Abstract
Background:
Approximately 250,000 new cases of breast cancer are diagnosed yearly in the U.S. resulting in more postmastectomy breast reconstructions (PMBRs). The acellular dermal matrix (ADM) expander-implant method became popular in the mid-2000s, but newer techniques such as the inferior deepithelialized flap (IDF) has more recently been described. We hypothesize that ADMs and IDFs provide comparable aesthetic outcomes, with no difference in complication rates and operative characteristics.
Methods:
A retrospective, single-institution study was performed between July 1, 2012, and June 30, 2014, examining all PMBR’s (ADM and IDF). Outcomes were categorized as clinical (e.g., complications requiring surgical intervention) or aesthetic.
Results:
A total of 65 patients (41 ADM; 24 IDF; mean age, 53.4 ± 10.7 years) were included, with 101 PMBR’s evaluated (63 ADM and 38 IDF). Patients who underwent IDFs had higher body mass index (32 versus 25; P < 0.01) and higher grades of breast ptosis. Major complication rates were similar between ADM and IDF groups (22% versus 31.5%; P = 0.34). There were no differences in aesthetic outcomes between groups (rater intraclass correlation, 0.92). The average IDF breast reconstruction took nearly 30 minutes longer per reconstructed side (192 minutes versus 166 minutes; P = 0.02), but operative costs were more expensive for the ADM breast reconstruction.
Conclusions:
The IDF procedure took 30 minutes longer for each reconstructed side, without significant differences in complications or aesthetic outcomes between the 2 PMBRs. IDF reconstructions may be more suitable for patients with grade 3 breast ptosis and higher body mass index. Further studies should focus on long-term outcomes and value-based approaches to PMBR.
INTRODUCTION
Breast cancer continues to have a global impact as a major public health issue.1–3 According to the National Breast Cancer Foundation, 1 in 8 women will develop breast cancer during their lifetime.4 Despite equivalent survival outcomes between mastectomy and breast conservation therapy for breast cancer, there has been an increasing trend for mastectomies.5–7
As the number for mastectomies increased, so did the demand for breast reconstruction (BR) operations, including the use of expanders or implants,8 pedicled flaps,9,10 and free flap options.8,11 Implant-based management continues to dominate, accounting for approximately 70% of BRs.12
Acellular dermal matrix (ADM) became popular in the mid-2000s, especially for the coverage of the inferior pole of the implant.13,14 This allows for faster tissue expansion filling time, greater immediate tissue expansion,13,15 and thus facilitates immediate implant-based postmastectomy BR (PMBR).16,17 A more recent technique has been described using an inferior deepithelialized flap (IDF) to cover the lower pole of the implant.18,19 Advantages of such a technique include autologous blood supply, thicker layer of tissue with a more natural consistency, reduced cost, and better tolerance to post-BR radiation.20,21
Common complications for ADM reconstructions include infections, seromas, and mastectomy skin flap necrosis.13,22,23 Among those, infections are most prominent; however, ADM alone is not an independent risk factor for infection.24 Literature regarding complications for dermal autografts remains sparse, with more data needed to better compare the ADM-assisted versus the IDF-based techniques. Aesthetic outcomes are among the most important metrics in BR. Despite this, data comparing aesthetic outcomes between ADM and IDF-assisted BR are lacking. We hypothesized that ADM and IDF provide comparable aesthetic outcomes, with no difference in complication rates and operative characteristics.
METHODS
A retrospective, single-institution study was performed between July 1, 2012, and June 30, 2014, examining all immediate expander BRs using ADM or IDF. Included were all patients who underwent an acellular dermis or IDF immediate PMBR, with or without radiotherapy treatment. Patients who were younger than 18 years of age were excluded. All the patients underwent immediate PMBR with tissue expanders and none with immediate implant-based reconstruction.
Abstracted data included demographics [age, body mass index (BMI), grade of ptosis), potential risk factors for postoperative morbidity (history of tobacco use, diabetes, pre-BR radiation therapy), and operative characteristics (type of operative procedure, laterality, duration, cost).
