Pediatric Musculoskeletal Imaging Guidelines (Ohio)
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Radiology imaging coverage determination guideline governing pediatric musculoskeletal imaging services for UnitedHealthcare Community Plan members in Ohio; defines application, development, and evidence standards used to evaluate medical necessity.
No material clinical or coverage changes in this revision.
Coverage Criteria — Pediatric Musculoskeletal Imaging
General criteria for medical necessity of advanced imaging
Covered when ALL of the following are met
Spine and musculoskeletal sections require x-rays from the current episode.
Repeat imaging only when evidence of progression, recurrence, or when repeat imaging will affect management.
See modality-specific sections for contrast and anesthesia considerations.
3D rendering considered indications
CPT 76376 or 76377 can be considered in the following clinical scenarios
See referenced Pelvis and Abdomen Imaging Guidelines for specific pelvic/abdominal indications.
Imaging guidance coding rules
Imaging guidance codes contain all imaging necessary to guide a needle or catheter; do not routinely bill diagnostic procedure codes in conjunction with a guidance procedure code.
See table of imaging guidance procedure codes.
Unit of service for guidance codes
Unit-of-service clarification
CPT 77013 is restricted to non-bone ablations; CPT 20982 includes CT guidance for bone tumor ablations.
Coverage and coding criteria
Inappropriate to bill guidance codes with open/excisional/incisional surgical codes.
Examples: neurosurgical navigation/planning, custom joint arthroplasty planning, positional acquisitions requiring different protocol.
No specific slice/sequence counts defined.
Whole-body low-dose skeletal CT is supported for multiple myeloma staging per Oncology Imaging Guidelines.
WBMRI reporting should use CPT 76498 when appropriate.
Whole-body MRI (WBMRI)
WBMRI coverage determination
Exceptions include interval WBMRI for select cancer predisposition syndromes and specific autoimmune conditions such as CRMO.
PET/MRI
PET/MRI coverage criteria
Report PET/MRI using CPT 78813 + 76498 when allowed; diagnostic MRI codes may be allowed concurrently when appropriate.
Prerequisites for Advanced Imaging
Covered when documentation supports clinical need and prior evaluation:
A meaningful technological contact (telehealth, phone, message) can satisfy evaluation in some cases.
Modality Selection
Modality selection guidance:
When multiple body areas are needed, obtain MRI of all necessary areas in the same session to minimize anesthesia.
CT contrast selection depends on the clinical question.
Ultrasound is operator dependent and limited by bone and large abnormality size.
Anesthesia and Contrast
Anesthesia and contrast considerations:
Weigh sedation risks versus diagnostic benefit.
Use caution in renal impairment and pregnancy per contrast rules.
Nuclear Medicine Indications
Specific nuclear medicine indications (covered when condition present):
Use CPT 78315, 78803, or 78830 as appropriate.
Use CPT 78102/78103/78104 and 78803/78830.
Acute Fracture
Acute Fracture (PEDMS-2.1): Covered when the following conditions apply
If x-rays are positive, additional advanced imaging usually not necessary unless fracture is complex or intra-articular.
3D rendering may sometimes be necessary for complex fracture repairs.
Bone scan is an alternative when indicated per stress/occult fracture guidance.
Joint-Adjacent Fracture
Joint-Adjacent Fracture (PEDMS-2.2): Covered when the following conditions apply
Growth Plate Injuries
Growth Plate Injuries (PEDMS-2.3): Covered when the following conditions apply
MRI is preferred for detecting some physeal abnormalities.
Osteochondral/Chondral Fractures
Osteochondral or Chondral Fractures (PEDMS-2.4): Covered when the following conditions apply
Stress/Occult Fracture
Stress/Occult Fracture (PEDMS-2.5): Covered when the following conditions apply
Follow-up plain x-rays often show progressive healing.
No conservative care delay required for these high-risk sites.
Compartment Syndrome
Compartment Syndrome (PEDMS-2.6): Covered when the following conditions apply
Physical Child Abuse
Physical Child Abuse (PEDMS-2.7): Cross-reference
Soft tissue and general imaging criteria
Covered when ALL of the following are met (general soft tissue mass considerations):
Evaluation by surgical specialist or oncologist is strongly recommended.
Even soft tissue masses benefit from plain film information.
CT may be used if MRI contraindicated.
MRI may be performed preoperatively.
Pathway for abnormal US or calcification on x-ray
Covered when ALL of the following are met (soft tissue mass with specific x-ray/US findings):
Bone lesion imaging criteria
Covered when ALL of the following are met (mass involving bone):
Entire bone radiographs help determine need for advanced imaging.
