Answer: Effective with discharges on or after August 1, 2020, new ICD-10-PCS codes have been implemented for the administration of three different drugs when used to treat COVID-19:
ICD-10-PCS Code | Description |
---|---|
XW033E5 | Introduction of remdesivir anti-infective into peripheral vein, percutaneous approach, new technology group 5 |
XW043E5 | Introduction of remdesivir anti-infective into central vein, percutaneous approach, new technology group 5 |
Oct 01, 2015 · 2022 ICD-10-PCS Procedure Code XW043E5; 2022 ICD-10-PCS Procedure Code XW043E5 Introduction of Remdesivir Anti-infective into Central Vein, Percutaneous Approach, New Technology Group 5. 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code. ICD-10-PCS XW043E5 is a specific/billable code that can be used to indicate a procedure.
ICD-10-PCS code XW033E5 is a billable procedure used to indicate the performance of introduction of remdesivir anti-infective into peripheral vein, percutaneous approach, new technology group 5. Code valid for the year 2022
Jul 31, 2020 · In addition to ICD-10-PCS codes for remdesivir and convalescent plasma, two other named substances have their own PCS codes. Each of the four substances has two codes apiece, because each substance can be administered via central or peripheral IV infusion. The eight substance-specific codes are below. Table XW0
4 rows · ICD-10-PCS Code Description; XW033E5: Introduction of remdesivir anti-infective into ...
Remdesivir may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
• nausea
• constipation
• pain, bleeding, bruising of the skin, soreness, or swelling near the place where the medication was injected
Benefits of Vaccination Outweigh the Risks Serious side effects that could cause a long-term health problem are extremely unusual following any vaccination, including COVID-19 vaccination.
Some people have no side effects. Many people have reported side effects, such as headache, fatigue, and soreness at the injection site, that are generally mild to moderate and go away within a few days.
Remdesivir is the only drug that is approved by the Food and Drug Administration (FDA) for the treatment of COVID-19. Ritonavir-boosted nirmatrelvir (Paxlovid), molnupiravir, and certain anti-SARS-CoV-2 monoclonal antibodies (mAbs) have received Emergency Use Authorizations from the FDA for the treatment of COVID-19.
Paxlovid is an oral antiviral pill that can be taken at home to help keep high-risk patients from getting so sick that they need to be hospitalized. So, if you test positive for the coronavirus and a health care provider writes you a prescription, you can take pills at home and lower your risk of going to the hospital.
In most situations, mRNA COVID-19 vaccines (Pfizer-BioNTech or Moderna) are preferred over the J&J/Janssen COVID-19 vaccine for primary and booster vaccination due to the risk of serious adverse events.
Introduction of Remdesivir Anti-Infective into Peripheral Vein, Percutaneous Approach New Technology Group 5
There are now a total of 42 questions with recommended coding for each. The last five questions discuss the new COVID-19 ICD-10-PCS codes just released. Other topics in the revised document include coding for re-admissions of COVID-19 patients, sequela and personal history of COVID-19 and multisystem inflammatory syndrome (MIS-C) due to COVID-19.
AMA released the CPT code 87426 for antigen testing in June 2020. Review our COVID-19 Explained article series, which dives into how to code the screening for suspected COVID-19 infection, how to code possible infection and symptoms, and the history and background on COVID-19.
The unprecedented events of the COVID-19 pandemic have resulted in another unprecedented event: the release of new ICD-10-PCS codes that will be put in use immediately – effective with discharges on or after August 1, 2020, rather than the usual effective date of October 1 (CMS, 2020). Immediate reporting of the new hospital procedure codes for COVID-19 will allow for tracking of the use and effectiveness of these therapies in treating inpatients for COVID-19 and provide valuable information as the nation continues to deal with the disease.
XW033E5 replaces the following previously assigned ICD-10-PCS code (s):
The ICD-10 Procedure Coding System (ICD-10-PCS) is a catalog of procedural codes used by medical professionals for hospital inpatient healthcare settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.
The codes are in section X New Technology of the ICD-10-PCS tables because, as CMS has stated at previous ICD-10 Coordination and Maintenance (C&M) Committee meetings, two types of procedures are typically included in Section X: 1) procedures that are not usually assigned a code on an inpatient record, and 2) procedures that require a new code (s) to uniquely identify the procedure for CMS’ New Technology Add-on Payment (NTAP) program. The new PCS codes fall under the first category. The new codes are designated with the qualifier New Technology Group 5, rather than designated New Technology Group 6 along with the new FY 2021 PCS codes posted on the CMS website on May 28, because they are valid on August 1 and so are retroactively included in the FY 2020 update. The new codes and associated official ICD-10-PCS content are posted in a separate set of addenda files.
