Department of Clinical Laboratory, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Department of Clinical Laboratory, Tongxiang First People's Hospital, Tongxiang, Zhejiang, China.
Front Cell Infect Microbiol. 2024 Jul 18;14:1395260. doi: 10.3389/fcimb.2024.1395260. eCollection 2024.
Patients with severe carbapenem-resistant (CRAB) infections currently face significant treatment challenges. When patients display signs of infection and the clinical suspicion of CRAB infections is high, appropriate treatment should be immediately provided. However, current treatment plans and clinical data for CRAB are limited. Inherent and acquired resistance mechanisms, as well as host factors, significantly restrict options for empirical medication. Moreover, inappropriate drug coverage can have detrimental effects on patients. Most existing studies have limitations, such as a restricted sample size, and are predominantly observational or non-randomized, which report significant variability in patient infection severity and comorbidities. Therefore, a gold-standard therapy remains lacking. Current and future treatment options of infections due to CRAB were described in this review. The dose and considerable side effects restrict treatment options for polymyxins, and high doses of ampicillin-sulbactam or tigecycline appear to be the best option at the time of initial treatment. Moreover, new drugs such as durlobactam and cefiderocol have substantial therapeutic capabilities and may be effective salvage treatments. Bacteriophages and antimicrobial peptides may serve as alternative treatment options in the near future. The advantages of a combination antimicrobial regimen appear to predominate those of a single regimen. Despite its significant nephrotoxicity, colistin is considered a primary treatment and is often used in combination with antimicrobials, such as tigecycline, ampicillin-sulbactam, meropenem, or fosfomycin. The Infectious Diseases Society of America (IDSA) has deemed high-dose ampicillin-sulbactam, which is typically combined with high-dose tigecycline, polymyxin, and other antibacterial agents, the best option for treating serious CRAB infections. A rational combination of drug use and the exploration of new therapeutic drugs can alleviate or prevent the effects of CRAB infections, shorten hospital stays, and reduce patient mortality.
目前,患有严重碳青霉烯类耐药(CRAB)感染的患者面临着巨大的治疗挑战。当患者出现感染迹象且临床高度怀疑 CRAB 感染时,应立即提供适当的治疗。然而,目前针对 CRAB 的治疗方案和临床数据有限。固有和获得性耐药机制以及宿主因素极大地限制了经验性用药的选择。此外,不适当的药物覆盖可能对患者产生不利影响。大多数现有研究存在局限性,例如样本量有限,主要是观察性或非随机的,报告患者感染严重程度和合并症存在显著差异。因此,仍然缺乏黄金标准的治疗方法。本文描述了针对 CRAB 感染的当前和未来的治疗选择。多黏菌素的剂量和严重副作用限制了其治疗选择,氨苄西林-舒巴坦或替加环素的高剂量似乎是初始治疗的最佳选择。此外,新的药物如达芦那韦和头孢他啶具有显著的治疗能力,可能是有效的挽救治疗方法。噬菌体和抗菌肽可能在不久的将来成为替代治疗选择。联合抗菌方案的优势似乎超过了单一方案。尽管多黏菌素具有显著的肾毒性,但它被认为是主要的治疗药物,通常与其他抗菌药物联合使用,如替加环素、氨苄西林-舒巴坦、美罗培南或磷霉素。美国传染病学会(IDSA)认为,高剂量氨苄西林-舒巴坦,通常与高剂量替加环素、多黏菌素和其他抗菌药物联合使用,是治疗严重 CRAB 感染的最佳选择。合理的药物联合使用和新治疗药物的探索可以减轻或预防 CRAB 感染的影响,缩短住院时间,降低患者死亡率。