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Low‐field MRI: Clinical promise and challenges

Thomas Campbell Arnold, Colbey W. Freeman, Brian Litt and 1 more

Journal of Magnetic Resonance Imaging · 2022 · Review · CC BY

doi:10.1002/jmri.28408

Abstract

Level of Evidence. 5

Technical Efficacy. Stage 6

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 18, 2026. Paragraph numbers are ours, so an answer can point at one.

Magnetic resonance imaging (MRI) is a mainstay of modern medicine and has led to significant advances in basic science and clinical patient care. MRI has superior soft tissue contrast and provides definitive diagnostic information throughout the body, particularly exceling in neuroimaging and musculoskeletal applications. MRI is widely utilized in high‐income countries (HICs), with 1.9 scans annually per 10 American Medicare enrollees. However, high costs and technical barriers have limited adoption in low‐ and middle‐income countries (LMICs). Worldwide, approximately 90% of people lack access to MRI, while two‐thirds lack even basic medical imaging., Even in HICs, MRI is unavailable in rural areas and to patients with disability or device constraints., Recent advances in lower‐field strength MRI offer potential solutions, with less expensive and portable devices. However, lower‐field MRI still faces significant challenges, and it remains to be seen how newer devices will be deployed clinically.

Most MRI units today use high‐field strength, cryogenically‐cooled, superconducting magnets, though low‐field permanent and resistive magnet designs have existed throughout MRI's history. Permanent magnets offer decreased cost and siting requirements but achieve lower magnetic field strengths, which impacts the signal‐to‐noise ratio (SNR) achieved per unit time during scanning. Lower‐field devices typically acquire lower resolution images to maintain clinically feasible scan times. Recent academic and industry efforts seek to leverage lower‐field strength advantages including lower cost, smaller device footprints, and fewer safety concerns while mitigating inherent disadvantages that contribute to lower image quality (Table 1). To balance these factors, lower‐field approaches are increasingly tailored to specific clinical questions and contexts. Selecting and validating appropriate use cases remains paramount.

In this review, we explore both the clinical promise and challenges of lower‐field MRI. We describe hardware and software advances as well as financial and practical considerations related to lower‐field device adoption. Next, we discuss five clinical domains where lower‐field MRI offers clinical promise: high acuity brain imaging, outpatient neuroimaging, MRI‐guided procedures, pediatric imaging, and musculoskeletal imaging. In each section, we provide a literature overview, examples of low‐field use, and a discussion of how new devices can integrate with current care standards. Although we cannot cover all use cases, our goal is to convey the technology's potential impact and stimulate further clinical translation.

Hardware & Software Advances

The definition of “low‐field” varies, sometimes referring to anything below 1.5T while other times indicating a narrow band between 0.01T and 0.1T. For this review, we refer to devices using the distinctions in Fig. 1. We use “lower‐field” to broadly describe devices below 1.5T and “higher‐field” for 1.5T and above. New levels of distinction will continue to be developed to better communicate; however, we can obviate confusion by defining terminology in our work or developing standards through professional societies, such as the International Society of Magnetic Resonance Medicine.

The distinction between low‐field and high‐field MRI appeared during MRI's infancy in the 1980s (Fig. 2). A citation gap emerged after 1985, when the first 1.5T scanners were introduced. The gap grew throughout the 1990s and widened significantly in the early 2000s, when 1.5T scanners became the clinical standard. High‐field scanners gained a dominant market share because of their higher SNR per unit time, which permits faster imaging, higher resolution, greater contrast sensitivity, and more advanced sequences. Commercial lower‐field devices have remained available over this time period, but many have been relegated to niche use cases or discontinued. Nevertheless, renewed commercial interest has led to FDA clearance of several lower‐field systems since 2018, including the 0.064T Hyperfine Swoop head scanner, 0.066T Promaxo prostate scanner, 0.5T Synaptive Evry intraoperative scanner, 0.55T Siemens Magnetom Free.Max general purpose scanner, and 1T Aspect Embrace neonatal scanner. While high‐field devices won market dominance based on higher image quality, two primary factors are driving this recent lower‐field renaissance: 1) lower scanner costs and 2) technological innovations resulting in image quality improvements.

Medical care costs in the United States have risen dramatically, with medical imaging contributing significantly. High‐field MRI devices are expensive, and their cost has increased over time. The largest component of MRI device cost is the magnet, with total high‐field device cost being roughly 1 million USD per Tesla. Lower‐field strength devices offer significant device cost savings. Although lower‐field MRI is associated with lower image quality, it is actually SNR per unit time that is proportionate to magnetic field strength. Stronger magnets reduce the time necessary to achieve a certain level of sensitivity. Given sufficient time, lower magnetic fields can produce high‐SNR images of diagnostic quality; however, patient tolerance and clinical expediency place practical constraints on acquisition times. Recent software and hardware advances have improved image quality obtained per unit time, making imaging at lower‐field strengths within clinically relevant quality and timeframe standards feasible.

