Prior Authorization Documentation Standards
BCBSRI is working to align applicable prior authorization documentation requirements with nationally standardized clinical documentation standards developed through AHIP and BCBSA. These standards are intended to promote consistency, improve transparency, and help providers understand what clinical information is needed when submitting prior authorization requests.
Please note the standards below only define the clinical documentation that may be requested to support prior authorization decision-making. BCBSRI Medical Policies, clinical review criteria and coverage determinations still apply. Prior authorization requirements can be found here.
Varicose Veins
Procedure Codes: 36465, 36466, 36468, 36470, 36471, 36473-36476, 36478, 36479, 36482, 36483, 37700, 37718, 37722, 37735, 37760, 37761, 37765, 37766, 37780, 37785
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 3 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 6 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 7 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 8 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 9 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 10 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 11 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 12 | Photographic Documentation | Include high-quality color photographs |
| 13 | Physical Examination | Physical examination and relevant findings |
| 14 | Treatment Plan | Details of the plan for treating the current condition |
Vascular Embolization
Procedure Codes: 37241-37244
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Procedure Type | Procedure being requested is diagnostic or postoperative |
| 3 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 4 | Imaging Special Considerations | Documentation of imaging related special considerations relevant to the condition targeted by requested service; provide severity and duration of each (e.g., pregnancy status, renal function, allergy to contrast, metal/indwelling devices) |
| 5 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 6 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 7 | Repeat Examinations | Reason for repeat, if performed in the past or additional services, provide dates and results |
| 8 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 9 | History of Malignancy | History of malignancy (Y/N) if yes, include specific diagnosis, date of diagnosis, and phase of treatment |
| 10 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 11 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 12 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 13 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 14 | Physical Examination | Physical examination and relevant findings |
| 15 | Treatment Plan | Details of the plan for treating the current condition |
Watchman Procedure
Procedure Codes: 33340
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Procedure Type | Procedure being requested is diagnostic or postoperative |
| 3 | Imaging Special Considerations | Documentation of imaging related special considerations relevant to the condition targeted by requested service; provide severity and duration of each (e.g., pregnancy status, renal function, allergy to contrast, metal/indwelling devices) |
| 4 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 5 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 6 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 7 | ECG Report | ECG report: include dates and findings demonstrating pathology that justifies the requested service |
| 8 | Stroke Risk | CHA2DS2 clinical risk score (>2) |
| 9 | Contraindication to Anticoagulation | List any/all contraindications to or previous complications from long-term anticoagulation |
| 10 | Treatment Plan | Documentation of performing physician specialty and experience with interventional cardiac procedures involving transeptal puncture through an intact septum. |
| 11 | Multidisciplinary Heart Team Evaluation | Documentation of Heart Team evaluation for the requested LAAC procedure, including participating provider specialties, clinical recommendation, and facility structural heart program qualifications or credentials, as applicable. |
| 12 | Shared Decision-Making | Documentation of shared decision-making between the patient and treating clinician, including treatment options discussed, risks and benefits reviewed, patient preferences, and rationale for the requested service. |
| 13 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
| 14 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 15 | Physical Examination | Physical examination and relevant findings |
Cosmetic & Reconstructive
Breast Reconstruction
Procedure Codes: 11920-11922, 11970, 11971, 13100-13102, 15271, 15272, 15734, 15769, 15771-15773, 15777, 15877, 19316, 19325, 19328, 19330, 19340, 19342, 19350, 19355, 19357, 19361, 19364, 19367-19371, 19380, 19396, 19499, S2066-S2068, S8950
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 3 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 6 | Photographic Documentation | Include high-quality color photographs |
| 7 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 8 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 9 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 10 | Surgical History | Relevant surgical history related to the target condition for which service is requested; include surgeries and dates performed |
| 11 | History of Malignancy | History of malignancy (Y/N) if yes, include specific diagnosis, date of diagnosis, and phase of treatment |
| 12 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 13 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 14 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 15 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 16 | Physical Examination | Physical examination and relevant findings |
| 17 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
Breast Reduction
Procedure Codes: 19318
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 3 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Photographic Documentation | Include high-quality color photographs |
| 6 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 7 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 8 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 9 | Surgical History | Relevant surgical history related to the target condition for which service is requested; include surgeries and dates performed |
| 10 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 11 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 12 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 13 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 14 | Physical Examination | Physical examination and relevant findings |
| 15 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
| 16 | For Revision - Indication | Reason for revision, including indication |
| 17 | For Revision - Treatment Plan | For revision, provide treatment plan |
Cochlear Implants
Procedure Codes: 69930, L8614-L8619, L8627, L8628, V5273
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Procedure Type | Procedure being requested is diagnostic or postoperative |
| 3 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 4 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 5 | Treatment Plan | Document: new, renewal, replacement, repair, modification or product change |