Primary outcomes were categorized into 2 groups: clinical and aesthetic. Clinical complications requiring surgical intervention postoperatively included hematoma, seroma, partial flap necrosis, tissue expander leakage/exposure, and inframammary fold displacement. Aesthetic outcomes were measured by 5 different variables that included BR volume, contour, placement, scarring, and inframammary fold appearance as described by Nguyen et al.20 The scale described was a 3-point scale with ratings from 0 to 2 with higher scores being more favorable (Table 1). Postoperative photographic data were scored by 2 blinded senior-level general surgery residents after being given explicit examples and instructions using the 3-point scale. None of the reviewers were involved with patient care.
Table 1.
Statistical analysis was performed using the student’s t test for normally distributed continuous variables, Mann-Whitney U test for nonnormally distributed continuous data, and Fisher’s exact test for categorical data. Statistical significance level was set at α = 0.05. SPSS 18 for Windows (IBM, Armonk, N.Y.) was used to perform analyses. Institutional review board approval was granted.
OVERVIEW OF SURGICAL TECHNIQUES
ADM
Our surgeon uses AlloMaxTM (Bard, Davol Inc., Warwick, R.I.) as the surgical biological graft. AlloMaxTM is a sterile, human-derived acellular dermal collagen with elastin fibers (Fig. 1). The ADM procedure consists of using the dermal matrix as an inferior sling for the tissue expander or implant.13,16,25 The inferolateral origin (margin) of the pectoralis major muscles is released and a piece of ADM is sutured into place between the inframammary fold and inferior border of the pectoralis major muscle to create an inferior sling for the tissue expander (Fig. 1A). The suture line extends the length of the ADM and follows the lateral contour of the pectoralis major muscle which re-creates a new inframammary fold and a pocket for the tissue expander or implant. A central pocket is left open where the tissue expander or implant will be inserted through. The tissue expander or implant is then securely placed below the pectoralis muscle superiorly and ADM sling inferiorly before the interface between the pectoralis and leading edge of the acellular dermis is completely closed over the expander (Fig. 1B–2C). Two drains were routinely placed, 1 in the subpectoral space and the other in the suprapectoral space.
IDF
The IDF procedure evolved later than the ADM procedure (Fig. 2). The concept behind this technique is the same as using the ADM; however, instead of using a biological graft, autologous tissue is used to make an inferior sling where the tissue expander or implant will stay. This newer technique utilizes a deepithelialized portion of the infero-lateral dermis as an infero-lateral sling.5,12,21 The first step to the procedure is deepithelializing the inferior portion of the mastectomy flap (Fig. 2B). Once the inferiorly based dermal flap is deepithelialized, the lateral attachments are taken down (Fig. 2C), to allow for a recreation of the inferior dermal sling where the lateral edge is sutured to the lateral mammary fold (Fig. 2D). As a result, the inframammary fold is already intact and a new one does not need to be recreated unlike the ADM procedure. The general dimensions of the inferior sling was patient dependent but ranged from 20 to 38 cm by 6 to 15 cm in this study. The tissue expander is then securely placed below the pectoralis muscle superiorly and autologous inferior dermal sling inferiorly before the interface between the pectoralis, and leading edge of the acellular dermis was completely closed over the expanders (Fig. 2E). SPY angiography was used at the discretion of the operating surgeon when there was concern for ischemic changes but not routinely used for all cases. Drain placement was the same as the ADM procedure.
RESULTS
A total of 65 patients underwent PMBR during the study period. The overall mean age was 53.4 ± 10.7 years. Of these, 41 patients underwent ADM-based procedure and 24 patients underwent IDF-based BR. Within the patient sample, there were 101 individual BRs (1.6 per patient). Looking at the 2 study subsets, there were 63 ADM-based BRs and 38 IDF-based reconstructions.