Technological developments spurring interest in lower‐field devices include hardware improvements (eg improved magnet, gradient, and coil designs) and software developments (eg deep learning reconstruction and post‐processing). Multiple research groups have pioneered the development of newer lower field devices, including the ultra‐low‐field 0.0065T electromagnet scanner at MGH, the 0.08T and 0.05T Halbach array devices respectively at MGH and the University of Leiden,, a fast field cycling scanner at the University of Aberdeen that can operate between 50μT and 0.2T, and the 0.05T and 0.055T permanent dipole systems at Chongqing University and the University of Hong Kong, respectively., A common theme is design simplification to facilitate scanner production, maintenance, and operation in low‐resource settings. Additionally, reduced weight and siting requirements enable some devices to be portable. At lower‐field strengths, coil noise is dominant, leading researchers to optimize wire diameter, spacing, and windings in low‐cost, 3D‐printed head coils. Portable systems must have lightweight radiofrequency (RF) shielding. Researchers eliminated bulky shielding by using passive coils to predict and remove electromagnetic noise., Another trend is reduced reliance on gradient coils, which require high amounts of power. Cooley et al designed a cylindrical Halbach array, a scanner composed of multiple small permanent magnets, with optimized magnet placement resulting in a built‐in readout field gradient with minimal stray flux. Importantly, this eliminates one gradient system, lowering the devices power and cooling requirements. Additionally, they leveraged a rotating scanner bore to collect 2D images without any gradient coils, thereby permitting silent imaging. Another approach has been to step‐down high‐field systems to operate at lower‐field strengths while maintaining state‐of‐the‐art commercial gradients and coils.,

Software advances have been facilitated by deep learning advancements, increased graphics processing unit availability, and the open‐source movement. With decreased SNR per unit time, lower‐field strengths accentuate the trade‐off between resolution and scan time. Lower‐field strength scanners can leverage reduced specific absorption rates (eg Transmit Array Spatial Encoding, shorter RF pulses, longer spin echo trains) and SNR efficient acquisition strategies (eg bSSFP, MR fingerprinting, long readout spiral imaging), to maximize image quality per unit time., Additionally, to reduce scan times researchers sought rapid imaging methods, such as sensor space subsampling; however, this results in noise and image artifacts after conventional reconstruction. Recently, compressed sensing and deep learning have enabled reconstruction from a smaller subset of k‐space., Deep learning reconstruction methods use neural networks to learn robust transformation mappings from sensor space to the image domain. Image postprocessing has also benefited from deep learning, with applications in super‐resolution,,, segmentation, simulation, denoising, and artifact rejection. However, analytical software development typically lags hardware advances. It may take several years for some software commonly used at high‐field to be adapted to low‐field scanners. The low‐field research community has engaged with the open‐source movement, most notably through the Open Source Imaging Initiative (OSI2: opensourceimaging.org),, which may facilitate faster development of both hardware and software applications.,,

While we must acknowledge the hardware and software innovations that have led to the lower‐field device resurgance, a full discussion is beyond the scope of this review. For more information, we recommend Wald et al & Marques et al.

Financial and Practical Considerations

Lower‐field MRI adoption requires an understanding of how device costs and implementation differs from traditional high‐field scanners. Lower‐field strength devices typically cost less and have reduced siting requirements, enabling them to be used for novel applications and in new settings. As MRI is expanded into new patient populations and care environments, it is crucial that researchers, device manufacturers, and care providers understand the relevant constraints in these settings. Here, we review practical and financial considerations that should guide appropriate clinical application selection.

One large advantage of lower‐field devices is reduced siting requirements compared to traditional high‐field systems (Table 1). High‐field devices are large, usually weighing over 5 tons and requiring two dedicated rooms with reinforced flooring and RF shielding. Most high‐field scanners use superconducting magnets, which require additional high‐power infrastructure and a quench pipe for cryogenic cooling. These devices are sensitive to vibrations and nearby ferromagnetic objects (eg ambulances, cars, trains). By contrast, many lower‐field strength devices weigh less, with several scanners reported between 0.05 and 0.25 tons. They require less or no RF shielding., Low‐field devices are often permanent magnets, reducing overall power demands and eliminating cryogenic cooling. Additionally, the 5 gauss safety line scales with magnetic field strength, enabling lower‐field devices to be in closer proximity to other scanners, medical equipment, and ferromagnetic objects. The lower siting requirements significantly reduces installation costs and overall device footprint, facilitating portability in some cases.

MRI resources tend to be concentrated in population centers, resulting in reduced imaging access in rural areas and introducing sampling bias into research studies. Tractor trailers have been retrofit with 1.5T magnets to increase access. Mobile scanners enable device cost sharing between hospitals and permit imaging in restricted populations. However, these devices cost millions of dollars and have complicated infrastructure, limiting their deployment. Recently, research groups have retrofit vans with lower‐field devices. Nakagomi et al placed a 0.2T magnet in a minivan for mobile extremity imaging. They envisioned deploying the device to sporting events or areas without MRI access. Deoni et al retrofit a Ford Transit van with a 0.064T magnet and demonstrated neuroimaging in pediatric and adult patients at their homes. The estimated project cost was 110,000 USD, a fraction of the cost to purchase a mobile 1.5T tractor trailer.

Increased healthcare costs in the United States have led to a critical evaluation of medical imaging expenditure. In addition to optimizing current practices, increased reliance on lower‐field devices may offer a cost‐effective means of enhancing MRI value. Japan, which has the highest concentration of MRI devices worldwide, has capped MRI reimbursement rates., This led to widespread adoption of low‐field devices, which offer lower cost per examination and thus increased profitability. While there are undoubtedly cases when high‐field MRI is more clinically appropriate, it may be reasonable to adopt a similar approach to Japan, where high‐field scanners are concentrated in healthcare centers and mid‐to‐low‐field devices are more widely available. While SNR per unit time is proportional to field strength, this may not be the best metric for determining how much value different MRI systems contribute to diagnostic accuracy, patient outcomes, and societal benefit. Low‐field devices may allow patient triage and reduce scheduling demands on high‐field scanners, resulting in decreased diagnostic delays and increased patient satisfaction.,

While low‐field devices may augment standard‐of‐care (SOC) imaging in HICs, they will likely play a more impactful role in LMICs. In 2016, an estimated 84 MRI units serviced West Africa, an area of over 370 million people. For comparison, in 2019, the United States had an estimated 13,000 devices to service ~330 million people. Low‐field devices already play a dominant role in MRI services in West African countries, with the majority (77.6%) of devices in Nigeria being low‐field strength (<0.3T)., Neuroimaging was the primary application, with one center reporting over 90% of studies requested were for brain (49.9%) or spine (45.6%) imaging. However, the average MRI cost was ~500 USD and services are typically paid by patients out‐of‐pocket, making even low‐field scanners beyond the reach of a significant portion of the population.

