Aetna considers magnetic resonance imaging (MRI) and computed tomography (CT) of the spine medically necessary when any of the following criteria is met:
Aetna considers MRI and CT of the spine experimental and investigational for all other indications because their clinical value for indications other than the ones listed above has not been established. Clinical guidelines, including those from the Agency for Healthcare Policy and Research, have consistently recommended against routine imaging studies for acute low back pain (Cho et al, 2009).
Aetna considers dynamic-kinetic MRI experimental and investigational for evaluation of the cervical spine because its effectiveness has not been established.
* Conservative therapy = moderate activity, analgesics, non-steroidal anti-inflammatory drugs, muscle relaxants.
Because of its complexity, the spine is probably the most difficult part of the skeletal system to evaluate radiologically. Improvement of computed tomography (CT) scanners and the advent of magnetic resonance imaging (MRI) have changed the approach to diagnostic imaging of the spine. Previously, invasive modalities were required to obtain information that is now available with non-invasive technologies.
The appropriate use of these new technologies is still somewhat unsettled. The focus is on which test will provide the most accurate and cost effective diagnostic information for each particular clinical situation. Computed tomographic scan, CT myelography, MRI and plain radiography all have their place in the diagnostic work-up of problems related to the spine.
Bulging intervertebral discs have been found in over half of all otherwise asymptomatic adults. It is therefore, important to perform MRI or CT at the right time and to interpret the results in the context of the clinical findings to ensure an accurate diagnosis and avoid unnecessary treatment of conditions that may not be the cause of a patient's symptoms.
According to accepted guidelines, MRI is the preferred method of imaging for each of the medically necessary indications listed in the Policy section, with the exception of (i) suspected spinal fracture or dislocation due to trauma, where CT scan is the preferred method of imaging if plain films are inconclusive, and (ii) evaluation of a patient with signs or symptoms of spinal stenosis, where MRI or CT are equally appropriate. For evaluation of recurrent symptoms after spinal surgery, MRI with and without gadolinium enhancement, is the preferred method of imaging.
Magnetic resonance imaging or CT evaluation of chronic mechanical low back pain (LBP) without radiculopathy or neurologic deficit, trauma, or clinical suspicion of systemic disorder (e.g., infectious process, metastatic disease) is not necessary unless back pain is severe (e.g., requiring hospitalization) or where symptoms are progressing despite conservative management (ICSI, 2002).
The American College of Physicians (2012) has recommended against obtaining imaging studies in patients with non-specific low back pain. In patients with back pain that cannot be attributed to a specific disease or spinal abnormality following a history and physical examination (e.g., non-specific low back pain), imaging with plain radiography, computed tomography (CT) scan, or magnetic resonance imaging (MRI) does not improve patient outcomes. The American Academy of Family Physicians (2012) recommends against do imaging for low back pain within the first six weeks, unless red flags are present. Red flags include, but are not limited to, severe or progressive neurological deficits or when serious underlying conditions such as osteomyelitis are suspected. Imaging of the lower spine before six weeks does not improve outcomes, but does increase costs. Low back pain is the fifth most common reason for all physician visits. The North American Spine Society (2013) has issued similar recommendations.
