Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA.
Division of Nephrology, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
J Pediatr. 2021 Apr;231:185-192.e4. doi: 10.1016/j.jpeds.2020.12.023. Epub 2020 Dec 17.
To determine incidence and severity of acute kidney injury (AKI) within 7 days of sepsis evaluation and to assess AKI duration and the association between AKI and 30-day mortality.
Retrospective, matched cohort study in a single-center level IV neonatal intensive care unit. Eligible infants underwent sepsis evaluations at ≥72 hours of age during calendar years 2013-2018. Exposed infants (cases) were those with culture-proven sepsis and antimicrobial duration ≥5 days. Nonexposed infants (controls) were matched 1:1 to exposed infants based on gestational and corrected gestational age, and had negative sepsis evaluations with antibiotic durations <48 hours. AKI was defined by modified neonatal Kidney Disease Improving Global Outcomes criteria. Statistical analysis included Mann-Whitney and χ tests, multivariable logistic regression, and Kaplan-Meier time-to-event analysis.
Among 203 episodes of late-onset sepsis, 40 (20%) developed AKI within 7 days after evaluation, and among 193 episodes with negative cultures, 16 (8%) resulted in AKI (P = .001). Episodes of sepsis also led to greater AKI severity, compared with nonseptic episodes (P = .007). The timing of AKI onset and AKI duration did not differ between groups. Sepsis was associated with increased odds of developing AKI (aOR, 3.0; 95% CI, 1.5-6.2; P = .002). AKI was associated with increased 30-day mortality (aOR, 4.5; 95% CI, 1.3-15.6; P = .017).
Infants with late-onset sepsis had increased odds of AKI and greater AKI severity within 7 days of sepsis evaluation, compared with age-matched infants without sepsis. AKI was independently associated with increased 30-day mortality. Strategies to mitigate AKI in critically ill neonates with sepsis may improve outcomes.
确定脓毒症评估后 7 天内急性肾损伤 (AKI) 的发生率和严重程度,并评估 AKI 持续时间以及 AKI 与 30 天死亡率之间的关系。
这是一项在单中心四级新生儿重症监护病房进行的回顾性匹配队列研究。2013 年至 2018 年期间,符合条件的婴儿在年龄≥72 小时时进行脓毒症评估。暴露组婴儿(病例)为培养阳性的脓毒症和抗生素持续时间≥5 天的婴儿。未暴露组婴儿(对照组)根据胎龄和校正胎龄与暴露组婴儿 1:1 匹配,且抗生素持续时间<48 小时,无脓毒症评估。AKI 采用改良新生儿肾脏病改善全球结局标准定义。统计分析包括曼-惠特尼和 χ 检验、多变量逻辑回归和 Kaplan-Meier 时间事件分析。
在 203 例晚发性脓毒症中,40 例(20%)在评估后 7 天内发生 AKI,在 193 例培养阴性的脓毒症中,16 例(8%)发生 AKI(P=.001)。与非脓毒症相比,脓毒症组 AKI 更严重(P=.007)。AKI 发病时间和 AKI 持续时间在两组之间无差异。脓毒症与 AKI 发生的几率增加相关(优势比,3.0;95%置信区间,1.5-6.2;P=.002)。AKI 与 30 天死亡率增加相关(优势比,4.5;95%置信区间,1.3-15.6;P=.017)。
与年龄匹配的无脓毒症婴儿相比,晚发性脓毒症婴儿在脓毒症评估后 7 天内发生 AKI 和 AKI 严重程度的几率增加。AKI 与 30 天死亡率独立相关。在脓毒症危重症婴儿中,减轻 AKI 的策略可能改善结局。