Increased geographical and financial access has been a primary motivator for ultra‐low‐field and very‐low‐field system development. This includes devices targeting pediatric hydrocephalus, which has a high prevalence in Africa., More targeted systems may be cheaper to produce and service, allowing for lower out‐of‐pocket costs. Ogbole et al noted that lack of technical support or service materials caused significant scanner downtime. When designing devices for LMICs, special consideration should be given to available resources and expertise., Additionally, many LMICs have a dearth of radiologists and radiographers. Remote readers or automated algorithms may provide diagnostic support, allowing countries to stretch scarce resources. For more details on imaging accessibility, the authors recommend Geethanath et al.

Equally important to proper device design is appropriate and equitable introduction of devices into society. Recently, working groups of researchers, clinicians, MR vendors, and local stakeholders have convened to provide guidelines and address key ethical, legal, and social questions surrounding portable MRI., Continued working group engagement will be essential for providing updated recommendations as new hardware and software are released.

The remainder of this review focuses on potential clinical applications of newer lower‐field MRI devices. While we focus on neuroimaging and musculoskeletal applications, lower‐field MRI offers opportunities throughout radiology, including adbominal, cardiac, and lung imaging.

For an introduction to additional applications not covered here, we recommend Campbell‐Washburn et al.

High Acuity Brain Imaging

High acuity brain imaging in critical care or emergency room patients primarily aims to identify acute problems that require immediate intervention, such as stroke, hemorrhage, edema, and mass effect. Importantly, transporting critically ill patients that require life‐sustaining equipment and continuous monitoring outside the intensive care unit (ICU) is difficult, time‐consuming, and poses risk of adverse events. Stroke is a leading cause of morbidity and mortality worldwide, causing an estimated 6.5 million deaths each year. The main stroke types are ischemic and hemorrhagic, with ischemic strokes accounting for 87% of United States cases. Quickly differentiating between ischemic and hemorrhagic strokes is an essential first step toward treatment. The irreversible infarct core enlarges over time, and evidence supports a 3–4.5‐hour treatment window for intravenous thrombolysis and a 24‐hour window for mechanical thrombectomy, after which outcomes are considerably worse.,

Computed tomography (CT) and MRI are the dominant methods for determining stroke subtype. Provided that MRI is readily accessible, the American Academy of Neurology recommends MRI over CT because it avoids ionizing radiation and has superior soft‐tissue contrast, facilitating detection of smaller infarcts., Diffusion‐weighted imaging (DWI) has exquisite sensitivity and specificity for ischemia detection, with other sequences, such as fluid‐attenuated inversion recovery (FLAIR) and gradient echo, providing complementary information., While MRI is diagnostically superior to CT, conventional MRI is more expensive, not always readily available, and is contraindicated in ~10% of patients (eg patients with foreign metal bodies, device implants, claustrophobia, etc.).

In the 1990s and early 2000s, several studies explored diffusion‐weighted and perfusion‐weighted sequence development for stroke diagnosis on lower‐field scanners (0.1–1.0T range). These studies employed fixed MRI systems with either permanent magnets (typically <0.35T) or superconducting magnets (typically >0.5T). While these systems could detect strokes, sensitivity was reduced compared to 1.5T systems or scan times were not clinically feasible.

At very‐low‐field strengths (<0.1T), there have been several recent clinical developments related to stroke imaging. The first report of portable MRI for stroke was published by Sheth et al in 2020., The authors used a 0.064T system to image 30 ICU patients with known intracranial abnormalities, including ischemic stroke, hemorrhagic stroke, subarachnoid hemorrhage, traumatic brain injury, and brain tumor. Bedside imaging was performed with medical equipment being actively used, including ventilators, dialysis machines, and patient monitoring equipment. The portable MRI detected intracranial abnormalities in 97% (28/29) of patients with SOC imaging findings, with one diffuse subarachnoid hemorrhage case missed. In a follow up study, researchers evaluated 144 portable MRI examinations with intracerebral hemorrhage (ICH, N = 56), non‐hemorrhagic acute ischemic stroke (AIS, N = 48), or healthy controls (N = 40). ICH classification accuracy was 90% (130/144), with 80% (45/56) sensitivity. AIS and healthy controls were correctly identified as parenchymal hemorrhage free in 97% (85/88) of cases. Manual hematoma segmentation volumes were strongly correlated between the 0.064T system and SOC imaging. Hematoma volume also correlated with cognitive status (ρ = 0.75/0.8, P < 0.001) and functional outcome at discharge (ρ = 0.59/0.64, P < 0.001). Figure 3 provides examples of ICH and AIS at 0.064T compared to 3T imaging. He et al also reported development of a 0.05T scanner with T1 and T2 weighted imaging in three stroke patients. The authors illustrated ischemic and hemorrhagic stroke cases and longitudinal monitoring of a hemorrhagic stroke with eight scans over 17 days.

The 0.064T system received FDA clearance early in the COVID‐19 pandemic. In their initial publication, Sheth et al imaged an additional 20 ICU patients diagnosed with COVID‐19 that presented with altered mental status. Abnormal findings were present in 40% (8/20) of patients. Turpin et al also described the use of portable MRI in ICU patients with COVID‐19, with abnormal findings present in 63% (12/19) of patients. The researchers highlighted that in five cases portable MRI led to changes in patient management. Importantly, portable MRI can aid in infection control by providing medical imaging to patients inside isolation wards, limiting infectious patient transport.

