Skip to main content

Ultrasound parameters of arteries and heart in normal fetuses

Abstract

Background

Currently, no normal ultrasound data of the fetuses during the 20–40 gestation have been obtained for references of fetal growth and development. If such ultrasound data existed for prenatal diagnosis of possible diseases and abnormalities, neonates would be able to get timely treatment immediately after birth. This study was thus performed to obtain ultrasound parameters of normal fetuses during the 20–40 week gestation and the distribution of ultrasound parameters with the gestational age for references of detecting potential fetal diseases and abnormalities.

Methods

Normal fetuses without any abnormalities were enrolled, and the ultrasound parameters of the general biology, arteries, and aorta were measured and analyzed.

Results

417 normal fetuses were enrolled. A significant (P < 0.05) negative correlation with the gestational age was detected in the peak systolic velocity/peak diastolic velocity (S/D), pulsatility index (PI) and resistance index (RI) of the umbilical artery (UA). A relatively stable relationship with the gestational age was detected in the fetal weight%, S/D, PI and RI of the middle cerebral artery (MCA), peak systolic velocity (PSV) and velocity time integral (VTI) of the intra-abdominal UA, fetal heart to chest ratio, mitral valve (MV)- and tricuspid valve (TV)-E/A peak flow velocity, aortic isthmic Z-score and displacement, distance between the brachiocephalic artery-left common carotid artery (BA-LCCA) and LCCA-left subclavian artery (LSA), Z-score of aorta, ascending aorta (AAO), pulmonary artery (PA), main pulmonary artery (MPA), and descending aorta (DAO). A significant (P < 0.05) positive correlation with the gestational age was detected in the fetal biological data, MCA PSV and VTI, free-UA PSV and VTI and cardio-thoracic ratio, cardiac parameters, ductus arteriosus (DA) and isthmus diameter, aortic parameters, PA and MPA diameter, MPA PSV and VTI, isthmus flow volume and velocity and PA flow volume, DA and BA parameters, and LCCA and LSA parameters (flow volume, PSV, and VTI).

Conclusion

A certain correlation and distribution trend is detected in the ultrasound parameters of normal fetuses, and the ratios among different parameters remain relative stable. These findings can be used for determination of abnormal growth of the fetuses in prenatal ultrasound scan.

Graphic Abstract

Peer Review reports

Authors:

Introduction

Both fetal size and growth velocity (change in size with time) have been used to assess fetal growth and development abnormalities [1,2,3,4,5,6,7,8,9,10]. Use of fetal size is common, and growth velocity evaluation is also a logical approach for fetal growth determination. For growth velocity, serial measurements of the fetuses are necessary over a large range of fetal age, however, strict serial evaluation of the fetuses may be difficult and only a limited number of studies have been conducted except for studies on individualized growth assessment [11,12,13]. Fetal growth velocity evaluation is focused on detection of growth abnormalities, and individualized growth assessment uses growth velocity mainly for evaluation of growth potential [14]. Measurement of the second trimester growth data can be used to specify the Rossavik size models to generate the expected third trimester size trajectories and birth features [11]. Good agreement has been achieved between the actual values and the expected data in fetuses and neonates with normal neonatal growth results as proved by the prenatal percent deviations and growth potential realization indexes in neonates [11, 14, 15]. Nonetheless, no normal ultrasound data of the fetuses during the 20–40 week gestation have been obtained for references of fetal growth and development. If such ultrasound data existed for prenatal diagnosis of possible diseases and abnormalities, neonates would be able to get timely treatment immediately after birth. This study was thus performed to obtain ultrasound parameters of normal fetuses during the 20–40 week gestation and the distribution of ultrasound parameters with the gestational age for references of detecting potential fetal diseases and abnormalities.

Materials and methods

Subjects

This prospective single-center study was approved by the ethics committee of the Fourth Hospital of Shijiazhuang with informed consent given by the pregnant women to participate. All methods were performed in accordance with the relevant guidelines and regulations. From May 2021 to May 2023, pregnant healthy women with antenatal sonography, regular menstruation, no genetic history, no pregnancy complications, 20–40 weeks of gestational age, and healthy neonates without abnormalities confirmed after birth were enrolled. The inclusion criteria were healthy pregnant women with known last menstrual time, no abnormalities by prenatal ultrasound screening, regular menstruation, 20–40 weeks of gestational age, antenatal sonography of the fetuses, delivery in our hospital, follow-up up to 6 months after birth, and no abnormalities confirmed by sonography and postpartum follow-up. The exclusion criteria were pregnant women with irregularity of menstruation, unknown time of last menstruation, genetic diseases, pregnancy complications, infectious diseases, and multiple pregnancies.

