Clinical Division and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven University Hospital, Leuven, Belgium.
Virtual Pediatric Systems, LCC, Los Angeles, CA.
Pediatr Crit Care Med. 2019 Feb;20(2):113-119. doi: 10.1097/PCC.0000000000001764.
The use of mortality prediction scores in clinical trials in the PICU is essential for comparing patient groups. Because of the decline in PICU mortality over the last decades, leading to a shift toward later deaths, recent trials use 90-day mortality as primary outcome for estimating mortality and survival more accurately. This study assessed and compared the performance of two frequently used PICU mortality prediction scores for prediction of PICU and 90-day mortality.
This secondary analysis of the randomized controlled Early versus Late Parenteral Nutrition in the Pediatric Intensive Care Unit trial compared the discrimination (area under the receiver operating characteristic curve) and calibration of the Pediatric Index of Mortality 3 and the Pediatric Risk of Mortality III scores for prediction of PICU and 90-day mortality.
Three participating PICUs within academic hospitals in Belgium, the Netherlands, and Canada.
One-thousand four-hundred twenty-eight critically ill patients 0-17 years old.
None.
Although Pediatric Index of Mortality 3 only includes information available at the time of PICU admission, thus before any intervention in the PICU, it showed good discrimination (area under the receiver operating characteristic curve, 0.894; 95% CI, 0.892-0.896) and good calibration (no deviation from the diagonal, p = 0.58) for PICU mortality. Pediatric Risk of Mortality III, which involves the worst values for the evaluated variables during the first 24 hours of PICU stay, was statistically more discriminant (area under the receiver operating characteristic curve, 0.920; 95% CI, 0.918-0.921; p = 0.04) but poor in calibration (significant deviation from the diagonal; p = 0.04). Pediatric Index of Mortality 3 and Pediatric Risk of Mortality III discriminated equally well between 90-day mortality and survival (area under the receiver operating characteristic curve, 0.867; 95% CI, 0.866-0.869 and area under the receiver operating characteristic curve, 0.882; 95% CI, 0.880-0.884, respectively, p = 0.77), but Pediatric Risk of Mortality III was not well calibrated (p = 0.04), unlike Pediatric Index of Mortality 3 (p = 0.34).
Pediatric Index of Mortality 3 performed better in calibration for predicting PICU and 90-day mortality than Pediatric Risk of Mortality III and is not influenced by intervention or PICU quality of care. Therefore, Pediatric Index of Mortality 3 seems a better choice for use in clinical trials with 90-day mortality as primary outcome.
在 PICU 临床试验中使用死亡率预测评分对于比较患者群体至关重要。由于过去几十年 PICU 死亡率下降,导致后期死亡人数增加,最近的试验使用 90 天死亡率作为主要结局来更准确地估计死亡率和生存率。本研究评估并比较了两种常用于预测 PICU 和 90 天死亡率的 PICU 死亡率预测评分的性能。
这项对早期与晚期肠外营养在儿科重症监护病房的随机对照试验的二次分析比较了儿科死亡率 3 指数和儿科死亡率风险 3 评分预测 PICU 和 90 天死亡率的区分度(接受者操作特征曲线下面积)和校准度。
比利时、荷兰和加拿大的三所参与学术医院的三个 PICU。
1428 名 0-17 岁的危重症患者。
无。
尽管儿科死亡率 3 指数仅包含 PICU 入院时可用的信息,因此在 PICU 内进行任何干预之前,它对 PICU 死亡率具有良好的区分度(接受者操作特征曲线下面积,0.894;95%CI,0.892-0.896)和良好的校准度(与对角线无偏差,p=0.58)。儿科死亡率风险 3 指数涉及 PICU 住院期间前 24 小时评估变量的最差值,在统计学上具有更高的区分度(接受者操作特征曲线下面积,0.920;95%CI,0.918-0.921;p=0.04),但校准度较差(与对角线有显著偏差;p=0.04)。儿科死亡率 3 指数和儿科死亡率风险 3 指数在 90 天死亡率和生存率之间的区分度相同(接受者操作特征曲线下面积,0.867;95%CI,0.866-0.869 和接受者操作特征曲线下面积,0.882;95%CI,0.880-0.884,p=0.77),但儿科死亡率风险 3 指数的校准度不佳(p=0.04),而儿科死亡率 3 指数则没有(p=0.34)。
儿科死亡率 3 指数在预测 PICU 和 90 天死亡率方面的校准性能优于儿科死亡率风险 3 指数,且不受干预或 PICU 护理质量的影响。因此,儿科死亡率 3 指数似乎是使用 90 天死亡率作为主要结局的临床试验的更好选择。