Medical Policy
Policy Num: 06.001.045
Policy Name: Positional Magnetic Resonance Imaging
Policy ID: [06.001.045] [Ar / B / M- / P-] [6.01.48]
Last Review: December 14, 2023
Next Review: Policy Archived
ARCHIVED
Related Policies:
06.001.039 - Dynamic Spinal Visualization and Vertebral Motion Analysis
Positional Magnetic Resonance Imaging
Population Reference No. | Populations | Interventions | Comparators | Outcomes |
1 | Individuals: · With position-dependent back or neck pain | Interventions of interest are: · Positional (eg, seated or standing) magnetic resonance imaging | Comparators of interest are: · Supine magnetic resonance imaging | Relevant outcomes include: · Test accuracy · Symptoms (eg, pain) · Functional outcomes · Quality of life |
Positional magnetic resonance imaging (MRI) permits imaging of a patient in various positions, including sitting and standing. This technology is being evaluated as a diagnostic tool for patients with position-dependent back pain.
For individuals who have position-dependent back or neck pain who receive positional MRI, the evidence includes comparative studies. Relevant outcomes are test accuracy, symptoms, functional outcomes, and quality of life. Comparisons of results from positional MRI with results from supine MRI or standing x-ray have indicated that positional MRI provides additional diagnostic data. However, no studies have been identified describing clinical outcomes of patients whose treatments were selected based on these new data. The clinical benefit of basing treatment decisions, including surgery, on these additional findings needs to be established. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
Not applicable.
The objective of this evidence review is to determine whether the use of positional magnetic resonance imaging improves the net health outcome in patients who have back or neck pain compared with supine magnetic resonance imaging.
Positional (nonrecumbent) magnetic resonance imaging is considered investigational, including its use in the evaluation of individuals with cervical, thoracic, or lumbosacral back pain.
Currently, there is no way to signify with coding that a magnetic resonance imaging (MRI) is open or positional. The service would be coded using the CPT code for the MRI scan (eg, codes 72141-72158 for MRI of the spine, codes 73221-73223 for any joint of the upper extremity).
See the Codes table for details.
BlueCard/National Account Issues
State or federal mandates (eg, Federal Employee Program) may dictate that certain U.S. Food and Drug Administration approved devices, drugs, or biologics may not be considered investigational, and thus these devices may be assessed only by their medical necessity.
Benefits are determined by the group contract, member benefit booklet, and/or individual subscriber certificate in effect at the time services were rendered. Benefit products or negotiated coverages may have all or some of the services discussed in this medical policy excluded from their coverage.
Determining the cause of back pain is a complex task. In some patients, extensive evaluation with various imaging modalities does not lead to a definitive diagnosis. Some studies have suggested that imaging the body in various positions with "loading" of the spine may lead to more accurate diagnoses. This loading can be accomplished by having the patient sit or stand upright. Also, imaging can be completed with the patient in the position that causes the symptom(s). This theory is being evaluated in suspected nerve root compression and in some cases of spondylolisthesis.
An open magnetic resonance imaging (MRI) system has been developed that allows imaging of a patient in various positions. Imaging can be conducted with partial or full weight-bearing. Dynamic-kinetic imaging (images obtained during movement) can also be obtained with this system. Conventional MRI of the spine is typically completed with a patient in a recumbent position. Weight-bearing can be simulated by imaging in the supine position with a special axial loading device.
One concern with positional MRI is the field strength of the scanners. Today's clinical MRI scanners may operate at a field strength between 0.1 to 3 tesla (T), and are classified as either low-field (<0.5 T), mid-field (0.5 to 1.0 T), or high-field (>1.0 T). Low-field MRI is typically used in open scanners. Open scanners are designed for use during interventional or intraoperative procedures, when a conventional design is contraindicated (eg, an obese or claustrophobic patient), or for changes in patient positioning.
In general, higher field strength results in an increase in signal-to-noise ratio, spatial resolution, contrast, and speed. Thus, low-field scanners produce poorer quality images compared with high-field scanners, and longer acquisition times with low-field scanners increases the possibility of image degradation due to patient movement. However, field strength has less of an effect on the contrast-to-noise ratio, which determines the extent to which adjacent structures can be distinguished from one another.
Several MRI systems have been cleared for marketing by the U.S. Food and Drug Administration (FDA) through the 510(k) process as open or total body systems for positional imaging. One such system is FONAR's Upright® MRI. FDA product code: LNH.
