Breast reconstruction with prosthetic devices remains the most popular option following mastectomy.1 Refinements in tumor treatment, mastectomy techniques, and reconstructive protocols have further broadened the indications for implant-based reconstructions. Rates of prosthetic reconstruction have increased in patients who were previously deemed to be high risk with comorbidities such as diabetes mellitus, advanced stage cancer, obesity, and prior radiotherapy.2 This fact can be attributed to a variety of factors such as improved newer generation silicone implants, the popularity and success of neoadjuvant chemotherapy, and developing mastectomy flaps containing the identified layer of subcutaneous tissue between the dermis and breast epithelium.3–6 As the indications for prosthetic-based reconstructions expand, reconstructive surgeons continue to develop new methods to improve upon adverse events, patient outcomes, and satisfaction. The evolution of prosthetic breast reconstruction has come full circle with its origins in the subcutaneous plane to its present-day prepectoral approach. Each technique aims to decrease pain, prevent animation deformity, and increase the projection and natural ptosis of the reconstruction. This article will highlight many of the advancements from an oncological and reconstructive perspective as we embark on this new paradigm.
SUBCUTANEOUS BREAST RECONSTRUCTION
The earliest descriptions of implant-based reconstructions were performed following subcutaneous mastectomy for benign disease in which a sufficient soft-tissue envelope was maintained.7 Subcutaneous reconstruction for malignant disease was later performed following radical mastectomy. Breast implants at that time were created with a thin shell and soft silicone gel and were prone to failure.8 Early studies following radical mastectomy and subcutaneous placement of implants demonstrated a 26% (13/50) and 31% (12/39) failure rate following immediate and delayed reconstruction, respectively. Nahai and Bostwick9 noted that “The problems of capsular contracture, implant exposure, and malposition of the mound…are seen commonly with subcutaneous placement of the implant…”9
TRANSITION TO SUBMUSCULAR PLANE
With the advent of the modified radical mastectomy and preservation of the pectoralis major muscle, submuscular breast reconstruction provided an extra layer of tissue for implant coverage. The original description of a total submuscular coverage, including partial elevation of the serratus anterior muscle was in 1981.10 In a review of 91 breast reconstructions, comparing 30 subcutaneous, 19 purely subpectoral, and 42 subserratus reconstructions, a 47% incidence of malposition for subcutaneous and prepectoral reconstructions, but only 19% for subserratus reconstructions was demonstrated.11 The introduction of the Radovan tissue expander in 1985 facilitated the process of prosthetic reconstruction.12 In their initial manuscript, all devices were placed in the subcutaneous or prepectoral position.
These early advancements were effective and improved outcomes; however, they did not alleviate all problems associated with subcutaneous implant placement such as capsular contracture. In a review of 76 patients following mastectomy with subcutaneous reconstruction, acute complications were noted in 39% of immediate and 16% following delayed reconstruction. Capsular contracture was demonstrated in 50% of submuscular and 100% of subcutaneous reconstructions.13 Subsequent comparisons of submuscular and subcutaneous reconstruction demonstrated capsular contracture rates of 55% and 58%, respectively.14
ACELLULAR DERMAL MATRICES
The introduction of acellular dermal matrices (ADM) into the realm of breast reconstruction has produced a major paradigm shift.15 Benefits of ADM include soft-tissue support, compartmentalization of implants, and control of the inferior position of the pectoralis major muscle during dual plane reconstruction.16 The ability of ADM to improve aesthetic outcomes was demonstrated by Ibrahim et al.17 in a review of 18 reconstructions with ADM and 20 without. Reconstructions incorporating ADM scored significantly higher in the categories of contour, implant placement, and in total aesthetic score.17 Forsberg et al.18 analyzed aesthetic outcomes in 183 implant-based breast reconstructions (58 with ADM, 125 total submuscular) demonstrating improved aesthetic outcomes with respect to, shape, symmetry, and overall outcome with the exception of contour and position.18 Salzberg et al.19 in a review of 1,584 reconstructions in 863 patients, demonstrated a grade 3/4 capsular contracture rate of 0.8% (12/1,584) at a mean follow-up of 4.7 years.19 In a recent meta-analysis of 15 studies using ADM, the rate of grade 3–4 capsular contracture ranged from 0% to 3.8%.20
Complications associated with ADM use are well studied and established. Chun et al.21 compared 269 submuscular reconstructions utilizing ADM and 146 reconstructions without ADM and demonstrated that the only statistically significant increase was for postoperative seroma with ADM use.21 Vardanian et al.22 compared 337 immediate implant-based reconstructions, of which 208 breasts had ADM and 129 did not, demonstrating no statistically significant increases in seroma, infection, dehiscence, or wound healing.22 In a meta-analysis of all articles providing outcomes of breast reconstructions with (2,037) and without (12,867) ADM, Kim et al.23 demonstrated no statistically significant difference in complications between the ADM and non-ADM cohorts. The overall complication rate was 15.4% versus 14.0%, seroma rate was 4.8% versus 3.5%, and infection rate was 5.3% versus 4.7%.23
MODERN PREPECTORAL BREAST RECONSTRUCTION
The modern era of prepectoral breast reconstruction differs in many ways from the subcutaneous reconstructions of old. Improvements in mastectomy techniques and outcomes have paralleled advancements in the field of plastic surgery. An increase in the propensity of many women, especially younger women, to elect for prophylactic mastectomy has allowed for better quality skin flaps during resection and a resurgence of prepectoral prosthetic reconstruction. The “prepectoral” space lies in the subcutaneous plane, but refers specifically to reconstruction utilizing modern techniques and devices.
