Skip to main content

Reduced right ventricular function on cardiovascular magnetic resonance imaging is associated with uteroplacental impairment in tetralogy of Fallot



Maternal right ventricular (RV) dysfunction (measured by echocardiography) is associated with impaired uteroplacental circulation, however echocardiography has important limitations in the assessment of RV function. We therefore aimed to investigate the association of pre-pregnancy RV and left ventricular (LV) function measured by cardiovascular magnetic resonance with uteroplacental Doppler flow parameters in pregnant women with repaired Tetralogy of Fallot (ToF).


Women with repaired ToF were examined, who had been enrolled in a prospective multicenter study of pregnant women with congenital heart disease. Clinical data and CMR evaluation before pregnancy were compared with uteroplacental Doppler parameters at 20 and 32 weeks gestation. In particular, pulsatility index (PI) of uterine and umbilical artery were studied.


We studied 31 women; mean age 30 years, operated at early age. Univariable analyses showed that reduced RV ejection fraction (RVEF; P = 0.037 and P = 0.001), higher RV end-systolic volume (P = 0.004) and higher LV end-diastolic and end-systolic volume (P = 0.001 and P = 0.003, respectively) were associated with higher uterine or umbilical artery PI. With multivariable analyses (corrected for maternal age and body mass index), reduced RVEF before pregnancy remained associated with higher umbilical artery PI at 32 weeks (P = 0.002). RVEF was lower in women with high PI compared to women with normal PI during pregnancy (44% vs. 53%, p = 0.022). LV ejection fraction was not associated with uterine or umbilical artery PI.


Reduced RV function before pregnancy is associated with abnormal uteroplacental Doppler flow parameters. It could be postulated that reduced RV function on pre-pregnancy CMR (≤2 years) is a predisposing factor for impaired placental function in women with repaired ToF.


Evidence that maternal cardiac function influences uteroplacental circulation, and consequently pregnancy outcome, is increasing [1,2,3]. In normal pregnancy, the uteroplacental circulation is a “low-resistance vessel-bed” [4], and uteroplacental Doppler flow investigation, in particular the Pulsatility Index (PI) of the uterine and umbilical arteries, provides insight into the placentation process. Abnormalities in placentation results in a high uteroplacental vascular resistance, reflected by abnormal uteroplacental Doppler patterns (high PI). These abnormal patterns are, in turn, associated with adverse maternal and neonatal outcome [5, 6]. To improve pregnancy counseling and monitoring in women with heart disease, more insight in the relationship between the heart and uteroplacental circulation is needed.

Interestingly, the number of studies that have examined placental function in patients with heart disease and failure is very limited, when compared to the large number of available data on organ dysfunction in patients with heart failure [7,8,9,10,11]. Indeed, in heart failure, specific effects on the kidney [7,8,9], the liver [10], and also the brain [11] have been reported. It could be hypothesized that during pregnancy in women with cardiac dysfunction or failure (for example women with repaired tetralogy of Fallot (ToF), the placenta also undergoes changes that can be (partly) seen as organ dysfunction.

It is generally accepted that organ dysfunction in patients with heart failure is mainly attributed to impaired perfusion (forward failure) due to decreased cardiac output (CO). However, venous congestion (backward failure) is also an important factor in organ dysfunction, as clearly shown in the kidney and liver [7, 9, 10]. The placenta can be seen as a temporary fetomaternal vascular organ. Therefore, similar hemodynamic interactions between the heart and the placenta may be present. Our previous studies in pregnant women with congenital heart diseases showed a consistent association between impaired right ventricular (RV) parameters and impaired uteroplacental Doppler parameters [1, 12,13,14]. However, these studies only focused on echocardiography parameters, which has known limitations, particularly in the assessment of RV function. Furthermore, CO measurements were not available and thus investigation of forward function was limited. Today, cardiovascular magnetic resonance (CMR) is the gold standard for the assessment of RV volume and function [15]. CMR evaluation could provide more insight in how RV function may influence uteroplacental circulation. In the present study, we therefore aimed to investigate the relationship of (pre-pregnancy) RV and left ventricular (LV) function measured by CMR with uteroplacental Doppler flow parameters during pregnancy in women with repaired ToF.


