Breast augmentation

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CHAPTER 53 Breast augmentation

Technical steps

Implant type

A significant consideration when planning augmentation mammaplasty is whether to utilize silicone or saline implants. Both types may be used to produce excellent results, with each possessing its merits and potential drawbacks.

The silicone implant resembles breast tissue to a greater extent, creating a more natural appearance and feel. This is often of primary consideration to the patient, and is reflected in the increased use of silicone since FDA reapproval. However, in view of the fact that the implants are pre-filled, they necessitate a somewhat larger incision. This is generally no more than a 1–2 cm variance, but is of course dependant upon implant size. Additionally, many women are still apprehensive about the perceived health risks associated with silicone. Despite the validation of safety regarding systemic autoimmune disease, the local inflammatory responses to free silicone from extracapsular rupture can produce cosmetic issues that may be challenging to manage. However, this has become much less of an issue in recent years with the additional barrier layer of the third generation silicone implants, and increased cross linking of the silicone for a more cohesive gel.

From 1992 to 2006, saline implants were the only prostheses available for use in the United States except for clinical trials, and operative techniques therefore advanced. Remote incisions such as those used in the transaxillary endoscopic approach have evolved with the use of saline implants, and become more popular during the time period of the silicone moratorium. A demographic of surgeons trained in laparoscopy also naturally contributed to this evolution. Implants can be placed through a relatively small incision, and this option allows the surgeon to intraoperatively adjust fill volumes to more readily correct asymmetries. They are also less costly than their gel counterparts, and are regarded by some to provide for more natural movement with activity. Saline implants are, on the other hand, more prone to rippling as well as spontaneous deflation. Regardless of implant type, proper selection must be a joint process between patient and surgeon. A biodimensional approach using the measurements of at the very least base diameter, tissue pinch, and nipple to inframammary fold discrepancies should be employed and are to be covered in another chapter of this text.

Placement

The breast pocket may be created in either the subglandular or subpectoral space (Fig. 53.1). The subglandular technique is usually reserved for patients who have substantial breast tissue or a mild degree of ptosis, since greater projection may be obtained. Also, women who are avid bodybuilders may prefer subglandular implants for the reason that placing them submuscularly, in some instances, may produce breast animation and distortion when the pectoral muscles are flexed. Increased risks of capsular contracture, rippling and implant palpability are typically issues discouraging the routine use of the subglandular plane.

In patients with a paucity of breast tissue and little to no ptosis, the subpectoral technique, in our opinion, produces optimum results. The pectoralis major drapes the superomedial aspect of the prosthesis, softening the transition, and thus creating a more anatomically shaped breast mound (Fig. 53.2). This method also achieves a natural feel, which is especially desirable when using saline implants. The submuscular plane additionally tends to be less vascular, and is associated with fewer sensory alterations of the nipple areolar complex. Also, rates of fibrous capsular contracture are demonstrably lowered with submuscular placement versus subglandular. In addition to improved aesthetic outcomes, there are moreover prospective functional advantages in regard to breast-feeding as well as cancer screening.

Surgical approach

Although numerous methods have been described in the literature, there are three preferred approaches for breast augmentation: inframammary, periareolar and transaxillary (Fig. 53.3). Dissections may be performed in either plane, with or without the aid of an endoscope.

The inframammary fold incision (Fig. 53.4) provides excellent results in terms of inconspicuous scars, accessibility for both implant types, and fold modifications (Fig. 53.5). This incision allows for optimal view of the pectoral muscle and breast parenchyma, which permits the surgeon to perform an accurate dissection in either, the submuscular or subglandular plane. The downsides of this approach are the potential increased risk of iatrogenic rupture during wound reapproximation, and implant exposure during the postoperative period given the weight of the implant on the healing incision. Additionally, the access incision must be carefully designed to avoid scar migration to the chest wall or inferior pole of the breast.

In patients not requiring fold adjustment, the incision is made at the inframammary fold and is approximately 2.5–3 cm in length, extended laterally from below the nipple, and carried deep until the lateral aspect of the pectoralis major muscle is reached. With the author’s preferred technique, if undertaking a subpectoral placement the inferior muscular attachments are freed by means of a fine mosquito clamp and cautery dissection. The pectoralis major can then be elevated from the chest wall using blunt finger dissection or an Agris–Dingman dissector, which is then replaced by a lighted retractor to allow assessment for hemostasis and the transection of any residual muscular bands via electrocautery. The only medial pectoralis muscle fibers transected are those that appear anomalous and medially displaced. Otherwise, purely inferior muscle fibers are released. In cases of ptosis or tuberous breast deformity, the dual plane technique as described by Tebbetts, may be utilized to aid in redraping the breast tissue over the implant.

