Since its early development in the 1980s, fetal echocardiography has been widely adopted as a screening technique for the prenatal diagnosis of congenital heart disease (CHD). The benefits of prenatal detection include the prevention of morbidity associated with neonatal hemodynamic instability, as well as providing families with a choice about whether to continue with a pregnancy in which the fetus is affected by a severe congenital heart malformation [1,2,3]. In a small minority of patients with the most severe forms of CHD, prenatal diagnosis may lead to families being offered fetal interventions aimed at improving the outcome of the malformation [4,5,6]. Ultrasound generally allows for excellent visualization of cardiac morphology and function, while Doppler can be used to characterize fetal cardiovascular physiology. The widespread availability of ultrasound in maternal fetal medicine clinics and the familiarity of fetal ultrasound techniques amongst perinatologists make it an ideal modality for detecting CHD [7]. However, in late gestation, fetal echocardiography can be hampered by technical limitations resulting from maternal obesity, oligohydramnios, adverse fetal position, multiple gestations and acoustic shadowing by the bony thorax, and this has led to interest in the development of fetal cardiovascular magnetic resonance (CMR) [8]. Of note, the image quality of fetal CMR actually improves in late gestation, especially when oligohydramnios or engagement of the fetus in the pelvis limits fetal body movement, thus limiting motion artifacts. Fetal CMR may therefore have a role as an adjunct to ultrasound when technical factors limit the diagnostic utility of fetal echocardiography [9, 10]. One of the strengths of magnetic resonance imaging (MRI) lies in its versatility in creating contrast between different tissues [11]. This has been exploited to reveal myocardial injury in a fetal sheep model [12]. Although concerns have been raised about the safety of MRI during embryogenesis and gadolinium-based contrast agents are contraindicated in pregnancy due to an increase in the risk of inflammatory conditions in children exposed to these agents in utero, fetal MRI is well tolerated and provided the equipment is used correctly, safe for mother and fetus [13]. To overcome the challenges imposed by maternal breathing and fetal body movements while attempting to image small cardiac structures beating at heart rates that are typically in the 130–150  beats per minute range, a number of modifications have been made to conventional post-natal CMR methods [14]. With the advent of accelerated imaging techniques, motion correction algorithms and a range of techniques for synchronization of image acquisition to the cardiac cycle, it is now possible to capture the anatomy and function of the fetal heart and measure blood flow and oxygen content within fetal vessels. This review aims to provide an update on the latest techniques available for imaging the fetal heart using MRI, emphasizing the unique information fetal CMR provides about fetal hemodynamics. In particular, we will focus on the potential clinical utility of fetal CMR in the setting of CHD.

Techniques and utility in fetal CMR

Fetal cardiovascular morphology and function

The most commonly used static CMR method for imaging fetal cardiac anatomy are balanced steady-state free precession “bright blood” sequences (bSSFP), which are referred to as TrueFISP, bFFE, FIESTA in vendor specific terminology. A single-shot fast spin echo “black blood” with half fourier transformation sequence is also useful for imaging mediastinal vascular anatomy and the airways and lungs (commercial names: HASTE, TSE, SSFSE). These sequences are well suited to fetal MRI because they offer relatively high spatial resolution with short acquisition times. However, they are subject to artifacts arising from cardiac motion, and provide no information about cardiac function [14]. In conventional postnatal CMR, high resolution cine imaging of the beating heart is achieved by triggering the image acquisition to the different phases of the cardiac cycle using the electrocardiographic (ECG) signal [15]. However, the fetal ECG is difficult to detect, particularly in the MRI environment. Non-invasive approaches to acquiring triggered cardiac imaging in the fetus include metric optimized gating (MOG), strategies based on “self-gating”, and Doppler Ultrasound gating (DUS) [16,17,18,19,20,21,22]. When gating is applied to cine bSSFP imaging, it is possible to obtain stacks of dynamic images of the heart that capture the details of cardiac structures and provide an assessment of ventricular contraction. However, each slice of gated bSSFP cine imaging requires several seconds of scan time, and this approach is therefore susceptible to artifacts arising from fetal body motion and maternal breathing movements. To overcome these artifacts, the acquisition can be accelerated using a combination of undersampling approaches such as golden angle radial trajectory k-space filling with an advanced reconstruction algorithm that employs compressed sensing. When combined with strategies for excluding data acquired during gross fetal movements and correcting for minor fetal and maternal respiratory movement using registration techniques, these accelerated imaging approaches result in consistently high quality cine imaging [14, 23,24,25]. An alternative approach to acquiring triggered fetal cine imaging that is feasible in animal models is to utilize an arterial blood pressure waveform obtained from a catheter placed in the carotid or femoral artery and connected to a blood pressure transducer. In combination with procedural anesthesia, this approach has yielded novel measurements of right and left systolic and diastolic ventricular volumes and ejection fractions in fetal sheep (Fig. 1) [26].