Cho et al (2009) reported the results of a systematic review and meta-analysis of imaging strategies for LBP without indications of serious underlying conditions. Inclusion criteria were randomized controlled trials that compared immediate, routine lumbar imaging (or routine provision of imaging findings) versus usual clinical care without immediate lumbar imaging (or not routinely providing results of imaging) for LBP without indications of serious underlying conditions. Primary outcomes were improvement in pain or function. Secondary outcomes were improvement in mental health, quality of life, patient satisfaction, and overall improvement. Outcomes were categorized as short-term (less than or equal to 3 months), long-term (greater than 6 months to less than or equal to 1 year), or extended (greater than 1 year). A total of 6 trials met the inclusion criteria: 4 assessed lumbar radiography and 2 assessed MRI or CT. Duration of follow-up ranged from 3 weeks to 2 years. One trial excluded patients with sciatica or other symptoms of radiculopathy, and 1 did not report the proportion of patients with such symptoms. In the other 4 trials, the proportion of patients with sciatica or radiculopathy ranged from 24 % to 44 %. Three trials compared immediate lumbar radiography with usual clinical care without immediate lumbar radiography, and 1 compared immediate lumbar radiography with a brief education intervention plus lumbar radiography, if no improvement was seen by 3 weeks. Patients (n = 1,804) enrolled in these trials had mainly acute or subacute (less than 12 weeks) LBP, and all trials were done in primary-care or urgent-care settings. Two studies assessed advanced imaging modalities. One study compared immediate MRI or CT with usual clinical care without advanced imaging in patients with mainly chronic LBP (82 % had LBP for greater than 3 months) referred to a surgeon, whereas in the other study all patients with LBP for less than 3 weeks underwent MRI, with randomization to routine notification of results within 48 hours versus notification of results only if clinically indicated. Patients were recruited from various settings (primary care, spine clinic, or emergency room). In both trials, the proportion of patients who underwent lumbar radiography before enrollment was not reported. The most frequent methodological shortcoming was lack of (or unclear use of) blinded outcome assessment (5 of 6 trials), followed by inadequate description of randomization method (4 of 6 trials). All trials excluded patients with features suggestive of a serious underlying condition, but exclusion criteria varied and trials did not indicate the number of patients excluded because of such factors. The authors found no significant difference between routine, immediate lumbar imaging and usual clinical care without immediate imaging for improvement in pain or function at short-term or long-term follow-up. In the trial that reported extended (2-year) follow-up data, immediate MRI or CT was not better than usual clinical care without immediate imaging on either the EuroQol-5D (mean difference 0.02, 95 % confidence interval: -0.02 to 0.07, 0 to 1 scale) or the SF-36 mental health score (-1.50, -4.09 to 1.09, 0 to 100 scale) in unadjusted analyses. The authors concluded that lumbar imaging forLBP without indications of serious underlying conditions does not improve clinical outcomes and that clinicians should refrain from routine, immediate lumbar imaging in patients with acute or subacute LBP and without features suggesting a serious underlying condition.
In a meta-analysis, Schoenfeld et al (2010) examined if adding an MRI would provide useful information that alters treatment when a CT scan reveals no evidence of injury in obtunded blunt trauma patients. Published studies from 2000 to 2008 involving patients undergoing MRI for the purposes of further cervical spine evaluation after a "negative" CT scan were identified via a literature search of online databases. Data from eligible studies were pooled and original scale meta-analyses were performed to calculate overall sensitivity, specificity, positive and negative predictive values, likelihood ratios, and relative risk. The Q-statistic p value was used to evaluate heterogeneity. A total of 11 studies met the inclusion criteria, yielding data on 1,550 patients with a negative CT scan after blunt trauma subsequently evaluated with a MRI. The MRI detected abnormalities in 182 patients (12 %). Ninety traumatic injuries were identified, including ligamentous injuries (86/182), fractures and dislocations (4/182). In 96 cases (6 % of the cohort), the MRI identified an injury that altered management. Eighty-four patients (5 %) required continued collar immobilization and 12 (1 %) required surgical stabilization. The Q-statistic p value for heterogeneity was 0.99, indicating the absence of heterogeneity among the individual study populations. The authors concluded that reliance on CT imaging alone to "clear the cervical spine" after blunt trauma can lead to missed injuries. The findings of this study supported the addition of MRI in evaluating patients who are obtunded, or unexaminable, despite a negative CT scan.
Callaghan et al (2012) examined diagnostic practice patterns as an early step in identifying opportunities to improve efficiency of care of patients with peripheral neuropathy. The 1996 to 2007 Health and Retirement Study Medicare claims-linked database was used to identify individuals with an incident diagnosis of peripheral neuropathy using International Classification of Diseases, Ninth Revision, codes and required no previous neuropathy diagnosis during the preceding 30 months. Focusing on 15 relevant tests, these investigators examined the number and patterns of tests and specific test utilization 6 months before and after the incident neuropathy diagnosis. Medicare expenditures were assessed during the baseline, diagnostic, and follow-up periods. Of the 12,673 patients, 1,031 (8.1 %) received a new International Classification of Diseases, Ninth Revision, diagnosis of neuropathy and met the study inclusion criteria. Of the 15 tests considered, a median of 4 (interquartile range, 2 to 5) tests were performed, with more than 400 patterns of testing. Magnetic resonance imaging of the brain or spine was ordered in 23.2 % of patients, whereas a glucose tolerance test was rarely obtained (1.0 %). Mean Medicare expenditures were significantly higher in the diagnostic period than in the baseline period ($14,362 versus $8,067, p < 0.001). The authors concluded that patients diagnosed as having peripheral neuropathy typically undergo many tests, but testing patterns are highly variable. Almost 25 % of patients receiving neuropathy diagnoses undergo high-cost, low-yield MRI, whereas few receive low-cost, high-yield glucose tolerance tests. Expenditures increase substantially in the diagnostic period. The authors stated that more research is needed to define effective and efficient strategies for the diagnostic evaluation of peripheral neuropathy.
