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May 2020

All Providers

Blue Cross and BCN take action to support providers and protect members during COVID‑19 pandemic

Days before the first Michigan cases of COVID‑19 were reported, Blue Cross Blue Shield of Michigan and Blue Care Network began taking action to support providers and protect members. Here are some of the temporary actions we’ve taken:

  • Waived authorization requirements and member cost sharing for diagnostic lab testing for COVID‑19
  • Waived member copayments, deductibles and coinsurance for COVID-19 treatment
  • Changed clinical review to plan notification for admissions to all Michigan acute care hospitals for all diagnoses and for the first three days of all skilled nursing facility transfers from acute care
  • Expanded laboratory testing for COVID-19 to any laboratory provider in Michigan, regardless of network status
  • Added influenza testing to physician in-office laboratory testing to rule out flu
  • Waived early refill limits on 30-day prescription maintenance medications with the exception of opioids
  • Facilitated the use of telehealth by revising our policies and creating an incentive for offices to participate in telehealth
  • Granted a 90-day extension to claim submission time limits for original claims with submission dates of Jan. 1, 2020, and after until further notice

Expanded use of telehealth

The COVID-19 pandemic brought a spotlight to telehealth as a method to safely provide medical care to patients who aren’t able to come in for a face-to-face office visit. Blue Cross and BCN have focused efforts on making telehealth easier for both our providers and our members. We have done this by:

  • Removing the BCN originating site requirement for telehealth
  • Waiving member cost sharing for telehealth services through at least June 30, 2020, on the most common medical office visits, hospitalization follow-up visits and common behavioral health therapy (see Telehealth procedure codes for COVID‑19)
  • Announcing that all Blue Cross and BCN members — including all self-funded groups — now have coverage for telemedicine services (those offered by our network providers). Most, but not all, members also have access to Blue Cross Online VisitsSM (operated by Amwell).
  • Expanding no-cost telehealth services to now include common behavioral health therapy for members with our behavioral health benefits
  • Temporarily relaxing HIPAA requirements to allow for alternative channels, such as Skype and Apple FaceTime
  • Expanding access to our 24-hour nurse hotline for members
  • Creating telehealth guides to help providers begin using telehealth
  • Introducing incentives through Blue Cross’ Physician Group Incentive Program to encourage physician offices to use telehealth, when applicable

If your office is not yet using telehealth, take a few minutes to learn how easy it can be to add a telehealth option. We have two guides that explain telehealth:

There’s also an eLearning available on our Coronavirus webpage.

Find more information

To find our telehealth guides and the latest developments on the COVID-19 pandemic, go to our Coronavirus (COVID-19) information updates for providers webpage, which is linked from BCBSM Newsletters and Resources as well as BCN Provider Publications and Resources within our secure provider website at bcbsm.com.

While the most comprehensive list of communications is available within our secure provider website, we also have a public webpage for providers who don’t have a login and password to our website and for out-of-state providers. This website is available at bcbsm.com/coronavirus. Click on For Providers.


Here are some COVID‑19 billing guidelines

The Centers for Disease Control and Prevention has introduced a new diagnosis code for confirmed COVID‑19 cases, effective April 1, 2020.

Diagnosis codes to use Through March 31, 2020 April 1, 2020, and after
For confirmed COVID‑19

J12.89, J20.8, J22 or J80 in the primary diagnosis field and B97.29 in the secondary diagnosis field

U07.1 as the primary diagnosis
For suspected COVID‑19

Z20.828 as the primary diagnosis

Z20.828

For more information, refer to the announcement from the CDC about the new ICD‑10‑CM code.

For the latest information about COVID‑19, including billing tips, go to our Coronavirus information updates for providers page. Log in to Provider Secured Services, click on BCBSM Provider Publications and Resources and then on Newsletters and Resources. (Or you can find it on BCN Provider Publications and Resources.) You can also find information at bcbsm.com/coronavirus by clicking on For Providers.


Clinical Quality Corner: Follow-up After Hospitalization for Mental Illness

The Follow‑up After Hospitalization for Mental Illness HEDIS® measure** looks at the percentage of discharges for members age 6 or older who were hospitalized in an acute inpatient setting for treatment of mental illness or intentional self-harm and who had an outpatient visit, intensive outpatient encounter or partial hospitalization with a mental health practitioner within seven and 30 days after discharge.

Follow-up visits can also include a community mental health center visit, telehealth visit, observation visit, transitional care management services or electroconvulsive therapy.

Why is this measure important?

Following up in a timely manner may:

  • Lower the chance of re‑hospitalization
  • Detect adverse responses to medications early on
  • Ensure progress made during hospitalization is retained
  • Offer continued support

How can I ensure my patients are getting follow‑up visits?

If you are the discharging hospital or the mental health practitioner accepting the patient for outpatient follow‑up:

  • Make sure the patient has a follow‑up visit scheduled within seven days before leaving your facility and that the outpatient provider has the capacity to see the patient within these seven days. Include this visit information in the discharge information that you send or share with Blue Cross Blue Shield of Michigan or Blue Care Network.
  • Educate the member about the importance of keeping the appointment so they can avoid readmission and continue to make progress.
  • Remember that patients are vulnerable after discharge from a psychiatric hospitalization. Continued care after stabilization in the hospital setting is important for them to maintain stability as they transition back into their environment.
  • Cooperate with efforts by Blue Cross, BCN or New Directions Behavioral Health (a company that provides behavioral health services for most Blue Cross members)  to confirm that follow-up appointments were made and kept. Case managers sometimes provide additional reminders or follow-up calls to ensure member compliance with these appointments.

For more information
Check out the recently updated 2020 HEDIS Tip Sheet for this measure. It’s also posted on web-DENIS in the Clinical Quality Corner section of BCBSM Newsletters and Resources. See the article, “HEDIS measure tip sheets updated for 2020,” also in this issue, for more details.

**HEDIS, which stands for Healthcare Effectiveness Data and Information Set, is a registered trademark of the National Committee for Quality Assurance, or NCQA.


We’re working to ensure providers are available to care for our Michigan members

During national emergencies, such as COVID-19, that are declared by the federal and state government, Blue Cross Blue Shield of Michigan and Blue Care Network — as directed by the government agencies — allow licensed practitioners to provide services to our members outside of their state of provider licensure. We’ve temporarily waived the requirement that out-of-state practitioners be licensed in Michigan when they are licensed in another state.

In addition, we’re relaxing certain requirements for enrollment and credentialing for practitioners joining multiple practice locations, as well as practitioners coming out of retirement to assist with the care of members.

These procedures are effective until the statewide emergency has been lifted.

Other important information

For in-state providers who plan to work at a different location and bill under a different Type 2 NPI or tax ID during this pandemic, the group bringing in the temporary physician will need to add him or her to their group through our enrollment self-service tool.

Follow these guidelines:

  • The originating practice should not delete the physician’s association with their group unless this is a permanent change.
  • We recommend that practices consider waiting one week before submitting new claims associated with a change. (This applies to in-state providers making changes through self-service.)
  • Be advised that sending in a paper form to execute this process will take longer than five business days.

For out-of-state providers

If you’re an out-of-state provider with questions about credentialing and enrollment, email Zachary Lucas at  zlucas@bcbsm.com.

When you receive confirmation on your submission, we recommend that you wait 10 business days before submitting claims for out-of-state providers. (This applies to out-of-state providers joining in-state groups.)


2020 second‑quarter CPT early release codes

Category III
Surgery

Code Change Coverage comments Effective date
0594T Added Not covered July 1, 2020
0614T Added Not covered July 1, 2020
0619T Added Not covered July 1, 2020

Category III
Surgery

Code Change Coverage comments Effective date
0617T Added Not covered July 1, 2020
0618T Added Not covered July 1, 2020

Category III
Surgery

Code Change Coverage comments Effective date
0616T Added Not covered July 1, 2020

Category III
Medicine

Code Change Coverage comments Effective date
0607T Added Not covered July 1, 2020
0608T Added Not covered July 1, 2020

Category III
Medicine

Code Change Coverage comments Effective date
0604T Added Not covered July 1, 2020

Category III
Medicine

Code Change Coverage comments Effective date
0605T Added Not covered July 1, 2020
0606T Added Not covered July 1, 2020

Category III
Laboratory

Code Change Coverage comments Effective date
0602T Added Not covered July 1, 2020
0603T Added Not covered July 1, 2020

Category III
Radiology

Code Change Coverage comments Effective date
0600T Added Not covered July 1, 2020
0601T Added Not covered July 1, 2020

Category III
Diagnostic services

Code Change Coverage comments Effective date
0598T Added Not covered July 1, 2020
0599T Added Not covered July 1, 2020

Category III
DME

Code Change Coverage comments Effective date
0596T Added Not covered July 1, 2020
0597T Added Not covered July 1, 2020

Category III
Medicine

Code Change Coverage comments Effective date
0615T Added Not covered July 1, 2020

Category III
Medicine

Code Change Coverage comments Effective date
0613T Added Not covered July 1, 2020

Category III
Diagnostic radiology

Code Change Coverage comments Effective date
0609T Added Not covered July 1, 2020
0610T Added Not covered July 1, 2020
0611T Added Not covered July 1, 2020
0612T Added Not covered July 1, 2020

Multianalyte assays with algorithmic analyses
Pathology and laboratory
Administrative codes

Code Change Coverage comments Effective date
0014M Added Not covered April 1, 2020

HCPCS update: New codes added, deleted

The Centers for Medicare & Medicaid Services has added several new codes as part of its quarterly Health Care Procedure Coding System updates. The codes, effective dates and Blue Cross Blue Shield of Michigan’s coverage decisions are below.

Annual
Physical/Occupational therapy visit

Code Change Coverage comments Effective date
G2168 Added Covered for facility only Jan. 1, 2020
G2169 Added Covered for facility only Jan. 1, 2020

First quarter
Professional/Data gathering codes

Code Change Coverage comments Effective date
G1000 Deleted Deleted March 31, 2020
G1012 Added Not covered April 1, 2020
G1013 Added Not covered April 1, 2020
G1014 Added Not covered April 1, 2020
G1015 Added Not covered April 1, 2020
G1016 Added Not covered April 1, 2020
G1017 Added Not covered April 1, 2020
G1018 Added Not covered April 1, 2020

First quarter
Injections C-codes

Code Change Coverage comments Effective date
C9053 Added Covered for facility only April 1, 2020
C9056 Added Covered for facility only April 1, 2020
C9057 Added Covered for facility only April 1, 2020
C9058 Added Covered for facility only April 1, 2020

None of the information included in this article is intended to be legal advice and, as such, it remains the provider’s responsibility to ensure that all coding and documentation are done in accordance with all applicable state and federal laws and regulations.


May is Mental Health Month

May is Mental Health Month, a good time to remind your patients of the important role that good mental health plays in overall wellness.

As we did last year, Blue Cross Blue Shield of Michigan will be supporting Mental Health Month in various ways. For example, you can:

  • Check out mibluesperspectives.com and the Mind section of ahealthiermichigan.org for blogs about depression, anxiety and other mental health issues.
  • Follow Blue Cross on Facebook and Twitter for up-to-date mental health information.
  • Access the educational materials and posters in the Mental Health Awareness section of the Engage page. While developed primarily for our group customers, the page offers many useful resources suitable for sharing with your patients.

New toolkit for providers
We also partnered with New Directions, a company that provides behavioral health services for most Blue Cross members, to develop a Primary Care Provider Toolkit. You can learn all about it in the article, “Help connect your patients to behavioral health resources with PCP toolkit,” also in this issue.


