儿童肺出血的临床概况和死亡危险因素:沙特阿拉伯的一项单中心研究

Annals of Saudi medicine Pub Date : 2025-07-01 Epub Date: 2025-08-07 DOI:10.5144/0256-4947.2025.235
Moath K Alabdulsalam, Robayeh A Asiry, Raghad T Alhuthil, Abdulaziz S Almusallam, Nora K Alhelali, Tareq M Alayed, Fahad B Aljofan, Fawaz A Alanzi, Tariq O Alofisan, Abdullah T Alturkia
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引用次数: 0

摘要

背景:肺出血是一种罕见的危及生命的事件,其特征是出血进入气道和肺实质。目的:探讨PH患者的临床特征,调查与死亡相关的危险因素,为这一人群的患者结局提供全面的了解。设计:回顾性队列研究。地点:沙特阿拉伯利雅得费萨尔国王专科医院和研究中心(KFSHRC)儿科重症监护室(PICU)。患者和方法:2014年1月至2019年9月住院的PH发作儿科患者(1个月至14岁)。主要结局指标:临床特征、结局和死亡相关危险因素。样本大小:80名儿童。结果:队列性别比例为1:1,中位年龄为24个月[四分位数范围:9-78]。病史包括骨髓移植(51.3%)、肿瘤病例(40.0%)、化疗(61.3%)、胸部感染(86.3%)和免疫抑制剂使用(71.3%)。此外,大多数患者(87.5%)在PH发作期间有急性呼吸窘迫综合征。在单变量分析中,PICU的总死亡率为82.5%(66/80),与血小板减少症、败血症、肾功能损害、肝功能障碍、多器官功能障碍和编码状态改变有关(均为P)。结论:报告的高死亡率强调需要有针对性的干预和提高警惕,特别是在免疫功能低下的儿童中。未来的研究将扩展这些发现,以完善当前的管理方案,并进一步改善儿科博士的患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical profiles and mortality risk factors in pediatric pulmonary hemorrhage: a singlecenter study in Saudi Arabia.

Clinical profiles and mortality risk factors in pediatric pulmonary hemorrhage: a singlecenter study in Saudi Arabia.

Clinical profiles and mortality risk factors in pediatric pulmonary hemorrhage: a singlecenter study in Saudi Arabia.

Clinical profiles and mortality risk factors in pediatric pulmonary hemorrhage: a singlecenter study in Saudi Arabia.

Background: Pulmonary hemorrhage (PH) is a rare, life-threatening event characterized by bleeding into the airways and lung parenchyma.

Objectives: To explore the clinical characteristics of PH patients and investigate mortality-related risk factors, providing a holistic understanding of patient outcomes in this population.

Design: A retrospective cohort study.

Settings: The Pediatric Intensive Care Unit (PICU) at King Faisal Specialist Hospital and Research Centre (KFSHRC), Riyadh, Saudi Arabia.

Patients and methods: Pediatric patients with PH episodes (aged 1 month to 14 years) who were admitted from January 2014 to September 2019.

Main outcomes measures: Clinical characteristics, outcomes, and mortality-related risk factors.

Sample size: 80 children.

Results: The cohort had a sex ratio of 1:1 and a median age of 24 months [interquartile range: 9-78]. Medical histories included bone marrow transplant (51.3%), oncology cases (40.0%), chemotherapy (61.3%), chest infection (86.3%), and immunosuppressant use (71.3%). Additionally, most patients (87.5%) had acute respiratory distress syndrome during the PH episode. The overall PICU mortality rate was 82.5% (66/80), and was associated with thrombocytopenia, sepsis, renal impairment, liver dysfunction, multiorgan dysfunction, and altered code status in univariable analysis (all P <.05). Multivariate analysis identified sepsis, multiorgan dysfunction, and altered code status as key predictors of PICU mortality (P <.05).

Conclusion: The high mortality rate reported emphasizes the need for tailored interventions and heightened vigilance, particularly in immunocompromised children. Future research will expand on these findings to refine current management protocols and further improve patient care in pediatric PH.

Limitations: Retrospective study, single-center.

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