Breast Reconstructive Surgery
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Defines Aetna's medical necessity, coverage stance, and coding guidance for reconstructive breast surgery following mastectomy/lumpectomy, autologous fat grafting, use of implants and flaps, and related procedures for members covered by Aetna.
No material clinical or coverage changes in this revision.
Coverage Criteria
Primary medical necessity
Aetna considers reconstructive breast surgery medically necessary when ANY of the following are met:
Supported by policy section 'Medical Necessity'
Covered reconstructive procedures
Medically necessary procedures include (when criteria above met):
Enumerated list of medically necessary procedures
Medically necessary acellular dermal matrices
The following acellular dermal matrices are considered medically necessary:
Named products supported as medically necessary
Cosmetic exclusion and exceptions
Cosmetic stance and exceptions:
Cosmetic exclusion with explicit exceptions
Experimental / investigational
The following are considered experimental and investigational (insufficient evidence):
Enumerated experimental/investigational procedures
Use of 3D volumetric imaging/printing for planning breast reconstruction
Evidence and findings reported in observational and small prospective studies — no standardized coverage criteria provided in these chunks.
Studies are small and heterogeneous; no standardized coverage criteria are established.
Nerve coaptation/neurotization for sensation improvement
Multiple observational studies, cadaver dissections, and systematic reviews report improved sensory recovery with neurotization techniques, but heterogeneity and limited standardized outcome measures remain.
Promising but heterogeneous evidence; further high‑quality standardized studies recommended before declaring standard of care.
Aetna considers breast reconstructive surgery to correct breast asymmetry to be cosmetic in all situations except the explicitly listed exceptions. Exceptions include: (1) surgical correction of chest wall deformity causing a functional deficit in Poland syndrome when criteria in CPB 0272 are met; and (2) repair of breast asymmetry that is the direct result of a medically necessary mastectomy or lumpectomy that produces a significant deformity. In those exception cases, procedures on the unaffected breast to achieve symmetry (for example, areolar/nipple reconstruction or tattooing, augmentation with an FDA‑approved internal breast prosthesis, implant removal/re‑implantation, reduction mammoplasty, mastopexy, capsulectomy, capsulotomy, and reconstructive revisions) are considered medically necessary when performed to produce a symmetrical appearance.
Autologous fat grafting (lipomodelling) is described as a technique to improve contour or restore volume but has variable effectiveness and important safety concerns. Case series report wide variability in outcomes (substantial improvement reported in 21%–86.5% of patients) and an approximate 7% rate of lipo‑necrotic lumps. These nodules, calcifications, cysts, and indurations can produce abnormalities on cancer screening and may impede future cancer detection; long‑term follow‑up and imaging (mammography, ultrasound, CT, MRI) are recommended after the procedure.
The “body lift” perforator flap technique — a layered or circumferential trunk donor approach to provide additional volume for autologous reconstruction in thin patients — has been reported in small case series but is currently judged to have insufficient evidence to support routine use for breast reconstruction. Major clinical reviews and UpToDate summaries do not describe this technique as a standard management option, and further well‑designed studies are needed to validate safety and outcomes.
Immediate expander‑implant breast reconstruction (EIBR) in patients with prior pre‑mastectomy external beam radiation therapy (XRT) is associated with substantially higher complication and failure rates compared with non‑irradiated patients. In one retrospective series, the EIBR failure rate was reported at 50.0% for the pre‑operative XRT group versus 13.3% in controls (p = 0.044). The authors recommend that patients with a history of pre‑mastectomy radiation strongly consider autologous reconstruction to avoid the higher risk of complications and implant loss with EIBR.
Evidence summaries and recent reviews note that 3D volumetric imaging and 3D‑printed templates have been evaluated in small observational series and may assist preoperative planning (for example, improved implant sizing prediction and reduced intraoperative perforator identification time). However, an UpToDate overview of breast reconstruction (Nahabedian, 2021) does not list 3D volumetric imaging among standard management tools, reflecting limited adoption in mainstream clinical references and the need for further validation before routine use.
