Premera Blue Cross · Identified Jun 18, 2026Medium impact
Medical Policy and Coding Updates - April 2018
Effective April 1, 2018, CAR T-cell therapy (Q2041), infliximab biosimilars (Q5103, Q5104), total artificial heart procedures (33927, 33928, 33929) and whole exome and whole genome sequencing (0036U) now require medical necessity review and prior authorization. Effective April 1, 2018, PMP22 peripheral neuropathy testing (81324, 81325, 81326) and non-cardiac SPECT brain imaging (78607) now require medical necessity review, intraoperative neurophysiologic monitoring (95925-95941 and G0453) now requires medical necessity review, and several urinary tumor marker, molecular panel and visual evoked potential services (0012M, 0013M, 0037U, 95930) are reviewed as investigational. Effective July 5, 2018, codes 43201, 43236 and 43257 are investigational for all uses, and effective April 1, 2018, bioimpedance spectroscopy (93702) and electrical or electromagnetic wound treatment codes (E0761, E0769, G0281, G0282, G0295, G0329) are removed from investigational review, while platelet-derived growth factor (S9055) is investigational and no longer requires medical necessity review or prior authorization. Pharmacy changes include a 7-day supply of short-acting opioids covered without prior authorization for opioid-naive patients effective April 15, 2018, and Neulasta Onpro added to the G-CSF policy with the same criteria as Neulasta.