Fig. 1
figure 1

Ventricular volumetry by post-processing a short-axis cine fetal CMR in fetal sheep. The top picture represents contoured 2-D cine images of the fetal heart and reconstructed into ventricular volumes (bottom picture). Re-produced from Cho et al. (58) with permission from Wiley

Fetal circulation

Fetal blood flow

The current gold standard approach to the non-invasive measurement of vessel blood flow in children and adults is by velocity-encoded cine phase-contrast (PC) CMR [27, 28]. Using similar cardiac gating approaches to those described above for myocardial cine imaging, cine PC CMR can be applied to the quantification of flow in fetal vessels, allowing for the measurement of the right and left ventricular output, and pulmonary and umbilical blood flow [16, 29,30,31]. Quantification of superior vena caval flow provides an approximation of cerebral blood flow [32], while calculations based on the conservation of flow can be used to estimate the shunt across the foramen ovale. Using multiplanar PC CMR, it is also possible to interrogate intracardiac flow dynamics. Thus, fetal MRI can be used to quantify the distribution of the fetal circulation and evaluate the impact of congenital cardiac malformations on fetal organ perfusion [33]. In animal models in which the imaging conditions can be further optimized through invasive gating and procedural sedation, complex flow dynamics such as the streaming of the umbilical venous return across the foramen ovale and the spiral trajectory of ductus venosus flow can be characterized by so-called four-dimensional cine PC CMR [34, 35].

Fetal blood oxygen content

One of the unique properties of the MRI signal is its sensitivity to changes in oxygen saturation and hemoglobin concentration. This can be exploited using quantitative relaxometry techniques known as T1 and T2 mapping to quantify the oxygen content of blood in fetal vessels, providing a completely novel approach to the assessment of fetal hemodynamics. Using modified versions of sequences developed for measuring T1 and T2 in the myocardium it has been shown that the paramagnetic effect of deoxyhemoglobin results in the time constant of the transverse relaxation of blood being proportional to its oxygen saturation, while its longitudinal recovery rate is primarily dependent on hematocrit. Interestingly, oxygen saturation also influences the relationship between T1 and hematocrit, while hematocrit affects the conversion of T2 to hematocrit. However, using a combination of T1 and T2 measurements from an individual vessel it is possible to calculate a unique solution for both hematocrit and oxygen saturation. Notwithstanding the negligible contribution of oxygen dissolved in plasma, oxygen content can then be quantified as the product oxygen saturation and hematocrit [36,37,38].