Billing chart: Blues highlight medical, benefit policy changes

You’ll find the latest information about procedure codes and Blue Cross Blue Shield of Michigan billing guidelines in the following chart.

This billing chart is organized numerically by procedure code. Newly approved procedures will appear under the New Payable Procedures heading. Procedures for which we have changed a billing guideline or added a new payable group will appear under Updates to Payable Procedures. Procedures for which we are clarifying our guidelines will appear under Policy Clarifications. New procedures that are not covered will appear under Experimental Procedures.

You will also see that descriptions for the codes are no longer included. This is a result of recent negotiations with the AMA on use of the codes.

We will publish information about new BCBS groups or changes to group benefits under the Group Benefit Changes heading.

For more detailed descriptions of the BCBSM policies for these procedures, please check under the Medical/Payment Policy tab in Explainer on web-DENIS. To access this online information:

  • Log in to web-DENIS.
  • Click on BCBSM Provider Publications & Resources.
  • Click on Benefit Policy for a Code.
  • Click on Topic.
  • Under Topic Criteria, click on the drop-down arrow next to Choose Identifier Type and then click on HCPCS Code.
  • Enter the procedure code.
  • Click on Finish.
  • Click on Search.
Code* BCBSM changes to:
Basic Benefit and Medical Policy, Group
Variations Payment Policy, Guidelines
NEW PAYABLE PROCEDURES

86316

Basic benefit and medical policy

Chromogranin A

Chromogranin A is considered medically necessary for the evaluation of suspected or known neuroendocrine tumors and to assess for disease progression, response to therapy or for recurrence after surgical resection.

Chromogranin A may also be used in the evaluation of occult primary cancer when medullary thyroid cancer is suspected.

All other uses are considered experimental.

Effective Dec. 1, 2019, this procedure will no longer require individual consideration.

Payment policy

Procedure 86316 is payable once per day. It isn’t payable in an office location, and modifiers 26 and TC don’t apply. It is payable to an independent laboratory when billed on a professional claim form.

UPDATES TO PAYABLE PROCEDURES

J3590

Basic benefit and medical policy

Kanjinti (trastuzumab-anns)

Effective June 13, 2019, Kanjinti (trastuzumab-anns) is payable for its U.S. Food and Drug Administration-approved indications. Kanjinti (trastuzumab-anns) should be reported with Not Otherwise Classified Code J3590 and National Drug Code 55513-0141-01 or 55513-0132-01 until a permanent code is established.
 
Kanjinti (trastuzumab-anns) is a biosimilar to Herceptin (trastuzumab) and a HER2/neu receptor antagonist indicated for the treatment of HER2 overexpressing breast cancer, HER2 overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma.

URMBT groups are excluded from coverage of this drug. 

Medical drug management doesn’t require prior authorization for this drug.

J3590

Basic benefit and medical policy

Ruxience (rituximab-pvvr)

Ruxience (rituximab-pvvr) is payable when billed for FDA-approved indications, effective July 23, 2019. Ruxience (rituximab-pvvr) should be reported with Not Otherwise Classified Code J3590 and the appropriate National Drug Code until a permanent code is established.

URMBT groups are excluded from coverage of this drug. 

Medical drug management doesn’t require prior authorization for this drug.

Ruxience (rituximab-pvvr) is a CD20-directed cytolytic antibody indicated for the treatment of adult patients with non-Hodgkin’s lymphoma -- relapsed or refractory, low grade or follicular, CD20-positive B-cell NHL as a single agent and chronic lymphocytic leukemia, previously untreated and previously treated CD20-positive CLL in combination with fludarabine and cyclophosphamide. It’s also for the treatment of granulomatosis with polyangiitis (Wegener’s granulomatosis) and microscopic polyangiitis in adult patients in combination with glucocorticoids.

POLICY CLARIFICATIONS

19303, 19350, 54520, 55970,** 55980,** 56805, 57291,** 57292,** 57335,** 58150, 58152, 58180, 58260, 58262, 58275, 58291, 58541, 58542, 58543, 58544, 58550, 58552, 58553, 58554 

Not covered:

11950, 11951, 11952, 11954, 15820, 15821, 15822, 15823, 15824, 15825, 15826, 15828, 15830, 15832, 15833, 15834, 15835, 15836, 15837, 15838, 15839, 15876, 15877, 15878, 15879, 17380,*** 21120, 21121, 21122, 21123, 21125, 21127, 30400, 30410, 30420, 30430, 30435, 30450

**Gender reassignment surgery may require prior authorization.

***17380 may be considered established when performed to prepare tissues prior to genital surgery – see inclusions.

Basic benefit and medical policy

Transgender services

The safety and effectiveness of selected medical and surgical treatments of gender dysphoria have been established. The established treatments of gender dysphoria include:

  • Puberty suppression in adolescents
  • Hormone therapy (for masculinization/feminization)
  • Medically necessary gender reassignment surgery:**
    • Genitalia reconstruction
    • Mastectomy in female-to-male transitions

(**Gender reassignment surgery may require prior authorization.)

Gender-specific services may be medically necessary for transgender people appropriate to their anatomy. Examples include:

  • Breast cancer screening for female-to-male transitioned people who haven’t undergone a mastectomy
  • Prostate cancer screening for male-to-female transitioned people who have retained their prostate
  • Cervical screening for female-to-male transitioned people, as needed
  • Obstetric services in female-to-male transitioned people

Criteria have been updated, effective May 1, 2020. 

Inclusions:
For University of Michigan Gender-Affirming Services (facial feminization, hair removal or chondrolaryngoplasty), reference the Medical Policy Partner document.

Assessment, diagnosis and treatment should be provided through a multidisciplinary gender services clinic or program affiliated with a major medical center. If this level of service is unavailable, there should be documentation that reflects a coordinated approach to care by specialists involved (mental health specialists, physicians, surgeons, etc.).

Puberty suppression**
Puberty suppression hormones for adolescents may be indicated for members that meet all the following inclusionary criteria:

Inclusions:

  • Onset of puberty to at least Tanner Stage 2.
  • The adolescent has demonstrated a long-lasting and intense pattern of gender nonconformity or gender dysphoria (whether suppressed or expressed).
  • Gender dysphoria emerged or worsened with the onset of puberty.
  • Any coexisting psychological, medical or social problems that could interfere with treatment (e.g., that may compromise treatment adherence) have been addressed, such that the adolescent’s situation and functioning are stable enough to start treatment.
  • The adolescent has given informed consent and, particularly when the adolescent hasn’t reached the age of medical consent, the parents, guardians or other legally authorized caretakers have consented to the treatment and are involved in supporting the adolescent throughout the treatment process.
  • The absence of contraindications to therapy in the judgment of the managing physician.

**Medications for puberty suppression may be managed under the member’s pharmacy benefit.

Hormone therapy**
Hormone therapy may be indicated for members that meet all the following inclusionary criteria:

Inclusions:

  • Persistent, well-documented gender dysphoria
  • Capacity to make a fully informed decision and to consent for treatments
  • 18 years of age or older (age of majority)
  • If significant medical or mental health concerns are present, they must be reasonably well-controlled.
  • The absence of contraindications to therapy in the judgment of the managing physician.

**Medications for hormone therapy may be managed under the member’s pharmacy benefit.

Gender reassignment surgery
Gender reassignment surgery may be indicated for members that meet all the following inclusionary criteria:

Inclusions:

  • Persistent, well-documented gender dysphoria
  • The provider must supply documentation that supports the member meets criteria for gender reassignment surgery:
    • For mastectomy in biological female-to-male patients, or for gender reassignment surgery, both of the following:
      • A (one) detailed psychological assessment by a mental health provider: either a psychiatrist, Ph.D.-prepared clinical psychologist or master’s prepared clinician who is licensed to practice independently in their state and has experience with gender dysphoria.
      • The psychological evaluation must be performed within a year of the surgery.
  • 18 years of age or older
  • Capacity to make a fully informed decision and to consent for treatment
  • If significant medical or mental health concerns are present, they must be controlled.
  • Twelve continuous months of hormone therapy** as appropriate to the patient’s gender role (unless there is a contraindication to hormonal therapy):
    • **Hormonal therapy is not required prior to mastectomy in biological female-to-male patients.
    • The aim of hormone therapy prior to gonadectomy is primarily to introduce a period of reversible estrogen or testosterone suppression, before the patient undergoes irreversible surgical intervention.
  • Twelve continuous months of living in a gender role that is congruent with their gender identity:
    • Living in a gender role congruent with gender identity for 12 continuous months is not required prior to mastectomy in biological female-to-male patients.

Electrolysis

  • If gender reassignment surgery is approved for a biological male transitioning to female, permanent hair removal (by electrolysis) may be considered established following medical review. Permanent hair removal is considered established only when the scrotal and surrounding tissues are used in the surgical construction of the vagina.
  • If gender reassignment surgery is approved for a biological female transitioning to male, permanent hair removal (by electrolysis) may be considered established following medical review. Permanent hair removal is considered established only when free flap or other donor tissues are used for phalloplasty performed in conjunction with vaginectomy and full-length urethroplasty.

Some patients receiving transgender services may require and benefit from ongoing behavioral health services, including psychotherapy.

Exclusions:

  • Transgender services aren’t covered if contract or certificate language contains specific exclusion of these services.
  • Reversal of transgender surgical procedures.
  • All procedures that are primarily cosmetic and not medically necessary, including but not limited to:**
    • Abdominoplasty
    • Blepharoplasty
    • Breast enhancements
    • Brow lift
    • Calf implants
    • Cheek/malar implants
    • Chin/nose implants
    • Chondrolaryngoplasty (Adam’s apple reduction)
    • Collagen injections
    • Drugs for hair loss or growth
    • Forehead lift
    • Hair removal (for exception: see electrolysis under inclusions)
    • Hair transplantation
    • Lip reduction
    • Liposuction
    • Mastopexy
    • Neck tightening
    • Pectoral implants
    • Removal of redundant skin
    • Rhinoplasty
    • Speech-language therapy
    • Non-covered services

**For University of Michigan Gender-Affirming Services (facial feminization, hair removal or chondrolaryngoplasty), reference the Medical Policy Partner document.

20240

Basic benefit and medical policy

Procedure code 20240

Procedure code 20240 is now payable to an oral surgeon.

Established
20979, E0760

Basic benefit and medical policy

Bone Growth Stimulation: Ultrasound Accelerated Fracture Healing Device policy

The safety and effectiveness of low-intensity ultrasound treatment for the treatment of specified fractures have been established. It’s a useful therapeutic option for patients at high risk for delayed fracture healing or nonunion.