Prepectoral reconstruction can be performed in 1 or 2 stages. Reported outcomes are similar for both methods with rates of capsular contracture, implant malposition, and rippling generally being less than 5%.24 , 25 Caution and proper patient selection must be strictly adhered to with 1-stage prepectoral reconstruction; otherwise, device removal may be more likely.26 Consideration for 1-stage requires optimal perfusion and thickness of the mastectomy skin flaps, whereas for 2 stage depends primarily on optimal perfusion. Excessive pressure on the mastectomy skin flaps associated with prefilled implants can result in skin flap necrosis and reconstructive failure. Strategies to offload pressure include the use of tissue expanders that are partially filled wit air rather than saline to avoid dependent pressure when standing and because air is evenly distributed within the tissue expander.
Prepectoral Reconstruction without Soft-tissue Support
Prepectoral breast reconstruction can be performed with or without additional soft-tissue support (Table 1). In a recent study of 107 women with prepectoral saline implants without ADM, the overall rate of implant failure was 5.6% (6/107), and the rate of capsular contracture was 20.6%.27 In a similar study of 155 patients and 250 breasts following nipple-sparing mastectomy and prepectoral tissue expander reconstruction without ADM, the rate of implant failure was 6.8%, and the rate of capsular contracture was 7.6%.28 These studies highlight the ongoing problem of capsular contracture despite the technical feasibility of prepectoral reconstruction.
Prepectoral Breast Reconstruction with Non-ADM Soft-tissue Support
In an attempt to further improve outcomes, surgeons have used adjunct materials to provide additional soft-tissue support (Table 2). Kobraei et al.29 performed 23 reconstructions in 13 patients utilizing a prepectoral sling made of Vicryl mesh, which was reinforced with ADM in 3 cases. No cases of capsular contracture were identified, and all other complications were reported within acceptable limits at 10-month follow-up.29 In a direct-to-implant study comparing reconstruction with a prepectoral titanium mesh wrap (n = 39) to subpectoral titanium sling (n = 34), there was only 1 implant failure in the prepectoral cohort. There were no significant differences between the 2 groups with any complication, including infection, implant loss, skin necrosis, hematoma, or reoperation at 1-year follow-up.30 Two-year follow-up demonstrated no capsular contracture in the prepectoral cohort and 12% in the partial subpectoral cohort.31 In a similarly designed tissue expander study using the same titanium mesh, the rate of implant loss was 0%, infection was 12%, and hematoma was 4%.32 To the authors’ knowledge, titanium mesh is not approved for use in breast reconstruction in the United States. These non-ADM adjuncts have demonstrated success with prepectoral breast reconstruction.