Except for BMI and grades of ptosis, the 2 groups were similar in all other aspects of general descriptive characteristics (Table 2). Patients who underwent IDFs had significantly higher BMI (32.2 versus 25.6; P < 0.01) and the majority of these patients had grade 3 breast ptosis (68%; Fig. 3). On the other hand, the majority of the patients who underwent the ADM procedure had grade 1 breast ptosis (50.8%). There were no significant differences between the groups in terms of tobacco use, diabetes, and pre-BR radiation therapy (Table 2). Majority of operative characteristics examined were similar between the 2 groups, including laterality. Self pay costs for the procedures differed significantly (Table 3). Average costs for a 192 minute and 166 minute procedures at our main campus are $8,105 and $6,745 respectively, which includes facility, anesthesia, and surgeon fees. However, the cost for an 8 × 16 cm piece of AlloMax is $3,411, resulting in the ADM BR procedure cost to be approximately $10,156. Although, the IDF cost was less than the ADM procedure, the average IDF procedure took nearly 30 minutes longer per reconstructed side (192 ± 45 minutes) than an average ADM procedure (166 ± 36 minutes; P = 0.02). Procedure times reflect the total operation time from start of the mastectomy procedures to the completion of the reconstruction.
Table 2.
Table 3.
Overall, major complication rates were similar between ADM and IDF groups (22% versus 31%; P = 0.34). Clinical complications requiring subsequent surgical intervention included hematoma, seroma, partial flap necrosis, tissue expander leakage/exposure, and inframammary fold. Outcomes for these categories are shown in Table 4. In addition, there were no cases of poor adherence of ADM or tissue necrosis of the IDF flap appreciated at the time of implant exchanges.
Table 4.
Finally, there were no significant differences in the aesthetic outcomes between the groups rated among our 2 reviewers (Figs. 4, 5). The 5 different aesthetic outcomes measured included BR volume, contour, placement, scarring, and inframammary fold appearance. Details regarding aesthetic outcomes are presented in Table 5. The intraclass correlation was calculated to be 0.92 (95% confidence interval, 0.89–0.94), indicating good rater agreement.
Table 5.
DISCUSSION
The demand for PMBR continues to increase for a number of reasons, including the large number of newly diagnosed cases of breast cancer and patient preference for mastectomy over breast conservation.1–3,5–7 BR options vary based on several factors, including breast size, BMI, and type of skin sparing mastectomies (e.g., categories I–IV).26
Of interest, the only parameter that reached statistical significance between the ADM and IDF reconstructed groups was BMI (32 versus 25, respectively). In addition, of importance, patients who underwent IDF reconstructed procedures were more likely to have grade 3 breast ptosis. Although the above finding is not surprising, it is important to note that BMI may play a role in breast cancer risk profile (both primary and recurrent).27,28 In smaller, less ptotic breasts and patients were lower BMIs, the IDF may not be feasible as there would not be sufficient tissue to create a dermal sling used to cover the tissue expander or implant.20,21
Operative characteristics and laterality were similar for the 2 groups. More specifically, the average IDF procedure took nearly 30 minutes longer per each BR than an average ADM procedure. Based on our operative experience, we attribute this increase in operative time to the deepithelialization process of the dermal flap as an extra step is necessary to create the inferior sling to harbor the tissue expander or implant. On the other hand, with ADM, depending on the product being used, cadaveric versus acellular human-derived tissue is readily available to create the inferior pocket. In terms of self pay costs, the ADM BR procedure was more expensive because of the use of AllomaxTM, despite the IDF procedure being a longer procedure. Granted, most of these procedures will be covered by insurance companies, but self pay costs give us a basis without the hyperinflation of charges that results when insurance companies are involved.