This evidence review was created in February 2007 and has been updated regularly with searches of the PubMed database. The most recent literature update was performed through July14, 2023.
Evidence reviews assess whether a medical test is clinically useful. A useful test provides information to make a clinical management decision that improves the net health outcome. That is, the balance of benefits and harms is better when the test is used to manage the condition than when another test or no test is used to manage the condition.
Promotion of greater diversity and inclusion in clinical research of historically marginalized groups (e.g., People of Color [African-American, Asian, Black, Latino and Native American]; LGBTQIA (Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, Asexual); Women; and People with Disabilities [Physical and Invisible]) allows policy populations to be more reflective of and findings more applicable to our diverse members. While we also strive to use inclusive language related to these groups in our policies, use of gender-specific nouns (e.g., women, men, sisters, etc.) will continue when reflective of language used in publications describing study populations.”
The first step in assessing a medical test is to formulate the clinical context and purpose of the test. The test must be technically reliable, clinically valid, and clinically useful for that purpose. Evidence reviews assess the evidence on whether a test is clinically valid and clinically useful. Technical reliability is outside the scope of these reviews, and credible information on technical reliability is available from other sources.
The purpose of positional magnetic resonance imaging (MRI) in patients with position-dependent back or neck pain is to inform a decision whether the pain can be attributed to changes in the spinal canal. For example, pressure on the spinal cord from a herniated disc may be increased with sitting when compared to standing.
The question addressed in this evidence review is: Does the use of positional MRI improve the net health outcome in patients who have position-dependent back or neck pain?
The following PICO was used to select literature relevant to the review.
The relevant population of interest are individuals being evaluated for position-dependent back or neck pain.
The intervention is positional MRI using seated or standing positions in neutral, extension, and flexion. Positional MRI is administered by referral to a spine specialist in back and neck pain.
The following test is currently being used to make decisions about managing position-dependent back or neck pain: conventional supine MRI, which is the reference standard. Studies comparing positional MRI with loaded supine MRI are also of interest.
In evaluating this approach to imaging, it is important to determine whether MRI adds actionable diagnostic information. However, it is also important to determine whether treatment of these additional findings results in improved outcomes. This additional step is important given reported concerns about described false-positive findings with MRI of the spine. For example, Jarvik et al (2001) reported that many MRI findings have a high prevalence in subjects without low back pain and that findings such as bulging discs and disc protrusion are of limited diagnostic use.1, The authors also reported that the less common findings of moderate or severe central stenosis, root compression, and disc extrusion were more likely to be clinically relevant. The health outcomes of interest include symptoms (eg, pain), self-reported functional outcomes, and quality of life measures.
The optimum interval to examine health outcomes would be after healing of surgical intervention, typically at 3 to 12 months postprocedure.
For the evaluation of the clinical validity of positional MRI, studies that met the following eligibility criteria were considered:
Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores)
Included a suitable reference standard (describe the reference standard)
Patient/sample clinical characteristics were described
Patient/sample selection criteria were described
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).
Dahabreh et al (2011) conducted a systematic review for the Agency for Healthcare Research and Quality that assessed emerging MRI technologies for musculoskeletal imaging under loading stress.2, Included were 36 studies that used positional weight-bearing MRI in patients with musculoskeletal conditions. Also included were studies evaluating axial compression devices. Most studies were cross-sectional or had case-control designs. The most commonly imaged body region was the lumbar spine. Four identified studies of lumbar spine imaging compared positional weight-bearing MRI with conventional MRI, myelography, or non-weight-bearing imaging in the same MRI device; however, these studies did not report the effect of the technology on patient outcomes. Two studies of foot imaging that compared weight-bearing MRI with MRI in the supine position with the same MRI device found that the 2 techniques provided similar information. Two studies of knee joint imaging found differences between weight-bearing MRI and non-weight-bearing MRI using the same device; no functional outcomes were reported. The potential effect on image quality of low magnetic field strengths (£0.6 tesla [T]) in weight-bearing MRI scanners was not assessed. Key studies not included in the systematic review are described next.
Lao et al (2014) and Lord et al (2014) both published systematic reviews assessing the literature on positional (kinetic) MRI, which consists primarily of examining anatomic changes in neutral, flexion, extension, and axial rotation.3,4, Kinetic MRI studies in healthy and symptomatic individuals identified changes in neuroforaminal size, cord compression, cord length, cross-sectional area, ligamentum flavum thickness, and motion at the index and adjacent levels.