The policy lists nerve coaptation / neurotization among procedures for which the current evidence is insufficient to establish clear effectiveness (classified as experimental and investigational in this CPB). Within the provided excerpt there is no explicit coverage exclusion or definitive payer stance on neurotization beyond its inclusion in the experimental/investigational list; the background summarizes promising but heterogeneous study results and calls for additional standardized research.
The excerpt contains no specific site‑exit coverage exclusions for additional procedures beyond those enumerated in the policy. The final chunk is a site‑exit disclaimer and does not state any further coverage restrictions or exclusions beyond the policy text already cited.
The policy references specific procedure and technology codes in its coverage discussion. Notably, CPT code 0694T (3‑dimensional volumetric imaging/reconstruction) is identified in the document as an item of concern (listed under experimental/not covered in the CPB), and nerve graft/allograft procedure codes 64910–64913 are discussed in the context of nerve repair/coaptation techniques. These code references are provided to guide billing and to indicate that these technologies/procedures are addressed in the policy.
Although neurotization (nerve coaptation) is discussed in the background and listed among experimental/investigational procedures in the policy, the excerpt does not contain any explicit statement designating neurotization procedures as not medically necessary. The document instead summarizes the existing evidence and notes heterogeneity and the need for standardized outcome measurement before establishing a definitive coverage determination.
Coding
| 11920 | Tattooing, intradermal introduction of insoluble opaque pigments to correct color defects of skin, including micropigmentation; 6.0 sq cm or less. |
| 11921 | 6.1 to 20.0 sq cm. |
| 11922 | each additional 20.0 sq cm (List separately in addition to code for primary procedure). |
| 11950 | Subcutaneous injection of filling material (eg, collagen). |
| 11971 | Removal of tissue expander without insertion of implant. |
| 15769 | Grafting of autologous soft tissue, other, harvested by direct excision (eg, fat, dermis, fascia). |
| 15771 | Grafting of autologous fat harvested by liposuction technique to trunk, breasts, scalp, arms, and/or legs; 50 cc or less injectate. |
| 15772 | each additional 50 cc injectate, or part thereof. |
| 15773 | Grafting of autologous fat harvested by liposuction technique to face, eyelids, mouth, neck, ears, orbits, genitalia, hands, and/or feet; 25 cc or less injectate. |
| 15774 | each additional 25 cc injectate, or part thereof. |
| 0694T | 3-dimensional volumetric imaging and reconstruction of breast or axillary lymph node tissue, each excised specimen. |
| 64910 | Nerve repair; with synthetic conduit or vein allograft (eg, nerve tube), each nerve. |
| 64911 | with autogenous vein graft (includes harvest of vein graft), each nerve. |
| 64912 | with nerve allograft, each nerve, first strand (cable). |
| 64913 | with nerve allograft, each additional strand (List separately in addition to code for primary procedure). |
| C1781 | Mesh (implantable) [Cortiva]. |
| C1789 | Prosthesis, breast (implantable). |
| C9358 | Dermal substitute, native, non- denatured collagen, fetal bovine origin (SurgiMend collagen matrix), per 0.5 square centimeters. |
| C9360 | Dermal substitute, native, non- denatured collagen, neonatal bovine origin (SurgiMend Collagen Matrix), per 0.5 square centimeters. |
| L8600 | Implantable breast prosthesis, silicone or equal. |
| Q4116 | Alloderm, per square centimeter. |
| Q4122 | Dermacell, dermacell awm or dermacell awm porous, per square centimeter. |
| Q4128 | Flex HD, Allopatch HD, or Matrix HD, per square centimeter. |
| Q4130 | Strattice TM, per sq cm. |
| S2066 | Breast reconstruction with gluteal artery perforator (GAP) flap, unilateral. |
| C50.011 - C50.929 | Malignant neoplasm of breast. |
| C79.81 | Secondary malignant neoplasm of breast. |
| D05.00 - D05.92 | Carcinoma in situ of breast. |
| N60.11 - N60.19 | Diffuse cystic mastopathy [severe fibrocystic disease]. |
| Z85.3 | Personal history of malignant neoplasm of breast. |
| Z90.10 - Z90.13 | Acquired absence of breast [following medically necessary mastectomy or lumpectomy resulting in significant deformity]. |
| R59.0 - R59.9 | Enlarged lymph nodes. |
| Z42.1 - Z42.8 | Encounter for plastic and reconstructive surgery following medical procedure or healed injury [breast reconstruction]. |
Provider Actions & Requirements
Prior Authorization Required
Prior authorization is required for covered reconstructive codes where the plan or member's benefit design specifies prior authorization. Providers should obtain prior authorization when applicable and submit appropriate clinical documentation supporting medical necessity.