Instruments and methods

Ultrasound scan was performed with the GE Voluson E10 Color Doppler ultrasound diagnostic instruments (General electric, Tiefenboch, AUSTRIA), quipped with 2D/3D transabdominal probes (frequency 2-5 MHz/4-8 MHz, probe model C1-6-D and RAB6-D, and power < 100 mW/cm2), STIC software package, and 4D View 7.0 Offline analysis. Under the fetal quiet state without influencing of breathing and movement, ultrasound scan and echocardiography were conducted to evaluate fetal growth, weight, and abnormalities. All the data were measured three times to obtain the average values by an experienced ultrasound physician with over 10 years of experience (Fig. 1).

Fig. 1
figure 1

Parameters measured on ultrasound images. A. The diameters of the transverse aorta (1) and the aortic isthmus (2) were measured on the 3 vessel trachea view, with the transverse aorta diameter of 0.35 cm and the isthmus diameter of 0.30 cm. B. The diameter of the aorta (AO) at the aortic valve annulus and the ascending aorta (AAO) was measured at the left ventricular outflow tract section, with the AO diameter (1) of 0.37 cm and the AAO diameter of 0.41 cm. C. The diameter of the aortic arch was measured at three locations: arch 1 before the brachiocephalic artery (BA), arch 2 before the left common carotid artery (LCCA) and arch 3 before the left subclavian artery (LSA). D. The ductus arteriosus (DA)-isthmus angle was measured on the HD Live Flow image on the sagittal view, with the DA-Isthmus angle of 35.02°. E. The DA-isthmus angle was measured on the HD Live Flow image viewed from the bird’s eye’s view, with the DA-Isthmus angle of 35.02°. F. The displacement (or distance) from the LSA origin to the DAO outer edge were measured on the 3D STICK-HD Live Flow image. MPA, main pulmonary artery; SVC, superior vena cava; ISTH, aortic isthmus

Ultrasound parameters

General biological data and ultrasound parameters were measured, including peak systolic velocity (PSV), pulsatility index (PI), resistance index (RI), S/D ratio (between the peak systolic velocity and peak diastolic velocity) and velocity time integral (VTI) of the middle cerebral artery (MCA) and umbilical artery (UA, both inside and outside the fetal abdomen before UA placental insertion). The heart axis, cardio-thoracic ratio (Area/Circumference), right and left atrium (end systole) and ventricle (end diastole) dimension, mitral valve A-peak flow velocity (MV-A), mitral valve E-peak flow velocity (MV-E), tricuspid valve A peak (TV-A), and tricuspid valve E peak (TV-E), were measured in the four-chamber view. Systolic aortic valve annular diameter, ascending aortic (AAO) inner diameter, aortic flow velocity and volume, pulmonary valve annular diameter, main pulmonary artery (MPA) inner diameter, and pulmonary artery (PA) flow velocity and volume were measured at the left and right ventricle outflow tract sections, with the spectrum automatic envelope to get the respective VTI and immediate heart rate. The left (LCO) and right (RCO) cardiac output, and combined cardiac output (CCO = LCO + RCO) were calculated according to the formula Q=(D/2)2 x 3.14 x VTI x HR (immediate heart rate). The diameter of ductus arteriosus (DA), transverse arch, and aortic isthmus was measured at the tracheal section of three vessels (3VTV). In the sagittal view of the aortic arch, the diameter of the aortic arch at three locations of arch 1–3, isthmus, descending aorta (DAO), three arch branches, the distance between the arch branches at the starting part, and the flow parameters were measured. The ratios among the parameters were calculated. The real-time 3D STIC mode was selected for 3D scanning. In the Color Render mode, the HD live flow imaging mode was applied to obtain the 3D image of the long axis of the aortic arch and catheter arch for relevant parameters (Fig. 1).

Statistical analysis

The JMP software (10.01.2, SAS Institute, Cary, NC, USA) was used for the statistical analysis. Continuous measurement data meeting the normal distribution requirement were presented as mean and standard deviation or as median and interquartile range if not meeting the normal distribution. Categorical data were expressed as frequency and percentage. The Chi square analysis was performed for the relationship of ultrasound parameters with the gestational age, with the R2 and F ratio calculated. The significant P value was set at < 0.05.