| 6 | Product Make And Model | Make and model of the product requested. Provide relevant codes (e.g., NDC codes), where applicable. |
| 7 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 8 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 9 | Vaccine Status | Vaccine history related to the target condition for which service is requested |
| 10 | Diagnostic Testing | Include results of relevant tests (e.g., audiology reports, laboratory tests) |
| 11 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 12 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 13 | Physical Examination | Physical examination and relevant findings |
| 14 | Cognitive Status | Ability to use auditory clues and a willingness to undergo an extended program of rehabilitation |
| 15 | Replacement or Upgrade | Documentation of the reason for replacement or upgrade, including device status, current functional limitations, impact on activities of daily living, and whether the existing device is no longer adequate, functional, or repairable. |
| 16 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
Eye Reconstructive
Procedure Codes: 15820-15823, 21280, 21282, 67900-67904, 67906, 67908, 67909, 67911, 67912, 67914-67917, 67921-67924, 67950, 67961, 67966
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Procedure Type | Procedure being requested is diagnostic or postoperative |
| 3 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 4 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 5 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 6 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 7 | Cause of Condition | Documentation of the condition etiology or circumstances, such as congenital, post-surgical, accident-related, injury-related, or other acquired cause. |
| 8 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 9 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 10 | Symptoms and Duration | Relevant symptoms, duration, frequency, and severity |
| 11 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 12 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 13 | Eye Exam Results | Results of relevant eye examination and vision testing (e.g., eye exam, visual acuity, visual field testing, marginal reflex distance) |
| 14 | Photographic Documentation | Include high-quality color photographs |
| 15 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
Musculoskeletal & Orthopedics
Artificial Disc Replacement - Cervical & Lumbar
Procedure Codes: 22856-22858, 22860-22862, 22865, 0095T, 0098T, 0164T, 0165T
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested Procedure Code(s) | Requested procedure codes |
| 2 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 3 | Spinal Level(s) | Include the number of spine levels being treated and their location |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Symptoms and Duration | Relevant symptoms, duration, frequency, and severity |
| 6 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 7 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 8 | Surgical History | Relevant surgical history related to the target condition for which service is requested; include surgeries and dates performed |
| 9 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 10 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 11 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 12 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 13 | Behavioral Health Disorder or Substance Use Disorder | Validated assessment and results for a behavioral health disorder and substance use disorder |
| 14 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 15 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 16 | Physical Examination | Physical examination and relevant findings |
| 17 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
Bone Stimulators
Procedure Codes: 20974, 20975, 20979, E0747-E0749, E0760
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested procedure code(s) | Requested procedure codes |
| 2 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 3 | Anatomic Area | Detail specific anatomic area(s) being evaluated/treated |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Medical History | Relevant history related to the target condition for which the service is requested; symptoms and function should be measured and reported using standardized tools, if any tools are listed below |
| 6 | History of Trauma and/or Accident | Reports of past injury relevant to the current service requested |
| 7 | Surgical History | Relevant surgical history related to the target condition for which service is requested; include surgeries and dates performed |
| 8 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 9 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 10 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 11 | Behavioral Health Disorder or Substance Use Disorder | Validated assessment and results for a behavioral health disorder and substance use disorder |
| 12 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates and duration, reason for discontinuation (if stopped), and therapeutic response |
| 13 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 14 | Prior Imaging Performed | Imaging reports (e.g., x-rays, CT, MRI, nuclear scans): include dates and reports demonstrating pathology that justifies the requested service (e.g., ACR-RADS) |
| 15 | Other Diagnostics | Results of relevant tests (e.g., laboratory studies, tests, procedures) |
| 16 | Physical Examination | Physical examination and relevant findings |
| 17 | Treatment Plan | Specific plan, including the type of implant and/or graft and pre- and post-service care to optimize outcomes |
| 18 | For Revision or Removal - Indication | Reason for revision or removal, including indication |
| 19 | For Revision or Removal - Treatment Plan | For revision or removal, provide treatment plan |
Hip Arthroscopy
Procedure Codes: 29860-29863, 29914-29916
| ID | Clinical Data Type | Clinical Documentation |
|---|---|---|
| 1 | Requested procedure code(s) | Requested procedure codes |
| 2 | Primary Diagnosis | Diagnosis codes of the condition or concern targeted by requested service |
| 3 | Laterality | Body part being treated; include laterality if relevant (left, right, or bilateral) |
| 4 | State-Specific Documentation | State-specific documentation applicable to the requested service, if any (e.g., regulatory, coverage, or program-specific criteria) |
| 5 | Functional Impairment | Functional impairment, related to the condition targeted by requested service, and interference with ADLs |
| 6 | Symptoms and Duration | Relevant symptoms, duration, frequency, and severity |
| 7 | Comorbidities | Documentation of comorbidities relevant to the condition targeted by the requested service; provide severity and duration of each |
| 8 | Nicotine Use | Nicotine history and status, including nicotine cessation, if applicable (e.g., smoking pack year history) |
| 9 | Surgical History | Relevant surgical history related to the target condition for which service is requested; include surgeries and dates performed |
| 10 | Conservative Treatment: Rx | List of medications (OTC and Rx) that have been tried, contraindicated, or not tolerated and the therapeutic response; include duration of use |
| 11 | Conservative Treatment: Non-Rx | Other than medications, list relevant prior therapies, treatments, or conservative management tried and/or contraindicated or not tolerated; include the dates |