August 2021 Anthem Blue Cross Provider News - California

Contents

AdministrativeCommercialAugust 1, 2021

Member grievance and appeals attestation requirement

AdministrativeCommercialAugust 1, 2021

Clearing up-coding confusion for retinal eye exams (DRE)

AdministrativeCommercialAugust 1, 2021

Register now for our August CME webinars!

Digital SolutionsCommercialAugust 1, 2021

Schedule appointments online through Availity

State & FederalMedicare AdvantageAugust 1, 2021

Preventing claims denials: Shingles vaccine

State & FederalMedicare AdvantageAugust 1, 2021

Infliximab Step Therapy – effective July 15, 2021

AdministrativeCommercialAugust 1, 2021

Member grievance and appeals attestation requirement

Anthem Blue Cross’ (Anthem) participating providers are REQUIRED to acknowledge (annually) that Member Grievance and Appeals forms, a description of grievance procedures, and assistance in filing grievances are readily available at each contracted provider location(s).

All pertinent information related to this requirement, including access to forms (in multiple languages) and procedures, is located on Anthem’s website at anthem.com/ca/forms.

  1. Go to View by Topic and Select the drop-down menu.
  2. Select Grievance & Appeals.
  3. Select the desired resource link.

 

To complete this year’s required attestation, by September 15, 2021, please follow the steps below.

The process takes approximately five (5) minutes.   

  1. Log into Availity: https://www.availity.com/
  2. Select Payer SpacesAnthem Blue Cross.
  3. On the landing page, select Access Your Custom Learning Center from the Applications
  4. Search (using keyword grievance) for the Member Grievance Form and Attestation
  5. Enroll and Complete the attestation.

 

Not yet registered for the Availity Portal?

  1. Visit https://www.availity.com/
  2. Select Register.
  3. Select your organization type.
  4. In the Registration wizard, follow the prompts to complete registration. 

 

For complete registration instructions Refer to these PDF documents. For any additional questions regarding the Availity Portal, call Client Services toll-free at 1-800-282-4548.

 

We appreciate your cooperation and support.For additional information regarding member grievance and appeals requirements, please see below.

 

The Department of Managed Health Care’s (DMHC) routine medical survey includes evaluation of a Health Plan’s compliance with California Health and Safety Code section 1368(a)(2); 28 CCR 1300.68(b)(6) and (7). These regulations require Health Plans to ensure that grievance forms, a description of grievance procedures, and assistance in filing grievances are readily available at each contracting provider’s office, contracting facility, or Plan facility.

Please review and distribute the Anthem grievance form to all your participating offices. It is important to implement processes to provide grievance forms and assistance to Anthem members promptly upon request.

 

Your agreement with Anthem requires you to comply with all applicable laws and regulations and to cooperate with Anthem’s administration of its grievance program which includes:

  • Annually attesting to Member Grievance and Appeals forms,
  • Provide a description of grievance procedures
  • Assistance in filing grievances are readily available (at each contracting provider’s office, contracting facility, or Plan facility)

 

Information can be accessed on the process of submitting member grievances and appeals, grievance forms in multiple languages, definitions and appeal rights, on Anthem’s website at anthem.com/ca/forms and within the Anthem Blue Cross Provider Manual.

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AdministrativeCommercialAugust 1, 2021

Telehealth visits can impact after-hospitalization follow-up care for mental illness

Telehealth visits are having a significant impact on missed appointments according to a study published in Counselling Psychology Quarterly. Prior to transitioning to telehealth, clinicians in the study “Psychotherapy at a public hospital in the time of COVID-19: telehealth and implications for practice,1” experienced a 14.25% missed appointment rate. After transitioning to telehealth, the missed appointment rate fell to 5.63%.




Rate of missed appointments before and after transitioning to telehealth
The graph below illustrates the changes in the average rate of missed appointments (cancellations and no-show) for each of the eight clinicians in the study between the periods before and after the transition to telehealth.

“While there are a number of limitations to consider regarding this data, [which is further discussed in the study], the statistically significant reduction in missed appointments pre-and-post [digital] transition is striking,” cited in the study report.

Telehealth and telephone visits with members after a behavioral health (BH) inpatient stay meet HEDIS® criteria for the measure: Follow-up after Hospitalization for Mental Illness (FUH). With transportation being one of the barriers to after hospitalization follow-up, telehealth visits could be an ideal solution.2

 

The FUH HEDIS measure evaluates:

  • Members (6 years and older) who were hospitalized for treatment of selected mental illness diagnoses and who had a follow-up visit with a mental health practitioner.

 

Two areas of importance for this HEDIS measure are:

  1. The percentage of behavioral health inpatient discharges for which the member received follow-up within 7 days after discharge.
  2. The percentage of behavioral health inpatient discharges for which the member received follow-up within 30 days after discharge.

