Kalache K D, Chaoui R, Hartung J, Wernecke K D, Bollmann R
Department of Obstetrics and Gynecology, Charité Medical Faculty, Humboldt-Universität zu Berlin, Germany.
Ultrasound Obstet Gynecol. 1998 Jul;12(1):27-32. doi: 10.1046/j.1469-0705.1998.12010027.x.
The purpose of this investigation was to examine the characteristics of breathing-related fluid flow in the trachea of human fetuses with congenital diaphragmatic hernia in the hopes of developing a standard for the prenatal diagnosis of the degree of severity of the resulting pulmonary hypoplasia. Our ultimate goal is the prediction of postnatal mortality in fetuses with congenital diaphragmatic hernia.
The study comprised six cases of isolated congenital diaphragmatic hernia (one on the right side; five on the left) varying in gestational age from 26 to 36 weeks. Four of the patients survived after surgical repair and two died during the neonatal period owing to lung hypoplasia. Color Doppler was used to visualize the fluid displacement in the trachea generated by fetal breathing movements. Spectral Doppler was then used to analyze the fluid flow velocity waveforms. More than 40 continuous breathing cycles (inspiration + expiration) were recorded for each case. We distinguished between regular and irregular patterns.
Only the regular breathing phases, defined as five or more consecutive cycles of symmetric appearance, were considered for analysis. The inspiration and expiration times, the peak velocity of inspired and expired fluid and the volume obtained by integration of the tracheal fluid flow displaced during fetal breathing were compared with those of five healthy fetuses for each gestational age. Only the tracheal volume flow was helpful in predicting outcome. In normal pregnancies this parameter increased from 0.21 +/- 0.10 ml/breath (mean +/- SD) at 26 weeks to 1.37 +/- 0.48 ml/breath at 36 weeks of gestation. A significantly low (p < 0.05) volume flow was found only in the fetuses with congenital diaphragmatic hernia with a lethal postnatal outcome, whereas this parameter was normal in all survivors.
Our preliminary observations suggest that the tracheal volume flow during fetal breathing activity is related to lung growth. In fetuses with severe lung hypoplasia one would expect a significant reduction in this parameter as an expression of deficient fetal lung growth. The displaced fluid volume per breath in the trachea of human fetuses as assessed by Doppler ultrasound may be a useful predictor of outcome in cases of isolated congenital diaphragmatic hernia.
本研究旨在探讨先天性膈疝胎儿气管内与呼吸相关的液体流动特征,以期制定先天性膈疝所致肺发育不全严重程度的产前诊断标准。我们的最终目标是预测先天性膈疝胎儿的出生后死亡率。
本研究包括6例孤立性先天性膈疝病例(右侧1例;左侧5例),孕周从26周至36周不等。4例患者术后修复存活,2例因肺发育不全在新生儿期死亡。使用彩色多普勒观察胎儿呼吸运动产生的气管内液体位移。然后用频谱多普勒分析液体流速波形。每例记录超过40个连续呼吸周期(吸气+呼气)。我们区分了规则和不规则模式。
仅将定义为五个或更多连续对称周期的规则呼吸阶段用于分析。将吸气和呼气时间、吸入和呼出液体的峰值流速以及胎儿呼吸期间气管内液体流动积分获得的体积与每个孕周的5例健康胎儿进行比较。只有气管体积流量有助于预测结果。在正常妊娠中,该参数从妊娠26周时的0.21±0.10 ml/呼吸(平均值±标准差)增加到妊娠36周时的1.37±0.48 ml/呼吸。仅在出生后有致命结局的先天性膈疝胎儿中发现显著低(p<0.05)的体积流量,而该参数在所有存活者中均正常。
我们的初步观察表明,胎儿呼吸活动期间的气管体积流量与肺生长有关。在严重肺发育不全的胎儿中,预计该参数会显著降低,作为胎儿肺生长不足的表现。通过多普勒超声评估的人胎儿气管内每呼吸的液体位移量可能是孤立性先天性膈疝病例预后的有用预测指标。