CT if MRI contraindicated.
Limping child — trauma and infection pathways
Covered when ALL of the following are met (limping child and suspected trauma or infection):
Many cases may be urgent.
If initial x-rays negative but symptoms persist, obtain follow-up x-rays in 7-10 days.
CT use is limited in this pathway.
DDH Screening Ultrasound
Screening studies - ultrasound
Routine screening of neonates/infants without risk factors is not recommended.
For children 4–6 months plain x-ray is preferred due to femoral head ossification.
Follow-up hip ultrasound
Follow-up/Diagnostic ultrasound
Postreduction and advanced imaging
Imaging modality selection when hip reduction or advanced evaluation needed
Plan imaging with attention to anesthesia risks.
AVN / Osteonecrosis imaging criteria
Osteonecrosis / AVN imaging
Suspected Child Physical Abuse - Imaging Criteria
Covered when specific clinical circumstances are present:
Repeat skeletal survey ~2 weeks if initial is abnormal/equivocal.
Body Area Imaging Criteria
Covered when clinical suspicion for injury to a specific body area exists:
CT should be performed with contrast unless absolute contraindication exists.
Screening of Contact Children
Covered screening for asymptomatic contact children depends on age:
Infection/Osteomyelitis Imaging Criteria
Covered when infection/osteomyelitis is suspected and MRI is not feasible or specific circumstances apply:
Ultrasound is not a prerequisite for other advanced imaging studies.
Leukocyte + marrow imaging is indicated in altered marrow distribution.
Foreign Body Imaging Criteria
Covered when foreign body suspected in soft tissue:
Foreign body imaging
Covered when ALL of the following apply (foreign body):
Common radiolucent foreign body: wood; radiopaque: glass and metal visible on x-ray.
Juvenile idiopathic arthritis (JIA) imaging
Covered when ALL of the following apply (JIA):
Chronic recurrent multifocal osteomyelitis (CRMO)
Covered when ANY of the following apply (CRMO evaluation and monitoring):
Characteristic lesions: juxtaphyseal/periphyseal tibia and femur, clavicle, thoracolumbar spine.
Inflammatory muscle diseases / Juvenile dermatomyositis
Covered when ALL of the following apply (Inflammatory muscle diseases / juvenile dermatomyositis):
Routine screening for occult neoplasm is not medically necessary.
Muscle/Tendon Unit Injuries (PEDMS-11)
Pediatric muscle/tendon injuries
Osgood-Schlatter Disease (PEDMS-12)
Osgood-Schlatter Disease imaging stance
Condition is self-limiting; treat conservatively.
Popliteal (Baker) Cyst (PEDMS-13)
Popliteal (Baker) cyst imaging in children
Ultrasound has high sensitivity and specificity and is preferred for children.
Consider sedation risks in young children.
Slipped Capital Femoral Epiphysis (PEDMS-14)
Slipped Capital Femoral Epiphysis (SCFE) imaging criteria
Presume SCFE in obese adolescents with limp and relevant pain.
Tarsal coalition
Tarsal coalition (PEDMS-16.1) — imaging coverage
Club foot
Club Foot (PEDMS-16.2) — imaging coverage
Vertical talus
Vertical Talus (PEDMS-16.3) — imaging coverage
Femoral anteversion and tibial torsion
Femoral anteversion and tibial torsion (PEDMS-16.4) — imaging coverage
Limb length discrepancy
Limb Length Discrepancy (PEDMS-15)
Imaging performed solely for research or data collection that is not used to guide an individual’s clinical management is not medically necessary. Requests for imaging obtained for clinical trials or investigational studies will be reviewed against these clinical guidelines; studies inconsistent with established clinical standards or requested only for data collection may be denied.
Imaging requested primarily to collect research data or for participation in clinical trials when the images do not influence direct patient care is excluded from coverage. Such requests are reviewed for consistency with evidence-based standards; if the imaging will not affect management decisions or is inconsistent with guideline expectations it is not medically necessary and may be denied.
CPT 76376 and 76377 (3D rendering) have explicit exclusions. They should not be reported in conjunction with procedures that inherently produce a 3D dataset or with listed modalities (for example CTA/MRA, PET, PET/CT, nuclear SPECT, stereotactic localization such as CPT 77011/70486, breast imaging, CT colonography, cardiac CT/MR). Reporting these 3D rendering codes together with those procedures is not appropriate.
Because stereotactic localization scans (e.g., CPT 77011 or equivalent diagnostic CT CPT 70486 when used) inherently generate a 3D dataset for navigation, 3D rendering codes (CPT 76376/76377) should not be reported for the same session. The stereotactic localization itself precludes separate reporting of 3D rendering for that acquisition.