Fetal oxygen transport

The combination of fetal vessel flow and oximetry data provides additional information regarding placental and fetal hemodynamics, fetal oxygen transport and fetal metabolism. Oxygen flow in a vessel is the product of oxygen content and blood flow. When this approach is applied in the umbilical vessel it can be used to quantify fetal oxygen delivery (umbilical vein oxygen content by umbilical vein flow). The combination of fetal oxygen delivery and oxygen content in the umbilical arteries (which is more easily measured in the descending aorta) yields fetal oxygen consumption, a measure of fetal metabolism, and fetal oxygen extraction, which may be increased in low output states [10, 39]. Using a similar approach, oxygen delivery and consumption of individual organs can be estimated using a combination of flow and oximetry measurements in fetal vessels. For example, cerebral oxygen delivery has been measured in fetal sheep using a combination of carotid blood flow measurements and oximetry measurements made in the superior vena cava and ascending aorta [40]. The same principle has been used to study the impact of the abnormal cardiac connections and obstructed blood flow that characterize CHD on fetal streaming, and the associated effect on cerebral oxygenation [41]. Measurements of umbilical vein oxygen saturation have also revealed evidence of subtle placental dysfunction in the setting of fetal CHD [42].

Fetal CMR as a clinical diagnostic tool

Over the past two decades, a number of studies have investigated the utility of fetal CMR for the diagnosis of CHD. Static, non-gated bSSFP imaging has been used to visualize the gross morphological structures of the fetal heart and great vessels. Fetal CMR has been used to define the viscero-atrial situs, cardiac position, atrio-ventricular and ventriculo-arterial concordance, systemic and pulmonary venous connections, great artery relationship, arch sidedness, and heart, chamber and vessel sizes in healthy and congenitally malformed hearts [43,44,45,46,47,48]. Studies have indicated there is a high degree of concordance between fetal CMR and echocardiography [44, 49,50,51]. Fetal CMR has also been used in the setting of cardiac tumours [52, 53]. In one study, fetal CMR had an 88% sensitivity and 96% specificity for the detection of CHD in relation to postnatal imaging, although the authors noted that MRI provided no additional diagnostic value over ultrasound [51]. By contrast, another study found fetal CMR was useful as an adjunct for the diagnosis of CHD when later confirmed by postnatal evaluation. In this cohort, 15% of cases were correctly diagnosed by CMR when echocardiography was incorrect. However, 18% of cases were correctly diagnosed by echocardiography when CMR was incorrect and 3% of cases were misdiagnosed by both echocardiography and CMR [54]. In a large retrospective study comparing fetal CMR with postnatal diagnosis at a single center in patients in whom there was some limitation of the ultrasound diagnosis, fetal CMR correctly diagnosed 99.2% of cases that had normal hearts, 60.6% of cases with CHD, and 87.9% of cases with other heart diseases [55]. Most of the misdiagnoses were attributed to atrial and ventricular septal defects, coarctation of the aorta, and patent ductus arteriosus. Several studies have focused on the diagnostic value of fetal CMR in vascular anomalies, in which it was reported to demonstrate high diagnostic accuracy, provide diagnostic value, and be superior to echocardiography [56,57,58,59,60,61,62]. It was suggested that the transverse aortic arch view by fetal CMR is relatively easy to obtain, to reproduce, and to interpret [58]. An alternative technique to visualize the entire fetal vasculature such as non-contrast magnetic resonance angiography using time-of-flight MRI has been feasible in late human pregnancy [63].

More recently, cardiac gated dynamic cine CMR imaging has been reported to deliver improved image quality of the cardiac anatomy while also providing a functional assessment of the fetal heart [18, 20, 23, 24, 64]. When compared to grey-scale cine sweeps by echocardiography, stacks of cine bSSFP CMR were reported to have superior image quality but lacked resolution for outflow tract abnormalities, small pulmonary arteries, and valvular morphology. Difficulties in visualizing the outflow tracts and pulmonary arteries were attributed to fetal movement and could often be shown by a repeat acquisition, which resulted in a longer scan [9]. Comparisons of measurements of various cardiac structures also suggest that cine fetal CMR imaging agrees well with measurements made using conventional echocardiography [19, 65, 66]. In one case report of an unbalanced atrioventricular septal defect, fetal CMR reliably detected significant aortic arch hypoplasia and excluded an interventricular communication, resulting in a more appropriate perinatal management plan [67]. Motion correction techniques have been successfully applied to multiplanar stacks of black-blood imaging to achieve very high resolution three-dimensional datasets, which have been used to generate exquisite volume rendered reconstructions of congenital cardiac abnormalities involving the great vessels and systemic and pulmonary veins. The motion corrected approach to reconstruction has been reported to improve fetal CMR visualization of the mediastinal vessels from 53 to 97%, with diagnostic imaging achieved in 90% of cases and good agreement with echocardiographic findings [25]. In one case, this approach to fetal CMR was used to successfully diagnose a double aortic arch with atresia of the aortic isthmus of the smaller arch [61].

