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治疗耐碳青霉烯类肠杆菌科细菌的方法。

Options for treating carbapenem-resistant Enterobacteriaceae.

作者信息

Rafailidis Petros I, Falagas Matthew E

机构信息

aAlfa Institute of Biomedical Sciences bDepartment of Internal Medicine, Athens Medical Center cDepartment of Internal Medicine - Infectious Diseases, Iaso General Hospital, Iaso Group, Athens, Greece dDepartment of Medicine, Tufts University School of Medicine, Boston, Massachusetts, USA.

出版信息

Curr Opin Infect Dis. 2014 Dec;27(6):479-83. doi: 10.1097/QCO.0000000000000109.

Abstract

PURPOSE OF REVIEW

To address the therapeutic management of carbapenem-resistant Enterobacteriaceae on the basis of literature of the last 12 months.

RECENT FINDINGS

Retrospective and prospective (nonrandomized noncontrolled) studies provide data regarding the management of infections due to carbapenem-resistant Enterobacteriaceae. The combination of a carbapenem with colistin or high-dose tigecycline or aminoglycoside or even triple carbapenem-containing combinations if the minimum inhibitory concentration (MIC) range of carbapenem (meropenem and imipenem) resistance is 8 mg/l or less seems to have an advantage over monotherapy with either colistin or tigecycline or fosfomycin. For Enterobacteriaceae with MIC for carbapenems over 8 mg/l, combination regimens involve colistin, tigecycline usually administered in a double dose than that suggested by its manufacturer, fosfomycin and aminoglycosides in various combinations.

SUMMARY

Suggestions based on the limited literature cannot be made safely. Combination regimens involving carbapenems for Enterobacteriaceae with MICs 8 mg/l or less for carbapenems (in dual combination with colistin or high-dose tigecycline or aminoglycoside or even triple combinations) seem to confer some therapeutic advantage over monotherapy. For Enterobacteriaceae with higher than the above-mentioned MICs, a combination of two or even three antibiotics among colistin, high-dose tigecycline, aminoglycoside and fosfomycin seems to confer decreased mortality.

摘要

综述目的

基于过去12个月的文献,探讨耐碳青霉烯类肠杆菌科细菌的治疗管理。

最新发现

回顾性和前瞻性(非随机非对照)研究提供了关于耐碳青霉烯类肠杆菌科细菌感染管理的数据。如果碳青霉烯类(美罗培南和亚胺培南)耐药的最低抑菌浓度(MIC)范围为8mg/L或更低,碳青霉烯类与黏菌素或高剂量替加环素或氨基糖苷类联合使用,甚至含三种碳青霉烯类的联合使用,似乎比单独使用黏菌素或替加环素或磷霉素具有优势。对于碳青霉烯类MIC超过8mg/L的肠杆菌科细菌,联合治疗方案包括黏菌素、通常以高于其生产商建议剂量的双倍剂量给药的替加环素、磷霉素和各种组合的氨基糖苷类。

总结

基于有限的文献无法安全地给出建议。对于碳青霉烯类MIC为8mg/L或更低的肠杆菌科细菌,含碳青霉烯类的联合治疗方案(与黏菌素或高剂量替加环素或氨基糖苷类双联或甚至三联组合)似乎比单一疗法具有一定的治疗优势。对于MIC高于上述水平的肠杆菌科细菌,黏菌素、高剂量替加环素、氨基糖苷类和磷霉素中的两种甚至三种抗生素联合使用似乎可降低死亡率。

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