THE NEW MACROLIDE ANTIBIOTICS - AZITHROMYCIN, CLARITHROMYCIN, DIRITHROMYCIN, AND ROXITHROMYCIN

被引:112
作者
BAHAL, N
NAHATA, MC
机构
[1] OHIO STATE UNIV,COLL PHARM,500 W 12TH AVE,COLUMBUS,OH 43210
[2] OHIO STATE UNIV,COLL MED,COLUMBUS,OH 43210
[3] AMER SOC HOSP PHARMACISTS,COLUMBUS,OH
[4] CHILDRENS HOSP,WEXNER INST PEDIAT RES,COLUMBUS,OH 43205
关键词
D O I
10.1177/106002809202600112
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the chemistry, antimicrobial spectrum, pharmacokinetics, clinical trials, adverse effects, and drug interactions of four new macrolide antibiotics: azithromycin, clarithromycin, dirithromycin, and roxithromycin. DATA SOURCES: Information was obtained from comparative clinical trials, abstracts, conference proceedings, and review articles. Indexing terms included azithromycin, clarithromycin, dirithromycin, erythromycin, roxithromycin, and macrolide antibiotics. STUDY SELECTION: Emphasis was placed on comparative clinical trials involving the new macrolide antibiotics. DATA EXTRACTION: Data from human studies published in the English language were evaluated. Trials were assessed by sample size, macrolide dosage regimen, and therapeutic response. DATA SYNTHESIS: The erythromycins have gained widespread use in treating a variety of infections. Although they are effective, limitations include the need to administer four times a day and the intolerable adverse gastrointestinal effects. Four of the more extensively studied agents, azithromycin, clarithromycin, dirithromycin, and roxithromycin, are currently being studied in patients. Based on the studies to date, the newer macrolides may offer several advantages over erythromycin, including: (1) greater antimicrobial activity against certain organisms; (2) longer elimination half-life, thus allowing less frequent administration; and (3) lower incidence of adverse gastrointestinal effects. CONCLUSIONS: The new macrolide antibiotics appear to offer an improvement over erythromycin. Definitive conclusions about the role of these drugs should await completion of ongoing clinical studies.
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页码:46 / 55
页数:10
相关论文
共 85 条
[21]  
CRAFT JC, 1990, 30TH INT C ANT AG CH
[22]  
DABERNAT H, 1990, 30TH INT C ANT AG CH
[23]  
DAUTZENBERG B, 1990, 30TH INT C ANT AG CH
[24]   AZITHROMYCIN (CP-62,993) IN ACUTE EXACERBATIONS OF CHRONIC-BRONCHITIS - AN OPEN CLINICAL, MICROBIOLOGICAL AND PHARMACOKINETIC STUDY [J].
DAVIES, BI ;
MAESEN, FPV ;
GUBBELMANS, R .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1989, 23 (05) :743-751
[25]  
DUBOIS J, 1990, 30TH INT C ANT AG CH
[26]   INVITRO AND INVIVO ACTIVITIES OF CLARITHROMYCIN AGAINST MYCOBACTERIUM-AVIUM [J].
FERNANDES, PB ;
HARDY, DJ ;
MCDANIEL, D ;
HANSON, CW ;
SWANSON, RN .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) :1531-1534
[27]  
FERNANDES PB, 1988, DRUG EXP CLIN RES, V14, P445
[28]  
FERRERO JL, 1990, DRUG METAB DISPOS, V18, P441
[29]   THE PHARMACOKINETICS OF AZITHROMYCIN IN HUMAN SERUM AND TISSUES [J].
FOULDS, G ;
SHEPARD, RM ;
JOHNSON, RB .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 25 :73-82
[30]  
FUTTERMAN M, 1990, 30TH INT C ANT AG CH