Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | L-114-005 |
Topic: | Pharmacogenomic Testing for Drug Toxicity and Response |
Section: | Laboratory |
Effective Date: | July 1, 2018 |
Issue Date: | July 2, 2018 |
Last Reviewed: | March 2018 |
For the purposes of this policy, pharmacogenomic tests are performed to assess a person’s response to therapy or risk for toxicity from drug treatment. Testing may be performed prior to treatment, in order to determine if the individual has genetic differences that could affect drug response and/or increase the risk for adverse drug reactions. Testing may also be performed during treatment, to assess whether an individual is having an adequate response or to investigate the cause of an unusual or adverse reaction. |
This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.
Policy Position Coverage is subject to the specific terms of the member’s benefit plan. |
Pharmacogenomic tests may be considered medically necessary when ALL of the following conditions are met:
Companion Diagnostic Testing may be considered medically necessary when ALL of the following conditions are met:
Limits:
Exclusions
The following pharmacogenomic tests are considered experimental/investigational and therefore non-covered due to lack of scientific-based evidence, professional guidelines and/or the FDA, or their use in medical management is deemed to be still evolving.
This list is not intended to be all inclusive.
Place of Service: Outpatient |
Experimental/Investigational (E/I) services are not covered regardless of place of service.
Pharmacogenomic testing for drug toxicity and response is typically an outpatient procedure which is only eligible for coverage as an inpatient procedure in special circumstances, including, but not limited to, the presence of a co-morbid condition that would require monitoring in a more controlled environment such as the inpatient setting.
The policy position applies to all commercial lines of business |
Denial Statements |
Services that do not meet the criteria of this policy will not be considered medically necessary. A network provider cannot bill the member for the denied service unless: (a) the provider has given advance written notice, informing the member that the service may be deemed not medically necessary; (b) the member is provided with an estimate of the cost; and (c) the member agrees in writing to assume financial responsibility in advance of receiving the service. The signed agreement must be maintained in the provider’s records.
Services that do not meet the criteria of this policy will be considered experimental/investigational (E/I). A network provider can bill the member for the experimental/investigational service. The provider must give advance written notice informing the member that the service has been deemed E/I. The member must be provided with an estimate of the cost and the member must agree in writing to assume financial responsibility in advance of receiving the service. The signed agreement must be maintained in the provider’s records.
Links |
05/2018, REMINDER: Molecular and Genomic Testing