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
A KFF analysis released Jan. 28 found that Medicare Advantage insurers made nearly 53 million prior authorization determinations in 2024, an increase…
Headline
Ji Im, system senior director of community and population health at CommonSpirit Health, explores why seamless navigation, community partnerships and…
Headline
The Centers for Medicare & Medicaid Services Jan. 26 released proposed changes to Medicare Advantage plan capitation rates and Part D payment policies for…
Headline
The AHA Jan. 26 expressed support and provided its perspective on certain provisions within the Centers for Medicare & Medicaid Services’ proposed…
Headline
The AHA Jan. 20 made recommendations to Congress on modernizing the Medicare Access and CHIP Reauthorization Act. Among the proposals, the AHA recommended…
Headline
The comment period for the Centers for Medicare & Medicaid Services' proposed rule for policies governing the Medicare Advantage and Part D programs for…