COVID-19 Updates & Alerts for Providers
Questions and Answers for California Wellcare Providers
Due to the rapidly changing environment as a result of COVID-19, the information included in this section is intended to serve as a guide for COVID-19-related information. This information and guidance is in response to the current state of COVID-19 and is subject to change, and may be retired at a future date. Unless stated otherwise, special coverage and waivers stated herein expire when the public emergency period ends. This section shall be updated as new information and guidance becomes available; however, providers should continue to refer to the Department of Managed Health Care (DMHC), Department of Health Care Services (DHCS), and the Centers for Medicare & Medicaid Services (CMS) websites for the most up-to-date information.
Please refer to the sections below for current plan information regarding COVID-19 vaccines and guidance.
Updated August 10, 2023
23-038G
COVID 19 - General Information
- COVID-19 Testing and Screening, Billing and Treatment Information (updated)
Information throughout the FAQs has been updated to reflect current guidance and information.
COVID-19 Therapeutic and Vaccine FAQs
What you need to know about current treatment
Communications & Resources
Stay informed on the latest news and help for you and your patients
COVID-19 General Information
What's covered, how to bill for treatment, telehealth guidance, and more
Historical Information
COVID-19 content that may be retired or no longer relevant to the public health emergency
Is there provider support for questions about COVID-19 testing and treatment?
All California health care providers can get confidential consultation support through the COVID-19 Therapeutics Warmline managed by the University of California, San Francisco (USCF) National Clinical Consultation Center (NCCC). Providers of any experience level can speak with a clinician or pharmacist:
- Call 866-268-4233 (866-COVID-CA). Monday – Friday, 6 a.m.–5 p.m. After- hours voice mail messages are returned the next business day.
- This support is in real-time and at no cost.
- No protected health information (PHI) is collected.
What resources are available about COVID-19 outpatient therapeutics?
Videos and resources are available from the Department of Health and Human Services’ Administration for Strategic Preparedness & Response (ASPR). The website covers the following topics and more:
- Compare COVID-19 Therapeutics and Patient Requirements
- Find, Order and Report COVID-19 Therapeutics
- Learn About COVID-19 Therapeutics
- Share Resources with Patients and Other Health Care Providers
The following videos are available through ASPR and cover:
- ASPR and the COVID Response
- Overview: COVID-19 Therapeutics
- COVID-19 Therapeutics Distribution
- Separate videos about therapeutics for: Paxlovid, Lagevrio, and Veklury
Note: The U.S. Food and Drug Administration (FDA) announced on January 26, 2023, that Evusheld is no longer authorized for emergency use in the United States against developing variants of the COVID-19 virus.
Additional resources
The Office of Communications for the California Department of Public Health (CDPH) has different material to download and print - from graphics and hand-outs to social messaging in English and Spanish. The goal is to educate patients and encourage use of COVID-19 therapeutics to treat symptoms before they become severe.
How to dispel misinformation about treatments
See the CDPH COVID-19 Therapeutics Myths and Facts sheet (PDF). It covers questions such as:
- I don't need medication for mild-to-moderate illness.
- I’m not high risk.
- Treatments have serious side effects.
- Rebound caused by treatments is common and can be dangerous.
Where can I get information for my patients about the COVID-19 Test to Treat Program?
More information about the Test to Treat Program can be found on the CDPH website. Patients who have COVID-19 symptoms can be seen by a health care provider and get treatment at a Test to Treat site during the same visit, if needed.
- This is available to adults and children over age 12.
- Uninsured individuals can access testing and treatment services at no cost at OptumServe locations.
Is coping assistance offered to members impacted by COVID-19?
Wellcare members impacted by COVID-19 may contact their participating physician group (PPG) for referrals to mental health counselors, local resources or telephonic consultations to help them cope with stress, grief, loss, or other trauma resulting from COVID-19.
Additional resources on how to mitigate the stress-related health outcomes anticipated with the COVID-19 emergency can be found at ACEs Aware.