Results

417 normal fetuses without any abnormalities were enrolled, and the ultrasound parameters of the fetal general biology, MCA, UA, DA, aortic isthmus, aorta, aortic arch, arch arterial branches (brachiocephalic artery or BA, LCCA or left common carotid artery, and LSA of left subclavian artery), PA, MPA, and DAO were obtained (Tables 1, 2 and 3), including the PI, RI, VTI, PSV, S/D, diameter, isthmus displacement, Z-score, flow velocity, flow volume, LCO, CCO, and ratios between different parameters.

Table 1 Biological, MCA, UA, and cardiac data
Table 2 Data of DA, isthmus, aorta, aortic arch, arch arteries, and pulmonary artery
Table 3 Data of cardiac output, PA, aorta, isthmus, and DA

Most of the ultrasound parameters were significantly (P < 0.05) correlated with the gestational age (Figs. 2, 3 and 4 and supplemental Figs. 1–8). The ratios of the MCA data to those of the UA both inside and outside the fetal abdomen, of the right to the left atrium or ventricle, and of the isthmus diameter and flow volume to those of the DA, aorta, AAO, DAO, and arch branches remained relatively stable (Figs. 1, 2 and 3). A significant (P < 0.05) negative correlation with the gestational age was detected in the intra-abdominal and free UA parameters (S/D, PI and RI) (Supplemental Fig. 1). Although significant (P < 0.05), a relatively stable correlation with the gestational age was detected in the parameters of fetal weight%, MCA S/D, PI and RI (Supplemental Fig. 1), intra-abdominal UA PSV and VTI, fetal cardio-thoracic ratio (Supplemental Fig. 2), MV- and TV-E/A (Supplemental Fig. 3), isthmus Z-score and displacement (Supplemental Fig. 4), BA-LCCA and LCCA-LSA distance, Z-score of aorta, AAO, PA, MPA, and DAO (Supplemental Fig. 5).

Fig. 2
figure 2

Trends of the ratios of the fetal MCA (middle cerebral artery) parameters to those of the intra-abdominal and free UA (umbilical artery) were shown with the gestational age. These ratios were in a narrow relatively-stable range

Fig. 3
figure 3

The trends with the gestational age were demonstrated in the ratios of between the right and left atrium and ventricle, MV (mitral valve)- and TV (tricuspid valve)-E/A peak flow velocity, ratio of isthmus to ductus arteriosus (DA), aorta, AAO and DAO diameter, ratio of LCCA-LSA distance to arch 3 diameter, and isthmus flow volume to the left cardiac output (LCO). These ratios were relatively stable

Fig. 4
figure 4

Relative stable trends with the gestational age were demonstrated in the ratios of the pulmonary artery (PA) and main pulmonary artery (MPA) to the ascending aorta (AAO) and descending aorta (DAO) diameter, of the isthmus flow volume to that of left cardiac output (LCO), combined cardiac output (CCO), ductus arteriosus (DA), aorta (AO), brachiocephalic artery (BA), left common carotid artery (LCCA), DAO, and left subclavian artery (LSA), and the BA-LCCA or LCCA-LSA distance

A significant (P < 0.05) positive correlation with the gestational age was detected in the fetal biological data (Supplemental Fig. 1), MCA PSV and VTI (Supplemental Fig. 1), free-UA PSV, VTI and perimeter ratio (Supplemental Fig. 2), left and right atrium and ventricle, MV- and TV-E, TV-A, DA and isthmus diameter (Supplemental Figs. 3 and 4), aortic arch and arch branch diameter (Supplemental Fig. 4), aortic diameter and flow volume and velocity, AAO diameter and VTI, PA and MPA diameter (Supplemental Fig. 5), MPA PSV and VTI, DAO parameters (diameter, flow velocity and volume, VTI, and PSV) (Supplemental Fig. 6), isthmus flow volume and velocity, PA flow volume, DA and BA parameters (flow volume, PSV and VTI) (Supplemental Figs. 7 and 8), LCCA and LSA parameters (flow volume, PSV, and VTI) (Supplemental Fig. 8).

