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Each year over 2 million women are diagnosed with breast cancer, the single-most common cancer diagnosis. Fortunately it is also among the most treatable with survival rates as high as 84% in 10 years. Nonetheless, definitive treatment, including mastectomy or breast-conserving therapy, may come at the cost of often significant psychosocial distress. Between 30% and 50% of women report symptoms of depression, loss of interest in or satisfaction from sexual intimacy, feeling less “feminine,” difficulty shopping for or wearing clothing, and overall cosmetic dissatisfaction.
Breast reconstruction has been demonstrated to ameliorate many of the psychosocial sequelae of mastectomy, improving quality of life in breast cancer survivors. These benefits can be offset by unexpected adverse events throughout the postoperative period, leading to prolonged healthcare interactions, delays in adjuvant therapies, compromised aesthetic outcomes, and symptoms of depression and psychosocial distress. As such, their prompt identification and management are of critical importance to improving patient care. In this chapter we review common complications in prosthetic breast reconstruction, presenting strategies for their identification, management, and prevention.
The risk of complications following prosthetic breast reconstruction is generally low, but can assume a wide range of values. Reports in the literature range from as low as 2% to 49% or higher depending on patient comorbidities, the timing of reconstruction, previous radiotherapy, implant and pocket selection, and use of acellular dermal matrices, to name a few variables. With such a broad range, it can be challenging to apply population-based measures of risk to the individual patient.
A statistical model that navigates these various patient- and surgery-specific variables would allow for a more evidence-based and patient-specific conversation of risk. In plastic surgery, the Breast Reconstruction Risk Assessment (BRA) Score ( Fig. 25.1 ) represents the first such attempt at developing such a risk calculator. The model has undergone multiple iterations and pulls data from several high-powered national registries to predict the risk of several potential complication. Clinically the utility of such a calculator is informing an objective discussion of the surgical risks, benefits, and alternatives; modifiable risk factors; and expected postoperative recovery. In a patient who smokes or with a high body mass index (BMI), risk calculations can more tangibly demonstrate the benefits of preoperative behavioral change. Similarly in a high-risk patient with a history of radiation or other non-modifiable risk factors, it allows surgeons to demonstrate how certain reconstructive options, delayed reconstruction, or even no reconstruction may best align with the patient’s stated goals. With so many reconstructive options at our disposal, a frank, evidence-based preoperative conversation may prevent complications in patients at increased risk for complications.
When a postoperative complication does occur, its rapid identification and intervention is crucial to preventing downstream morbidity and the final aesthetic result. An untreated insult to the already tenuous postoperative milieu of the healing mastectomy flap will almost invariably increase the risk of poor wound healing, infections, and/or explantation ( Fig. 25.2 ). Within the early postoperative periods, mastectomy flap necrosis or seromas can beget infection or even explantations. Hematomas can place undue tension on skin flaps and increase the risk of necrosis and implant exposure. Even when the final reconstruction has healed uneventfully, issues with cosmesis may become evident, including rippling, lateral or inferior malposition, or other asymmetries. Several years to decades out from their procedure, patients may experience issues related to implant rupture and capsular contracture. Patients undergoing implant-based reconstruction require follow-up, not only in the immediate postoperative period but long-term to appropriately identify and treat complications and to minimize their deleterious downstream sequelae.
Although all surgical procedures carry an inherent risk of postoperative bleeding, the development of a hematoma following implant-based reconstruction carries significant acute and long-term sequelae including infection and capsular contracture. Despite meticulous hemostasis, hematomas have been reported to occur in between 1% and 7% of immediate breast reconstructions. Mastectomy creates a large wound bed of raw tissue with numerous vessels with the potential to open up and extravasate into the large cavity left by mastectomy. Long operative times also allow for fluctuations in blood pressure related to anesthesia and fluid shifts and is further compounded by the need for two separate surgical teams.
Tumescent mastectomy technique creates a relatively hemostatic hydrodissection plane facilitating a rapid, sharp elevation of mastectomy skin flaps by the breast surgery team. The tumescent solution typically includes 1 mL of 1% epinephrine, leading some surgeons to hypothesize that it may constrict vessels intra-operatively, which subsequently bleed once the epinephrine has worn off. Despite this theoretical concern, several studies, including a recent meta-analysis, have not demonstrated a significant difference in hematoma rates with tumescent mastectomy. Intravenous ketorolac, a potent nonsteroidal anti-inflammatory drug, has also not demonstrated an increased propensity for hematoma following breast surgery, although many surgeons anecdotally continue to avoid its use.