 

These two consecutive follow-up appointments are paramount to positive outcomes as well as meeting this HEDIS measure. Telehealth visits can greatly increase the likelihood of keeping follow-up appointments leading to reduced numbers of rehospitalization and more favorable outcomes for these patients. To learn more about the FUH HEDIS measure, visit the NCQA website.

 

HEDIS® is a registered trademark of the National Committee for Quality Assurance (NCQA).

 

1 Counselling Psychology Quarterly. Psychotherapy at a public hospital in the time of COVID-19: telehealth and implications for practice https://www.tandfonline.com/doi/full/10.1080/09515070.2020.1777390

2 Traveling towards disease: transportation barriers to health care access. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265215/#:~:text=Transportation%20barriers%20are%20often%20cited,and%20thus%20poorer%20health%20outcomes


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AdministrativeCommercialAugust 1, 2021

Clearing up-coding confusion for retinal eye exams (DRE)

The Comprehensive Diabetes Care HEDIS® Measure Retinal Eye Exam (DRE) valuates the percent of adult members ages 18 to 75, with diabetes (type 1 and type 2), who had a retinal eye exam during the measurement year.

Changes to 3072F

The definition for the code 3072F (negative for retinopathy) has been redefined to: Low risk for retinopathy (no evidence of retinopathy in the prior year). This can be particularly confusing because it would not be used at the time of the exam. It would be used the following year, along with the exam coding for the current year, to indicate that retinopathy was not present the previous year.

A simpler coding solution

Using these three codes count toward the DRE measurement if they are billed in the current measurement year, or the prior year. This means you can submit the appropriate code at the time of the exam, and it covers both years:

·         2023F

Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist documented and reviewed; without evidence of retinopathy (DM)

·         2025F

7 standard field stereoscopic retinal photos with interpretation by an ophthalmologist or optometrist documented and reviewed: without evidence of retinopathy (DM)

·         2033F

Eye imaging validated to match diagnosis from 7 standard field stereoscopic retinal photos results documented and reviewed: without evidence of retinopathy (DM)

 


For more about diabetic retinopathy, visit CMS.gov or use this link to read more

Meeting the measurement for all diabetes care

These exams are also important in evaluating the overall health of diabetic patients, as well as meeting the Comprehensive Diabetes Care HEDIS measure:

  • Hemoglobin A1c (HbA1c) testing
  • HbA1c poor control (>9.0%)
  • HbA1c control (<8.0%)
  • Retinal Eye exam performed
  • Blood Pressure control (<140/90 mm Hg)

 

Record your efforts in the member’s medical records for the HbA1c tests and results, retinal eye exam, blood pressure, urine creatinine test and the estimated glomerular filtration rate test. Meeting the mark and closing gaps in care is key to good health outcomes.

HEDIS® is a registered trademark of the National Committee for Quality Assurance (NCQA).

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AdministrativeCommercialAugust 1, 2021

Register now for our August CME webinars!

Overview:

Join us throughout the year in a new Continuing Medical Education (CME) webinar series as we share practices and success stories to overcoming barriers in achieving clinical quality goals, attaining better patient outcomes and improving STARs ratings.

 

Program objectives:

  • Learn strategies to help you and your healthcare team improve your performance across a range of clinical areas.
  • Apply the knowledge you gain from the webinars to improve your organization’s quality and STARs ratings.

 

Attendees will receive one CME credit upon completion of a program evaluation at the conclusion of each webinar.

 

REGISTER HERE for our upcoming clinical quality webinars!

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Digital SolutionsCommercialAugust 1, 2021

Schedule appointments online through Availity

We’re making it even easier for you to schedule online appointments through the Appointment Scheduler App on Availity.  The Appointment Scheduler App gives you secure access to new appointment requests. You’ll also receive digital access to the member’s ID number, contact information and any special health information.

Appointment Scheduler App features include:

  • Manage appointment requests
  • Configure appointment availability
  • Notifications for new visit requests on your Availity dashboard
  • Members are automatically notified by text or email when appointments are confirmed



Administrators, administrator assistants and users with the role of “office staff” will have access to the Appointment Scheduler App.

To access Appointment Scheduler, log onto Availity.com and select Anthem from Payer Spaces. The Appointment Scheduler App will be located in your Applications menu. To learn more about the new App, go to Custom Learning Center in Availity.

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Reimbursement PoliciesCommercialAugust 1, 2021

Reimbursement policy update: Claims requiring additional documentation (facility)

In our May Provider News, we announced a threshold increase for the itemized bill requirement for outpatient facility claims.  This requirement will remain; however effective August 1, 2021, Anthem Blue Cross will remove the threshold amount from the policy language for outpatient facility claims and inpatient stay claims.