Adverse Childhood Experiences (ACEs) resources and information for Medi-Cal can be found at California Department of Health Care Services Trauma Screenings and Trauma-Informed Care Provider Trainings.
As a health care provider, you play an integral role with COVID-19 vaccinations. For regular and frequent updates on the vaccine information and distribution in California, visit Vaccinate ALL 58.
Important! Enroll to get your California Immunization Information System (IIS) ID
The California Department of Public Health (CDPH) is overseeing the registration for the COVID-19 vaccination program in California. Program enrollment is currently focused on small physician practices who routinely vaccinate their patients as well as providers that are prioritized for vaccine allocation by local health departments.
Step 1: Get your IIS ID
Enroll in your local registry to receive your Immunization Information System (IIS) ID for enrollment in CalVax. County-specific information is below.
County | Website |
---|---|
San Joaquin | www.myhealthyfutures.org |
Other Counties | www.cairweb.org/join-cair |
Step 2: Enroll in myCAvax
Make sure you meet all the requirements before enrolling. Use the Provider Enrollment Worksheet to gather information needed ahead of time to complete enrollment in myCAvax.
Refer to the Readiness Checklist: Quick Start Guide (PDF) for additional steps to help providers onboard to the COVID-19 Vaccination Program.
More information that can help you share clear and accurate information about COVID-19 vaccines and address common questions from patients can be found in Communication Resources for Healthcare Providers and Staff from the Centers for Disease Control and Prevention (CDC).
Is there a current COVID-19 vaccination schedule?
The CDC develops age-specific immunization schedules that give guidance based on age and medical conditions including dosage for different vaccines and interval periods between doses. Age and condition specific up-to date COVID-19 guidance is also available for:
Where can I find the latest guidance for the COVID-19 vaccine?
What are the codes to report and bill the COVID-19 vaccines?
The American Medical Association (AMA) has published updates to the Current Procedural Terminology (CPT®) code set that includes new vaccine-specific codes to report immunizations for the novel coronavirus (SARS-CoV-2). The code set will continue to be updated as additional vaccines receive EUA approval by the U.S. Food & Drug Administration (FDA).
The following codes have been published; however, they will not be billable or payable until the specific vaccine receives official EUA approval or after the EUA is revoked.
Current vaccine-specific code sets with FDA EUAs:
Code | CPT Short Descriptor | Labeler Name | Vaccine/Procedure Name |
---|---|---|---|
91312 |
SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine – Booster |
0124A |
ADM SARSCV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Administration – Booster |
91315 (eff. August 31, 2022) |
SARSCOV2 VAC 10MCG/0.2ML TRS-SUCR |
Pfizer | Pfizer-BioNTech Covid-19 Vaccine – Booster ages 5 years – 11 years |
0154A (eff. August 31, 2022) |
ADM SARSCV2 10MCG/0.2ML TRS-SUCR 3 |
Pfizer | Pfizer-BioNTech Covid-19 Vaccine Administration – Booster ages 5 years – 11 years |
91317 (eff December 8, 2022) |
SARSCOV2 VAC BVL 3MCG/0.2ML |
Pfizer | Pfizer-BioNTech COVID-19 Vaccine, Bivalent Product ages 6 months through 4 years (Maroon cap) |
0173A (eff December 8, 2022) |
ADM SARSCV2 BVL 3MCG/0.2ML 3 |
Pfizer | Pfizer-BioNTech Covid-19 Pediatric Vaccine (ages 6 months through 4 years) (Maroon cap) Administration - Third Dose |
91313 |
SARS-COV2 |
Moderna |
Moderna COVID-19 Vaccine – Bivalent Booster |
0134A |
ADM SARSCOV2 VAC |
Moderna |
Moderna COVID-19 Vaccine Administraton – Bivalent Booster |
91314 (eff. August 31, 2022) |
SARS-COV2 25MCG/0.25 ML IM |
Moderna | Moderna COVID-19 Vaccine – Bivalent Booster ages 6 years – 11 years |
0144A (eff. August 31, 2022) |
