Department of Paediatrics and Child Health, University of the Free State Faculty of Health Sciences School of Medicine Bloemfontein, South Africa.
Paediatric Intensive Care Units, Universitas Academic and Pelonomi Tertiary Hospitals, Bloemfontein, South Africa.
Pediatr Crit Care Med. 2021 Sep 1;22(9):813-821. doi: 10.1097/PCC.0000000000002693.
To evaluate the performance of the Pediatric Index of Mortality 3 as mortality risk assessment model.
This prospective study included all admissions 30 days to 18 years old for 12 months during 2016 and 2017. Data gathered included the following: age and gender, diagnosis and reason for PICU admission, data specific for the Pediatric Index of Mortality 3 calculation, PICU outcomes (death or survival), and length of PICU stay.
Nine units that care for children within tertiary or quaternary academic hospitals in South Africa.
All admissions 30 days to 18 years old, excluding premature infants, children who died within 2 hours of admission, or children transferred to other PICUs, and those older than 18 years old.
None.
There were 3,681 admissions of which 2,253 (61.3%) were male. The median age was 18 months (interquartile range, 6-59.5 mo). There were 354 deaths (9.6%). The Pediatric Index of Mortality 3 predicted 277.47 deaths (7.5%). The overall standardized mortality ratio was 1.28. The area under the receiver operating characteristic curve was 0.81 (95% CI 0.79-0.83). The Hosmer-Lemeshow goodness-of-fit test statistic was 174.4 (p < 0.001). Standardized mortality ratio for all age groups was greater than 1. Standardized mortality ratio for diagnostic subgroups was mostly greater than 1 except for those whose reason for PICU admission was classified as accident, toxin and envenomation, and metabolic which had an standardized mortality ratio less than 1. There were similar proportions of respiratory patients, but significantly greater proportions of neurologic and cardiac (including postoperative) patients in the Pediatric Index of Mortality 3 derivation cohort than the South African cohort. In contrast, the South African cohort contained a significantly greater proportion of miscellaneous (including injury/accident victims) and postoperative noncardiac patients.
The Pediatric Index of Mortality 3 discrimination between death and survival among South African units was good. Case-mix differences between these units and the Pediatric Index of Mortality 3 derivation cohort may partly explain the poor calibration. We need to recalibrate Pediatric Index of Mortality 3 to the local setting.
评估儿科死亡率指数 3 作为死亡率风险评估模型的性能。
这项前瞻性研究包括 2016 年和 2017 年期间 12 个月内 30 天至 18 岁的所有入住 PICU 患者。收集的数据包括:年龄和性别、入住 PICU 的诊断和原因、儿科死亡率指数 3 计算的具体数据、PICU 结局(死亡或存活)以及 PICU 住院时间。
南非三级或四级学术医院内的 9 个儿童护理单位。
所有 30 天至 18 岁的入住患者,不包括早产儿、入院后 2 小时内死亡的患儿或转至其他 PICU 的患儿以及年龄大于 18 岁的患儿。
无。
共纳入 3681 例患儿,其中 2253 例(61.3%)为男性。中位年龄为 18 个月(四分位距,6-59.5 个月)。共有 354 例死亡(9.6%)。儿科死亡率指数 3 预测死亡 277.47 例(7.5%)。总体标准化死亡率比为 1.28。受试者工作特征曲线下面积为 0.81(95%CI 0.79-0.83)。Hosmer-Lemeshow 拟合优度检验统计量为 174.4(p<0.001)。所有年龄组的标准化死亡率比均大于 1。诊断亚组的标准化死亡率比除了因意外、毒素和毒液以及代谢而入住 PICU 的患儿外,大多大于 1,这些患儿的标准化死亡率比小于 1。呼吸科患儿的比例相似,但儿科死亡率指数 3 推导队列中神经科和心脏科(包括术后)患儿的比例显著大于南非队列。相比之下,南非队列中包含比例显著更高的其他(包括损伤/意外受害者)和非心脏术后患者。
儿科死亡率指数 3 在南非各单位区分死亡与存活的能力较好。这些单位与儿科死亡率指数 3 推导队列之间的病例组合差异可能部分解释了校准效果不佳。我们需要对儿科死亡率指数 3 进行重新校准以适应当地情况。