An implant sizer may be placed to aid in prosthesis selection, and can also be over filled for intraoperative tissue expansion, as well as its tamponade effect to facilitate hemostasis. Using an antibiotic solution, the selected prostheses are bathed and the pockets are irrigated prior to insertion. The implants are placed, and the patient is raised in an upright seated position to assess contour and symmetry. Once any final adjustments have been made, the patient is then returned to the supine position and the incisions are closed in a layered fashion with 3-0 and 4-0 Monocryl (Ethicon, Somerville, NJ). For additional tissue support in the inframammary approach, we also employ a running, subcuticular 3-0 Prolene (Ethicon, Somerville, NJ), which may be removed later in the postoperative course without sequelae.

The periareolar incision (Fig. 53.6) requires a somewhat higher degree of technical skill, but provides a central point of access for pocket development as well as radial release. This incision is especially suitable for those who have an ill defined fold, constricted breast tissue, or require nipple-areolar resizing. It also allows for conservative excision of redundant lower pole skin. In order to achieve discrete scars, the patient must have a sufficiently sized nipple-areolar complex to accommodate the selected implant, a well-defined areolar edge, and differentiation of pigment (Figs 53.7, 53.8). The approach is generally limited to smaller silicone implants, but this is less of an issue with saline prostheses. Given the proximity of the incision to the lactiferous ducts, it may however, be a less favorable choice for patients who desire to breastfeed. Also, there may be an increased likelihood of nipple dysesthesias due to proximity of the dissection.

The incision lies on the lower border of the areola, and is approximately 3.0–4.0 cm long from 3 o’clock to 9 o’clock. This length may vary depending upon the individual anatomy, but should generally not extend beyond one half of the areolar circumference. After the initial incision is made, the breast parenchyma is dissected down to the fascia of the pectoralis major muscle in an inferior direction towards the breast base. If subpectoral placement is desired, the muscle is carefully released allowing entry into the subpectoral space. The pectoralis muscle is then elevated, thus creating the breast pocket.

Using a lighted retractor for visualization, electrocautery is employed to detach the muscle edge from the inferior chest wall and provide a hemostatic environment. Once the pockets have been adequately dissected, they are irrigated with antibiotic solution and the implants are placed. The patient is then maneuvered to a sitting position allowing the surgeon to evaluate the aesthetic effect and further fine tune any pocket modifications before closing. Again, we use 3-0 and 4-0 Monocryl for the deeper layers, while 5-0 running nylon is employed on the skin.

The transaxillary endoscopic technique (Fig. 53.9) is ideal for patients with minimal glandular tissue, little or no ptosis and an ill-defined inframammary fold. The incision is best suited for saline implants that can be filled once they have been placed, but silicone implants may be placed with extension of the incision up to 4 cm. The main advantage of this technique is that there are no scars created on the breast (Fig. 53.10). However, as the breast pocket is further away from the incision, it is more difficult to precisely alter the inframammary fold and correct asymmetries. Inadequate muscle release with this technique may lead to persistently high riding implants. This approach is not appropriate for patients with tubular breast deformities, and although possible, is impractical for subglandular placement. Also, revision surgeries may require an alternate counterincision if substantial modifications are to be made.

A 2.5–3 cm transverse incision is made posterior to the anterior axillary fold and inferior to the apex of the axilla, following the lines of Langer in an axillary crease. Blunt dissecting scissors are used to create a subcutaneous plane from the incision to the lateral pectoral fascia. It is important that this dissection is carried out superficially to avoid injury to the intercostobrachial nerve, which traverses this area. Once the lateral edge of the muscle has been raised, the inferior and lateral subpectoral spaces are digitally dissected much as possible. Following this, an Agris–Dingman dissector is utilized to develop the remaining subpectoral pocket. Care must be employed with this maneuver to avoid avulsion of the medial perforators and/or entry into the pleural space. If the use of an endoscopic retractor is desired, it may be introduced into the pocket at this point for precision of muscle release inferiorly along the inframammary fold.

To achieve this, we utilize an angled retractor, which accommodates a 10 mm, 30-degree endoscope, along with a standard breast endoscopic instrumentation set. Snowden Pencer (Cardinal Health, Dublin, OH) has provided us with the most effective instrumentation for this procedure. For optimal results, the dissection should be performed bilaterally prior to implant placement. Once the pockets have been irrigated and the implants inserted, the patient is elevated to a sitting position to assess cosmesis as well as symmetry, and allow the surgeon to make any final adjustments prior to closing. The wound is then sutured in a layered fashion using 3-0 and 4-0 Monocryl, with running 5-0 Nylon for skin.

Complications

See Table 53.1.

