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Cardiac magnetic resonance (CMR) Imaging techniques provide noninvasive assessments of the newborn circulation with high accuracy and repeatability.
Cine CMR produces three-dimensional assessments of chamber volumes and myocardial mass.
Phase contrast CMR can quantify blood flow in any major vessel.
CMR techniques have provided normative ranges for neonatal left and right ventricular development and quantification of PDA shunt volume and have guided optimization of echo techniques.
This chapter describes the evolving role of cardiovascular magnetic resonance (CMR) in the assessment of neonatal hemodynamics. Although CMR currently occupies only a niche role in circulatory assessments in the neonatal intensive care unit (NICU), the technique has begun to demonstrate its value in providing highly detailed insights into the pathophysiology of the fetal and neonatal circulations.
CMR has become a standard imaging modality in assessments of structural congenital heart disease. A 2022 consensus statement, endorsed among others by the Society of Cardiovascular Magnetic Resonance, American Society of Echocardiography, and the American Heart Association, describes recent advances in CMR capabilities as “spectacular” and highlights the value of a single imaging modality in providing noninvasive assessments of cardiac structure, function, and blood flow.
The evolution of brain magnetic resonance imaging (MRI) from a research tool into a core clinical imaging modality shows the potential path forward for CMR in the newborn. The widespread use of brain MRI can also facilitate the growth of CMR, as NICU team members have become comfortable with MR technology, clinical monitoring in the scanner environment, and the widespread use of non-pharmacologic approaches to obtain usable images.
CMR assessments of neonatal hemodynamic function are neither simple nor inexpensive but are highly detailed, highly accurate, and entirely noninvasive. This chapter summarizes areas of neonatal hemodynamics where there is residual uncertainty over pathophysiology and management, provides a background to application of CMR in adults and newborns, discusses the current and emerging CMR techniques, and describes areas where CMR has already advanced understanding of developmental cardiovascular physiology and where in the future it may contribute to changes in the care of critically ill preterm and term neonates with cardiovascular compromise.
Our hope is that as co-location of MRI technology within NICUs becomes more common, CMR will fulfill its significant promise to advance clinical research and support improvements in mortality and morbidity in the vulnerable newborn through enhanced hemodynamic monitoring and support.
As discussed in a number of chapters in this book, the most prematurely born infants remain at high risk of death and disability. While in the past respiratory disease was the primary cause of death, high-quality research has improved preterm respiratory care, such that an increasing proportion of deaths occur due to episodes of sepsis or necrotizing enterocolitis, where impaired myocardial function and failing peripheral vascular control often make circulatory failure the final mechanism of death.
Circulatory failure is also central to the pathophysiology of the key morbidities of premature birth. The long-term sequelae of preterm birth carry an estimated annual socioeconomic burden of >£3 billion in the UK and >$26 billion in the United States. Failing cardiac function causes cerebral hypoperfusion, and episodes of low cerebral blood flow are central to the pathophysiology of preterm brain injury, which causes long-term disability ( Chapters 7 and 8 ). Limitations in clinicians’ ability to adequately assess circulatory function impair both the ability to tailor care in individual infants and the conduct of adequate trials of the impact of potential therapies. Improving circulatory management is therefore a research priority in preterm infants.
All circulatory function relies on the interplay of preload, contractility, and afterload ( Chapter 1 ). The preterm transitional circulation is further complicated by the persistence of fetal shunt pathways (foramen ovale and ductus arteriosus), which may alter circulatory dynamics. A robust assessment of the newborn circulation therefore needs to quantify preload, contractility, afterload, and systemic and organ perfusion.
Unfortunately, the current methods fall short of this ideal; in particular, routine clinical monitoring of circulatory status in the neonatal unit still relies heavily on arterial blood pressure. , However, systemic arterial blood pressure is the product of systemic blood flow and systemic vascular resistance, but it cannot itself distinguish between the two. While clinicians presumably feel that monitoring systemic blood pressure is a screening tool for low systemic perfusion, in fact, blood pressure in itself is at best weakly predictive of volume of blood flow, and some studies have suggested no, or even an inverse, relationship between blood pressure and flow in newborn preterm infants. Other clinical assessments, such as capillary refill time or volume of urine output, also have limited value in indicating circulatory health.
A range of technologies are now entering “prime time” for hemodynamic assessment in the neonatal unit. Point of care cardiac ultrasound/echocardiography ( Chapter 9, Chapter 10, Chapter 11 ) leads the way, has produced important advances in the understanding of circulatory physiology, and has an increasing role in the assessment of circulatory status at the bedside. Established techniques are being improved upon , and newer modalities are emerging and undergoing optimization. , Bedside cardiac imaging currently provides only snapshots of hemodynamic status, so continuous monitoring techniques such as impedance monitoring ( Chapter 12 ) and near-infrared spectroscopy are also reaching the point of clinical utility. Finally, the evolving systems capable of real-time, comprehensive, and mostly noninvasive, continuous cardiorespiratory and neurocritical care monitoring and data acquisition at the bedside provide an approach with the potential of addressing many of the presently unanswered questions and unresolved controversies ( Chapter 14 ). CMR will again play a key role in helping to improve our understanding of the interplay among important hemodynamic factors during transition and in pathological conditions, as well as assessing the response to various treatment approaches in neonates with hemodynamic compromise.
A key step for all new modalities is robust validation in the population of interest. In the current absence of a gold-standard assessment of cardiac function in the premature infant, CMR has a role as a validation tool – its accuracy and repeatability in newborns are consistently outperforming that of cardiac ultrasound, near-infrared spectroscopy, and impedance monitoring. Outside the early newborn period (where transfer of a sick newborn to an MRI scanner, even one located on the NICU, is challenging), the accuracy of CMR in quantifying volume of blood flow and myocardial mass provides valuable insights into circulatory physiology and cardiac development.
