Department of Pediatric Pulmonology, Faculty of Medicine Erciyes University, Kayseri, Turkey
Department of Pediatric Pulmonology, Meram Medical School Necmettin Erbakan University, Konya, Turkey
Balkan Med J. 2022 Sep 9;39(5):366-373. doi: 10.4274/balkanmedj.galenos.2022.2022-3-46.
Pulmonary embolism is a clinical condition caused by the obstruction of the pulmonary artery and its branches with endogenous, exogenous embolism, or local thrombus formation. It is a rare but potentially life-threatening event in the pediatric population. Pediatric pulmonary embolism has many unknown characteristics.
To evaluate clinical features, genetic and acquired risk factors, diagnostic imaging, and treatment strategies with long-term results in children with pulmonary embolism.
A retrospective multicenter clinical trial.
Patients aged 0-18 years who were diagnosed with pulmonary embolism with computed tomography pulmonary angiography (CTPA) findings (intraluminal filling defect in the lobar or main pulmonary artery) in 3 university hospitals between 2006 and 2021 were included in the study. A form was created for data standardization, and variables were collected retrospectively through medical record review. In addition to the features given above, we also evaluated in situ pulmonary artery thrombosis (ISPAT) and patients' Wells scores. Follow-up CTPA results were evaluated for patient response to treatment. Complete recovery means that there were no lesions, incomplete recovery if there was still embolism, and no response if there was no change.
Twenty-four patients (female:13, male:11) were included in the study. The mean age was 13.5 years. All patients but one had at least one or more genetic or acquired risk factors. Factor V Leiden mutation (16.6%) was the most common genetic risk factor. Six of 16 patients with Doppler ultrasonography were diagnosed with ISPAT because there was no sign of thromboembolic thrombosis. Nine (41.6%) patients had a Wells score of >4 (pulmonary embolism clinically strong), and 15 (58.4%) patients scored <4 (pulmonary embolism clinically likely weak), indicating that an alternative diagnosis was more likely than pulmonary embolism (sensitivity %37.5). The mean follow-up period was 23 (±17) months. Complete and incomplete recovery was observed in 15 (62.5%) and 7 (29.1%) patients, respectively, among the patients who underwent follow-up evaluation. No response was obtained in 2 patients (8.3%) who died.
The Wells scoring system seems insufficient to diagnose pulmonary embolism in children and should be improved by adding new parameters. ISPAT may be more common in children with congenital heart disease and systemic disease.
肺栓塞是一种由内源性、外源性栓塞或局部血栓形成导致肺动脉及其分支阻塞的临床病症。它是儿科人群中一种罕见但潜在危及生命的事件。儿科肺栓塞有许多未知的特征。
评估儿童肺栓塞的临床特征、遗传和获得性危险因素、诊断影像学以及治疗策略,并评估长期结果。
回顾性多中心临床试验。
本研究纳入了 2006 年至 2021 年间 3 所大学医院通过计算机断层肺动脉造影(CTPA)检查(肺段或主肺动脉腔内充盈缺损)诊断为肺栓塞的 0-18 岁患者。创建了一个表格来进行数据标准化,并通过病历回顾回顾性地收集变量。除了上述特征外,我们还评估了原位肺动脉血栓形成(ISPAT)和患者的 Wells 评分。评估随访 CTPA 结果以了解患者对治疗的反应。完全恢复是指无病变,不完全恢复是指仍有栓塞,无反应是指无变化。
本研究纳入了 24 名患者(女性 13 名,男性 11 名)。平均年龄为 13.5 岁。除 1 名患者外,所有患者均有至少 1 个或多个遗传或获得性危险因素。因子 V Leiden 突变(16.6%)是最常见的遗传危险因素。16 名患者中有 6 名通过多普勒超声诊断为 ISPAT,因为没有血栓栓塞的迹象。9 名(41.6%)患者的 Wells 评分>4(肺栓塞临床高度可能),15 名(58.4%)患者的 Wells 评分<4(肺栓塞临床低度可能),表明替代诊断比肺栓塞更有可能(敏感性为 37.5%)。患者的平均随访时间为 23(±17)个月。在接受随访评估的患者中,15 名(62.5%)患者完全恢复,7 名(29.1%)患者不完全恢复。2 名(8.3%)死亡的患者未得到任何反应。
Wells 评分系统似乎不足以诊断儿童肺栓塞,应通过添加新参数进行改进。ISPAT 在先天性心脏病和全身性疾病的儿童中可能更为常见。