Azithromycin in the treatment of Legionella pneumonia requiring hospitalization

被引:46
作者
Plouffe, JF
Breiman, RF
Fields, BS
Herbert, M
Inverso, J
Knirsch, C
Kolokathis, A
Marrie, TJ
Nicolle, L
Schwartz, DB
机构
[1] Ohio State Univ, Columbus, OH 43210 USA
[2] Mt Carmel Med Ctr, Columbus, OH USA
[3] Ctr Dis Control & Prevent, Atlanta, GA USA
[4] Pfizer, New York, NY USA
[5] Albany VA Hosp, Albany, NY USA
[6] Univ Alberta, Edmonton, AB, Canada
[7] Univ Manitoba, Winnipeg, MB, Canada
关键词
D O I
10.1086/379329
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Azithromycin is highly active against Legionella pneumophila and has been shown to be efficacious in animal models and in clinical studies of patients with legionnaires disease. This open, prospective, multicenter trial evaluated azithromycin for the treatment of legionnaires disease. Twenty-five hospitalized patients with community-acquired pneumonia and a positive result of a L. pneumophila serogroup 1 urinary antigen assay received monotherapy with intravenous azithromycin (500 mg/day) for 2-7 days, followed by oral azithromycin (1500 mg administered over the course of 3 or 5 days). The mean total duration of intravenous plus oral therapy was 7.92 days. The overall cure rate among clinically evaluable patients was 95% (20 of 21 patients) at 10 14 days after therapy and 96% (22 of 23 patients) at 4-6 weeks after therapy. The results of this study support previously reported data demonstrating that azithromycin is both safe and efficacious for the treatment of hospitalized patients with legionnaires disease.
引用
收藏
页码:1475 / 1480
页数:6
相关论文
共 42 条
[1]  
ANDREWS JM, 1990, AM REV RESPIR DIS, V141, pA598
[2]   THE FUTURE-ROLE AND IMPORTANCE OF MACROLIDES [J].
BALL, P .
JOURNAL OF HOSPITAL INFECTION, 1991, 19 :47-59
[3]  
Bartlett John G., 2000, Clinical Infectious Diseases, V31, P347, DOI 10.1086/313954
[4]   Therapy for Legionnaires disease -: In response [J].
Edelstein, PH .
ANNALS OF INTERNAL MEDICINE, 1999, 130 (10) :864-864
[5]   INVITRO ACTIVITY OF AZITHROMYCIN AGAINST CLINICAL ISOLATES OF LEGIONELLA SPECIES [J].
EDELSTEIN, PH ;
EDELSTEIN, MAC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (01) :180-181
[6]   NEW AND EMERGING ETIOLOGIES FOR COMMUNITY-ACQUIRED PNEUMONIA WITH IMPLICATIONS FOR THERAPY - A PROSPECTIVE MULTICENTER STUDY OF 359 CASES [J].
FANG, GD ;
FINE, M ;
ORLOFF, J ;
ARISUMI, D ;
YU, VL ;
KAPOOR, W ;
GRAYSTON, JT ;
WANG, SP ;
KOHLER, R ;
MUDER, RR ;
YEE, YC ;
RIHS, JD ;
VICKERS, RM .
MEDICINE, 1990, 69 (05) :307-316
[7]  
File TM, 1999, CLIN INFECT DIS, V29, P426, DOI 10.1086/520227
[8]   The role of atypical pathogens: Mycoplasma pneumoniae, Chlamydia pneumoniae, and Legionella pneumophila in respiratory infection [J].
File, TM ;
Tan, JS ;
Plouffe, JF .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 1998, 12 (03) :569-+
[9]   A multicenter, randomized study comparing the efficacy and safety of intravenous and/or oral levofloxacin versus ceftriaxone and/or cefuroxime axetil in treatment of adults with community-acquired pneumonia [J].
File, TM ;
Segreti, J ;
Dunbar, L ;
Player, R ;
Kohler, R ;
Williams, RR ;
Kojak, C ;
Rubin, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (09) :1965-1972
[10]   A COMPARISON OF THE EFFICACY OF AZITHROMYCIN AND CLARITHROMYCIN IN ORAL-THERAPY OF EXPERIMENTAL AIRBORNE LEGIONNAIRES-DISEASE [J].
FITZGEORGE, RB ;
LEVER, S ;
BASKERVILLE, A .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 :171-176