The supplemental file 1. shows an example of how fetal CMR was helpful in the management of a fetus presenting in late gestation with a large congenital diaphragmatic hernia. The echocardiographic windows were extremely challenging, and although there was a suspicion of CHD, no diagnosis could be made. Fetal CMR was performed at 35 weeks and provided reasonable views of the heart, confirming the presence of balanced ventricles with a large ventricular septal defect and a single outlet to an overriding aorta with no central pulmonary arteries. Postnatal echocardiography in this case confirmed the presence of tetralogy of Fallot with pulmonary atresia and major aorto-pulmonary collateral arteries. Given the complexity of the cardiac diagnosis combined with the severity of the diaphragmatic hernia, the family opted for palliative management, and the infant died soon after birth. In this example, the fetal CMR provided additional information over the echocardiogram which helped with fetal counselling and helped the family in their decision making about the postnatal management.

Assessment of the fetal circulation

Our modern understanding of fetal circulatory physiology is largely based on experiments performed in fetal sheep. Adopting techniques for catheterizing exteriorized fetal sheep developed by Barcroft and Dawes [68, 69], Rudolph et al. developed an approach to measuring the distribution of the fetal sheep circulation using radioactive microspheres injected into the different venous compartments, the concentrations of which could then be measured where they become lodged in the microcirculation of each organ supplied by the right and left heart [70]. This approach was combined with conventional blood gas samples and pressure measurements obtained from intravascular catheters to define the hemodynamics of the fetal circulation. A number of human ultrasound studies have since provided estimates of the distribution of the human fetal circulation [71,72,73,74,75]. However, through a combination of blood flow and oximetry measurements, fetal CMR has provided a more definitive picture of late gestational human fetal hemodynamics, confirming many similarities with the fetal sheep [29, 76]. In the human fetal circulation, just as in the sheep, the circulation operates in parallel, with shunts and the foramen ovale and the ductus arteriosus which allow blood to bypass the lungs. This is tolerated in fetal life because gas exchange occurs at the placenta. Thus, the highest oxygen saturations in the fetal circulation are found in the umbilical vein (85%). As a result of streaming of the umbilical venous return via the ductus venosus and foramen ovale, the oxygen saturation in the left heart and aorta is higher (68%) than in the right heart and main pulmonary artery (49%). The oxygen saturation in the descending aorta lies between these values (57%), being derived from both right and left ventricles, giving an arteriovenous difference across the fetal side of the placenta of 28%. The combined ventricular output (CVO) in the late gestation human is 465 ml/min/kg, which is comprised of contributions of 57% from the right ventricle and 43% from the left ventricle. Pulmonary blood flow is higher in the human than the sheep, accounting for 16% of the CVO, while umbilical flow is 29% and foramen ovale shunt is 27%. Despite the lower umbilical flow (135 ml/min/kg) present in the human fetal circulation, fetal oxygen delivery (25 ml/min/kg) and consumption (6.8 ml/min/kg) are very similar to sheep, due to the higher hematocrit present in the human (15.5 g/dL) [40]. The unique streaming mechanism responsible for relatively well-oxygenated blood reaching the left heart and being supplied to the metabolically active heart and brain, while more deoxygenated blood is delivered to the lungs and placenta via the right heart, ductus arteriosus can clearly be visualized in fetal sheep using a “four dimensional” cine phase contrast CMR acquisition, often referred to as 4D flow (Fig. 2) [34]. This approach has also revealed a spiral trajectory of blood flow through the ductus venosus, which may account for the lack of mixing between the two streams as they flow towards the right atrium in the inferior vena cava (Fig. 3) [35]. With the advent of increasingly sophisticated approaches to image acquisition and processing, approaches similar to 4D flow are now being used to interrogate complex flow dynamics in human fetuses [77, 78].