ADM SARSCOV2 VAC 25MCG/0.25ML BST |
Moderna | Moderna COVID-19 Vaccine Administration – Bivalent Booster ages 6 years – 11 years |
91316 (eff December 8, 2022) |
SARSCOV2 VAC BVL 10MCG/0.2M |
Moderna | Moderna COVID-19 Vaccine, Bivalent Product ages 6 months through 5 years (Dark pink cap and a label with a yellow box) |
0164A (eff December 8, 2022) |
ADM SRSCV2 BVL 10MCG/0.2ML B |
Moderna | Moderna COVID-19 Vaccine, Bivalent ages 6 months through 5 years (Dark pink cap and label with a yellow box) Administration – Booster Dose |
91304 |
SARS-COV2 |
Novavax |
Novavax COVID-19 Vaccine |
0041A |
ADM SARSCOV2 5MCG/0.5ML First dose |
Novavax |
Novavax COVID-19 Vaccine |
0041B |
ADM SARSCOV2 5MCG/0.5ML Second dose |
Novavax |
Novavax COVID-19 Vaccine |
0044A (eff. October 19, 2022) |
ADM SARSCOV2 5MCG/0.5ML BST |
Novavax | Novavax Covid-19 Vaccine, Adjuvanted Administration - Booster |
91303 |
SARSCOV2 VAC |
Janssen |
Janssen COVID-19 Vaccine |
0031A |
ADM SARSCOV2 |
Janssen |
Janssen COVID-19 Vaccine Administration |
0034A |
ADM SARSCOV2 |
Janssen |
Janssen CVOID-19 Vaccine |
Prior vaccine-specific code sets with FDA Emergency Use Authorization revoked:
Code | CPT Short Descriptor | Labeler Name | Vaccine/Procedure Name |
---|---|---|---|
91300 |
SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech COVID-19 Vaccine |
0001A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech COVID-19 Vaccine |
0002A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech COVID-19 Vaccine |
0003A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech COVID-19 Vaccine |
0004A |
ADM SARSCOV2 30MCG/0.3ML BST |
Pfizer |
Pfizer-BioNTech COVID-19 Vaccine |
91305 |
SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pre-Diluted (Gray Cap) |
0051A |
ADM SARSCV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pre-Diluted (Gray Cap) |
0052A |
ADM SARSCV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pre-Diluted (Gray Cap) |
0053A |
ADM SARSCV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pre-Diluted (Gray Cap) |
0054A |
ADM SARSCV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pre-Diluted (Gray Cap) |
91307 |
SARSCOV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0071A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0072A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0073A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pediatric Administration – Third Dose |
0074A |
ADM SARSCOV2 VAC 10MCG/0.2ML TRS-SUCR B |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine Pediatric Administration – |
91308 |
SARSCOV2 |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0081A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0082A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
0083A |
ADM SARSCOV2 VAC |
Pfizer |
Pfizer-BioNTech Covid-19 Vaccine |
91301 |
SARSCOV2 VAC |
Moderna |
Moderna COVID-19 Vaccine |
0011A |
ADM SARSCOV2 VAC |
Moderna |
Moderna COVID-19 Vaccine |
0012A |
ADM SARSCOV2 VAC |
Moderna |
Moderna COVID-19 Vaccine |
0013A |
ADM SARSCOV2 VAC |
Moderna |
Moderna COVID-19 Vaccine |
91306 |
SARSCOV2 VAC 50MCG/0.25ML IM |
Moderna |
Moderna COVID-19 Vaccine (Low Dose) |
0064A |
ADM SARSCOV2 50MCG/0.25ML BST |
Moderna |
Moderna COVID-19 Vaccine (Low Dose) Administration – Booster |
0091A |
ADM SARSCOV2 50MCG/0.5ML 1ST |
Moderna |
Moderna COVID-19 Vaccine |
0092A |
ADM SARSCOV2 50MCG/0.5ML 2ND |
Moderna |
Moderna COVID-19 Vaccine Administration – Pediatric ages 6–11 |
0093A |
ADM SARSCOV2 50MCG/0.5ML 3RD |
Moderna |
Moderna COVID-19 Vaccine |
0113A |
AMD SARSCOV2 25MCG/0.25ML 3RD |
Moderna |
Moderna COVID-19 Vaccine |
91309 |
SARSCOV2 VAC 50MCG/0.5ML IM |
Moderna |
Moderna COVID-19 Vaccine – Booster |
0094A |
ADM SARSCOV2 50MCG/0.5ML BST |
Moderna |
Moderna COVID-19 Vaccine |
91311 |
SARSCOV2 |
Moderna |
Moderna COVID-19 Vaccine |
0111A |
IMM ADMN SARSCOV2 |
Moderna |
Moderna COVID-19 Vaccine |
0112A |
IMM ADMN SARSCOV2 |
Moderna |
Moderna COVID-19 Vaccine |
What are the reporting requirements for the COVID-19 vaccine?