Study design and patient selection

All women in the present study were pregnant women with repaired ToF who had been enrolled in the prospective multicenter observational cohort ZAHARA II or ZAHARA III study (2008–2015) [1, 14, 16]. In the present (sub-) study, women who also underwent CMR ≤ 2 years before their pregnancy were identified. Pregnant women with repaired ToF, aged ≥18 years, presenting in one of the participating centers ≤20 weeks gestation were thus eligible for enrollment in the current study.

Pre-pregnancy baseline data were collected from the medical records. These included maternal age, additional heart defects, cardiovascular history, pre-pregnancy cardiac status (including New York Heart Association (NYHA) functional class, modified World Health Organization (WHO) risk class before pregnancy (risk classification of maternal cardiovascular risk during pregnancy [17]), Electrocardiogram (ECG), laboratory results and echocardiographic recordings) and relevant medication use. Women were excluded if they had a surgical or transcatheter pulmonary valve intervention between the CMR study and their pregnancy. The study protocol was approved by the Research Ethics Committee of the participating centers and all participating women gave written informed consent.

Uteroplacental Doppler flow measurements

Routine evaluation of uteroplacental circulation in second and third trimester was performed at 20 and 32 weeks gestation by uteroplacental Doppler flow measurements consisting the PI of the uterine and umbilical arteries, according to the guidelines of the International Society of Ultrasound in Obstetrics and Gynaecology [18, 19]. Uterine or umbilical artery PI was considered high if the value exceeded the 95th percentile reference values according to gestational age in healthy pregnant women [20, 21].

CMR imaging

CMR protocols for the acquisition of cardiac volumes, functional parameters and flow have been previously published by our group [22, 23]. In brief, CMR assessments were performed using a 1.5 T CMR scanner. ECG-triggered cine loop images were obtained during end-expiratory breath holds, using a retrospectively gated balanced steady-state free precession sequence. The four-chamber view was used for long-axes slices and short-axis were acquired covering both ventricles from base to apex. A 2-D gradient echo Fast Low Angle Shot (FLASH) was used to perform two dimensional velocity encoded CMR flow measurements, perpendicular and ± 1.5 cm cranial to the pulmonary and aortic valve, and were acquired during normal respiration with retrospective cardiac gating.

CMR analysis

All CMR studies were analyzed offline using dedicated software (QMass 7.6, Medis, Leiden, The Netherlands) to quantify ventricular function, volume and mass and to analyze pulmonary artery and aortic flow. The assessments were performed by one observer (A.S.S.) and reviewed by another observer (T.M.G.) In case of disagreement, CMR studies were also reviewed by a certified level 3 trained cardiovascular radiologist (T.P.W.). Endo - and epicardial borders of the LV and RV were manually traced in end-diastolic and end-systolic phases. On the most basal slice, both atria, the aorta and the pulmonary artery were excluded. The RV outflow tract was included until the pulmonary valve. The papillary muscle and trabeculae were excluded from ventricular volumes, by using semi-automatic threshold-based segmentation software (MassK Mode®, Medis, Leiden, The Netherlands) [24]. End-diastolic and end-systolic volumes were automatically calculated by the summation of slices multiplied by slice thickness method. Stroke volume, ejection fraction (EF), ventricular mass and RV/LV volume ratio were calculated using standard formulas.

Pulmonary artery and aortic flow were analyzed using Qflow 5.6 (Medis, Leiden, The Netherlands). Pulmonary and aortic contours were generated semi-automatically on the standard magnitude images, and thereafter manually adjusted for each phase image. Forward and backward flow of the aortic and pulmonary valve were measured and used to calculate CO and regurgitation fraction using standard formulas. All absolute volumes and masses were indexed for body surface area measured at the time of CMR. LV and RV dysfunction were defined as EF < 50 and < 45%, respectively [25, 26].

