endstream endobj startxref This period (such as 30, 60, 90 days, 6 months, etc.) Turn to the AMA for timely guidance on making the most of medical residency. Yes, COVID-19 vaccines are available for everyone at no cost, including the booster dose. %PDF-1.6 % A. These NDCs will not be manufactured. CMS and the AMA developed this code structureto make claims processingfor administration of COVID-19 vaccines and monoclonal antibody infusions that get FDA EUA or FDA approval more efficient. @LeD8BAz^atUgy@JEAM0 0-z Individuals can self-report that they are eligible and receive a booster shot wherever vaccines are provided. The FDA issued its initial Emergency Use Authorization for the Janssen (Johnson & Johnson) COVID-19 vaccine on Saturday February 27, 2021. A written appeal must be filed with the New York State Health Department. A physician who fails to comply can be subject to disciplinary action by the New York State Health Department. We'll issue specific code descriptors in the future. A patient over age 12 may be advised of a records request and, if he or she objects, the provider . endstream endobj 159 0 obj <>/Subtype/Form/Type/XObject>>stream received. Prior authorization in health care is a requirement that a provider (physician, hospital, etc.) Recognizing that some institutions may not have IRBs, or that some IRBs may not have the expertise needed to review research that requires consideration of risks to privacy, the Privacy Rule permits the covered entity to accept documentation of waiver of authorization from an alternative body called a Privacy Boardwhich could have fewer members, and members with different expertise than IRBs. Explore the seven key steps physicians and teams can take to use SMBP with patients with high blood pressure and access links to useful supporting resources. Explore top articles, videos, research highlights and more from the AMAyour source for clear, evidence-based news and guidance during the pandemic. When a physician denies you access, he or she must provide you with a form explaining the appeals process. Therefore, covered entities can continue to disclose protected health information to report adverse events to the Office for Human Research Protections either with patient authorization as provided at 45 CFR 164.508, or without patient authorization for public health activities as permitted at 45 CFR 164.512(b). The AMA promotes the art and science of medicine and the betterment of public health. If your client application is throwing HTTP 403 (Forbidden) errors, a likely cause is that the client is using an expired Shared Access Signature (SAS) when it sends a storage request (although other possible causes include clock skew, invalid keys, and empty headers). These cookies may also be used for advertising purposes by these third parties. Many of these codes are placeholders and aren't currently effective, is specifically assigned. Signature Thats why Baptist Health Medical Group is readjusting how they tackle burnout systemwide. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 50 mcg/0.25 mL dosage, for intramuscular use, 100 mcg/0.5 mL for adult 18+ (Same formulation and concentration as EUA product), FDA EUA update of 04/18/2023 rescinds use of this monovalent vaccine. Yes. Information the physician believes may cause substantial harm to the patient or others. There are some restrictions on what may be obtained and fees may be charged by physicians, other health care professionals and facilities for providing copies. s> _:9ID/ngz[i>Oir,O0]mX+M|^Kqz'5h4N*"{LTdVHMQ Moderna is actively assessing demand signals to activate supply plans and working closely with USG partners to collect official demand requirements., Moderna COVID-19 Vaccine Bivalent Booster, 0.5 mL dose of Original and Omicron COVID-19 strains, Moderna Statement: NDC codes 80777-280-99 and 80777-280-05 were provided in anticipation of FDA authorization under EUA for a bivalent booster vaccine (Moderna COVID-19 Vaccine, Bivalent). A patient over age 12 may be advised of a records request and, if he or she objects, the provider may deny the request. The pandemic has affected everyone differently. The FDA issued its initial Emergency Use Authorization for the Novavax COVID-19 vaccine on Wednesday July 13, 2022. Immunocompromised individuals 5 years of age and older who have received one dose of a bivalent COVID-19 vaccine: An additional dose with Pfizer-BioNTech COVID-19 Vaccine, Bivalent may be . Information disclosed to the practitioner under the condition that