Providers must record details of the vaccination into their system of record within 24 hours, and into the applicable public health system within 72 hours.
How will the COVID-19 vaccine be covered for members?
Similar to other preventive immunizations, the COVID-19 vaccines are offered at no cost to members. In addition:
- For Calendar Years (CYs) 2020 and 2021, payment for the COVID-19 vaccine administration for Medicare Advantage plan members will be made through the original fee-for-service Medicare program. The vaccine itself is available from the federal government free of charge.
- For CY 2022 forward, CMS no longer directly reimburses providers for COVID-19 vaccines including their administration. Vaccine related claims should be billed like other Medicare covered vaccines. Send claims to the delegated at-risk provider groups of Wellcare.
Updated 5/11/23
Effective February 11, 2023, Health and Human Services (HHS) Secretary Xavier Becerra renewed the COVID-19 Public Health Emergency for a final time with a 90-day notice. This extends flexibilities and funding tied to the public health emergency (PHE) to continue through May 11, 2023, at which time the PHE will expire. California state law adds six months to the federal PHE requirements on health plans to continue covering COVID-19 tests, vaccines and therapeutics from any licensed provider (in- or out-of-network) with no prior authorization or enrollee cost sharing.
Does Wellcare allow access to telehealth services to increase access to care? And what is the reimbursement rate?
To limit members' risk of COVID-19 infection, Wellcare encourages use of telehealth to deliver care when medically appropriate and capable through telehealth modalities for covered services.
Wellcare's coverage for telehealth services will follow guidance released by CMS, which includes telecommunications involving audio and video technology and audio only technology.
- Services that cannot be appropriately delivered remotely are not eligible for telehealth coverage and reimbursement.
- Capitated physician groups are required to support, cover and enable telehealth services and to abide by regulatory requirements for coverage and payment of telehealth services as outlined above. Claims processing risk will follow the in-person location place of service where the service would have been delivered in lieu of telehealth.
In addition to telehealth services offered through our network of providers, Wellcare has expanded access to telehealth services through third parties.
What are the guidelines for telehealth services specific to risk adjustment?
Providers should follow the guidance in the communication from the Centers for Medicare and Medicaid Services (CMS) dated April 10, 2020, regarding the Applicability of diagnoses from telehealth services for risk adjustment (PDF).
How do I bill for telehealth services?
Providers should bill in accordance with CMS requirements found at Telehealth.HHS.GOV
Examples of benefits or services not appropriate for telehealth delivery:
Below are some examples (not exhaustive) of benefits or services that would not be appropriate for delivery via a telehealth modality.
- Performed in an operating room or while the patient is under anesthesia
- Requiring direct visualization or instrumentation of bodily structures
- Involving sampling of tissue or insertion/removal of medical device
- Requiring the in-person presence of the patient for any reason
Are there member cost shares for Medicare network provider telehealth services?
