Computer analysis of three-dimensional power angiography images of foetal cerebral, lung and placental circulation in normal and high-risk pregnancy.

Three-dimensional (3-D) ultrasound (US) has greatly improved evaluation of organ circulation. The aim of this study was to explore the possible use of this new technique in normal and high-risk pregnancies. Fetal brain, lung and placenta 3-D power Doppler signal intensity were recorded in 115 normal singleton pregnancies (24 to 42 weeks gestation) and in 67 high-risk pregnancies. Mean image pixel signal intensity was calculated for each organ and a brain-lung ratio. In normal pregnancy, placental and lung signal intensity increased until 33, with a rapid decrease after 38, weeks of gestation. Fetal cerebral signal intensity increased with gestational age. Placental and fetal lung signal intensity was significantly lower in high-risk pregnancies than in the control group, with increased fetal brain and brain-lung ratios. The present results suggest a reduction of placental perfusion after 38 weeks of gestation in normal pregnancy, with redistribution of fetal circulation. Lung signal intensity increased abruptly at 32 weeks of gestation, which might reflect lung maturity. The new method showed signs of centralization of fetal circulation at the end of gestation. The results might suggest a possible clinical use for fetal surveillance in high-risk pregnancies.

[1]  D O Cosgrove,et al.  Development of three-dimensional power Doppler ultrasound imaging of fetoplacental vasculature. , 2001, Ultrasound in medicine & biology.

[2]  K. Maršál,et al.  Fetal and placental power Doppler imaging in normal and high-risk pregnancy. , 1999, European journal of ultrasound : official journal of the European Federation of Societies for Ultrasound in Medicine and Biology.

[3]  A. Kurjak,et al.  The assessment of ovarian tumor angiogenesis: what does three‐dimensional power Doppler add? , 1998, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[4]  K. Kalache,et al.  Application of three‐dimensional power Doppler ultrasound in prenatal diagnosis , 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[5]  M. Heymann,et al.  Cardiovascular responses to hypoxemia and acidemia in fetal lambs. , 1974, American journal of obstetrics and gynecology.

[6]  D. H. King,et al.  The Quantitative Analysis of Occlusive Peripheral Arterial Disease By a Non-Intrusive Ultrasonic Technique , 1971, Angiology.

[7]  L. Valentin,et al.  Factors affecting color Doppler energy ultrasound recordings in an in-vitro model. , 1998, Ultrasound in medicine & biology.

[8]  G. Lingman,et al.  Fetal central blood circulation in the third trimester of normal pregnancy--a longitudinal study. I. Aortic and umbilical blood flow. , 1986, Early human development.

[9]  K Marsál,et al.  Umbilical Artery and Uteroplacental Blood Flow Velocity Waveforms in Normal Pregnancy — A Cross‐Sectional Study , 1988, Acta obstetricia et gynecologica Scandinavica.

[10]  K. Maršál,et al.  Uterine artery color Doppler assisted veloeimetry and perinatal outcome , 1996, Acta obstetricia et gynecologica Scandinavica.

[11]  E. Jauniaux,et al.  Sonographic, stereological and Doppler flow velocimetric assessments of placental maturity , 1995, British journal of obstetrics and gynaecology.

[12]  W Kuhn,et al.  3D Color Power Angio™ imaging: a new method to assess intracervical vascularization in benign and pathological conditions , 1998, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[13]  L. Peeters,et al.  Blood flow to fetal organs as a function of arterial oxygen content. , 1979, American journal of obstetrics and gynecology.

[14]  L. Longo,et al.  Fetal and newborn cerebral vascular responses and adaptations to hypoxia. , 1991, Seminars in perinatology.

[15]  L. Peeters,et al.  Redistribution of cardiac output and oxygen delivery in the hypoxemic fetal lamb. , 1979, American journal of obstetrics and gynecology.

[16]  J. Wladimiroff,et al.  Cerebral Doppler Ultrasound of the Human Fetus , 1989 .

[17]  R. Thompson,et al.  Umbilical artery flow velocity waveforms and placental resistance: the effects of embolization of the umbilical circulation. , 1987, American journal of obstetrics and gynecology.

[18]  R L Berkowitz,et al.  The ultrasonic changes in the maturing placenta and their relation to fetal pulmonic maturity. , 1979, American journal of obstetrics and gynecology.

[19]  R. Deter,et al.  Middle cerebral artery flow velocity waveforms in normal and small-for-gestational-age fetuses. , 1992, American journal of obstetrics and gynecology.

[20]  J. Huhta,et al.  Fetal branch pulmonary arterial vascular impedance during the second half of pregnancy. , 1996, American journal of obstetrics and gynecology.

[21]  C. Carl Jaffe Vascular and Doppler ultrasound , 1984 .

[22]  K. Maršál,et al.  Betamethasone treatment and fetal lung perfusion evaluated with color Doppler energy imaging , 1997, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.