新生儿败血症的流行病学和疗效:澳大利亚三级新生儿重症监护室的经验。

Neonatology Pub Date : 2024-01-01 Epub Date: 2024-06-18 DOI:10.1159/000539174
Cheryl Anne Mackay, Elizabeth A Nathan, Michelle Claire Porter, Damber Shrestha, Rolland Kohan, Tobias Strunk
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引用次数: 0

摘要

导言:新生儿败血症与严重的死亡率和发病率有关。中低收入国家受到的影响尤为严重,但在高收入国家,仍有多达 20% 的新生儿在 28 周后出现晚发型败血症(LOS)。了解特定地区的数据对于指导管理至关重要:珀斯爱德华国王纪念医院(KEMH)开展了一项回顾性队列研究。研究纳入了 2012 年 1 月至 2022 年 6 月期间入院的婴儿。数据提取自常规电子数据库。研究确定了败血症的发病率和病因,并分析了败血症与新生儿预后的关系:在研究期间,共有 23,395 名新生儿入院,中位妊娠期为 37 周,出生体重为 2,800 克。6 per 1,000 live births),主要是无乳链球菌(35 例,34.3%)和大肠杆菌(27 例,26.5%);268 例为 LOS(0.9 per 1,000 inpatient days),主要是凝固酶阴性葡萄球菌(CONS)(156 例,57.6%)和大肠杆菌(30 例,11.1%)。从2012年到2022年,LOS的发生率有所下降(p = 0.002)。患 EOS 的婴儿脑损伤(25.7% 对 4.1%;p = 0.002)和死亡率(18.8% 对 1.6%;p < 0.001)增加。住院时间(中位数 95 天 vs. 15 天;p < 0.001)、死亡率(15.3% vs. 1.6%;p = 0.018)、坏死性小肠结肠炎(NEC)(7.4% vs. 0.5%;p < 0.001)和慢性肺病(CLD)(58.1% vs. 5.9%;p = 0.005)均有所增加。与未感染的婴儿相比,患有败血症的28周婴儿出现神经发育障碍的风险更高(43.2% vs. 30.9%,p = 0.027):虽然我们观察到 LOS 的发生率有所下降,但败血症仍与较高的死亡率相关,幸存者的住院时间更长,脑损伤、NEC、CLD 和神经发育障碍的风险也更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology and Outcomes of Neonatal Sepsis: Experience from a Tertiary Australian NICU.

Introduction: Neonatal sepsis is associated with significant mortality and morbidity. Low-middle-income countries are disproportionately affected, but late-onset sepsis (LOS) still occurs in up to 20% of infants <28 weeks in high-income countries. Understanding site-specific data is vital to guide management.

Methods: A retrospective cohort study was conducted at King Edward Memorial Hospital (KEMH), Perth. Infants admitted between January 2012 and June 2022 were included. Data were extracted from routine electronic databases. Incidence and aetiology of sepsis were determined and the association of sepsis with neonatal outcomes analysed.

Results: During the study period, 23,395 newborns were admitted with a median gestation of 37 weeks and birth weight of 2,800 g. There were 370 sepsis episodes in 350 infants; 102 were early-onset sepsis (EOS) (1.6 per 1,000 live births), predominantly Streptococcus agalactiae (35, 34.3%) and Escherichia coli (27, 26.5%); 268 were LOS (0.9 per 1,000 inpatient days), predominantly coagulase-negative staphylococci (CONS) (156, 57.6%) and E. coli (30, 11.1%). The incidence of LOS declined from 2012 to 2022 (p = 0.002). Infants with EOS had increased brain injury (25.7% vs. 4.1%; p = 0.002) and mortality (18.8% vs. 1.6%; p < 0.001). Those with LOS had increased hospital stay (median 95 vs. 15 days; p < 0.001), mortality (15.3% vs. 1.6%; p = 0.018), necrotising enterocolitis (NEC) (7.4% vs. 0.5%; p < 0.001), and chronic lung disease (CLD) (58.1% vs. 5.9%; p = 0.005). Infants <28 weeks with sepsis were at increased risk of neurodevelopmental impairment compared to those without infection (43.2% vs. 30.9%, p = 0.027).

Conclusions: While we observed a reduction in LOS incidence, sepsis remains associated with higher mortality, and in survivors with longer hospital stay and increased risk of brain injury, NEC, CLD, and neurodevelopmental impairment.

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