POTENTIAL IMPROVEMENTS IN THERAPEUTIC OPTIONS FOR MYCOPLASMAL RESPIRATORY-INFECTIONS

被引:18
作者
BEBEAR, C [1 ]
DUPON, M [1 ]
RENAUDIN, H [1 ]
DEBARBEYRAC, B [1 ]
机构
[1] HOP PELLEGRIN,SERV MALAD INFECTIEUSES & MED INTERNE,F-33076 BORDEAUX,FRANCE
关键词
D O I
10.1093/clinids/17.Supplement_1.S202
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrolides and tetracyclines are the most active antibiotics against mycoplasmas in vitro. In particular, erythromycin has been widely used for the treatment of infections caused by Mycoplasma pneumoniae. However, improvements in therapy are needed to accommodate specific characteristics of the microorganism or unusual manifestations of the illness it causes. Because no rapid microbiological. technique is available for the diagnosis of M. pneumoniae infections, empirical treatment must be effective against other relevant pathogens as well. Macrolides and fluoroquinolones have recently undergone substantial development. The newer macrolides have more favorable pharmacokinetic properties and are better tolerated than older agents of this class, while the newer fluoroquinolones exhibit a broadened spectrum of in vitro activity that in some instances includes M. pneumoniae and Streptococcus pneumoniae. Although the existing data on in vivo efficacy are only preliminary, the newer macrolides and fluoroquinolones are promising agents for the treatment of M. pneumoniae infection and, more generally, for that of community-acquired pneumonia.
引用
收藏
页码:S202 / S207
页数:6
相关论文
共 49 条
[21]   NEW DIRECTIONS FOR MACROLIDE ANTIBIOTICS - STRUCTURAL MODIFICATIONS AND INVITRO ACTIVITY [J].
KIRST, HA ;
SIDES, GD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) :1413-1418
[22]   NEW DIRECTIONS FOR MACROLIDE ANTIBIOTICS - PHARMACOKINETICS AND CLINICAL EFFICACY [J].
KIRST, HA ;
SIDES, GD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) :1419-1422
[24]  
KOBAYASHI H, 1987, AM J MED, V82, P169
[25]   ASSOCIATION OF THE VIRUS-LIKE INFECTIOUS AGENT ORIGINALLY REPORTED IN PATIENTS WITH AIDS WITH ACUTE FATAL DISEASE IN PREVIOUSLY HEALTHY NON-AIDS PATIENTS [J].
LO, SC ;
DAWSON, MS ;
NEWTON, PB ;
SONODA, MA ;
SHIH, JW ;
ENGLER, WF ;
WANG, RYH ;
WEAR, DJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1989, 41 (03) :364-376
[26]   CURRENT STATUS OF ANTIBIOTIC-TREATMENT FOR MYCOPLASMA-PNEUMONIAE INFECTIONS [J].
MCCRACKEN, GH .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1986, 5 (01) :167-171
[27]   PHAGOCYTE UPTAKE AND TRANSPORT OF AZITHROMYCIN [J].
MCDONALD, PJ ;
PRUUL, H .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1991, 10 (10) :828-833
[28]   ISOLATION OF MYCOPLASMA-PNEUMONIAE FROM CHILDREN WITH LOWER-RESPIRATORY-TRACT INFECTIONS [J].
NAGAYAMA, Y ;
SAKURAI, N ;
YAMAMOTO, K ;
HONDA, A ;
MAKUTA, M ;
SUZUKI, R .
JOURNAL OF INFECTIOUS DISEASES, 1988, 157 (05) :911-917
[29]   ISOLATION OF MYCOPLASMA-PNEUMONIAE FROM PLEURAL FLUID AND OR CEREBROSPINAL-FLUID - REPORT OF 4 CASES [J].
NAGAYAMA, Y ;
SAKURAI, N ;
TAMAI, K ;
NIWA, A ;
YAMAMOTO, K .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1987, 19 (05) :521-524
[30]   INVITRO DEVELOPMENT OF RESISTANCE TO ERYTHROMYCIN, OTHER MACROLIDE ANTIBIOTICS, AND LINCOMYCIN IN MYCOPLASMA-PNEUMONIAE [J].
NIITU, Y ;
HASEGAWA, S ;
KUBOTA, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1974, 5 (05) :513-519