Whole-body CT or ‘LifeScan’ screening of asymptomatic individuals is an explicit exclusion and not a covered benefit. Routine screening CT examinations of healthy people are not supported by validity evidence and carry radiation risk, so such claims risk denial.
Whole-body MRI (WBMRI) is generally not medically necessary for broad cancer screening or routine use because of lack of standardized technique and insufficient evidence of improved outcomes; when performed it should be reported using CPT 76498. Exceptions exist for select cancer predisposition syndromes and certain autoimmune conditions where WBMRI may be appropriate.
CT should not be substituted for MRI solely to avoid sedation unless a condition‑specific guideline explicitly recommends CT for that purpose. Modality selection should be determined by the clinical question and guideline‑based recommendations.
When plain radiographs demonstrate a simple fracture, further advanced imaging is generally unnecessary. Advanced imaging (CT or MRI) is reserved for complex, displaced, or intra-articular fractures that require preoperative planning. Conversely, acute compartment syndrome is a clinical diagnosis and advanced imaging is not medically necessary.
Advanced imaging is not indicated for clearly benign superficial soft‑tissue entities such as ganglion cysts, sebaceous cysts, uncomplicated hematomas, and subcutaneous lipomas. These lesions do not routinely require MRI unless surgery is planned or other clinical features justify cross‑sectional imaging.
Hip ultrasound is not medically necessary for infants older than 6 months of age because femoral head ossification on plain x‑ray becomes more reliable. Ultrasound screening is reserved for infants 4 weeks to 4 months with risk factors or as otherwise indicated by the treating provider.
Routine imaging of asymptomatic contact children older than 24 months is not medically necessary. Age‑based screening rules apply: contacts <12 months require neuroimaging plus skeletal survey, 12–24 months require skeletal survey, and >24 months do not require routine imaging if asymptomatic.
For juvenile idiopathic arthritis (JIA), MRI of the most symptomatic joint is appropriate when ultrasound is inconclusive and MRI findings will change management; however, routine MRI for follow‑up is not medically necessary except for annual TMJ screening (MRI CPT 70336) to detect silent temporomandibular disease.
Osgood‑Schlatter disease is a clinical diagnosis confirmed by x‑ray and is managed conservatively; advanced imaging is generally not indicated and not medically necessary for routine evaluation.
When advanced imaging (MRI or CT) is otherwise indicated based on clinical evaluation and prior studies, ultrasound is not required as a mandatory prerequisite. If MRI or CT is the appropriate next‑step for diagnosis or surgical planning, ultrasound need not be performed first.
Requests for imaging that are inconsistent with established clinical standards or are submitted primarily for data collection without impact on patient care carry a high risk of denial. Providers should document how the requested imaging will affect management and ensure prior, guideline‑recommended evaluations (for example plain x‑rays) have been performed.
Appropriate Uses and Indications
Ultrasound appropriate uses
Operator-dependent; limited by bone and large abnormality size.
CT appropriate uses
Contrast decisions depend on indication; avoid routine CT without and with contrast except when supported.
MRI appropriate uses
Consider contraindications (pacemakers, certain implants) and contrast cautions.
PET/CT appropriate uses
Unbundling PET/CT into separate PET and diagnostic CT codes is not medically necessary.
3D rendering for complex bony and preoperative planning scenarios
3D rendering considered for specific pelvic and abdominal indications
See Pelvis and Abdomen Imaging Guidelines for details.
Whole-body imaging
See condition-specific Oncology Imaging Guidelines and CRMO guidance.
Cancer predisposition syndrome surveillance
Examples include Li-Fraumeni, NF1/NF2, Rhabdoid Tumor Predisposition, HPP, CMMRD, Bloom Syndrome; see referenced PEDONC sections.
Multiple myeloma staging/restaging
Chronic recurrent multifocal osteomyelitis (CRMO)
Characteristic MR lesions include juxtaphyseal/periphyseal tibia/femur, clavicle, thoracolumbar spine.
Infant hip dysplasia evaluation
Screening indicated for infants 4 weeks–4 months with risk factors.
Acute fracture
Bone scan is an alternative when indicated for stress/occult fracture pathway.
Suspected stress/occult fracture
Soft tissue mass
CT if MRI contraindicated.
Abnormal ultrasound with negative x-ray
Calcified soft tissue mass on x-ray
Limping child — suspected fracture or soft tissue injury
CT use is limited.
Hip pain — suspected septic arthritis
DDH screening and diagnostic ultrasound
Suspected osteonecrosis/AVN/Legg-Calvé-Perthes
Imaging modalities matched to clinical suspicion by body region and availability
Repeat survey ~2 weeks if initial equivocal/abnormal.
