Morrissey Ian, Maher Kirsty, Williams Laura, Shackcloth Jemma, Felmingham David, Reynolds Rosy
Quotient Bioresearch Limited, Microbiology, 7-9 William Road, London NW1 3ER, UK.
J Antimicrob Chemother. 2008 Nov;62 Suppl 2:ii97-103. doi: 10.1093/jac/dkn356.
To determine the antimicrobial susceptibility of Haemophilus influenzae and Moraxella catarrhalis causing community-acquired respiratory tract infections in the UK and Ireland from 1999/2000 to 2006/07.
Sentinel laboratories across the UK and Ireland contributed up to a fixed quota of isolates of defined organisms per annum. A central laboratory confirmed the isolates' identities, measured MICs by the BSAC agar dilution method and undertook further testing by standard methods. The variability of the MIC method was assessed by repeated annual testing of control isolates. BSAC and EUCAST breakpoints were used. Statistical analysis adjusted for inter-centre variation by random effects logistic regression.
A total of 7371 H. influenzae and 2529 M. catarrhalis isolates were investigated. Over 90% of the H. influenzae isolates were susceptible to most of the antimicrobials tested, the exceptions being ampicillin (84.6% susceptible), trimethoprim (84.0%), cefuroxime (82.9%), amoxicillin (77.2%) and cefaclor (11.7%). For M. catarrhalis, resistance was solely due to beta-lactamase (prevalence over 91%) reducing susceptibility to penicillins only. There was little evidence of decreased antimicrobial susceptibility between 1999 and 2007 in either pathogen, except for a reduction in susceptibility to trimethoprim in H. influenzae (90.3% to 82.6%, P < 0.00001). On the other hand, tetracycline susceptibility in H. influenzae increased over this period in the UK and Ireland (96.5 to 98.8%, P = 0.00008).
Despite increased resistance in respiratory pathogens from other parts of the world, the susceptibility of H. influenzae and M. catarrhalis to all agents, except tetracycline and trimethoprim in the case of H. influenzae, has remained constant during this longitudinal study.
确定1999/2000年至2006/07年期间在英国和爱尔兰引起社区获得性呼吸道感染的流感嗜血杆菌和卡他莫拉菌的抗菌药物敏感性。
英国和爱尔兰的哨点实验室每年提供固定配额的特定微生物分离株。一个中央实验室确认分离株的身份,通过英国抗菌化疗学会(BSAC)琼脂稀释法测量最低抑菌浓度(MIC),并采用标准方法进行进一步检测。通过对对照分离株进行年度重复检测来评估MIC方法的变异性。使用BSAC和欧洲抗菌药物敏感性试验委员会(EUCAST)的断点。通过随机效应逻辑回归对中心间变异进行统计分析。
共调查了7371株流感嗜血杆菌和2529株卡他莫拉菌。超过90%的流感嗜血杆菌分离株对大多数测试抗菌药物敏感,例外的是氨苄西林(84.6%敏感)、甲氧苄啶(84.0%)、头孢呋辛(82.9%)、阿莫西林(77.2%)和头孢克洛(11.7%)。对于卡他莫拉菌,耐药性仅归因于β-内酰胺酶(流行率超过91%),仅降低了对青霉素的敏感性。除了流感嗜血杆菌对甲氧苄啶的敏感性有所降低(从90.3%降至82.6%,P<0.00001)外,在1999年至2007年期间,这两种病原体的抗菌药物敏感性几乎没有下降的证据。另一方面,在此期间,英国和爱尔兰流感嗜血杆菌对四环素的敏感性有所增加(从96.5%增至98.8%,P = 0.00008)。
尽管世界其他地区呼吸道病原体的耐药性有所增加,但在这项纵向研究期间,流感嗜血杆菌和卡他莫拉菌对所有药物的敏感性保持不变,流感嗜血杆菌对四环素和甲氧苄啶除外。