Member cost shares for covered services delivered via telehealth will be subject to the cost sharing provisions of a member's benefit plan for particular covered service delivered.
Capitated Physician Groups:
Capitated physician groups are required to support, cover and enable telehealth services and to abide by regulatory requirements for coverage and payment of telehealth services as outlined above.
What is Wellcare's strategy to support telehealth services for providers and members?
Wellcare is committed to supporting your relationship with your patients. We continuously encourage members to first take advantage of the telehealth services provided by their primary care provider before considering Wellcare's contracted vendors.
What additional telehealth options are available to my patients?
Wellcare offers additional telehealth services through Teladoc® to enhance access to care for your patients. These services supplement, but do not replace, the personal care you provide to your patients.
Providers can also refer to Telehealth Platforms for Providers for a variety of telehealth platforms that optimize the availability of telehealth capabilities to our providers. These platforms accommodate most medical conditions, including COVID-19, and allow for a compliant way to administer health care services to your patients.
What support will Teladoc provide to me if my patients use them?
Teladoc supports the PCP and their relationship with their patient. Teladoc services include:
- Visit summaries sent to the PCP for close communication and continuity of care, at the member's request.
- Referring patients back to the assigned PCP for follow-up appointments.
- Prescribing of non-scheduled, non-lifestyle medications.
- Availability of the member's medical records through the Teladoc application.
Is Wellcare requiring prior authorization, precertification, prior notification, or step therapy protocols for COVID-19 screening and testing? Will cost shares be applied?
After the PHE expires on May 11, 2023, the application of member cost share, prior authorization and out of network coverage rules will apply per the member’s posted benefit plan design.
Updated 8/10/2023
What billing codes should be used to bill for COVID-19 testing?
CMS updated the list of valid HCPCS codes used for COVID-19 related testing and billing effective May 12, 2023. Claims after that date must reflect a valid HCPCS code for reimbursement.
Specimen Collection - Valid codes:
- HCPCS C9803 - Hospital outpatient clinic visit specimen collection for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]).
- CPTs 99000, 99001, or 99211 when billed with a COVID-19 related diagnosis code.
Invalid specimen collection codes for billing dates of service on or after May 12, 2023:
- HCPCS G2023
- HCPCS G2024
Active Virus Testing - Valid codes:
- HCPCS U0001 - For CDC developed tests only: 2019-nCoV Real-Time RT-PCR Diagnostic Panel.
- HCPCS U0002 - For all other commercially available tests: 2019-nCoV Real-Time RT-PCR Diagnostic Panel.
- CPT 87635 – (effective March 13, 2020): Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]), amplified probe technique. The industry standard for reporting of novel coronavirus tests across the nation’s health care system.
- CPT 0202U – (effective May 20, 2020): Infectious disease (bacterial or viral respiratory tract infection), pathogen specific nucleic acid (DNA or RNA), 22 targets including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), qualitative RT-PCR, nasopharyngeal swab, each pathogen reported as detected or not detected.
- CPT 0223U (effective June 25, 2020) Infectious disease (bacterial or viral respiratory tract infection), pathogen-specific nucleic acid (DNA or RNA), 22 targets including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), qualitative RT-PCR, nasopharyngeal swab, each pathogen reported as detected or not detected.
- CPT 87426 (effective June 25, 2020) Infectious agent antigen detection by immunoassay technique, (eg, enzyme immunoassay [EIA], enzyme-linked immunosorbent assay [ELISA], immunochemiluminometric assay [IMCA]) qualitative or semi-quantitative, multiple-step method; severe acute respiratory syndrome coronavirus (e.g., SARS-CoV, SARS-CoV-2 [COVID-19]).
- CPT 0225U (effective September 8, 2020) Infectious disease (bacterial or viral respiratory tract infection) pathogen-specific DNA and RNA, 21 targets, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), amplified probe technique, including multiplex reverse transcription for RNA targets, each analyte reported as detected or not detected.
