Spanish Network for Research in Infectious Diseases (REIPI), Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.
Infectious Diseases (GC-03) and Clinical and Molecular Microbiology (GC-24) Groups, Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofía University Hospital, University of Cordoba, Cordoba, Spain.
Transpl Infect Dis. 2022 Aug;24(4):e13881. doi: 10.1111/tid.13881. Epub 2022 Jun 28.
Infections caused by multidrug-resistant gram-negative bacilli (MDR GNB), in particular extended-spectrum β-lactamase-producing (ESBL-E) and carbapenem-resistant Enterobacterales (CRE), pose a major threat in solid organ transplantation (SOT). Outcome prediction and therapy are challenging due to the scarcity of randomized clinical trials (RCTs) or well-designed observational studies focused on this population.
Narrative review with a focus on the contributions provided by the ongoing multinational INCREMENT-SOT consortium (ClinicalTrials identifier NCT02852902) in the fields of epidemiology and clinical management.
The Spanish Society of Transplantation (SET), the Group for Study of Infection in Transplantation of the Spanish Society of Infectious Diseases and Clinical Microbiology (GESITRA-SEIMC), and the Spanish Network for Research in Infectious Diseases (REIPI) recently published their recommendations for the management of MDR GNB infections in SOT recipients. We revisit the SET/GESITRA-SEIMC/REIPI document taking into consideration new evidence that emerged on the molecular epidemiology, prognostic stratification, and treatment of post-transplant ESBL-E and CRE infections. Results derived from the INCREMENT-SOT consortium may support the therapeutic approach to post-transplant bloodstream infection (BSI). The initiatives devoted to sparing the use of carbapenems in low-risk ESBL-E BSI or to repurposing existing non-β-lactam antibiotics for CRE in both non-transplant and transplant patients are reviewed, as well as the eventual positioning in the specific SOT setting of recently approved antibiotics.
Due to the clinical complexity and relative rarity of ESBL-E and CRE infections in SOT recipients, multinational cooperative efforts such as the INCREMENT-SOT Project should be encouraged. In addition, RCTs focused on post-transplant serious infection remain urgently needed.
多药耐药革兰氏阴性杆菌(MDR GNB)引起的感染,特别是产超广谱β-内酰胺酶(ESBL-E)和耐碳青霉烯肠杆菌科(CRE),对实体器官移植(SOT)构成了重大威胁。由于缺乏针对该人群的随机临床试验(RCT)或精心设计的观察性研究,因此预后预测和治疗具有挑战性。
以正在进行的多国 INCREMENT-SOT 联盟(ClinicalTrials 标识符 NCT02852902)在流行病学和临床管理领域的贡献为重点进行叙述性综述。
西班牙移植学会(SET)、西班牙传染病学会和临床微生物学移植研究组(GESITRA-SEIMC)以及西班牙传染病研究网络(REIPI)最近发布了他们关于 MDR GNB 感染的管理建议。我们考虑到新出现的关于移植后 ESBL-E 和 CRE 感染的分子流行病学、预后分层和治疗的新证据,重新审视了 SET/GESITRA-SEIMC/REIPI 文件。来自 INCREMENT-SOT 联盟的结果可能支持移植后血流感染(BSI)的治疗方法。审查了旨在减少低危 ESBL-E BSI 中碳青霉烯类药物使用或重新利用现有非β-内酰胺抗生素治疗非移植和移植患者的 CRE 的举措,以及最近批准的抗生素在特定 SOT 环境中的最终定位。
由于 SOT 受者中 ESBL-E 和 CRE 感染的临床复杂性和相对罕见性,应鼓励开展 INCREMENT-SOT 等多国合作努力。此外,仍迫切需要针对移植后严重感染的 RCT。