Prepectoral Reconstruction with ADMs
ADM is the most common material used for prepectoral breast reconstruction and can be applied with a partial or circumferential lining of the mastectomy pocket. In general, the preferred thickness of ADM is 2–3 mm; however, 1–2 mm thickness can also be used. Becker et al.33 using an adjustable saline implant in the prepectoral space lined with Flex HD in 52 breasts (Musculoskeletal Transplant Foundation, Edison, N.J.) or vicryl in 10 breasts demonstrated high patient satisfaction and low complications that included a seroma (1/62, 1.6%), implant loss (2/62, 3.2%), and capsular contracture (2/62, 3.6%).33 Caputo et al.34 utilized wise pattern skin resection with an inferior dermal sling and a superior lining that consisted of a porcine ADM (Native; MBP, Neustadt-Glewe, Germany). After a mean follow-up of 14.7 months, there was no implant loss and no capsular contracture.34 Reitsamer and Peintinger35 utilized another porcine ADM, Strattice (LifeCell Corporation, Bridgewater, N.J.) to perform a complete wrap of the prepectoral implant in 13 patients (22 breasts). Six-month follow-up demonstrated 1 hematoma and no capsular contractures.35 Figures 1–6 illustrate a patient following nipple-sparing mastectomy followed by immediate 2-stage prepectoral prosthetic breast reconstruction.
Several European studies have utilized a porcine ADM, Braxon (MBP, Neustadt-Glewe, Germany) for prepectoral implant reconstruction (Table 3). Berna et al.36 used Braxon in 25 patients demonstrating a seroma rate of 20%, of which 12% required explantation with the remaining 8% being managed conservatively.36 Vidya et al.37 conducted a multicenter trial of 100 patients utilizing Braxon mesh for prepectoral reconstruction with a low complications that included seroma (5%), implant loss (2%), and no infection.37 Onesti et al.38 reported on 64 direct-to-implant reconstructions utilizing Braxon with a 3.1% incidence of explantation. Serial ultrasound examination revealed an initial fluid layer between the ADM and the implant and the ADM and the skin flap that resolved by 12 months in all patients.38
The most widely used ADM for breast reconstruction in the United States is Alloderm (LifeCell Corporation, Bridgewater, N.J.). Down and Hedges26 performed 79 prepectoral direct-to-implant reconstructions in 45 patients utilizing an Alloderm wrap. Complications included implant loss in 17.7% (11 due to skin necrosis, 3 due to infection) and capsular contracture in 10.1%.26 Sigalove et al.24 performed 353 reconstructions in 207 patients utilizing Alloderm for total implant coverage. Complications included infection in 4.5%, seroma in 2%, skin necrosis in 2.5%, and no clinically significant capsular contracture at 6- to 26-month follow-up. Contraindications to prepectoral reconstruction included a body mass index > 40, poor quality mastectomy flaps, active smokers, or those patients with deep tumors24 (Table 4).
INCORPORATING PREPECTORAL BREAST RECONSTRUCTION
Patient selection is arguably the most important criteria for prepectoral breast reconstruction. Contraindications include poorly controlled diabetes mellitus, active tobacco use, and chronic immunosuppression. Increased risk is associated with prior radiation and morbid obesity. Determinants of success include well-perfused mastectomy skin flaps without visible dermis. Intraoperatively, skin flaps should be assessed clinically and when possible, intraoperative fluorescent angiography. If the flaps cannot be excised and closed without significant tension, the reconstruction should be delayed or converted to another reconstructive method.
ADMs are commonly utilized in the setting of prepectoral reconstruction to increase the soft-tissue support and provide optimal implant position and pocket control. The ADM should cover at least the entire anterior surface of the implant, but can be wrapped to include ADM on its posterior surface. ADM fenestration can improve incorporation and reduce fluid accumulation.
Postoperative care does not differ substantially from other forms of implant-based breast reconstruction. Antibiotic use is at the discretion of the surgeon. Patients should be followed closely for delayed healing or mastectomy flap skin necrosis. Areas of necrosis should be excised and closed immediately. Drain use is recommended for all patients with removal based on output and time. Expansion may be started within 3 weeks of implant placement, provided there are no issues with wound healing. Fat grafting is an important adjunct to prepectoral reconstructions. Fat grafting donor sites should be assessed at the initial consultation and a treatment plan should be formulated at that time.
Implant-based breast reconstruction continues to be the primary type of reconstruction offered by plastic surgeons. Early experience with subcutaneous reconstruction was fraught with reconstructive failure due to aggressive mastectomy and early generation implants that were prone to rupture and encapsulate. Prepectoral reconstruction is now possible based on the recent advancements in breast oncology and reconstruction. Skin and nipple-sparing mastectomy is considered safe and effective and has improved aesthetic outcomes. Accurate assessment of mastectomy skin flap perfusion is now possible and predictive of tissue survival. ADM has decreased the rate of capsular contracture and implant exposure without significantly increasing the risk for seroma, infection, or other untoward complications. Improvement in the quality of implants with regard to silicone gel cohesivity and shell durability have improved outcomes and decreased rippling and wrinkling. The use of autologous fat grafting has provided the ability to expand the thickness and enhance the quality of mastectomy skin flaps. We now reside in the era of the bioengineered breast, and prepectoral breast reconstruction represents a paradigm shift in our reconstructive algorithm. It is the hope of the authors that this technique will continue to be adopted, studied, and reported upon to further optimize the patient experience and surgical results.