Inclusions:

  • Low-intensity ultrasound treatment may be considered established when used as an adjunct to conventional management (e.g., closed reduction and cast immobilization) for the treatment of fresh, closed fractures in skeletally mature individuals. A fracture is most commonly defined as “fresh” for seven days after the fracture occurs. Candidates for ultrasound treatment are those at high risk for delayed fracture healing or nonunion. These risk factors may include either locations of fractures or patient comorbidities and include the following:
    • Patient comorbidities:
      • Diabetes
      • Steroid therapy
      • Osteoporosis
      • History of alcoholism
      • History of smoking
    • Fracture locations:
      • Jones fracture (fracture in the meta-diaphyseal junction of the fifth metatarsal of the foot)
      • Fracture of navicular bone in the wrist (also called the scaphoid)
      • Closed fractures of the distal radius (Colles fracture)
      • Closed or grade I open, tibial diaphyseal fractures
      • Fracture of metatarsal
      • Fractures associated with extensive soft tissue or vascular damage
  • Low-intensity ultrasound treatment may be considered established when used as a treatment of delayed union of bones, excluding the skull and vertebra. Delayed union is defined as a decelerating healing process as determined by serial X-rays, together with a lack of clinical and radiologic evidence of union, bony continuity or bone reaction at the fracture site for no less than three months from the index injury or the most recent intervention.
  • Low-intensity ultrasound treatment may be considered established for non-unions of the appendicular skeleton (non-skull or vertebrae) if there has been no X-ray evidence of progression of healing for three or more months despite appropriate fracture care, and all the following criteria are met:
    • Bone is noninfected
    • Bone is stable on both ends by means of cast or fixation
    • The two portions of the involved bone are separated by less than 1cm
    • Nonunion isn’t related/secondary to malignancy

Exclusions:
Other applications of low-intensity ultrasound treatment are experimental, including, but not limited to, treatment of:

  • Congenital pseudarthroses
  • Open fractures
  • Fresh surgically treated closed fractures in patients who aren’t at high risk for delayed fracture healing or nonunion stress fractures
  • Stress fractures
  • Arthrodesis
  • Failed arthrodesis

This policy is effective May 1, 2020.

Established
21120, 21121, 21122, 21123, 21141, 21196, 21198, 21199, 21685, 42140, 42145, 64568, 0466T, 0467T, 0468T

Experimental, not medically necessary 41512, 41530, 42299, S2080

Basic benefit and medical policy

Obstructive Sleep Apnea and Snoring – Surgical Treatment policy

The criteria have been updated for the Obstructive Sleep Apnea and Snoring — Surgical Treatment policy. The policy is effective May 1, 2020.

Inclusions:

  • Palatopharyngoplasty (e.g., uvulopalatopharyngoplasty, uvulopharyngoplasty, uvulopalatal flap, expansion sphincter pharyngoplasty, lateral pharyngoplasty, palatal advancement pharyngoplasty, relocation pharyngoplasty) for the treatment of clinically significant** obstructive sleep apnea syndrome in adult patients who haven’t responded to or don’t tolerate continuous positive airway pressure or failed an adequate trial of an oral appliance
  • Hyoid suspension, surgical modification of the tongue, or maxillofacial surgery, including mandibular-maxillary advancement in adult patients with clinically significant** OSA and objective documentation of hypopharyngeal obstruction who haven’t responded to or don’t tolerate CPAP or failed an adequate trial of an oral appliance
  • Adenotonsillectomy in pediatric patients with OSA, hypertrophic tonsils and one of the following:
    • AHI or RDI of at least five per hour
    • AHI or RDI of at least 1.5 per hour in a patient with excessive daytime sleepiness, behavioral problems or hyperactivity

**Clinically significant OSA is defined as patients who have AHI or RDI of 15 or more events per hour, or AHI or RDI of at least five events per hour with one or more signs or symptoms associated with OSA (e.g., excessive daytime sleepiness, hypertension, cardiovascular heart disease or stroke).

  • Hypoglossal nerve stimulation, all the following:
    • Member is 22 years of age or older
    • AHI is ≥15 events per hour
    • Total number of central and mixed apneas are less than 25% of the total AHI
  • Member has a minimum of 30 days of CPAP documentation monitoring that:
    • Demonstrates CPAP failure (AHI ≥15 despite usage of four or more hours per night, five nights per week), or
    • Demonstrates CPAP intolerance (usage is less than four hours per night, five nights per week), and
    • Non-concentric retropalatal obstruction on drug-induced sleep endoscopy, and
    • Body mass index is less than 32 kg/m2, and
    • The sleep study used for the AHI is performed within 24 months of the first consultation for the hypoglossal nerve stimulator
  • Adolescent or young-adult member with Down syndrome must meet all the following:
    • Member is 10 to 21 years of age
    • Member had a prior adenotonsillectomy:
      • AHI is greater than 10 and less than 50
      • Total number of central and mixed apneas are less than 25% of the total AHI following adenotonsillectomy
    • Member has one of the following:
      • A tracheostomy
      • An ineffective treatment with CPAP due to noncompliance, discomfort, undesirable side effects, persistent symptoms despite compliant use or refusal to use the device
    • Body mass index at the 95th percentile or lower for age
    • Non-concentric retropalatal obstruction on drug-induced sleep endoscopy

Exclusions:

  • Laser-assisted palatoplasty, or LAUP
  • Midline glossectomy, or MLG
  • Palatal stiffening procedures (e.g., cautery-assisted and injection snoreplasty)
  • Palatal implants
  • Radiofrequency volumetric tissue reduction, or RVTR of the tongue
  • Radiofrequency reduction of the palatal tissues (e.g., Somnoplasty)
  • Tongue base suspension (e.g., Repose system)
  • All other minimally invasive surgical procedures not described above
  • All interventions for the treatment of snoring in the absence of documented OSA; snoring alone isn’t considered a medical condition

Exclusions for hypoglossal nerve stimulator:

  • Any anatomical finding that would compromise the performance of the device
  • Any condition or procedure that has compromised neurological control of the upper airway
  • Members who are unable or don’t have the necessary assistance to operate the sleep remote
  • Members who are pregnant or plan to become pregnant
  • Members who are known to require magnetic resonance imaging (this doesn’t apply to a model that is MR-compatible)
  • Members with an implantable device that may be susceptible to unintended interaction with the device

Implantable hypoglossal nerve stimulators for those not meeting the inclusion criteria are considered experimental.

Implantable hypoglossal nerve stimulators that aren’t FDA-approved are considered experimental.

Established
64566, 97014, 97032, 0587T, 0588T, 0589T, 0590T

Experimental, not medically necessary
64999

Basic benefit and medical policy

Measurement Percutaneous Tibial Nerve Stimulation policy

The safety and effectiveness of posterior tibial nerve stimulation for non-neurogenic urinary dysfunction have been established. It may be considered a useful therapeutic option when indicated.

Inclusions:

Posterior tibial nerve stimulation, known as PTNS, is established in patients with non-neurogenic urinary dysfunction who meet all the following criteria:

  • There is a diagnosis of urinary frequency, nocturia or urinary urgency.
  • Active urinary tract infections and anatomical abnormalities of the lower urinary tract have been excluded as a cause of urinary dysfunction.
  • The patient has tried and failed conservative behavioral therapies (e.g., biofeedback, fluid management, pelvic floor exercises) for at least a sufficient duration to fully assess its efficacy.
  • There is documented failure or intolerance of pharmacologic treatment (anti-cholinergic drugs or a combination of an anti-cholinergic and a tricyclic anti-depressant).
  • PTNS treatment consists of 30-minute weekly sessions for 12 treatments.
  • After weekly 12 sessions, treatments may continue at a frequency of one per month, up to a total of two years. The two-year time period begins with the initiation of PTNS treatment.

Note: For continuation of treatment, patients should report an improvement in symptoms of urinary frequency, nocturia or urinary urgency within the initial six weeks (six sessions) of PTNS treatment. PTNS should be discontinued if symptoms don’t improve within the initial six treatment sessions.

Exclusions:

  • PTNS isn’t established for all other indications, including stress and neurogenic incontinence.
  • PTNS hasn’t been established for fecal incontinence.
  • PTNS treatment beyond two years hasn’t been extensively studied and is therefore not established for long-term use.

This policy is effective May 1, 2020.

80145, 80230, 80280, 84999

Basic benefit and medical policy

Measurement of antibodies

Measurement of antibodies to selected biologic agents in patients receiving this treatment either alone or as a combination test that includes the measurement of serum agent levels, is considered experimental. The use of these tests hasn’t been clinically proven to improve patient clinical outcomes or alter patient management. This policy statement was updated, effective May 1, 2020.
81401, 81271, 81274

Basic benefit and medical policy

Genetic Testing for Huntington’s Disease  policy

The safety and effectiveness of genetic testing for Huntington’s disease have been established. It may be considered a useful diagnostic option when indicated.

Inclusions:

  • Genetic testing for Huntington’s disease to confirm the diagnosis of Huntington’s disease when clinical signs, symptoms and imaging results are consistent with Huntington’s disease

Table 1. Symptoms of Huntington’s disease

Neurologic

Psychiatric

Cognitive

Chorea

Apathy

Poor judgment

Dystonia

Irritability

Inflexibility of thought

Eye movement slowing

Depression

Loss of insight

Hyperreflexia

Delusions

Decreased concentration

Gait abnormality

Aggression

Memory loss

 

Anxiety

Subcortical dementia

Parkinsonism (late stages)

Disinhibition

 

 

Paranoia        

 

Source: Suchowersky, O. Huntington disease: clinical features and diagnosis. UpToDate. November 2019.

  • Testing in asymptomatic first- or second-degree relatives of a person with a genetically confirmed diagnosis of Huntington’s disease.
  • Prenatal testing in fetuses from families in which there is a history of Huntington’s disease

Neuroimaging: Axial MRI images through the lateral ventricles demonstrate caudate atrophy, defined by the loss of the normal protrusion of the caudate head into the lateral ventricle in late-stage Huntington’s disease. Caudate atrophy, quantified by simple analysis of linear caudate measurements, correlates with change in cognitive function. Functional imaging using positron-emission tomography, or PET, and MRI also show abnormal metabolic changes in the caudate. 

Exclusions:

  • Genetic testing for HD for routine screening

This policy is effective May 1, 2020.

J3490
J3590

Basic benefit and medical policy

Adakveo (crizanlizumab-tmca)

Beginning Dec. 5, 2019, Adakveo (crizanlizumab-tmca) is considered established to reduce the frequency of vaso-occlusive crises in adults and pediatric patients aged 16 and older with sickle cell disease when all the following criteria are met:

  • Diagnosis of sickle cell disease
  • Prescribed by or in consultation with a hematologist 
  • FDA-approved age
  • Patient has experienced two or more sickle cell-related crises in the past 12 months 
  • If using hydroxyurea concurrently, patient must have been using the drug for at least six months and on a stable dose for the past three months
  • Must not be using long-term red blood cell transfusion therapy

The service requires prior authorization by the Medical Pharmacy Prior Authorization program.

The URMBT doesn’t cover this drug.

J3490
J3590

Basic benefit and medical policy

Ervebo (Ebola Zaire vaccine, live)

Beginning Dec. 19, 2019, Ervebo (Ebola Zaire vaccine, live) is considered established when used for the prevention of disease caused by Zaire ebolavirus in individuals 18 years of age and older.

Limitations of use

  • The duration of protection conferred by Ervebo is unknown.
  • Ervebo doesn’t protect against other species of Ebolavirus or Marburgvirus.
  • Effectiveness of the vaccine when administered concurrently with antiviral medication, immune globulin, or blood or plasma transfusions is unknown.
The URMBT doesn’t cover this service.

J3590
J3490

Basic benefit and medical policy

Padcev (enfortumab vedotin-ejfv)

Padcev (enfortumab vedotin-ejfv) is considered established for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a programmed death receptor-1, known as PD-1, or programmed death-ligand 1, known as PD-L1, inhibitor, and a platinum-containing chemotherapy in the neoadjuvant/adjuvant, locally advanced or metastatic setting.

This policy is effective Dec. 18, 2019.
J9271

Basic benefit and medical policy

Keytruda (pembrolizumab)

Effective June 10, 2019, Keytruda (pembrolizumab) is covered for the following new FDA indication: endometrial carcinoma. Effective Sept. 17, 2019, Keytruda (pembrolizumab) is payable for the updated indications for head and neck squamous cell cancer.

