Thiart Marí, Nel Pieter, du Toit Jacques, Burger Marilize, Ferreira Nando
Division of Orthopaedic Surgery, Department of Surgical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg Campus, Cape Town, South Africa.
Division of Microbiology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg Campus, Cape Town, South Africa.
J Child Orthop. 2025 Jun 24:18632521251346650. doi: 10.1177/18632521251346650.
A subset of children with acute haematogenous osteomyelitis become severely ill. This study aimed to define a severe and standard course and identify potential risk factors on admission for a severe course as well as the cumulative incidence.
This retrospective cohort study included all children under 16 years with acute haematogenous osteomyelitis between January 2018 and September 2021. The outcome parameters included >2 surgical debridements, C-reactive protein level not halving in 48 h, extraosseous involvement and hospital stay >14 days. Predictor variables (delayed presentation (>5 days), C-reactive protein >250 mg/L on admission, >1 bone segment and need for intensive care unit on admission) were tested against the outcome of a severe clinical course using univariate logistic regression analysis (using < 0.2).
One hundred and twenty-one patients were included. Thirty-nine patients (32.2%) had a complicated course. Patients admitted to intensive care unit had a 2.8-times higher risk of a severe course compared to those not requiring intensive care unit (risk ratio 2.8; 95% confidence interval 1.6-4.8); having a C-reactive protein >250 mg/L on admission increased the risk of a severe course 1.7 times (risk ratio 1.71, 95% confidence interval 1.3-2.3). Having more than one bone segment involved and a delayed presentation of >5 days increased risk of a severe course by 2.4 (risk ratio 2.4, 95% confidence interval 1.6-3.6) and 1.3 times (risk ratio 1.3, 95% confidence interval 1.3-1.3), respectively, compared to the alternative. The cumulative incidence of acute haematogenous osteomyelitis ranged between 4.0% and 5.0% per year.
Four risk factors present on admission were identified and are suggested to modify the risk of a severe disease as well as change treatment protocols.
一部分患有急性血源性骨髓炎的儿童病情严重。本研究旨在确定严重和标准病程,并确定入院时严重病程的潜在风险因素以及累积发病率。
这项回顾性队列研究纳入了2018年1月至2021年9月期间所有16岁以下患有急性血源性骨髓炎的儿童。结局参数包括>2次手术清创、48小时内C反应蛋白水平未减半、骨外受累以及住院时间>14天。预测变量(就诊延迟(>5天)、入院时C反应蛋白>250mg/L、>1个骨段以及入院时需要重症监护病房)使用单因素逻辑回归分析(使用<0.2)针对严重临床病程的结局进行测试。
共纳入121例患者。39例患者(32.2%)病程复杂。入住重症监护病房的患者严重病程风险比不需要重症监护病房的患者高2.8倍(风险比2.8;95%置信区间1.6 - 4.8);入院时C反应蛋白>250mg/L使严重病程风险增加1.7倍(风险比1.71,95%置信区间1.3 - 2.3)。与其他情况相比,累及多个骨段和就诊延迟>5天分别使严重病程风险增加2.4倍(风险比2.4,95%置信区间1.6 - 3.6)和1.3倍(风险比1.3,95%置信区间1.3 - 1.3)。急性血源性骨髓炎的累积发病率每年在4.0%至5.0%之间。
确定了入院时存在的四个风险因素,建议这些因素可改变严重疾病风险并更改治疗方案。