Although rare, there is an estimated 0.5% incidence of hematoma following breast augmentation surgery (Baker, 1998). This postoperative complication is typically heralded by the onset of unilateral pain with progressive enlargement and ecchymosis. Risks are minimized by careful hemostasis intraoperatively as well as limiting hypertension and excessive activity in the postoperative period. Infection is also a potential complication, typically caused by flora indigenous to breast tissue. Intraoperatively, this is addressed with antibiotic irrigation and appropriate in travenous antibiotic prior to the incision being made. Nipple and areola sensation may be affected by breast surgery, resulting in hyperesthesia or dysesthesia. The vast majority of these changes are temporary, and tend to resolve over time. Capsular contracture may arise, and is commonly believed to be associated with residual blood or subclinical bacterial contamination, although the predisposing factors are still frequently debated. Again meticulous hemostasis, triple antibiotic pocket irrigation and the use of antimicrobial prophylaxis are certainly helpful, and a daily postoperative massage regimen may also be advantageous. If subglandular placement is planned, the use of a textured implant may be of benefit as has been previously suggested by the plastic surgery literature. However, downsides to textured implants include their thicker shell and potential palpability in patients with thin tissues.

Pearls & pitfalls

Summary of steps

1. After informed consent has been obtained, the patient is marked in an upright position using a surgical pen. These markings, at minimum, should reflect the midline below the sternal notch, as well as an outline of the inframammary folds and proposed breast pockets with incisions.

2. Intravenous access is established and antibiotic prophylaxis is administered prior to commencing with the operation.

3. The patient is placed in the supine position and anesthetized under general endotracheal anesthesia, or by means of a laryngeal mask airway. The author prefers this to local anesthesia with sedation, as it allows for optimal muscular relaxation and subsequently a more precise pocket dissection.

4. The arms are secured on arm boards at 90 degrees, and at the level of the shoulders. Joint surfaces are inspected and padded.

5. The proposed access incisions and inframammary fold are injected with an approximate total of 50 mL image% lidocaine with epinephrine in a 1 : 200,000 ratio.

6. The patient is then widely prepped and draped in a sterile fashion, with a chest-breast or split sheet, allowing access both above and below the arm boards.

7. An incision is made, and one of the three approaches previously discussed is used.

8. Once the dissection is carried out to the pectoral fascia, a breast pocket is created in either the submuscular or subglandular plane, and hemostasis is attained. The author prefers a partial submuscular or dual plane technique in the vast majority of cases.

9. In moderate to severe cases of asymmetry using saline implants, and in most cases of asymmetry using silicone implants, an implant sizer is placed to determine size (and then overfilled with saline for intraoperative tissue expansion and tamponade).

10. Attention is then directed to the contralateral breast, and the operation is repeated in a similar manner.

11. After the appropriate implant has been selected, the sizers are removed.

12. The breast pockets are then copiously irrigated with an antibiotic solution, and again assessed for hemostasis. Triple antibiotic solution with bacitracin, cefazolin and gentamicin is preferred.

13. The prostheses are dispensed to the sterile field, bathed in the antibiotic solution, and prepared as required.

14. Once the implants have been placed, the patient is maneuvered into a sitting position to assess contour and symmetry, allowing the surgeon to make any final modifications. Assessment of the shoulders and clavicles is necessary to ensure proper positioning and therefore symmetry.

15. When completed, the patient is returned to the supine position and the surgical wounds are closed in a layered fashion.

16. Steri Strips are applied to the incisions, and a 6-inch elastic wrap is placed circumferentially, prior to emergence and transfer to the Recovery Room.

Further reading

Adams WP, Jr., Rios JL, Smith SJ. Enhancing patient outcomes in aesthetic and reconstructive breast surgery using triple antibiotic breast irrigation: Six year prospective clinical study. Plast Reconstr Surg Adv Breast Augment. 2006;118((7S) Suppl):46S–52S.

Baker JL, Jr. Chapter 63. In: Spear SL, ed. Augmentation mammaplasty, surgery of the breast principles and art. Philadelphia: Lippincott-Raven; 1998:845–854.

Bostwick J, III. Plastic and reconstructive breast surgery, 2nd edn. St Louis: MO: Quality Medical Publishing; 2000.

Burkhardt BR, Demas CP. The effect of siltex texturing and povidone-iodine irrigation on capsular contracture around saline-inflatable breast implants. Plast Reconstr Surg. 1994;93(1):123–130.

FDA approves silicone gel-filled breast implants after in-depth evaluation news release. http://www.fda.gov/bbs/topics/NEWS/2006/NEW01512.html, 16 November 2006.

Hidalgo DA. Breast augmentation: Choosing the optimal incision, implant, and pocket plane. Plast Reconstr Surg. 2000;105(6):2202–2216.

Muzaffar AR, Rohrich RJ. The silicone gel-filled breast implant controversy: An update. Plast Reconstr Surg. 2004;109(2):742–748.

Netter FH. Atlas of human anatomy. Basle: Ciba-Geigy Corporation; 1989.

Takayanagi S, Chisato N, Sugimoto Y. Augmentation mammaplasty: Where should the implant be placed? Aesthet Plast Surg. 2004;28:83–88.

Tebbetts JB. Dual plane breast augmentation: Optimizing implant–soft tissue relationships in a wide range of breast types. Plast Reconstr Surg. 2001;107(5):1255–1272.