Jones Ronald N, Mendes Caio, Turner Philip J, Masterton Robert
JMI Laboratories, North Liberty, IA 52317, USA.
Diagn Microbiol Infect Dis. 2005 Dec;53(4):247-56. doi: 10.1016/j.diagmicrobio.2005.10.006.
This overview provides a summary of the Meropenem Yearly Susceptibility Test Information Collection (MYSTIC) Program over an 8-year period from 1997 to 2004. The evolution of the MYSTIC Program is described, as well as its design compared with other surveillance programs. In addition, the global MYSTIC Program data, published to date, are summarized, and the empiric use of carbapenems, their current indications, and meropenem usage versus resistance was discussed. From 1997 to 2004, 120 medical centers that were actively prescribing meropenem in 32 countries worldwide participated in the program. The MYSTIC Program results demonstrate the sustained potency and continued effectiveness of meropenem globally against clinically relevant Gram-negative and Gram-positive pathogens including extended spectrum beta-lactamase- and AmpC beta-lactamase-producing organisms, which may also display resistance to the fluoroquinolones and/or aminoglycosides. Furthermore, in centers actively prescribing meropenem, resistance to meropenem is not increasing despite greater resistance among the comparator antimicrobial agents. Thus, antipseudomonal carbapenems such as meropenem and imipenem remain an effective treatment option.
本概述总结了1997年至2004年这8年间美罗培南年度药敏试验信息收集(MYSTIC)项目。描述了MYSTIC项目的发展历程,以及与其他监测项目相比它的设计情况。此外,总结了迄今为止已发表的全球MYSTIC项目数据,并讨论了碳青霉烯类药物的经验性使用、它们目前的适应证以及美罗培南的使用与耐药情况。1997年至2004年,全球32个国家中120个积极使用美罗培南的医疗中心参与了该项目。MYSTIC项目结果表明,美罗培南在全球范围内对临床相关的革兰阴性和革兰阳性病原体持续保持效力且疗效持久,这些病原体包括产超广谱β-内酰胺酶和AmpCβ-内酰胺酶的菌株,它们可能对氟喹诺酮类药物和/或氨基糖苷类药物也有耐药性。此外,在积极使用美罗培南的医疗中心,尽管对照抗菌药物的耐药性有所增加,但美罗培南的耐药性并未上升。因此,像美罗培南和亚胺培南这样的抗假单胞菌碳青霉烯类药物仍然是一种有效的治疗选择。