The Fetal Heart Program at Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Circ Cardiovasc Imaging. 2010 Mar;3(2):172-8. doi: 10.1161/CIRCIMAGING.109.848432. Epub 2009 Dec 31.
Cardiopulmonary interactions play an important role in the pathophysiology of hypoplastic left heart syndrome (HLHS). Pulmonary vasculopathy has been identified, especially in those with restrictive/intact atrial septum. Responsiveness of the pulmonary vasculature to maternal hyperoxygenation (MH) may provide a tool to assess the degree of pulmonary vasculopathy present before birth.
Doppler echocardiography was performed in 27 normal and 43 HLHS fetuses. In HLHS, sampling was repeated after 10 minutes of MH with 60% FiO(2) and after 5 minutes of recovery. Sampling was performed in the proximal, midportion, and distal branch pulmonary artery (PA). Pulsatility index (PI) was used as a measure of vascular impedance. Of the HLHS fetuses, 34 had an open interatrial septum and 9 had a restrictive/intact atrial septum. At birth, 5 fetuses underwent immediate intervention on the interatrial septum. Middle cerebral artery PI was lower in HLHS versus normal fetuses (P<0.001). There was no difference in UA, DA, or branch PA PI between normal fetuses and those with HLHS. MH led to a significant decrease in PI at each of the PA sites sampled in fetuses with an open atrial septum (P<0.001); however, there no was significant change in the PI in fetuses that required immediate intervention on the atrial septum at birth. Using a cutoff value of <10% vasoreactivity, the sensitivity of MH testing for determining need for immediate intervention at birth is 100% (0.46 to 1.0); specificity, 94% (0.78 to 0.99); positive predictive value, 71% (0.30 to 0.95); and negative predictive value, 100% (0.86 to 1.0). No untoward effects were seen with MH.
PA vasoreactivity to MH occurs in the fetus with HLHS. MH testing accurately identifies fetuses requiring urgent postnatal intervention at birth and may be used to select candidates for fetal atrial septoplasty.
心肺相互作用在左心发育不全综合征(HLHS)的病理生理学中起着重要作用。已经确定了肺血管病变,特别是在那些具有限制性/完整房间隔的患者中。肺血管对母体高氧血症(MH)的反应性可能提供了一种评估出生前肺血管病变程度的工具。
对 27 例正常胎儿和 43 例 HLHS 胎儿进行了多普勒超声心动图检查。在 HLHS 中,在 MH 后 10 分钟(FiO2 为 60%)和恢复 5 分钟后重复采样。在肺动脉近端、中段和远端分支处进行采样。搏动指数(PI)用作血管阻抗的度量。在 HLHS 胎儿中,34 例有开放的房间隔,9 例有限制性/完整的房间隔。出生时,5 例胎儿立即进行了房间隔介入。大脑中动脉 PI 在 HLHS 胎儿中低于正常胎儿(P<0.001)。正常胎儿和 HLHS 胎儿之间的 UA、DA 或分支 PA PI 没有差异。在开放房间隔的胎儿中,MH 导致每个采样的 PA 部位的 PI 显著降低(P<0.001);然而,在出生时需要立即进行房间隔介入的胎儿中,PI 没有明显变化。使用<10%血管反应性的截断值,MH 测试确定出生时是否需要立即干预的灵敏度为 100%(0.46 至 1.0);特异性为 94%(0.78 至 0.99);阳性预测值为 71%(0.30 至 0.95);阴性预测值为 100%(0.86 至 1.0)。MH 没有引起不良反应。
HLHS 胎儿的 PA 对 MH 有血管反应性。MH 测试准确识别出生时需要紧急产后干预的胎儿,并可用于选择胎儿房间隔成形术的候选者。