Keytruda (pembrolizumab) is a programmed death receptor-1 (PD-1)-blocking antibody.

Endometrial carcinoma

  • In combination with lenvatinib, for the treatment of patients with advanced endometrial carcinoma that is not MSI-H or dMMR, who have disease progression following prior systemic therapy and aren’t candidates for curative surgery or radiation

Head and neck squamous cell cancer

  • In combination with platinum and FU for the first-line treatment of patients with metastatic or with unresectable, recurrent HNSCC
  • As a single agent for the first-line treatment of patients with metastatic or with unresectable, recurrent HNSCC whose tumors express PD-L1 (combined positive score ≥1) as determined by an FDA-approved test 
  • As a single agent for the treatment of patients with recurrent or metastatic HNSCC with disease progression on or after platinum-containing chemotherapy

Dosage information:

  • Endometrial carcinoma: 200 mg every three weeks with lenvatinib 20 mg orally once daily for tumors that aren’t MSI-H or dMMR
  • HNSCC: 200 mg every three weeks 

Pharmacy doesn’t require prior authorization of this drug.

S1040, 97799

Basic benefit and medical policy

Cranial Orthosis (Helmet or Band Therapy) policy

The safety and effectiveness of cranial orthoses (helmets) have been established as a treatment of plagiocephaly. Cranial orthoses may be considered a useful therapeutic option when indicated.

Criteria have been updated, effective May 1, 2020.

Inclusions:

A custom cranial orthosis may be a therapeutic option if all the following conditions are met:

  • For synostotic plagiocephaly or non-synostotic plagiocephaly, the cranial orthosis must be an FDA-approved device intended for the treatment of deformational plagiocephaly (including plagiocephalic, brachycephalic and scaphocephalic shaped heads) to provide a reasonable assurance of safety and effectiveness
  • Following corrective surgery for synostotic plagiocephaly or the infant is from age 3 to 18 months with persistent non-synostotic plagiocephaly who has failed conservative treatment, (e.g., positional changes)

Note: Cranial orthoses require multiple fittings as the infant’s skull grows to make room for the brain.

Exclusions:

All other indications not listed in inclusions

Established
S0157

Experimental, not medically necessary
0232T, G0460, P9020, S9055

Basic benefit and medical policy

Recombinant and autologous platelet-derived growth factors

The criteria have been updated for the Recombinant and Autologous Platelet-Derived Growth Factors as a Treatment of Wound Healing and Other Non-Orthopedic Conditions policy.

This policy is effective May 1, 2020.

Inclusions:

Recombinant platelet-derived growth factor (Regranex®) when used as an adjunct to standard wound management for the following indications:

  • When used according to the U.S. Food and Drug Administration-labeled indication, (i.e., neuropathic diabetic ulcers extending into the subcutaneous tissue)
  • As a treatment of pressure ulcers extending into the subcutaneous tissue

Exclusions:

Recombinant platelet-derived growth factor (Regranex®) for:

  • Ischemic ulcers
  • Venous stasis ulcers
  • Ulcers not extending through the dermis into the subcutaneous tissue

The use of platelet-rich plasma (i.e., autologous blood-derived growth factors or autologous platelet gel [e.g., Aurix/Autologel and SafeBlood®]) for the treatment of acute or chronic wounds, including surgical wounds and nonhealing ulcers, is considered experimental.

J3590

Basic benefit and medical policy

Polivy (polatuzumab vedotin- piiq)

Polivy (polatuzumab vedotin- piiq) is considered established, effective June 10, 2019.

Polivy (polatuzumab vedotin-piiq) is considered covered when the following criteria are met:

  • POLIVY is a CD79b-directed antibody-drug conjugate indicated in combination with bendamustine and a rituximab product for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma, not otherwise specified, after at least two prior therapies.
  • Accelerated approval was granted for this indication based on complete response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.

Dosing information:

Polivy (polatuzumab vedotin- piiq) is for injection: 140 mg of polatuzumab vedotin-piiq as a lyophilized powder in a single-dose vial

  • The recommended dose of POLIVY is 1.8 mg/kg as an intravenous infusion over 90 minutes every 21 days for six cycles in combination with bendamustine and a rituximab product. Subsequent infusions may be administered over 30 minutes if the previous infusion is tolerated.
  • Premedicate with an antihistamine and antipyretic before POLIVY.
  • See Full Prescribing Information for instructions on preparation and administration.

Pharmacy doesn’t require preauthorization of this drug.

This drug isn’t a benefit for URMBT.

The National Drug Code is 50242-0105-01.
J3590

Basic benefit and medical policy

Zirabev-(bevacizumab-bvzr)

Zirabev-(bevacizumab-bvzr) is considered established effective June 27, 2019.

Zirabev is a vascular endothelial growth factor inhibitor indicated for the treatment of:

  • Metastatic colorectal cancer, in combination with intravenous fluorouracil-based chemotherapy for first- or second-line treatment
  • Metastatic colorectal cancer, in combination with fluoropyrimidineirinotecan- or fluoropyrimidine-oxaliplatin-based chemotherapy for second-line treatment in patients who have progressed on a first-line bevacizumab product-containing regimen

Limitations of use: Zirabev isn’t indicated for adjuvant treatment of colon cancer. 

  • Unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer, in combination with carboplatin and paclitaxel for first-line treatment
  • Recurrent glioblastoma in adults
  • Metastatic renal cell carcinoma in combination with interferon alfa
  • Persistent, recurrent or metastatic cervical cancer, in combination with paclitaxel and cisplatin or paclitaxel and topotecan

Dosing information:

Don’t administer Zirabev for 28 days following major surgery and until surgical wound is fully healed.

Metastatic colorectal cancer:

  • 5 mg/kg every two weeks with bolus-IFL
  • 10 mg/kg every two weeks with FOLFOX4
  • 5 mg/ kg every two weeks or 7.5 mg/kg every three weeks with fluoropyrimidine-irinoteca or fluoropyrimidine-oxaliplatin based chemotherapy after progression on a first-line bevacizumab product-containing regimen

First-line non-squamous non-small cell lung cancer:

  • 15 mg/kg every three weeks with carboplatin and paclitaxel

Recurrent glioblastoma:

  • 10 mg/kg every two weeks

Metastatic renal cell carcinoma:

  • 10 mg/kg every two weeks with interferon alfa

Persistent, recurrent, or metastatic cervical cancer:

  • 15 mg/kg every three weeks with paclitaxel and cisplatin or paclitaxel and topotecan
  • Administer as an intravenous infusion

Pharmacy doesn’t require prior authorization of this drug.

This drug isn’t a benefit for URMBT. 

The National Drug Code isn’t available.
S0317

Basic benefit and medical policy

Pediatric feeding programs

The safety and effectiveness of pediatric feeding programs have been established. The multidisciplinary, integrated programs may be considered a useful therapeutic option when indicated.

Criteria have been updated, effective May 1, 2020. 

Inclusions:

Intensive outpatient day feeding programs may be considered established in children when all the following criteria have been met:

  • Referral by qualified medical professional experienced in the care of children after a thorough medical and nutritional evaluation has been completed to identify potentially treatable underlying conditions (endocrine disorders, thyroid disease, etc.)
  • A pattern of significant malnutrition or failure-to-thrive exists that is believed to be related to inadequate dietary intake resulting from an abnormal relationship to food (aversion, swallowing dysregulation, etc.)
  • Age-appropriate growth charts or body mass index tables may be used to document growth and weight gain.**
  • A 3- to 4-month trial of traditional outpatient approaches to improve dietary intake and growth has failed.

Intensive inpatient admission for pediatric intensive feeding program services may be considered established when facility-based care is required and all the following criteria have been met:

  • All of the above (intensive outpatient) criteria have been met.
  • Member is deemed medically unstable as evidence by one or more of the following:
    • Bradycardia
    • Congestive heart failure
    • Dehydration (documented clinically and on labs)
    • Electrolyte abnormalities
    • Hypotension
    • Hypothermia
    • Other clinical circumstances where cardiac, pulmonary, hepatic, metabolic or renal status are at risk in the judgment of the attending physician

Exclusions:

  • Patients who have mild to moderate feeding difficulties who continue to meet normal growth and developmental milestones
  • Services provided by professionals within a pediatric feeding program shouldn’t be duplicated concurrently by providers outside of the feeding program. Such services are duplicative and “not a covered benefit.”
  • Maintenance programs

**Special growth charts for selected genetic syndromes should be used when indicated (e.g., Down syndrome, Turner syndrome, etc.).

Q5107

Basic benefit and medical policy

Mvasi (bevacizumab-awwb)

Effective June 24, 2019, Mvasi (bevacizumab-awwb) is covered for the following new U.S. Food and Drug Administration indication: recurrent glioblastoma in adults.

Mvasi is a vascular endothelial growth factor inhibitor indicated for the treatment of:

  • Metastatic colorectal cancer, in combination with intravenous fluorouracil-based chemotherapy for first- or second-line treatment.
  • Metastatic colorectal cancer, in combination with fluoropyrimidine-irinotecan- or fluoropyrimidine-oxaliplatin-based chemotherapy for second-line treatment in patients who have progressed on a first-line bevacizumab product-containing regimen.

Limitations of use:

Mvasi isn’t indicated for adjuvant treatment of colon cancer.

  • Unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer, in combination with carboplatin and paclitaxel for first-line treatment
  • Recurrent glioblastoma in adults
  • Metastatic renal cell carcinoma in combination with interferon-alfa
  • Persistent, recurrent or metastatic cervical cancer, in combination with paclitaxel and cisplatin or paclitaxel and topotecan

Dosing information:

Don’t administer Mvasi for 28 days following major surgery and until surgical wound is fully healed. 

Metastatic colorectal cancer:

  • 5 mg/kg every two weeks with bolus-IFL
  • 10 mg/kg every two weeks with FOLFOX4
  • 5 mg/kg every two weeks or 7.5 mg/kg every three weeks with fluoropyrimidine-irinotecan or fluoropyrimidine-oxaliplatin based chemotherapy after progression on a first-line bevacizumab product-containing regimen

First-line non-squamous non-small cell lung cancer:

  • 15 mg/kg every three weeks with carboplatin and paclitaxel

Recurrent glioblastoma:

  • 10 mg/kg every two weeks

Metastatic renal cell carcinoma:

  • 10 mg/kg every two weeks with interferon-alfa

Persistent, recurrent, or metastatic cervical cancer:

  • 15 mg/kg every three weeks with paclitaxel and cisplatin or paclitaxel and topotecan

Administer as an intravenous infusion.

Pharmacy doesn’t require prior authorization of this drug.
EXPERIMENTAL PROCEDURES
20560, 20561, 20999

Basic benefit and medical policy

Dry Needling of Myofascial Trigger Points policy

Dry needling of myofascial trigger points is experimental. It hasn’t been scientifically demonstrated to improve patient clinical outcomes.

This policy is effective May 1, 2020.

81333

Basic benefit and medical policy

Gene analysis for corneal dystrophies

The peer-reviewed medical literature hasn’t demonstrated the clinical utility of gene analysis for corneal dystrophies. Therefore, this service is experimental; policy is effective May 1, 2020.

Professional

Help connect your patients to behavioral health resources with PCP toolkit

As a primary care physician, you’re most likely working with your patients to improve their mental health as well as their physical health. Addressing mental health concerns while managing medical treatment is important to the overall well-being of your patients. Consider these statistics:**

  • 1 in 5 primary care visits address mental health concerns.
  • 10 to 20% of the general population will consult a primary care doctor for a mental health problem in the course of a year.
  • 10 to 40% of primary care patients have a diagnosable mental disorder.
  • 40 to 50% of primary care patients who are high utilizers exhibit significant psychological distress.