1. Albornoz CR, Bach PB, Mehrara BJ, et al. A paradigm shift in U.S. breast reconstruction: increasing implant rates. Plast Reconstr Surg. 2013;131:15–23.
2. Albornoz CR, Cordeiro PG, Pusic AL, et al. Diminishing relative contraindications for immediate breast reconstruction: a multicenter study. J Am Coll Surg. 2014;219:788–795.
3. Maxwell GP, Gabriel A. The evolution of breast implants. Clin Plast Surg. 2009;36:1–13. doi:10.1016/j.cps.2008.08.001.
4. Santoro S, Loreti A, Cavaliere F, et al. Neoadjuvant chemotherapy is not a contraindication for nipple sparing mastectomy. Breast. 2015;24:661–666.
5. Robertson SA, Rusby JE, Cutress RI. Determinants of optimal mastectomy skin flap thickness. Br J Surg. 2014;101:899–911.
6. Larson DL, Basir Z, Bruce T. Is oncologic safety compatible with a predictably viable mastectomy skin flap? Plast Reconstr Surg. 2011;127:27–33.
7. Glatt BS, Afifi G, Noone RB. Long-term follow-up of a sponge breast implant and review of the literature. Ann Plast Surg. 1999;42:196–201.
8. Snyderman RK, Guthrie RH. Reconstruction of the female breast following radical mastectomy. Plast Reconstr Surg. 1971;47:565–567.
9. Nahai F, Bostwick J 3rd.. Aesthetic aspects of breast reconstruction. Aesthetic Plast Surg. 1982;6:61–67.
10. Apfelberg DB, Laub DR, Maser MR, et al. Submuscular breast reconstruction—indications and techniques. Ann Plast Surg. 1981;7:213–221.
11. Gruber RP, Kahn RA, Lash H, et al. Breast reconstruction following mastectomy: a comparison of submuscular and subcutaneous techniques. Plast Reconstr Surg. 1981;67:312–317. Available at http://www.ncbi.nlm.nih.gov/pubmed/7232564
13. Slade CL. Subcutaneous mastectomy: acute complications and long-term follow-up. Plast Reconstr Surg. 1984;73:84–90.
14. Holzgreve W, Beller FK. Surgical complications and follow-up evaluation of 163 patients with subcutaneous mastectomy. Aesthetic Plast Surg. 1987;11:45–48.
15. Zenn MR, Salzberg CA. A direct comparison of alloderm-ready to use (RTU) and DermACELL in immediate breast implant reconstruction. Eplasty. 2016;16:e23.
16. Nahabedian MY. Acellular dermal matrices in primary breast reconstruction: principles, concepts, and indications. Plast Reconstr Surg. 2012;130:44S–53S. doi:10.1097/PRS.0b013e31825f2215.
17. Ibrahim AM, Koolen PG, Ganor O, et al. Does acellular dermal matrix really improve aesthetic outcome in tissue expander/implant-based breast reconstruction? Aesthetic Plast Surg. 2015;39:359–368.
18. Forsberg CG, Kelly DA, Wood BC, et al. Aesthetic outcomes of acellular dermal matrix in tissue expander/implant-based breast reconstruction. Ann Plast Surg. 2014;72:S116–S120.
19. Salzberg CA, Ashikari AY, Berry C, et al. Acellular dermal matrix-assisted direct-to-implant breast reconstruction and capsular contracture: a 13-year experience. Plast Reconstr Surg. 2016;138:329–337.
20. Basu CB, Jeffers L. The role of acellular dermal matrices in capsular contracture: a review of the evidence. Plast Reconstr Surg. 2012;130:118S–124S.
21. Chun YS, Verma K, Rosen H, et al. Implant-based breast reconstruction using acellular dermal matrix and the risk of postoperative complications. Plast Reconstr Surg. 2010;125:429–436.
