首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >In Vitro Activity of Doripenem a Carbapenem for the Treatment of Challenging Infections Caused by Gram-Negative Bacteria against Recent Clinical Isolates from the United States
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In Vitro Activity of Doripenem a Carbapenem for the Treatment of Challenging Infections Caused by Gram-Negative Bacteria against Recent Clinical Isolates from the United States

机译:多利培南(一种碳青霉烯类药物用于治疗革兰氏阴性细菌引起的挑战性感染)针对美国最近的临床分离株的体外活性。

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摘要

Doripenem, a 1β-methylcarbapenem, is a broad-spectrum antibiotic approved for the treatment of complicated urinary tract and complicated intra-abdominal infections. An indication for hospital-acquired pneumonia including ventilator-associated pneumonia is pending. The current study examined the activity of doripenem against recent clinical isolates for the purposes of its ongoing clinical development and future longitudinal analysis. Doripenem and comparators were tested against 12,581 U.S. clinical isolates collected between 2005 and 2006 including isolates of Staphylococcus aureus, coagulase-negative staphylococci, Streptococcus pneumoniae, Enterobacteriaceae, Pseudomonas aeruginosa, and Acinetobacter spp. MICs (μg/ml) were established by broth microdilution. By MIC90, doripenem was comparable to imipenem and meropenem in activity against S. aureus (methicillin susceptible, 0.06; resistant, 8) and S. pneumoniae (penicillin susceptible, ≤0.015; resistant, 1). Against ceftazidime-susceptible Enterobacteriaceae, the MIC90 of doripenem (0.12) was comparable to that of meropenem (0.12) and superior to that of imipenem (2), though susceptibility of isolates exceeded 99% for all evaluated carbapenems. The activity of doripenem was not notably altered against ceftazidime-nonsusceptible or extended-spectrum β-lactamase screen-positive Enterobacteriaceae. Doripenem was the most potent carbapenem tested against P. aeruginosa (MIC90/% susceptibility [%S]: ceftazidime susceptible = 2/92%S, nonsusceptible = 16/61%S; imipenem susceptible = 1/98.5%S, nonsusceptible = 8/56%S). Against imipenem-susceptible Acinetobacter spp., doripenem (MIC90 = 2, 89.1%S) was twice as active by MIC90 as were imipenem and meropenem. Overall, doripenem potency was comparable to those of meropenem and imipenem against gram-positive cocci and doripenem was equal or superior in activity to meropenem and imipenem against Enterobacteriaceae, including β-lactam-nonsusceptible isolates. Doripenem was the most active carbapenem tested against P. aeruginosa regardless of β-lactam resistance.
机译:多立培南是一种1β-甲基卡巴培南,是一种广谱抗生素,被批准用于治疗复杂的尿路和复杂的腹腔内感染。医院获得性肺炎(包括呼吸机相关性肺炎)的适应症正在等待中。本研究检查了多瑞培南对近期临床分离株的活性,以对其进行中的临床开发和未来的纵向分析进行研究。在2005年至2006年期间,对多立培南和比较剂进行了针对12581种美国临床分离株的测试,其中包括金黄色葡萄球菌,凝固酶阴性葡萄球菌,肺炎链球菌,肠杆菌科,铜绿假单胞菌和不动杆菌属。通过肉汤微量稀释建立MIC(μg/ ml)。通过MIC90,多瑞培南在抗金黄色葡萄球菌(易感甲氧西林,0.06;抗药性,8)和肺炎链球菌(易感青霉素,≤0.015;抗药性,1)方面与亚胺培南和美罗培南相当。对于头孢他啶敏感性肠杆菌科细菌,多立尼姆的MIC90(0.12)与美罗培南(0.12)相当,并且优于亚胺培南(2),尽管所有评估的碳青霉烯的分离物敏感性均超过99%。对头孢他啶不敏感或广谱β-内酰胺酶筛选阳性肠杆菌科,多瑞培南的活性没有明显改变。多瑞培南是针对铜绿假单胞菌测试的最有效的碳青霉烯(MIC90 /%磁化率[%S]:头孢他啶敏感= 2/92%S,不敏感= 16/61%S;亚胺培南敏感= 1 / 98.5%S,不敏感= 8 / 56%S)。对于易受亚胺培南敏感的不动杆菌属,多立培南(MIC90 = 2,89.1%S)的活性是亚胺培南和美罗培南的两倍。总体而言,多立培南对革兰氏阳性球菌的效力与美洛培南和亚胺培南相当,而多立培南在抗肠杆菌科细菌(包括β-内酰胺不敏感分离株)方面的活性与美洛培南和亚胺培南相同或更高。不论β-内酰胺抗药性如何,多瑞培南是针对铜绿假单胞菌测试的最活跃的碳青霉烯。

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