To help you coordinate behavioral health care, Blue Cross Blue Shield of Michigan has partnered with New Directions to create a PCP toolkit for behavioral health. Using this toolkit, you can help your patients address mental health and substance use issues, with resources that include:

  • Screening tools to determine patient treatment and referral needs
  • Physician Help Line for psychiatry (medication) consults
  • Resources for patient referrals and augmented treatment options, such as behavioral health care management services
  • Condition-specific tools to identify and appropriately treat patients who exhibit:
    • Depression
    • Anxiety
    • Suicidal thoughts
    • Substance abuse
    • Chronic pain
    • PTSD

To learn more, go to ndbh.com/PCP*** or call 1-877-233-3262.

**Statistics are from the Centers for Disease Control and Prevention and the National Academy of Sciences.

***Blue Cross Blue Shield of Michigan doesn’t own or control this website


We’re making a professional payment policy change for select procedures done in ambulatory surgical facilities

Blue Cross Blue Shield of Michigan recognizes that for certain procedures, additional effort is required and additional costs are incurred when performed outside of a hospital setting. Effective July 1, 2020, the PPO physician reimbursement policy will increase allowed amounts by 15% for select procedures when done in an ambulatory surgical facility. For a preliminary list of the CPT codes for these procedures, click here.

We’ll continue to closely monitor our list of eligible procedures and adjust it based on provider input and other factors, including the effectiveness of the policy. Any other procedures not listed will be paid at the published rate.


Update: Providers must submit authorization requests to TurningPoint for musculoskeletal surgical procedures scheduled on or after July 1 for certain members

As we reported in previous issues of The Record, providers will need to submit authorization requests through TurningPoint Healthcare Solutions LLC for Blue Care Network commercial, BCN AdvantageSM and Medicare Plus BlueSSM PPO members.

Due to the COVID-19 pandemic, we’re delaying the date on which TurningPoint will begin managing authorizations. TurningPoint will now begin managing authorizations for dates of service on or after July 1, 2020.

Providers must submit authorization requests for all surgical procedures related to musculoskeletal conditions to TurningPoint. This is effective for procedures scheduled on or after July 1, 2020.

See this article in the March Record for detailed information.

You’ll be able to submit authorization requests to TurningPoint starting on June 1, 2020. For information about the duration of authorizations during the COVID-19 pandemic, see the Changes to authorization durations for elective and non-urgent procedures, including PT, OT and ST, during the COVID-19 pandemic message that we posted to our public website at bcbsm.com/coronavirus.

We’ll continue to offer webinar training for providers and facilities.

Use the links below to register for webinars:

Important information for facilities

Facilities should have an authorization before scheduling surgery.

Facility providers won’t be able to access the TurningPoint portal until fourth-quarter 2020 to get a status on authorization requests. In the meantime, we’re recommending that the ordering physicians secure the required authorization and provide the authorization numbers to the rendering facilities or providers.

Facilities can look up the status of an authorization request by checking on ereferrals.bcbsm.com. The authorization will show in our system one business day after TurningPoint has made a decision. To check the status of an authorization request directly with TurningPoint, call 1-833-217-9670.

Include only procedure codes authorized for musculoskeletal procedures on your claims

For inpatient professional claims, make sure to include only the procedure codes TurningPoint authorized on your claim.

On a quarterly basis, Blue Cross Blue Shield of Michigan and Blue Care Network will review paid inpatient claims from professional providers to ensure that the procedure codes on the claims match the procedure codes TurningPoint authorized. If we find overpayments because the claim included codes that TurningPoint didn’t authorize, we’ll pursue payment recoveries as necessary.

You can request that TurningPoint add procedure codes to an authorization, but you must do this prior to submitting your claim. For more information about updating procedure codes on an authorization, see the FAQ document referenced below.

Where to find more information

For more information about TurningPoint, see the Blue Cross or BCN Musculoskeletal Services pages on the ereferrals.bcbsm.com website. On these pages, you can find procedure codes for orthopedic and spinal procedures managed by TurningPoint. The links are below:

You can also refer to the frequently asked questions document on these pages.


Collaborative care codes now payable with no member cost sharing

Effective July 1, 2020, we’ll reimburse medical practices that perform collaborative care, and there will be no member cost share for collaborative care services. These changes apply to the following collaborative care codes for treating Blue Cross Blue Shield of Michigan commercial, Blue Care Network commercial, BCN AdvantageSM and Medicare Plus BlueSM members:

*99492
*99493
*99494
*99484 (the general behavioral health integration code)

Collaborative care includes mental and behavioral health and substance abuse services provided in a primary care setting with the assistance of psychiatric consultations. Case managers coordinate the services and interventions of providers outside the primary care setting so that the entire team is working for the best possible outcomes for members.

“These codes allow for reimbursement to the medical practice for behavioral health case management and psychiatric consultation to the practice to coordinate the best holistic care for members’ medical and behavioral health needs,” said William Beecroft, M.D., BCN medical director.

Collaborative care is designed to improve outcomes, while empowering patients and their families, Beecroft said. This style of practice has been shown to alleviate provider burnout, increase behavioral health access and improve outcomes for members’ medical and behavioral health issues, leading to improvement in their health and quality of life.

Check web-DENIS for benefits, eligibility and policy limitations.


Quarterly update: Requirements changed for some commercial medical benefit drugs

Blue Cross Blue Shield of Michigan and Blue Care Network encourage proper utilization of high-cost medications covered under the medical benefit. As part of this effort, we maintain a comprehensive list of requirements for both PPO and HMO commercial members.

During January, February and March 2020, the following medical drugs had authorization requirement updates, site-of-care updates or both for Blue Cross’ PPO members:

HCPCS code Brand name Generic name
J3590** Adakveo® crizanlizumab-tmca
J3490** Vyondys 53 golodirsen
J3590** Avsola infliximab-axxqJ
J3490** Givlaari givosiran
J7170 Hemlibra® emicizumab-kxwh
J0222 Onpattro® patisiran
J1303 Ultomiris® avulizumab‑cwvz
J3111 Evenity® romosozumab-aqqg
J0178 Eylea® aflibercept
J2778 Lucentis® ranibizumab
J0179 Beovu® brolucizumab-dbll
J2503 Macugen® pegaptanib sodium
**Will become a unique code.

For a detailed list of requirements, see the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

Additional notes

The authorization requirements apply only to groups currently participating in the standard commercial Medical Drug Prior Authorization Program for drugs administered under the medical benefit. To view the list of PPO groups that don’t require members to participate in the program, see the Specialty Pharmacy Prior Authorization Master Opt-in/out Group List. This list is available on the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

These changes don’t apply to Federal Employee Program® Service Benefit Plan members.

An authorization approval isn’t a guarantee of payment. Health care providers need to verify eligibility and benefits for members.


Medicare Part B medical specialty drug prior authorization list changing in June

We’re adding medications to the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members. These specialty medications are administered by health care professionals in outpatient sites of care, such as physician’s offices, members’ homes, off-campus outpatient hospitals or ambulatory surgical centers (sites of care 11, 12, 19, 22 and 24).

For dates of service on or after June 15, 2020, the following medications will require prior authorization through NovoLogix®:

  • J1428 Exondys 51®
  • J3490 Vyondys 53
  • J3490 Givlaari®
  • J3590 Tepezza
  • J3590 Vyepti

How to bill

For Medicare Plus Blue and BCN Advantage, we require authorization for all outpatient sites of care when you bill these medications as a professional service or as an outpatient facility service:

  • Electronically through an 837P transaction or on a professional CMS-1500 claim form
  • Electronically through an 837I transaction or by using the UB04 claim form for a hospital outpatient type of bill 013x

Important reminder

For these drugs, submit authorization requests through the NovoLogix online tool. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For Medicare Plus Blue, if you have a Type 1 individual NPI and you checked the Medical Drug PA box when you completed the Provider Secured Access Application form, you already have access to NovoLogix. If you didn’t check that box, you can complete an Addendum “P" form to request access to NovoLogix and fax it to the number on the form.
  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.

If you need to request access to Provider Secured Services, complete the Provider Secured Access Application form and fax it to the number on the form.

List of requirements

For a list of requirements related to drugs covered under the medical benefit, see the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members.


Starting May 1, 2020, we’ll change how we cover some drugs for HIV-1 PrEP

The U.S. Preventive Services Task Force has recommended that providers offer pre-exposure prophylaxis with effective antiretroviral therapy to people at high risk for HIV. The Centers for Disease Control and Prevention reports that when taken daily, PrEP is highly effective for preventing HIV-1.

In complying with this recommendation, Blue Cross Blue Shield of Michigan and Blue Care Network will change how we cover Truvada® and Descovy®, the only two drugs indicated for HIV-1 pre-exposure prophylaxis. Members currently on Descovy won’t be affected by this change.

If a member is newly prescribed Descovy for PrEP on or after May 1, 2020, we won’t cover the prescription unless prior authorization criteria are met. In such situations, prescribers should submit a prior authorization request. Otherwise, the prescription claim won’t be covered at the pharmacy.

We’ll only approve a PA for Descovy for PrEP if there is documentation of:

  • A creatinine clearance, or CrCl, <60 mL/min
  • Osteoporosis 

Members using Descovy to treat HIV will receive their medication for their applicable copay.

Effective July 1, 2020, Blue Cross will cover Truvada for PrEP at $0 cost share for commercial members at high risk. We’ll cover generic Truvada for PrEP at $0 cost share when it is available.

Truvada and Descovy are very similar and both contain tenofovir and emtricitabine. Each tenofovir component is formulated as a prodrug. After administration, it’s metabolized within the body into an active drug.

Differences in prodrug formulation and subsequent half-life differences don’t affect efficacy but can affect side-effect profiles. Descovy demonstrated non-inferiority to Truvada in the DISCOVER trial, which means both drugs are equally efficacious in preventing the transmission of HIV-1.

Both drugs are contraindicated as PrEP in patients with unknown or positive HIV status. Using Descovy or Truvada for PrEP without confirmation of negative HIV status may increase the risk of developing HIV-1 resistance substitutions.


We’ll pay inpatient facility claims for Zulresso for Blue Cross members, starting July 1

Starting July 1, 2020, we’ll pay only inpatient facility claims for Zulresso (brexanolone), HCPCS code C9055, for Blue Cross Blue Shield of Michigan commercial members.

We’ll deny Blue Cross commercial claims that indicate a place of service other than an inpatient facility.

This applies only to our in-state providers.


We made changes to coverage for infliximab biosimilar products for Medicare Advantage members

Blue Cross Blue Shield of Michigan removed authorization requirements for certain infliximab biosimilar drugs and designated preferred infliximab biosimilar drugs for Medicare Plus BlueSM and BCN AdvantageSM members. This change started in April 2020.

Removing authorization requirements

For dates of service on or after April 3, 2020, we no longer require authorization for the following infliximab biosimilars for Remicade® for Medicare Plus Blue and BCN Advantage members:

  • Q5103 Inflectra®
  • Q5104 Renflexis®

Designating preferred biosimilar drugs

Since April 20, 2020, we’ve designated the following drugs as preferred infliximab biosimilar products for Medicare Plus Blue and BCN Advantage members:

  • J3590 Avsola
  • Q5103 Inflectra
  • Q5104 Renflexis

As part of our shared commitment to keeping health care affordable for all, we encourage you to switch members to one of the preferred infliximab biosimilar products.