Ferreiro Perez et al (2007) compared recumbent with upright sitting positions in 89 patients who had disc herniation or spondylolisthesis (cervical or lumbar spine).5, Using a 0.6-T Upright MRI system for both positions, pathology (disc herniation or spondylolisthesis) was identified in 68 (76%) patients. Images from 18 (20%) patients were not interpretable due to motion artifact. Pathologic features were better identified (ie, either only evident or seen to be enlarged) in 52 (76%) of the 68 patients when in the sitting position; 10 of these were only observed in the sitting position. Pathologic features were better identified in the recumbent position in 11 (16%) of the 68 patients. The overall underestimation rate was calculated to be 62% for patients in the recumbent position and 16% for those in the upright-seated position. This research would suggest that there may be advantages when the position during imaging is matched with the positional symptoms of the patient. However, a more appropriate comparison group would be a standard recumbent clinical MRI system (eg, field strength >0.6 T). In addition, technical problems with motion artifact were due to poor stabilization in an upright sitting position.
In a study by Tarantino et al (2013), 57 patients with low back pain when standing (50% also had back pain in the supine position) received an MRI in both upright and recumbent positions using a 0.25-T tilting system.6, A table tilt of 82° was used to reproduce the orthostatic position without the patient instability associated with standing at 90°. Compared with the supine position, there was a significant decrease in intervertebral disc thickness (11.2 mm vs. 12.9 mm) along with changes in other measures and a qualitative increase in the volume of disc protrusions and/or spondylolisthesis in the upright position.
In a study by Charoensuk et al (2021), 54 patients suspected of having spinal stenosis underwent both standing MRI and MRI plus axial loading using a compression device.7, Primary outcome measures included measures of the intervertebral disc (ie, cross-sectional area [DA], disc height [DH], and anteroposterior distance [DAP]), dural sac (cross-sectional area [DCSA]), spinal curvature (ie, lumbar lordosis [LL] and L1-L3-L5 angle [LA]), and total lumbar spine height (LH). Results showed that there was a major difference observed with LL, but minor differences observed in DCSA, DAP, DA, LA, and LH. This suggests that the standing position might be adequately simulated while recumbent by utilizing an axial-loaded MRI using a compression device.
A study by Madsen et al (2008) compared vertical (standing) MRI with recumbent MRI plus axial loading in patients who had lumbar spinal stenosis.8, Sixteen patients with neurogenic claudication, experienced mainly during walking or in an erect position, were recruited for this phase of the study. Each patient underwent 4 scans with a 0.6-T Upright MRI system, consisting of vertical, horizontal with compression at a load of 40% of body weight, horizontal with no load, and horizontal with a 50% axial load. All horizontal scans were conducted with a cushion placed below the lower back to induce the extension of the lumbar spine. Results showed a similar DCSA between the 2 positions, suggesting that the standing position might be adequately simulated while recumbent by axial loading and lordosis. Results were not correlated with patient symptoms in this study.
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, more effective therapy, or avoid unnecessary testing or therapy.
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from randomized controlled trials (RCTs).
No evidence from RCTs was identified to support the use of positional MRI for position-dependent back or neck pain. Moreover, the systematic review by Dahabreh et al (2011) concluded that, despite a large number of available studies, considerable uncertainty remained about the utility of this technique for the clinical management of musculoskeletal conditions.2,
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility.
Because the clinical validity of positional MRI for diagnosis of position-dependent back or neck pain has not been established, a chain of evidence cannot be constructed.
For individuals who have position-dependent back or neck pain who receive positional MRI, the evidence includes comparative studies. Relevant outcomes are test accuracy, symptoms, functional outcomes, and quality of life. Comparisons of results from positional MRI with results from supine MRI or standing x-ray have indicated that positional MRI provides additional diagnostic data. However, no studies have been identified describing clinical outcomes of patients whose treatments were selected based on these new data. The clinical benefit of basing treatment decisions, including surgery, on these additional findings needs to be established. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
[ ] Medically Necessary | [X] Investigational |
The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.
While the various physician specialty societies and academic medical centers may collaborate with and make recommendations during this process, through the provision of appropriate reviewers, input received does not represent an endorsement or position statement by the physician specialty societies or academic medical centers, unless otherwise noted.