Fig. 2
figure 2

Blood flow through a 3-D reconstructed cardiovascular system using 4-D flow CMR in fetal sheep. The left picture represents the 3-D reconstruction of the major fetal vessels and cardiac shunts with rings representing where blood flow was assessed. The top left graph represents the blood flow of inflow vessels and cardiac shunts of the heart. The bottom left graph represents the blood flow of outflow vessels and cardiac shunts of the heart. UV, umbilical vessel; DV, ductus venosus; IVCd/p, distal/proximal inferior vena cava; SVC, superior vena cava; FO, foramen ovale; AAo, ascending aorta; BT brachiocephalic trunk; DA, ductus arteriosus; DAo, descending aorta; MPA, main pulmonary artery; PBF, pulmonary blood flow. Re-produced from Schrauben et al. (27) used under CC BY 4.0

Fig. 3
figure 3

Blood flow through a 3-D reconstructed ductus venosus – inferior vena cava junction using 4-D flow CMR in fetal sheep. The left picture represents the 3-D reconstruction major hepatic veins and inferior vena cava with rings representing where blood flow was assessed. The right graph represents the blood flow across each vessel interrogated. UV, umbilical vein; PS, portal sinus; DV, ductus venosus; L/RHV, left/right hepatic vein; IVCd/p. distal/proximal inferior vena cava. Re-produced from Schrauben et al. (61) with permission from Wiley

The application of cine PC CMR and MR oximetry in fetuses with CHD has provided an opportunity to confirm many of the observations made about the impact of the abnormal cardiac anatomy on fetal cardiovascular physiology. For example, in the setting of obstruction of blood flow across one side of the heart, the output of the contralateral ventricle increases. However, in the setting of single ventricle physiology, the increase does not entirely compensate, resulting in a reduction in combined ventricular output [79]. This is most profound in the setting of severe atrioventricular valve regurgitation such as in fetuses with severe forms of Ebstein’s anomaly, in which reductions are seen in pulmonary, cerebral and umbilical perfusion [80]. In other forms of CHD, cerebral blood flow appears to be preserved, or even increased in the setting of transposition of the great arteries [81]. However, in severe forms of left heart obstruction, perfusion of head and neck vessels is achieved via retrograde arch flow via the ductus arteriosus [79]. The interruption of the normal streaming mechanism in all major forms of CHD results in more desaturated blood reaching the cerebral and coronary circulations, which may account for the impaired brain growth and development that is typical of newborns with CHD [41]. In fetuses with CHD associated with left atrial hypertension, such as hypoplastic left heart syndrome with an intact or highly restrictive atrial septum, pulmonary blood flow is impaired [79]. Similarly, pulmonary blood flow is reduced in fetuses in which the pulmonary circulation is supplied retrograde via the ductus arteriosus including those with pulmonary atresia and severe forms of Ebstein’s anomaly [80]. Umbilical blood flow is reduced in the setting of fetal CHD that is associated with lower cardiac output, and this further impacts fetal oxygen delivery [41]. The presence of CHD also appears to be associated with subtle decrements in placental function which result in reduced umbilical venous oxygen saturations [42]. Thus, the fetus with CHD is subject to a suboptimal fetal environment, while individual organs may be underperfused and hypoxemic as a result of the heart disease, potentially leading to issues with fetal development included brain dysmaturation and pulmonary vascular disease.

