MedicaidCoverageMedium impact
Continuity of Care (Revised)
Humana·LA · Pharmacy·Medicaid
Effective date
May 27, 2026
We identified it
Jun 25, 2026
Summary
Humana Medicaid Louisiana updated its Continuity of Care policy (revised May 27, 2026) to clarify when utilization management overrides (step therapy, prior authorization, non-preferred edits) apply to patients newly enrolled or transitioning to the plan. Members stable on pre-existing medications within 90 days of eligibility start qualify for override, EXCEPT for select medications with off-label use potential, fraud/abuse risk, or non-preferred generics. Claims for off-label or off-evidence uses will be denied.
Action Required
REQUIREMENTS:
- Effective immediately (policy revised May 27, 2026): Billing and prior authorization teams must apply the 90-day continuity of care window based on member eligibility start date, not enrollment date.
- For all new or transitioning Medicaid Louisiana members: Verify eligibility start date is within previous 90 days before applying step therapy, prior authorization, or non-preferred edits to current medications.
- CRITICAL: Do NOT override utilization management for the select list of medications (off-label use potential, high fraud/waste/abuse risk, or non-preferred generics with preferred AB-rated alternatives). These require standard review per SSA Title 19 requirements.
- Prior authorization staff must document in claims system: (1) member stability on therapy, (2) compendia-supported diagnosis, (3) eligibility start date confirmation, (4) whether medication falls on the excepted medications list.
- Deny claims for any off-label or off-evidence medication uses. Flag prescriptions for non-FDA-approved indications or those lacking peer-reviewed literature support for medical director review.
- Update PA request forms and system workflows to capture eligibility start date and confirm medication stability (note: sample medications alone do NOT constitute stability).
- Verify current medication list at time of claim—transition fills remain subject to appropriate review per state mandate.
- Training: Educate billing, PA, and claims staff on the distinction between off-label (FDA-approved drug for non-approved use) vs. off-evidence (insufficient safety/efficacy data) to ensure correct denials.
- Consequences of inaction: Claims inappropriately subject to step therapy or PA within the 90-day window may trigger member complaints and appeal denials; conversely, approving off-label/off-evidence uses violates federal Medicaid rules and may result in overpayments and compliance violations.