Effective Date:03/01/2010 |
Title:Allergy Testing
|
Revision Date:07/01/2020
|
Document:BI111:00
|
CPT Code(s):86001, 86003, 86005, 86008, 95004, 95012, 95017, 95018, 95024, 95027, 95028, 95044, 95052, 95056, 95060, 95065, 95070, 95071, 95076, 95079, 0178U, 94617, 94618
|
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.
Allergy testing requires preauthorization except for the following:
a.
Percutaneous (scratch, prick or puncture) testing
b.
Intradermal testing
c.
Patch testing up to first 80 units.
d.
In vitro testing (certain types of blood tests) is covered when performed
by Allergist, for one set, up to 70 tests; additional in vitro testing requires
pre-authorization.
2.
Other allergy tests that require preauthorization include patch testing
for more than 80 units, intradermal dilution testing, oral challenge testing and
pulmonary function testing.
3.
For pulmonary function testing, please refer to BI542.
4.
Tests that are considered Experimental and Investigational are not
covered and are listed under the Limits section.
|
Medical Statement
|
For pulmonary function testing, please refer to
BI542.
1)
The following forms of
allergy testing are considered medically necessary and do not require
pre-authorization:
A)
Percutaneous
(scratch, prick or puncture) skin testing (95004) has a maximum limit of 70
units per 12 months and is considered medically necessary when IgE-mediated
reactions occur to any of the
following:
i.
Inhalants; or
ii.
Foods; or
iii.
Hymenoptera (stinging insects); or
iv.
Specific drugs (penicillin’s and macromolecular agents).
B)
Intradermal (Intracutaneous) allergy testing (95024, 95028) is performed when
percutaneous tests are negative.
Intradermal
allergy testing has a maximum combined limit of 40
units per 12 months; any
additional units require pre-authorization. Intradermal
allergy testing is considered medically necessary
when IgE-mediated reactions occur to
any of the following:
i.
Inhalants; or
ii.
Foods; or
iii.
Hymenoptera (stinging insects); or
iv.
Specific drugs (penicillin’s and macromolecular agents).
C)
Allergen Specific IgE (in
vitro) Testing
(86003 –
86008) requires evaluation by an
Immunologist or Dermatologist and
has a
limit of
up to 70 tests per year;
any additional tests require pre-authorization.
Allergen specific testing
is considered medically necessary under the following guidelines:
i.
When percutaneous testing of IgE-mediated allergies cannot be done for:
a.
Inhalant allergy; or
b.
Food allergy;
1.
Due to
any of the following reasons:
·
Member has severe Dermatographism, ichthyosis, or generalized eczema;
or
·
Member is unable to discontinue antihistamines but is in need of allergy
testing; or
·
Difficulty in testing uncooperative members (e.g., small children or individuals
with mental or physical impairments); or
·
When clinical history suggests an unusually greater risk of anaphylaxis from
skin testing than usual; or
·
Direct skin testing is inconclusive.
ii.
Also as an alternative to percutaneous testing for:
a.
The evaluation of cross-reactivity between insect venoms;
or
b.
As adjunctive laboratory tests for disease activity of allergic bronchopulmonary
aspergillosis (ABPA) and certain parasitic diseases.
D)
Skin Patch Testing
(95044) for diagnosing contact allergic dermatitis. The first 80 units are
covered without pre-authorization; any additional units require
pre-authorization.
E)
Skin Endpoint Titration (SET)
or Intradermal Dilutional testing (IDDT) (95017, 95018, 95027)
is covered for a cumulative total of 80 units per calendar year
for determining the starting dose for immunotherapy for members highly allergic
to:
i.
Inhalant allergy (95027); or
ii.
Hymenoptera venom allergy (95017); or
iii.
Drugs/biological allergy (95018).
It is
inappropriate to use SET or IDDT (95027) in place of skin testing and it is not
eligible for benefits unless skin
testing has been performed.
2)
The following tests require pre-authorization:
A)
Photo Patch Testing (95052)
for diagnosing photo allergy (e.g., photo-allergic contact dermatitis to be
requested by an Allergist or Dermatologist)
B)
Photo Tests
(95056) for evaluating photosensitivity disorders, to be requested by an
Allergist or Dermatologist.
C)
Exercise Challenge Testing
(94617, 94618) for exercise-induced bronchospasm, to be requested by Allergist
or Pulmonologist.
D)
Bronchial Challenge Test (95070 –
95071) for testing with
methacholine, histamine or antigens in defining asthma or airway hyperactivity
when any of the following conditions
are met:
i.
Asthma is a serious possibility and spirometry performed
before and after administration of a bronchodilator, have not established or
eliminated the diagnosis; or
ii.
To identify new allergens for which skin or blood testing
has not been validated; or
iii.
When skin testing is unreliable;
AND
iv.
When requested by a
Pulmonologist or Allergist.
E)
Ingestion (Oral) Challenge Test
(95076 – 95079)
for
any of the following:
i.
Food or other substances (i.e., Metabisulfite);
or
ii.
