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Clinical characteristics and prognosis of bloodstream infections with carbapenem-resistant Gram-negative organisms in patients with hematological malignancies: A multicenter case-control study in China - 06/12/24

Doi : 10.1016/j.jinf.2024.106331 
Junxin Zhou a, b, c, 1, Jian Sun a, b, c, 1, Shanshan Lu a, b, c, Xinhong Han d, Jintao He e, Ping Zhang a, b, c, Huangdu Hu f, Yuke Zhang a, b, c, Yanfei Wang a, b, c, Qin Yang g, Shujuan Ji a, b, c, Zhihui Zhou a, b, c, Xiaoting Hua a, b, c, Xueqing Wu a, b, c, Yan Jiang a, b, c, Xiaoxing Du a, b, c, Yunsong Yu a, b, c,
a Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China 
b Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou, China 
c Regional Medical Center for National Institute of Respiratory Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China 
d Department of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China 
e Centre of Laboratory Medicine, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China 
f Department of Infectious Diseases, Centre for General Practice Medicine, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China 
g Department of Laboratory Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China 

Correspondence to: No. 3, East Qingchun Rd, Shangcheng District, Hangzhou 310016, China.No. 3, East Qingchun Rd, Shangcheng DistrictHangzhou310016China

Summary

Objective

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.

Methods

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.

Results

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, blaKPC-2 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. blaKPC-2 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.

Conclusions

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.

Le texte complet de cet article est disponible en PDF.

Highlights

The epidemiological and molecular characteristics of HM patients with CRO BSI in China in 2018-2020 were studied.
The overall in vitro activity of novel antimicrobials against CRO strains was poor.
The proportion of IEAT was high but not associated with the prognosis of HM patients with concomitant CRO BSI.
Our findings help to drive rationalization of CRO BSI antimicrobial drug therapy in HM patients and prognostic improvement.

Le texte complet de cet article est disponible en PDF.

Keywords : Carbapenem-resistant Gram-negative organism, Bloodstream infection, Hematological malignancy, Risk factor


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Vol 89 - N° 6

Article 106331- décembre 2024 Retour au numéro
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