Pediatric Intensive Care Unit, Jeanne de Flandre University Hospital, Lille, France.
Crit Care Med. 2013 Jul;41(7):1761-73. doi: 10.1097/CCM.0b013e31828a2bbd.
Multiple organ dysfunction syndrome is the main cause of death in adult ICUs and in PICUs. The PEdiatric Logistic Organ Dysfunction score developed in 1999 was primarily designed to describe the severity of organ dysfunction. This study was undertaken to update and improve the PEdiatric Logistic Organ Dysfunction score, using a larger and more recent dataset.
Prospective multicenter cohort study.
Nine multidisciplinary, tertiary-care PICUs of university-affiliated hospitals in France and Belgium.
All consecutive children admitted to these PICUs (June 2006-October 2007).
None.
We collected data on variables considered for the PEdiatric Logistic Organ Dysfunction-2 score during PICU stay up to eight time points: days 1, 2, 5, 8, 12, 16, and 18, plus PICU discharge. For each variable considered for the PEdiatric Logistic Organ Dysfunction-2 score, the most abnormal value observed during time points was collected. The outcome was vital status at PICU discharge. Identification of the best variable cutoffs was performed using bivariate analyses. The PEdiatric Logistic Organ Dysfunction-2 score was developed by multivariable logistic regressions and bootstrap process. We used areas under the receiver-operating characteristic curve to evaluate discrimination and Hosmer-Lemeshow goodness-of-fit tests to evaluate calibration. We enrolled 3,671 consecutive patients (median age, 15.5 mo; interquartile range, 2.2-70.7). Mortality rate was 6.0% (222 deaths). The PEdiatric Logistic Organ Dysfunction-2 score includes ten variables corresponding to five organ dysfunctions. Discrimination (areas under the receiver-operating characteristic curve = 0.934) and calibration (chi-square test for goodness-of-fit = 9.31, p = 0.317) of the PEdiatric Logistic Organ Dysfunction-2 score were good.
We developed and validated the PEdiatric Logistic Organ Dysfunction-2 score, which allows assessment of the severity of cases of multiple organ dysfunction syndrome in the PICU with a continuous scale. The PEdiatric Logistic Organ Dysfunction-2 score now includes mean arterial pressure and lactatemia in the cardiovascular dysfunction and does not include hepatic dysfunction. The score will be in the public domain, which means that it can be freely used in clinical trials.
多器官功能障碍综合征是成人 ICU 和儿科 ICU 死亡的主要原因。1999 年制定的儿科 Logistic 器官功能障碍评分主要用于描述器官功能障碍的严重程度。本研究旨在使用更大、更新的数据集对儿科 Logistic 器官功能障碍评分进行更新和改进。
前瞻性多中心队列研究。
法国和比利时 9 家多学科、三级儿童重症监护病房。
这些儿科重症监护病房(2006 年 6 月至 2007 年 10 月)连续收治的所有患儿。
无。
我们收集了在儿科重症监护病房住院期间考虑用于儿科 Logistic 器官功能障碍-2 评分的变量的数据,最多可达 8 个时间点:第 1、2、5、8、12、16 和 18 天,加上儿科重症监护病房出院。对于儿科 Logistic 器官功能障碍-2 评分考虑的每个变量,均采集时间点观察到的最异常值。结局为儿科重症监护病房出院时的存活状态。使用双变量分析确定最佳变量截止值。通过多变量逻辑回归和自举过程开发儿科 Logistic 器官功能障碍-2 评分。我们使用受试者工作特征曲线下面积评估鉴别能力,Hosmer-Lemeshow 拟合优度检验评估校准。我们共纳入 3671 例连续患儿(中位年龄 15.5 个月;四分位间距 2.2-70.7)。死亡率为 6.0%(222 例死亡)。儿科 Logistic 器官功能障碍-2 评分包括对应于五个器官功能障碍的十个变量。儿科 Logistic 器官功能障碍-2 评分的鉴别力(受试者工作特征曲线下面积=0.934)和校准(拟合优度卡方检验=9.31,p=0.317)良好。
我们开发并验证了儿科 Logistic 器官功能障碍-2 评分,该评分可使用连续量表评估儿科重症监护病房中多器官功能障碍综合征的严重程度。儿科 Logistic 器官功能障碍-2 评分现在包括心血管功能障碍中的平均动脉压和乳酸血症,不包括肝功能障碍。该评分将公开发布,这意味着可以在临床试验中自由使用。