The Defense Health Agency, relying on medical laboratory experts and existing authority to conduct medical “demonstrations,” will restore Tricare coverage this month for up to 40 genetic tests used in patient care.
Many of these laboratory-developed tests – also called molecular pathology tests – are viewed as medically necessary. But Tricare had stopped reimbursing for more than 100 such tests in January 2013, believing it lacked authority to cover them if ordered by civilian physicians treating patients through Tricare provider networks.
Military treatment facilities have continued to order and pay for such tests routinely, which created a startling disparity of coverage between military direct care and purchased care contracts. Senior DHA officials acknowledged the coverage gap last February and vowed to close it.
The first step to do so will occur July 18 when “30 to 40” genetic tests, those “most commonly performed” across U.S. medicine, will become reimbursable again under Tricare, as part of a three-year medical demonstration project, said Army Maj. Gen. Richard W. Thomas, chief medical officer and director of healthcare operations for DHA.
Among genetic tests to be restored to Tricare coverage is one that determines if a woman who is pregnant or desires to become pregnant carries a genetic marker for cystic fibrosis. That marker would indicate increased risk that a newborn would have CF.
Tricare stopped paying for this and many more laboratory-developed tests after the American Medical Association changed its procedural codes for such lab work and clarified that these tests are “medical devices.”
Tricare, in turn, concluded that under current support contracts it cannot pay for medical devices if not certified as safe and effective by the Federal Drug Administration. Because the FDA doesn’t review or approve genetic tests, Tricare officials decided they had to stop coverage.
Civilian physicians continued to order such tests, but after December 2012, Tricare quietly began denying payments. For a time, many impacted laboratories absorbed the costs. But for some of the more costly tests ordered, Tricare patients began receiving unexpected bills.
In a phone interview, Thomas explained that DHA earlier this year formed its own panel of experts, the Joint Lab Working Group, and began conducting its own review of safety and effectiveness of genetic tests. It used forensic science and other criteria to screen tests. One factor was whether major health insurance companies covered the tests, Thomas said.
Restored Tricare coverage for up to 40 LDTs will occur under what DHA calls its Non-FDA-Approved Laboratory Test Demonstration Project, described in the June 18 Federal Register. A full list of genetic testing to be approved for Tricare hasn’t been released yet, but coverage will be retroactive to Jan. 1, 2013, Thomas said, so laboratories and patients will be able to apply for reimbursements of newly cleared tests that they had paid for back to that date. DHA already has reimbursed impacted laboratories $3.5 million, mostly for prenatal CF testing the last 18 months.
During the demonstration, DHA would like to see Congress pass legislation to give it permanent genetic test review authority. The Senate Armed Services Committee’s version of the fiscal 2015 defense authorization bill contains such language, so it could be enacted into law by year’s end.
Besides closing its coverage gap, DHA plans to use the demonstration to better manage for military medicine the recent “explosion” in genetic testing, Thomas said. It will seek to hold down costs by using military labs with genetic testing capability when possible. Such labs now operate at military medical centers in Texas, Mississippi and Washington states.
DHA also wants to impose more “discipline and clarity” on use of such testing, whether by military health care providers or network civilian doctors.
“We’ve got to be flexible enough in our system that we can address these tests and certainly offer them, as appropriate, if they have proven clinical merit, are efficacious and safe,” Thomas said.
Prenatal cystic fibrosis testing is a good example. For now, DHA will extend coverage, acknowledging that such tests are recommended by the American College of Obstetricians and Gynecologists. But during the demonstration, military patient outcomes will be studied to determine if CF testing provides real medical benefits or simply adds to the cost of care.
DHA officials had argued earlier this year that awareness that a fetus is at higher risk of cystic fibrosis usually has no impact on management of labor, delivery or neonatal care. Also, they noted, that, at birth, infants are tested for a host of health conditions immediately, including for CF.
Thomas described guidelines from ACOG as “deliberately opaque” on the benefits of prenatal CF screening. Yet because ACOG strongly recommends such screening, the tests have become a “standard of practice” though not yet “a standard of care,” Thomas said.
Karen Ruedisueli, a health care advocate for National Military Family Association, said NFMA is pleased to see Tricare restore coverage of some genetic tests, particularly prenatal cystic fibrosis screening, which represents the “bulk of genetic test denials” by Tricare since early 2013.
But NMFA, she said, wants to learn why the DHA panel did not clear for restored Tricare coverage more than 60 other genetic tests.
“That over half of those tests will continue to be denied coverage is concerning,” Ruedisueli said. “Because it’s our understanding the vast majority of those tests are covered by commercial insurance carriers as well as by other government plans.”
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