Additional studies characterized midline shift (MLS) in stroke patients on the 0.064T system., In a 102 patient cohort, low‐field MRI had 93% sensitivity and 96% specificity for detecting MLS presence when compared to SOC imaging based on manual identification of midline structures. In a follow‐up study, the commercial AI‐based method for assessing MLS (Fig. 3a), which is available at the point‐of‐care, was non‐inferior to neuroradiologists (P < 1e‐5). Automated, quantitative biomarkers in lower‐field, point‐of‐care imaging have potential to facilitate interpretation and may extend services to sites where radiologists are not readily available, provided findings are actionable in that context.

In stroke cases time is brain. Mobile stroke units were developed in 2015 to deliver appropriate therapy as quickly as possible. These vehicles are equipped with point‐of‐care lab testing, a CT scanner, and personnel trained in stroke therapy. A recent study with over 1000 patients found mobile stroke units with onboard CT improved patient disability outcomes, reduced time from stroke onset to tissue plasminogen activator administration by 34%, and decreased mortality rate from 11.9% to 8.9%. While MRI has not previously been integrated into mobile stroke units because of siting and cost issues, new portable low‐field MRI systems have been placed in vehicles for remote imaging., Mobile stroke units combined with portable MRI could offer rapid stroke imaging with the high tissue contrast and safety benefits of MRI.

Image quality for some sequences at very‐low‐field are currently below clinical expectations. In a recent study, two neurosurgeons and a neuroradiologist rated image quality of a portable MRI system using a 5‐point scale, 5 being the lowest quality. FLAIR (2.19 ± 0.98), T1‐weighted (T1w) (2.6 ± 0.98), T2‐weighted (T2w)‐axial (2.47 ± 0.99), and T2w‐coronal (2.88 ± 0.99) sequences had similar quality ratings with approximately 85% of images deemed adequate for interpretation. However, only 27% of DWI were sufficient for interpretation and images had a correspondingly lower average quality rating (4.13 ± 1.02). This highlights that DWI, which is the gold‐standard for stroke imaging, remains challenging at very‐low‐field, as this sequence must be fast to avoid motion effects and requires strong gradients with rapid shifting. However, researchers noted DWI quality improved as newer software and hardware versions were released throughout data collection. In addition, Mazurek et al illustrated several false‐negative cases where pathology could be seen upon closer examination, indicating neuroradiologists may require training on lower‐field images to become accustomed to their appearance. Protocols have been described for integrating portable, very‐low‐field devices into ICU, emergency department (ED), and COVID‐19 care settings.,

At stroke centers, vascular imaging also guides acute and chronic management. Both CT angiography and high‐field time‐of‐flight and contrast‐enhanced MR angiography exquisitely depict cerebrovascular anatomy. Facilitated by artificial intelligence based processing, CT perfusion determination of infarct core, penumbra, and collateral flow has also become integrated into decision‐making for mechanical thrombectomy. At very‐low‐field strengths, vascular and perfusion imaging will be challenging and gadolinium contrast will be less effective. Alternative agents, such as superparamagnetic iron oxide nanoparticles, demonstrate high sensitivity even at ultra‐low‐field strengths (<0.01T). These agents have been used for vascular imaging at higher field strength, though clinical translation is limited by off‐label use and cumbersome administration requirements.,, In preliminary studies we investigated vascular imaging using ferumoxytol, an iron oxide agent that is FDA approved for treatment of iron deficiency anemia. With high T1 and T2/T2* relaxivity and prolonged intravascular time, this agent represents a best‐case scenario for vascular enhancement. Anemia patients were imaged on the portable 0.064T scanner before and after ferumoxytol administration. Visual enhancement of dural venous sinuses and large arteries was observed (Fig. 4), although additional studies of dose and sequence optimization are needed.

To date, ICU stroke imaging is the most well studied clinical application for the new generation of very‐low‐field devices. While there are technical challenges that must be overcome (Table 2), the technology has been integrated into clinical workflows and demonstrated high stroke sensitivity. Although diffusion sequences on earlier low‐field scanners had reduced sensitivity and longer scan times, newer lower‐field machines are equipped with state‐of‐the‐art gradient systems, which could improve DWI and increase utility for stroke imaging.,,, In high resource settings, ED and ICU care are areas where we are likely to see lower‐field MRI integrated into SOC practices because of lower device costs, increased device portability, and MR compatibility. First, lower‐field scanners are often less expensive to purchase and operate. Several research groups have reported developing systems for under 20,000 USD and commercial systems are available for ~75,000 USD/year.,, Portability of lower‐field systems can also increase availability. Portable CT scanners provide an alternative in some centers, but portable MRI could still offer lower cost, more definitive imaging for stroke, with potential for frequent follow‐up imaging without ionizing radiation. Finally, many patients with conventional MRI contraindications (eg pacemakers, defibrillators, implants, foreign metal bodies) can be safely imaged on some lower‐field systems. Given that stroke patients may be incapacitated during imaging, reduced screening requirements could be a substantial benefit. For more details on stroke imaging on lower‐field MRI the authors recommend Bhat et al.

Outpatient Neuroimaging

While portable MRI applications have centered on the neuro ICU, evidence is emerging regarding their efficacy for outpatient neurology use cases. Neurological disorders affect 1 billion people worldwide. They are the leading cause of disability and the second leading cause of death, killing an estimated 9 million people annually. Many neurological disorders require frequent imaging and longitudinal monitoring. In this section, we review emerging clinical evidence for lower‐field devices in outpatient settings and discuss how reduced costs and increased portability could impact when and where patients receive neuroimaging.

