先天性心脏病患儿肺动脉和右心房压力的超声心动图估算:一项全面的前瞻性研究和新方程的引入。

Q2 Medicine
Elaheh Malakan Rad, Reza Elhamian, Keyhan Sayadpour Zanjani, Reza Shabanian, Ehsan Aghaei Moghadam, Mohamad Taghi Majnoon, Aliakbar Zeinaloo
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引用次数: 0

摘要

背景:小儿肺动脉高压(PH)的特征是平均肺动脉压超过 20 mmHg。关于基于成人的方法是否适用于估测小儿肺动脉高压的研究十分有限。本研究采用成人的既定公式,旨在评估先天性心脏病(CHD)患儿超声心动图估测的收缩压、舒张压和平均肺动脉压与平均右心房压之间的相关性:我们进行了一项前瞻性研究,研究对象是接受心导管检查但未进行过心脏手术的先天性心脏病患儿。我们使用超声心动图估算肺动脉压和右心房压,并将其与有创测量值进行比较。我们建立了四个可靠的回归方程来估算收缩压、舒张压、平均肺动脉压和平均右心房压。确定了预测 PH 发生的临界值。通过线性回归、Bland-Altman 分析和接收者操作特征曲线分析来评估超声心动图的准确性并确定 PH 的诊断阈值:该研究涉及 55 名 1 至 192 个月大的无囊性心脏病患儿(23 名肺动脉压正常,32 名 PH)。为检测肺动脉高压制定了四个方程,肺动脉收缩压的临界值为 32.9,肺动脉舒张压的临界值为 14.95,肺动脉平均压的临界值为 20.7。结果表明,该方法具有较高的灵敏度和适度的特异性,但在压力较高时有低估收缩压和平均肺动脉压的趋势:本研究为使用基于成人的超声心动图公式估测无瓣膜性心脏病儿科患者的 PH 提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Echocardiographic estimation of pulmonary arterial and right atrial pressures in children with congenital heart disease: a comprehensive prospective study and introduction of novel equations.

Background: Pediatric pulmonary hypertension (PH) is characterized by a mean pulmonary arterial pressure exceeding 20 mmHg. There is limited research on the suitability of adult-based methods for estimating PH in pediatric populations. Using established formulas for adults, this study aimed to evaluate the correlation between echocardiographic estimates of systolic, diastolic, and mean pulmonary arterial pressures, and mean right atrial pressures in children with congenital heart disease (CHD).

Methods: A prospective study was conducted involving children with CHD undergoing cardiac catheterization without prior cardiac surgery. We used echocardiography to estimate pulmonary and right atrial pressures and compared these with invasively measured values. Four reliable regression equations were developed to estimate systolic, diastolic, and mean pulmonary arterial pressures, and mean right atrial pressures. Cutoff values were determined to predict the occurrence of PH. Linear regression, Bland-Altman analysis, and receiver operating characteristic curve analysis were performed to assess the accuracy of echocardiography and establish diagnostic thresholds for PH.

Results: The study involved 55 children (23 with normal pulmonary arterial pressure and 32 with PH) with acyanotic CHD aged 1 to 192 months. Four equations were developed to detect high pulmonary arterial pressures, with cutoff values of 32.9 for systolic pulmonary arterial pressure, 14.95 for diastolic pulmonary arterial pressure, and 20.7 for mean pulmonary arterial pressure. The results showed high sensitivity and moderate specificity but a tendency to underestimate systolic and mean pulmonary arterial pressures at higher pressures.

Conclusions: The study provides valuable insights into the use of adult-based echocardiographic formulas for estimating PH in pediatric patients with acyanotic CHD.

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来源期刊
Journal of Cardiovascular Imaging
Journal of Cardiovascular Imaging Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.40
自引率
0.00%
发文量
42
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