Suspected soft-tissue foreign body
Juvenile idiopathic arthritis (JIA)
MRI (except annual TMJ) is not medically necessary for routine follow-up.
Chronic recurrent multifocal osteomyelitis (CRMO)
Inflammatory muscle diseases / Juvenile dermatomyositis
Avoid routine CT/bone scan screening for occult neoplasm.
Popliteal (Baker) cyst
Ultrasound sensitivity/specificity high; MRI adds detail for intraarticular pathology when clinically relevant.
Osgood-Schlatter Disease
Conservative treatment is recommended.
Slipped Capital Femoral Epiphysis (SCFE)
MRI without contrast is also medically necessary for preoperative planning if MRI was not completed for diagnosis.
Suspected tarsal coalition
Infant clubfoot evaluation
Ultrasound is not required prior to MRI/CT if MRI/CT are appropriate.
Preoperative femoral/tibial torsion assessment
Coding — CPT/HCPCS Guidance
| C9791 | MRI utilizing Xenon Xe 129 (contrast) referenced as CPT C9791 (considered investigational) |
| 19085 | Biopsy, breast, with placement of breast localization device(s), when performed, and imaging of the biopsy specimen, when performed, percutaneous; first lesion, including MR guidance |
| 19086 | Biopsy, breast, with placement of breast localization device(s), when performed, and imaging of the biopsy specimen, when performed, percutaneous; each additional lesion, including MR guidance |
| 75989 | Imaging guidance for percutaneous drainage with placement of catheter (all modalities) |
| 76942 | Ultrasonic guidance for needle placement |
| 77011 | CT guidance for stereotactic localization |
| 77012 | CT guidance for needle placement |
| 77013 | CT guidance for, and monitoring of parenchymal tissue ablation |
| 77021 | MR guidance for needle placement |
| 77022 | MR guidance for, and monitoring of parenchymal tissue ablation |
| C8001 | 3D anatomical segmentation imaging for preoperative planning, data preparation and transmission, obtained from previous diagnostic CT or MR examination of the same anatomy |
| 77011 | Stereotactic localization - procedure inherently generates 3D dataset; 3D rendering should not be reported with it |
| 77013 | CT guidance for needle electrode — include initial guidance, monitoring, multiple ablations, confirmation of coagulative necrosis (use only for non-bone ablation procedures) |
| 77022 | MR guidance for needle electrode — includes guidance and monitoring as described |
| 20982 | Includes CT guidance for bone tumor ablations |
| 77012 | CT guidance (alternative guidance code referenced) |
| 77021 | MR guidance (alternative guidance code referenced) |
| 76942 | Ultrasound guidance |
| 77002 | Fluoroscopy guidance (reference range 77002-77003) |
| 77003 | Fluoroscopy guidance (see above) |
| 76380 | Limited or follow-up CT scan — for CT scans where full diagnostic code work is not performed |
| 76140 | Interpretation of an outside study (secondary interpretation) |
| Category III mpMRI quantitative codes | Category III CPT codes for quantitative analysis of multiparametric MRI data (used with/without diagnostic MRI) |
| HCPCS (C/S codes) | HCPCS codes may be used by hospitals; many correspond to Level-III CPT codes (e.g., C8931 similar to CPT 72159) |
| S8042 | MRI low-field — non-specific HCPCS code; redirect to a specific CPT when possible |
| 76498 | Unlisted MRI procedure (used to report whole-body MRI) |
| 73218 | MRI Upper Extremity non-joint without contrast |
| 73219 | MRI Upper Extremity non-joint with contrast |
| 73220 | MRI Upper Extremity non-joint without and with contrast |
| 73221 | MRI Upper Extremity joint without contrast |
| 73222 | MRI Upper Extremity joint with contrast |
| 73223 | MRI Upper Extremity joint without and with contrast |
| 73718 | MRI Lower Extremity non-joint without contrast |
| 73719 | MRI Lower Extremity non-joint with contrast |
| 73720 | MRI Lower Extremity non-joint without and with contrast |
| 73721 | MRI Lower Extremity joint without contrast |
| 76885 | Ultrasound, infant hips; dynamic (requiring physician manipulation) |
| 76886 | Ultrasound, infant hips; limited, static (not requiring physician manipulation) |
| 76882 | Ultrasound, axilla |
| 76604 | Ultrasound, upper back |
| 76705 | Ultrasound, lower back |
| 76999 | Ultrasound, other soft tissue areas not otherwise specified |
