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儿童心脏病后血栓形成综合征的特征。

Characterization of Post-Thrombotic Syndrome in Children with Cardiac Disease.

机构信息

Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada.

Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

J Pediatr. 2019 Apr;207:42-48. doi: 10.1016/j.jpeds.2018.10.064. Epub 2018 Dec 7.

Abstract

OBJECTIVE

To assess the validity of existing clinical scales assessing the presence of physical and functional abnormalities for diagnosing post-thrombotic syndrome (PTS) in children, including specific evaluation of use in children with congenital heart disease (CHD).

STUDY DESIGN

One hundred children aged >2 years (average age, 6 years), including 33 with CHD and previously proven extremity deep vein thrombosis (DVT), 37 with CHD and no previous DVT, and 30 healthy siblings, were blindly assessed for PTS using the modified Villalta Scale (MVS). All patients aged <6 years underwent neurodevelopmental testing and an age-appropriate quality of life assessment.

RESULTS

The MVS identified mild PTS in 20 children and moderate PTS in 1 child (including 14 of 33 [42%] in the CHD/DVT group, 5 of 37 [14%] in the CHD/no DVT group, and 2 of 30 controls [7%]). The diagnosis of PTS was confirmed clinically in 14 patients, all of whom had previous thrombosis and 1 of whom was MVS-negative. MVS had an accuracy of 91% and performed reasonably well as a screening tool but poorly as a diagnostic tool. MVS reliability was acceptable. Children with PTS had similar quality of life as those without PTS but had higher rates of neurodevelopmental delays in gross motor skills (70% vs 24%; P = .02) and problem-solving indicators (60% vs 15%; P = .008).

CONCLUSIONS

Using the MVS scale for PTS screening in children with CHD is feasible and reliable, and the scale has good correlation with a clinical diagnosis of PTS despite a high prevalence of false-positive findings. Further research is needed to determine the clinical relevance of PTS in this population.

摘要

目的

评估现有的评估物理和功能异常以诊断儿童血栓后综合征(PTS)的临床量表的有效性,包括专门评估在先天性心脏病(CHD)儿童中的应用。

研究设计

100 名年龄>2 岁的儿童(平均年龄 6 岁),包括 33 名患有 CHD 且之前已确诊肢体深静脉血栓形成(DVT)的儿童、37 名患有 CHD 且之前无 DVT 的儿童和 30 名健康的兄弟姐妹,使用改良 Villalta 量表(MVS)对 PTS 进行盲法评估。所有年龄<6 岁的患者均进行神经发育测试和适合年龄的生活质量评估。

结果

MVS 发现 20 名儿童存在轻度 PTS,1 名儿童存在中度 PTS(包括 CHD/DVT 组的 14 名[42%]、CHD/no DVT 组的 5 名[14%]和对照组的 2 名[7%])。14 名患者的 PTS 诊断得到临床证实,所有患者均有既往血栓形成,其中 1 名 MVS 阴性。MVS 的准确率为 91%,作为筛查工具表现相当不错,但作为诊断工具表现不佳。MVS 的可靠性可接受。患有 PTS 的儿童与无 PTS 的儿童的生活质量相似,但在粗大运动技能方面出现神经发育迟缓的发生率较高(70%比 24%;P=0.02)和解决问题指标(60%比 15%;P=0.008)。

结论

在患有 CHD 的儿童中使用 MVS 量表进行 PTS 筛查是可行且可靠的,尽管存在大量假阳性发现,但该量表与 PTS 的临床诊断具有良好的相关性。需要进一步研究来确定 PTS 在该人群中的临床相关性。

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