Hydrocephalus is a condition in which the brain's fluid‐filled ventricles become abnormally enlarged. It is readily managed by placing a sunt to relieve the abnormal accumulation of cerebrospinal fluid but requires imaging for diagnosis and to monitor for under or over shunting. MRI easily depicts the ventricles and offers an ionizing radiation free alternative to serial CT, particularly for children. Researchers have desinged ultra‐low‐field scanners for the treatment and monitoring of hydrocephalus, though scanning has been limited to phantoms thus far. At our center, we collected paired SOC and portable very‐low‐field data from 22 adult hydrocephalus patients and compared ventricle volume estimates to high‐field imaging (Fig. 5a). Radiologists were able to accurately categorize patient ventricle sizes as small, large, mixed, or within normal limits. Ventricle volumes measured at 0.064T and high‐field were strongly correlated. Figure 5a illustrates an example of automated ventricular segmentation provided by the point‐of‐care scanner. In many patients, neurosurgeons implant programmable shunts so fluid drainage can be adjusted non‐invasively. Programmable shunts use a magnetic mechanism for drainage adjustment that can be reset by high‐field MRI and must be checked by the neurosurgical team after scanning. Lower field strength devices might have reduced interference with shunt settings, but we found that shunt settings were altered by the very‐low‐field MRI.

Point‐of‐care scanners have also been used to study multiple sclerosis (MS), a demyelinating disease affecting the brain and spinal cord. Mateen et al used a 0.08T portable scanner to visualize demyelinating lesions in two MS patients. They noted cortical atrophy in one patient with advanced disease, a finding that has applicability in other neurodegenerative diseases, such as dementia. In a cohort of 36 MS patients, our group probed the sensitivity of a very‐low‐field device using paired 3T and 0.064T data. We found the portable 0.064T device was sensitive to white matter (WM) lesions, with both radiologists and automated algorithms able to detect lesions (Fig. 5b). Lower resolution for a given scan time and uncertain benefits from conventional gadolinium contrast are challenges facing very‐low‐field MRI for MS and other applications that track lesions over time (eg metastases). Initial reports have begun exploring contrast enhancement on very‐low‐field devices (Fig. 6), but larger studies are needed to optimize sequences and contrast dosage.

In recent decades, researchers have identified MRI biomarkers for neurodegenerative and psychiatric disorders., Disease‐specific patterns of brain atrophy can be evident on imaging prior to symptom onset, such as hippocampal volume loss in Alzheimer's disease. The presence of other features, such as WM hyperintensities, can further aid in the differential diagnosis. Imaging biomarkers can also serve as endpoints for clinical trials. Reduced image resolution in lower‐field devices has proven problematic for some conventional neuroimaging pipelines, which could impact biomarker analysis. To address this, Iglesias et al developed a super‐resolution algorithm (SynthSR) that takes lower resolution images and synthesizes a 1 mm isotropic T1w MPRAGE to use for subsequent postprocessing. The group has demonstrated high correlation for key brain regions (eg hippocampus, thalamus, ventricles, cortical gray matter [GM]) between 3T and SynthSR‐enhanced lower‐field images., Deoni et al demonstrated the ability to generate 1.5 mm isotropic T2w images by registering and averaging three orthogonal slice plane acquisitions. Although high‐field biomarkers have yet to be validated on very‐low‐field imaging, these initial super‐resolution results provide a promising avenue.

In summary, although lower‐field devices are not indicated for all applications, growing literature supports the use of in specific cases, such as hydrocephalus and MS. Potential use cases including longitudinal volume tracking (eg hydrocephalus, subdural hematoma) and more frequent MS follow up. Rapid advances in this lower‐field technology, aided by machine learning, may expand clinical applications over time (Table 3).

Intraoperative MRI and MRI‐Guided Procedures

MRI is an integral part of neurosurgery, allowing surgeons to plan procedures and monitor for complications. Accurate localization of structures is perhaps the most important problem at the interface of neuroimaging and surgery. In the 1980s, frame‐based stereotaxy became the first widely used systematic method for localizing intracranial structures. These systems fix the patient's head in a physical frame to relate a coordinate system and have largely been replaced by frameless neuronavigational systems, which rely on fiducial markers. Today, frameless neuronavigational systems are the most widely‐deployed localization method used in HICs.

Despite their physical differences, both frame‐based and frameless methods for neuronavigation rely on preoperative imaging. However, significant anatomical distortions occur as tissue is removed and cerebrospinal fluid (CSF) is lost during surgery and neither method permits intraoperative monitoring for complications, such as hemorrhage. In the late 1990s, researchers began developing intraoperative MRI (iMRI) approaches using low‐field scanners. Two initial iMRI approaches were developed: the Boston concept, where surgery is performed in the scanner, and the Heidelberg concept, where the patient is transported to a nearby scanner. Later, the idea of bringing the scanner to the patient was explored using both high‐field and low‐field devices. Approaches where the patient or the scanner are moved to acquire imaging have become more widely adopted because they permit higher field‐strength magnets, unrestricted patient access, and traditional ferromagnetic surgical instruments.

iMRI has largely been pioneered in neurosurgery for brain tumor resections,,, where the superior soft tissue contrast and 3D visualization of MRI facilitates maximal tumor resection, minimal healthy tissue removal, and monitoring for surgical complications. Other common uses for iMRI include accounting for brain shift during surgery, biopsy needle guidance, functional MR guidance to avoid eloquent cortex, tractography to avoid major WM tracts, thermal ablation guidance and temperature monitoring, seizure focus resection, and intracranial device placement. Several innovative approaches in mid‐to‐low‐field iMRI have been developed, including the original 0.5T Signa SP (GE) pioneered by Black et al, the 0.2T Magnetom Open (Siemens) pioneered by Tronnier et al where patients were moved intraoperatively, and the semi‐portable 0.12–0.3T PoleStar N‐10, N‐20, and N‐30 systems (Odin Medical, later Medtronic). While studies using mid‐to‐low‐field devices demonstrated improvements over standard surgery, including improvements in gross total resection, remission rate,, survival time,, there have also been reports of tumor remnants found postoperatively using high‐field imaging.,,