According to an announcement posted July 30 on the CMS website, “In response to the COVID-19 pandemic, the Centers for Medicare & Medicaid Services (CMS) is implementing 12 new procedure codes to describe the introduction or infusion of therapeutics, including remdesivir and convalescent plasma, into the International Classification of Diseases, Tenth Revision, Procedure Coding System (ICD-10-PCS), effective August 01, 2020. ”
On October 22, 2020, the FDA approved remdesivir (Veklury) for the treatment of COVID-19 for adults and certain pediatric patients requiring hospitalization. On November 19, 2020, the FDA issued an EUA for the use of baricitinib (Olumiant), in combination with remdesivir (Veklury), for the treatment of suspected or laboratory confirmed COVID-19 in ...
NCTAP claims are those that are eligible for the 20% add-on payment under Section 3710 of the CARES Act. Eligible claims have both of the following:
CMS issued an Interim Final Rule with Comment Period that established the New COVID-19 Treatments Add-on Payment (NCTAP) under the Medicare Inpatient Prospective Payment System (IPPS). The NCTAP, designed to mitigate potential financial disincentives for hospitals to provide new COVID-19 treatments, is effective from November 2, 2020, until the end of the COVID-19 public health emergency (PHE).
Through the NCTAP, the Medicare Program will provide an enhanced payment for eligible inpatient cases that use certain new products with current FDA approval or emergency use authorization (EUA) to treat COVID-19, including the following: On August 23, 2020, the FDA issued (reissued on November 30, 2020, and revised on March 9, ...
Hospitals shouldn’t report charges for products they got for free. A hospital shouldn't seek additional payment on the claim for drugs or biologicals to treat patients with known or suspected COVID-19 that the government purchased or provided for free.
It can also be used to treat children with polyarticular juvenile idiopathic arthritis or systemic juvenile idiopathic arthritis.
Convalescent plasma (also called immune plasma or hyperimmune plasma) is similar to fresh frozen plasma. The major difference from other plasma is that convalescent plasma is obtained from donors who have recovered from a specific infection – in this case, COVID-19. The hope is that convalescent plasma contains antibodies to COVID-19 at a level high enough to provide passive immunity to the recipient of the plasma.
phase 3 clinical trial of the study of Kevzara in COVID-19 patients on a mechanical ventilator was stopped when it failed to show improvements in patients or failed to prevent death.
A concurrent approach is important so that this information is surfaced before discharge, and coding and billing of the record is not delayed. The clinical documentation specialist (CDS) will most likely have reviewed the clinical care provided, especially since patients receiving these treatments are more complex cases and have longer lengths of stay.
CDI and coding teams have standardized and refined their processes and procedures over many years, and incorporated technology as their programs have grown and matured. Although the CMS announcement may be viewed as a disruptive event, CDI and coding professionals are well-prepared to incorporate these new codes with relative ease. This pandemic has exposed many painful inadequacies within our healthcare delivery system—the clinical documentation improvement and coding process is not one of them.
The Food and Drug Administration (FDA) has authorized the emergency use of remdesivir to treat hospitalized patients with suspected or confirmed COVID-19. Remdesi vir is not approved anywhere globally for any use and the safety and efficacy for the treatment of COVID-19 are not proven.
It is currently being evaluated in several phase 3 clinical trials to determine the efficacy of using tocilizumab in hospitalized adult patients with pneumonia related to COVID-19.
The Centers for Medicare & Medicaid Services (CMS) released two International Classification of Diseases, 10 th Revision, Procedure Coding System (ICD-10-PCS) codes, effective August 1, 2020 to report the administration of Remdesivir.
The decision to charge separately for infusion of drugs, including Remdesivir, for hospital inpatients should be determined by each hospital and outlined in a policy and procedure.
CMS has not indicated a specific revenue code assignment ; in the absence of specific guidance, revenue code reporting should represent the code where the costs will be reported on the facility’s cost report.
Answer: The Secretary of the Department of Health and Human Services declared a public health emergency that justifies the emergency use of Ve klury® to treat coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 infection. In response, the U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) ...
