Past administration of β-lactam antibiotics and increase in the emergence of β-lactamase-producing bacteria in patients with orofacial odontogenic infections

被引:64
作者
Kuriyama, T
Nakagawa, K
Karasawa, T
Saiki, Y
Yamamoto, E
Nakamura, S
机构
[1] Kanazawa Univ, Sch Med, Dept Oral & Maxillofacial Surg, Kanazawa, Ishikawa 9208640, Japan
[2] Kanazawa Univ, Sch Med, Dept Bacteriol, Kanazawa, Ishikawa 9208640, Japan
来源
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY | 2000年 / 89卷 / 02期
关键词
D O I
10.1067/moe.2000.102040
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Objective. The purpose of this study was to determine the current status of beta-lactamase-producing bacteria in orofacial odontogenic infections. Study design. Microbiologic data regarding purulent exudate from ill cases with orofacial odontogenic infections were analyzed in relation to the past administration of beta-lactams. Results. beta-lactamase-producing bacteria were isolated more frequently from the beta-lactam-administered group (38.5%) than from the beta-lactam-nonadministered group (10.9%; P < .005), and they were isolated more frequently as the duration of administration increased. The predominant bacteria isolated included Prevotella (the most frequent isolate), viridans streptococci, Peptostreptococcus, and Fusobacterium, and 7.1% of total isolates produced beta-lactamase. Penicillin and cefazolin worked well with beta-lactamase-nonproducing Prevotella but were remarkably affected by beta-lactamase-producing Prevotella. Cefmetazole, sulbactam/cefoperazone, and imipenem worked well against both types of Prevotella, Conclusions. beta-lactams are still suitable for the first antimicrobial therapy in the treatment of these infections. However, because past beta-lactam administration increases the emergence of beta-lactamase-producing bacteria, beta-lactamase-stable antibiotics should be prescribed to patients with unresolved infections who have received beta-lactams.
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页码:186 / 192
页数:7
相关论文
共 46 条
[1]
SUSCEPTIBILITIES OF 394 BACTEROIDES-FRAGILIS, NON-B-FRAGILIS GROUP BACTEROIDES SPECIES, AND FUSOBACTERIUM SPECIES TO NEWER ANTIMICROBIAL AGENTS [J].
APPELBAUM, PC ;
SPANGLER, SK ;
JACOBS, MR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (06) :1214-1218
[2]
BETA-LACTAMASE PRODUCTION AND SUSCEPTIBILITIES TO AMOXICILLIN, AMOXICILLIN-CLAVULANATE, TICARCILLIN, TICARCILLIN-CLAVULANATE, CEFOXITIN, IMIPENEM, AND METRONIDAZOLE OF 320 NON-BACTEROIDES-FRAGILIS-BACTEROIDES ISOLATES AND 129 FUSOBACTERIA FROM 28 UNITED-STATES CENTERS [J].
APPELBAUM, PC ;
SPANGLER, SK ;
JACOBS, MR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (08) :1546-1550
[3]
Baker K A, 1994, Dent Clin North Am, V38, P689
[4]
AEROBIC AND ANAEROBIC MICROBIOLOGY OF PERIAPICAL ABSCESS [J].
BROOK, I ;
FRAZIER, EH ;
GHER, ME .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1991, 6 (02) :123-125
[5]
EMERGENCE OF BETA-LACTAMASE-PRODUCING AEROBIC AND ANAEROBIC-BACTERIA IN THE OROPHARYNX OF CHILDREN FOLLOWING PENICILLIN CHEMOTHERAPY [J].
BROOK, I ;
GOBER, AE .
CLINICAL PEDIATRICS, 1984, 23 (06) :338-341
[6]
BROOK I, 1988, LARYNGOSCOPE, V98, P428
[7]
Present status of therapy for anaerobic infections [J].
Finegold, SM ;
Wexler, HM .
CLINICAL INFECTIOUS DISEASES, 1996, 23 :S9-S14
[8]
THE DEVELOPMENT OF PENICILLIN-RESISTANT ORAL STREPTOCOCCI AFTER REPEATED PENICILLIN PROPHYLAXIS [J].
FLEMING, P ;
FEIGAL, RJ ;
KAPLAN, EL ;
LILJEMARK, WF ;
LITTLE, JW .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1990, 70 (04) :440-444
[9]
Flynn TR, 1991, ORAL MAXILLOFAC SURG, V3, P311
[10]
OROFACIAL ODONTOGENIC INFECTIONS - REVIEW OF MICROBIOLOGY AND CURRENT TREATMENT [J].
GILL, Y ;
SCULLY, C .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 1990, 70 (02) :155-158