Aetna modified CPB 0611 for fecal incontinence, effective February 27, 2026. Here's what billing teams need to know about coverage criteria, affected codes, and what Aetna now considers experimental.
Aetna, a CVS Health company, updated its fecal incontinence coverage policy under CPB 0611 Aetna system. This policy governs medical necessity for a wide range of diagnostic, conservative, and surgical interventions — from anorectal manometry through sacral nerve stimulation (CPT 64561, 64581) and the Acticon Neosphincter. If your practice treats fecal incontinence and bills Aetna, this update touches nearly every layer of your coding and documentation workflow.
Quick-Reference Table
| Field | Detail |
|---|---|
| Payer | Aetna, a CVS Health company |
| Policy | Fecal Incontinence – CPB 0611 |
| Policy Code | CPB 0611 |
| Change Type | Modified |
| Effective Date | February 27, 2026 |
| Impact Level | High |
| Specialties Affected | Colorectal surgery, gastroenterology, urology, general surgery, physical therapy, nutrition/dietetics |
| Key Action | Audit your documentation for the 3-month conservative treatment trial before billing any invasive procedure under CPB 0611 |
Aetna Fecal Incontinence Coverage Criteria and Medical Necessity Requirements 2026
Aetna's fecal incontinence coverage policy draws a hard line between conservative and invasive treatment. You cannot bill for surgery, neuromodulation, or artificial sphincter implantation without documented evidence of a failed conservative trial first.
The policy requires a 3-month trial of two or more traditional treatments before any invasive intervention is considered medically necessary. Those traditional treatments include biofeedback (CPT 90912, +90913), bowel training, defecation programs, diet modification, and pharmacotherapy. If your chart doesn't show this trial, Aetna will deny the claim.
Diagnostic tests covered under medical necessity:
| # | Covered Indication |
|---|---|
| 1 | Anorectal manometry (see Aetna CPB 0616) |
| 2 | Anorectal ultrasonography |
| 3 | Rectal sensory testing |
These diagnostics do not require the 3-month conservative trial. Bill them with the appropriate ICD-10-CM code from the R15.x range (R15.0 through R15.9) to support medical necessity.
Invasive procedures covered when criteria are met:
Aetna defines "severe" fecal incontinence as involuntary loss of solid or liquid stool on a weekly or more frequent basis. That definition matters for prior authorization. If you're submitting a prior auth for sphincter repair, colostomy, the Acticon Neosphincter, or sacral nerve stimulation, document severity using that specific standard — not just a general diagnosis of incontinence.
Anal sphincter repair (CPT 46750, 46751, 46760, 46761) is covered for members with severe fecal incontinence who have failed, or cannot attempt, medical interventions such as biofeedback, dietary management, pharmacotherapy, or strengthening exercises.
Colostomy is covered for members with severe fecal incontinence who have failed medical interventions and surgical sphincter repair options, including post-anal repair, sphincteroplasty, or total pelvic floor repair.
The Acticon Neosphincter artificial bowel sphincter is covered for members 18 years of age or older with severe fecal incontinence — weekly or more frequent involuntary stool loss — who have failed both medical interventions and surgical sphincter repair.
Sacral nerve stimulation (sacral neuromodulation) is covered via a two-stage process for members with chronic fecal incontinence who have had an inadequate response to conservative treatments and who have a weak but structurally intact anal sphincter. First, a temporary percutaneous peripheral nerve electrode (CPT 64561) must be placed. Then, if the member achieves 50% or greater improvement in incontinence symptoms over at least 48 hours of testing, implantation of a permanent pulse generator (CPT 64590) is covered. Aetna notes this can be administered via InterStim. CPT 64581 — the open incisional approach to electrode lead implantation — is the surgical alternative to percutaneous placement via CPT 64561. Both are covered when selection criteria are met. The HCPCS codes for the hardware — C1767, C1778, C1787, C1820, L8679, L8680, L8685, L8686, L8687, L8688 — all fall under the same criteria gate. If the temporary trial doesn't meet the 50% threshold, the permanent implant is considered experimental.
The reimbursement path for sacral neuromodulation is clear, but it's also sequential. Don't bill for the permanent generator (CPT 64590) before you have documentation showing the temporary trial result. That's a clean denial waiting to happen.
Aetna Fecal Incontinence Exclusions and Non-Covered Indications
This section is where fecal incontinence billing gets expensive if your team isn't paying attention. Aetna's list of experimental, investigational, or unproven designations is long — and several of these codes are in active use at many practices.
Injectable bulking agents are explicitly experimental. That means CPT 11950, 11951, 11952, 11953, 11954 (subcutaneous injection of filling material) and CPT 0963T (anoscopy with directed submucosal injection of bulking agent) are not covered for fecal incontinence under this policy. HCPCS L8605 (dextranomer/hyaluronic acid copolymer implant) is also in the non-covered group. If you've been billing these, stop — or expect denials.
