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Effective Date: 01/01/2022 |
Title: Polymerase Chain Reaction Respiratory Viral Panel Testing
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Revision Date:
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Document: BI685:00
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CPT Code(s): 87631, 87632, 87633
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Public Statement
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Please Note:
QualChoice reserves the right to
conduct audits on any provider and/or facility to ensure compliance with the
guidelines stated in this policy. Services that are provided outside of
following guidelines may not meet coverage criteria and may lead to recoupment
of payment.
It is better and often less costly to
get care from doctors who are in QualChoice network. If the member gets care
from an out-of-network Health care provider, even if care is given at a network
doctor’s office or facility, the member’s cost may be higher.
Public
Statement:
Effective Date:
a)
This policy will apply to
all services performed on or after the above revision date which will become the
new effective date.
b)
For all services referred
to in this policy that were performed before the revision date, contact customer
service for the rules that would apply.
1)
Respiratory viral panels
(RVPs) testing for five (5) pathogens or less are considered medically necessary
and are covered without prior authorization.
2)
Respiratory viral panels
(RVPs) testing for 6 or more pathogens are considered medically necessary in a
healthcare setting that cares for critically ill patients, such as the emergency
department or inpatient hospital, including those in observation status.
3)
RVPs are considered not
medically necessary for all other indications.
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Medical Statement
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The diagnostic role and importance of the multi-pathogen panels in
identifying specific viruses in the setting of a respiratory infection is
limited because the care and management of the patient is not altered based upon
the pathogen identified.
1)
Respiratory viral panels
(CPT 87631) testing for 5 or less pathogens are considered medically necessary
and are covered without prior authorization.
2)
Respiratory viral panels
(CPT 87632 and 87633) testing for 6 or more pathogens are considered medically
necessary for critically ill members only when performed in an inpatient
facility, observation or emergency room settings.
3)
RVPs testing for 6 or
more pathogens are considered not medically necessary for any other places of
service.
Codes
Used In This BI:
87631
Infectious agent detection by nucleic acid (DNA or
RNA); respiratory virus (e.g., adenovirus, influenza virus, coronavirus,
metapneumovirus, parainfluenza virus, respiratory syncytial virus, rhinovirus),
includes multiplex reverse transcription, when performed, and multiplex
amplified probe technique, multiple types or subtypes, 3-5 targets.
87632 Infectious agent detection by
nucleic acid (DNA or RNA); respiratory virus (eg, adenovirus, influenza virus,
coronavirus, metapneumovirus, parainfluenza virus, respiratory syncytial virus,
rhinovirus), includes multiplex reverse transcription, when performed, and
multiplex amplified probe technique, multiple types or subtypes, 6-11 targets.
87633
Infectious agent detection by nucleic acid (DNA or
RNA); respiratory virus (eg, adenovirus, influenza virus, coronavirus,
metapneumovirus, parainfluenza virus, respiratory syncytial virus, rhinovirus),
includes multiplex reverse.
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Limits
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Respiratory viral panels
PCR testing in an outpatient place of service is reimbursable only when
performed as part of the diagnostic work-up for a patient admitted for
Observation.
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Background
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Polymerase chain reaction (PCR) respiratory viral panels (RVP) may detect the
RNA or DNA of multiple types of respiratory viruses as a single test, often
through a nasal, nasopharyngeal, or oropharyngeal swab. Viral pathogens are the
most common cause of respiratory tract infections. PCR testing is effective for
confirming respiratory viral infections with very high sensitivity and
specificity. Rhinovirus, parainfluenza virus, coronavirus, adenovirus,
respiratory syncytial virus, Coxsackie virus, human metapneumovirus, and
influenza virus account for most cases of viral respiratory infections.
Multiplex PCR testing can detect numerous respiratory viruses; that number
varies with the type and brand of testing being performed. However, the
diagnostic role and importance of these multi-pathogen panels in identifying
specific viruses in the setting of a respiratory infection is quite limited
because the care and management of the patient is not altered based upon the
pathogen identified, if any. For example, the child with a URI, cough, and
wheezing who might be positive for RSV would not be managed any differently than
the child with parainfluenza virus, adenovirus, rhinovirus, human
metapneumovirus, enterovirus, Coxsackie virus, or coronavirus.
Infectious Disease Society of America (IDSA)
The
IDSA recommends that “clinicians should use multiplex RT-PCR assays targeting a
panel of respiratory pathogens, including influenza viruses, in hospitalized
immunocompromised patients.” Further, “clinicians can consider using multiplex
RT-PCR assays targeting a panel of respiratory pathogens, including influenza
viruses, in hospitalized patients who are not immunocompromised if it might
influence care (e.g., aid in cohorting decisions, reduce testing, or decrease
antibiotic use).”
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Reference
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1)
Hill AT, et al. and the
CHEST Expert Cough Panel. Adult Outpatients with Acute Cough Due to Suspected
Pneumonia or Influenza: CHEST Guideline and Expert Panel Report. CHEST 2019;
Volume 155, Issue 1, Pages 155–167.
2)
Noridian Local Coverage
Determination. L37315 MolDX: Multiplex Nucleic Acid Amplified Tests for
Respiratory Viral Panels. Revision effective 10/1/2019.
3)
Hayes Precision Medicine
Research Brief, “FilmArray Respiratory Panel and FilmArray Respiratory Panel 2
(BioFire Diagnostics LLC),” September 2019
4)
Uyeki TM, et al. Clinical
Practice Guidelines by the Infectious Diseases Society of America: 2018 Update
on Diagnosis, Treatment, Chemoprophylaxis, and Institutional Outbreak Management
of Seasonal Influenza. Clin Inf Dis 2019; Volume 68, Issue 6, Pages e1–e47,
https://doi.org/10.1093/cid/ciy866.
5)
Ralston SL, et al.
Clinical practice guideline: the diagnosis, management, and prevention of
bronchiolitis. American Academy of Pediatrics. Pediatrics 2014; Volume 134,
Issue 5, Pages e1474- 502. doi: 10.1542/peds.2014-2742.
6)
Esposito S, et al.
Multiplex Platforms for the Identification of Respiratory Pathogens: Are They
Useful in Pediatric Clinical Practice? Front Cell Infect Microbiol. 2019 Jun
4;9:196. doi: 10.3389/fcimb.2019.00196.
7)
Busson L, et al.
Contribution of the FilmArray Respiratory Panel in the management of adult and
pediatric patients attending the emergency room during 2015–2016 influenza
epidemics: An interventional study. Int J Infect Dis. 2019 Jun;83:32-39. doi:
10.1016/j.ijid.2019.03.027.
8)
Echavarria M, et al.
Clinical impact of rapid molecular detection of respiratory pathogens in
patients with acute respiratory infection. J Clin Virol. 2018 Nov;108:90-95.
doi: 10.1016/j.jcv.2018.09.009.
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Application to Products
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This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet. Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail. State and federal mandates will be followed as they apply.
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Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
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