it would be kept confidential. The IRB or Privacy Board could be created by the covered entity or the recipient researcher, or it could be an independent board. The codes for these vaccines are also included in the vaccine code set files unless otherwise noted in the table. In response to the spread of COVID-19, the Centers for Medicare & Medicaid Services (CMS) now allows more qualified nonphysician health care professionals, including SLPs, to report communication technology-based services (CTBS), such as e-visits, virtual check-ins, and telephone assessments, for Medicare Part B (outpatient) beneficiaries. Authorized by WHO 10/19/2022 Counted toward immunity in US, Pfizer COVID-19 Bivalent, Original + BA.1 (Non-US Tradename COMIRNATY Bivalent), SARS-COV-2 (COVID-19) vaccine SP, protein-based, adjuvanted, B.1.351 strain (VidPrevtyn Beta), Sanofi-GSK, COVID-19 SP, protein-based, adjuvanted (VidPrevtyn Beta), Sanofi-GSK, COVID-19 Moderna EUA Recipient-Caregiver Fact Sheet all ages 6 months and older, COVID-19 Pfizer BioNTech EUA Recipient-Caregiver Fact Sheet all ages 6 months and older, COVID-19 Janssen Vaccine EUA Recipient-Caregiver Fact Sheet, COVID-19 Novavax EUA Recipient-Caregiver Fact Sheet, Centers for Disease Control and Prevention. However, an individual cannot be denied access to information solely because he or she is unable to pay. The COVID-19 vaccine-related codes are provided in anticipation of potential vaccine availability under an EUA. Most individuals with certain kinds of immunocompromise who have received a bivalent COVID-19 vaccine may receive a single additional dose of a bivalent COVID-19 vaccine at least 2 months . If the appeal is denied, the individual can seek disclosure through the courts. ( patient has right to appear in person or by phone at review meeting before a health care Washington, D.C. 20201 A covered entity may use or disclose protected health information without individuals authorizations for the creation of a research database, provided the covered entity obtains documentation that an IRB or Privacy Board has determined that the specified waiver criteria were satisfied. The request should indicate that a qualified person is making the request and should be as precise as possible. The law also permits access by other "qualified persons." Only the SPIKEVAX NDCs 80777-100-99 and 80777-100-11 will be manufactured at this time., Download the Preview Table for Non-US vaccine administration only: Excel Version. These NDC codes are not included in CDC Vaccine Code Set files at this time. Get reliable information on developments in the authorization, distribution and administration of COVID-19 vaccines. Authorizations, if needed, should be obtained before treatment is rendered. Turn around time for Dental Authorization review is 30 days after all required information has been received. Expedited (jeopardize patient's health): 72 hours. Reddit and its partners use cookies and similar technologies to provide you with a better experience. I recently got an appointment at Walgreens to receive the vaccine. Used to record Moderna vaccines administered in the US and in non-US locations (includes tradename Spikevax), Moderna COVID-19 Vaccine (non-US Spikevax), SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 30 mcg/0.3mL dose, EUA 12/11/2020, 2-dose vaccine. Under state law, failure to provide medical records requested by a qualified individual is misconduct. and our If you do not allow these cookies we will not know when you have visited our site, and will not be able to monitor its performance. Im wondering if these are not required in the state of MI, but I couldnt find any information about it. The Ohio Department of Health repealed authorization for the monovalent COVID-19 vaccines from Moderna and Pfizerthe same type of vaccines many Americans received during the start of the pandemic. Thats why Baptist Health Medical Group is readjusting how they tackle burnout systemwide. AMA members can get $1,000 off any Volvo pure electric, plug-in hybrid or mild hybrid model. I got my first dose on Tuesday through Walgreens . CMS is planning for the end of the COVID-19 public health emergency (PHE), which is expected to occur on May 11, 2023. Review this page for information about Medicare coding for administering COVID-19 vaccines during and after the PHE. A total of 10,334 patients diagnosed with osteonecrosis of the femoral head and having received hip surgery were identified from a nationwide database between 1 January 2010 and 31 December 