Drugs when all of the following are met:
a)
History of allergy to a particular drug;
and
b)
Treatment with that drug class is essential;
and
c)
There is no effective alternative drug;
and
d)
Requested by an Allergist.
F)
Peanut allergen-specific quantitative assessment (0178U) for documented severe
anaphylactic reaction to minimal peanut exposure.
Codes Used In This BI:
86001
|
Allergen specific IgG; quantitative/semi quantitative, ea allergen
|
86003
|
Allergen specific IgE; quantitative/semi quantitative, ea allergen
|
86005
|
qualitative, multiallergen screen
|
86008
|
quantitative/semi quantitative, recombinant or purified component, each
(new code 1/1/2018)
|
95004
|
Percut tests w/allergenic extracts, immed type reaction, incl test
interpret & rpt, specify # of tests
|
95012
|
Nitric oxide expired gas determination
|
95017
|
Allergy Testing, any combo of percut & intracut, seq & incrmntl,
w/venoms, immed type reaction, incl test interp & rpt, specify # tests
|
95018
|
Allergy Testing, any combo of percut & intracut, seq & incrmntl, w/drugs
or biologicals, immed type reaction, incl test interp & rpt, specify #
tests
|
95024
|
Intracut tests w/allergenic extracts, immed type reaction, incl test
interpret & rpt, specify # of tests
|
95027
|
Intracut tests, sequential & incremental, w/allergenic extracts for
airborne allergens, immed type reaction, incl test interpret & rpt,
specify # of tests (SET or IDDT)
|
95028
|
Intracutaneous tests, w/allergenic extracts, delayed type reaction, incl
reading, specify # of tests
|
95044
|
Patch or application test(s), specify # of tests
|
95052
|
Photo Patch Test(s), specify # of tests
|
95056
|
Photo tests
|
95060
|
Ophthalmic mucous membrane tests
|
95065
|
Direct nasal mucous membrane test
|
95070
|
Inhalation bronchial challenge testing; w/histamine, methacholine, or
similar compounds
|
95071
|
w/antigens or gases, specify
|
95076
|
Ingestion challenge test; initial 120 mn of testing
|
95079
|
each addtl 60 mn
|
94617
|
Exercise test for bronchospasm, including pre- and post-spirometry and
pulse oximetry; with electrocardiographic recording(s)
|
94618
|
Pulmonary stress testing (eg, 6-minute walk test), including measurement
of heart rate, oximetry, and oxygen titration, when performed
|
0178U
|
Peanut allergen-specific quantitative assessment of multiple epitopes
using enzyme-linked immunosorbent assay (ELISA), blood, report of
minimum eliciting exposure for a clinical reaction (new code eff
7/1/2020)
|
|
Limits
|
The following
tests are considered experimental and investigational as they have not been
proven to be effective:
A.
Exhaled nitric oxide measurement.
B. ALCAT test
C. IgG RAST/ELISA
Testing
D.
Candidiasis test
E. Chlorinated
pesticides (serum)
F. Complement
(total or components); (may be appropriate in autoimmune disorders, complement
component deficiencies, hereditary angioedema, vasculitis)
G. C-reactive
protein (may be appropriate in inflammatory diseases)
H. Cytotoxic food
testing (Bryans Test, ACT)
I.
Electrodermal acupuncture
J. ELISA/ACT
K. Food immune
complex assays (FICA)
L. Immune
complex assay (may be appropriate in autoimmune disorders, systemic lupus
erythematosus, vasculitis)
M. Leukocyte
histamine release test
N. Lymphocytes (B
or T subsets); (may be appropriate for collagen vascular disease, immune
deficiency syndromes, leukemia, lymphomas)
O. Mediator
release test (MRT)
P. Testing for
multiple chemical sensitivity syndrome (a.k.a., idiopathic environmental
intolerance (IEI), clinical ecological illness, clinical ecology, environmental
illness, chemical AIDS, environmental/chemical hypersensitivity disease, total
allergy syndrome, cerebral allergy, 20th century disease)
Q. Muscle strength
testing or measurement (kinesiology) after allergen ingestion
R. Ophthalmic
mucous membrane tests/conjunctival challenge tests
S. Direct nasal
mucous membrane testing/provocative nasal test
T.
Prausnitz-Kustner or P-K testing - passive cutaneous transfer test
U.
Provocation-neutralization testing (Rinkel Test) either subcutaneously or
sublingually
V. Pulse test
(pulse response test, Reaginic pulse test)
W. Rebuck skin
window test
X. Sublingual
provocative neutralization testing and treatment with hormones
Y. Venom blocking
antibodies
Z.
Volatile chemical panels (blood testing for chemicals).
|
Reference
|
1.
American Academy of Allergy,
Asthma and Immunology. What is allergy testing? Available at
http://www.aaaai.org/patients/publicedmat/tips/whatisallergytesting.stm
2.
Leow YH, Goh CL. Contact
allergy in Singapore.
Asian Pac J Allergy Immunol. 1999; 17(3):207-217.
3.