Development and monitoring of fetal interventions

The demonstration of reduced fetal oxygen delivery and cerebral hypoxemia in fetuses with CHD has led to interest in the potential of maternal hyperoxygenation as a neuroprotective strategy in fetuses with CHD [41]. It has long been known that increasing maternal fraction of inspired oxygen (FiO2) results in an increase in fetal PaO2 and SaO2, and several randomized controlled trials performed in the 1990s suggested that chronic maternal hyperoxygenation was associated with improved outcomes in growth restricted fetuses [82]. Acute maternal hyperoxygenation results in an increase in umbilical vein oxygen saturation in fetuses with normal hearts, and in those with CHD [42]. In pregnant sheep ventilated with an FiO2 of 1.0, we observed no change in uterine or cerebral blood flow and 20% increase in cerebral oxygen delivery (unpublished data). We are currently conducting a pilot safety and feasibility study of chronic maternal hyperoxygenation in fetuses with single ventricle CHD (NCT03136835). The pulmonary vasodilator effect of maternal hyperoxygenation has also resulted in interest in intermittent doses as an approach to increasing venous return to the underdeveloped left ventricle [83,84,85]. In one case of borderline left ventricular hypoplasia, the impact of acute maternal hyperoxygenation was assessed by PC-CMR, revealing no increase in ascending aortic flow despite a doubling of pulmonary blood flow, which may explain why the response to chronic maternal hyperoxygenation is inconsistent and likely related to the degree of anatomical restriction imposed by morphologic abnormalities versus underfilled left heart structures [86]. In cases of Ebstein Anomaly with circular shunting, fetal CMR revealed an improvement in systemic and cerebral blood flow following constriction of ductus arteriosus flow induced by transplacental treatment with non-steroidal anti-inflammatory drugs (NSAID) [80]. In this case series, severely diminished cardiac output and cerebral oxygen delivery and consumption identified by CMR contributed to decision making about the timing of delivery, highlighting the potential clinical value of fetal CMR in cases of severe hemodynamic compromise.

An example of how fetal CMR can be used to aid decision-making around fetal cardiac intervention, and monitor the impact of an in utero procedure is provided in the case illustrated in Table 1 and Fig. 4. The presence of an intact or highly restrictive atrial septum has been shown to be an important prognostic factor in fetuses with transposition of the great arteries [87]. In recognition of the potential for severe hypoxemia following birth in this setting, we have reported the use of late gestational balloon atrial septostomy to achieve a more stable transition from fetal to postnatal circulation [88]. In a second fetal case of transposition in which we suspected a restrictive atrial communication we recently performed fetal CMR. The results of the CMR revealed that unlike in most fetuses with TGA, in which streaming results in higher oxygen saturations in the left heart and main pulmonary artery than the right ventricle and aorta, in this fetus the oxygen saturations were actually slightly higher in the right ventricle than the left (Fig. 5a), while the PC CMR assessment of the distribution of blood flow indicated there was a diminutive shunt across the foramen ovale (Fig. 6). Following percutaneous in utero balloon atrial septostomy, the flow assessment indicated a significant increase in flow across the atrial septum with equalization of oxygen saturations in the right and left heart (Fig. 5b). The supplemental files 2 and 3 shows the application of PC-CMR and cine imaging to assess fetal blood flow and the four-chamber view heart structure, respectively, after intervention. The baby was born 7 days later with arterial oxygen saturations of 70% and successfully underwent repeat balloon atrial septostomy and arterial switch. Of note, the pre-procedural flow assessment was also suggestive of significant aortopulmonary collateral flow, which may account for the relative preservation of oxygen saturations in the left ventricle despite the lack of shunting at atrial level. The presence of significant aortopulmonary collaterals has previously been reported in fetuses with transposition with atrial septal restriction and could be a contributing factor to the development of pulmonary vascular disease in these patients [81, 89].