While iMRI has explored a range of field strengths, today most devices are 1.5T or 3T. Higher‐field strengths are favored because they permit higher image quality with faster acquisition times, allow for a greater resection extent, and have increased sensitivity to enhancing neoplasm,, which is a primary predictor of surgical outcome. High‐field systems have demonstrated clinical and economic benefits, while evidence for low‐field systems has been mixed. However, high‐field devices have disadvantages associated with their increased magnetic field strength, including increased susceptibility artifact, hardware interactions, shielding requirements, a larger 5‐gauss line, increased safety precautions, and MR compatibility issues (eg device heating, projectile risk, and image artifacts). Additionally, iMRI systems require significant capital investment, more staff training, and longer procedure times, which has likely slowed adoption.

Newer lower‐field devices may overcome some disadvantages of high‐field scanners while improving upon shortcomings from prior lower‐field iterations. With a sufficiently low magnetic field, surgeries can be performed using traditional implements without moving the patient or scanner. Additionally, staff training burden and safety precautions are reduced. Some researchers have advocated for the development of mid‐field systems equipped with the latest technology developed for high‐field systems.,,, Campbell‐Washburn et al modified a 1.5T Siemens Magnetom Aera to operate at 0.55T while maintaining gradient performance and using a 16‐channel head coil. A similar design is now commercially available as the 0.55T Siemens Magnetom Free.Max. Campbell‐Washburn et al described seven patients that underwent successful MRI‐guided right heart catheterization using the mid‐field scanner and demonstrated reduced RF‐induced heating in guidewires, catheters, and pacemakers previously deemed unsafe at 1.5T (Fig. 7)., Synaptive Medical offers the 0.5T Evry system, which was designed for iMRI applications. Preliminary studies report reduced risk of RF‐induced heating and have demonstrated gradient specifications (max amplitude = 100 mT/m, max slew = 400 T/m/sec) that enable high‐quality diffusion tensor imaging.,, Additionally, MRIdian's 0.35T ViewRay system for MRI‐guided linac radiation therapy received FDA‐clearance in 2014. This device combines low‐field MRI with an MR compatible radiation therapy system to permit precise tumor localization and monitoring during treatment. To our knowledge, no publications have reported new mid‐field scanners being used for peri‐neurosurgical or neurointerventional procedures to date, but their increased surgical precision and MR compatibility alongside the potential for reduced iMRI costs merit further investigation.

At very‐low‐field strengths, the 0.066T Promaxo system has been proposed as a point‐of‐care method for guiding prostate biopsies by urologists., Prior to the procedure, high‐field imaging is collected to identify biopsy targets. Very‐low‐field imaging is collected during the procedure and registered to high‐field imaging to provide needle guidance. In phantom studies, needle guidance error was less than 3 mm on average. In early in‐vivo reports, MRI guidance increased sensitivity to prostate cancer by 37% over blinded systematic biopsy (MRI‐guided: 12/16, blinded systematic biopsy: 6/16). To date, there are no reports of new lower‐field systems for neurosurgical applications. However, prior iterations, such as the discontinued PoleStar system, had operational cost of approximately 750,000 USD annually. New lower‐cost scanners have potential to change the cost‐benefit analysis and may drive iMRI adoption in areas previously deemed cost‐prohibitive.

Although new low‐to‐mid field devices offer reduced scanner costs and have improved in image quality, they still face significant challenges (Table 4). Device sensitivity is the most critical question. Prior studies of low‐field devices frequently reported tumor remnants on high‐field follow‐up. Gadolinium contrast is proportional to magnetic field strength, which is another concern. While conventional contrast usage may be adequate for mid‐field scanners, to achieve sufficient contrast at even lower field strengths we may need to increase dosages or develop higher relaxivity agents. Finally, magnet and coil configurations must be designed to accommodate surgical implements, monitoring equipment, and staff needs during surgery. For more details on iMRI applications, the authors recommend Hall et al.

Pediatrics

Pediatric MR imaging is increasingly used for clinical and research purposes given concerns of ionizing radiation exposure from CT and x‐ray. There are unique challenges associated with imaging pediatric patients, including safety concerns, image acquisition obstacles, and differences in image analysis. These barriers can prevent direct translation of research or clinical practices from adult to pediatric populations and highlight the importance of evaluating each step of neuroimaging pipelines with the target population in mind. Here, we highlight some features of pediatric neuroimaging and discuss lower‐field MRI contributions.

Ultrasound (US), CT, and MRI are the dominant modalities for pediatric neuroimaging. US is primarily used to diagnose disorders such as hydrocephalus and intracranial hemorrhage in the first 6 months of life, prior to anterior fontanelle closure. CT is commonly used for trauma‐related neuroimaging because it offers fast imaging with good contrast between blood, bone, and brain. CT acquisition times are short so sedation of pediatric patients is rarely required. However, CT has less soft tissue contrast and exposes patients to ionizing radiation, making it less desirable for repeated imaging, such as monitoring shunted hydrocephalus patients., While MRI offers superior soft tissue contrast and non‐ionizing radiation, it is more expensive and less widely available than CT. This is particularly relevant in rural areas and in many LMICs. MRI acquisition times are longer than CT, often necessitating patient sedation which poses safety risks. Finally, MRI hardware, such as head coils, needs to be optimized for pediatric patients.

