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. 2015 Jun;4(3):270–276. doi: 10.3978/j.issn.2227-684X.2015.01.07

Use of latissimus dorsi muscle onlay patch alternative to acellular dermal matrix in implant-based breast reconstruction

Jeeyeon Lee 1, Youngtae Bae 2,
PMCID: PMC4461708  PMID: 26161312

Abstract

Background

An acellular dermal matrix (ADM) is applied to release the surrounding muscles and prevent dislocation or rippling of the implant. We compared implant-based breast reconstruction using the latissimus dorsi (LD) muscle, referred to as an “LD muscle onlay patch,” with using an ADM.

Method

A total of 56 patients (60 breasts) underwent nipple sparing mastectomy with implant-based breast reconstruction using an ADM or LD muscle onlay patch. Cosmetic outcomes were assessed 4 weeks after chemotherapy or radiotherapy, and statistical analyses were performed.

Results

Mean surgical time and hospital stay were significantly longer in the LD muscle onlay patch group than the ADM group. However, there were no statistically significant differences between groups in postoperative complications. Cosmetic outcomes for breast symmetry and shape were higher in the LD muscle onlay patch group.

Conclusions

Implant-based breast reconstruction with an LD muscle onlay patch would be a feasible alternative to using an ADM.

Keywords: Breast, latissimus dorsi muscle, reconstruction

Introduction

Implant-based breast reconstruction is the most frequently utilized surgical technique. The breast volume can be adjusted based on remained breast tissue and volume of inserted implant. Usually, the implant is inserted underneath the pectoralis muscle. However, a displacement or rippling of the implant can occur, because the chest wall and pectoralis muscle has strong tension which makes limited space between them (1). In addition, the capsular contracture after radiotherapy sometimes may result in respiratory discomfort (2,3).

Acellular dermal matrix (ADM) has been used to cover and support the inferior aspect of the breast pocket, and prevent capsular contracture or dislocation of the implant. Although ADM allowed the reconstructed breast to maintain its natural contour and shape (4-7), it has some complications, such as infection and postoperative seroma (8-14). There are some reports that autologous tissue has been used for full muscle coverage instead of an ADM (15). When implant-based breast reconstruction is performed with a latissimus dorsi (LD) muscle flap, the additional coverage by the LD muscle will thicken the overlying flap which might be positive to the appearance and feeling of the breast.

This study was undertaken to compare immediate implant-based breast reconstruction using a LD muscle flap, which is referred as “LD muscle onlay patch,” and implant-based breast reconstruction using an ADM.

Methods

We reviewed a database of patients with breast tumors between January 2009 and December 2011. Fifty-six patients (60 breasts) underwent implant-based breast reconstruction using either the ADM (n=28) or LD muscle onlay patch (n=32).

All data were collected and analyzed retrospectively, and included clinicopathologic characteristics, volumes of the resected breast and implant, treatment modalities, complications, and cosmetic outcomes. The questionnaire survey for cosmetic outcomes was conducted by patients and physicians after 4 weeks from radiotherapy based on a 4-point scoring system, which included the following items: overall satisfaction, breast symmetry, shape, softness, and tension with movement.

Both groups underwent nipple sparing mastectomy with implant-based breast reconstruction. After the breast tumor was removed with safety margin, the pectoralis major muscle was dissected from the chest wall from the lateral to the medial and inferior margins of the muscle. A triangular window composed of the lateral margins of pectoralis, anterior serratus muscle, and the lateral side of inframammary line was covered with the ADM or LD muscle onlay patch (Figure 1). In the ADM group, the implant was inserted into the breast pocket and the window was covered with ADM (Surgimend®, TEI Biosciences Inc. Boston, MA, USA). And in the LD onlay patch group, the window was enveloped with the LD muscle after an appropriate volume of the implant was positioned. The extent of the patch is decided after considering the volume of the breast prosthesis. Then, anchoring sutures were inserted to fix the muscle and prevent displacement of the implant. Anchoring sutures should be inserted at 1-cm intervals to prevent the escape of the implant and to avoid damaging the vasculature of the LD muscle. These sutures should avoid the vascular structures of the LD muscle, because damage to the vascularity may cause necrosis or stiffness of the flap (Figure 2).

Figure 1.

Figure 1

Implant-based breast reconstruction. (A,C) An acellular dermal matrix (black arrow) and (B,D) the latissimus dorsi muscle (dots) are used to cover the triangular window.

Figure 2.

Figure 2

Transverse views of a completed implant-based breast reconstruction. (A) An acellular dermal matrix (black arrow) is placed between the inferior border of pectoralis muscle and the inframammary line; (B) the latissimus dorsi muscle onlay patch (dot arrow) is fixed with anchoring sutures on the inferior border of the pectoralis muscle and the chest wall at the inframammary line.