Statistical analysis

Continuous variables with normal distribution are presented as mean with standard deviation (±SD), non-normally distributed data as median with interquartile ranges [Q1-Q3], dichotomous variables as absolute numbers with percentages. Correlations were calculated using Pearson’s product moment if variables were continuous and Spearman’s rank–order correlation if either of the variables was ordinal. For the primary endpoint, univariable and multivariable linear regression were used to associate baseline characteristics (age, body mass index (BMI) and parity) and CMR parameters (RV and LV function, volume and mass and RV/LV volume ratio) with uterine and umbilical PI at 20 and 32 weeks gestation. For multivariable analysis, known predisposing factors for poor placentation (age and BMI [27]) and RV function (RVEF) based on our previous results were selected [1, 12,13,14]. To maintain model validity, variables were kept to a maximum of 3 due to the small study sample. Multivariable Lasso regression with penalized selection of variables was performed to identify the most parsimonious model and to confirm results of the univariable analyses. Logistic regression analyses were performed to associate baseline CMR parameters with high PI of uterine or umbilical artery during pregnancy (indicative for abnormal placentation). High or normal PI during pregnancy was established in women with complete follow-up data available of uterine and umbilical artery PI at 20 and 32 weeks gestation. Comparison of continuous variables between groups (high vs. normal PI) was performed with the Student t-test or Mann-Whitney U test, depending on distribution.

For internal validation, because of the time gap between CMR evaluation and pregnancy, linear univariable regression were used to associate echocardiographic parameters of ventricular function (LVEF, tricuspid annular plane systolic excursion (TAPSE), S′) and chamber dimensions during pregnancy (at 20 and 32 weeks) with uteroplacental Doppler flow parameters. A p-value < 0.05 was considered statistically significant. Statistical analyses were performed using the SPSS version 23.0 software package (Statistical Package for the Social Sciences, International Business Machines, Inc., Armonk, New York, USA) and STATA software package (version 13, Stata Corporation, College Station, Texas, USA).


Pre-pregnancy characteristics

In the ZAHARA II and III study 66 repaired ToF women were included. For the present study, women were excluded because of miscarriage (n = 3), no CMR evaluation available because of a pacemaker (n = 3) or no CMR evaluation available within 2 years before pregnancy (n = 29), resulting in a total study population of 31 repaired ToF women (median time between the CMR evaluation and date of conception was 8 [3–14] months).

Pre-pregnancy characteristics are presented in Table 1. One woman had a history of arrhythmia and one woman had a history of heart failure. None of the women had hypertension before pregnancy. Because of atrial tachyarrhythmia or reduced LV function, five (16.1%) women were on beta-blocker therapy before pregnancy. One woman was on angiotensin converting enzyme inhibitor therapy and no diuretics were used. Ventricular volume and function data are outlined in Table 2.

Table 1 Baseline characteristics (prior to pregnancy)
Table 2 Pre-pregnancy cardiac magnetic resonance imaging

Relationship between pre-pregnancy CMR parameters and uteroplacental circulation

Median time between pre-pregnancy CMR evaluation and uteroplacental flow measurements at 20 weeks and 32 weeks gestation were 12 [7–19] months and 15 [10–23] months, respectively. Uteroplacental flow measurements (PI) were available in 26 (83.9%) ToF women at 20 weeks and in 28 (90.3%) ToF women at 32 weeks gestation. Univariable and multivariable associations of pre-pregnancy CMR parameters, uterine artery PI at 20 weeks and umbilical artery PI at 32 weeks gestation of ToF women are reported in Tables 3 and 4. Reduced RVEF, higher indexed LV end diastolic volume (EDV) and LV end systolic volume (ESV) were associated with impaired uterine artery PI at 20 weeks with univariable analyses (P = 0.037, P = 0.001 and P = 0.003, respectively). Higher maternal age, reduced RV EF and higher indexed RV ESV were associated with impaired umbilical artery PI at 32 weeks with univariable analyses (P = 0.037, P = 0.001 and P = 0.004, respectively). A negative correlation was found between RVEF and indexed LV ESV (P = 0.016). No correlation was found between RVEF and pulmonary regurgitation fraction.

