Mountain State Medical Policy Bulletin |
Section: | Laboratory |
Number: | L-34 |
Topic: | Genetic Testing |
Effective Date: | August 1, 2005 |
Issued Date: | August 1, 2005 |
Date Last Reviewed: | 07/2005 |
Indications and Limitations of Coverage
Genetic testing performed to diagnose patients with signs and symptoms of possible genetic disease is generally covered. In addition, the test results must have a direct effect on the patient's treatment. Genetic testing performed on patients with no current evidence or manifestation of genetic disease (i.e., asymptomatic) is considered genetic screening and is noncovered except for those groups/programs that specifically identify coverage in benefits. This includes genetic testing performed to determine susceptibility or predisposition to diseases such as cancer and heart disease and genetic testing for carrier identification to determine if a person is a "carrier" of an abnormal gene. The following testing is covered for symptomatic patients. The testing is also covered for asymptomatic patients when the patient's contract covers genetic screening. This is not an all-inclusive list.
Genetic testing for diagnosis or risk assessment of Alzheimer's disease (S3852) is considered experimental/investigational and therefore, not covered and not eligible for payment. This includes, but is not limited to, testing for the apolipoprotein E epsilon 4 allele, presenilin genes, or amyloid precursor gene. There is no evidence that testing for genetic mutations improves the sensitivity or specificity of clinical criteria and would not alter diagnostic testing for other causes of dementia. A participating, preferred, or network provider can bill the member for the denied service. Date Last Reviewed: 08/2004 Genetic testing is a complex process. The results depend on reliable laboratory procedures and accurate interpretation of results. When no code exists, molecular diagnostic testing (codes 83890-83906) and cytogenetic testing (codes 88230-88289) may be reported for genetic testing. Different combinations of the codes may be reported depending on the clinical circumstances. In some cases, certain codes may be reported multiple times. Genetic counseling (S0265) is generally provided in conjunction with genetic testing. Counseling usually occurs when the results of the tests are provided to the patient and intervention strategies are discussed. Coverage for genetic counseling is determined according to individual or group customer benefits. When genetic testing is noncovered, the counseling performed in conjunction with the testing is also noncovered.
Description Genetic diseases are conditions resulting in abnormalities of DNA. Some genetic diseases are transmitted from parents to their children, and in other circumstances, genetic diseases may occur spontaneously, as in mutations. |
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83890 | 83891 | 83892 | 83893 | 83894 | 83896 |
83897 | 83898 | 83901 | 83902 | 83903 | 83904 |
83905 | 83906 | 88230 | 88233 | 88235 | 88237 |
88239 | 88240 | 88241 | 88245 | 88248 | 88249 |
88261 | 88262 | 88263 | 88264 | 88267 | 88269 |
88271 | 88272 | 88273 | 88274 | 88275 | 88280 |
88283 | 88285 | 88289 | S0265 | S3818 | S3819 |
S3820 | S3822 | S3823 | S3828 | S3829 | S3830 |
S3831 | S3833 | S3834 | S3835 | S3837 | S3840 |
S3841 | S3842 | S3843 | S3844 | S3845 | S3846 |
S3847 | S3848 | S3849 | S3850 | S3851 | S3852 |
S3853 |
PRN References 12/1999, Blue Shield explains genetic testing coverage |
National Blue Cross Blue Shield Association Medical Policy 2.04.02, Genetic Testing for Inherited BRCA1 or BRCA2 Mutations, 03/2002 National Blue Cross Blue Shield Association Medical Policy 2.04.05, Genetic Testing for Germline Mutations of the RET Proto-Oncogene in Medullary Carcinoma of the Thyroid, 11/1998 National Blue Cross Blue Shield Association Medical Policy 2.04.08, Genetic Testing for Inherited Susceptibility to Colon Cancer Including Microsatellite Instability, 03/2002 National Blue Cross Blue Shield Association Medical Policy 2.04.13, Genetic Testing for Familial Alzheimer's Disease, 10/2000 |