- CPT 0226U (effective September 8, 2020) Surrogate viral neutralization test (sVNT), severe acute respiratory syndrome coronavirus 2 (SARSCoV-2) (Coronavirus disease [COVID-19]), ELISA, plasma, serum.
- CPT 0240U (effective October 6, 2020) Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 3 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B), upper respiratory specimen, each pathogen reported as detected or not detected.
- CPT 0241U (effective October 6, 2020) Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 4 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B, respiratory syncytial virus [RSV]), upper respiratory specimen, each pathogen reported as detected or not detected.
- CPT 87636 (effective October 6, 2020) Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]) and influenza virus types A and B, multiplex amplified probe technique.
- CPT 87637 (effective October 6, 2020) Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]), influenza virus types A and B, and respiratory syncytial virus, multiplex amplified probe technique.
- CPT 87811 (effective October 6, 2020) Infectious agent antigen detection by immunoassay with direct optical (i.e., visual) observation; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]).
- CPT 87913 (effective February 21, 2022) Infectious agent genotype analysis by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), mutation identification in targeted region(s).
Invalid active virus testing codes for billing dates of service on or after May 12, 2023:
- HCPCS U0003
- HCPCS U0004
- HCPCS U0005 (Note: This code was not covered by Medi-Cal prior to May 12, 2023, as well)
Antibody (serologic) Testing
- CPT 86318 Immunoassay for infectious agent antibody(ies), qualitative or semi quantitative, single step method (e.g., reagent strip); (EXISTING PARENT CODE NOT SPECIFIC TO COVID 19).
- CPT 86328 Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), (Coronavirus disease [COVID-19]), (For severe acute respiratory syndrome, coronavirus 2 [SARS-CoV-2] [Coronavirus, disease {COVID-19}] antibody testing using multiple-step method, use 86769).
- CPT 86769 Antibody; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]) (For severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] [Coronavirus disease {COVID-19}] antibody testing using single step method, use 86328).
- CPT 0224U (effective June 25, 2020) Antibody, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]), includes titer(s), when performed.
- CPT 86408 (effective August 10, 2020) Neutralizing antibody, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]); screen.
- CPT 86409 (effective August 10, 2020) Neutralizing antibody, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]); titer.
- CPT 86413 (effective September 8, 2020) Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]) antibody, quantitative.
CDC Antibody Testing Guidance: View the Interim Guidelines for COVID-19 Antibody Testing
What diagnosis codes should be used to bill for services related to COVID-19 screening and testing?
For complete and up-to-date diagnosis coding for COVID-19, visit the CDC National Center for Health Statistics website.
The following diagnosis codes can be used to bill for screening and testing services related to COVID-19.
- Z11.52 - Encounter for screening for COVID-19.
- Z20.822 - Contact with and (suspected) exposure to COVID-19.
Can providers balance bill members for fees related to screening and testing for COVID-19?
Balance billing is strictly prohibited by state and federal law and Wellcare's PPA. Providers may not bill members for any fees related to screening and testing for COVID-19.
Is Wellcare waiving cost-share requirements for COVID-19 related therapeutics?
Coverage for Medicare members will follow existing program guidelines.
What COVID-19 ICD-10 diagnoses codes are approved for use in treatment?
- U07.1: 2019-nCoV - Confirmed by lab testing (effective April 1, 2020)
- M35.81: Multisystem Inflammatory Syndrome (MIS) (effective January 1, 2021)
Does Wellcare cover monoclonal antibody infusion treatment for COVID-19?
For dates of service prior to June 1, 2021, COVID-19 monoclonal antibody treatments available under an FDA Emergency Use Authorization (EUA) are covered benefits with no cost share or prior authorization required. The medications are available from the federal government at no cost to providers. After June 1, 2021, normal cost shares and prior authorization guidelines, if any, will apply.
The following codes have been published; however, they are not billable or payable until after the specific treatment received official EUA approval.