Table 3 Univariable and multivariable regression analysis pre-pregnancy CMR parameters and uterine artery PI at 20 weeks gestation
Table 4 Univariable and multivariable regression analysis pre-pregnancy CMR parameters and umbilical artery PI at 32 weeks gestation

With multivariable analyses (corrected for age and BMI), reduced RVEF before pregnancy remained significantly associated with higher umbilical artery PI at 32 weeks gestation. Lasso regression analysis including all parameters (as shown in Tables 3 and 4) at 20 weeks selected RVEF and indexed LV EDV and at 32 weeks selected age, BMI, RVEF and RVESVI in the aforementioned models. The associations between RVEF, LVEF and uteroplacental flow (PI) are shown in Fig. 1. High PI (at 20 or 32 weeks) was reported in 6 (30.0%) of the 20 women with complete evaluation available of uterine and umbilical PI during pregnancy. Only RVEF was associated with high PI values (odds ratio = 0.85, P = 0.045). As shown in Fig. 1, RVEF was significantly lower in women with high PI values, compared to women with normal PI during pregnancy (44% vs. 53%, p = 0.022).

Fig. 1

Associations between cardiac function and uteroplacental circulation. a + b Regression plots between right ventricular (RV) ejection fraction (EF), left ventricular (LV) EF and umbilical artery pulsatility index (PI) at 32 weeks of pregnancy. c + d relation between RVEF, LVEF and normal PI vs. high PI of uterine or umbilical artery during pregnancy (at 20 or 32 weeks gestation). *Patients included with complete follow-up data available of uterine and umbilical artery PI at 20 and 32 weeks

Univariable analyses of echocardiographic parameters during pregnancy with uteroplacental flow showed that reduced RV function (S′), higher index RV diameter (basal) and outflow tract dimension at 20 weeks were associated with impaired umbilical artery PI at 32 weeks (P = 0.045, P = 0.047 and P = 0.008, respectively). For internal validation, correlation was assessed between preconception CMR and echocardiography data during pregnancy. A correlation was found between pre-pregnancy RV volume measured by CMR (RV EDV) and RV echocardiographic dimensions (basal diameter and outflow tract) at 20 weeks gestation (Pearson = 0.794, P < 0.001 and Pearson = 0.624, P = 0.013, respectively). A trend was shown in the correlation between pre-pregnancy RVEF and RV S′ at 20 weeks gestation (Pearson = 0.425, P = 0.070).


The main finding of the present CMR study is that a reduced RV function before pregnancy is associated with impaired uteroplacental Doppler parameters during pregnancy in women with repaired ToF. These findings suggest that impaired RV function might be a predisposing factor for poor placental function, which is known to be associated with adverse maternal and neonatal outcome.

The current study combining CMR with PI confirms our previous findings that pre-existing reduced RV function is associated with impaired uteroplacental circulation [1, 12,13,14]. In our previous echocardiographic studies, we were limited in the assessment of RV function and CO measurements due to the specific modality. In the present study, we used CMR, i.e. the accepted gold standard assessment of cardiac function resulting in more robust information about RV and LV function.