Posterior tibial nerve stimulation (CPT 64566) is also in the experimental bucket. Some practices use this as an alternative neuromodulation approach. Aetna does not cover it for fecal incontinence under CPB 0611.
Graciloplasty is experimental. So are anal slings, pubo-rectal slings, and the Fenix Continence Restoration System. HCPCS A4563 (rectal control system for vaginal insertion) sits in the same non-covered group.
Autologous muscle cell therapy — CPT 1001T — is also experimental. Same for mesenchymal stem cell injections. The codes 38205, 38206, 38240, and 38241 (hematopoietic progenitor cell harvesting and transplantation) appear in the experimental group as well.
Category III codes 0587T, 0588T, 0589T, and 0590T — covering integrated single-device neurostimulation systems — are non-covered under this policy. These are newer technology codes. Aetna is not convinced yet.
The Acticon Neosphincter is also non-covered if the member has any of these contraindications: an irreversibly obstructed proximal bowel segment, or being a poor candidate for surgery or anesthesia due to physical or mental conditions. Even if all other criteria are met, these contraindications flip the coverage status.
Coverage Indications at a Glance
| Indication | Status | Relevant Codes | Notes |
|---|---|---|---|
| Anorectal manometry | Covered | See CPB 0616 | No trial required |
| Anorectal ultrasonography | Covered | ICD-10 R15.x | No trial required |
| Rectal sensory testing | Covered | ICD-10 R15.x | No trial required |
| Biofeedback | Covered | CPT 90912, +90913 | See CPB 0132 |
| Bowel training / defecation programs / diet modification / pharmacotherapy | Covered | CPT 97110, 97530, 97802–97804, S9470, J0745 | Conservative first-line |
| Anal sphincter repair | Covered (criteria met) | CPT 46750, 46751, 46760, 46761 | Requires 3-month trial + severe FI |
| Colostomy | Covered (criteria met) | ICD-10 R15.x | Requires failure of medical AND surgical repair |
| Acticon Neosphincter | Covered (criteria met) | Age ≥18, severe FI, failed medical + surgical repair | Non-covered with listed contraindications |
| Sacral nerve stimulation – temporary trial | Covered | CPT 64561, 64581; HCPCS A4290 | Member must have weak but structurally intact anal sphincter; temporary trial must precede permanent implant |
| Sacral nerve stimulation – permanent implant | Covered (criteria met) | CPT 64590, 64595; HCPCS C1767, C1778, L8679, L8685–L8688 | Requires ≥50% improvement from trial over ≥48 hours; member must have weak but structurally intact anal sphincter |
| SNS electronic analysis | Covered (criteria met) | CPT 95970, 95971, 95972 | Post-implant follow-up |
| Injectable bulking agents | Experimental | CPT 0963T, 11950–11954; HCPCS L8605 | Not covered for fecal incontinence |
| Posterior tibial nerve stimulation | Experimental | CPT 64566 | Not covered under CPB 0611 |
| Graciloplasty | Experimental | — | No covered code path |
| Anal sling / pubo-rectal sling / Fenix System | Experimental | HCPCS A4563 | Not covered |
| Autologous muscle cell therapy | Experimental | CPT 1001T | Not covered |
| Integrated neurostimulation system (Category III) | Experimental | CPT 0587T, 0588T, 0589T, 0590T | Not covered |
| Mesenchymal stem cell injection | Experimental | CPT 38205, 38206, 38240, 38241 | Not covered for this indication |
Aetna Fecal Incontinence Billing Guidelines and Action Items 2026
This update has real claim denial risk if your charge capture and documentation workflows don't reflect the current criteria. Here's what to do before billing under CPB 0611.