Table 1 Fetal PC-CMR blood flow assessment demonstrating the hemodynamic changes in TGA with IVS and RAS before and after fetal balloon atrial septostomy. TGA transposition of the great arteries, IVS intact ventricular septum, RAS restricted atrial septum, MPA main pulmonary artery, AAo ascending aorta, SVC superior vena cava, DAo descending aorta, UV umbilical vein, DA ductus arteriosus, PBF pulmonary blood flow, CVO combined ventricular output, FO foramen ovale
Fig. 4
figure 4

Echocardiography of the fetal heart in TGA IVS and RAS before and after fetal balloon atrial septostomy (BAS). Panel A and C represents limited blood flow across the small FO prior to BAS. Panel B and D represents blood flow across the restrictive FO and additional superior atrial communication (AC) after BAS. Panel A and B were acquired using 2-D echocardiography and Panel C and D were acquired using 3-D echocardiography. TGA, transposition of the great arteries; IVS, intact ventricular septum; RAS, restricted atrial septum; FO, foramen ovale; SVC, superior vena cava; TV, tricuspid valve

Fig. 5
figure 5

Oxygen saturations of the four-chamber view in TGA with IVS and RAS before intervention (a) and after intervention (b) by fetal CMR Color T2 mapping. TGA; transposition of the great arteries; IVS, intact ventricular septum; RAS, restricted atrial septum

Fig. 6
figure 6

Fetal blood flow distribution and oxygen content before and after fetal balloon atrial septostomy in TGA with IVS and RAS by fetal CMR. TGA; transposition of the great arteries; IVS, intact ventricular septum; RAS, restricted atrial septum

Fetal CMR has also been used to investigate the impact of potential fetal pharmacologic strategies aimed at improving fetal development in animal models. Examples include the investigation of the impact of an umbilical vein infusion of prostaglandin I2 (PGI2) on fetal circulatory physiology, which revealed an increase in ductus venosus shunting of substrate-rich blood from the placenta to the heart. However, the administration of PGI2 was also associated with vasodilation of the pulmonary circulation, which decreased FO shunting, resulting in no increase in cerebral oxygen delivery [90]. In another set of experiments, CMR was used to measure uterine blood flow in pregnant sheep exposed to resveratrol to demonstrate an increase in uterine blood flow and fetal weight (unpublished data).

Future directions and current limitations

The examples provided above give a sense of how, in a few academic centers, fetal CMR is beginning to find a role in selected fetal congenital heart disease cases. It would appear possible that just as postnatal CMR is now used by most large paediatric units caring for patients with CHD, fetal CMR may ultimately be used in specialist centers for rare cases like those described above, when echocardiography is so limited that additional diagnostic information is required in order to determine a safe perinatal management plan, or when a fetal intervention is being contemplated or followed up. It is also possible that fetal CMR will continue to be used by researchers interested in studying fetal cardiovascular physiology or developing new fetal treatments.

However, despite our enthusiasm for an increased role for fetal CMR, we recognize there remain significant limitations and barriers to wider adoption of the technique. Importantly, fetal CMR is currently only useful in the third trimester, while many of the critical management decisions about a fetus with CHD are often made during the second trimester. Even in late gestation, current fetal CMR techniques continue to be degraded by motion artifacts, and while substantial advances have been made in overcoming these artifacts, the techniques required currently involve several postprocessing steps and significant investments in terms of computer science and manual analyses steps. Indeed, any form of MRI remains relatively expensive and inaccessible in comparison to ultrasound. Further work and collaboration with the MRI vendors is needed to make these postprocessing steps more automated and less time consuming before they are feasible for most clinical settings.


In summary, fetal CMR represents an exciting new imaging modality for characterizing the morphology and physiology of fetal CHD. Many of the initial barriers to imaging the fetal heart and cardiovascular system have been overcome through technical innovations involving accelerated imaging strategies and approaches to motion correction. As a result, fetal CMR is providing new insights into the impact of cardiac malformations on fetal development, and may be helpful for visualizing the anatomy when conventional echocardiographic imaging is limited, and in patients requiring a sophisticated approach to perinatal management.