Recently some groups have begun to explore tranexamic acid (TXA) to prevent hematoma formation. TXA inhibits the activation of fibrinogen thus preventing degradation of fibrin clots and blocks the activation of platelets by plasmin thereby preserving platelets for clot formation. A recent retrospective cohort study in implant-based breast reconstruction demonstrated a significantly lower hematoma rate (0.46% vs. 2.9%) when TXA was used after controlling for age, hypertension, and implant pocket location.
In the postoperative period, hematomas may present as ecchymosis, fluctuant expansion of the skin envelope, increased and bloody drain output, and/or hemodynamic instability ( Fig. 25.3 ). Initial management should revolve around ensuring the stability of the patient, and can include obtaining a hemoglobin, ensuring intravenous access, and resuscitation with fluids and/or blood products as indicated. Small hematomas may be managed with gentle compression and observation, although this must be weighed against potential decreased perfusion to the mastectomy skin flaps. Imaging is typically not indicated; however, a bedside ultrasound with or without aspiration may be useful in differentiating between hematomas or other fluid collections, particularly in the setting of a late or unusual presentation.
For a rapidly expanding hematoma, urgent operative intervention is typically indicated to control the blood loss. Even in less severe cases, a hematoma in the breast pocket may further compromise the already tenuous mastectomy flap perfusion, serve as a culture medium for bacterial proliferation, and/or potentially contribute to the development of capsular contracture, justifying the need for surgical intervention. The incisions are re-opened and all clotted blood is evacuated from the pocket. The wound bed is copiously irrigated with several liters of warm irrigation and all bleeding vessels are identified and controlled. Placement of a large bore drain is recommended by most surgeons.
A seroma is defined as a fluid collection that occurs at the surgical site around the tissue expander or permanent implant. Although many patients are likely to have small fluid accumulations following surgical drain removal, few persist and/or become large enough to be clinically significant. As such, variations in definitions have made it challenging to determine its incidence. Reported values range between 0.2% and 20%.
Commonly reported risk factors for seroma formation include a high BMI and the use of an acellular dermal matrix (ADM). Surgical trauma to the wound bed results in lymphatic disruption, tissue injury, and niduses of non-viable tissue and fatty debris that trigger inflammatory pathways. This is further exacerbated by the foreign body response to the implant and ADM ( ) and potential subclinical microbial contamination. A meta-analysis of the risks of ADM use in immediate tissue expander-based breast reconstruction demonstrated a relative risk of 2.7 in the ADM group compared to those undergoing reconstruction without ADM. Advances in the types and processing of ADM materials appears to affect seroma formation with several studies reporting differences in complication rates among the various devices.
Egress of the serous fluid into the wound bed is initially controlled with the use of postoperative drains, although there is sparse literature to guide evidence-based decisions on the number of drains and the optimal duration of use. Following drain removal, if the rate of fluid production is greater than its resorption, a seroma will begin to form ( Fig. 25.4 ). This has the greatest potential to become clinically significant in high BMI patients with larger skin flaps as there is a greater volume of dead space in which the seroma can accumulate.
Several techniques have also been reported to minimize seroma formation. Dead space following mastectomy is particularly common in the lateral breast gutter in obese patients or those with extensive lymph node dissection. Judicious intra-operative expander fill and/or appropriate implant volume selection can fill this dead space – although this must be weighed against the risk of mastectomy flap necrosis. Similarly, gentle external compression with bandages or a soft surgical bra may be helpful to moderate fluid accumulation. New implant technologies including dual-port tissue expanders provide a means for surgeons to safely aspirate fluid out of the breast pocket. Additional recommendation within the literature include ensuring the appropriate “polarity” of the ADM to facilitate its incorporation and soaking it prior to implantation to remove proinflammatory additives. Although there is a relatively extensive body of evidence on the use of quilting sutures and fibrin glues in the setting of abdominoplasty and latissimus dorsi donor sites, these strategies have not been rigorously studied in implant-based breast reconstruction.
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