| 93922 | Limited bilateral noninvasive physiologic studies of upper or lower extremity arteries |
| 93923 | Complete bilateral noninvasive physiologic studies of upper or lower extremity arteries |
| 93930 | Duplex scan of upper extremity arteries or arterial bypass grafts; complete bilateral |
| 93931 | Duplex scan of upper extremity arteries or arterial bypass grafts; unilateral or limited |
| 78315 | Bone scan (triple phase bone scan) |
| 78803 | Distribution of Radiopharmaceutical Agent SPECT |
| 78831 | Distribution of Radiopharmaceutical Agent SPECT (alternate code listed) |
| 78830 | SPECT/CT |
| 78102 | Nuclear medicine bone marrow imaging |
| 78103 | Nuclear medicine bone marrow imaging |
| 78104 | Nuclear medicine bone marrow imaging |
| 76881 | Ultrasound, extremity, nonvascular; limited |
| 76882 | Ultrasound, extremity, nonvascular; complete |
| 78300 | Bone imaging, whole body; single study (listed in document as an option) |
| 78305 | Bone imaging, whole body; additional code listed in document |
| 78306 | Bone imaging, whole body; additional code listed in document |
| 78315 | Bone imaging, limited area (used for stress/occult fracture) |
| 78830 | SPECT/CT, bone |
| 78803 | Distribution of radiopharmaceutical agent SPECT |
| 76881 | Ultrasound, complete, joint/area (hip/soft tissue) (CPT® cited) |
| 76882 | Ultrasound, limited, joint/area (hip/soft tissue) (CPT® cited) |
| 73721 | MRI lower extremity without contrast (CPT® cited) |
| 73723 | MRI lower extremity without and with contrast (CPT® cited) |
| 78300 | Bone imaging (radionuclide) (CPT® cited) |
| 78305 | Bone imaging (radionuclide) (CPT® cited) |
| 78306 | Whole body bone scan (radionuclide) (CPT® cited) |
| 78315 | Radionuclide bone imaging (CPT® cited) |
| 78803 | SPECT (single photon) (CPT® cited) |
| 78830 | SPECT/CT (CPT® cited) |
| 76885 | Ultrasound, hip, static (e.g., Graf) (screening) |
| 76886 | Ultrasound, hip, limited or follow-up (dynamic or screening) |
| 73721 | MRI lower extremity joint without contrast (hip) |
| 73723 | MRI lower extremity joint without and with contrast (hip) |
| 73700 | CT lower extremity, hip, without contrast |
| 78300 | Bone imaging, for example, three-phase bone scan (general nuclear bone scan codes listed) |
| 78305 | Bone imaging, additional nuclear code |
| 78306 | Bone imaging, additional nuclear code |
| 78803 | Bone imaging, limited area |
| 78830 | SPECT/CT |
| 78300 | Bone/soft tissue imaging (as listed in document) |
| 78305 | Bone/soft tissue imaging |
| 78306 | Bone/soft tissue imaging |
| 78315 | Bone/soft tissue imaging |
| 78830 | SPECT/CT (Distribution of Radiopharmaceutical Agent SPECT listed) |
| 78803 | Distribution of Radiopharmaceutical Agent SPECT |
| 70450 | CT Head without contrast |
| 70551 | MRI Brain without contrast |
| 70553 | MRI Brain without and with contrast |
| 72141 | MRI Cervical Spine without contrast |
| 70336 | Magnetic resonance imaging, temporomandibular joint (TMJ) |
| 76498 | Magnetic resonance imaging, whole body |
| 73700 | CT Lower Extremity without contrast (as referenced for tarsal coalition, club foot residuals, vertical talus, torsion measurements) |
| 73718 | MRI Lower Extremity without contrast (as referenced for tarsal coalition, club foot residuals, vertical talus, femoral anteversion/tibial torsion) |
| 76881 | Ultrasound, limited, joint — referenced for infant clubfoot evaluation |
| 76882 | Ultrasound, complete, joint — referenced for infant clubfoot evaluation |
Provider Actions, Documentation, and Prior Authorization
State-specific medical necessity review (Ohio)
This guideline applies to Ohio; services described as unproven or subject to coverage/quantity limits will be reviewed for medical necessity under Ohio Administrative Code 5160-1-01.
CPT inclusion does not imply prior authorization
Presence of a CPT code in these guidelines does not mean the code requires prior authorization; inclusion is not evidence that PA is required.
Prior authorization may be required for 3D rendering (CPT 76376/76377)
Providers may be required to obtain prior authorization for CPT 76376 and 76377 even when the underlying ultrasound/echocardiography or base modality does not require PA; document concurrent physician supervision as defined.