| # | Action Item |
|---|---|
| 1 | Audit your documentation for the 3-month conservative treatment trial. Before billing any invasive procedure — sphincter repair, colostomy, Acticon, or sacral nerve stimulation — confirm the record shows a minimum 3-month trial of two or more conservative treatments. Missing this is the single most common reason for denial on these claims. Pull any pending authorizations and verify documentation completeness now, not after the claim drops. |
| 2 | Remove CPT 0963T, 11950–11954, and 64566 from your fecal incontinence charge capture. These codes are experimental under CPB 0611. If your billing team has been routinely billing injectable bulking agents or posterior tibial nerve stimulation for fecal incontinence against Aetna, those claims will deny. Review your charge master and any order sets tied to R15.x diagnoses. |
| 3 | Confirm the two-stage documentation pathway for sacral nerve stimulation before submitting CPT 64590. The permanent pulse generator is only covered after a temporary trial (CPT 64561 or 64581) shows ≥50% improvement in symptoms over at least 48 hours. You must also document that the member has a weak but structurally intact anal sphincter — this is a hard eligibility criterion under CPB 0611, not an optional clinical note. Document the trial dates, the symptom assessment method, the percentage improvement, and the sphincter status explicitly. If your operative reports don't capture this data, work with your clinical team to update the template before the next case. |
| 4 | Verify prior authorization requirements before scheduling sacral nerve stimulation or Acticon Neosphincter procedures. These are high-cost interventions with multiple clinical gates. Aetna's coverage policy is clear on criteria, but prior auth processes vary by plan and region. Call to confirm what documentation Aetna's utilization management team expects before you submit. |
| 5 | Map your ICD-10-CM codes correctly. Aetna covers fecal incontinence billing under the R15.x range — R15.0 through R15.9. Make sure your coders are using the most specific subcategory available, and that the diagnosis code in your claim aligns with the severity documented in the chart. "Severe" fecal incontinence — weekly or more frequent involuntary stool loss — is what unlocks the invasive procedures. |
| 6 | Flag Category III codes 0587T–0590T in your system. These codes for integrated single-device neurostimulation are non-covered under CPB 0611. If your practice has recently adopted newer InterStim or similar technology and has been billing these codes, check your payer contract and get your compliance officer involved before your next billing cycle. The potential reimbursement exposure here is significant. |
If you're unsure how this coverage policy applies to your specific payer mix or plan types, talk to your compliance officer before the effective date of February 27, 2026.
| Previous Version | Current Version |
|---|---|
| Coverage is considered experimental and investigational for all indications | Coverage is considered medically necessary when specific criteria are met |
| Prior authorization is not required | Prior authorization is required for initial treatment |
| Documentation must include clinical history | Documentation must include clinical history |
| Re-review every 24 months | Re-review every 12 months with updated clinical documentation |
CPT, HCPCS, and ICD-10 Codes for Fecal Incontinence Under CPB 0611
Covered CPT Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| 64561 | CPT | Percutaneous implantation of neurostimulator electrode array; sacral nerve (transforaminal placement) |
| 64581 | CPT | Incision for implantation of neurostimulator electrodes; sacral nerve (transforaminal placement) |
| 64590 | CPT | Insertion or replacement of peripheral or gastric neurostimulator pulse generator or receiver |
| 64595 | CPT | Revision or removal of peripheral or gastric neurostimulator pulse generator or receiver |
| 95970 | CPT | Electronic analysis of implanted neurostimulator pulse generator system |
| 95971 | CPT | Simple spinal cord, or peripheral neurostimulator pulse generator programming |
| 95972 | CPT | Electronic analysis of implanted neurostimulator pulse generator system (complex) |
Other CPT Codes Related to CPB 0611
| Code | Type | Description |
|---|---|---|
| 46750 | CPT | Sphincteroplasty, anal, for incontinence or prolapse; adult |
| 46751 | CPT | Sphincteroplasty, anal, for incontinence or prolapse; child |
| 46760 | CPT | Sphincteroplasty, anal, for incontinence, adult; muscle transplant |
| 46761 | CPT | Sphincteroplasty, anal, for incontinence, adult; levator muscle imbrication |
| 90912 | CPT | Biofeedback training, perineal muscles, anorectal or urethral sphincter, including EMG and/or manometry |
| +90913 | CPT | Each additional 15 minutes of biofeedback training, perineal muscles |
| 97110 | CPT | Therapeutic procedure; therapeutic exercises to develop strength |
| 97530 | CPT | Therapeutic activities, direct (one-on-one) patient contact |
| 97802 | CPT | Medical nutrition therapy (initial) |
| 97803 | CPT | Medical nutrition therapy (follow-up) |
| 97804 | CPT | Medical nutrition therapy (group) |
Not Covered / Experimental CPT Codes
| Code | Type | Description | Reason |
|---|---|---|---|
| 0587T | CPT | Percutaneous implantation or replacement of integrated single device neurostimulation system including electrode array and pulse generator | Experimental — integrated neurostimulation |
