In addition to the seven new 2022 ICD-10 procedure codes announced in November, the Centers for Medicare & Medicaid Services on April 1 will implement two new ICD-10 procedure codes for reporting COVID-19 therapeutics. The new codes are for describing the infusion of tixagevimab and cilgavimab monoclonal antibody (code XW023X7), and the infusion of other new technology monoclonal antibody (code XW023Y7).
Jan 13, 2022 · In addition to the seven new 2022 ICD-10 procedure codes announced in November, the Centers for Medicare & Medicaid Services on April 1 will implement two new ICD-10 procedure codes for reporting COVID-19 therapeutics. The new codes are for describing the infusion of tixagevimab and cilgavimab monoclonal antibody (code XW023X7), and the …
Mar 03, 2022 · What ICD-10 diagnosis code should be billed for the COVID-19 vaccine or mAb infusion? Diagnosis code Z23 is the primary diagnosis required for the COVID-19 vaccine. The mAb infusion billing enter the appropriate diagnosis coded to highest level of specificity (U071 - use as appropriate).
If you administer COVID-19 monoclonal antibodies to Medicare patients in traditional health care locations (for example, a hospital outpatient infusion clinic or freestanding infusion clinic), continue to bill HCPCS codes M0240, M0243, M0245, M0247, or M0222, as applicable.
Oct 01, 2021 · Z01.84 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM Z01.84 became effective on October 1, 2021. This is the American ICD-10-CM version of Z01.84 - other international versions of ICD-10 Z01.84 may differ.
CMS developed two procedure codes, M0239 and M0243. When coverage criteria were established by CMS for these codes, no professional component was “split out” to allow both professional and institutions to billed for the same code as other outpatient procedure codes. In the situation described, the physician attending to the patient care should bill the appropriate evaluation and management code and the hospital bills for the mAb infusion.
During the PHE, we would anticipate this circumstance to be a common occurrence, and physicians and non-physician practitioners furnishing these services on the same day should add modifier “25” to the E/M code to identify it as a medically necessary E/M service furnished on the same day that another service is furnished by the same physician or other supplier. Similarly, hospital outpatient departments furnishing separately identifiable office visits on the same day a vaccine or mAb infusion is administered should also add modifier “25” to identify a medically necessary E/M service furnished on the same day as another service.
mAB may only be administered in settings in which health care providers have immediate access to medications to treat a severe infusion reaction, such as anaphylaxis, and the ability to activate the emergency medical system, as necessary. Reference: Monoclonal Antibody COVID-19 Infusion. 6.
The DR condition code is not required.
At this time the mAb infusions currently are not on the NCCI edit files and should not impact claims when the patient is receiving other infusions. The NCCI edit files are updated quarterly so be sure to review the current files.
On November 9, 2020, the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the investigational monoclonal antibody therapy, bamlanivimab, for the treatment of mild-to-moderate COVID-19 in adults and pediatric patients with positive COVID-19 test results who are at high risk for progressing to severe COVID-19 and/or hospitalization. Bamlanivimab may only be administered in settings in which health care providers have immediate access to medications to treat a severe infusion reaction, such as anaphylaxis, and the ability to activate the emergency medical system (EMS), as necessary. Review the Fact Sheet for Health Care Providers EUA of Bamlanivimab regarding the limitations of authorized use.
Bamlanivimab may only be administered in settings in which health care providers have immediate access to medications to treat a severe infusion reaction, such as anaphylaxis, and the ability to activate the emergency medical system (EMS), as necessary.
The 2022 edition of ICD-10-CM Z01.84 became effective on October 1, 2021.
Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00 -Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways:
Ever since a public health emergency (PHE) for COVID-19 was declared on Jan. 27, 2020, there has been several new HCPCS Level II codes created for monoclonal antibody (mAb) products and administration.
Here are the most current codes for investigational monoclonal antibody therapies with emergency use authorization (EUA) and applicable administration codes:
Medicare will pay for COVID-19 mAb under the Medicare Part B vaccine benefit through the end of the calendar year that the PHE ends — so at least Dec. 31, 2022. Medicare payment is typically at reasonable cost or at 95 percent of the average sales price (ASP). See payment allowance limits for Medicare Part B drugs, effective Jan.
CPT® defines a therapeutic, prophylactic, or diagnostic injection (96372) as requiring “direct physician supervision” and, typically, “special consideration to prepare, dose or dispose of … practice training and competency for staff who administer infusions, and … periodic patient assessment.”.
Code 96401 may be used for a variety of drugs, including: non-radionuclide anti-neoplastic drugs. anti-neoplastic agents provided for treatment of noncancer diagnoses. certain monoclonal antibody agents and other biologic response modifiers. CPT® does not specifically identify those “certain monoclonal antibody agents and other biologic response ...
CPT® does not specifically identify those “certain monoclonal antibody agents and other biologic response modifiers” that would qualify under 96401.
Medicare Advantage claims for the COVID-19 vaccine and mAb infusions, require the condition code (CC) 78 to be reported on the claim to avoid the claim from rejecting.
For tocilizumab, roster billing cannot be used to report multiple units or infusions. Submit individual claims for the tocilizumab product and infusions when reporting multiple units of the product and/or the first and second infusions.
Under the terms of the EUA, tocilizumab may only be infused in the hospital setting (TOB 12X). CMS pays for tocilizumab based on the number of units administered, so include the total number of units administered on the claim per day. For example: