CHU de Caen, Microbiologie & Centre National de Référence de la Résistance aux Antibiotiques (laboratoire associé Entérocoques et résistances particulières des bactéries à Gram positif), Caen, France ; CHU de Caen, Service de Microbiologie - Niveau 3, Avenue de la Côte de Nacre-CS30001, 14033 Caen, Cedex 9, France.
Pfizer Inc, Collegeville, PA USA.
Antimicrob Resist Infect Control. 2014 Dec 1;3(1):36. doi: 10.1186/2047-2994-3-36. eCollection 2014.
Clinically important Gram-positive and -negative isolates were collected from patients in France between 2004 and 2012 as a part of the Tigecycline Evaluation and Surveillance Trial.
MICs were determined using methodology described by the Clinical and Laboratory Standards Institute.
In total, 17,135 isolates were contributed by 29 medical centres; respiratory (25.1%) and cardiovascular (20.3%) sources predominated. High susceptibility was observed among Enterococcus spp. and Staphylococcus aureus (including methicillin-resistant S. aureus [MRSA]) to linezolid (100%), tigecycline (≥99.8%) and vancomycin (≥94.6%). The percentage of MRSA decreased from 34.3% in 2004 to 20.0% in 2009 before increasing to 34.7% in 2012. Vancomycin, linezolid, levofloxacin and carbapenems were highly active (≥99.6%) against Streptococcus pneumoniae; 3.2% were PRSP. Escherichia coli showed peak susceptibility to the carbapenems (≥99.9%), tigecycline (99.3%) and amikacin (97.9%); significant (p < 0.01) decreases in susceptibility were observed for ampicillin, cefepime and ceftriaxone between 2004 and 2012. ESBL production among E. coli increased from 3.0% (2004) to 14.9% (2012). High susceptibility was noted among Haemophilus influenzae to levofloxacin (100%), amoxicillin-clavulanate (99.2%), carbapenems (≥98.7%) and ceftriaxone (98.5%); β-lactamase production fluctuated with no notable trend between 18.1% (2007) and 27.7% (2011). Klebsiella spp. were highly susceptible to carbapenems (≥99.6%) and amikacin (≥96.4%); significant (p < 0.01) decreases in amoxicillin-clavulanate, cefepime, ceftriaxone, levofloxacin, piperacillin-tazobactam and tigecycline susceptibility were observed among K. pneumoniae between 2004 and 2012. Only imipenem was highly active (96.5% susceptible) against Acinetobacter baumannii. Imipenem and amikacin (87.7% and 87.1% susceptible) were the most active agents against P. aeruginosa; 10.2% of isolates were categorized as multidrug resistant.
Carbapenems, linezolid, tigecycline and vancomycin conserved good in vitro activity against most pathogens (according to their spectrum of activity) in France between 2004 and 2012.
2004 年至 2012 年期间,从法国的患者中收集了具有临床重要性的革兰氏阳性和革兰氏阴性分离株,作为替加环素评估和监测试验的一部分。
使用临床和实验室标准协会描述的方法确定 MIC。
总共由 29 个医疗中心提供了 17135 株分离株;呼吸道(25.1%)和心血管(20.3%)来源占主导地位。肠球菌属和金黄色葡萄球菌(包括耐甲氧西林金黄色葡萄球菌[MRSA])对利奈唑胺(100%)、替加环素(≥99.8%)和万古霉素(≥94.6%)具有高度敏感性。MRSA 的百分比从 2004 年的 34.3%下降到 2009 年的 20.0%,然后在 2012 年上升到 34.7%。万古霉素、利奈唑胺、左氧氟沙星和碳青霉烯类对肺炎链球菌具有高度活性(≥99.6%);3.2%为 PRSP。大肠杆菌对碳青霉烯类(≥99.9%)、替加环素(99.3%)和阿米卡星(97.9%)表现出最高的敏感性;2004 年至 2012 年间,对氨苄西林、头孢吡肟和头孢曲松的敏感性显著(p<0.01)下降。大肠杆菌中产 ESBL 的比例从 2004 年的 3.0%(2004 年)增加到 2012 年的 14.9%。流感嗜血杆菌对左氧氟沙星(100%)、阿莫西林-克拉维酸(99.2%)、碳青霉烯类(≥98.7%)和头孢曲松(98.5%)具有高度敏感性;β-内酰胺酶的产生在 18.1%(2007 年)至 27.7%(2011 年)之间波动,没有明显趋势。克雷伯菌属对碳青霉烯类(≥99.6%)和阿米卡星(≥96.4%)具有高度敏感性;2004 年至 2012 年间,对阿莫西林-克拉维酸、头孢吡肟、头孢曲松、左氧氟沙星、哌拉西林-他唑巴坦和替加环素的敏感性显著(p<0.01)下降。只有亚胺培南对鲍曼不动杆菌具有高度活性(96.5%敏感)。亚胺培南和阿米卡星(87.7%和 87.1%敏感)是对铜绿假单胞菌最有效的药物;10.2%的分离株被归类为多药耐药。
2004 年至 2012 年期间,在法国,碳青霉烯类、利奈唑胺、替加环素和万古霉素对大多数病原体(根据其活性谱)保持良好的体外活性。