儿童重症监护病房收治的自身免疫性炎症性风湿病儿童和青少年的死亡率

IF 2.8 3区 医学 Q1 PEDIATRICS
Tinnapat Buranapattama, Suwannee Phumeetham, Nuntawan Piyaphanee, Maynart Sukharomana, Sirirat Charuvanij
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引用次数: 0

摘要

背景:本研究旨在描述儿童和青少年自身免疫性炎症性风湿性疾病(AIIRD)入住儿科重症监护病房(PICU)的特点和结局。探讨儿童死亡风险(PRISM) III和儿童死亡指数(PIM) 3评分预测死亡率的准确性。方法:回顾性队列研究。纳入2011年7月至2021年6月期间在泰国最大的大学转诊中心入住PICU的年龄≤18岁的aird儿童和青少年。结果:74例患者入院PICU 122例;平均年龄12.0±4.3岁,女性74.3%。AIIRD以系统性红斑狼疮(SLE)居多(83.8%),其次为系统性幼年特发性关节炎(5.4%)、幼年皮肌炎(JDM)(2.7%)和显微镜下多血管炎(2.7%)。入院原因以感染合并疾病发作为主(29.5%)。肺炎是感染的主要部位。鲍曼不动杆菌是最常见的病原体。8例(6.5%)患者出现巨噬细胞激活综合征。PICU入院患者死亡18例,死亡率14.8%;17例SLE, 1例JDM。机械通气(aOR 24.07, 95%CI:1.33 ~ 434.91, P= 0.031)、气胸(aOR 24.08, 95%CI:1.76 ~ 328.86, P= 0.017)和血小板减少(aOR 8.34, 95%CI:1.31 ~ 53.73, P= 0.025)与死亡率相关。PRISM III评分预测的死亡率风险随着评分≥9而增加。对于PIM 3评分,如果评分≥3,死亡风险增加。PRISM III和PIM 3评分的ROC曲线下面积分别为0.741 (95%CI: 0.633 ~ 0.849), P = 0.001和0.804 (95%CI: 0.685 ~ 0.924), P结论:SLE是需要入住PICU的主要aird。机械通气、气胸和血小板减少与儿童AIIRD患者的死亡率相关。PRISM III和PIM 3评分具有较好的校准性,而PIM 3评分在预测儿童AIIRD死亡率方面具有较好的判别能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mortality in children and adolescents with autoimmune inflammatory rheumatic diseases admitted to the pediatric intensive care unit.

Background: This study aimed to describe the characteristics and outcomes of children and adolescents with autoimmune inflammatory rheumatic diseases (AIIRD) who were admitted to the pediatric intensive care unit (PICU). The accuracy of the Pediatric Risk of Mortality (PRISM) III and Pediatric Index of Mortality (PIM) 3 scores to predict the mortality were investigated.

Methods: This was a retrospective cohort study. Children and adolescents with AIIRD aged ≤ 18 years who were admitted to the PICU at the largest university-based referral center in Thailand during July 2011 to June 2021 were included.

Results: There were 122 PICU admissions from 74 patients; mean age of 12.0 ± 4.3 years, 74.3% female. Majority of AIIRD were systemic lupus erythematosus (SLE) (83.8%), followed by systemic juvenile idiopathic arthritis (5.4%), juvenile dermatomyositis (JDM) (2.7%) and microscopic polyangiitis (2.7%). The main cause of admission was combined infection and disease flare (29.5%). Pneumonia was the main site of infection. Acinetobacter baumanii was the most common causative agent. Macrophage activation syndrome occurred in 8 (6.5%) admissions. The mortality rate of PICU admissions was 14.8% from 18 deaths; 17 with SLE and 1 with JDM. Mechanical ventilation (aOR 24.07, 95%CI:1.33-434.91, P= 0.031), pneumothorax (aOR 24.08, 95%CI:1.76-328.86, P = 0.017 and thrombocytopenia (aOR 8.34, 95%CI:1.31-53.73, P = 0.025) were associated with mortality. The risk of mortality rate as predicted by the PRISM III score increased with a score ≥ 9. For the PIM 3 score, the risk of mortality increased if the score ≥ 3. The area under the ROC curve for the PRISM III and PIM 3 scores was 0.741 (95%CI: 0.633-0.849), P = 0.001 and 0.804 (95%CI: 0.685-0.924), P < 0.001, respectively. The model calibration using the Hosmer-Lemeshow goodness of fit test demonstrated a chi-square of 4.335, P = 0.826 for PRISM III and 7.987, P = 0.435 for PIM 3.

Conclusion: SLE was the main AIIRD that required admission to the PICU. Mechanical ventilation, pneumothorax and thrombocytopenia were associated with mortality in pediatric patients with AIIRD. The PRISM III and PIM 3 scores demonstrated good calibration, while the PIM 3 score provided better discrimination ability in the prediction of mortality for pediatric AIIRD.

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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