已发表论文

血液系统恶性肿瘤患者血流感染碳青霉烯类耐药铜绿假单胞菌的临床特征及预后

 

Authors Yuan F, Xiao W, Wang X, Fu Y, Wei X

Received 27 April 2023

Accepted for publication 26 July 2023

Published 31 July 2023 Volume 2023:16 Pages 4943—4952

DOI https://doi.org/10.2147/IDR.S419064

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Professor Suresh Antony

Objective: To analyze the clinical characteristics and prognostic risk factors of carbapenem-resistant Pseudomonas aeruginosa (CRPA) bloodstream infections in patients with hematologic malignancies.
Methods: Medical records and drug susceptibility data of patients with hematologic malignancies complicated by CRPA bloodstream infections admitted to the Cancer Hospital of Zhengzhou University between January 1, 2018, and December 31, 2022, were retrospectively analyzed.
Results: A total of 64 patients were included in the study, with a mortality rate of 37.5% (24/64) at 28 days after the occurrence of CRPA bloodstream infection. In Cox regression analysis, an absolute neutrophil count < 0.5× 109/L at discharge (HR 0.039, 95% CI 0.006 ~ 0.258, =0.001), admission to the intensive care unit (HR 7.546, 95% CI 1.345 ~ 42.338, = 0.022), and a higher Pitt bacteremia score (HR 0.207, 95% CI 0.046 ~ 0.939, = 0.041) were independent risk factors associated with 28-day mortality. Survival analysis showed that patients receiving ceftazidime-avibactam-based (HR 0.368, 95% CI 0.107~ 1.268, = 0.023) or polymyxin B (HR 2.561, 95% CI 0.721 ~ 9.101, = 0.015) therapy had a higher survival rate.
Conclusion: Patients with hematologic neoplasms had high mortality from CRPA bloodstream infections, and admission to the intensive care unit, higher Pitt bacteremia score (PBS) scores, granulocyte deficiency, and granulocyte deficiency at discharge were independently associated with higher mortality. Early anti-infective treatment with ceftazidime-avibactam or polymyxin B may improve the clinical prognosis of patients.
Keywords: Pseudomonas aeruginosa , carbapenem resistance, bloodstream infection, hematologic neoplasm, risk factors