Require prior clinical evaluation and documentation before advanced imaging
Obtain and document a pertinent clinical evaluation (history, exam) and prior imaging (plain x‑ray) showing that advanced imaging will affect management before requesting advanced studies.
- Submit history, physical exam, relevant labs, and prior imaging performed since symptom onset/change
- Plain x‑ray results from the current episode must be available to justify advanced imaging
Use specified nuclear medicine codes as alternatives to MRI/CT when justified
When MRI is contraindicated or not feasible, selected bone scan/SPECT CPT codes (e.g., 78300/78305/78306/78315; 78803/78830) are documented alternatives for stress/occult fractures and infection — follow plan PA rules when applicable.
Expectation to obtain prior authorization for advanced imaging when required
Advanced cross-sectional or nuclear imaging should only be ordered after required initial plain radiographs and when medical necessity criteria are met; obtain prior authorization per payer rules when required.
- Ensure plain x‑rays are performed and available prior to MRI/CT/nuclear studies
- Document clinical indications (size, growth, persistent symptoms, abnormal ultrasound) to support PA
Prior authorization required per payer rules for advanced imaging modalities
Per payer rules, prior authorization is required for advanced modalities (MRI, CT, nuclear medicine/SPECT/CT) when used for diagnosis, preoperative planning, or when MRI is contraindicated/unavailable; follow plan-specific authorization processes.
- PA typically required when advanced imaging is for diagnosis or surgical planning
- Follow payer/InterQual processes for authorization
Obtain prior authorization when advanced imaging is indicated and coverage criteria met
When an advanced imaging study is listed as medically necessary for a specific indication, ensure documentation meets coverage criteria (clinical indication, age, prior imaging) and obtain PA per plan rules if required.
- Document clinical indication and patient age
- Obtain PA when required by the treating plan
Whole‑body MRI for CRMO — prior authorization likely
Whole‑body MRI (CPT 76498) may be medically necessary for CRMO in specific situations (to avoid biopsy or for monitoring every 6–12 months); prior authorization is likely per payer rules.
- Report WBMRI using CPT 76498
- Document indication (suspected CRMO where MR findings would preclude biopsy or monitoring need)
Follow modality sequencing — ultrasound first for Baker cyst, MRI only if needed
Sequence imaging as directed: ultrasound (CPT 76881/76882) is the indicated initial study for Baker cyst; MRI (CPT 73721/73723) is medically necessary only for non‑diagnostic ultrasound or preoperative planning.
Use InterQual and payer-specific prior authorization processes
Follow payer and InterQual authorization processes when submitting requests; InterQual is used for primary medical/surgical criteria and UnitedHealthcare policies apply when InterQual is not available.
- Use InterQual criteria when applicable
- Check payer-specific submission processes for PA
No explicit prior authorization requirements in this excerpt — check plan rules
No additional explicit PA procedures are specified in these document excerpts; follow plan-specific PA requirements and check governing benefit rules.
- Confirm plan PA requirements as they may vary
- Refer to federal/state/contractual rules if conflicts arise
Clinician judgment may override guideline recommendations with documentation
Guidelines do not replace clinician judgment; physicians may override guidelines when clinically appropriate and must document the reason for deviation.
- Document clinical rationale when overriding guideline recommendations
- Use independent medical judgment considering individual circumstances
Stepwise imaging approach — obtain initial tests and try conservative care first
Use a stepwise imaging approach: obtain results of initial diagnostic tests (history, exam, plain x‑ray, ultrasound) and continue conservative care if improving before ordering advanced imaging unless results will change management.
- Obtain initial test results before advanced imaging
- Continue conservative therapy when appropriate; advanced imaging required if it will change management
Conservative care should precede advanced imaging when clinical improvement is occurring
Continue conservative therapy prior to advanced imaging when the patient is improving; order advanced imaging when results are expected to affect management or when guideline exceptions permit earlier imaging.
- Advanced imaging is indicated when it will change immediate treatment decisions
- For many stress/occult fractures, follow-up plain x‑rays after 10–14 days of conservative care are expected unless high‑risk site
Follow-up plain x‑ray interval guidance (10–14 days) for stress/occult fractures
Follow-up plain x‑ray intervals for suspected stress/occult fractures: obtain repeat x‑rays typically at 10–14 days (often 10 days; some sites 14 days) before advanced imaging except for high‑risk locations where immediate MRI/CT is allowed.