Also, an UpToDate review on "Overview of polyneuropathy" (Rutkove, 2012) does not mention the use of MRI or CT in the diagnostic evaluation of individuals with polyneuropathy.
The Institute for Clinical Systems Improvement clinical practice guideline on “Adult acute and subacute low back pain” (ICSI, 2012) stated that imaging (CT, MRI, or x-ray) is not recommended for non-specific low-back pain [strong recommendation, moderate quality evidence].
el Barzouhi et al (2013) noted that MRI is frequently performed during follow-up in patients with known lumbar-disk herniation and persistent symptoms of sciatica. The association between findings on MRI and clinical outcome is controversial. These investigators studied 283 patients in a randomized trial comparing surgery and prolonged conservative care for sciatica and lumbar-disk herniation. Patients underwent MRI at baseline and after 1 year. These researchers used a 4-point scale to assess disk herniation on MRI, ranging from 1 for "definitely present" to 4 for "definitely absent". A favorable clinical outcome was defined as complete or nearly complete disappearance of symptoms at 1 year. These investigators compared proportions of patients with a favorable outcome among those with a definite absence of disk herniation and those with a definite, probable, or possible presence of disk herniation at 1 year. The area under the receiver-operating-characteristic (ROC) curve was used to assess the prognostic accuracy of the 4-point scores regarding a favorable or unfavorable outcome, with 1 indicating “perfect discriminatory value” and 0.5 or less indicating “no discriminatory value”. At 1 year, 84 % of the patients reported having a favorable outcome. Disk herniation was visible in 35 % with a favorable outcome and in 33 % with an unfavorable outcome (p = 0.70). A favorable outcome was reported in 85 % of patients with disk herniation and 83 % without disk herniation (p = 0.70). Assessment of disk herniation by means of MRI did not distinguish between patients with a favorable outcome and those with an unfavorable outcome (area under ROC curve, 0.48). The authors concluded that MRI performed at 1-year follow-up in patients who had been treated for sciatica and lumbar-disk herniation did not distinguish between those with a favorable outcome and those with an unfavorable outcome. Moreover, they stated that further research is needed to evaluate the value of MRI in clinical decision-making for patients with persistent or recurrent sciatica.
Steffens et al (2014) systematically reviewed whether MRI findings of the lumbar spine predict future LBP in different samples with and without LBP. MEDLINE, CINAHL and EMBASE databases were searched. Included were prospective cohort studies investigating the relationship between baseline MRI abnormalities of the lumbar spine and clinically important LBP outcome at follow-up. These researchers excluded cohorts with specific diseases as the cause of their LBP. Associations between MRI findings and LBP pain outcomes were extracted from eligible studies. A total of 12 studies met the inclusion criteria; 6 studies presented data on participants with current LBP; 1 included a sample with no current LBP, 3 included a sample with no history of LBP and 2 included mixed samples. Due to small sample size, poor overall quality and the heterogeneity between studies in terms of participants, MRI findings and clinical outcomes investigated, it was not possible to pool findings. No consistent associations between MRI findings and outcomes were identified. Single studies reported significant associations for Modic changes type 1 with pain, disc degeneration with disability in samples with current LBP and disc herniation with pain in a mixed sample. The authors concluded that the limited number, heterogeneity and overall quality of the studies do not permit definite conclusions on the association of MRI findings of the lumbar spine with future LBP
Weber et al (2014) evaluated the incremental diagnostic value of spine MRI evaluated separately from and combined with sacroiliac joint (SIJ) MRI in non-radiographic axial spondyloarthritis (nr-axSpA) compared with SIJ MRI alone. The study sample comprised 2 independent cohorts A/B of 130 consecutive patients aged less than or equal to 50 years with back pain, newly referred to 2 university clinics, and 20 healthy controls. Patients were classified according to clinical examination and pelvic radiographs as having nr-axSpA (n = 50), ankylosing spondylitis (n = 33), or non-specific back pain (n = 47). Four readers assessed SIJ and spine MRI separately 6 months apart, and 1 to 12 months later both scans simultaneously using standardized modules. Readers recorded presence/absence of SpA and their level of confidence in this conclusion on a 0 to 10 scale (0 = definitely not; 10 = definite). These researchers analyzed differences between SIJ MRI versus spine MRI alone, and SIJ MRI alone versus combined MRI, descriptively by the number/percentage of subjects according to the mean of 4 readers. In cohorts A/B, 15.8 %/24.2 % of patients with nr-axSpA having a negative SIJ MRI were re-classified as being positive for SpA by global evaluation of combined scans. However, 26.8 %/11.4 % of non-specific back pain controls and 17.5 % of healthy volunteers with a negative SIJ MRI were falsely re-classified as having SpA by combined MRI. Low confidence in a diagnosis of SpA by SIJ MRI increased to high confidence by combined MRI in 6.6 %/7.3 % of patients with nr-axSpA. The authors concluded that combined spine and SIJ MRI added little incremental value compared with SIJ MRI alone for diagnosing patients with nr-axSpA and enhancing confidence in this diagnosis.
