Antibiotic susceptibility profiles for group B streptococci isolated from neonates, 1995-1998

被引:83
作者
Lin, FYC
Azimi, PH
Weisman, LE
Philips, JB
Regan, J
Clark, P
Rhoads, GG
Clemens, J
Troendle, J
Pratt, E
Brenner, RA
Gill, V
机构
[1] NICHHD, NIH, Bethesda, MD 20892 USA
[2] NIH, Dept Clin Pathol, Warren G Magnuson Clin Ctr, Microbiol Serv, Bethesda, MD 20892 USA
[3] Westat, Rockville, MD USA
[4] Childrens Hosp, Med Ctr, Oakland, CA 94609 USA
[5] Baylor Coll Med, Houston, TX 77030 USA
[6] Univ Alabama, Birmingham, AL USA
[7] Columbia Univ Hlth Sci, New York, NY USA
[8] Univ Florida, Gainesville, FL USA
[9] Univ Med & Dent New Jersey, Piscataway, NJ 08854 USA
关键词
D O I
10.1086/313936
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibiotic susceptibility profiles were analyzed for 119 invasive and 227 colonizing strains of group B streptococci isolated from neonates at 6 US academic centers, All strains were susceptible to penicillin, vancomycin, chloramphenicol, and cefotaxime, The rate of resistance to erythromycin was 20.2% and to clindamycin was 6.9%. Resistance to erythromycin increased in 1997, Type V strains were more resistant to erythromycin than were type Ia (P = .003) and type Tb (P = .004) strains and were more resistant to clindamycin than were type Ia (P < .001), type Tb (P = .01), and type III (P = .001) strains. Resistance rates varied with geographic region: in California, there were high rates of resistance to erythromycin and clindamycin (32% and 12%, respectively), and low rates in Florida (8.5% and 2.1%, respectively). Penicillin continues to be the drug of choice for treatment of group B streptococcus infection. For women who are penicillin intolerant, however, the selection of an alternative antibiotic should be guided by contemporary resistence patterns observed in that region.
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收藏
页码:76 / 79
页数:4
相关论文
共 15 条
[1]   PERINATAL GROUP-B STREPTOCOCCAL COLONIZATION AND INFECTION [J].
ALLARDICE, JG ;
BASKETT, TF ;
SESHIA, MMK ;
BOWMAN, N ;
MALAZDREWICZ, R .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1982, 142 (06) :617-620
[2]  
[Anonymous], 1996, MMWR Recomm Rep, V45, P1
[3]   Inhibition enzyme-linked immunosorbent assay for serotyping of group B streptococcal isolates [J].
Arakere, G ;
Flores, AE ;
Ferrieri, P ;
Frasch, CE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (08) :2564-2567
[4]   ANTIMICROBIAL SUSCEPTIBILITY OF GROUP-B STREPTOCOCCI ISOLATED FROM A VARIETY OF CLINICAL SOURCES [J].
BAKER, CJ ;
WEBB, BJ ;
BARRETT, FF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1976, 10 (01) :128-131
[5]   ANTIBIOTIC-RESISTANCE PATTERNS OF GROUP-B STREPTOCOCCI IN PREGNANT-WOMEN [J].
BERKOWITZ, K ;
REGAN, JA ;
GREENBERG, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (01) :5-7
[6]   PREVENTION OF EARLY-ONSET NEONATAL GROUP-B STREPTOCOCCAL DISEASE WITH SELECTIVE INTRAPARTUM CHEMOPROPHYLAXIS [J].
BOYER, KM ;
GOTOFF, SP .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (26) :1665-1669
[7]   GROUP-B STREPTOCOCCAL CARRIAGE AND DISEASE - A 6-YEAR PROSPECTIVE-STUDY [J].
DILLON, HC ;
KHARE, S ;
GRAY, BM .
JOURNAL OF PEDIATRICS, 1987, 110 (01) :31-36
[8]   Antimicrobial susceptibilities of group B streptococci isolated between 1992 and 1996 from patients with bacteremia or meningitis [J].
Fernandez, M ;
Hickman, ME ;
Baker, CJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) :1517-1519
[9]   REDUCTION OF MORBIDITY AND MORTALITY-RATES FOR NEONATAL GROUP-B STREPTOCOCCAL DISEASE THROUGH EARLY DIAGNOSIS AND CHEMOPROPHYLAXIS [J].
LIM, DV ;
MORALES, WJ ;
WALSH, AF ;
KAZANIS, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 23 (03) :489-492
[10]   Change in antibiotic resistance of group B Streptococcus:: Impact on intrapartum management [J].
Morales, WJ ;
Dickey, SS ;
Bornick, P ;
Lim, DV .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1999, 181 (02) :310-312