The right atrium and ventricle were significantly (P < 0.05) greater than the left atrium (1.27 ± 0.35 vs. 1.17 ± 0.29 cm, P < 0.001) and ventricle (1.18 ± 0.34 vs. 1.17 ± 0.31 cm, P = 0.001), respectively (Table 1). The PA/AAO diameter ratio was 0.91–1.45(1.15 ± 0.09). The LCO (AO flow volume) was significantly smaller than the RCO (PA flow volume) (329.37 ± 193.87 ml vs. 430.46 ± 275.39 ml, P < 0.001). The LCO was in a significant (P < 0.05) positive correlation with RCO, CCO, and the flow volume of BA, LCCA, LSA, isthmus, and DAO, whereas the RCO was significantly positively correlated with the CCO and the flow volume of DA and DAO (Fig. 5). In normal condition, the RCO contributed more to the CCO and DAO flow volume, whereas the LCO contributed more to the isthmus flow volume.

Fig. 5
figure 5

The left cardiac output (LCO) was in a significant (P < 0.05) positive correlation with right cardiac output (RCO), combined cardiac output (CCO), and the flow volume of brachiocephalic artery (BA), left common carotid artery (LCCA), left subclavian artery (LSA), isthmus, and descending aorta (DAO), and the RCO was significantly positively correlated with the CCO and the flow volume of ductus arteriosus (DA) and DAO. In normal condition, the RCO contributed more to the CCO and DAO flow volume, whereas the LCO contributed more to the isthmus flow volume

Discussion

In this study exploring the normal range and distribution trend of ultrasound parameters with the gestational age in normal fetuses, a certain correlation was found in the ultrasound parameters of normal fetuses with the gestational age, and the ratios among different parameters remained relative stable. These findings could be used for determination of abnormal growth of the fetuses in prenatal ultrasound scan.

In fetuses with prenatal restricted growth, blood flow is redistributed from the peripheral tissues and organs to the brain, and Doppler ultrasound examination of the UA and fetal cerebral arteries (MCA in particular) can be applied to evaluate the relevant changes [16]. In these fetuses, the UA PI is increased while the MCA PI is decreased. The nomograms of the MCA PI and PSV with advanced gestational age have been reported, and decreased MCA PI has been reported in fetuses with congenital heart disease or at risk of perinatal mortality and morbidity [16,17,18,19]. Lower MCA PI and cerebral placental ratio (MCA PI/UA PI) and increased UA PI were reported in fetal hypoplastic left heart syndrome and isolated coarctation of the aorta (CoA), and the MCA PI is associated with changed fetal cerebral blood flow and positively correlates with head development [20]. The MCA PSV has been found to increase as a good indicator for perinatal mortality in a group of fetuses with restricted growth [16, 21]. Our study provided the ultrasound parameters of fetal biology, MCA and UA both inside and outside the fetal abdomen of normal fetuses as references to diagnose potential abnormalities of fetal growth. The fetal biparietal diameter, head circumference, abdomenal circumference, femur length, humerus length, estimated body weight positively correlated with the gestational age, and the ratios of the MCA data to those of the UA both inside and outside the fetal abdomen remained relatively stable during the 20–40 week gestaion investigated in our study.

The Prenatal Growth Assessment Score (PGAS) has been developed to detect different kinds of fetal growth issues except those of tissue abnormalities [22], and the PGAS was based on the head circumference, abdominal circumference, femur diaphysis length, mid-thigh circumference, and estimated weight. Nonetheless, this score is limited by reference ranges determined from all the 20–40 week gestation data without considering age-specific differences and was initially proposed for only one combination of anatomical parameters [22,23,24]. Our study provided the reference ranges of the fetuses during the 20–40 weeks and could be used as references for normal growth.