On behalf of the Tufts Medical Center Evidence-based Practice Center, Dahabreh and colleagues (2011) performed a systematic review of emerging MRI technologies for musculoskeletal imaging under loading stress for the Agency for Healthcare Research and Quality (AHRQ). The review included 57 studies about MRI under physiologic loading stress performed in an upright or sitting position or under axial loading by using a compression device. The most commonly imaged regions were the spine (33 studies) and knee (13 studies). Most studies had a cross-sectional (n = 37) or case-control (n = 13) design and reported on anatomical measurements rather than patient-relevant end points. Studies were generally small: The median (25th, 75th percentile) number of case patients was 26 (17, 45), and the median (25th, 75th percentile) number of control participants was 13 (12, 20 for case-control studies). Fifteen of 57 studies used at least 2 imaging tests and reported on diagnostic or patient-relevant outcomes, but did not report meaningful information on the relative performance of the tests. In 10 studies that included information on adverse effects, 5 % to 15 % of participants reported new-onset or worsening pain and neuropathy during MRI under loading stress. The authors concluded that available evidence is insufficient to support the clinical utility of MRI under loading stress for musculoskeletal conditions.
Lord et al (2014) reviewed the body of literature related to kinetic MRI (kMRI) of the cervical spine. A review of literature related to kMRI was performed using PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. These researchers included 16 prospective and retrospective studies of symptomatic and asymptomatic patients who underwent kMRI of the cervical spine. The authors concluded that data suggested that kMRI is able to provide meaningful information regarding changes in the cervical spine in both normal and pathologic segments. Moreover, they stated that a prospective study comparing MRI and kMRI is needed to confirm clinically utility of this technology.
Also, an UpToDate review on “Evaluation of the patient with neck pain and cervical spine disorders” (Isaac and Anderson, 2014) states that “Magnetic resonance imaging (MRI) should be the first-line imaging study performed in patients with progressive signs or symptoms of neurologic disease. MRI should also be obtained if there is a suspicion for infection or malignancy and if there are moderate to severe neck symptoms beyond six weeks, even if plain films are negative …. A non-contrast MRI is sufficient in the majority of cases. The addition of gadolinium contrast intravenously allows better diagnosis of infection, tumor, or post-surgical epidural fibrosis, and can be ordered subsequently if the non-contrast study is inconclusive”. It does not mention the use of dynamic-kinetic MRI.