To the extent of our knowledge, this is the first study to investigate both reduced CO and RV dysfunction in relation to abnormal uteroplacental Doppler flow parameters. Our findings suggest that pre-existing impaired RV function, rather than impaired LV function, has a negative effect on placentation. Venous congestion could play a central role in this effect. This has previously been shown for other organs in patients with heart failure. Indeed, in such patients, it is well known that kidney and liver failure are associated with impaired organ perfusion. Interestingly, venous congestion seems to be a more important hemodynamic determinant for deterioration of renal and liver function than reduced perfusion [7, 10]. Furthermore, RV dysfunction is a strong predictor of renal impairment in patients with decompensated heart failure [28, 29]. The same could possibly be true for impaired placental circulation. Evidence that RV dysfunction plays a prominent role in placental development and uteroplacental flow regulation is increasing. The question that remains is whether RV dysfunction is a direct cause of abnormal uteroplacental circulation parameters, and if so, what is the underlying pathophysiological mechanism. Could it be that RV dysfunction leads to venous congestion resulting in defective placentation or is the RV unable to increase CO during pregnancy due to worse functional reserve? To answer this question, other conditions could possibly give us some insight. For instance, there is increasing evidence that venous congestion plays a role in pre-eclampsia. Despite widespread consensus that pre-eclampsia is a predominant placental disorder (associated with abnormal uteroplacental flow patterns), maladaptation of the maternal cardiovascular system to pregnancy might be the primary mechanism leading to placental dysfunction [27]. Interestingly in women with pre-eclampsia, both RV dysfunction and abnormal maternal venous hemodynamics have been shown [30, 31]. These changes may lead to further increased venous pressure on the placenta which might impair trophoblast invasion resulting in abnormal placentation, as previously postulated by Gyselaers et al. [32] These data support the view that venous congestion, a typical consequence of RV dysfunction, is a critical factor in the relation between the heart and placental dysfunction. A multicenter prospective study to investigate RV function, venous hemodynamics and CO in pregnant women with ToF, including serial CMR evaluation at preconception, during pregnancy and post-partum, is currently underway to further elucidate the pathophysiological mechanism and its clinical consequence (Netherlands trial register id: NL7890). Furthermore, the pathophysiology of placental dysfunction is most likely multifactorial and therefore studies to other possible factors (e.g. endothelial dysfunction) are also needed. Lastly, since non-contrast CMR is considered to be a safe imaging modality in pregnancy for both the mother and fetus [33], CMR could also be very useful for evaluation of placental and foetal blood flow and deserves further investigation [34, 35].

Until these pathophysiological mechanisms are clarified, frequent monitoring of the placental circulation during pregnancy seems reasonable in women with pre-existing RV dysfunction due to their higher risk of impaired placental function and thus worse pregnancy outcome. If the association between venous congestion and worse RV function would be confirmed in pregnant women, then it could be worth studying the therapeutic use of medications to reduce venous congestion, such as diuretics, on placental circulation.


The number of women in the present study was relatively small, which limits the multivariable regression analyses. However, with additional Lasso regression analyses [36], the findings were confirmed which supports our findings. We acknowledge this point, but unfortunately, rather few CMR studies in this population are performed and we believe that despite this, we are still able to draw some conclusions. Second, although ZAHARA was a prospective study, CMR data were collected retrospectively. Third, it would have been interesting to have CMR data (of RV function and CO) at the same time as the uteroplacental circulation measurements, but CMR studies during pregnancy were not available in the current study. Having said this, CMR data pre-pregnancy did correlate with echocardiography data measured during pregnancy. In addition, internal validation, using echocardiography data for reduced RV function and uteroplacental flow impairment correlation, showed similar patterns. At last, not all women had complete evaluation of uteroplacental circulation at both time points during pregnancy (20 and 32 weeks), since measurements could be technically difficult depending on the location of the fetus during evaluation and therefore missing data was unavoidable.


The present CMR study shows that reduced RV function before pregnancy is associated with abnormal uteroplacental Doppler flow parameters. It could be postulated that reduced RV function on pre-pregnancy CMR (≤2 years) is a predisposing factor for impaired placental function in women with repaired ToF.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.