For more information about this policy, visit the reimbursement policy page at anthem.com/ca.

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PharmacyCommercialAugust 1, 2021

Specialty dose rounding program for certain oncology medications

Providers treating members covered by Anthem plans will be asked in selective circumstances to voluntarily reduce the requested dose to the nearest whole vial for over 40 oncology medications (see list below). Reviews for these oncology drugs will continue to be administered by AIM Specialty Health® (AIM).

As part of the online prior authorization process, providers will be asked about the dosage of the medication being requested in pop-up questions:

 

  • Whether or not the recommended dose reduction is acceptable
  • If the patient is considered unable to have his or her dose reduced, then a second question will appear asking for the provider’s clinical reasoning.

 

For prior authorization requests made outside of the online AIM Provider Portal (i.e. via phone or fax) the same questions will be asked by the registered nurse or medical director reviewing the request.  Since this program is voluntary, the decision made regarding dose reduction will not affect the final decision on the prior authorization.

 

The dose reduction questions will appear only if the originally requested dose is within 10 percent of the nearest whole vial. This threshold is based on the current medical literature and recommendations from the Hematology and Oncology Pharmacists Association (HOPA) it is appropriate to consider dose rounding within 10 percent. Click here to view the HOPA recommendations.

The voluntary dose reduction program only applies to the specific oncology drugs listed below. Providers can view prior authorization requirements for Anthem members on the Medical Policy & Clinical UM Guidelines page at anthem.com.


Drug Name

HCPCS Code

Drug Name

HCPCS Code

Abraxane (paclitaxel protein-bound)

J9264

Kadcyla (ado-trastuzumab emtansine)

J9354

Actimmune (interferon gamma-1B)

J9216

Kanjinti (trastuzumab-anns)

Q5117

Adcetris (brentuximab vedotin)

J9042

Keytruda (pembrolizumab)

J9271

Alimta (pemetrexed)

J9305

Kyprolis (carfilzomib)

J9047

Asparlas (calaspargase pegol-mknl)

J9118

Lumoxiti (moxetumomab pasudotox-tdfk)

J9313

Avastin (bevacizumab)

J9035

Mvasi (bevacizumab-awwb)

Q5107

Bendeka (bendamustine)

J9034

Mylotarg (gemtuzumab ozogamicin)

J9203

Besponsa (inotuzumab ozogamicin)

J9229

Neupogen (filgrastim)

J1442

Blincyto (blinatumomab)

J9039

Ogivri (trastuzumab-dkst)

Q5114

Cyramza (ramucirumab)

J9308

Oncaspar (pegaspargase)

J9266

Darzalex (daratumumab)

J9145

Ontruzant (trastuzumab-dttb)

Q5112

Doxorubicin liposomal

Q2050

Opdivo (nivolumab)

J9299

Elzonris (tagraxofusp-erzs)

J9269

Padcev (enfortumab vedotin-ejfv)

J9177

Empliciti (elotuzumab)

J9176

Polivy (polatuzumab vedotin-piiq)

J9309

Enhertu (fam-trastuzumab deruxtecan-nxki)

J9358

Riabni (rituximab-arrx)

Q5123

Erbitux (cetuximab)

J9055

Rituxan (rituximab)

J9312

Erwinase (asparginase)

J9019

Ruxience (rituximab-pvvr)

Q5119

Ethyol (amifostine)

J0207

Sarclisa (isatuximab-irfc)

J9227

Granix (tbo-filgrastim)

J1447

Sylvant (siltuximab)

J2860

Halaven (eribulin mesylate)

J9179

Trazimera (trastuzumab-qyyp)

Q5116

Herceptin (trastuzumab)

J9355

Treanda (bendamustine)

J9033

Herzuma (trastuzumab-pkrb)

Q5113

Truxima (rituximab-abbs)

Q5115

Imfinzi (durvalumab)

J9173

Vectibix (panitumumab)

J9303

Istodax (romidepsin)

J9315

Yervoy (ipilimumab)

J9228

Ixempra (ixabepilone)

J9207

Zaltrap (ziv-aflibercept)

J9400

Jevtana (cabazitaxel)

J9043

Zirabev (bevacizumab-bvzr)

Q5118


Note: In some plans “dose reduction to nearest whole vial” or another term “waste reduction” may be the term used in benefit plans, provider contracts or other materials instead of or in addition to “dose reduction to nearest whole vial” and in some plans, these terms may be used interchangeably.  For simplicity, we will hereafter use “dose reduction (to nearest whole vial).”

 

Providers should continue to verify eligibility and benefits for all members prior to rendering services.

If you have questions, please call the Provider Service phone number on the back of the member’s ID card.