Open scanner designs and reduced scanner noise are appealing advantages of lower‐field systems. Patient compliance can be particularly challenging for children under 6 years old, who often require sedation. With open scanner designs, claustrophobia is less of a problem. Sedation usage may also decrease, as parents or providers can access children during scanning. Rupprecht et al compared sedation and anesthesia requirements of 274 pediatric patients imaged on a 0.2 tesla open bore MRI (Magnetom Open, Siemens) to 111 patients imaged on a standard high‐field, closed bore system. In the open system, only 27% (74/274) of patients required sedation compared to 47% (52/111) on the closed system. The effect was most pronounced in children under 10 years old. The authors also reported using lower sedation doses and that monitoring patients was easier. Moreover, lower‐field devices have reduced acoustic noise, which is particularly useful for imaging infants, who are often asleep during scans or require ear protection.,

Lower‐field systems have been deployed for thoracic, orthopedic, and neurosurgical applications, and have been integrated into pediatric and neonatal ICU settings to reduce patient transport risk., In the early 2000s, Whitby et al compared SOC imaging (US) to a 0.17T (InnerVision MRI Ltd, London, UK) in 134 neonatal patients (89 controls & 43 with suspected pathology). In 56% (24/43) of patients, MRI provided additional clinical information beyond US findings. In 40% (17/43) of cases, the US read was normal, while MRI detected five subdural hematomas cases, five hypoxic ischemia cases, and seven additional findings. Whitby et al noted device cost (~£150,000 in the United Kingdom) and relative cost per treatment (~£60) were similar between US and MRI. More recently, Aspect Imaging received FDA clearance for their 1T Embrace neonatal MRI system, which is designed to be embedded in the NICU. Thiim et al compared the 1T system to US in the NICU and conventional 3T scanning with patient transport outside the NICU. Compared to US, the 1T scanner provided significant clinical benefit, with abnormal findings identified in 15 additional cases (1T MRI: 59, US: 44). The authors reported greater sensitivity to WM injury (1T MRI: 17, US: 7), hypoxic ischemia (1T MRI: 2, US: 0), and hemorrhage (1T MRI: 25, US: 20). For 32 patients, 3T comparison imaging was collected. Reports of brain injury were largely concordant between 3T and 1T, with two notable exceptions: one case of punctate susceptibility foci noted at 3T but not 1T and one polymicrogyria case noted at 1T but not 3T. Figure 8 illustrates example images of neonatal patients on the 1T scanner.

Portable very‐low‐field systems have also been applied to pediatric neuroimaging. Deoni et al described the first use of a portable 0.064T MRI to track neurodevelopment in a cohort of 42 healthy children (age range: 6 weeks to 16 years). The researchers calculated brain volume estimates for GM, WM, and CSF and replicated known developmental trajectories from 3T imaging studies. The authors reported greater scan success rates at 0.064T (89%) than 3T (75%), presumably related to the open bore design. However, researchers noted that some sequences and analytical software may require optimization to work in pediatric populations. The team's volumetric analyses were performed on T2w sequences, which offered superior anatomical contrast, instead of the T1w sequences typically used in morphometrics. WM myelination changes rapidly during childhood, and developing brains have higher water content in unmyelinated WM. Both water content and magnetic field strength influence tissue relaxivity properties., The researchers used sequences designed for adult imaging, which need to be optimized based on pediatric patient age to provide better tissue contrast. Additionally, the researchers utilized two common neuroimaging analysis software packages, Advanced Normalization Tools and FreeSurfer. They noted that FreeSurfer failed to process the low‐resolution data accurately, although this may improve with sequence optimization, super‐resolution approaches, and further software development., Finally, the researchers only replicated group‐level developmental trajectories, and it remains to be seen if accurate volume estimates can be obtained for individual patients.

The Deoni et al study highlights how expanded access to low‐cost scanners could change how large neuroimaging studies are conducted. These devices could enable larger sample sizes by reducing per patient scanning costs and shift recruitment focus away from academic hospitals in HICs to include more children from rural areas and LMICs. A group at Queen Elizabeth Central Hospital in Malawi recently reported scanning 260 patients with a 0.064T portable MRI, including examples of malarial encephalopathy and subdural empyema, a collection of purulent material around the brain. Research applying low‐field MRI in LMICs is likely to increase in coming years with increasing investment in the field.

Despite the many advantages lower‐field MRI offers for pediatric neuroimaging, there are significant barriers that must be overcome before the technology can be widely adopted (Table 5). Foremost, sequences, hardware, and analytic software need to be optimized for pediatric populations. Multiple researchers have reported that T1w and DWI sequences require quality improvements and optimization for pediatric patients.,, Many current lower‐field systems contain hardware designed for adults, which may require alterations for pediatric patients. Additionally, on scanners below mid‐field strength some sequences used for neurodevelopmental research are difficult to obtain, including functional, perfusion, and high‐angle‐diffusion sequences. In lower resolution images, it may be more feasible to place individuals on growth trajectories, measure macroscale volumes, and characterize patterns of neurodegeneration rather than to quantify the volume of smaller brain structures. Finally, because of the reduced SNR per unit time at lower magnetic field strengths, sequences are often longer, which reduces patient compliance and exacerbates motion issues.

Musculoskeletal Imaging

Orthopedics and musculoskeletal imaging (MSK) were early adopters of low‐field MRI and remain one of the few specialties in HICs where low‐field is relatively common in clinical practice today. Low‐field scanners are particularly attractive to orthopedics were metal implants are common and unique scanner designs (eg open bores, extremity specific scanners, and vertical scanners for weight‐bearing studies) offer more clinically tailored imaging. Several manufacturers, including FONAR, Esaote, and Paramed currently offer low‐field MRI scanners targeted at orthopedic and spinal applications. These devices focus on minimizing imaging costs or feature rotating tables which permit weight‐bearing and kinematic imaging. Unlike conventional closed‐bore systems, extremity specific and open bore scanner configurations permit central positioning of limbs in the magnetic field, which increases image quality. Although these advantages have given low‐field scanners some traction in orthopedics, due to their lower resolution they are predominantly used for niche applications.

