Berger-Kulemann Vanessa, Berger Rudolf, Mlczoch Elisabeth, Sternal Daniel, Mailath-Pokorny Mariella, Hachemian Nilouparak, Prayer Daniela, Weber Michael, Salzer-Muhar Ulrike
Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, AKH, Waehringer Guertel 18-20, 1090, Vienna, Austria,
Pediatr Cardiol. 2015 Aug;36(6):1287-93. doi: 10.1007/s00246-015-1159-8. Epub 2015 Apr 18.
This study assessed whether the presence of tetralogy of Fallot (TOF) affects fetal lung development and whether these fetuses are at risk of pulmonary hypoplasia (PH). Furthermore, we investigated whether the degree of the concomitant pulmonary valve (PV) stenosis or a stenosis in the branch pulmonary arteries correlates with the fetal lung volume. Lung volumetry was performed in 16 fetuses with TOF who underwent MRI between gestational weeks 21 and 35 and in 22 controls. Fetal biometric data and the diameters of the PVs were evaluated by ultrasound. PV and branch pulmonary artery diameters were standardized (z-scores), and fetal lung volume/fetal body weight (FLV/FBW) ratios (ml/g) were calculated. The mean FLV/FBW ratio (0.031 ± 0.009 ml/g) in the TOF group was statistically significantly lower than in the control group (0.041 ± 0.009 ml/g; P = 0.003). None of the fetuses with TOF met the criterion for PH. FLV did not correlate with the degree of PV stenosis, but rather with the presence of a significant stenosis in at least one branch pulmonary artery. The presence of TOF moderately affects fetal lung growth, which is apparently not dependent on the degree of the PV stenosis. However, only an additional stenosis in at least one branch pulmonary artery was associated with a small FLV, but not with PH. Thus, reduced pulmonary blood flow may be offset by additional factors, such as the ability to establish a sufficient collateral system and to alter structural vascular size and, thus, pulmonary vascular resistance.
本研究评估法洛四联症(TOF)的存在是否会影响胎儿肺发育,以及这些胎儿是否存在肺发育不全(PH)的风险。此外,我们还研究了合并存在的肺动脉瓣(PV)狭窄程度或分支肺动脉狭窄是否与胎儿肺容积相关。对16例孕21至35周期间接受磁共振成像(MRI)检查的TOF胎儿及22例对照胎儿进行了肺容积测定。通过超声评估胎儿生物测量数据及PV直径。对PV和分支肺动脉直径进行标准化(Z评分),并计算胎儿肺容积/胎儿体重(FLV/FBW)比值(ml/g)。TOF组的平均FLV/FBW比值(0.031±0.009 ml/g)在统计学上显著低于对照组(0.041±0.009 ml/g;P = 0.003)。没有TOF胎儿符合PH的标准。FLV与PV狭窄程度无关,而是与至少一支分支肺动脉存在明显狭窄相关。TOF的存在对胎儿肺生长有中度影响,这显然不依赖于PV狭窄程度。然而,只有至少一支分支肺动脉存在额外狭窄与较小的FLV相关,但与PH无关。因此,肺血流量减少可能会被其他因素抵消,如建立足够侧支循环的能力以及改变血管结构大小从而改变肺血管阻力的能力。