2019, by using the International Classification of Disease, the Ninth/Tenth revision (ICD-9/10) codes. Documentation of IRB or Privacy Board approval of an alteration or waiver of individual authorization is only needed before a covered entity may use or disclose protected health information under 45 CFR 164.512(i)(1)(i). A researcher is a covered health care provider if he or she furnishes health care services to individuals, including the subjects of research, and transmits any health information in electronic form in connection with a transaction covered by the Transactions Rule. You have the right to have access to or request a copy of your own health records. A. These cookies perform functions like remembering presentation options or choices and, in some cases, delivery of web content that based on self-identified area of interests. Therefore, covered entities can continue to disclose protected health information to the Office for Human Research Protections for such compliance investigations either with patient authorization as provided at 45 CFR 164.508, or without patient authorization for health oversight activities as permitted at 45 CFR 164.512(d). Authorization forms under the HIPAA privacy rule should include the following components: The covered entity is responsible for providing the authorization form and obtaining the patient's signature. CVX code 500 should be used to record Non-US vaccine where product is not known. CVX and MVX codes are identified for vaccines that have received emergency authorization from the World Health Organization (WHO), US Food and Drug Administration (FDA) or both. Normally, a payer that authorizes a service prior to an encounter assigns an authorization number that you need to include on the claim when you submit it for payment. If the committee finds that the records should be made available, the practitioner must comply. EUA-authorized for ages 5 yrs to < 12 yrs. before enrollment is called the "look-back" period. Visit our online community or participate in medical education webinars. The vaccines are also providing protection against the Delta variant. Web Design System. Ages 6 mos to < 6 yrs: Used to record Pfizer vaccines administered in the US and in non-US locations (includes tradename Comirnaty), Pfizer-BioNTech COVID-19 Vaccine (US-EUA), COMIRNATY (US-BLA), COMIRNATY (Non-US), SARS-COV-2 (COVID-19) vaccine, vector non-replicating, recombinant spike protein-ChAdOx1, preservative free, 0.5 mL, COVID-19 vaccine, vector-nr, rS-ChAdOx1, PF, 0.5 mL, WHO authorized pandemic vaccine. Secure .gov websites use HTTPS Payment. Learn more: Part of the AMAsCOVID-19 CPT guidance, the Find your COVID-19 Vaccine CPT Codes resource, helps you determine the appropriate CPT code combination for the type and dose of vaccine that you are using. Subscribe now to stay in the loop on continued CPT reform. The NDCs related to the Carton of 10 7.5mL vials (80777-100-98/80777-100-15) will not be manufactured. The law defines personal notes and observations as "a practitioner's speculations, impressions (other than a tentative or actual diagnosis) and reminders". Officials and members gather to elect officers and address policy at the 2023 AMA Annual Meeting being held in Chicago, June 9-14, 2023. Information obtained from other physicians who are still in practice. Only bivalent booster should be administered. A federal government website managed and paid for by the U.S. Centers for Medicare & Medicaid Services. Yes, both flu vaccine and COVID-19 boosters can be administered at the same visit. Discuss & share news about Coronavirus in Michigan. Information regarding the Moderna vaccines as well as both the EUA Provider Fact Sheet and the EUA Recipient and Caregiver Fact Sheets is now available on the following FDA web site link: https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/moderna-covid-19-vaccines. FDA EUA updated 04/18/2023. Under the Privacy Rule, a covered entity may use or disclose protected health information pursuant to a copy of a valid and signed Authorization, including a copy that is received by facsimile or electronically transmitted. FDA EUA update of 04/18/2023 rescinds use of this monovalent vaccine. CVX and MVX codes are identified for vaccines that have received emergency authorization from the World Health Organization (WHO), US Food and Drug Administration (FDA) or both. Required prior authorization or precertification was not obtained; . Transitioningfrom medical student to resident can be a challenge. obtains