In response to requests, input was received from 1 physician specialty society and 1 academic medical center while the policy was under review in 2008. Both reviewers agreed that positional magnetic resonance imaging is considered investigational.
Guidelines or position statements will be considered for inclusion in ‘Supplemental Information’ if they were issued by, or jointly by, a US professional society, an international society with US representation, or National Institute for Health and Care Excellence (NICE). Priority will be given to guidelines that are informed by a systematic review, include strength of evidence ratings, and include a description of management of conflict of interest.
No guidelines or statements were identified.
Not applicable.
There is no national coverage determination. In the absence of a national coverage determination, coverage decisions are left to the discretion of local Medicare carriers.
A search of ClinicalTrials.gov in July 2023 did not identify any ongoing or unpublished trials that would likely influence this review.
Codes | Number | Description |
---|---|---|
CPT | No specific code to indicate positional, code range in Policy Guidelines Section | |
72141 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, cervical; without contrast material | |
72142 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, cervical; with contrast material(s) | |
72146 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, thoracic; without contrast material | |
72147 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, thoracic; with contrast material(s) | |
72148 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, lumbar; without contrast material | |
72149 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, lumbar; with contrast material(s) | |
72156 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, without contrast material, followed by contrast material(s) and further sequences; cervical | |
72157 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, without contrast material, followed by contrast material(s) and further sequences; thoracic | |
72158 | Magnetic resonance (eg, proton) imaging, spinal canal and contents, without contrast material, followed by contrast material(s) and further sequences; lumbar | |
73221 | Magnetic resonance (eg, proton) imaging, any joint of upper extremity; without contrast material(s) | |
73222 | Magnetic resonance (eg, proton) imaging, any joint of upper extremity; with contrast material(s) | |
73223 | Magnetic resonance (eg, proton) imaging, any joint of upper extremity; without contrast material(s), followed by contrast material(s) and further sequences | |
ICD-10-CM | Investigational for all diagnoses | |
M45.0-M45.9 | Ankylosing spondylitis code range | |
M47.01-M47.9 | Spondylosis code range | |
M50.00-M50.93 | Cervical disc disorders code range | |
M51.04-M51.9 | Thoracic, thoracolumbar, and lumbosacral intervertebral disc disorders code range | |
M51.A0 | Intervertebral annulus fibrosus defect, lumbar region, unspecified size | |
M51.A1 | Intervertebral annulus fibrosus defect, small, lumbar region | |
M51.A2 | Intervertebral annulus fibrosus defect, large, lumbar region | |
M51.A3 | Intervertebral annulus fibrosus defect, lumbosacral region, unspecified size | |
M51.A4 | Intervertebral annulus fibrosus defect, small, lumbosacral region | |
M51.A5 | Intervertebral annulus fibrosus defect, large, lumbosacral region | |
M54.00-M54.9 | Dorsalgia code range | |
ICD-10-PCS | ICD-10-PCS codes are only used for inpatient services. There is no specific ICD-10-PCS code for this imaging.The following codes might be used. | |
BR30Y0Z, BR30YZZ, BR30ZZZ, BR31Y0Z, BR31YZZ, BR31ZZZ, BR32Y0Z, BR32YZZ, BR32ZZZ, BR33Y0Z, BR33YZZ, BR33ZZZ, BR37Y0Z, BR37YZZ, BR37ZZZ, BR39Y0Z, BR39YZZ, BR39ZZZ | Imaging, axial skeleton, magnetic resonance imaging (MRI), code by body part, use of contrast and whether enhanced or not | |
Type of service | Radiology | |
Place of service | Outpatient/inpatient |
Date | Action | Description |
12/14/23 | Replace Policy | Policy archived. |
10/12/23 | Annual Review | Policy updated with literature review through July 14, 2023; no references added. Policy statement unchanged. |
10/05/22 | Annual Review | Policy updated with literature review through August 10, 2022; references added. Minor editorial refinements to policy statements; intent unchanged |
10/05/21 | Annual Review | Policy updated with literature review through July 20, 2021; no references added. Policy statement unchanged. |
10/13/20 | Annual Review | Policy updated with literature review through July 17, 2020; no references added. Policy statement unchanged. |
10/01/19 | Annual Review | Policy updated with literature review through July 8, 2019; no references added. Policy statement unchanged |
10/19/17 | | |
06/09/16 | | |
09/22/15 | | |
04/30/14 | | |
04/17/13 | | |
10/25/10 | Created | New policy |