Important: Remicade won’t be considered a preferred biosimilar and will continue to require authorization for Medicare Plus Blue and BCN Advantage members.

List of requirements

We’ve updated the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus Blue PPO and BCN Advantage members with these changes.

The specialty medications on this list can be administered in outpatient sites of care, a physician’s office, an outpatient facility or a member’s home.


Sign up for training webinar

Provider Experience is continuing its series of training webinars for health care providers and staff. The webinars are designed to help you work more efficiently with Blue Cross Blue Shield of Michigan and Blue Care Network.

Register for the upcoming training webinar:

Webinar name Date and time Registration
Blue Cross 101: Understanding the Basics

Tuesday, May 12, 10 to 11:30 a.m.

Click here to register

As additional training webinars become available, we’ll communicate about them through web-DENIS, The Record or BCN Provider News.


HEDIS measure tip sheets updated for 2020

We’ve updated our HEDIS® tip sheets** for 2020 and posted them on the Clinical Quality Corner page of web-DENIS, along with a series of Star Measure Tips that were posted earlier this year. The tip sheets were developed to assist health care providers and their staff in their efforts to improve overall health care quality and prevent or control diseases and chronic conditions.

The Star Measure Tips highlight select measures related to the Centers for Medicare & Medicaid Services’ five-star quality rating system. Most of the Star measures are also HEDIS measures. HEDIS is one of the most widely used performance improvement tools in the U.S.

Accessing the tip sheets

These HEDIS Measure Tip Sheets and the Star Measure Tips are housed on the Clinical Quality Corner page of web-DENIS. You can get there by following these steps:

  • From the homepage of web-DENIS, click on BCBSM Provider Publications and Resources in the left column. (You can also access them from the BCN Provider Publications and Resources section of web-DENIS.)
  • Click on Newsletters & Resources.
  • Click on Clinical Quality Corner on the left-hand side of the page under Other Resources.

**HEDIS®, which stands for Healthcare Effectiveness Data and Information Set, is a registered trademark of the National Committee for Quality Assurance, or NCQA.


Two UAW groups have similar names, causing some confusion

There continues to be some confusion among providers about whether the UAW Retiree Health Care Trust (sometimes referred to as URHCT) requires prior authorization from AIM Specialty Health® for select outpatient medical diagnostic services. The answer is that it does not. Neither does the UAW International Staff.

However, the UAW Retiree Medical Benefits Trust, commonly referred to as URMBT, does require prior authorization for select outpatient medical diagnostic services for their commercial members. Any confusion among providers may be the result of the UAW Retiree Medical Benefits Trust and UAW Retiree Health Care Trust having similar names.

The following needs to be considered when determining prior authorization requirements for AIM:

Prior authorization not required from AIM

  • UAW Retiree Health Care Trust, or URHCT — group number 70605
  • UAW International Staff — group number 71714

Prior authorization required from AIM

  • UAW Retiree Medical Benefits Trust, or URMBT — group numbers 71400, 71435 and 71436

The information above is provided as a guide to help eliminate confusion. As always, you should check eligibility and benefits through web-DENIS.


We’ve updated the guidelines for cosmetic and reconstructive surgery

The Joint Uniform Medical Policy Committee, known as JUMP, updated the guidelines for the Cosmetic and Reconstructive Surgery medical policy. This policy is effective May 1, 2020.

Medical policy statement

Reconstructive surgery is an established service when it involves the restoration of a patient to a normal functional status, or when it is done to repair a defect arising from congenital defects, developmental abnormalities, trauma, infection, involutional defects, tumors or disease. It may be a therapeutic option when indicated.

Cosmetic surgery is performed solely to preserve or enhance appearance or self-esteem. It is considered not medically necessary.

Guidelines

In the absence of a functional deficit, reconstructive surgery may be used to restore a patient’s appearance to the state of normalcy that existed before the illness, traumatic injury or surgery.

Declaration of medical necessity to justify surgery should be supported by medical documentation. Categories of conditions that may be included as part of the contractual definition of reconstructive services include the following:

  • Post-surgery (including breast reconstruction)
  • Accidental trauma or injury
  • Diseases
  • Congenital anomalies
  • Post-chemotherapy
  • Massive weight loss causing functional impairment. This includes, but isn’t limited to, severe rashes or intertrigo, skin ulceration or pain (such as backache due to a large panniculus) that hasn’t responded to conventional therapy.

The following procedures may be considered either cosmetic or reconstructive in nature based on the indications for the surgery. (Note: This list is not all-inclusive.)

Procedure Cosmetic vs. reconstructive
Abdominoplasty/ panniculectomy
  • Reconstructive if patient meets policy guidelines.  See Abdominoplasty joint policy.
Blepharoplasty of lower lids
  • Cosmetic
Blepharoplasty of upper lids
  • Cosmetic when done to improve appearance only.
  • Reconstructive if criteria are met. Refer the Blepharoplasty and Repair of Brow Ptosis policy.
Breast augmentation**/ reconstruction
  • Cosmetic if done solely to improve appearance
  • Reconstructive if done following prophylactic mastectomy in high-risk patients. May also be considered reconstructive following medically necessary mastectomy. This would include reconstruction of the nipple and areolar complex. Reconstruction/revision of the contralateral breast may be necessary to provide symmetry between the breasts.
  • **See the medical policy titled Reconstructive Breast Surgery/Management of Breast Implants for tattooing the breast/nipple in conjunction with breast reconstruction.
Breast reduction
  • Cosmetic if done to improve appearance in the absence of functional deficits
  • Reconstructive if policy guidelines are met. See the Breast Reduction Mammoplasty joint policy.
Chemical peels**
  • Cosmetic when done for aging skin (e.g., skin damage due to overexposure to sun, etc.), wrinkles, acne scarring, or when using chemical peel and hydrating agents that don’t require physician supervision for application
  • Reconstructive when guidelines are met:
    Chemical peels performed no more than three to four times in a 12-month period are appropriate as follows:
    • Dermal (medium and deep) chemical peels, up to four times per in a 12-month period, used to treat patients with numerous (>10) actinic keratoses or other premalignant skin lesions
    • Epidermal (superficial) peels, up to six times in a 12-month period, to treat active acne in patients who have failed other therapy
**Note: Requests for chemical peels should be carefully evaluated to determine if the request is primarily cosmetic in nature. Refer to the Chemical Peels joint policy.
Cheek (malar) or chin (genioplasty) implants
  • Cosmetic
Correction of telangiectasias or spider veins
  • Cosmetic
Cryotherapy for skin conditions
  • Cosmetic when used to treat acne scarring or other dermatologic conditions in which the primary purpose is to change or improve appearance when there is no specific functional deficit or imminent health risk. Cryotherapy isn’t recommended for the treatment of active acne vulgaris.
  • Reconstructive when used to treat actinic keratosis or other pre-cancerous skin lesions.
Dermabrasion/ microdermabrasion
  • Cosmetic when used for treatment of wrinkling, hyperpigmentation or acne scarring. Dermabrasion and microdermabrasion are not recommended for the treatment of active acne vulgaris.
  • Reconstructive when used to treat actinic keratosis or other pre-cancerous skin lesions.
Dermal fillers
  • Cosmetic when used to improve appearance.
Diastasis recti repair absent a true midline hernia
  • Cosmetic
Electrolysis
  • Cosmetic
Excision of excessive skin of the thigh, leg, hip, buttock, arm, forearm, hand, submental fat pad or other areas
  • Cosmetic if the primary purpose is to change or improve appearance when there is no specific functional deficit (e.g., interference with ADLs) or imminent health risk (e.g., infection) that can be removed or improved by the procedure.
  • Reconstructive if done to correct a functional problem, including but not limited to, severe rashes or intertrigo, skin ulceration or pain, etc., that hasn’t responded to conventional medical therapy (e.g., topical antifungals, topical or systemic corticosteroids, or local or systemic antibiotics)
Excision of glabellar frown lines
  • Cosmetic
Fat grafts
  • Cosmetic
Hairplasty for any form of alopecia
  • Cosmetic. Coverage may be available only for the treatment of the underlying condition. Refer to the Alopecia Treatment joint policy.
Insertion or injection of prosthetic material to replace absent adipose tissue
  • Reconstructive only when used to repair a significant deformity from accidental injury, surgery or trauma.
Laser resurfacing of the skin
  • Cosmetic when done to treat wrinkling or aging skin, acne scars, telangiectasias or other skin conditions in which the primary purpose is to change or improve appearance when there is no specific functional deficit or imminent health risk. Laser resurfacing isn’t recommended for the treatment of active acne vulgaris.
  • Reconstructive when done to treat patients with numerous (>10) actinic keratoses or other pre-malignant or nonmalignant skin lesions when treatment of the individual lesions would be impractical.
Laser resurfacing of burn scars (ablative/non-ablative fractional and micro-fractional CO2 laser resurfacing)
  • Reconstructive when used to help correct the abnormal texture and pliability of burn scars
Laser treatment of port wine stains
  • Reconstructive if done due to functional impairment related to the port wine stain (e.g., bleeding).
Liposuction/suction-assisted lipectomy
  • Cosmetic if it is the sole procedure done.
    • Commonly performed on the abdomen (the tummy), buttocks (behind), hips, thighs, knees, chin, upper arms, back and calves.
    • Long-term effectiveness of treatment of lower extremity lymphedema hasn’t been established.
  • Reconstructive if done in conjunction with covered reconstruction surgery. For example, if a covered breast reduction is done by conventional means, there may be a need for minor liposuction to smooth the edges of the incisions.
Otoplasty
  • Cosmetic when done to treat psychological symptomatology or psychosocial complaints related to one’s appearance
  • Reconstructive in following circumstances: when done to correct absent or deformed ears due to congenital deformity/absence, trauma or accidental injury.
Poly-L-lactic acid injection (e.g., Sculptra®)
  • Cosmetic for all indications, including HIV lipoatrophy
Reduction of labia majora and minora, or labiaplasty
  • Cosmetic. In situations where there is discomfort from the condition, these symptoms can be managed with personal hygiene and avoidance of form-fitting clothes.
Rhinoplasty
  • Cosmetic if done to improve appearance only
  • Reconstructive if done for repair of nasal deformity due to trauma, accidental injury or chronic condition affecting the nasal structures (e.g., Wegener’s granulomatosis).
Salabrasion (a technique in which salt or a salt solution is used to abrade the skin, e.g., to remove the pigment from a tattoo or permanent makeup)
  • Cosmetic
Scar revision
  • Cosmetic if scars are asymptomatic
  • Reconstructive for the revision of symptomatic scars
Tattoo removal
  • Cosmetic if done for the removal of decorative tattoos
  • Reconstructive if done for the removal of hyperpigmentation resulting from trauma, surgery or other procedures
Testicular prostheses
  • Reconstructive for replacement of congenitally absent testes or testes lost due to disease, injury or surgery.
Voice-lifting procedures (e.g., Restylane injections)
  • Cosmetic. Implants or injections of fat or collagen are used to bring vocal cords closer together or to plump cords in an attempt to restore elasticity of vocal cords and reinstate a youthful quality to the patient’s voice

Reminder: Additional radiology procedures for commercial and Medicare Plus Blue members to require prior authorization

The PPO Radiology Management Program, administered by AIM Specialty Health®, will require prior authorization for additional radiology procedures beginning May 1, 2020. This change will apply to Blue Cross Blue Shield of Michigan commercial, Blue Care Network commercial and Medicare Plus BlueSM members.