- Usual follow-up interval: 10–14 days depending on site
- High‑risk sites (pelvis, sacrum, hip, femur, tibia, tarsal navicular, proximal 5th metatarsal, scaphoid) may proceed directly to MRI/CT
Preferred imaging sequence: plain x‑ray → ultrasound (if needed) → MRI/CT as indicated
Begin evaluation with clinical exam and plain radiographs; if x‑ray is negative proceed to ultrasound for superficial masses and to MRI (preferred) or CT when indicated per criteria.
MRI preferred when available; CT/nuclear as acceptable alternatives when MRI unavailable/contraindicated
When MRI is available and not contraindicated, MRI without contrast is preferred over CT or nuclear studies for pediatric musculoskeletal imaging; CT or nuclear studies are acceptable alternatives only if MRI is contraindicated or unavailable.
- Prefer MRI without contrast for soft tissue and bone marrow evaluation
- Use CT or nuclear modalities only if MRI is contraindicated/unavailable
When MRI unavailable for infection, obtain bone scan or SPECT/CT as next step
If MRI cannot be performed for suspected osteomyelitis or multifocal infection, bone scan or SPECT/CT is an accepted next step; combine labeled leukocyte and marrow imaging when altered marrow distribution is present.
Denial risk for investigational/clinical‑trial imaging and data‑collection studies
Requests for services stated as unproven or for data collection (e.g., clinical trial imaging not used in direct care) will be evaluated and may be denied as not medically necessary under Ohio Administrative Code review.
- Imaging for data collection not used in direct clinical management is not medically necessary
- Clinical trial imaging may be denied if inconsistent with clinical standards
Clinical trial/investigational imaging — denial risk
Imaging inconsistent with established clinical standards or requested solely for research/data collection is not medically necessary and may be denied.
Overutilization and duplicate imaging — denial risk
Requests for duplicate, questionably necessary, or 'double contrast' CT studies, and MRI ordered solely to avoid radiation, may be scrutinized and denied for overutilization.
- Avoid duplicate imaging if prior study answers the clinical question
- Do not order CT without and with contrast ('double contrast') unless clearly indicated
Denial risk for unnecessary repeat or pre‑operative imaging
Repeat imaging or pre‑operative imaging that is not medically necessary (for example when the underlying surgery is not medically necessary) may lead to denial.
- Ensure surgery/procedure is medically necessary before approving pre‑operative imaging
- Document how repeat imaging will affect management
Whole‑body CT screening for asymptomatic individuals is not covered
Whole‑body CT or LifeScan for screening asymptomatic individuals is not a covered benefit; such claims will be denied.
Denial risk for WBMRI outside select indications; use CPT 76498 when allowed
Requests for whole‑body MRI are likely to be denied except for select cancer predisposition syndromes or specific autoimmune indications (e.g., CRMO); WBMRI must be reported with CPT 76498.
- WBMRI generally not medically necessary outside select indications
- Report whole‑body MRI using CPT 76498 when allowed
Denial risk if pre‑imaging clinical evaluation or basic imaging is not documented
Advanced imaging may be denied if there is no documented pertinent clinical evaluation (history, exam, labs, and basic imaging) demonstrating need prior to the study.
- Submit history, physical, labs, and prior x‑rays when requesting advanced imaging
- A meaningful technological contact may satisfy evaluation in some cases
Denial risk if plain x‑ray not performed or documented before advanced imaging for fractures
Failure to perform or document an initial plain x‑ray prior to advanced imaging for suspected acute, stress, or occult fractures may lead to denial unless guideline exceptions for high‑risk sites are met.
- Plain x‑rays should be performed and documented before advanced imaging except for listed high‑risk sites
- If x‑rays are negative but suspicion persists, document why advanced imaging is needed
Imaging sequence requirement — plain x‑ray required before many advanced studies
Advanced imaging without prior appropriate clinical evaluation and plain radiographs may not meet guideline expectations; plain x‑rays are required before advanced imaging for soft tissue masses and bone lesions.
- Plain x‑rays of the entire bone containing a lesion are required prior to advanced imaging for bone masses
- For soft tissue masses, document location, size, and pain association before MRI
Ultrasound screening eligibility for DDH — strict age/risk criteria
Screening hip ultrasound is indicated only for infants aged 4 weeks to 4 months with risk factors (breech, family history, abnormal exam); routine ultrasound screening in neonates/infants without risk factors may be denied.
- Eligible screening age: 4 weeks–4 months with listed risk factors
- For 4–6 months use plain x‑ray as initial modality
Screening limits for asymptomatic contact children (>24 months not indicated)
No routine imaging is medically necessary in asymptomatic contact children older than 24 months; requests for routine imaging in this group may be denied.
