Timing of corticosteroid initiation and severe in-hospital outcomes in pediatric Mycoplasma pneumoniae pneumonia: a propensity score-matched cohort study.
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引用次数: 0
Abstract
Background: Among hospitalized children with Mycoplasma pneumoniae pneumonia (MPP) who received systemic corticosteroids, the association between treatment timing and subsequent in-hospital outcomes remains uncertain. We evaluated whether earlier initiation was associated with a more favorable hospital course.
Methods: We conducted a retrospective propensity score-matched cohort study at a tertiary pediatric center in China between January 2023 and August 2025. Children aged 1-18 years with confirmed MPP who received systemic corticosteroids 3-14 days after symptom onset were included. Symptom onset was adjudicated by chart abstraction from caregiver-reported histories documented in the electronic medical record. All included patients received macrolide-based first-line antibiotics. Patients were grouped by corticosteroid initiation timing as early (3-7 days) or late (> 7 days). The propensity model used prespecified pre-treatment demographic, clinical-course, admission respiratory, inflammatory, radiographic, comorbidity, and resistance variables. The primary outcome was a severe composite endpoint; secondary outcomes included fever duration after corticosteroid initiation, hospital stay, oxygen therapy, ICU admission, pleural effusion, and antibiotic escalation. Exploratory analyses compared 3-5, 6-7, and > 7 days, with initiation day additionally modeled continuously for trend.
Results: Among 902 eligible patients, 482 received early corticosteroids and 420 received late corticosteroids. After 1:1 matching, 299 pairs were analyzed; 183 early initiators and 121 late initiators were unmatched and excluded from the matched cohort. Early initiation was associated with lower odds of the severe composite outcome than late initiation (12.0% vs. 19.4%; OR 0.57, 95% CI 0.36-0.89; P = 0.018), less oxygen therapy (8.7% vs. 13.7%; OR 0.59, 95% CI 0.35-0.99), less antibiotic escalation (9.4% vs. 15.7%; OR 0.56, 95% CI 0.34-0.91; P = 0.019), shorter fever after corticosteroid initiation (3 [IQR 2-4] vs. 4 [3-5] days), and shorter hospitalization (7 [6-9] vs. 9 [7-11] days; both P < 0.001). In exploratory timing analyses, only initiation on days 3-5 was associated with lower odds of severe outcomes (OR 0.35, 95% CI 0.18-0.68), whereas initiation on days 6-7 was not (OR 0.83, 95% CI 0.48-1.43). Continuous modeling suggested a graded association between later initiation day and worse outcomes (P for trend = 0.021).
Conclusion: Among corticosteroid-treated hospitalized children with MPP, earlier corticosteroid initiation-particularly on days 3-5 after symptom onset-was associated with a more favorable in-hospital course. Because residual confounding, potential collider bias, and time-dependent bias cannot be excluded, these findings should be interpreted as associative and require prospective confirmation.
背景:在接受全身皮质类固醇治疗的肺炎支原体肺炎(MPP)住院儿童中,治疗时机与随后的住院结局之间的关系仍不确定。我们评估了早期开始治疗是否与更有利的住院治疗相关。方法:我们于2023年1月至2025年8月在中国一家三级儿科中心进行了一项回顾性倾向评分匹配队列研究。年龄1-18岁确诊MPP的儿童在症状出现后3-14天接受全身性皮质类固醇治疗。通过从电子病历中记录的护理人员报告的病史中提取图表来判断症状的发作。所有患者均接受大环内酯类一线抗生素治疗。患者按皮质类固醇起始时间分为早(3-7天)或晚(10 -7天)。倾向模型使用预先指定的治疗前人口统计学、临床病程、入院呼吸、炎症、放射学、合并症和耐药性变量。主要终点是严重的复合终点;次要结局包括皮质类固醇起始治疗后的发热持续时间、住院时间、氧疗、ICU入院、胸腔积液和抗生素剂量增加。探索性分析比较了3-5、6-7和bbb7天,并对起始日进行了连续建模。结果:902例患者中,482例接受早期皮质激素治疗,420例接受晚期皮质激素治疗。1:1配对后,共分析299对;183例早期启动者和121例晚期启动者不匹配,被排除在匹配队列之外。早期开始治疗与较晚开始治疗相比,出现严重复合结局的几率较低(12.0%比19.4%;OR 0.57, 95% CI 0.36-0.89; P = 0.018),较少的氧疗(8.7%比13.7%;OR 0.59, 95% CI 0.35-0.99),较少的抗生素升级(9.4%比15.7%;OR 0.56, 95% CI 0.34-0.91; P = 0.019),皮质类固醇开始治疗后发热时间较短(3 [IQR 2-4]比4[3-5]天),住院时间较短(7[6-9]比9[7-11]天;结论:在接受皮质类固醇治疗的MPP住院儿童中,更早开始使用皮质类固醇-特别是在症状出现后3-5天-与更有利的住院病程相关。由于残留混杂、潜在碰撞偏倚和时间相关偏倚不能排除,这些发现应被解释为关联性,需要前瞻性确认。
期刊介绍:
BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.