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1996 - 1997年冬季比利时肺炎球菌耐药性监测

Surveillance of pneumococcal resistance in Belgium during winter 1996-1997.

作者信息

Vanhoof R, Carpentier M, Glupczynski Y, Gordts B, Magerman K, Mans Y, Nyssen H J, Simon A, Surmont I, Van De Vyvere M, Van Landuyt H, Van Nimmen L, Van Noyen R

机构信息

Eenheid Antibiotica-onderzoek, Pasteurinstituut-Brussel.

出版信息

Acta Clin Belg. 1998 Aug;53(4):275-81. doi: 10.1080/17843286.1998.11754175.

Abstract

This study tested 212 pneumococcal isolates from 9 institutions for their susceptibilities to penicillin, ampicillin, amoxycillin, amoxycillin/clavulanate, cefaclor, cefuroxime, cefotaxime, imipenem, tetracycline, erythromycin, and clarithromycin using NCCLS-standardized microdilution. Penicillin-insusceptibility was 12.3% [5.7% intermediate (0.12-1 microgram/ml) and 6.6% high-level (> or = 2 micrograms/ml)], tetracycline-insusceptibility (> or = 4 micrograms/ml) 31.1%, and erythromycin-insusceptibility (> or = 0.5 microgram/ml) 31.1% as well. Erythromycin-insusceptible isolates showed cross-insusceptibility to clarithromycin. Penicillin-susceptible isolates were susceptible to all beta-lactams. MICs of all beta-lactams rose with those of penicillin for penicillin-insusceptible isolates. Ampicillin and penicillin were equally potent against penicillin-insusceptible isolates, imipenem, cefotaxime, and amoxycillin +/- clavulanate were more potent (generally 5, 1, and 1 doubling dilution, respectively), and cefuroxime and cefaclor less potent (generally 1 and 6 doubling dilutions, respectively). Most penicillin-insusceptible isolates were high-level resistant to cefaclor (> or = 32 micrograms/ml). Although MICs of all beta-lactams rose with those of penicillin, resistance to penicillin was not absolute in terms of cross-resistance. Most penicillin-intermediate and high-level penicillin-resistant isolates remained fully susceptible and intermediate, respectively, to amoxycillin +/- clavulanate, cefotaxime, and imipenem, but not to cefuroxime. Penicillin-susceptible isolates were 76.9%, 42.3%, and 34.6% co-insusceptible to tetracycline, erythromycin, and tetracycline plus erythromycin, respectively. Most penicillin-, tetracycline-, and erythromycin-insusceptible isolates were of capsular types 23 >> 6 > 19 > 32, 19 > 6 > 28 > 23, and 19 > 6 > 14 > 23, respectively. Compared to winter 1994-1995, insusceptibility to penicillin, tetracycline, and erythromycin rose by some 4%, 4%, and 13%, respectively.

摘要

本研究采用美国国家临床实验室标准化委员会(NCCLS)标准化微量稀释法,检测了来自9个机构的212株肺炎球菌分离株对青霉素、氨苄西林、阿莫西林、阿莫西林/克拉维酸、头孢克洛、头孢呋辛、头孢噻肟、亚胺培南、四环素、红霉素和克拉霉素的敏感性。青霉素不敏感率为12.3%[5.7%为中介水平(0.12 - 1微克/毫升),6.6%为高水平(≥2微克/毫升)],四环素不敏感率(≥4微克/毫升)为31.1%,红霉素不敏感率(≥0.5微克/毫升)也为31.1%。对红霉素不敏感的分离株对克拉霉素也表现出交叉不敏感。对青霉素敏感的分离株对所有β-内酰胺类药物均敏感。对于对青霉素不敏感的分离株,所有β-内酰胺类药物的最低抑菌浓度(MIC)均随青霉素MIC的升高而升高。氨苄西林和青霉素对青霉素不敏感分离株的抗菌效力相当,亚胺培南、头孢噻肟和阿莫西林±克拉维酸的抗菌效力更强(通常分别为5倍、1倍和1倍稀释倍数),而头孢呋辛和头孢克洛的抗菌效力较弱(通常分别为1倍和6倍稀释倍数)。大多数对青霉素不敏感的分离株对头孢克洛高水平耐药(≥32微克/毫升)。尽管所有β-内酰胺类药物的MIC均随青霉素MIC的升高而升高,但就交叉耐药而言,对青霉素的耐药并非绝对。大多数青霉素中介水平和高水平耐药的分离株对阿莫西林±克拉维酸、头孢噻肟和亚胺培南仍分别保持完全敏感和中介水平敏感,但对头孢呋辛不敏感。对青霉素敏感的分离株对四环素、红霉素以及四环素加红霉素的共同不敏感率分别为76.9%、42.3%和34.6%。大多数对青霉素、四环素和红霉素不敏感的分离株分别属于23型>>6型>19型>32型、19型>6型>28型>23型和19型>6型>14型>23型。与1994 - 1995年冬季相比,对青霉素、四环素和红霉素的不敏感率分别上升了约4%、4%和13%。

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