Early deaths associated with community-acquired and healthcare-associated bloodstream infections: a population-based study, Finland, 2004 to 2018.

Keiju Sk Kontula, Kirsi Skogberg, Jukka Ollgren, Asko Järvinen, Outi Lyytikäinen
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引用次数: 1

Abstract

BackgroundBloodstream infections (BSI) cause substantial morbidity and mortality.AimWe explored the role of causative pathogens and patient characteristics on the outcome of community-acquired (CA) and healthcare-associated (HA) BSI, with particular interest in early death.MethodsWe used national register data to identify all BSI in Finland during 2004-18. We determined the origin of BSI, patients´ underlying comorbidities and deaths within 2 or 30 days from specimen collection. A time-dependent Cox model was applied to evaluate the impact of patient characteristics and causative pathogens on the hazard for death at different time points.ResultsA total of 173,715 BSI were identified; 22,474 (12.9%) were fatal within 30 days and, of these, 6,392 (28.4%) occurred within 2 days (7.9 deaths/100,000 population). The 2-day case fatality rate of HA-BSI was higher than that of CA-BSI (5.4% vs 3.0%). Patients who died within 2 days were older than those alive on day 3 (76 vs 70 years) and had more severe comorbidities. Compared with other BSI, infections leading to death within 2 days were more often polymicrobial (11.8% vs 6.3%) and caused by Pseudomonas aeruginosa (6.2% vs 2.0%), fungi (2.9% vs 1.4%) and multidrug-resistant (MDR) pathogens (2.2% vs 1.8%), which were also predictors of death within 2 days in the model.ConclusionsOverrepresentation of polymicrobial, fungal, P. aeruginosa and MDR aetiology among BSI leading to early death is challenging concerning the initial antimicrobial treatment. Our findings highlight the need for active prevention and prompt recognition of BSI and appropriate antimicrobial treatment.

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与社区获得性和医疗保健相关的血液感染相关的早期死亡:2004年至2018年芬兰一项基于人群的研究
血液感染(BSI)引起大量的发病率和死亡率。我们探讨了致病病原体和患者特征对社区获得性(CA)和卫生保健相关(HA) BSI结果的作用,特别是对早期死亡的兴趣。方法我们使用国家登记数据来确定2004-18年间芬兰所有的BSI。我们确定了BSI的起源、患者潜在的合并症和标本采集后2天或30天内的死亡情况。采用时间依赖的Cox模型评估不同时间点患者特征和致病病原体对死亡危险的影响。结果共检出BSI 173,715例;22,474例(12.9%)在30天内死亡,其中6,392例(28.4%)在2天内死亡(每10万人中有7.9例死亡)。HA-BSI的2天病死率高于CA-BSI (5.4% vs 3.0%)。2天内死亡的患者比第3天存活的患者年龄大(76岁vs 70岁),并且有更严重的合并症。与其他BSI相比,导致2天内死亡的感染更多是多微生物感染(11.8%比6.3%),由铜绿假单胞菌(6.2%比2.0%)、真菌(2.9%比1.4%)和多药耐药(MDR)病原体(2.2%比1.8%)引起,这些也是模型中2天内死亡的预测因子。结论多微生物、真菌、铜绿假单胞菌和耐多药等病因在导致BSI早期死亡的初步抗菌治疗中具有代表性。我们的研究结果强调了积极预防和及时识别BSI以及适当的抗菌治疗的必要性。
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