Statistical analyses were performed using SPSS ver. 12 (SPSS, Inc., Chicago, Ill, USA). For comparisons of the ADM and LD muscle onlay patch groups, Pearson’s chi-square test, Fisher’s exact test, and the Wilcoxon-Mann-Whitney test were performed. The chi-square and Fisher’s exact tests were applied for unadjusted categorical variables, and the Mann-Whitney test was used for nonparametric categorical variables. Continuous data were described as the mean ± the standard deviation (SD), and P value less than 0.05 was considered statistically significant.

Results

The mean age of the patients was 46 years (range, 24-64 years), and the mean body mass index was 21.8 kg/m2 (range, 16.4-30.6 kg/m2). The mean follow-up period was 35.5 months (range, 18.7-53.5 months), and the mean interval period between surgery and chemotherapy or radiotherapy was 21.3 days (range, 15-32 days).

Clinical characteristics are listed in Table 1; there were statistically significant differences between groups in terms of implant volume (P=0.022), surgical time (P=0.003), and hospital stay (P=0.010). However, the mean volume loss of the breast and incidence of complications were not statistically different between groups.

Table 1. Comparison of patient characteristics between using acellular dermal matrix group and latissimus dorsi muscle onlay patch group.

Characteristics ADM* (n=28) LD muscle onlay patch (n=32) P value
Age (years, SD) 36.8±11.31 45.8±11.99 0.284
Body mass index (kg/m2, SD) 19.0±2.76 23.4±3.43 0.065
Volume loss (g, SD) 153.9±120.29 299.7±116.03 0.275
Implant volume (cc, SD) 194.5±49.50 155.2±74.25 0.022
OP time (minutes, SD) 198.0±86.06 342.5±54.7 0.003
Hospital stay (days, SD) 6.9±1.52 8.7±1.56 0.010
Follow-up period (mo, SD) 36.2±8.48 34.9±8.60 0.244
Interval period (days, SD) 19.9±6.24 27.9±7.58 0.992
Chemotherapy, n (%) 16 (57.1) 25 (78.1) 0.167
Radiotherapy, n (%) 23 (82.1) 31 (96.9) 0.454
Complication, n (%) 4 (14.3) 1 (3.1) 0.175

*, acellular dermal matrix; , latissumus dorsi.

Pathological characteristics were analyzed with regard to tumor size, type, multicentricity, overall stage, microcalcification of the tumor, differentiation of tumor cells, perineural and lymphovascular invasion of tumor cells, and hormone receptor status. No tumor characteristics showed a significant difference between groups (Table 2).

Table 2. Comparison of clinicopathologic characteristics between using acellular dermal matrix group and latissimus dorsi muscle onlay patch group.

Characteristics ADM* (n=28) LD muscle onlay patch (n=32) P value
Mean tumor size (cm, SD) 2.0±1.43 3.8±2.27 0.483
Tumor type, n (%) 0.095
  Atypical ductal hyperplasia 4 (14.3) 0
  Carcinoma in situ 6 (21.4) 7 (21.9)
  Invasive carcinoma 18 (64.3) 25 (78.1)
Multicentricity, n (%) 3 (10.7) 1 (3.1) 0.331
Stage, n (%) 0.673
  0 6 (21.4) 7 (21.9)
  I 3 (10.7) 0
  IIA 7 (25.0) 9 (28.1)
  IIB 6 (21.4) 10 (31.3)
  IIIA 2 (7.1) 2 (6.3)
  IIIB 0 4 (12.5)
Microcalcification on mammography, n (%) 2 (7.1) 3 (9.4) 0.982
Differentiation, n (%) 0.378
  Well 7 (25.0) 3 (9.4)
  Moderately 9 (32.1) 16 (50.0)
  Poorly 2 (7.1) 6 (18.8)
Perineural invasion, n (%) 0.736
  Positive 1 (3.6) 1 (3.1)
  Negative 17 (60.7) 24 (75.0)
Lymphovascular invasion, n (%) 0.637
  Positive 1 (3.6) 3 (9.4)
  Negative 17 (60.7) 22 (68.8)
Estrogen receptor, n (%) 0.754
  Positive 15 (53.6) 21 (65.6)
  Negative 9 (32.1) 11 (34.4)
Progesterone receptor, n (%) 0.126
  Positive 13 (46.4) 15 (46.9)
  Negative 11 (39.3) 17 (53.1)
c-erbB2 protein, n (%) 0.446
  Positive 5 (17.9) 7 (21.9)
  Negative 19 (67.9) 25 (78.1)
Triple negative, n (%) 1 (3.6) 3 (9.4) 0.387

*, acellular dermal matrix; , latissumus dorsi.

The postoperative complications occurred in four out of 28 in the ADM group and one out of 32 in the LD muscle onlay patch group. A severe infection of the ADM occurred in the ADM group. We removed both the cohesive gel implant and ADM immediately, because methicillin-resistant staphylococcus aureus (MRSA) was detected in tissue culture. Other complications were capsular contracture after radiotherapy, inflammation, and seroma of the implant cavity, which were confirmed by breast MRI. In the LD muscle onlay patch group, only one seroma of the implant cavity was detected by breast MRI (Table 3). The patient, who was diagnosed the second degree of capsular contracture in MRI, had no previous surgical history or radiotherapy. This contracture occurred on 4 months after surgery and 3 months after radiotherapy.

