Zhou Junxin, Sun Jian, Lu Shanshan, Han Xinhong, He Jintao, Zhang Ping, Hu Huangdu, Zhang Yuke, Wang Yanfei, Yang Qin, Ji Shujuan, Zhou Zhihui, Hua Xiaoting, Wu Xueqing, Jiang Yan, Du Xiaoxing, Yu Yunsong
Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China; Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou, China; Regional Medical Center for National Institute of Respiratory Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China.
J Infect. 2024 Dec;89(6):106331. doi: 10.1016/j.jinf.2024.106331. Epub 2024 Oct 25.
To investigate clinical characteristics of hematological malignancy (HM) patients with carbapenem-resistant gram-negative organism (CRO) bloodstream infections (BSI) in China, and to elucidate the prognostic risk factors of CRO BSI.
We conducted a multicenter case-control study of 201 HM patients with CRO BSI between 2018-2020. Antimicrobial susceptibility testing and whole genome sequencing were performed for CRO isolates. Independent risk factors for 28-day crude mortality were analyzed using Cox proportional hazards regression models. The subgroups of major species were also evaluated.
The pathogens responsible for CRO BSI in HM patients dominated by ST11 CRKP, ST167 CREC and ST463 CRPA. Most isolates produced carbapenemases with KPC and NDM being the main. CRO isolates had resistance rates to conventional antimicrobials ranging from 55%-100% and poor susceptibility to novel antimicrobials related to carbapenemases and species. The 28-day crude mortality was 24.2%. Non-Hodgkin lymphoma, heart disease, bla positive, empirical antibiotic therapy with linezolid, Pitt bacteremia score >3.5 were risk factors for 28-day mortality and appropriate definitive antibiotic therapy, tigecycline-containing therapy and aminoglycoside-containing therapy were protective factors. bla positive in CRKP and ST463 in CRPA were associated with Pitt bacteremia score >3.5. Solid tumor and other site infections before BSI were risk factors for ST463 CRPA BSI and pulmonary infection before BSI was risk factor for KPC-KP BSI.
The antimicrobial resistance of CRO isolates for BSI in HM patients is critical. HM patients with CRO BSI should be treated with appropriate definitive antibiotic therapy based on early clarification of pathology and their antimicrobial susceptibility.
探讨中国血液系统恶性肿瘤(HM)患者合并耐碳青霉烯类革兰阴性菌(CRO)血流感染(BSI)的临床特征,并阐明CRO BSI的预后危险因素。
我们对2018年至2020年间201例合并CRO BSI的HM患者进行了一项多中心病例对照研究。对CRO分离株进行了药敏试验和全基因组测序。使用Cox比例风险回归模型分析28天粗死亡率的独立危险因素。还对主要菌种的亚组进行了评估。
HM患者CRO BSI的病原体以ST11型耐碳青霉烯类肺炎克雷伯菌、ST167型耐碳青霉烯类大肠埃希菌和ST463型耐碳青霉烯类铜绿假单胞菌为主。大多数分离株产生碳青霉烯酶,主要为KPC和NDM。CRO分离株对传统抗菌药物的耐药率为55%-100%,对与碳青霉烯酶和菌种相关的新型抗菌药物敏感性较差。28天粗死亡率为24.2%。非霍奇金淋巴瘤、心脏病、bla阳性、利奈唑胺经验性抗生素治疗、皮特菌血症评分>3.5是28天死亡率的危险因素,而适当的确定性抗生素治疗、含替加环素治疗和含氨基糖苷类治疗是保护因素。CRKP中的bla阳性和CRPA中的ST463与皮特菌血症评分>3.5相关。BSI前的实体瘤和其他部位感染是ST463 CRPA BSI的危险因素,BSI前的肺部感染是KPC-KP BSI的危险因素。
HM患者CRO分离株对BSI的抗菌耐药性至关重要。合并CRO BSI的HM患者应在早期明确病原体及其药敏情况的基础上,接受适当的确定性抗生素治疗。