Aldardeer Namareq F, Labban Hatun M, Alhuthil Raghad T, Aljahdali Seham H, Alharbi Moataz H, Alharbi Riham A, Al Musawa Mohammed I, Almalki Abdulrahman A, Almangour Thamer A
Critical Care Clinical Pharmacy Consultant, Medical and Clinical Affairs Department, King Faisal Specialist Hospital and Research Center, P.O. Box 40047, Jeddah, 21499, Saudi Arabia.
Pediatric Antimicrobial Stewardship Clinical Pharmacist , King Saud Medical City, Riyadh, Saudi Arabia.
BMC Infect Dis. 2024 Dec 22;24(1):1455. doi: 10.1186/s12879-024-10365-5.
The World Health Organization (WHO) has identified carbapenem-resistant Pseudomonas aeruginosa (CRPA) as one of the three critical priority pathogens. There is scarce literature evaluating the treatment outcomes in patients with CRPA infections treated with traditional non-carbapenem β-lactam (NCBL) agents. Thus, this study aims to assess the effectiveness of traditional NCBL compared to novel β-lactam agents (NVL) for treating non-carbapenem β-lactam -susceptible CRPA.
A single-center retrospective cohort study was conducted between January 2016 and December 2022. The study included adult patients 18 years and older with infection due to CRPA who were treated based on microbiology sensitivity with traditional NCBL or NVL for more than 48 h. The primary outcome was 30-day mortality.
124 patients were included: 98 (79%) in the NCBL group and 26 (20.9%) in the NVL group. 78 (62.9%) patients were male. The median (interquartile range (IQR)) age of included patients was 64 (45, 77) years. A total of 84 (67.7%) patients were critically ill, with an overall median (IQR) APACHE II score of 18 (13.5, 23). The rates of 30-day mortality in NCBL and NVL groups were 41 (41.8%) and 12 (46.2%), respectively; P = 0.692.
In patients with CRPA infections susceptible to traditional NCBL, there was no statisticallly significant difference in 30-day mortality among patients who were treated with traditional NCBL compared with NVL. Further studies with larger sample sizes are needed to confirm these findings.
世界卫生组织(WHO)已将耐碳青霉烯类铜绿假单胞菌(CRPA)确定为三种关键优先病原体之一。评估使用传统非碳青霉烯类β-内酰胺(NCBL)药物治疗CRPA感染患者的治疗结果的文献很少。因此,本研究旨在评估传统NCBL与新型β-内酰胺类药物(NVL)治疗对非碳青霉烯类β-内酰胺敏感的CRPA的有效性。
于2016年1月至2022年12月进行了一项单中心回顾性队列研究。该研究纳入了18岁及以上因CRPA感染而根据微生物敏感性接受传统NCBL或NVL治疗超过48小时的成年患者。主要结局是30天死亡率。
纳入124例患者:NCBL组98例(79%),NVL组26例(20.9%)。78例(62.9%)患者为男性。纳入患者的年龄中位数(四分位间距(IQR))为64(45,77)岁。共有84例(67.7%)患者病情危重,APACHE II评分的总体中位数(IQR)为18(13.5,23)。NCBL组和NVL组的30天死亡率分别为41例(41.8%)和12例(46.2%);P = 0.692。
在对传统NCBL敏感的CRPA感染患者中,接受传统NCBL治疗的患者与接受NVL治疗的患者在30天死亡率方面无统计学显著差异。需要更大样本量的进一步研究来证实这些发现。