- Submit applicable CPT/HCPCS/ICD-10 codes listed in the policy and ensure selection criteria are met (see Applicable codes section).
- Obtain prior authorization when the member’s plan requires it for reconstructive procedures.
ADM Use — Documentation Required
When acellular dermal matrices (ADMs) or biologic implants are used, document product selection and clinical rationale in the medical record. Include details that may affect complication risk and choice of material.
- Record the specific ADM product (e.g., AlloDerm, DermACELL, Cortiva, SurgiMend) and lot if available.
- Document indication for ADM use, anticipated benefit, and any product-specific considerations (e.g., prior radiation, infection risk).
- Include intraoperative findings and how ADM contributed to reconstruction.
Artia (porcine collagen mesh) — Coding/Coverage Note
Artia is classified by the FDA as a collagen mesh (porcine). CMS has stated Artia is not suitable for Level II HCPCS coding for ambulatory use and would be bundled for inpatient hospital payment; providers should be aware of coding and billing implications.
- Artia: porcine collagen mesh; FDA classification as collagen mesh.
- CMS (2019) guidance: not appropriate for Level II HCPCS coding for outpatient use; inpatient use may be bundled in hospital payment.
- Contact payer coding services for billing guidance and consider pass-through coding avenues per CMS guidance.
Prior Authorization Not Specified for Certain Adjuncts in Excerpt
The provided excerpt does not specify explicit prior authorization requirements for 3D printing/templates, neurotization (nerve coaptation), or some other adjunctive techniques. Providers should verify member-specific prior authorization requirements with the plan.
- 3D volumetric analysis, 3D-printed templates, and nerve coaptation procedures are discussed in evidence sections but no uniform prior authorization rule is stated in the excerpt.
- Confirm prior authorization requirements with member’s benefit and local medical policy before scheduling.
Autologous Fat Grafting — Safety Concerns
Autologous fat grafting carries safety concerns including formation of lipo-necrotic lumps, calcifications, cysts, and indurations that can impede future cancer detection. Patients should be counseled about these risks and followed long-term with appropriate imaging.
- Document informed consent discussing risk of calcification, cyst formation, palpable induration, and potential impacts on breast cancer screening.
- Plan and document post-procedure imaging and long-term follow-up (mammography, ultrasound, MRI as indicated).
Radiation History — Increased EIBR Failure Risk
Prior radiation increases failure and complication risk for immediate expander-implant breast reconstruction (EIBR). Consider autologous reconstruction in patients with pre-mastectomy radiation and document radiation history in the record.
- Document history and timing of external beam radiation therapy (pre- or post-operative).
- Discuss increased risk of EIBR failure with the patient; document shared decision-making and consideration of autologous options.
Obesity — Increased Complication Risk
Obesity is associated with higher rates of surgical and medical complications and re-operation after breast reconstruction. Document BMI and counsel regarding increased peri-operative risk; consider weight optimization when clinically appropriate.
- Record BMI and discuss specific risks (higher wound complications, fat necrosis, re-operation rates).
- Consider and document any preoperative optimization steps or rationale for proceeding despite elevated BMI.