The procedures, which include myocardial imaging and positron emission tomography, involve the following procedure codes:

  • *78429
  • *78430
  • *78431
  • *78432
  • *78433

These codes will require preauthorization for both office settings and hospital outpatient locations. A list of the codes is available at aimspecialtyhealth.com.** You can also refer to Blue Cross’ online provider manuals.

Providers can get authorization through the provider portal or by contacting AIM at 1-800-728-8008.

Reminder: Keep in mind that not all our members require prior authorization through AIM. Benefit Explainer will let you know if a service requires authorization when you enter the patient’s contract number and the procedure code for a service.

**Blue Cross Blue Shield of Michigan and Blue Care Network don’t own or control this website.


Help FEP members avoid emergency room costs for non‑emergency care

Emergency rooms are an important part of our health care system but can be costly.  When members choose the right level of care, they save time and out-of-pocket costs.

FEP members’ choices for care

The Federal Employee Program® provides care choices for members in multiple settings. Members can speak to a health care provider by phone, online or in person.

Print and distribute the Know Where to Go guide to FEP Service Benefit Plan members to help them decide which level of care is best suited for their health care needs. The guide also provides information on a member’s copayment for each benefit option.

If members have questions about their care options, they can call Customer Service at 1-800-482-3600.

Facility

We’re making a professional payment policy change for select procedures done in ambulatory surgical facilities

Blue Cross Blue Shield of Michigan recognizes that for certain procedures, additional effort is required and additional costs are incurred when performed outside of a hospital setting. Effective July 1, 2020, the PPO physician reimbursement policy will increase allowed amounts by 15% for select procedures when done in an ambulatory surgical facility. For a preliminary list of the CPT codes for these procedures, click here.

We’ll continue to closely monitor our list of eligible procedures and adjust it based on provider input and other factors, including the effectiveness of the policy. Any other procedures not listed will be paid at the published rate.


Update: Providers must submit authorization requests to TurningPoint for musculoskeletal surgical procedures scheduled on or after July 1 for certain members

As we reported in previous issues of The Record, providers will need to submit authorization requests through TurningPoint Healthcare Solutions LLC for Blue Care Network commercial, BCN AdvantageSM and Medicare Plus BlueSSM PPO members.

Due to the COVID-19 pandemic, we’re delaying the date on which TurningPoint will begin managing authorizations. TurningPoint will now begin managing authorizations for dates of service on or after July 1, 2020.

Providers must submit authorization requests for all surgical procedures related to musculoskeletal conditions to TurningPoint. This is effective for procedures scheduled on or after July 1, 2020.

See this article in the March Record for detailed information.

You’ll be able to submit authorization requests to TurningPoint starting on June 1, 2020. For information about the duration of authorizations during the COVID-19 pandemic, see the Changes to authorization durations for elective and non-urgent procedures, including PT, OT and ST, during the COVID-19 pandemic message that we posted to our public website at bcbsm.com/coronavirus.

We’ll continue to offer webinar training for providers and facilities.

Use the links below to register for webinars:

Important information for facilities

Facilities should have an authorization before scheduling surgery.

Facility providers won’t be able to access the TurningPoint portal until fourth-quarter 2020 to get a status on authorization requests. In the meantime, we’re recommending that the ordering physicians secure the required authorization and provide the authorization numbers to the rendering facilities or providers.

Facilities can look up the status of an authorization request by checking on ereferrals.bcbsm.com. The authorization will show in our system one business day after TurningPoint has made a decision. To check the status of an authorization request directly with TurningPoint, call 1-833-217-9670.

Include only procedure codes authorized for musculoskeletal procedures on your claims

For inpatient professional claims, make sure to include only the procedure codes TurningPoint authorized on your claim.

On a quarterly basis, Blue Cross Blue Shield of Michigan and Blue Care Network will review paid inpatient claims from professional providers to ensure that the procedure codes on the claims match the procedure codes TurningPoint authorized. If we find overpayments because the claim included codes that TurningPoint didn’t authorize, we’ll pursue payment recoveries as necessary.

You can request that TurningPoint add procedure codes to an authorization, but you must do this prior to submitting your claim. For more information about updating procedure codes on an authorization, see the FAQ document referenced below.

Where to find more information

For more information about TurningPoint, see the Blue Cross or BCN Musculoskeletal Services pages on the ereferrals.bcbsm.com website. On these pages, you can find procedure codes for orthopedic and spinal procedures managed by TurningPoint. The links are below:

You can also refer to the frequently asked questions document on these pages.


Quarterly update: Requirements changed for some commercial medical benefit drugs

Blue Cross Blue Shield of Michigan and Blue Care Network encourage proper utilization of high-cost medications covered under the medical benefit. As part of this effort, we maintain a comprehensive list of requirements for both PPO and HMO commercial members.

During January, February and March 2020, the following medical drugs had authorization requirement updates, site-of-care updates or both for Blue Cross’ PPO members:

HCPCS code Brand name Generic name
J3590** Adakveo® crizanlizumab-tmca
J3490** Vyondys 53 golodirsen
J3590** Avsola infliximab-axxqJ
J3490** Givlaari givosiran
J7170 Hemlibra® emicizumab-kxwh
J0222 Onpattro® patisiran
J1303 Ultomiris® avulizumab‑cwvz
J3111 Evenity® romosozumab-aqqg
J0178 Eylea® aflibercept
J2778 Lucentis® ranibizumab
J0179 Beovu® brolucizumab-dbll
J2503 Macugen® pegaptanib sodium
**Will become a unique code.

For a detailed list of requirements, see the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

Additional notes

The authorization requirements apply only to groups currently participating in the standard commercial Medical Drug Prior Authorization Program for drugs administered under the medical benefit. To view the list of PPO groups that don’t require members to participate in the program, see the Specialty Pharmacy Prior Authorization Master Opt-in/out Group List. This list is available on the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

These changes don’t apply to Federal Employee Program® Service Benefit Plan members.

An authorization approval isn’t a guarantee of payment. Health care providers need to verify eligibility and benefits for members.


Medicare Part B medical specialty drug prior authorization list changing in June

We’re adding medications to the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members. These specialty medications are administered by health care professionals in outpatient sites of care, such as physician’s offices, members’ homes, off-campus outpatient hospitals or ambulatory surgical centers (sites of care 11, 12, 19, 22 and 24).

For dates of service on or after June 15, 2020, the following medications will require prior authorization through NovoLogix®:

  • J1428 Exondys 51®
  • J3490 Vyondys 53
  • J3490 Givlaari®
  • J3590 Tepezza
  • J3590 Vyepti

How to bill

For Medicare Plus Blue and BCN Advantage, we require authorization for all outpatient sites of care when you bill these medications as a professional service or as an outpatient facility service:

  • Electronically through an 837P transaction or on a professional CMS-1500 claim form
  • Electronically through an 837I transaction or by using the UB04 claim form for a hospital outpatient type of bill 013x

Important reminder

For these drugs, submit authorization requests through the NovoLogix online tool. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For Medicare Plus Blue, if you have a Type 1 individual NPI and you checked the Medical Drug PA box when you completed the Provider Secured Access Application form, you already have access to NovoLogix. If you didn’t check that box, you can complete an Addendum “P" form to request access to NovoLogix and fax it to the number on the form.
  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.

If you need to request access to Provider Secured Services, complete the Provider Secured Access Application form and fax it to the number on the form.

List of requirements

For a list of requirements related to drugs covered under the medical benefit, see the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members.


We’ve added site-of-care requirements for Adakveo, Givlaari for Blue Cross’ PPO members

The site-of-care program for specialty drugs covered under the medical benefit has expanded as of April 1, 2020. This applies to Blue Cross Blue Shield of Michigan’s PPO members for the following drugs:

  • Adakveo® (crizanlizumab-tmca, HCPCS code C9053)
  • Givlaari® (givosiran, HCPCS code C9056)

Providers should encourage Blue Cross’ PPO members to select one of the following infusion locations instead of an outpatient hospital facility:

  • A doctor’s or other health care provider’s office
  • An ambulatory infusion center
  • The member’s home, from a home infusion therapy provider

If Blue Cross’ PPO members currently receive infusions for these drugs at a hospital outpatient facility, providers must:

  • Obtain prior authorization for that location.
  • Check the directory of participating home infusion therapy providers and infusion centers to see where the member may be able to continue infusion therapy.

If the infusion therapy provider can accommodate the member, the provider will work with the member and the member’s practitioner to make this change easy. The member may also contact the ordering practitioner directly for help with the change.

More about the authorization requirements

The authorization requirements apply only to groups that are currently participating in the standard commercial Medical Drug Prior Authorization Program for drugs administered under the medical benefit. These changes don’t apply to members covered by the Federal Employee Program® Service Benefit Plan.

Authorization isn’t a guarantee of payment. Health care practitioners need to verify eligibility and benefits for members.

List of requirements

For a list of requirements related to drugs covered under the medical benefit, see the Blue Cross and BCN utilization management medical drug list document located on the Blue Cross Medical Benefit Drugs – Pharmacy webpage of our ereferrals.bcbsm.com website.


We’ll pay inpatient facility claims for Zulresso for Blue Cross members, starting July 1

Starting July 1, 2020, we’ll pay only inpatient facility claims for Zulresso (brexanolone), HCPCS code C9055, for Blue Cross Blue Shield of Michigan commercial members.

We’ll deny Blue Cross commercial claims that indicate a place of service other than an inpatient facility.

This applies only to our in-state providers.


We made changes to coverage for infliximab biosimilar products for Medicare Advantage members

Blue Cross Blue Shield of Michigan removed authorization requirements for certain infliximab biosimilar drugs and designated preferred infliximab biosimilar drugs for Medicare Plus BlueSM and BCN AdvantageSM members. This change started in April 2020.

Removing authorization requirements

For dates of service on or after April 3, 2020, we no longer require authorization for the following infliximab biosimilars for Remicade® for Medicare Plus Blue and BCN Advantage members:

  • Q5103 Inflectra®
  • Q5104 Renflexis®

Designating preferred biosimilar drugs

Since April 20, 2020, we’ve designated the following drugs as preferred infliximab biosimilar products for Medicare Plus Blue and BCN Advantage members:

  • J3590 Avsola
  • Q5103 Inflectra
  • Q5104 Renflexis

As part of our shared commitment to keeping health care affordable for all, we encourage you to switch members to one of the preferred infliximab biosimilar products.

Important: Remicade won’t be considered a preferred biosimilar and will continue to require authorization for Medicare Plus Blue and BCN Advantage members.

List of requirements

We’ve updated the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus Blue PPO and BCN Advantage members with these changes.

The specialty medications on this list can be administered in outpatient sites of care, a physician’s office, an outpatient facility or a member’s home.


Sign up for training webinar

Provider Experience is continuing its series of training webinars for health care providers and staff. The webinars are designed to help you work more efficiently with Blue Cross Blue Shield of Michigan and Blue Care Network.

Register for the upcoming training webinar:

Webinar name Date and time Registration
Blue Cross 101: Understanding the Basics

Tuesday, May 12, 10 to 11:30 a.m.

Click here to register

As additional training webinars become available, we’ll communicate about them through web-DENIS, The Record or BCN Provider News.


Two UAW groups have similar names, causing some confusion

There continues to be some confusion among providers about whether the UAW Retiree Health Care Trust (sometimes referred to as URHCT) requires prior authorization from AIM Specialty Health® for select outpatient medical diagnostic services. The answer is that it does not. Neither does the UAW International Staff.