approval from your health insurance plan before prescribing a specific medication for you or performing a particular medical procedure. A research year during medical school affords students more time to follow their scholarly pursuits. With the rapidly expanding availability of different vaccines coming to market, understanding the appropriate reporting for the vaccine that physicians and qualified health care professionals plan to deliver to patients is critical. For dates of service on or after August 24, 2021, if you administer the vaccine to fewer than 10 Medicare patients at the same group living location on that date, report the HCPCS Level II code M0201 for each Medicare patient vaccinated in an individual home that day, and up to a maximum of 5 times if multiple Medicare patients are vaccinated in the same home or communal space, Report the appropriate product-and dose-specific COVID-19 vaccine administration CPT code for each Medicare patient vaccinated in the home that day. CMS and the American Medical Association (AMA) collaborated on a new approach to report use of COVID-19 vaccines. Pfizer-BioNTech, Moderna and Johnson & Johnson COVID-19 booster shots are all available now. Use HCPCS Level II code M0201 to bill for the additional payment for administering the COVID-19 vaccine to Medicare patients in their homes under certain circumstances. You will be subject to the destination website's privacy policy when you follow the link. 471-May a covered entity use or disclose a patient's entire medical record based on the patient's signed authorization 472-Does the Privacy Rule permit a covered entity to use or disclose protected health information 473-May a valid authorization list categories of persons who may use or discloseinformation 10 mcg/0.2 mL for primary series, IC 3rd dose, booster, SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 10 mcg/0.2 mL dose, tris-sucrose formulation, COVID-19, mRNA, LNP-S, PF, 10 mcg/0.2 mL dose, tris-sucrose, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 10 mcg/0.2 mL dosage, diluent reconstituted, tris-sucrose formulation, for intramuscular use, FDA EUA update 04/18/2023 rescinds use of this monovalent vaccine.EUA-authorized for ages 6 mo to <5 yrs, SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 3 mcg/0.2 mL dose, tris-sucrose formulation, COVID-19, mRNA, LNP-S, PF, 3 mcg/0.2 mL dose, tris-sucrose, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 3 mcg/0.2 mL dosage, diluent reconstituted, tris-sucrose formulation, for intramuscular use. endstream endobj 156 0 obj <>/Metadata 19 0 R/Outlines 39 0 R/PageLabels 151 0 R/PageLayout/OneColumn/Pages 153 0 R/PieceInfo<>>>/StructTreeRoot 45 0 R/Type/Catalog/ViewerPreferences<>>> endobj 157 0 obj <>/ExtGState<>/Font<>/ProcSet[/PDF/Text/ImageC]/XObject<>>>/Rotate 0/StructParents 0/Tabs/S/Type/Page>> endobj 158 0 obj <>/Subtype/Form/Type/XObject>>stream Featured updates: COVID-19 resource center, Get the news you need with AMA Update on YouTube, Stay informed on the latest COVID-19 vaccine updates, COVID-19 Vaccine Script for Patient Inquiries, AMA Recovery Plan for America's Physicians. For more information, please see our It may not be the same as the EUA authorization date or the date embedded in the Document Barcode String. People ages 18 to 49 years who are at high risk for severe COVID-19 due to certain, People ages 18 to 64 years who are at increased risk for COVID-19 exposure and transmission because of. To support this effort, the CDC is working closely with data partners responsible for the creation and distribution of vaccine codes and drug compendia publishers to coordinate the release of codes in advance of potential EUAs to enable systems and users that require these codes to prepare in advance. A lock (LockA locked padlock) or https:// means youve safely connected to the .gov website. See how the CCB recommends changes to the AMA Constitution and Bylaws and assists in reviewing the rules, regulations and procedures of AMA sections. When requesting prior authorization, please provide the following information: Member name and ID number Cookie Notice With expert resources and tireless advocacy, the AMA is your powerful ally against COVID-19. A physician can deny you access to the following: A. "It doesn't do anybody any good if the patient has the test, but the hospital has to write it off or the patient has to pay for it," says Lestina. The list of vaccines not authorized by the WHO may be incomplete. Moderna has provided the following statement