Body mass index


Cardiovascular magnetic resonance


Cardiac output




End-diastolic volume


End-diastolic volume index


Ejection fraction


End-systolic volume


End-systolic volume index


Left ventricle/left ventricular


Left ventricular ejection fraction


New York Heart Association


Pulsatility index


Right ventricle


Right ventricular ejection fraction


Tricuspid annular plane systolic excursion


Tetralogy of Fallot


World Health Organization


  1. 1.

    Pieper PG, Balci A, Aarnoudse JG, et al. Uteroplacental blood flow, cardiac function, and pregnancy outcome in women with congenital heart disease. Circulation. 2013;128(23):2478–87.

    CAS  PubMed  Google Scholar 

  2. 2.

    Kampman MAM, Bilardo CM, Mulder BJM, et al. Maternal cardiac function, uteroplacental Doppler flow parameters and pregnancy outcome: a systematic review. Ultrasound Obstet Gynecol. 2015;46(1):21–8.

    CAS  PubMed  Google Scholar 

  3. 3.

    Thilaganathan B. Placental syndromes: getting to the heart of the matter. Ultrasound Obstet Gynecol. 2017;49(1):7–9.

    CAS  PubMed  Google Scholar 

  4. 4.

    Osol G, Moore LG. Maternal uterine vascular remodeling during pregnancy. Microcirculation. 2014;21(1):38–47.

    PubMed  Google Scholar 

  5. 5.

    Brosens I, Pijnenborg R, Vercruysse L, et al. The "great obstetrical syndromes" are associated with disorders of deep placentation. Am J Obstet Gynecol. 2011;204(3):193–201.

    PubMed  Google Scholar 

  6. 6.

    Aardema MW, Oosterhof H, Timmer A, et al. Uterine artery Doppler flow and uteroplacental vascular pathology in normal pregnancies and pregnancies complicated by pre-eclampsia and small for gestational age fetuses. Placenta. 2001;22(5):405–11.

    CAS  PubMed  Google Scholar 

  7. 7.

    Mullens W, Abrahams Z, Francis GS, et al. Importance of venous congestion for worsening of renal function in advanced decompensated heart failure. J Am Coll Cardiol. 2009;53(7):589–96.

    PubMed  PubMed Central  Google Scholar 

  8. 8.

    Damman K, Navis G, Smilde TD, et al. Decreased cardiac output, venous congestion and the association with renal impairment in patients with cardiac dysfunction. Eur J Heart Fail. 2007;9(9):872–8.

    PubMed  Google Scholar 

  9. 9.

    Damman K, van Deursen VM, Navis G, et al. Increased central venous pressure is associated with impaired renal function and mortality in a broad spectrum of patients with cardiovascular disease. J Am Coll Cardiol. 2009;53(7):582–8.

    PubMed  Google Scholar 

  10. 10.

    van Deursen VM, Damman K, Hillege HL, et al. Abnormal liver function in relation to hemodynamic profile in heart failure patients. J Card Fail. 2010;16(1):84–90.

    PubMed  Google Scholar 

  11. 11.

    Erkelens CD, van der Wal HH, de Jong BM, et al. Dynamics of cerebral blood flow in patients with mild non-ischaemic heart failure. Eur J Heart Fail. 2017;19(2):261–8.

    CAS  PubMed  Google Scholar 

  12. 12.

    Kampman MAM, Siegmund AS, Bilardo CM, et al. Uteroplacental Doppler flow and pregnancy outcome in women with tetralogy of Fallot. Ultrasound Obstet Gynecol. 2017;49(2):231–9.

    CAS  PubMed  Google Scholar 

  13. 13.

    Siegmund AS, Kampman MAM, Bilardo CM, et al. Pregnancy in women with corrected aortic coarctation: Uteroplacental Doppler flow and pregnancy outcome. Int J Cardiol. 2017;249:145–50.

    PubMed  Google Scholar 

  14. 14.

    Siegmund AS, Kampman MAM, Oudijk MA, et al. Maternal right ventricular function, uteroplacental circulation in first trimester and pregnancy outcome in women with congenital heart disease. Ultrasound Obstet Gynecol. 2019;54(3):359–66.