However, the UAW Retiree Medical Benefits Trust, commonly referred to as URMBT, does require prior authorization for select outpatient medical diagnostic services for their commercial members. Any confusion among providers may be the result of the UAW Retiree Medical Benefits Trust and UAW Retiree Health Care Trust having similar names.

The following needs to be considered when determining prior authorization requirements for AIM:

Prior authorization not required from AIM

  • UAW Retiree Health Care Trust, or URHCT — group number 70605
  • UAW International Staff — group number 71714

Prior authorization required from AIM

  • UAW Retiree Medical Benefits Trust, or URMBT — group numbers 71400, 71435 and 71436

The information above is provided as a guide to help eliminate confusion. As always, you should check eligibility and benefits through web-DENIS.


Reminder: Additional radiology procedures for commercial and Medicare Plus Blue members to require prior authorization

The PPO Radiology Management Program, administered by AIM Specialty Health®, will require prior authorization for additional radiology procedures beginning May 1, 2020. This change will apply to Blue Cross Blue Shield of Michigan commercial, Blue Care Network commercial and Medicare Plus BlueSM members.

The procedures, which include myocardial imaging and positron emission tomography, involve the following procedure codes:

  • *78429
  • *78430
  • *78431
  • *78432
  • *78433

These codes will require preauthorization for both office settings and hospital outpatient locations. A list of the codes is available at aimspecialtyhealth.com.** You can also refer to Blue Cross’ online provider manuals.

Providers can get authorization through the provider portal or by contacting AIM at 1-800-728-8008.

Reminder: Keep in mind that not all our members require prior authorization through AIM. Benefit Explainer will let you know if a service requires authorization when you enter the patient’s contract number and the procedure code for a service.

**Blue Cross Blue Shield of Michigan and Blue Care Network don’t own or control this website.

Pharmacy

Quarterly update: Requirements changed for some commercial medical benefit drugs

Blue Cross Blue Shield of Michigan and Blue Care Network encourage proper utilization of high-cost medications covered under the medical benefit. As part of this effort, we maintain a comprehensive list of requirements for both PPO and HMO commercial members.

During January, February and March 2020, the following medical drugs had authorization requirement updates, site-of-care updates or both for Blue Cross’ PPO members:

HCPCS code Brand name Generic name
J3590** Adakveo® crizanlizumab-tmca
J3490** Vyondys 53 golodirsen
J3590** Avsola infliximab-axxqJ
J3490** Givlaari givosiran
J7170 Hemlibra® emicizumab-kxwh
J0222 Onpattro® patisiran
J1303 Ultomiris® avulizumab‑cwvz
J3111 Evenity® romosozumab-aqqg
J0178 Eylea® aflibercept
J2778 Lucentis® ranibizumab
J0179 Beovu® brolucizumab-dbll
J2503 Macugen® pegaptanib sodium
**Will become a unique code.

For a detailed list of requirements, see the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

Additional notes

The authorization requirements apply only to groups currently participating in the standard commercial Medical Drug Prior Authorization Program for drugs administered under the medical benefit. To view the list of PPO groups that don’t require members to participate in the program, see the Specialty Pharmacy Prior Authorization Master Opt-in/out Group List. This list is available on the Blue Cross Drugs Covered Under the Medical Benefit page at ereferrals.bcbsm.com.

These changes don’t apply to Federal Employee Program® Service Benefit Plan members.

An authorization approval isn’t a guarantee of payment. Health care providers need to verify eligibility and benefits for members.


Medicare Part B medical specialty drug prior authorization list changing in June

We’re adding medications to the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members. These specialty medications are administered by health care professionals in outpatient sites of care, such as physician’s offices, members’ homes, off-campus outpatient hospitals or ambulatory surgical centers (sites of care 11, 12, 19, 22 and 24).

For dates of service on or after June 15, 2020, the following medications will require prior authorization through NovoLogix®:

  • J1428 Exondys 51®
  • J3490 Vyondys 53
  • J3490 Givlaari®
  • J3590 Tepezza
  • J3590 Vyepti

How to bill

For Medicare Plus Blue and BCN Advantage, we require authorization for all outpatient sites of care when you bill these medications as a professional service or as an outpatient facility service:

  • Electronically through an 837P transaction or on a professional CMS-1500 claim form
  • Electronically through an 837I transaction or by using the UB04 claim form for a hospital outpatient type of bill 013x

Important reminder

For these drugs, submit authorization requests through the NovoLogix online tool. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For Medicare Plus Blue, if you have a Type 1 individual NPI and you checked the Medical Drug PA box when you completed the Provider Secured Access Application form, you already have access to NovoLogix. If you didn’t check that box, you can complete an Addendum “P" form to request access to NovoLogix and fax it to the number on the form.
  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.

If you need to request access to Provider Secured Services, complete the Provider Secured Access Application form and fax it to the number on the form.

List of requirements

For a list of requirements related to drugs covered under the medical benefit, see the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus BlueSM PPO and BCN AdvantageSM members.


We’ve added site-of-care requirements for Adakveo, Givlaari for Blue Cross’ PPO members

The site-of-care program for specialty drugs covered under the medical benefit has expanded as of April 1, 2020. This applies to Blue Cross Blue Shield of Michigan’s PPO members for the following drugs:

  • Adakveo® (crizanlizumab-tmca, HCPCS code C9053)
  • Givlaari® (givosiran, HCPCS code C9056)

Providers should encourage Blue Cross’ PPO members to select one of the following infusion locations instead of an outpatient hospital facility:

  • A doctor’s or other health care provider’s office
  • An ambulatory infusion center
  • The member’s home, from a home infusion therapy provider

If Blue Cross’ PPO members currently receive infusions for these drugs at a hospital outpatient facility, providers must:

  • Obtain prior authorization for that location.
  • Check the directory of participating home infusion therapy providers and infusion centers to see where the member may be able to continue infusion therapy.

If the infusion therapy provider can accommodate the member, the provider will work with the member and the member’s practitioner to make this change easy. The member may also contact the ordering practitioner directly for help with the change.

More about the authorization requirements

The authorization requirements apply only to groups that are currently participating in the standard commercial Medical Drug Prior Authorization Program for drugs administered under the medical benefit. These changes don’t apply to members covered by the Federal Employee Program® Service Benefit Plan.

Authorization isn’t a guarantee of payment. Health care practitioners need to verify eligibility and benefits for members.

List of requirements

For a list of requirements related to drugs covered under the medical benefit, see the Blue Cross and BCN utilization management medical drug list document located on the Blue Cross Medical Benefit Drugs – Pharmacy webpage of our ereferrals.bcbsm.com website.


Starting May 1, 2020, we’ll change how we cover some drugs for HIV-1 PrEP

The U.S. Preventive Services Task Force has recommended that providers offer pre-exposure prophylaxis with effective antiretroviral therapy to people at high risk for HIV. The Centers for Disease Control and Prevention reports that when taken daily, PrEP is highly effective for preventing HIV-1.

In complying with this recommendation, Blue Cross Blue Shield of Michigan and Blue Care Network will change how we cover Truvada® and Descovy®, the only two drugs indicated for HIV-1 pre-exposure prophylaxis. Members currently on Descovy won’t be affected by this change.

If a member is newly prescribed Descovy for PrEP on or after May 1, 2020, we won’t cover the prescription unless prior authorization criteria are met. In such situations, prescribers should submit a prior authorization request. Otherwise, the prescription claim won’t be covered at the pharmacy.

We’ll only approve a PA for Descovy for PrEP if there is documentation of:

  • A creatinine clearance, or CrCl, <60 mL/min
  • Osteoporosis 

Members using Descovy to treat HIV will receive their medication for their applicable copay.

Effective July 1, 2020, Blue Cross will cover Truvada for PrEP at $0 cost share for commercial members at high risk. We’ll cover generic Truvada for PrEP at $0 cost share when it is available.

Truvada and Descovy are very similar and both contain tenofovir and emtricitabine. Each tenofovir component is formulated as a prodrug. After administration, it’s metabolized within the body into an active drug.

Differences in prodrug formulation and subsequent half-life differences don’t affect efficacy but can affect side-effect profiles. Descovy demonstrated non-inferiority to Truvada in the DISCOVER trial, which means both drugs are equally efficacious in preventing the transmission of HIV-1.

Both drugs are contraindicated as PrEP in patients with unknown or positive HIV status. Using Descovy or Truvada for PrEP without confirmation of negative HIV status may increase the risk of developing HIV-1 resistance substitutions.


We’ll pay inpatient facility claims for Zulresso for Blue Cross members, starting July 1

Starting July 1, 2020, we’ll pay only inpatient facility claims for Zulresso (brexanolone), HCPCS code C9055, for Blue Cross Blue Shield of Michigan commercial members.

We’ll deny Blue Cross commercial claims that indicate a place of service other than an inpatient facility.

This applies only to our in-state providers.


We made changes to coverage for infliximab biosimilar products for Medicare Advantage members

Blue Cross Blue Shield of Michigan removed authorization requirements for certain infliximab biosimilar drugs and designated preferred infliximab biosimilar drugs for Medicare Plus BlueSM and BCN AdvantageSM members. This change started in April 2020.

Removing authorization requirements

For dates of service on or after April 3, 2020, we no longer require authorization for the following infliximab biosimilars for Remicade® for Medicare Plus Blue and BCN Advantage members:

  • Q5103 Inflectra®
  • Q5104 Renflexis®

Designating preferred biosimilar drugs

Since April 20, 2020, we’ve designated the following drugs as preferred infliximab biosimilar products for Medicare Plus Blue and BCN Advantage members:

  • J3590 Avsola
  • Q5103 Inflectra
  • Q5104 Renflexis

As part of our shared commitment to keeping health care affordable for all, we encourage you to switch members to one of the preferred infliximab biosimilar products.

Important: Remicade won’t be considered a preferred biosimilar and will continue to require authorization for Medicare Plus Blue and BCN Advantage members.

List of requirements

We’ve updated the Medical Drug and Step Therapy Prior Authorization List for Medicare Plus Blue PPO and BCN Advantage members with these changes.

The specialty medications on this list can be administered in outpatient sites of care, a physician’s office, an outpatient facility or a member’s home.

DME

Bypass the manual review requirement for medically necessary insulin pumps

Effective March 1, 2020, health care providers must append the KX and TW modifiers to avoid the manual review process for a medically necessary replacement insulin pump.

To avoid the manual review process, all the following must apply:

  • Insulin pump malfunctioned
  • Manufacturer’s warranty has expired
  • Blue Cross Blue Shield of Michigan’s five-year reasonable useful lifetime, or RUL, hasn’t been reached

By appending the KX and TW modifiers, you are certifying that the member’s insulin pump has malfunctioned after the manufacturer’s warranty period but before the five-year RUL and that the member meets Blue Cross medical criteria for an insulin pump.


Blue Cross to reject certain HCPCS codes for arch supports starting in June

Starting on June 1, 2020, Blue Cross Blue Shield of Michigan’s systems won’t consider certain HCPCS codes for arch supports a benefit. On June 1, Blue Cross systems will be updated to reject the following:

  • L3040
  • L3050
  • L3060
  • L3070
  • L3080
  • L3090
  • L3100

No portion of this publication may be copied without the express written permission of Blue Cross Blue Shield of Michigan, except that BCBSM participating health care providers may make copies for their personal use. In no event may any portion of this publication be copied or reprinted and used for commercial purposes by any party other than BCBSM.

*CPT codes, descriptions and two-digit numeric modifiers only are copyright 2019 American Medical Association. All rights reserved.