Effective Date:10/01/2010 |
Title:Airway Clearance Devices
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Revision Date:01/01/2019
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Document:BI268:00
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CPT Code(s):A7025, A7026,E0480, E0484, E0482, E0483, S8185, E0481
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Public Statement
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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)
Several forms
of mechanical devices are used to help clear secretions in persons who have
severe lung disease such as cystic fibrosis.
2)
These devices
require pre-authorization.
3)
When
approved, they are covered under the DME benefit.
4)
Intrapulmonary percussive ventilators (IPV) are considered experimental and
investigational as there is insufficient evidence supporting their
effectiveness.
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Medical Statement
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1)
The
following airway clearance devices are considered medically necessary durable
medical equipment (DME) to assist in mobilizing respiratory tract secretions for
members with the following conditions:
a)
Airway
oscillating devices (e.g., Flutter and Acapella) are considered medically
necessary for cystic fibrosis (E84.0), bronchitis (J41.0 – J42), bronchiectasis
(Q33.4, J47.0 – J47.9), and asthma (J44.0 – J45.998).
b)
Mechanical
percussors (e.g., Fluid Flo and Frequencer) are considered medically necessary
for cystic fibrosis (E84.0), chronic bronchitis (J41.0 – J42), bronchiectasis
(Q33.4, J47.0 – J47.9), immotile cilia syndrome (J39.8), and asthma (J44.0 –
J45.998).
c)
Positive
expiratory pressure (PEP) mask is considered medically necessary for cystic
fibrosis (E84.0), chronic bronchitis (J41.0 – J42), asthma (J44.0 – J45.998),
and chronic obstructive pulmonary disease (J44.9).
2)
High-frequency chest compression systems (the SmartVest, the MedPulse
Respiratory Vest System, the Vest Airway Clearance System, the ABI Vest, and the
InCourage Vest/System) are considered medically necessary in lieu of chest
physiotherapy for the following indications, where there is a documented failure
of standard treatments to adequately mobilize retained secretions, including
chest physiotherapy:
a)
Bronchiectasis (Q33.4, J47.0-J47.9), confirmed by CT scan, characterized by
daily productive cough for at least 6 continuous months or by frequent (i.e.,
more than 2 times per year) exacerbations requiring antibiotic therapy; or
b)
Cystic
fibrosis (E84.0); or
c)
The member
has one of the following neuromuscular disease diagnoses:
1.
Acid
maltase deficiency (E74.00)
2.
Anterior
horn cell diseases (G12.0 – G12.9)
3.
Hereditary
muscular dystrophy (G71.0)
4.
Multiple
sclerosis (G35)
5.
Myotonic
disorders (G71.11-G71.19)
6.
Other
myopathies (G71.3 – G71.9, G72.81 – G72.9)
7.
Paralysis
of the diaphragm (J98.6)
8.
Post-polio
(G14)
9.
Quadriplegia (G82.50 – G82.54)
d)
Lung
transplant recipients, within the first 6 months post-operatively, who are
unable to tolerate standard chest physiotherapy.
e)
High-frequency chest compression systems are considered experimental and
investigational for other indications (e.g., alpha 1-antitrypsin deficiency,
coma, kyphosis, leukodystrophy, and scoliosis).
3)
Mechanical
in-exsufflation devices are considered medically necessary DME for persons with
a neuromuscular disease (e.g., amyotrophic lateral sclerosis, high spinal cord
injury with quadriplegia) that is causing a significant impairment of chest wall
and/or diaphragmatic movement and for whom standard treatments (e.g., chest
percussion and postural drainage, etc.) have not been successful in adequately
mobilizing retained secretions.
Codes
Used In This BI:
A7025 |
High freq
chest wall oscillation syst vest, rplcmt for use w/ pt-owned equipmt, ea |
A7026 |
High freq
chest wall oscillation syst hose, rplcmt for use w/ pt-owned equipmt, ea |
E0480 |
Percussor,
electric or pneumatic, home model |
E0481 |
Intrapulmonary
percussive ventilation syst & related accessories |
E0482 |
Cough
stimulating device, alternating positive & negative airway pressure |
E0483 |
High freq
chest wall oscillation syst, (incl all access & suppl), ea
(code revised 1/1/19) |
E0484 |
Oscillatory
positive expiratory pressure dvc, nonelec, any type, ea |
S8185 |
Flutter device |
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Limits
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Intrapulmonary percussive ventilators (IPV) are considered experimental and
investigational as there is insufficient evidence supporting their
effectiveness.
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Reference
|
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Van Hengstum M, Festen J,
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Bellone A, Spagnolatti L,
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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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