    CAS  PubMed  Google Scholar 

  15. 15.

    Kilner PJ, Geva T, Kaemmerer H, et al. Recommendations for cardiovascular magnetic resonance in adults with congenital heart disease from the respective working groups of the European Society of Cardiology. Eur Heart J. 2010;31(7):794–805.

    PubMed  PubMed Central  Google Scholar 

  16. 16.

    Balci A, Sollie KM, Mulder BJM, et al. Associations between cardiovascular parameters and uteroplacental Doppler (blood) flow patterns during pregnancy in women with congenital heart disease: Rationale and design of the Zwangerschap bij Aangeboren Hartafwijking (ZAHARA) II study. Am Heart J. 2011;161(2):269–75.

    PubMed  Google Scholar 

  17. 17.

    Regitz-Zagrosek V, Roos-Hesselink JW, Bauersachs J, Blomstrom-Lundqvist C, Cifkova R, De Bonis M, et al. 2018 ESC guidelines for the management of cardiovascular diseases during pregnancy. Eur Heart J. 2018;39(34):3165–241.

    PubMed  Google Scholar 

  18. 18.

    Bhide A, Acharya G, Bilardo CM, et al. ISUOG practice guidelines: use of Doppler ultrasonography in obstetrics. Ultrasound Obstet Gynecol. 2013;41(2):233–9.

    CAS  PubMed  Google Scholar 

  19. 19.

    Aardema MW, Lander M, Oosterhof H, et al. Doppler ultrasound screening predicts recurrence of poor pregnancy outcome in subsequent pregnancies, but not the recurrence of PIH or preeclampsia. Hypertens Pregnancy. 2000;19(3):281–8.

    CAS  PubMed  Google Scholar 

  20. 20.

    Acharya G, Wilsgaard T, Berntsen GK, et al. Reference ranges for serial measurements of umbilical artery Doppler indices in the second half of pregnancy. Obstet Gynecol. 2005;192(3):937–44.

    Google Scholar 

  21. 21.

    Gomez O, Figueras F, Fernandez S, et al. Reference ranges for uterine artery mean pulsatility index at 11-41 weeks of gestation. Ultrasound Obstet Gynecol. 2008;32(2):128–32.

    CAS  PubMed  Google Scholar 

  22. 22.

    Freling HG, van Wijk K, Jaspers K, et al. Impact of right ventricular endocardial trabeculae on volumes and function assessed by CMR in patients with tetralogy of Fallot. Int J Card Imaging. 2013;29(3):625–31.

    Google Scholar 

  23. 23.

    Freling HG, Willems TP, van Melle JP, et al. Effect of right ventricular outflow tract obstruction on right ventricular volumes and exercise capacity in patients with repaired tetralogy of fallot. Am J Cardiol. 2014;113(4):719–23.

    PubMed  Google Scholar 

  24. 24.

    Jaspers K, Freling HG, van Wijk K, et al. Improving the reproducibility of MR-derived left ventricular volume and function measurements with a semi-automatic threshold-based segmentation algorithm. Int J Card Imaging. 2013;29(3):617–23.

    Google Scholar 

  25. 25.

    Ponikowski P, Voors AA, Anker SD, et al. 2016 ESC guidelines for the diagnosis and treatment of acute and chronic heart failure: the task force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC) developed with the special contribution of the heart failure association (HFA) of the ESC. Eur Heart J. 2016;37(27):2129–200.

    Google Scholar 

  26. 26.

    Petersen SE, Aung N, Sanghvi MM, et al. Reference ranges for cardiac structure and function using cardiovascular magnetic resonance (CMR) in Caucasians from the UK biobank population cohort. J Cardiovasc Magn Reson. 2017;19(1):18 -017-0327-9.

    PubMed  PubMed Central  Google Scholar 

  27. 27.

    Thilaganathan B. Pre-eclampsia and the cardiovascular-placental axis. Ultrasound Obstet Gynecol. 2018;51(6):714–7.

