Empiric treatment of community-acquired pneumonia with fluoroquinolones, and delays in the treatment of tuberculosis

被引:97
作者
Dooley, KE
Golub, J
Goes, FS
Merz, WG
Sterling, TR
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Epidemiol, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Div Infect Dis, Baltimore, MD 21205 USA
[5] Maryland Dept Hlth & Mental Hyg, Baltimore, MD USA
[6] Baltimore City Dept Hlth, Eastern Chest Clin, Baltimore, MD USA
关键词
D O I
10.1086/340618
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fluoroquinolones, which are widely used to treat community-acquired pneumonia, also have excellent in vitro activity against Mycobacterium tuberculosis. A retrospective cohort study was conducted among adults with culture-confirmed tuberculosis to assess the effect of empiric fluoroquinolone therapy on delays in the treatment of tuberculosis. Sixteen (48%) of 33 patients received fluoroquinolones for presumed bacterial pneumonia before tuberculosis was diagnosed and treated. There were no differences between the group who did and the group who did not receive fluoroquinolones, except that patients who received fluoroquinolones were more likely to present with shortness of breath. Among patients treated empirically with fluoroquinolones, the median time between presentation to the hospital and initiation of antituberculosis treatment was 21 days (interquartile range, 5-32 days); among those who were not, it was 5 days (interquartile range, 1-16 days; P = .04). Initial empiric therapy with a fluoroquinolone was associated with a delay in the initiation of appropriate antituberculosis treatment.
引用
收藏
页码:1607 / 1612
页数:6
相关论文
共 21 条
[1]  
[Anonymous], 2000, SCOTT LEV PHYS DRUG
[2]  
Bartlett John G., 2000, Clinical Infectious Diseases, V31, P347, DOI 10.1086/313954
[3]   INVITRO ACTIVITY OF 6 FLUORINATED QUINOLONES AGAINST MYCOBACTERIUM-TUBERCULOSIS [J].
BERLIN, OGW ;
YOUNG, LS ;
BRUCKNER, DA .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1987, 19 (05) :611-615
[4]  
*CDCP, 1999, MMWR-MORBID MORTAL W, V48, P732
[5]   COMPARATIVE INVITRO ACTIVITY OF 5 FLUOROQUINOLONES AGAINST MYCOBACTERIA [J].
DAVIES, S ;
SPARHAM, PD ;
SPENCER, RC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1987, 19 (05) :605-609
[6]   Global burden of tuberculosis - Estimated incidence, prevalence, and mortality by country [J].
Dye, C ;
Scheele, S ;
Dolin, P ;
Pathania, V ;
Raviglione, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (07) :677-686
[7]   Evaluation of an intensive intermittent-induction regimen and duration of short-course treatment for human immunodeficiency virus-related pulmonary tuberculosis [J].
El-Sadr, WM ;
Perlman, DC ;
Matts, JP ;
Nelson, ET ;
Cohn, DL ;
Salomon, N ;
Olibrice, M ;
Medard, F ;
Chirgwin, KD ;
Mildvan, D ;
Jones, BE ;
Telzak, EE ;
Klein, O ;
Heifets, L ;
Hafner, R .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (05) :1148-1158
[8]   EARLY BACTERICIDAL AND STERILIZING ACTIVITIES OF CIPROFLOXACIN IN PULMONARY TUBERCULOSIS [J].
KENNEDY, N ;
FOX, R ;
KISYOMBE, GM ;
SARUNI, AOS ;
UISO, LO ;
RAMSAY, ARC ;
NGOWI, FI ;
GILLESPIE, SH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (06) :1547-1551
[9]   Randomized controlled trial of a drug regimen that includes ciprofloxacin for the treatment of pulmonary tuberculosis [J].
Kennedy, N ;
Berger, L ;
Curram, J ;
Fox, R ;
Gutmann, J ;
Kisyombe, GM ;
Ngowi, FI ;
Ramsay, ARC ;
Saruni, AOS ;
Sam, N ;
Tillotson, G ;
Uiso, LO ;
Yates, M ;
Gillespie, SH .
CLINICAL INFECTIOUS DISEASES, 1996, 22 (05) :827-833
[10]  
KiaNoury D, 2000, INT J TUBERC LUNG D, V4, P1092