A recent meta-analysis showed that infections, hematomas, and seromas may occur more frequently in ADM-based BRs.29 However, our study suggests that there is no difference in complications between the 2 groups; however, our sample size is relatively small, and definitive conclusions cannot be made. In theory, autologous tissue should be less immunogenic and more compatible, suggesting perhaps that there should be a lower complication especially with regard to infection rates.30 However, we speculated that the increased technical skill and longer operative time required for the deepithelialization process of the inferior flap in the IDF procedure mitigated the differences in complication rates between the 2 procedures.
In addition to complication rates, aesthetics also have a major impact on BR outcomes.31 The optimal result in breast cancer is predicated on elimination of the malignancy and the achievement of satisfactory aesthetic outcome, including the recreation of a natural breast appearance.32 Aesthetic outcomes are difficult to measure objectively due to their inherent subjectivity. Past studies have used overall outcome of reconstruction as an aesthetic endpoint for ADM-assisted closures but lacked quantitative measures.33,34 In our study, the appearance of PMBR was subjectively measured for both groups by third-party reviewers and not the patients’ themselves. Any definitive conclusion about aesthetic outcomes cannot be made, as our scale lacks objective measures and patient satisfaction measures. Overall findings of this study suggest that both options provide similar and adequate aesthetic outcomes. However, this may differ over longer term follow-up, and a more complete study with the subjective opinion of the patient’s overall satisfaction may provide more insight in this matter. One study used patient-reported satisfaction measures and examined aesthetic outcomes between prosthetic and autogenous reconstruction.35 This study studied short-term (< 5 years), intermediate (6–8 years) and long-term (> 8 years) patient-reported aesthetic outcomes and interestingly found that satisfaction was similar between prosthetic and autogenous aesthetic outcomes during short-term follow-up.35 However, in the long-term follow-up group, autogenous tissue reconstruction patients were significantly more satisfied with their aesthetic outcomes.35
Limitations to this study include the inherent retrospective nature of the study. In addition, it is a relatively small study conducted in a single institution by a single surgeon, and an increase in sample size plus a multicenter study may demonstrate a statistical difference in the complication rates between the 2 groups. A power calculation was performed that showed that our sample size would need to be approximately 364 patients to potentially determine a difference between the 2 groups, reiterating a larger study may be of benefit. Aesthetic outcome postoperative grading measures among the patients were performed over a period of 3–32 months. Granted the patients who required additional operations secondary to complication rates had longer follow ups, a more standardized methodology for aesthetic outcome measurements at set intervals should be considered for future research. In addition, the aesthetic outcomes scale used in this study was a subjective one, and physical, photographic, 3-dimensional imaging scales, and patient satisfaction scales should be considered. As well, a long-term follow-up study greater than 5 years after the reconstructive procedures with regard to aesthetic outcomes may be of benefit including patient satisfaction. Future directions should also evaluate capsular contracture and whether or not the use of ADM decreased the rate of capsular contracture, when compared with IDF.
CONCLUSIONS
Our study suggests that there are no significant differences in major complications or aesthetic outcomes between the ADM and the IDF approach to immediate expander BR, but no definitive conclusions can be made, given that our sample size was relatively small. Although these preliminary results are favorable, data from additional prospective, randomized multicenter trials would be beneficial. However, our data suggest that IDF may be more suitable for patients with higher grades of breast ptosis (2 or 3) and higher BMIs. On the other hand, ADM may be more appropriate for patients with less available autologous tissue for BR. On average, the ADM procedure took significantly less time for each reconstructed side, but costs were more expensive secondary to the use of the biological graft. As a result, the duration in the operating room must be balanced against the cost of biological graft. The results from this study are preliminary, and further studies are warranted in this area, focusing on complication rates, patient satisfication, long-term outcomes and value-based approaches to BR.
ACKNOWLEDGMENTS
We would like to thank Crystal Corredera for facilitation of patient information.
Footnotes
Presented at the 11th Annual Academic Surgical Congress, February 2–4, 2016, Jacksonville, Fla.
Disclosure: The authors have no financial interest to declare in relation to the content of this article. The Article Processing Charge was paid for by the authors.
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