Current monoclonal antibody treatments with FDA EUA's
Code | CPT Short Descriptor | Labeler Name | Vaccine/Procedure Name |
---|---|---|---|
Q0249 (eff. June 24, 2021) |
Tocilizumab for COVID-19 |
Genentech |
Injection, tocilizumab, for hospitalized adults and pediatric patients (ages 2 years and older) with COVID-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) only, 1 mg |
M0249 (eff. June 24, 2021) |
Adm Tocilizu COVID-19 1st |
Genentech |
Intravenous infusion, tocilizumab, for hospitalized adults and pediatric patients (ages 2 years and older) with COVID-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) only, includes infusion and post administration monitoring, first dose |
M0250 (eff. June 24, 2021) |
Adm Tocilizu COVID-19 2nd |
Genentech |
Intravenous infusion, tocilizumab, for hospitalized adults and pediatric patients (ages 2 years and older) with COVID-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) only, includes infusion and post administration monitoring, second dose |
Q0220 (eff Dec 8, 2021) |
Tixagevimab & Cilgavimab (EVUSHELD), 300mg |
AstraZeneca | Injection, tixagevimab and cilgavimab, for the pre-exposure prophylaxis only, for certain adults and pediatric individuals (12 years of age and older weighing at least 40kg) with no known sars-cov-2 exposure, who either have moderate to severely compromised immune systems or for whom vaccination with any available covid-19 vaccine is not recommended due to a history of severe adverse reaction to a covid-19 vaccine(s) and/or covid-19 vaccine component(s), 300 mg |
Q0221 (eff Feb 24, 2022) |
Tixagevimab & Cilgavimab (EVUSHELD), 600mg |
AstraZeneca | Injection, tixagevimab and cilgavimab, for the pre-exposure prophylaxis only, for certain adults and pediatric individuals (12 years of age and older weighing at least 40kg) with no known sars-cov-2 exposure, who either have moderate to severely compromised immune systems or for whom vaccination with any available covid-19 vaccine is not recommended due to a history of severe adverse reaction to a covid-19 vaccine(s) and/or covid-19 vaccine component(s), 600 mg |
M0220 (eff Dec 8, 2021) |
Tixagevimab & Cilgavimab (EVUSHELD) Admin |
AstraZeneca | Injection, tixagevimab and cilgavimab, for the pre-exposure prophylaxis only, for certain adults and pediatric individuals (12 years of age and older weighing at least 40kg) with no known sars-cov-2 exposure, who either have moderate to severely compromised immune systems or for whom vaccination with any available covid-19 vaccine is not recommended due to a history of severe adverse reaction to a covid-19 vaccine(s) and/or covid-19 vaccine component(s), includes injection and post administration monitoring |
M0221 (eff Dec 8, 2021) |
Tixagevimab & Cilgavimab (EVUSHELD) Admin Home |
AstraZeneca | Injection, tixagevimab and cilgavimab, for the pre-exposure prophylaxis only, for certain adults and pediatric individuals (12 years of age and older weighing at least 40kg) with no known sars-cov-2 exposure, who either have moderate to severely compromised immune systems or for whom vaccination with any available covid-19 vaccine is not recommended due to a history of severe adverse reaction to a covid-19 vaccine(s) and/or covid-19 vaccine component(s), includes injection and post administration monitoring in the home or residence; this includes a beneficiary’s home that has been made provider-based to the hospital during the covid-19 public health emergency |
Prior treatments with FDA Emergency Use Authorization revoked
Code | CPT Short Descriptor | Labeler Name | Vaccine/Procedure Name |
---|---|---|---|
Q0239* |
bamlanivimab-xxxx |
Eli Lilly |
Injection, bamlanivimab, 700 mg |
M0239 (FDA’s EUA ended April 16, 2021) |
