For future public health emergencies, the Centers for Medicare & Medicaid Services should improve how it sets Medicare rates for clinical diagnostic laboratory tests under the Clinical Laboratory Fee Schedule and communicates with stakeholders involved in setting the rates, the Department of Health and Human Services’ Office of Inspector General advised last week. When CMS was working to increase testing capacity during the COVID-19 PHE, CMS’s standard rate setting procedures did not allow Medicare Administrative Contractors to set rates that were adequate to cover the cost of conducting COVID-19 viral tests for all laboratories, OIG said. In addition, OIG said CMS may have missed opportunities to obtain important information from laboratory associations and MAC pricing coordinators when it made decisions about the new CDLT rates.

Related News Articles

Headline
The Food and Drug Administration May 16 announced it cleared the first blood test to diagnose Alzheimer’s disease. The test, created by Fujirebio Diagnostics,…
Headline
The Centers for Medicare & Medicaid Services May 12 released draft guidance for the third round of negotiations for the Medicare Drug Price Negotiation…
Headline
Zaira Khalid, M.D., senior staff geriatric psychiatrist at Henry Ford Behavioral Health Hospital, discusses the unique physical, emotional and social needs of…
Headline
An estimated 7.2 million Americans are living with Alzheimer's disease, according to the latest annual report by the Alzheimer's Association. Nearly two-thirds…
Headline
Leaders from the Centers for Medicare & Medicaid Services at the 2025 AHA Annual Membership Meeting May 5 discussed issues on the agency’s agenda in a…
Headline
The AHA April 30 released a report highlighting how hospitals and health systems continue to experience significant financial headwinds that can challenge…