22. Vardanian AJ, Clayton JL, Roostaeian J, et al. Comparison of implant-based immediate breast reconstruction with and without acellular dermal matrix. Plast Reconstr Surg. 2011;128:403e–410e.
23. Kim JY, Davila AA, Persing S, et al. A meta-analysis of human acellular dermis and submuscular tissue expander breast reconstruction. Plast Reconstr Surg. 2012;129:28–41.
24. Sigalove S, Maxwell GP, Sigalove NM, et al. Prepectoral implant-based breast reconstruction: rationale, indications, and preliminary results. Plast Reconstr Surg. 2017;139:287–294.
25. Sbitany H, Piper M, Lentz R. Prepectoral breast reconstruction: a safe alternative to submuscular prosthetic reconstruction following nipple-sparing mastectomy. Plast Reconstr Surg. 2017;140:432–443. doi:10.1097/PRS.0000000000003627.
26. Downs RK, Hedges K. An alternative technique for immediate direct-to-implant breast reconstruction—a case series. Plast Reconstr Surg Glob Open. 2016;4:e821.
27. Benediktsson K, Perbeck L. Capsular contracture around saline-filled and textured subcutaneously-placed implants in irradiated and non-irradiated breast cancer patients: five years of monitoring of a prospective trial. J Plast Reconstr Aesthet Surg. 2006;59:27–34.
28. Salibian AH, Harness JK, Mowlds DS. Staged suprapectoral expander/implant reconstruction without acellular dermal matrix following nipple-sparing mastectomy. Plast Reconstr Surg. 2017;139:30–39.
29. Kobraei EM, Cauley R, Gadd M, et al. Avoiding breast animation deformity with pectoralis-sparing subcutaneous direct-to-implant breast reconstruction. Plast Reconstr Surg Glob Open. 2016;4:e708.
30. Casella D, Bernini M, Bencini L, et al. TiLoop® bra mesh used for immediate breast reconstruction: comparison of retropectoral and subcutaneous implant placement in a prospective single-institution series. Eur J Plast Surg. 2014;37:599–604.
31. Bernini M, Calabrese C, Cecconi L, et al. Subcutaneous direct-to-implant breast reconstruction: surgical, functional, and aesthetic results after long-term follow-up. Plast Reconstr Surg Glob Open. 2015;3:e574.
32. Casella D, Calabrese C, Bianchi S, et al. Subcutaneous tissue expander placement with synthetic titanium-coated mesh in breast reconstruction: long-term results. Plast Reconstr Surg Glob Open. 2015;3:e577.
33. Becker H, Lind JG 2nd, Hopkins EG. Immediate implant-based prepectoral breast reconstruction using a vertical incision. Plast Reconstr Surg Glob Open. 2015;3:e412.
34. Caputo GG, Marchetti A, Dalla Pozza E, et al. Skin-reduction breast reconstructions with prepectoral implant. Plast Reconstr Surg. 2016;137:1702–1705.
35. Reitsamer R, Peintinger F. Prepectoral implant placement and complete coverage with porcine acellular dermal matrix: a new technique for direct-to-implant breast reconstruction after nipple-sparing mastectomy. J Plast Reconstr Aesthet Surg. 2015;68:162–167.
36. Berna G, Cawthorn SJ, Papaccio G, et al. Evaluation of a novel breast reconstruction technique using the Braxon® acellular dermal matrix: a new muscle-sparing breast reconstruction. ANZ J Surg. 2017;87:493–498.
37. Vidya R, Masià J, Cawthorn S, et al. Evaluation of the effectiveness of the prepectoral breast reconstruction with Braxon dermal matrix: first multicenter European report on 100 cases. Breast J. 2017.
38. Onesti MG, Maruccia M, Di Taranto G, et al. Clinical, histological, and ultrasound follow-up of breast reconstruction with one-stage muscle-sparing “wrap” technique: a single-center experience. J Plast Reconstr Aesthet Surg. 2017;70:1527–1536.
39. Schlenker JD, Bueno RA, Ricketson G, et al. Loss of silicone implants after subcutaneous mastectomy and reconstruction. Plast Reconstr Surg. 1978;62:853–861.
40. Eskenazi LB. New options for immediate reconstruction: achieving optimal results with adjustable implants in a single stage. Plast Reconstr Surg. 2007;119:28–37.
41. Woo A, Harless C, Jacobson SR. Revisiting an old place: single-surgeon experience on post-mastectomy subcutaneous implant-based breast reconstruction. Breast J. 2017;23:545–553.