01Billing team must review and implement the following Aetna coverage restrictions in the claims submission system:
1. RESTRICTIONS BY PLAN TYPE:
- For HMO plans: Do NOT bill foot drop splints/recumbent positioning devices or related interfaces.
02Do NOT bill static/dynamic positioning AFOs when used solely for heel pressure ulcer prevention/treatment.
03- Ensure billing system flags HMO claims with these codes for denial/rejection before submission.
042. SPECIFIC COVERAGE DENIALS (All plan types):
- Air-stirrups (e.g., Air Cast): Deny when billed for chronic ankle instability or re-injury prevention.
05Approve only after acute ankle injury (fractures/sprains).
06- Elastic ankle sleeves: Deny for chronic ankle instability or re-injury prevention.
07Approve only for acute injury (acute and rehabilitative stages).
08- Orthoplast ankle stirrups: Deny for chronic instability or re-injury prevention.
09Approve only after acute injury.
10- Rigid ankle casts: Deny for ankle sprains, chronic instability, or re-injury prevention.
11Approve only for ankle fractures.
12- Semi-rigid ankle casts: Deny for ankle fractures, chronic instability, or re-injury prevention.
13Approve only for ankle sprains.
14- Unna boots: Deny for ankle fractures, chronic instability, or re-injury prevention.
15Approve only for ankle sprains and soft tissue injuries.
16- Static/dynamic positioning AFOs with knee/hip components: Deny (experimental/unproven).
17- AFO additions: Deny if base orthosis is not medically necessary.
18- AFOs in ambulatory members for edema or heel pressure ulcer prevention/treatment: Deny.
193. APPROVAL REQUIREMENTS:
- All orders must be prescribed by eligible providers (physician, NP, podiatrist, or qualified health professional per state law).
20- Verify prescriber is licensed/certified as required by state.
21- Confirm orthotic provider is certified by ABC or BOC, or licensed by state.
22- For custom molded AFOs in ambulatory patients: Verify medical necessity documentation in chart.
23- For static/dynamic positioning AFOs (contracture splints): Verify goniometer measurement documenting at least 10-degree dorsiflexion on passive ROM testing, documented stretching program, and contracture impact on function.
24- For post-operative ankle braces: Confirm application within 6 weeks of surgery.
25- For all orders: Verify provision within 6 months of prescription date.
264. DOCUMENTATION REQUIREMENTS:
- Instruct providers to document clinical indication (acute vs. chronic) on prescription/order.
27- For contracture splints: Require pre-treatment ROM measurements and stretching program details in medical record before billing.
28- Ensure medical records show physical examination supporting functional improvement/restoration of ADLs.
295. SYSTEM UPDATES:
- Update billing software edit rules to flag claims for non-approved indications.
30- Create denial reason codes mapping to each excluded indication.
31- Add billing alerts for HMO plan type restrictions.
32Consequences of inaction: Claims will be denied for lack of medical necessity, requiring rework and appeals.
33Systematic billing of non-covered indications may trigger audits.