Evidence Summaries Present — Authorization Details Not Specified
The excerpt includes evidence and background summaries (e.g., ADM comparative studies, neurotization outcomes, 3D volumetric planning) but does not always translate these into explicit authorization or billing requirements. Providers should use the evidence to support medical necessity documentation where applicable.
- When relying on evidence summaries to support authorization, include study-relevant clinical details in the request (e.g., prior radiation, flap type, complication risks).
- If the evidence section suggests higher risk subgroups (e.g., smokers, prior XRT, high initial expander fill), document these factors in the clinical record.
No Explicit Authorization/Denial Triggers in Excerpt
In the provided excerpt there are background and evidence sections without direct provider-action mandates. Where no explicit authorization or denial triggers are listed, providers should still document clinical rationale and confirm payer-specific requirements.
- Examples include sections on neurotization and 3D planning where clinical evidence is described but no coverage rule is given.
- Verify member coverage for adjunctive or emerging techniques.
No Denial-Risk Statements in Administrative Links
The excerpt does not contain explicit denial-risk statements tied to external links or administrative content. External resources and site links are informational only.
- Reference links (glossary, program provisions, disclosures) are provided for convenience and do not constitute coverage guidance.
- For coverage determinations rely on the policy, benefit booklet, and payer prior authorization processes.
Post-procedure Imaging and Follow-up — Document Plan
Post-procedure follow-up and imaging should be documented following autologous fat grafting and other reconstructive procedures. Long-term surveillance may include mammography, ultrasound (echography), CT, or MRI as clinically indicated.
- Document a follow-up plan including timing and modality of imaging.
- Record findings from postoperative imaging and any interventions prompted by imaging abnormalities.
Volumetric Planning — Document Assessments
Pre-operative volumetric planning (3D surface imaging, MRI, mastectomy specimen weight) can support implant selection and improve symmetry. Document any volumetric assessments used to plan reconstruction.
- Record method used for volumetric assessment (3D surface imaging, MRI, CTA, or mastectomy specimen weight) and results.
- If 3D-printed molds or templates are used, document purpose, how they informed intraoperative decisions, and related outcomes.
Suggested Clinical Documentation Elements
Suggested clinical documentation elements from studies include 3D surface imaging, mastectomy specimen weight, BREAST-Q scores, and perforator imaging (CTA) for flap planning. Include these when available to support medical necessity and expected outcomes.
- Include objective pre- and post-operative assessments (3D volumes, mastectomy specimen weight).
- Document patient-reported outcomes (BREAST-Q) when used.
- For perforator flap planning, include CTA or other imaging reports and how they affected surgical approach.
Use Evidence to Support Authorization Requests
The document excerpt provides evidence summaries on multiple adjuncts (ADMs, 3D planning, neurotization, fat grafting) but does not always stipulate coverage criteria for emerging products or techniques. Use evidence to inform clinical justification when requesting authorization.
- When submitting prior authorization requests, include relevant codes and clinical rationale tied to policy-listed medically necessary indications.
- No step therapy or sequencing requirements are specified in the provided excerpt; verify if member-specific benefits impose such requirements.
Reference Resources
Reference resources and external links are provided in the excerpt for additional information on benefits, program provisions, and legal notices. These are informational and do not replace policy or benefit determinations.
- Use the Aetna glossary and program provisions for definitions and benefit guidance.
- For coverage decisions consult the full policy, member benefit booklet, and prior authorization tools.
Background
Breast reconstruction rebuilds breast shape after mastectomy using implants or autologous tissue and may require multiple staged procedures including nipple/areolar reconstruction and tattooing. Staged approaches include use of tissue expanders followed by implant placement or autologous flap reconstruction (eg, TRAM, DIEP, SIEA, GAP flaps). The policy notes that when reconstruction is medically necessary after mastectomy or lumpectomy, associated staged procedures and related services (including nipple/areolar reconstruction and tattooing) are part of the reconstructive plan and may be considered medically necessary when selection criteria are met.
Definitions
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