Carbapenem resistance and mortality in pediatric Acinetobacter bloodstream infections: determinants from a 12-year tertiary-care cohort study.

IF 2.9 3区 医学 Q1 PEDIATRICS
Suleyman Emre Karauzum, Ece Erci, Gulizar Koc, Pinar Yazici Ozkaya, Ezgi Kiran Tasci, Miray Karakoyun, Gulcihan Ozek, Eda Ataseven, Demet Terek, Melike Yasar Duman, Fatma Feriha Cilli, Zumrut Sahbudak Bal, Gulhadiye Avcu
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引用次数: 0

Abstract

Carbapenem-resistant (CR) Acinetobacter spp. bloodstream infections (BSIs) are difficult to treat in children, yet pediatric data on factors associated with resistance and mortality remain limited. We aimed to identify factors associated with carbapenem resistance and 30-day mortality in pediatric Acinetobacter BSIs. We retrospectively analyzed children with monomicrobial Acinetobacter BSIs at a tertiary-care university hospital between January 2014 and September 2025. Factors associated with carbapenem resistance were assessed using co-primary logistic regression analyses in the full cohort and within A. baumannii; 30-day mortality was assessed using Cox regression. Among 128 episodes, median age was 2.0 years (IQR 0.76-8.01), 60.2% (77/128) were male and 90.6% (116/128) had comorbidities. Carbapenem resistance was identified in 54/128 episodes (42.2%), all caused by A. baumannii (54/87, 62.1%). Increasing age, longer hospitalization before BSI onset, mechanical ventilation (MV), and prior meropenem exposure were associated with resistance in both co-primary models. Adjusted ORs for MV were 23.77 (95% CI, 7.54-74.92) in the full cohort and 23.20 (95% CI, 5.39-99.95) within A. baumannii. Overall 30-day mortality was 13.3% (17/128) and was higher in CR than carbapenem-susceptible episodes (22.2% versus 6.8%; p = 0.011). Exploratory comparisons across CR A. baumannii treatment categories were inconclusive (exact p = 0.256). Thrombocytopenia (aHR, 6.12; 95% CI, 2.13-17.61) and carbapenem resistance (aHR, 3.01; 95% CI, 1.04-8.71) were associated with mortality in the primary Cox model.

Conclusion:  Thrombocytopenia and carbapenem resistance were associated with 30-day all-cause mortality in the primary adjusted analysis; the resistance association was not statistically significant in A. baumannii-restricted and first-episode-only sensitivity analyses.

What is known: • Acinetobacter BSIs mainly affect medically complex hospitalized children. • Pediatric evidence on factors associated with carbapenem resistance and mortality remains scarce.

What is new: • Increasing age, longer hospitalization before BSI onset, mechanical ventilation, and prior meropenem exposure were associated with carbapenem resistance in both the full Acinetobacter cohort and within A. baumannii. • Carbapenem resistance was associated with 30-day mortality in the primary model, but this finding was not consistently supported in sensitivity analyses; thrombocytopenia remained associated with mortality.

碳青霉烯耐药性和儿童不动杆菌血流感染的死亡率:一项为期12年的三级保健队列研究的决定因素。
碳青霉烯耐药(CR)不动杆菌(Acinetobacter sp .)血流感染(bsi)在儿童中很难治疗,但与耐药和死亡率相关因素的儿科数据仍然有限。我们的目的是确定与小儿不动杆菌BSIs中碳青霉烯类耐药性和30天死亡率相关的因素。我们回顾性分析了2014年1月至2025年9月间一家三级大学医院的单菌不动杆菌bsi患儿。在整个队列和鲍曼不动杆菌中使用共一级logistic回归分析评估与碳青霉烯类耐药性相关的因素;采用Cox回归评估30天死亡率。128例患者中位年龄为2.0岁(IQR 0.76-8.01), 60.2%(77/128)为男性,90.6%(116/128)有合并症。54/128例(42.2%)对碳青霉烯类耐药,均由鲍曼不动杆菌(54/87,62.1%)引起。在两种共原发模型中,年龄增加、BSI发病前住院时间延长、机械通气(MV)和既往美罗培南暴露与耐药相关。在整个队列中,MV的调整ORs为23.77 (95% CI, 7.54-74.92),在鲍曼不动杆菌中为23.20 (95% CI, 5.39-99.95)。总体30天死亡率为13.3% (17/128),CR高于碳青霉烯敏感发作(22.2% vs 6.8%; p = 0.011)。跨鲍曼杆菌治疗类别的探索性比较没有结论性(精确p = 0.256)。在初级Cox模型中,血小板减少症(aHR, 6.12; 95% CI, 2.13-17.61)和碳青霉烯类药物耐药性(aHR, 3.01; 95% CI, 1.04-8.71)与死亡率相关。结论:在初步校正分析中,血小板减少和碳青霉烯耐药性与30天全因死亡率相关;在鲍曼不动杆菌限制型和首发型敏感性分析中,耐药相关性无统计学意义。已知情况:•不动杆菌bsi主要影响医疗复杂的住院儿童。•与碳青霉烯耐药性和死亡率相关因素的儿科证据仍然很少。新发现:•在整个不动杆菌群和鲍曼不动杆菌群中,年龄增加、BSI发病前住院时间延长、机械通气和既往美罗培南暴露与碳青霉烯类耐药有关。在初级模型中,碳青霉烯耐药性与30天死亡率相关,但这一发现在敏感性分析中并未得到一致支持;血小板减少症仍与死亡率相关。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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