regarding the SPIKEVAX branded NDCs and labels: EUA-authorized for ages 6 years to < 12 years, 50 mcg/0.50 mL pediatric primary series for ages 6 yrs to <12 years, Moderna Statement: These codes have been provided in anticipation of FDA authorization and need. The Privacy Rule permits, but does not require, a covered entity voluntarily to obtain patient consent for uses and disclosures of protected health information for treatment, payment, and health care operations. SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 50 mcg/0.5 mL dose, COVID-19, mRNA, LNP-S, PF, 50 mcg/0.5 mL dose, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 50 mcg/0.5 mL dosage, for intramuscular use, 25 mcg/0.25 mL dose For pediatric primary series and IC doses for ages 6 mo to <6 years, SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, pediatric 25 mcg/0.25 mL dose, COVID-19, mRNA, LNP-S, PF, pediatric 25 mcg/0.25 mL dose, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 25 mcg/0.25 mL dosage, for intramuscular use. However, over time, public health experts are starting to see reduced protection against mild and moderate diseases as COVID-19 variants continue to change. Review the list of candidates to serve on the AMA Board of Trustees and councils. FDA EUA updated 04/18/2023. According to an AMA survey, respondents reported an "average of 14.6 hours (approximately two business days) spent each week by the physician/staff" to complete this prior authorizations workload. Document the informed consent conversation and the patient's (or surrogate's) decision in the medical record in some manner. See how the CCB recommends changes to the AMA Constitution and Bylaws and assists in reviewing the rules, regulations and procedures of AMA sections. In contrast, an individuals informed consent, as required by the Common Rule and the Food and Drug Administrations (FDA) human subjects regulations, is a consent to participate in the research study as a whole, not simply a consent for the research use or disclosure of protected health information. Authorizes dosing for Dose 3 and additional doses for ages 6 mo to < 6 yrs, SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, bivalent, preservative free, 10 mcg/0.2 mL dose, COVID-19, mRNA, LNP-S, bivalent, PF, 10 mcg/0.2 mL, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, bivalent, preservative free, 10 mcg/0.2 mL dosage, for intramuscular use, FDA EUA update 04/18/2023 rescinds use of this monovalent vaccine.EUA-authorized for ages 12 yrs +. Yes. All rights reserved. Information that the practitioner believes should not be disclosed regarding the treatment of a minor. 0013A - Immunization administration by intramuscular injection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 100 mcg/0.5 mL dosage; third dose. Information about you will not be released without your authorization unless permitted by law (an example of this is State public health reporting). .gov The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. ) These vaccines are listed separately because they represent NDCs that will not be manufactured or made available in the near term even if authorized. Yes, COVID-19 booster doses are the same formulation as the COVID-19 vaccines used for the primary series. @-92d~#AO,a0510I((#0H}/t:9|oVXc:YURTk^M/ The Privacy Rule allows those doctors, nurses, hospitals, laboratory technicians, and other health care providers that are covered entities to use or disclose protected health information, such as X-rays, laboratory and pathology reports, diagnoses, and other medical information for treatment purposes without the patients authorization. Review the reports and resolutions submitted for consideration at the 2023 Annual Meeting of the AMA House of Delegates. An authorization, sometimes referred to as 'preauthorization' or 'precertification', is the approval from a patient's health insurance for treatment by a specialist, deeming it medically necessary. 30 mcg/0.3 mL for primary series, IC 3rd dose and boosters. Code 1975 27-3A-5 2 business days of receipt of request and all necessary info . Certification Number or Treatment Authorization Number. Why are booster shots needed? The CPT codes, updated by the CPT Editorial Panel, will be effective for use now that a third dose shot of the Pfizer and Moderna COVID-19 vaccines have received emergency use authorization from the U.S. Food and Drug Administration (FDA) for certain patients with compromised immune systems. 