Sen. Hicks wins Senate approval for rapid whole-genome sequencing for vulnerable children

OKLAHOMA CITY – Sen. Carri Hicks has won full Senate approval for a bipartisan measure increasing access to rapid whole-genome sequencing (rWGS) for critically ill infants. Assistant Democratic Leader Hicks, D-Oklahoma City, is the Senate principal author of House Bill 1567, and House Majority Leader Mark Lawson, R-Sapulpa, is principal author in his chamber. The legislation would ensure Medicaid coverage of rWGS for babies whose conditions might not otherwise be correctly diagnosed in a timely way, if at all.

“Rapid whole-genome sequencing can be life-changing for families facing rare diseases,” Hicks said. “It gives doctors answers sooner, helping parents make informed decisions and sparing children from painful, unnecessary procedures. This legislation offers real hope for Oklahoma’s most vulnerable babies.”

Studies have demonstrated the value of genome sequencing tests for critically ill children, and there are currently 18 states where Medicaid provides coverage for rWGS.

“House Bill 1576 gives doctors the tools needed to save Oklahoma’s most vulnerable patients when every minute counts,” Lawson said. “Rapid whole-genome sequencing provides critical answers in hours, improving outcomes and reducing costs. This bill is a lifeline for families desperate for answers and for health care professionals trying to make the right call under extreme pressure.”

HB 1576 next moves to a conference committee for further consideration.