Mark KA, Brancaccio RR,
Soter NA, et al. Allergic contact and photo allergic contact dermatitis to plant
and pesticide allergens. Arch Dermatol. 1999; 135(1):67-70.
4.
Oliveira HS, Goncalo M,
Figueiredo AC. Photosensitivity to lomefloxacin. A clinical and photo biological
study. Photodermatol Photoimmunol Photomed. 2000; 16(3):116-120.
5.
Lane AP, Pine HS, Pillsbury
HC 3rd. Allergy testing and immunotherapy in an academic otolaryngology
practice: a 20-year review. Otolaryngol Head Neck Surg. 2001; 124(1):9-15.
6.
Parker F. Skin diseases of
general importance. In: Cecil Textbook of Medicine. 21st ed. L Goldman, JC
Bennett, eds. Philadelphia, PA: W.B. Saunders Co; 2000: 2277, 2295-2296.
7.
Parker F. Examination of
the skin and an approach to diagnosing skin disease. In: Cecil Textbook of
Medicine. 21st ed. L Goldman, JC Bennett, eds.
Philadelphia,
PA: W.B. Saunders Co; 2000: 2271.
8.
No authors listed. American
Gastroenterological Association medical position statement: Guidelines for the
evaluation of food allergies. Gastroenterology. 2001; 120(4):1023-1025.
9.
Teuber SS, Porch-Curren C.
Unproved diagnostic and therapeutic approaches to food allergy and intolerance.
Curr Opin Allergy Clin Immunol. 2003; 3(3):217-221.
10.
Somerville M. Immunotherapy for seasonal rhinitis,
asthma and bee sting venom allergy. Bazian Ltd., eds. London,
UK: Wessex Institute for
Health Research and Development,
University
of Southampton; 2002.
11.
BlueCross BlueShield Association (BCBSA) Technology Evaluation
Center. Serial Endpoint
Testing for the Diagnosis and Treatment of Allergic Disorders July 2002.
Available at:
http://www.bcbs.com/tec/vol17/17_06.html
12.
Arkansas Blue Cross Blue Shield. Coverage Policy Manual,
RAST Tests. Available at:
http://www.arkbluecross.com/members/ex_report.asp?ID=1997188
13.
Senna G, Passalacqua G, Lombardi C, Antonicelli L.
Position paper: Controversial and unproven diagnostic procedures for food
allergy. Allergy Immunol (Paris).
2004; 36(4):139-145.
14.
Klein R, Schwenk M, Heinrich-Ramm R, Templeton DM.
Diagnostic relevance of the lymphocyte transformation test for sensitization to
beryllium and other metals. IUPAC Technical Report. Pure Appl Chem. 2004;
76(6):1269-1281.
15.
Barna BP, Culver DA,
Yen-Lieberman B, et al. Clinical application of beryllium lymphocyte
proliferation testing. Clin Diagnose Lab Immunol. 2003; 10(6):990-994.
Addendum:
1)
Effective 04/01/2017: Specified coverage limits for
percutaneous and intracutaneous allergy testing. Clarified under limits that IgG
testing (86001) is considered experimental and investigational. Added coverage
for Bronchial Challenge testing with pre-authorization.
Removed CPT codes 95010 & 95015 from policy. These codes were deleted 1/1/13 &
replaced with 95017 & 95018. Also added the following CPT codes corresponding
with Bronchial Challenge Testing coverage:
94070, 94150, 94200, 94350, 94360, 94620, 94621, 94680, 94681, 94690,
94720, & 94770.
Retroactive to 01/01/2017
–
No PA needed for the following CPT codes: 94010, 94060, and 94375.
2)
Effective 09/01/2017:
Removed CPT codes for PFT from BI and added the following statement: “For
pulmonary function testing, please refer to BI542. Also updated “Codes Used in
This BI” section to reflect updated changes.
3)
Effective 11/01/2017:
Skin Patch Testing: first 80 units is covered without prior authorization.
Additional units require pre-authorization.
4)
Effective 3/8/2018:
Added new code for 2018.
5)
Effective 10/01/2018:
95024 and 95028 have a maximum combined limit of 40 units per 12 months. Any
additional units require prior authorization. Removed PA requirements for 95017,
95018 and 95027 (Skin serial endpoint titration (SET) for determination of a
safe starting dose for testing or immunotherapy): are covered for a cumulative
total of 80 units per calendar year. Some types of allergy testing require
evaluation by specialists.
6)
Effective 02/01/2019:
Updated codes in Medical Policy Statement
section to align with system configuration.
7)
Effective 07/01/2020:
Added new code (0178U) with pre-authorization.
8)
Deleted code 95071
(eff 01-01-2021),
updated revised code 95070 (eff 01-01-2021) and
added codes 94617 and 94618 that were
in the medical statement requiring PA and added to search box as well as
description of codes in the codes used in this BI.
|
Application to Products
|
This policy applies to all health plans and products 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) or Certificate of Coverage (COC) for those plans or products insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC or COC, the SPD, EOC, or COC, as applicable, will prevail. State and federal mandates will be followed as they apply.
|
Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
|
|
|