| 0588T | CPT | Revision or removal of integrated single device neurostimulation system including electrode array and pulse generator | Experimental — integrated neurostimulation |
| 0589T | CPT | Electronic analysis with simple programming of implanted integrated neurostimulation system | Experimental — integrated neurostimulation |
| 0590T | CPT | Electronic analysis with complex programming of implanted integrated neurostimulation system | Experimental — integrated neurostimulation |
| 0963T | CPT | Anoscopy with directed submucosal injection of bulking agent into anal canal | Experimental — injectable bulking agents |
| 1001T | CPT | Autologous muscle cell therapy, injection of muscle progenitor cells into the external anal sphincter | Experimental — autologous muscle cell therapy |
| 11950 | CPT | Subcutaneous injection of filling material (e.g., collagen), 1 cc or less | Experimental — injectable bulking agents |
| 11951 | CPT | Subcutaneous injection of filling material, 1.1 to 5.0 cc | Experimental — injectable bulking agents |
| 11952 | CPT | Subcutaneous injection of filling material, 5.1 to 10.0 cc | Experimental — injectable bulking agents |
| 11953 | CPT | Subcutaneous injection of filling material, over 10.0 cc | Experimental — injectable bulking agents |
| 11954 | CPT | Subcutaneous injection of filling material (additional) | Experimental — injectable bulking agents |
| 38205 | CPT | Blood-derived hematopoietic progenitor cell harvesting; allogeneic | Experimental — mesenchymal stem cell injection |
| 38206 | CPT | Blood-derived hematopoietic progenitor cell harvesting; autologous | Experimental — mesenchymal stem cell injection |
| 38240 | CPT | Hematopoietic progenitor cell; allogeneic transplantation per donor | Experimental — mesenchymal stem cell injection |
| 38241 | CPT | Hematopoietic progenitor cell; autologous transplantation | Experimental — mesenchymal stem cell injection |
| 64566 | CPT | Posterior tibial neurostimulation, percutaneous needle electrode, single treatment | Experimental — pudendal nerve / posterior tibial stimulation |
Covered HCPCS Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| A4290 | HCPCS | Sacral nerve stimulation test lead, each |
| C1607 | HCPCS | Neurostimulator, integrated (implantable), rechargeable with all implantable and external components |
| C1767 | HCPCS | Generator, neurostimulator (implantable), non-rechargeable |
| C1778 | HCPCS | Lead, neurostimulator (implantable) |
| C1787 | HCPCS | Patient programmer, neurostimulator |
| C1816 | HCPCS | Receiver and/or transmitter, neurostimulator (implantable) |
| C1820 | HCPCS | Generator, neurostimulator (implantable), with rechargeable battery and charging system |
| C1883 | HCPCS | Adaptor/extension, pacing lead or neurostimulator lead (implantable) |
| C1897 | HCPCS | Lead, neurostimulator test kit (implantable) |
| L8679 | HCPCS | Implantable neurostimulator, pulse generator, any type |
| L8680 | HCPCS | Implantable neurostimulator electrode, each |
| L8681 | HCPCS | Patient programmer (external) for use with implantable programmable neurostimulator pulse generator |
| L8682 | HCPCS | Implantable neurostimulator radiofrequency receiver |
| L8683 | HCPCS | Radiofrequency transmitter (external) for use with implantable neurostimulator radiofrequency receiver |
| L8684 | HCPCS | Radiofrequency transmitter (external) for use with implantable sacral root neurostimulator receiver |
| L8685 | HCPCS | Implantable neurostimulator pulse generator, single array, rechargeable, includes extension |
| L8686 | HCPCS | Implantable neurostimulator pulse generator, single array, non-rechargeable, includes extension |
| L8687 | HCPCS | Implantable neurostimulator pulse generator, dual array, rechargeable, includes extension |
| L8688 | HCPCS | Implantable neurostimulator pulse generator, dual array, non-rechargeable, includes extension |
| L8689 | HCPCS | External recharging system for battery (internal) for use with implantable neurostimulator |
| L8695 | HCPCS | External recharging system for battery (external) for use with implantable neurostimulator |
Not Covered / Experimental HCPCS Codes
| Code | Type | Description | Reason |
|---|---|---|---|
| A4563 | HCPCS | Rectal control system for vaginal insertion, for long term use | Experimental — anal sling / Fenix system |
| L8605 | HCPCS | Injectable bulking agent, dextranomer/hyaluronic acid copolymer implant, anal canal, 1 ml | Experimental — injectable bulking agents |
Other HCPCS Codes Related to CPB 0611
| Code | Type | Description |
|---|---|---|
| E0740 | HCPCS | Incontinence treatment system, pelvic floor stimulator, monitor, sensor and/or trainer |
| E0746 | HCPCS | Electromyography (EMG), biofeedback device |
| G0283 | HCPCS | Electrical stimulation (unattended), to one or more areas |
| J0745 | HCPCS | Injection, codeine phosphate, per 30 mg |
| S9470 | HCPCS | Nutritional counseling, dietitian visit |
Key ICD-10-CM Diagnosis Codes
| Code | Description |
|---|---|
| R15.0 | Fecal incontinence |
| R15.1 | Fecal incontinence |
| R15.2 | Fecal incontinence |
| R15.3 | Fecal incontinence |
| R15.4 | Fecal incontinence |
| R15.5 | Fecal incontinence |
| R15.6 | Fecal incontinence |
| R15.7 | Fecal incontinence |
| R15.8 | Fecal incontinence |
| R15.9 | Fecal incontinence |
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