In fetuses suspected of CoA, the right heart structures (atrium and ventricle) are larger than the left ones, the TV is larger than the MV, and the PA/AAO diameter ratio is greater than 1.60 at the 3VTV view, with the presence of a narrowed aortic isthmus, hypoplastic transverse aortic arch, and CoA shelf [25,26,27]. Transverse aortic arch hypoplasia and elevated PA valve and PA diameters have also been reported in neonates with CoA, which may suggest reduced aortic arch flow and raised PA and DA flow in fetuses [28]. In our study, normal fetuses showed greater right heart structures than the left ones, but a smaller ratio of the PA/AAO diameter (range 0.91–1.45 and mean 1.15 ± 0.09), with no presence of CoA shelf, hypoplastic transverse aortic arch, or a narrowed isthmus. The right heart structures are larger than the left ones because the major blood flow of the fetus comes from the right heart. A prenatal definitive diagnosis of congenital fetal diseases like CoA can influence and decrease the mortality rate [26, 29]. Definition of the normal ultrasound parameters is helpful for detection of possible congenital fetal diseases. Antenatal ultrasound parameters have been applied for the diagnosis of CoA [30,31,32,33,34,35], including diameter of the PA or the aorta at the aortic valve, aortic isthmus, and AAO, and a ratio between the DA and aortic isthmus. The Z-scores of the aortic isthmus and AAO had been reported to be significantly lower in neonates with CoA [36, 37]. The MPA and TV Z-scores significantly rose while the mean Z-scores of the MV and the aortic isthmus significantly dropped in CoA fetuses [30]. A significant increase in the LCCA-LSA distance and aortic arch-DAO angle was also reported in CoA positive fetuses [38]. In our study, these ultrasound parameters were investigated in normal fetuses and can be used as references for detection of potential diseases.

Cardiac remodeling manifests as alterations in mass, size, geometry, and function of the heart in response to injury or load [9, 39]. This process can cause impairment in the cardiac ejection and/or relaxation ability as clinical or subclinical cardiac dysfunction. Cardiac structure dysfunction and remodeling have been described in some antenatal conditions but are scarcely described in fetuses with congenital heart diseases [9, 40]. With the cardiac ultrasound parameters obtained in normal fetuses, correct prenatal diagnosis of some congenital heart diseases can be reached earlier. In normal fetuses, the left ventricle develops under a low volume load and normal pressure condition, and after birth, the left ventricle changes to a globular shape and the filling velocities are increased because of elevated pulmonary venous return and closed foramen ovale to support the system flow. This is why the left cardiac structures, including the atrium and ventricle, were significantly smaller than the right ones in the normal fetuses as revealed by our study. This significant difference between the right and left cardiac structures may require to reach a certain degree for the diagnosis of a diseased status. Our study also found that the LCO was significantly smaller than the RCO (329.37 ± 193.87 ml vs. 430.46 ± 275.39 ml, P < 0.001), with the RCO contributing more to the CCO and DAO flow volume while the LCO contributing more to the isthmus flow volume.

This study had some limitations such as a relatively small cohort of fetuses, Chinese subjects enrolled only, one-center study design, and no control, which may all result in publication bias and affect the generalization of the outcome. Future prospective, multi-center studies with a lot of fetuses enrolled and multiple races and ethnicities involved will have to be conducted for better outcomes.

Conclusion

In summary, a certain correlation exists in the ultrasound parameters of normal fetuses with the gestational age, and the ratios among different parameters remain relative stable. The right heart structures are significantly larger than the left ones in normal fetuses, with the right cardiac output contributing more to the CCO and DAO flow volume while the left cardiac output contributing more to the isthmus flow volume. These findings can be used for determination of abnormal growth of the fetuses in prenatal ultrasound scan.

Data availability

The datasets generated and/or analyzed during the current study are not publicly available due to the restriction by the hospital policy but are available from the corresponding author on reasonable request.

Abbreviations

2D:

Two dimension

3D:

Three dimension

PSV:

Peak systolic velocity

PI:

Pulsatility index

RI:

Resistance index

S/D:

Peak systolic velocity/peak diastolic velocity

VTI:

Velocity time integral

MCA:

Middle cerebral artery

UA:

Umbilical artery

MV-A:

Mitral valve A peak flow velocity

TV-E:

Tricuspid valve E peak flow velocity

AO:

Aorta

AAO:

Ascending aorta

MPA:

Main pulmonary artery

PA:

Pulmonary artery

LCO:

Left cardiac output

RCO:

Right cardiac output

CCO:

Combined cardiac output

DA:

Ductus arteriosus

3VTV:

3 vessel tracheal view

DAO:

Descending aorta

LCCA:

Left common carotid artery

BA:

Brachiocephalic artery

LSA:

Left subclavian artery

CoA:

Coarctation of the aorta

PGAS:

Prenatal growth assessment score

GA:

Gestational age

BPD:

Biparietal diameter

HC:

Head circumference

AC:

Abdomen circumference

FL:

Femur length

HL:

Humerus length

SV:

Sagittal view

ZS:

Z-score

AAD:

Ascending aortic inner diameter

AD:

Aortic inner diameter

SVC:

Superior vena cava

ISTH:

Aortic isthmus

References

  1. Deter RL, Dicker P, Lee W, Tully EC, Cody F, Malone FD, Flood KM. Growth patterns and cardiovascular abnormalities in SGA fetuses: 2. Normal growth and progressive growth restriction. J Matern Fetal Neonatal Med. 2022;35(14):2818–27.

