Enhanced Outcomes in Bacteremia Through Rapid Phenotype Identification of Carbapenemase-Producing Organisms.

IF 1.7 4区 医学 Q4 INFECTIOUS DISEASES
Surgical infections Pub Date : 2026-05-01 Epub Date: 2025-12-01 DOI:10.1177/10962964251403441
Huajian Ren, Yitian Teng, Zhihao Xu, Caiqing Yang, Jiayang Li, Jiajie Wang, Jinjian Huang, Jinpeng Zhang, Shuai Hao, Zhiwu Hong, Zherui Zhang, Jianan Ren
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引用次数: 0

Abstract

Objective: The treatment of carbapenemase-producing organisms (CPOs) causing bacteremia in patients with intra-abdominal infections remains challenging. The early detection of CPOs from blood specimens is critical for guaranteeing the timely selection of appropriate antibiotics and achieving favorable outcomes. Our aim was to evaluate whether the rapid identification of CPOs can improve clinical outcomes.

Patients and methods: Between January 2019 and January 2024, we conducted a retrospective study of all bacteremia patients admitted to the Intestinal Fistulae and Intra-abdominal Infection Center at Jinling Hospital. A subset of patients underwent screening for CPOs using lateral flow immunoassays (LFIA) method.

Results: A total of 163 patients were enrolled, with 96 in the 30-day survivors group and 67 in the 30-day non-survivors group. LFIA was performed in 76 patients, revealing the identification of 64 carbapenemases in four classes: bla Klebsiella pneumoniae carbapenemases (KPC) (45/76, 59.2%), bla NDM (11/76, 14.5%), bla oxacillinase (OXA)-48 (6/76, 7.9%), and bla imipenemase (IMP) (2/45, 2.2%). The most prevalent CPOs cultured were carbapenem-resistant Klebsiella pneumoniae (104/163, 63.8%), followed by carbapenem-resistant Acinetobacter baumannii (36/163, 22.1%), carbapenem-resistant Pseudomonas aeruginosa (32/163, 19.6%), carbapenem-resistant Escherichia coli (19/163, 11.7%), and others (28/163, 17.2%). Univariable analysis revealed that risk factors related to mortality included outbreaks in the intensive care unit or community, sources from the respiratory tract, mechanical ventilation, Pitt score of ≥4, and active therapy before blood culture collection. Multivariable logistic regression analysis indicated that outbreaks in the intensive care unit or community, sources from the respiratory tract, and mechanical ventilation were independent predictors of clinical failure. In addition, LFIA test was associated with decreased 30-day mortality.

Conclusions: The LFIA method can rapidly detect the presence of CPOs in patients with bacteremia, thereby improving clinical outcomes. Future multicenter randomized controlled trial (RCT) studies are warranted to investigate the benefits of LFIA detection in bacteremia.

通过碳青霉烯酶产生生物的快速表型鉴定提高菌血症的预后。
目的:腹内感染患者中碳青霉烯酶产生生物(CPOs)引起菌血症的治疗仍然具有挑战性。血液标本中CPOs的早期检测对于保证及时选择合适的抗生素和获得良好的治疗效果至关重要。我们的目的是评估快速识别CPOs是否可以改善临床结果。患者和方法:2019年1月至2024年1月,我们对金陵医院肠瘘和腹腔内感染中心收治的所有菌血症患者进行了回顾性研究。一部分患者采用侧流免疫测定法(LFIA)筛查CPOs。结果:共纳入163例患者,其中30天存活组96例,30天非存活组67例。对76例患者进行LFIA,共鉴定出4类64种碳青霉烯酶:bla肺炎克雷伯菌碳青霉烯酶(KPC)(45/76, 59.2%)、bla NDM(11/76, 14.5%)、bla oxacillinase (OXA)-48(6/76, 7.9%)和bla亚胺烯酶(IMP)(2/45, 2.2%)。最常见的CPOs培养为耐碳青霉烯肺炎克雷伯菌(104/163,63.8%),其次为耐碳青霉烯鲍曼不动杆菌(36/163,22.1%)、耐碳青霉烯铜绿假单胞菌(32/163,19.6%)、耐碳青霉烯大肠杆菌(19/163,11.7%)和其他(28/163,17.2%)。单变量分析显示,与死亡相关的危险因素包括重症监护病房或社区暴发、呼吸道来源、机械通气、Pitt评分≥4分以及采血前的积极治疗。多变量logistic回归分析表明,重症监护病房或社区暴发、呼吸道来源和机械通气是临床失败的独立预测因素。此外,LFIA试验与降低30天死亡率相关。结论:LFIA法可快速检测出菌血症患者中CPOs的存在,从而改善临床疗效。未来的多中心随机对照试验(RCT)研究有必要调查LFIA检测在菌血症中的益处。
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来源期刊
Surgical infections
Surgical infections INFECTIOUS DISEASES-SURGERY
CiteScore
3.80
自引率
5.00%
发文量
127
审稿时长
6-12 weeks
期刊介绍: Surgical Infections provides comprehensive and authoritative information on the biology, prevention, and management of post-operative infections. Original articles cover the latest advancements, new therapeutic management strategies, and translational research that is being applied to improve clinical outcomes and successfully treat post-operative infections. Surgical Infections coverage includes: -Peritonitis and intra-abdominal infections- Surgical site infections- Pneumonia and other nosocomial infections- Cellular and humoral immunity- Biology of the host response- Organ dysfunction syndromes- Antibiotic use- Resistant and opportunistic pathogens- Epidemiology and prevention- The operating room environment- Diagnostic studies
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