bamlanivimab-xxxx infusion | Eli Lilly | Intravenous infusion, bamlanivimab-xxxx, includes infusion and post administration monitoring |
Q0240 (eff. July 30, 2021; FDA’s EUA ended Jan 24, 2022) |
Casirivi and imdevi 600 mg | Regeneron | Injection, casirivimab and imdevimab, 600 mg |
M0240 (eff. July 30, 2021; FDA’s EUA ended Jan 24, 2022) |
Casiri and imdev repeat | Regeneron | Intravenous infusion or subcutaneous injection, casirivimab and imdevimab includes infusion or injection, and post administration monitoring, subsequent repeat doses |
M0241 (eff. July 30, 2021; FDA’s EUA ended Jan 24, 2022) |
Casiri and imdev repeat hm | Regeneron | Intravenous infusion or subcutaneous injection, casirivimab and imdevimab includes infusion or injection, and post administration monitoring in the home or residence. This includes a beneficiary’s home, subsequent repeat doses |
Q0243* (FDA’s EUA ended Jan 24, 2022) |
casirivimab and imdevimab | Regeneron | Injection, casirivimab and imdevimab, 2400 mg |
Q0244 (eff. June 3, 2021; FDA’s EUA ended Jan 24, 2022) |
casirivimab and imdevimab | Regeneron | Injection, casirivimab and imdevimab, 1200 mg |
M0243 (FDA’s EUA ended Jan 24, 2022) |
casirivi and imdevi infusion | Regeneron | Intravenous infusion, casirivimab and imdevimab includes infusion and post administration monitoring |
M0244 (eff May 6, 2021; FDA’s EUA ended Jan 24, 2022) |
casirivi and imdevi infusion home | Regeneron | Intravenous infusion, casirivimab and imdevimab includes infusion and post administration monitoring in the home or residence |
Q0245* (FDA’s EUA ended Jan 24, 2022) |
bamlanivimab and etesevimab | Eli Lilly | Injection, bamlanivimab and etesevimab, 2100 mg |
M0245 (FDA’s EUA ended Jan 24, 2022) |
bamlan and etesev infusion | Eli Lilly | Intravenous infusion, bamlanivimab and etesevimab, includes infusion and post administration monitoring |
M0246 (FDA’s EUA ended Jan 24, 2022) |
bamlan and etesev infusion home | Eli Lilly | Intravenous infusion, bamlanivimab and etesevimab, includes infusion and post administration monitoring in the home or residence |
Q0247 (eff. May 26 2021 – ended April 5, 2022**) |
Sotrovimab | GSK | Injection, sotrovimab, 500 mg |
M0247 (eff. May 26 2021 – ended April 5, 2022**) |
Sotrovimab infusion | GSK | Intravenous infusion, sotrovimab, includes infusion and post administration monitoring |
M0248 (eff. May 26 2021 – ended April 5, 2022**) |
Sotrovimab inf, home admin | GSK | Intravenous infusion, sotrovimab, includes infusion and post administration monitoring in the home or residence |
Q0222 (eff Feb 11, 2022; FDA’s EUA ended Nov 30, 2022) |
Bebtelovimab 175 mg | Eli Lilly | Injection, bebtelovimab, 175 mg |
M0222 (eff Feb 11, 2022; FDA’s EUA ended Nov 30, 2022) |
Bebtelovimab injection admin | Eli Lilly | Intravenous injection, bebtelovimab, includes injection and post administration monitoring |
M0223 (eff Feb 11, 2022; FDA’s EUA ended Nov 30, 2022) |
Bebtelovimab injection admin, home | Eli Lilly | Intravenous injection, bebtelovimab, includes injection and post administration monitoring in the home or residence; this includes a beneficiary’s home that has been made provider-based to the hospital during the covid-19 public health emergency |
*medication code not payable
Effective January 1, 2022, the medication and infusion's administration fee is billable to the appropriate payor based on Wellcare’s existing division of financial responsibility with the capitated physician group/IPA. Medication that is available free from the federal government is not reimbursable. Prior to 2022, the medication and infusion's administration fee is billable to CMS directly for both Original Medicare and Medicare Advantage members.