    Article  PubMed  Google Scholar 

  2. Deter RL, Lee W, Dicker P, Tully EC, Cody F, Malone FD, Flood KM. Third-trimester growth diversity in small fetuses classified as appropriate-for-gestational age or small-for-gestational age at birth. Ultrasound Obstet Gynecol. 2021;58(6):882–91.

    Article  CAS  PubMed  Google Scholar 

  3. Deter RL, Lee W, Kingdom JCP, Romero R. Fetal growth pathology score: a novel ultrasound parameter for individualized assessment of third trimester growth abnormalities. J Matern Fetal Neonatal Med. 2018;31(7):866–76.

    Article  PubMed  Google Scholar 

  4. Gardosi J. Customized fetal growth standards: rationale and clinical application. Semin Perinatol. 2004;28(1):33–40.

    Article  PubMed  Google Scholar 

  5. Hugh O, Cowan J, Butler E, Gardosi J. Fetal size vs growth: comparative analysis of three models of growth velocity based on third trimester estimated fetal weights for identifying stillbirth risk. Am J Obstet Gynecol 2023.

  6. Hugh O, Gardosi J. Fetal weight projection model to define growth velocity and validation against pregnancy outcome in a cohort of serially scanned pregnancies. Ultrasound Obstet Gynecol. 2022;60(1):86–95.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Lees CC, Romero R, Stampalija T, Dall’Asta A, DeVore GA, Prefumo F, Frusca T, Visser GHA, Hobbins JC, Baschat AA, et al. Clinical opinion: the diagnosis and management of suspected fetal growth restriction: an evidence-based approach. Am J Obstet Gynecol. 2022;226(3):366–78.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Mula C, Hidalgo J, Peguero A, Mazarico E, Martinez J, Figueras F, Meler E. Third-trimester uterine artery Doppler for prediction of adverse outcome in late small-and adequate for-gestational-age fetuses. Minerva Obstet Gynecol. 2023;75(5):440–8.

    Article  PubMed  Google Scholar 

  9. Soveral I, Crispi F, Walter C, Guirado L, Garcia-Canadilla P, Cook A, Bonnin A, Dejea H, Rovira-Zurriaga C, Sanchez, de Toledo J et al. Early cardiac remodeling in aortic coarctation: insights from fetal and neonatal functional and structural assessment. Ultrasound Obstet Gynecol. 2020;56(6):837–849.

  10. Stampalija T, Wolf H, Mylrea-Foley B, Marlow N, Stephens KJ, Shaw CJ, Lees CC. authors T-FS: Reduced fetal growth velocity and weight loss are associated with adverse perinatal outcome in fetuses at risk of growth restriction. Am J Obstet Gynecol. 2023;228(1):71 e71-71 e10.

  11. Deter RL, Lee W, Sangi-Haghpeykar H, Tarca AL, Yeo L, Romero R. Individualized fetal growth assessment: critical evaluation of key concepts in the specification of third trimester size trajectories. J Matern Fetal Neonatal Med. 2014;27(6):543–51.

    Article  PubMed  Google Scholar 

  12. Deter RL, Lee W, Yeo L, Erez O, Ramamurthy U, Naik M, Romero R. Individualized growth assessment: conceptual framework and practical implementation for the evaluation of fetal growth and neonatal growth outcome. Am J Obstet Gynecol. 2018;218(2S):S656–78.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Sherwin E, Deter R, Joudi N, Trepman P, Lee W, El-Sayed YY, Girsen AI, Datoc I, Hintz SR, Blumenfeld YJ. Individualized growth assessment in pregnancies complicated by fetal gastroschisis. J Matern Fetal Neonatal Med. 2022;35(25):6842–52.

    Article  CAS  PubMed  Google Scholar 

  14. Deter RL, Lee W, Kingdom J, Romero R. Second trimester growth velocities: assessment of fetal growth potential in SGA singletons. J Matern Fetal Neonatal Med. 2019;32(6):939–46.

    Article  PubMed  Google Scholar 

  15. Deter RL, Lee W, Sangi-Haghpeykar H, Tarca AL, Yeo L, Romero R. Fetal growth cessation in late pregnancy: its impact on predicted size parameters used to classify small for gestational age neonates. J Matern Fetal Neonatal Med. 2015;28(7):755–65.

