Clinical characteristics and treatment outcomes of Acinetobacter baumannii bloodstream infections in a setting with high carbapenem susceptibility among isolates.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Jinghao Nicholas Ngiam, Matthew Chung Yi Koh, Ka Lip Chew
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引用次数: 0

Abstract

In most settings, carbapenem-resistant Acinetobacter baumannii (CRAB) infections predominate over carbapenem-susceptible Acinetobacter baumannii (CSAB). Treatment guidelines focus on the management of CRAB and do not describe the optimal antibiotic choice for CSAB. We describe the clinical characteristics and outcomes in both CRAB and CSAB. We examined consecutive episodes of CRAB or CSAB bloodstream infections in our institution from February 2022 to July 2024. Clinical, laboratory, and microbiological data were tabulated, and adverse outcomes were defined as the need for intensive care (ICU) or all-cause in-hospital mortality. We compared (i) CRAB to CSAB, and among patients with CSAB, (ii) we evaluated if the definitive antibiotic choice was associated with adverse outcomes, after adjusting for C-reactive protein levels. We identified 71 unique episodes of bacteremia, of which a majority (52/71, 73.2%) were nosocomial onset. A minority were CRAB (15/71, 21.1%). These patients often had ICU onset, prior carbapenem exposure, and were more likely to experience mortality (73.3% versus 16.1%, P < 0.001). Only a minority of patients (7/71, 9.9%) received dual antibiotic therapy. Among the 56 patients with CSAB, only 11/56 (19.6%) experienced adverse outcomes. On multivariable analysis, after adjusting for elevated C-reactive protein, the use of carbapenems as the definitive antibiotic choice remained independently associated with adverse outcomes (adjusted odds ratio 7.34, 95% CI 1.25-43.01, P = 0.027). CSAB was far more common than CRAB in our setting. Prior carbapenem exposure and ICU onset were important risk factors for CRAB, which had higher mortality than CSAB. Carbapenem-sparing options may be considered as the definitive antibiotic choice for CSAB.

Importance: In our setting, carbapenem-susceptible Acinetobacter baumannii (CSAB, n = 56/71, 78.9%) bloodstream infections (BSIs) were far more common than with carbapenem-resistant isolates (CRAB). CRAB BSI was associated with intensive care onset, prior carbapenem use, and had higher mortality (73.3% versus 16.1%). In CSAB BSI, after adjusting for elevated C-reactive protein, the definitive use of carbapenems for treatment remained independently associated with adverse outcomes (adjusted odds ratio 7.34, 95%CI 1.25-43.01). These findings may suggest that carbapenem-sparing regimens may be effective alternative antibiotic choices for CSAB. Although treatment guidelines focus on CRAB, future prospective studies should also evaluate optimal treatment strategies for CSAB.

高碳青霉烯敏感性环境中鲍曼不动杆菌血流感染的临床特征和治疗结果
在大多数情况下,耐碳青霉烯鲍曼不动杆菌(CRAB)感染高于碳青霉烯敏感鲍曼不动杆菌(CSAB)。治疗指南侧重于螃蟹的管理,而没有描述CSAB的最佳抗生素选择。我们描述了螃蟹和CSAB的临床特征和结果。我们检查了从2022年2月到2024年7月在我们机构连续发作的螃蟹或CSAB血液感染。将临床、实验室和微生物学数据制成表格,并将不良结果定义为需要重症监护(ICU)或全因住院死亡率。我们比较了(i) CRAB和CSAB,在CSAB患者中,(ii)在调整c反应蛋白水平后,我们评估了明确的抗生素选择是否与不良结果相关。我们确定了71例独特的菌血症发作,其中大多数(52/71,73.2%)是医院发病的。少数为螃蟹(15/71,21.1%)。这些患者通常有ICU发病,既往碳青霉烯暴露,更有可能出现死亡率(73.3%对16.1%,P < 0.001)。只有少数患者(7/71,9.9%)接受了双重抗生素治疗。56例CSAB患者中,仅有11/56(19.6%)出现不良结局。在多变量分析中,在调整了升高的c反应蛋白后,碳青霉烯类抗生素作为最终的抗生素选择仍然与不良结局独立相关(调整后的优势比为7.34,95% CI 1.25-43.01, P = 0.027)。在我们的环境中,CSAB比CRAB更常见。既往碳青霉烯暴露和ICU发病是螃蟹的重要危险因素,螃蟹死亡率高于CSAB。碳青霉烯保留方案可能被认为是CSAB的最终抗生素选择。重要性:在我们的研究中,碳青霉烯敏感鲍曼不动杆菌(CSAB, n = 56/71, 78.9%)血液感染(bsi)远比碳青霉烯耐药分离株(CRAB)更常见。CRAB BSI与重症监护发作、既往碳青霉烯类药物使用相关,且死亡率较高(73.3%对16.1%)。在CSAB BSI中,在调整了升高的c反应蛋白后,碳青霉烯类药物的最终使用仍然与不良结局独立相关(调整后的优势比为7.34,95%CI为1.25-43.01)。这些发现可能表明碳青霉烯保留方案可能是CSAB有效的替代抗生素选择。虽然治疗指南侧重于螃蟹,但未来的前瞻性研究还应评估CSAB的最佳治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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