A comprehensive discussion of magnetic resonance (MR) physics is beyond the scope of this textbook, but a few basic principles may be pertinent. The underlying principle of MR relies upon the fact that certain atomic nuclei possess an intrinsic magnetic moment, if they contain an odd number of protons or neutrons. This is also identified as nuclei having the property of non-zero spin. When placed in a strong magnetic field, these nuclei align either with, or against, the field; a slightly higher proportion align with rather than against the field, leading to a net magnetization. The effect is proportional to the field strengh and ultimately leads to the level of signal available in MRI, hence the drive to increase field strength magnets in clinical imaging. The resulting net magnetization rotates or “precesses around the axis of the feld at a set rate, depending on the field strength and the gyromagnetic ratio of the nuclei. This rate of precession (or resonance) is known as the Larmor frequency.
The aligned equilibrium magnetization can be manipulated by radiofrequency (RF) pulses applied at the resonant frequency; subsequently, the perturbed magnetization will then emit its own RF signal as it rotates in the magnetic field; this is measured using closely coupled receiver coils. Images are produced by localizing the abundance of spins by use of magnetic field gradients. Hydrogen atoms, consisting of a single proton, provide the strongest signal of all relevant atoms and are also the most abundant in the body. Image contrast may be based on the concentrations of protons or how they interact with their magnetic environment, which is detected by changes in their relaxation rate. In-flow effects can provide additional contrast; this is particularly useful to CMR, where blood flow provides “fresh” magnetization compared to saturated signal of more static tissue. Alternatively, in phase contrast (PC) MR spins are “labeled” according to their velocity by applying additional encoding magnetic field gradients, producing a signal dependent on their velocity through the direction of the applied field, analogous to that achieved with Doppler ultrasound.
Cardiac magnetic resonance techniques have significantly advanced understanding of cardiovascular physiology and pathophysiology in adults and are now considered the gold-standard functional assessment tool. These noninvasive assessments of cardiac health are now being gained faster, in more detail, and with greater sophistication than ever before. The range of techniques available have been summarized in recent reviews. , The key benefits of CMR in the adult population are the ability to quantify the component factors of circulatory function and the improved repeatability over echocardiography for assessment of quantitative measures. Critically, improved repeatability also translates into a reduction in the patient numbers required to prove a hypothesis in research studies.
It is clear that functional CMR will not become a routine clinical assessment tool for the sick newborn infant in the foreseeable future – imaging acutely ill children and infants remains challenging. It is more feasible, especially for more stable newborns, when an MR scanner is located within the neonatal unit – a growing number of centers are installing either dedicated neonatal , or full-size adult scanners, bringing “point-of-care MRI” closer to reality. It is now well established that MR scans can safely be performed in the newborn population while maintaining respiratory, circulatory, and thermal stability. We have now performed cardiac MR examinations in over 350 newborn preterm and term infants without any adverse events. Functional CMR images have been successfully obtained in infants weighing under 600 g and at 25 weeks’ corrected gestation.
Our belief is that virtually all infants undergoing CMR imaging can lay still after they have been fed and allowed to fall into a natural sleep after a feed. A recent systematic review of this “feed and wrap” approach reports very high success rates. Infants should be scanned with oxygen saturation, heart rate, and continuous temperature monitoring; a pediatrician/neonatologist or trained neonatal nurse should be in attendance throughout each scan. Protection from acoustic noise is achieved by applying moldable dental putty or ear plugs and then covering with neonatal ear muffs. Application of an acoustic hood can further reduce disturbance from scanner noise. Scans can be performed free-breathing or, with the provision of mechanical ventilation, with nasal continuous positive airway pressure and high-flow or low-flow oxygen therapy as clinically indicated. In older subjects respiratory motion causes significant image degradation requiring breath-holds, use of image navigators to coordinate acquisition with diaphragmatic movement, or advanced post-processing to account for respiratory motion. In neonates relatively high-quality cardiac images are obtainable without the use of respiratory navigation, presumably due to the relatively small degrees of diaphragmatic excursion. However, the widespread implementation of free-breathing techniques in older subjects is making their application in newborns feasible (see below).
Gating of scan acquisitions to the infant’s cardiac cycle remains vital for adequate imaging. This is relatively easily achieved using a four-lead vector cardiogram (VCG) (standard three-lead ECGs tend to be significantly degraded by the magnetic fields in the MRI environment). VCG gating can be carried out prospectively or retrospectively. In general, retrospective gating is preferred as this technique allows imaging throughout the entire cardiac cycle and gives additional flexibility to adapt to the variable heart rate seen in the newborn. Novel approaches to cardiac self-gating and real-time sequences are emerging, which may have particular benefits in newborns with unpredictable heart rates and whole-body motion patterns.
Adult CMR studies are increasingly performed at higher (3.0 Tesla) field strengths. Discussion on the specific challenges faced when imaging at higher field strengths is outside the scope of this review. However, in brief, the main drive to higher field systems comes from the increased signal offered as field strength increases, which may confer a substantial benefit for imaging small neonates. The major challenges faced in performing CMR in neonates arise from the need to significantly increase image resolution, both spatially – due to the size of the heart – and temporally – due to the rapid heart rates. These requirements place significant increased demands on the scanner hardware. In addition, the standard imaging protocols applied to adults may not be directly transferable and thus require modification to be used for scanning small neonates. The initial process of image optimization which we have undergone to improve image quality has previously been described. ,
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