- Contacts <12 months: neuroimaging + skeletal survey required
- Contacts 12–24 months: skeletal survey required; >24 months: no routine imaging
Pre‑imaging clinical evaluation must be documented to avoid denial
Advanced imaging should be considered only after a pertinent clinical evaluation including detailed history, exam, and plain x‑rays; failure to document these prior steps may result in denial.
- Document detailed history, physical exam, and plain x‑rays prior to advanced imaging requests
- Show how imaging results will affect immediate treatment decisions
Denial risk for MRI for Baker cyst without prior non‑diagnostic ultrasound
Ordering MRI for a Baker cyst without first obtaining ultrasound or documenting that ultrasound was non‑diagnostic may risk denial; document prior ultrasound results.
Denial risk for MRI in SCFE without required plain radiographs documented
Requesting MRI for SCFE without documented AP and lateral (frog‑leg or cross‑table lateral) radiographs of both hips may be denied unless clinical notes justify MRI after negative films.
Check governing benefit rules (federal/state/contractual) before applying policy
Coverage decisions must reference applicable federal, state (OAC) or contractual benefit rules; conflicts are governed by those requirements which may change coverage determinations.
- Check federal/state/contractual requirements before using this policy
- In case of conflict, federal/state/contractual rules govern
No explicit denial/authorization procedures in excerpt — verify plan processes
No specific denials or authorization procedures are detailed in these excerpts; providers should verify plan‑specific PA and denial processes.
- Confirm plan PA and denial workflows with payer
- Refer to full policy and plan documents for detailed procedures
Contrast considerations — renal impairment, pregnancy, allergy (GFR <30 mL/min)
When contrast is a concern (renal impairment, pregnancy, allergy), follow guideline rules: CT without contrast for renal insufficiency or elevated BUN/creatinine; GFR <30 mL/min indicates contrast risk for both CT and MRI.
- Use CT without contrast for individuals with renal insufficiency or elevated BUN/creatinine
- GFR <30 mL/min is a contrast risk threshold for CT and MRI
Gadolinium contrast — limit use and document necessity
Limit gadolinium‑based contrast agent exposure: reserve GBCA use for situations where contrast provides additional necessary diagnostic information and assess need for repetitive GBCA‑enhanced MRIs.
- Weigh GBCA risks and document necessity when ordering contrast MRI
- If anesthesia IV access present, consider performing without and with contrast in same session to avoid repeat anesthesia
Frequency Limits and Units of Service
Contrast Use and Safety Considerations
Definitions and Key Terms
Not Covered / Investigational Services
MRI techniques utilizing Xenon Xe 129 (CPT C9791) are considered investigational/experimental and are not covered. In addition, PET/MRI is generally not medically necessary except where condition‑specific criteria are met or when PET/CT criteria are met but PET/CT is unavailable and PET/MRI is requested as an alternative.
Advanced imaging is not medically necessary for the diagnosis of acute compartment syndrome, which is a clinical diagnosis requiring direct compartment pressure measurement and urgent surgical management.
Two‑dimensional reformatting and standard 2D reconstructions are included in cross‑sectional imaging base codes and should not be billed separately. Reporting separate CPT codes for routine 2D reformatting is not appropriate.
As above, 2D reformatting that is part of the diagnostic CT/MR technical component is not separately billable; providers should not submit separate charges for routine 2D reformats in addition to the base study codes.
Separate billing for basic 2D post‑processing is not allowed when those reconstructions are customarily included in the performed cross‑sectional study; such coding practices can lead to claim denial.
Standard two‑dimensional reformatting and routine reconstructions are considered part of the primary CT/MR service and should not be itemized or billed as additional 2D reformatting services.
Providers should not bill separate 2D reformatting codes when those functions are performed as part of the cross‑sectional imaging examination; such charges are generally considered included in the base code.
Billing for routine two‑dimensional reconstructions in addition to the primary CT or MR study is inappropriate because these reformats are incorporated into the imaging service.
Routine 2D image reformatting is part of the diagnostic study and should not be billed separately; providers should reserve additional reconstruction codes for distinct, documented, and atypical processing that exceeds usual practice.
Background and Scope
These guidelines evaluate a range of advanced imaging modalities and aim to align imaging selection with evidence and specialty recommendations to optimize patient outcomes while minimizing unnecessary testing and radiation exposure. They are based on peer‑reviewed literature, specialty guidance, and expert input and are intended to guide appropriate imaging selection without supplanting clinician judgment.
Prior Authorization Notes
Policy History and Versioning
Interim evidence-based updates to the guideline (Policy version V2.0.2026).
Annual evidence-based updates to the guideline.
Annual evidence-based updates to the guideline.
Interim evidence-based updates to the guideline.
Annual evidence-based updates to the guideline.
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