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首页> 外文期刊>Clinical transplantation. >Multidrug‐resistant Gram‐negative bacterial infections in solid organ transplant recipients—Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice
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Multidrug‐resistant Gram‐negative bacterial infections in solid organ transplant recipients—Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice

机译:固体器官移植受者的多药革兰阴性细菌感染 - 来自美国移植学会传染病界的指导

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摘要

Abstract These updated guidelines from the Infectious Diseases Community of Practice of the American Society of Transplantation review the diagnosis, prevention, and management of infections due to multidrug‐resistant (MDR) Gram‐negative bacilli in the pre‐ and post‐transplant period. MDR Gram‐negative bacilli, including carbapenem‐resistant Enterobacteriaceae, MDR Pseudomonas aeruginosa , and carbapenem‐resistant Acinetobacter baumannii, remain a threat to successful organ transplantation. Clinicians now have access to at least five novel agents with activity against some of these organisms, with others in the advanced stages of clinical development. No agent, however, provides universal and predictable activity against any of these pathogens, and very little is available to treat infections with MDR nonfermenting Gram‐negative bacilli including A?baumannii. Despite advances, empiric antibiotics should be tailored to local microbiology and targeted regimens should be tailored to susceptibilities. Source control remains an important part of the therapeutic armamentarium. Morbidity and mortality associated with infections due to MDR Gram‐negative organisms remain unacceptably high. Heightened infection control and antimicrobial stewardship initiatives are needed to prevent these infections, curtail their transmission, and limit the evolution of MDR Gram‐negative pathogens, especially in the setting of organ transplantation.
机译:摘要这些已更新的传染病群落的实践界,美国移植学会审查了在预移植后和移植后期的多药抗性(MDR)革兰尼杆菌引起的诊断,预防和管理。 MDR革兰阴性杆菌,包括耐药肠道菌,MDR假单胞菌铜绿假西亚群岛和耐鲤鱼抗性的肺炎鲍曼氏菌,对成功的器官移植造成威胁。临床医生现在可以通过临床开发的先进阶段获得至少五种具有针对这些生物的活动的新药。然而,没有代理人为任何这些病原体提供普遍和可预测的活动,并且很少可用于治疗MDR纯革兰氏阴性杆菌,包括a?baumannii。尽管有进展,但经验丰富的抗生素应根据局部微生物学和靶向方案量身定制,应对易患性定制。源控制仍然是治疗盔甲的重要组成部分。与MDR革兰氏阴性生物体引起的感染相关的发病率和死亡率仍然不可接受。需要提高的感染控制和抗微生物管道举措以防止这些感染,缩短其传播,并限制MDR革兰阴性病原体的演变,尤其是在器官移植的设置中。

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