    CAS  PubMed  Google Scholar 

  28. 28.

    Mukherjee M, Sharma K, Madrazo JA, et al. Right-sided cardiac dysfunction in heart failure with preserved ejection fraction and worsening renal function. Am J Cardiol. 2017;120(2):274–8.

    PubMed  Google Scholar 

  29. 29.

    Van Aelst LNL, Arrigo M, Placido R, et al. Acutely decompensated heart failure with preserved and reduced ejection fraction present with comparable haemodynamic congestion. Eur J Heart Fail. 2018;20(4):738–47.

    PubMed  Google Scholar 

  30. 30.

    Vaught AJ, Kovell LC, Szymanski LM, et al. Acute cardiac effects of severe pre-Eclampsia. J Am Coll Cardiol. 2018;72(1):1–11.

    PubMed  Google Scholar 

  31. 31.

    Gyselaers W, Staelens A, Mesens T, et al. Maternal venous Doppler characteristics are abnormal in pre-eclampsia but not in gestational hypertension. Ultrasound Obstet Gynecol. 2015;45(4):421–6.

    CAS  PubMed  Google Scholar 

  32. 32.

    Gyselaers W, Peeters L. Physiological implications of arteriovenous anastomoses and venous hemodynamic dysfunction in early gestational uterine circulation: a review. J Matern Fetal Neonatal Med. 2013;26(9):841–6.

    PubMed  Google Scholar 

  33. 33.

    Expert Panel on MR Safety, Kanal E, Barkovich AJ, Bell C, et al. ACR guidance document on MR safe practices: 2013. J Magn Reson Imaging. 2013;37(3):501–30.

    Google Scholar 

  34. 34.

    Shao X, Liu D, Martin T, et al. Measuring human placental blood flow with multidelay 3D GRASE pseudocontinuous arterial spin labeling at 3T. J Magn Reson Imaging. 2018;47(6):1667–76.

    PubMed  Google Scholar 

  35. 35.

    Tsai-Goodman B, Zhu MY, Al-Rujaib M, et al. Foetal blood flow measured using phase contrast cardiovascular magnetic resonance--preliminary data comparing 1.5 T with 3.0 T. J Cardiovasc Magn Reson. 2015;17:30–015–0132-2.

    Google Scholar 

  36. 36.

    Tibshirani R. Regression shrinkage and selection via the lasso: a retrospective. J R Statist Soc B. 2011;73(3):273–82.

    Google Scholar 

Download references


Not applicable.


The ZAHARA II study was supported by a grant from The Netherlands Heart Foundation (2007B75); the ZAHARA III study was supported by a grant from ZonMW (91210050).

Author information




ASS, TPW, PGP, CMB, TMG, BJB, MRMJ, GTjS, JWR-H, APJD and MGD contributed to collection, analysis and interpretation of data; PGP, CMB, DJvV, and MGD contributed to data conception, design and approval of the article. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Michael G. Dickinson.

Ethics declarations

Ethics approval and consent to participate

The ZAHARA II study was approved by the Medical Ethical Committee of the University Medical Center Groningen (METc2007/192) and the ZAHARA III study was approved by the Medical Ethical Committee of Amsterdam Medical Center (2011_138). All subjects provided informed consent for research participation.

Consent for publication

Not applicable, non-identifiable data only included.

Competing interests

None declared.

Additional information

Publisher’s Note

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

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 The Creative Commons Public Domain Dedication waiver ( 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

Verify currency and authenticity via CrossMark

Cite this article

Siegmund, A.S., Willems, T.P., Pieper, P.G. et al. Reduced right ventricular function on cardiovascular magnetic resonance imaging is associated with uteroplacental impairment in tetralogy of Fallot. J Cardiovasc Magn Reson 22, 52 (2020).

Download citation


  • Congenital heart disease
  • Pregnancy
  • Right ventricular function
  • Uteroplacental circulation