100 mcg/0.5 mL for adult primary series and IC dose 12+ (existing product), SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 100 mcg/0.5mL dose or 50 mcg/0.25mL dose, COVID-19, mRNA, LNP-S, PF, 100 mcg/0.5mL dose or 50 mcg/0.25mL dose, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) vaccine, mRNA-LNP, spike protein, preservative free, 100 mcg/0.5 mL dosage, for intramuscular use. The Privacy Rule requires that an Authorization contain either an expiration date or an expiration event that relates to the individual or the purpose of the use or disclosure. On 8/31/2022, EUA rescinded for adult monovalent booster. You can review and change the way we collect information below. Authorization through the ACRC for the hospital admission does not remove the need for prior authorization (PA) required by Medicaid for specific services. Moderna received FDA BLA license on January 31, 2022, for its COVID-19 vaccine SPIKEVAX (COVID-19 Vaccine, mRNA) for use in individuals 18 and older. Albany, New York 12204-2719. or call (800) 663-6114. c. the patient's insurance payer d. the physician performing the procedure or service. Download AMA Connect app for Avoid "No Auth" Claims Denials June 1, 2016 When a physician orders a procedure to be performed in a surgical setting at Birmingham, AL-based UAB Hospital, patient access staff start the process of obtaining required authorizations. CDC twenty four seven. A code given to . A. Receive the latest updates from the Secretary, Blogs, and News Releases. Once your request is received, a physician or health care facility has 10 days to provide you with an opportunity to inspect your records. A. Health systems science is key to creating a new generation of physicians better equipped to deliver great team care. We take your privacy seriously. No, no charge may be imposed for providing, releasing, or delivering your records or copies of your records when requested for the purpose of supporting an application, claim or appeal for any government benefit or program, provided that, where a provider maintains your records in electronic form, the provider must provide the copy in either electronic or paper form, as required by the government benefit or program, or at the patients request. Authorizes bivalent vaccine dosing for ages 6 mo and older. r ``8*EX Your plan may contract with a pharmacy benefits management company to process prior authorization requests for certain prescription drugs or specialty drugs. What doctors wish patients knew about the What doctors wish patients knew about COVID-19 People 65 years and older and residents ages 18 years and older of long-term care settings should receive a booster dose at least 6 months after their primary series. The CPT codes will facilitate the updating of health care electronic systems across the U.S. Questions on CPT coding and content should be directed to the CPT Network, the authoritative source for CPT coding answers. Coding for COVID-19 Vaccine Shots After the FDA issues an emergency use authorization (EUA) or approves licensure of each COVID-19 vaccine product, CMS will identify the following for Medicare payment: Vaccine code (s), by dose if necessary Vaccine administration code (s) for each dose Information regarding the Janssen vaccines as well as both the EUA Provider Fact Sheet and the EUA Recipient and Caregiver Fact Sheets is now available on the following FDA web site link: https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/janssen-covid-19-vaccine#additional. Yes, as long as the Authorization describes, among other things, the information to be used or disclosed by the covered entity in a. Turn to the AMA for timely guidance on making the most of medical residency. New concentration, 50 mcg/0.50 mL for booster dose adults 18+ yrs, also authorized for primary series and IC doses for ages 6 years to <12 years. "People have to understand the ramifications of this." The obvious problem is that payers can and do refuse to pay if the authorization wasn't obtained prior to service. 7500 Security Boulevard, Baltimore, MD 21244, An official website of the United States government. It's possible thatwe won't use all codes. No. hb```b``b`e`: ,@Q :%MH0yDoq*OKPD2(( B. So, for example, if you had surgery at age 11 and want your records at age 18, the law requires that the physician and the hospital have them. Reactions reported after the booster dose were similar to that of the primary series. canadian shield climate graph, eric and ariel simple living alaska, pete nelson family photos,
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