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PharmacyCommercialAugust 1, 2021

Specialty dose rounding program for certain non-oncology medications beginning August 1, 2021

Effective with dates of service on or after August 1, 2021, providers treating members covered by Anthem Blue Cross (Anthem) Commercial plans may be asked to consider voluntarily reducing the requested dose to avoid vial wastage for select non-oncology specialty medications The dose reduction suggestion will only be made if the originally requested dose is within 10% of the nearest whole vial.

 

Since this program is voluntary, the decision to participate will not affect the final decision on the prior authorization. 

 

Reviews for these specialty drugs will continue to be administered by IngenioRx®.

 

As part of the prior authorization process, providers may be asked the following questions:

  • Whether the suggested dose reduction is clinically acceptable
  • Clinical reasoning if the dose reduction is not appropriate

 

Providers can view prior authorization requirements for Anthem members on the Medical Policy & Clinical UM Guidelines page at anthem.com.

 

Providers should continue to verify eligibility and benefits for all members prior to rendering services.

 

If you have questions, please call the Provider Service phone number on the back of the member’s ID card.

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PharmacyCommercialAugust 1, 2021

Anthem Blue Cross to update formulary lists for commercial health plan pharmacy benefit, October 1, 2021

Effective with dates of service on and after October 1, 2021, and in accordance with the IngenioRx Pharmacy and Therapeutics (P&T) process, Anthem Blue Cross will update its drug lists that support commercial health plans.

 

  • Updates include changes to drug tiers and the removal of medications from the formulary.

 

  • Please note, this update does not apply to the Select Drug List and does not impact Medicaid and Medicare plans.

 

To ensure a smooth member transition and minimize costs, providers should review these changes and consider prescribing a drug on formulary or on a lower tier, if appropriate.

 

View a summary of changes here.  


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PharmacyCommercialAugust 1, 2021

Immune globulin adjusted body weight dosing program beginning August 1, 2021

Commercial plans may be asked to consider voluntarily using adjusted body weight (AdjBW) dosing compared to actual body weight (ABW) dosing for immune globulin medications. The dose change using AdjBW will only be made if the member’s actual body weight is more than 20% of the ideal body weight (IBW).

 

Since this program is voluntary, the decision to participate will not affect the final decision on the prior authorization. 

 

Reviews for the immune globulin medications will continue to be administered by IngenioRx® as these will specifically target specialty non-oncology indications.

 

As part of the prior authorization process, providers may be asked the following questions:

  • Whether the suggested use of AdjBW and change in dose is clinically acceptable
  • Clinical reasoning if the dose change (using AdjBW) is not appropriate

 

Providers can view prior authorization requirements for Anthem members on the Medical Policy & Clinical UM Guidelines page at anthem.com.

 

Providers should continue to verify eligibility and benefits for all members prior to rendering services.

 

If you have questions, please call the Provider Service phone number on the back of the member’s ID card.

 

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PharmacyCommercialAugust 1, 2021

Pharmacy information available on anthem.com/ca

For more information on copayment/coinsurance requirements and their applicable drug classes, drug lists and changes, prior authorization criteria, procedures for generic substitution, therapeutic interchange, step therapy or other management methods subject to prescribing decisions, and any other requirements, restrictions, or limitations that apply to using certain drugs, visit anthem.com/pharmacyinformation. The commercial and marketplace drug lists are posted to the web site quarterly (the first of the month for January, April, July and October).

To locate “Marketplace Select Formulary” and pharmacy information, scroll down to “Select Drug Lists.” This drug list is also reviewed and updated regularly as needed.

 

FEP Pharmacy updates and other pharmacy related information may be accessed at www.fepblue.org > Pharmacy Benefits.


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State & FederalMedicare AdvantageAugust 1, 2021

Preventing claims denials: Shingles vaccine

We want you to have the information you need when filing claims for our Medicare Advantage members, so your payments are received quickly and effortlessly. The shingles vaccine and the administration of the vaccine is commonly billed in error under the member’s Medicare Part B medical benefit. The shingles vaccination is a Medicare Part D pharmacy benefit, which requires the member to pay in advance of reimbursement. The member then submits the prescription drug claim form to their Medicare Part D plan for reimbursement. 

 

You can also refer the member to the pharmacy for the vaccine. The claim is usually filed for the member by the pharmacy provider using a clearinghouse platform that enables Medicare Part D claims transactions. Or, if you have access to clearinghouse platforms that enable you to file pharmacy transactions, that is another option for administering the vaccination in your office and for further serving the member.

 

The Centers for Medicare & Medicaid Services (CMS) has a helpful resource, MLN Fact Sheet: Medicare Part D Vaccines, that offers an all-inclusive look into patient access, vaccine administration, and reimbursement. Use this link to download a copy

 

We want you to have all the information you need to know best. For more information about filing claims, visit this link.

 

ABCCARE-0599-21

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