While low‐field MRI offers a cost‐effective method for orthopedic imaging, there remain significant challenges that must be overcome before scanners become more widely adopted. The three primary obstacles are user perceptions of low‐field image quality, developing the full range of clinically necessary sequences, and loss of quality control by radiologists. User perception of image quality and its impact on diagnostic value is perhaps the most important problem facing lower‐field MRI. In the 1990s and early 2000s, low‐field MRI scanners were directly compared to standard high‐field systems across a range of orthopedic applications. In shoulder imaging, most studies found equivalent performance between scanners, with the notable exception of Magee et al, who reported that subsequent high‐field scans changed reviewer interpretations in 9/40 patients. However, as noted by Thomsen et al, their results were for a single low‐field system and may not generalize to low‐field devices more broadly. In knee imaging, most studies reported equivalence, although a meta‐analysis including 29 knee MRI studies identified a significant reduction in diagnostic performance for anterior cruciate ligament (ACL) tears. Low‐field scanners were evaluated for numerous other orthopedic applications, including the elbow, hand, and foot. While many studies reported equivalent diagnostic performance between low‐field and high‐field scanners, there remained significant concern that the lower SNR per unit time would translate to missed diagnoses and perhaps legal liability.

In the first report describing knee scans on the portable 0.064T scanner, raters visualized the quadriceps tendon, patellar tendon, and posterior cruciate ligament easily, but had more difficulty with the ACL, iliotibial band, medial collateral ligament, and lateral collateral ligament. Some sequences may need optimization to provide sufficient visualization of key knee anatomy. In the mid‐field range, Khodarahmi et al compared artifacts in 0.55T and 1.5T imaging of patients with hip implants. They found a 45%–64% reduction in image artifact when using 0.55T compared to 1.5T, even when 1.5T scanners used a slice encoding for metal artifact correction protocol, though there was a modest 17%–28% reduction in SNR at 0.55T.

Another challenge at low‐field is fat suppression, which increases contrast when evaluating cartilage, menisci, or bone marrow. Many fat suppression techniques rely on the chemical shift between lipids and water, which is proportional to magnetic field strength. Bellisari et al demonstrated a fat suppression technique on a 0.25T low‐field scanner and found comparable diagnostic performance to 1.5T (Fig. 9). Although this shows promise, such techniques may not transfer to even lower field strengths and represents only a single sequence among multiple that still need to be replicated and optimized for low‐field scanners.

As scanners become increasingly used by non‐radiologists and in nontraditional health care settings, there is significant concern that radiologists will lose quality control oversight or be unavailable for image interpretation. Portable, very‐low‐field devices could be deployed in field hospital or sports arena sidelines for musculoskeletal imaging. Guallart‐Naval et al reported the use of a 0.07T device to scan a patient with a knee implant in various nontraditional setting (eg indoors vs. outdoors) and conditions (eg power via wall outlet vs. gas generator). SNR was most affected in outdoor settings using gas generator power, although even under these conditions SNR was considered acceptable by the authors. Additionally, there was minimal artifact near the participant's knee implant in all imaging settings. Ownership of imaging quality control may need to be re‐evaluated as devices move to nontraditional settings.

The idea of providing diagnostic support to low‐field scanners in remote settings has been gaining traction. Raman et al used a neural network to perform binary classification of knee effusion in simulated low‐field images. Their network had comparable accuracy to radiologists (47.2% vs. 41.7%, respectively), indicating that such technology could provide diagnostic feedback when a physician is not readily available. Automated methods for segmenting knee anatomy at low‐field also show promise for providing diagnostic support. While this could further be mitigated by telehealth, it remains unclear how health systems will adapt to increased imaging outside the radiologist's realm.

Although lower‐field devices offer advantages for musculoskeletal imaging and have a demonstrated history in clinical practice, there are significant challenges that the field must still be overcome (Table 6). For more details on low‐field orthopedic applications, the authors recommend Ghazinoor et al.

Conclusion

In conclusion, we have reviewed potential clinical applications for lower‐field MRI, discussing how the technology can be deployed to complement existing high‐field devices and expand access to imaging where it was previously not economically feasible. When thinking about appropriate clinical applications, opportunities for lower‐field strength devices center around their advantages, most notably lower cost and portability. Although this review promotes the clinical translation of lower‐field scanners, we must acknowledge that there are outstanding questions surrounding the appropriate implementation of these devices which are scientific, practical, legal, ethical, economic, and cultural. How should new lower‐field scanners be integrated with other imaging in high‐resource settings? How should devices be utilized in low‐resource settings, where they may be the only option available? With the advent of portable systems, who will control point‐of‐care imaging? Can clinicians adjust their expectations around MRI and the level of image quality necessary to answer clinical questions? Can lower‐field devices be used for triage or will they simply contribute to more imaging? Finally, for the industry, does economic viability require broader use of lower‐field devices in HICs to support dissemination in lower‐resource settings? Despite the questions and challenges facing low‐field MRI, the technology demonstrates immense clinical promise with potential to increase medical imaging access and improve patient care worldwide.

Conflict Of Interest

Joel M. Stein has received support from sponsored research agreements with Hyperfine and consulting income from Centaur Diagnostics, Inc. Brian Litt is a co‐founder of Liminal Science and serves on the Medical and Scientific Advisory Boards of Hyperfine and as a result has equity in the company.

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