Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave MLC 2005, Cincinnati, OH, 45229, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, 3230 Eden Ave, Cincinnati, OH, 45267, USA.
Crit Care. 2023 Nov 28;27(1):463. doi: 10.1186/s13054-023-04746-6.
Acute kidney injury (AKI) occurs commonly in pediatric septic shock and increases morbidity and mortality. Early identification of high-risk patients can facilitate targeted intervention to improve outcomes. We previously modified the renal angina index (RAI), a validated AKI prediction tool, to improve specificity in this population (sRAI). Here, we prospectively assess sRAI performance in a separate cohort.
A secondary analysis of a prospective, multicenter, observational study of children with septic shock admitted to the pediatric intensive care unit from 1/2019 to 12/2022. The primary outcome was severe AKI (≥ KDIGO Stage 2) on Day 3 (D3 severe AKI), and we compared predictive performance of the sRAI (calculated on Day 1) to the original RAI and serum creatinine elevation above baseline (D1 SCr > Baseline +). Original renal angina fulfillment (RAI +) was defined as RAI ≥ 8; sepsis renal angina fulfillment (sRAI +) was defined as RAI ≥ 20 or RAI 8 to < 20 with platelets < 150 × 10/µL.
Among 363 patients, 79 (22%) developed D3 severe AKI. One hundred forty (39%) were sRAI + , 195 (54%) RAI + , and 253 (70%) D1 SCr > Baseline + . Compared to sRAI-, sRAI + had higher risk of D3 severe AKI (RR 8.9, 95%CI 5-16, p < 0.001), kidney replacement therapy (KRT) (RR 18, 95%CI 6.6-49, p < 0.001), and mortality (RR 2.5, 95%CI 1.2-5.5, p = 0.013). sRAI predicted D3 severe AKI with an AUROC of 0.86 (95%CI 0.82-0.90), with greater specificity (74%) than D1 SCr > Baseline (36%) and RAI + (58%). On multivariable regression, sRAI + retained associations with D3 severe AKI (aOR 4.5, 95%CI 2.0-10.2, p < 0.001) and need for KRT (aOR 5.6, 95%CI 1.5-21.5, p = 0.01).
Prediction of severe AKI in pediatric septic shock is important to improve outcomes, allocate resources, and inform enrollment in clinical trials examining potential disease-modifying therapies. The sRAI affords more accurate and specific prediction than context-free SCr elevation or the original RAI in this population.
急性肾损伤(AKI)在儿科感染性休克中很常见,增加了发病率和死亡率。早期识别高危患者可以促进有针对性的干预,以改善预后。我们之前修改了肾脏绞痛指数(RAI),这是一种经过验证的 AKI 预测工具,以提高该人群的特异性(sRAI)。在这里,我们前瞻性地评估了 sRAI 在另一组人群中的表现。
对 2019 年 1 月至 2022 年 12 月期间入住儿科重症监护病房的感染性休克儿童进行的前瞻性、多中心、观察性研究的二次分析。主要结局是第 3 天(D3 严重 AKI)的严重 AKI,我们比较了 sRAI(在第 1 天计算)与原始 RAI 和血清肌酐基线升高(D1 SCr > 基线 +)的预测性能。原始肾脏绞痛满足(RAI +)定义为 RAI ≥ 8;脓毒症肾脏绞痛满足(sRAI +)定义为 RAI ≥ 20 或 RAI 8 至 <20 且血小板 <150 × 10/µL。
在 363 名患者中,79 名(22%)发生 D3 严重 AKI。140 名(39%)为 sRAI +,195 名(54%)为 RAI +,253 名(70%)为 D1 SCr > 基线 +。与 sRAI-相比,sRAI +的 D3 严重 AKI 风险更高(RR 8.9,95%CI 5-16,p < 0.001)、肾脏替代治疗(KRT)(RR 18,95%CI 6.6-49,p < 0.001)和死亡率(RR 2.5,95%CI 1.2-5.5,p = 0.013)。sRAI 预测 D3 严重 AKI 的 AUC 为 0.86(95%CI 0.82-0.90),特异性(74%)优于 D1 SCr > 基线(36%)和 RAI +(58%)。在多变量回归中,sRAI +与 D3 严重 AKI(aOR 4.5,95%CI 2.0-10.2,p < 0.001)和 KRT 需求(aOR 5.6,95%CI 1.5-21.5,p = 0.01)相关。
预测儿科感染性休克严重 AKI 对于改善预后、分配资源和告知潜在疾病修正治疗的临床试验入组非常重要。sRAI 在该人群中的预测准确性和特异性均优于无背景 SCr 升高或原始 RAI。