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J Korean Med Sci. 2013;28(3):378-82.

Clinical effects of gemifloxacin on the delay of tuberculosis treatment.

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제1저자 김서윤 · 교신저자 김덕겸

소속 (1)
  1. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine and Lung Institute of Medical Research Center, Seoul National University College of Medicine, Seoul, Korea.

Abstract

Although gemifloxacin has low in vitro activity against Mycobacterium tuberculosis, the effect of gemifloxacin on the delay of tuberculosis (TB) treatment has not been validated in a clinical setting. The study group included patients with culture-confirmed pulmonary TB who initially received gemifloxacin for suspected community-acquired pneumonia (CAP). Two control groups contained patients treated with other fluoroquinolones or nonfluoroquinolone antibiotics. Sixteen cases were treated with gemifloxacin for suspected CAP before TB diagnosis. Sixteen and 32 patients were treated with other fluoroquinolones and nonfluoroquinolones, respectively. The median period from the initiation of antibiotics to the administration of anti-TB medication was nine days in the gemifloxacin group, which was significantly different from the other fluoroquinolones group (35 days). The median times for the nonfluoroquinolone group and the gemifloxacin group were not significantly different. There were no significant differences between the gemifloxacin and other fluoroquinolone group in terms of symptomatic and radiographic improvements. However, the frequency of radiographic improvement in the other fluoroquinolones group tended to be higher than in the gemifloxacin group. Gemifloxacin might be the preferred fluoroquinolone for treating CAP, to alleviate any concerns about delaying TB treatment.

Keywords

FluoroquinolonesPneumoniaTuberculosis

Figures

Fig. 1
Fig. 1 The time interval from the initiation of antibiotics until the administration of anti-TB drugs. The median time intervals from the initiation of antibiotics until the administration of anti-TB medications were nine days (range, 7-72 days) in the gemifloxacin group, 35 days in the other fluoroquinolones group (range, 14-72 days) and 7 days in the nonfluoroquinolone group (range, 3-63 days). *P value < 0.05.
Fig. 2
Fig. 2 Differences in the proportions of patients with symptomatic improvements. Symptomatic improvement was defined when more than one symptom of the followings was improved: febrile sense, cough, dyspnea, general weakness and pleuritic chest pain. The proportions of subjects with symptomatic improvements were 50% in the gemifloxacin group and the other fluoroquinolones group and 31% in the nonfluoroquinolone group.
Fig. 3
Fig. 3 Differences in the proportions of patients with radiographic improvement. Radiographic improvement was defined when radiograhic improvement was detected on a follow-up chest radiograph within 1-4 weeks after antibiotic treatment. Seven patients (44%) in the other fluoroquinolones group had improved follow-up radiographs, while four patients (25%) had improvements in the gemifloxacin group. Radiographic improvement was observed in only 12% of patients treated with nonfluoroquinolone antibiotics. *P value < 0.05.

그림 출처: PubMed Central 공개 논문 (PMC3594600)

그 밖의 정보
출판 형태
Controlled Clinical Trial, Journal Article
저널
Journal of Korean medical science · eISSN 1598-6357
전자 출판
2013-03-04
MeSH
Adult · Aged · Anti-Bacterial Agents / therapeutic use · Case-Control Studies · Fluoroquinolones / therapeutic use · Gemifloxacin · Humans · Middle Aged · Naphthyridines / therapeutic use · Pneumonia / complications / diagnosis · Radiography · Tuberculosis / complications / diagnostic imaging / drug therapy
Substances
Anti-Bacterial Agents · Fluoroquinolones · Naphthyridines · Gemifloxacin
참고문헌
21편