    Article  PubMed  Google Scholar 

  16. Mari G, Hanif F, Kruger M, Cosmi E, Santolaya-Forgas J, Treadwell MC. Middle cerebral artery peak systolic velocity: a new Doppler parameter in the assessment of growth-restricted fetuses. Ultrasound Obstet Gynecol. 2007;29(3):310–6.

    Article  CAS  PubMed  Google Scholar 

  17. Mari G, Deter RL. Middle cerebral artery flow velocity waveforms in normal and small-for-gestational-age fetuses. Am J Obstet Gynecol. 1992;166(4):1262–70.

    Article  CAS  PubMed  Google Scholar 

  18. Mari G, Adrignolo A, Abuhamad AZ, Pirhonen J, Jones DC, Ludomirsky A, Copel JA. Diagnosis of fetal anemia with doppler ultrasound in the pregnancy complicated by maternal blood group immunization. Ultrasound Obstet Gynecol. 1995;5(6):400–5.

    Article  CAS  PubMed  Google Scholar 

  19. Man T, He Y, Zhao Y, Sun L, Liu X, Ge S. Cerebrovascular hemodynamics in fetuses with congenital heart disease. Echocardiography. 2017;34(12):1867–71.

    Article  PubMed  Google Scholar 

  20. Yamamoto Y, Khoo NS, Brooks PA, Savard W, Hirose A, Hornberger LK. Severe left heart obstruction with retrograde arch flow influences fetal cerebral and placental blood flow. Ultrasound Obstet Gynecol. 2013;42(3):294–9.

    Article  CAS  PubMed  Google Scholar 

  21. Ozcan T, Sbracia M, d’Ancona RL, Copel JA, Mari G. Arterial and venous doppler velocimetry in the severely growth-restricted fetus and associations with adverse perinatal outcome. Ultrasound Obstet Gynecol. 1998;12(1):39–44.

    Article  CAS  PubMed  Google Scholar 

  22. Deter RL, Stefos T, Harrist RB, Hill RM. Detection of intrauterine growth retardation in twins using individualized growth assessment: I. evaluation of growth outcome at birth. J Clin Ultrasound. 1992;20(9):573–7.

    Article  CAS  PubMed  Google Scholar 

  23. Deter RL, Lee W, Sangi-Haghpeykar H, Tarca AL, Yeo L, Romero R. A modified prenatal growth assessment score for the evaluation of fetal growth in the third trimester using single and composite biometric parameters. J Matern Fetal Neonatal Med. 2015;28(7):745–54.

    Article  PubMed  Google Scholar 

  24. Hata T, Deter RL, Hill RM. Individual growth curve standards in triplets: prediction of third-trimester growth and birth characteristics. Obstet Gynecol. 1991;78(3 Pt 1):379–84.

    CAS  PubMed  Google Scholar 

  25. Slodki M, Rychik J, Moszura T, Janiak K, Respondek-Liberska M. Measurement of the great vessels in the mediastinum could help distinguish true from false-positive coarctation of the aorta in the third trimester. J Ultrasound Med. 2009;28(10):1313–7.

    Article  PubMed  Google Scholar 

  26. Slodki M, Rizzo G, Augustyniak A, Seligman NS, Zych-Krekora K, Respondek-Liberska M, International Prenatal Cardiology Collaboration G. Retrospective cohort study of prenatally and postnatally diagnosed coarctation of the aorta (CoA): prenatal diagnosis improve neonatal outcome in severe CoA. J Matern Fetal Neonatal Med. 2020;33(6):947–51.

    Article  PubMed  Google Scholar 

  27. Akalin M, Demirci O, Yucel IK, Erol N. Fetal echocardiographic findings to Predict Early Surgical repair and neonatal outcomes in fetuses with isolated Coarctation of the Aorta. Am J Perinatol 2022.

  28. Morrow WR, Huhta JC, Murphy DJ Jr., McNamara DG. Quantitative morphology of the aortic arch in neonatal coarctation. J Am Coll Cardiol. 1986;8(3):616–20.

    Article  CAS  PubMed  Google Scholar 

  29. Polyviou S, Charakida M, Miller OI, Rscn TW, Vigneswaran TV, Zidere V, Day TG, Lloyd DFA, Sharland GK, Simpson JM. Outcome and impact of Associated Left-Sided Cardiac lesions in Coarctation of the Aorta diagnosed during fetal life. Am J Cardiol. 2022;166:114–21.