On October 22, 2020, the FDA approved remdesivir (Veklury) for the treatment of COVID-19 for adults and certain pediatric patients requiring hospitalization. On November 19, 2020, the FDA issued an EUA for the use of baricitinib (Olumiant), in combination with remdesivir (Veklury), for the treatment of suspected or laboratory confirmed COVID-19 in ...
NCTAP claims are those that are eligible for the 20% add-on payment under Section 3710 of the CARES Act. Eligible claims have both of the following:
The NCTAP, designed to mitigate potential financial disincentives for hospitals to provide new COVID-19 treatments, is effective from November 2, 2020, until the end of the COVID-19 public health emergency (PHE).
Hospitals shouldn’t report charges associated with the product received at no cost. A hospital should not seek additional payment on the claim for drugs or biologicals that a governmental entity procured or provided to a provider at no cost to the provider to diagnose or treat patients with known or suspected COVID-19.
HHS is committed to making its websites and documents accessible to the widest possible audience, including individuals with disabilities. We are in the process of retroactively making some documents accessible. If you need assistance accessing an accessible version of this document, please reach out to the Section 508 Help Desk.
Hospitals should report the ICD-10-PCS code (s) for all products administered during the stay, even if the hospital got the product for free. Hospitals shouldn’t report charges for products they got for free.
The device is an interbody fusion implant that stabilizes the lumbar spinal column and facilitates fusion during lumbar fusion procedures indicated for the treatment of spinal deformity. The applicant states that the implant device is custom made for patient-specific features, by using patient CT scans to create 3D virtual models of the deformity. Made of Titanium Alloy. The device is used during anterior lumbar interbody fusion, lateral lumbar interbody fusion, transforaminal lumbar interbody fusion, or standalone anterior lumbar interbody fusion procedures. The maximum payment a hospital can receive for this is $20,475 as a new technology add on payment FY2022. orthoworld.com/carlsmed-aprevo-interbody-gains-fda-clearance-breakthrough-device-designation/ Approved.
Section “X” is a separate place within ICD-10-PCS for certain new technology procedures (such as new technology drugs). Section “X” does not introduce any new coding concepts or unusual guidelines for correct coding and maintains continuity with the other sections in ICD-10-PCS. The same root operation and body part values are used in section “X” as in other sections. The seventh character in section “X” is used to indicate the new technology group. This is a number that changes each year that new technology codes are added. It is only used to indicate the year the code was created and all codes for that update year will have the same qualifier. The new technology drugs for FY2022 will have the qualifier/seventh character of “7” since this is the seventh year of ICD-10-PCS. You will see other new technology codes with numbers from previous years that are still being paid.
FY2022 Medicare will make an add-on payment equal to the lesser of: (1) 75 percent medical product (65 % for new technology) of the costs of the new medical service or technology; or (2) 75 percent of the amount by which the costs of the case exceed the standard DRG payment.
Code C34 for malignancy of bronchus and lung tor Z51.11/Z51.12 for admit for chemo or immunotherapy. Hospital will get $8,622.90 as a new technology add on payment FY2022.
VEKLURY® (remdesivir) VEKLURY® is a nucleotide analog that inhibits viral RNA-dependent RNA polymerases, demonstrat ing activity counter ing viral path ogens such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19). Approved for patients 12 years or older. Hospital will get $2,028 as a new technology add on payment FY2022.
StrataGraftTM Skin Tissue It is described as a viable, bioengineered, regenerative skin construct (BRSC) consisting of an epidermal layer of viable, fully stratified, allogeneic human NIKS®603 keratinocytes growing on a dermal layer composed of viable human dermal fibroblasts embedded in a collagen-rich matrix. The applicant noted that StrataGraftTM is intended for the treatment of adult patients with severe thermal burns that contain intact dermal elements and require surgical intervention (hereinafter referred to as severe thermal burns [STB]). Hospital will get $44,200 as a new technology add on payment FY2022.
ABECMA® (idecabtagene vicleucel) Idecabtagene viclecuel is a, B-cell maturation antigen (BCMA)-directed genetically modified autologou s chimeric antigen receptor (CAR) T-cell immunotherapy for the treatment of adult patients with relapsed or refractory (RR) multiple myeloma (MM) (RRMM) who have received at least four prior therapies including an immunomodulatory agent (IMiD), a proteasome inhibitor (PI), and an anti-CD38 antibody (for example, triple-class-exposed). Idecabtagene vicleucel is expected to be a 5th line plus (5L+) treatment. Codes C90.00 and C90.02 for diagnoses. The maximum payment a hospital can receive for this is $272,675.00 as a new technology add on payment FY2022.