|CPT Codes / HCPCS Codes / ICD-10 Codes|
|Information in the [brackets] below has been added for clarification purposes.  Codes requiring a 7th character are represented by "+":|
|ICD-10 codes will become effective as of October 1, 2015 :|
|CPT codes covered if selection criteria are met:|
|72125||Computed tomography, cervical spine; without contrast material|
|72126||with contrast material|
|72127||without contrast material, followed by contrast material(s) and further sections|
|72128||Computed tomography, thoracic spine; without contrast material|
|72129||with contrast material|
|72130||without contrast material, followed by contrast material(s) and further sections|
|72131||Computed tomography, lumbar spine; without contrast material|
|72132||with contrast material|
|72133||without contrast material, followed by contrast material(s) and further sections|
|72141||Magnetic resonance (e.g., proton) imaging, spinal canal and contents, cervical; without contrast material|
|72142||with contrast material(s)|
|72146||Magnetic resonance (e.g., proton) imaging, spinal canal and contents, thoracic; without contrast material|
|72147||with contrast material(s)|
|72148||Magnetic resonance (e.g., proton) imaging, spinal canal and contents, lumbar; without contrast material|
|72149||with contrast material(s)|
|72156||Magnetic resonance (e.g., proton) imaging, spinal canal and contents, without contrast material, followed by contrast material(s) and further sequences; cervical|
|Other CPT codes related to the CPB:|
|76390||Magnetic resonance spectroscopy|
|HCPCS codes covered if selection criteria are met:|
|A9575||Injection, gadoterate meglumine, 0.1 ml|
|A9576||Injection, gadoteridol, (ProHance multipack), per ml|
|A9577||Injection, gadobenate dimeglumine (MultiHance), per ml|
|A9578||Injection, gadobenate dimeglumine (MultiHance multipack), per ml|
|A9579||Injection, gadolinium based magnetic resonance contrast agent, not otherwise specified, per ml|
|Q9953||Injection, iron-based magnetic resonance contrast agent, per ml|
|Q9954||Oral magnetic resonance contrast agent, per 100 ml|
|ICD-10 codes covered if selection criteria are met:|
|A18.01, A18.03||Tuberculosis of spine and other bones|
|C41.2||Malignant neoplasm of vertebral column|
|C41.4||Malignant neoplasm of pelvic bones, sacrum, and coccyx|
|C70.1||Malignant neoplasm of spinal meninges|
|C72.0 - C72.1||Malignant neoplasm of spinal cord|
|C79.51 - C79.52||Secondary malignant neoplasm of bone and bone marrow|
|D16.6||Benign neoplasm of vertebral column, excluding sacrum and coccyx|
|D16.8||Benign neoplasm of pelvic bones, sacrum and coccyx|
|D32.1||Benign neoplasm of spinal meninges|
|D33.4||Benign neoplasm of spinal cord|
|D42.0 - D42.9||Neoplasm of uncertain behavior of meninges|
|D43.0 - D43.2, D43.4||Neoplasm of uncertain behavior of brain and spinal cord|
|D48.0||Neoplasm of uncertain behavior of bone and articular cartilage|
|D48.1 - D48.2||Neoplasm of uncertain behavior of connective and other soft tissue|
|G00.0 - G03.9||Meningitis|
|G04.00 - G04.91||Encephalitis, myelitis, and encephalomyelitis|
|G06.1||Intraspinal abscess and granuloma|
|G11.0 - G12.9||Spinocerebellar disease, anterior horn cell disease, and other diseases of spinal cord|
|G56.00 - G56.92
G58.0 - G58.9
|Mononeuritis of upper limb and mononeuritis multiplex|
|G57.00 - G57.92||Mononeuritis of lower limb and unspecified site|
|G83.4||Cauda equina syndrome|
|M40.00 - M41.9||Kyphosis and lordosis|
|M46.20 - M46.39, M86.08, M86.18
M86.28, M86.38, M86.48, M86.58
M86.68, M86.8x8, M86.9, M89.68
|Osteomyelitis, periostitis, and other infections involving bone, other specified sites|
|M48.00 - M48.09||Spinal stenosis|
|M50.00 - M50.03
M51.04 - M51.07
|Intervertebral disc disorder with myelopathy|
|M50.10 - M50.13||Cervical disc disorder with radiculopathy|
|M50.20 - M50.23, M50.90 - M50.93
M51.24 - M51.27
|Displacement of intervertebral disc|
|M51.14 - M54.17, M54.14 - M54.17||Thoracic or lumbosacral neuritis or radiculopathy, unspecified|
|M54.10 - M54.18, M79.2||Neuralgia, neuritis, and radiculitis, unspecified|
|M54.30 - M54.32||Sciatica|
|M54.40 - M54.5||Lumbago|
|Q04.9, Q06.9, Q07.9||Congenital malformations of brain, spinal cord, and nervous system, unspecified|
|Q05.0 - Q05.9||Spina bifida|
|Q06.0 - Q06.9||Other congenital malformations of spinal cord|
|Q07.0 - Q07.9||Other congenital malformations of nervous system|
|Q27.9||Congenital malformation of peripheral vascular system, unspecified|
|Q76.0 - Q76.49||Congenital malformations of spine|
|S12.000+ - S12.9xx+
S22.000+ - S22.089+
S32.000+ - S32.2xx+
|Fracture of vertebral column|
|S13.100+ - S13.29
S23.100+ - S23.171+
S33.100+ - S33.39x+
|Dislocation of vertebra|
|S14.101+ - S14.159+
S24.101+ - S24.159+
S34.101+ - S34.139+
|Spinal cord injury|
|S14.2xx+ - S14.3xx+, S24.2xx+
S34.21x+ - S34.22x+, S34.4xx+
|Injury to nerve roots and spinal plexus|