    Article  PubMed  Google Scholar 

  30. Familiari A, Morlando M, Khalil A, Sonesson SE, Scala C, Rizzo G, Del Sordo G, Vassallo C, Elena Flacco M, Manzoli L, et al. Risk factors for Coarctation of the aorta on prenatal Ultrasound: a systematic review and Meta-analysis. Circulation. 2017;135(8):772–85.

    Article  PubMed  Google Scholar 

  31. Lee A, Reddy M, Chai M, Grange Sobe I, Green E, Rolnik DL, Rao SJV, Teoh M. Subjective and objective Sonographic Assessment for the prenatal detection of neonatal coarctation of the Aorta. Fetal Diagn Ther. 2023;50(2):98–105.

    Article  PubMed  Google Scholar 

  32. Matsui H, Mellander M, Roughton M, Jicinska H, Gardiner HM. Morphological and physiological predictors of fetal aortic coarctation. Circulation. 2008;118(18):1793–801.

    Article  PubMed  Google Scholar 

  33. Power A, Nettel-Aguirre A, Fruitman D. Fetal right ventricular prominence: Associated Postnatal Abnormalities and Coarctation Clinical Prediction Tool. Pediatr Cardiol. 2017;38(7):1471–7.

    Article  PubMed  Google Scholar 

  34. Jowett V, Aparicio P, Santhakumaran S, Seale A, Jicinska H, Gardiner HM. Sonographic predictors of surgery in fetal coarctation of the aorta. Ultrasound Obstet Gynecol. 2012;40(1):47–54.

    Article  CAS  PubMed  Google Scholar 

  35. Anuwutnavin S, Satou G, Chang RK, DeVore GR, Abuel A, Sklansky M. Prenatal Sonographic predictors of neonatal coarctation of the Aorta. J Ultrasound Med. 2016;35(11):2353–64.

    Article  PubMed  Google Scholar 

  36. Contro E, Cattani L, Balducci A, Prandstraller D, Perolo A, Larcher L, Reggiani MLB, Farina A, Donti A, Gargiulo GD, et al. Prediction of neonatal coarctation of the aorta at fetal echocardiography: a scoring system. J Matern Fetal Neonatal Med. 2022;35(22):4299–305.

    Article  PubMed  Google Scholar 

  37. Wang H, Lei W, Liu J, Yang B, Li H, Huang D. The diastolic and systolic velocity-time integral ratio of the aortic isthmus is a sensitive Indicator of aortic coarctation in fetuses. J Am Soc Echocardiogr. 2019;32(11):1470–6.

    Article  PubMed  Google Scholar 

  38. Arya B, Bhat A, Vernon M, Conwell J, Lewin M. Utility of novel fetal echocardiographic morphometric measures of the aortic arch in the diagnosis of neonatal coarctation of the aorta. Prenat Diagn. 2016;36(2):127–34.

    Article  PubMed  Google Scholar 

  39. Cohn JN, Ferrari R, Sharpe N. Cardiac remodeling–concepts and clinical implications: a consensus paper from an international forum on cardiac remodeling. Behalf of an International Forum on Cardiac Remodeling. J Am Coll Cardiol. 2000;35(3):569–82.

    Article  CAS  PubMed  Google Scholar 

  40. Crispi F, Bijnens B, Figueras F, Bartrons J, Eixarch E, Le Noble F, Ahmed A, Gratacos E. Fetal growth restriction results in remodeled and less efficient hearts in children. Circulation. 2010;121(22):2427–36.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

Study design: Guihong Chen, Jie Mi; Data collection: Guihong Chen, Pin Wang, Yanhong Zhang, Na Li, Liman Fu, Yu Chen1, Xuna Geng, Yongfeng Han, Lu Qin; Data analysis: Guihong Chen, Bulang Gao; Supervision: Guihong Chen, Tianxiao Yu; Approval: All authors.

Corresponding authors

Correspondence to Tianxiao Yu or Jie Mi.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chen, G., Wang, P., Zhang, Y. et al. Ultrasound parameters of arteries and heart in normal fetuses. Cardiovasc Ultrasound 22, 9 (2024). https://doi.org/10.1186/s12947-024-00328-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12947-024-00328-w

Keywords