical or radiological improvement (216 participants, 2 trials). Substituting ciprofloxacin into first‐line regimens in drug‐sensitive tuberculosis led to a higher incidence of relapse (RR 7.17, 95% CI 1.33 to 38.58; 384 participants, 3 trials) and longer time to sputum culture conversion (MD 0.50 months, 95% CI 0.18 to 0.82; 168 participants, 1 trial), although this was confined to HIV‐positive participants. Substituting for ethambutol in first‐line regimens led to a higher incidence of total number of adverse events (RR 1.34, 95% CI 1.05 to 1.72; 492 participants, 2 trials). Adding or substituting levofloxacin to basic regimens in drug‐resistant areas had no effect. A comparison of sparfloxacin versus ofloxacin added to regimens showed no statistically significant difference in cure (184 participants, 2 trials), treatment failure (149 participants, 2 trials), or the total number of adverse events (253 participants, 3 trials).

Authors' conclusions

Only ciprofloxacin, ofloxacin, levofloxacin, sparfloxacin and moxifloxacin have been tested in randomized controlled trials for treating tuberculosis. We cannot recommend ciprofloxacin in treating tuberculosis. Trials of newer fluoroquinolones for treating tuberculosis are needed and are ongoing. No difference has been demonstrated between sparfloxacin and ofloxacin in drug‐resistant tuberculosis.

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Plain language summary

disponible en

Substituting or adding fluoroquinolones to established first‐line antituberculous drug regimens gives no additional benefit or risks

Fluoroquinolones have antituberculous activity, but are not one of the standard antituberculous medicines. Ciprofloxacin, ofloxacin, levofloxacin, sparfloxacin, and moxifloxacin have been tested in randomized controlled trials. Ciprofloxacin should not be used as a substitute drug in the standard antituberculous regimen as more people with drug‐sensitive tuberculosis had relapses and it took longer for them to be cured. However, it was no different in terms of cure or number of adverse events. Sparfloxacin was no better than ofloxacin when added to antituberculous regimens in drug‐resistant tuberculosis. Further trials are warranted.