Table 3. Comparison of the incidence of postoperative complications between using acellular dermal matrix group and latissimus dorsi muscle onlay patch group.

Postoperative complications, n (%) ADM* (n=28) LD muscle onlay patch (n=32)
Inflammation in cavity 1 (3.6) 0
Seroma in cavity 1 (3.6) 1 (3.1)
Capsular contracture (grade II) 1 (3.6) 0
Severe infection of covering material 1 (3.6) 0

*, acellular dermal matrix; , latissumus dorsi.

The scores of each item for cosmetic outcomes are shown in Table 4 and Figure 3. The LD muscle onlay patch group had a greater degree of satisfactory than the ADM group in terms of breast symmetry (P<0.001) and breast shape (P=0.008). However, in terms of overall satisfaction, breast softness and tension with movement were similar between groups.

Table 4. Comparision of cosmesic outcomes between using acellular dermal matrix group and latissimus dorsi muscle onlay patch group.

ADM* (n=28) (%)
LD muscle onlay patch (n=32) (%)
P value
Excellent Good Fair Poor Excellent Good Fair Poor
Overall satisfaction 9 (32.1) 15 (53.6) 2 (7.1) 2 (7.1) 16 (50.0) 11 (34.4) 5 (15.6) 0 0.429
Breast symmetry 5 (17.9) 14 (50.0) 9 (32.1) 0 20 (62.5) 11 (34.4) 1 (3.1) 0 <0.001
Breast shape 9 (21.1) 13 (46.4) 6 (21.4) 0 16 (50.0) 13 (40.6) 3 (9.4) 0 0.008
Breast softness 7 (25.0) 16 (57.1) 4 (14.3) 1 (3.6) 13 (40.6) 15 (46.9) 3 (9.4) 1 (3.1) 0.217
Tension with movement 17 (60.7) 8 (28.6) 2 (7.1) 1 (3.6) 24 (75.0) 5 (15.6) 3 (9.4) 0 0.450

*, acellular dermal matrix; latissumus dorsi.

Figure 3.

Figure 3

Cosmetic outcomes after implant-based breast reconstruction. (A,C,E) Pre- and (B,D,F) post-operative views after implant-based breast reconstruction with latissimus dorsi muscle onlay patch.

Discussion

Oncoplastic breast surgery has been performed with autologous flaps or artificial implants. In cases of breast reconstruction after mastectomy or nipple sparing mastectomy, implant-based breast reconstruction is primarily performed. Because an excessive movement or displacement of the implant can occur when the implant is put into the breast cavity, the implant should be inserted under the muscle in a fixed position. However, the full muscle coverage for the implant does not only limit the space for the implant but is usually not possible to be achieved, because the pectoralis muscle anatomically does not reach so far down to cover the lower lateral part of the implant. Even with additional intraoperative lifting of the serratus muscle a full coverage in the lower lateral aspect of the breast is hardly to achieve. Thus, breast surgeons have used an ADM to cover and support the lateral and inferior aspects of the cavity, allowing expansion of the space and prevention for displacement of implant (1,7,10,14).

A single stage reconstruction is beneficial regarding postoperative capsule fibrosis then this could also be achieved with an implant only reconstruction straight underneath the skin too, or with a reconstruction with the use of LD muscle flap (3,11,16). Implant-based breast reconstruction with ADM allows a natural breast contour with the formation of a neo-inframammary fold. However, postoperative seroma or infection is the most frequent complication (10). When, a severe infection occurred, the ADM or prosthesis should be removed immediately. In our study, there was one case of methicillin-resistent staphyllococcus aureus infection of the ADM. We removed the ADM and prosthesis immediately and delayed breast reconstruction was planned after chemotherapy and radiotherapy. Although this complication arose before adjuvant treatment in our study, we might expect the higher incidence of infection in patients who received chemotherapy or radiotherapy.

When breast symmetry cannot be achieved with an autologous flap, such as using a transversus rectus abdominis myocutaneous flap, or is impossible because of old age or underlying disease, implant-based breast reconstruction can be planned. However, breast symmetry would not be acceptable only with large volume of implant in ptotic breasts, because the reconstructed breast would be firm and elastic compared to the contralateral breast (17). To obtain high-quality of breast symmetry and shape, breast reconstruction should be performed with an autologous flap and any insufficient breast volume can be filled with the implant. In implant-based breast reconstruction using an LD muscle flap, a triangular window can be covered with a LD muscle flap instead of an ADM. And it is able to reduce the incidence of postoperative infection, even in patients who received chemotherapy or radiotherapy. And because the LD muscle onlay patch is thicker than ADMs, it can also prevent radiotherapy-induced capsular contracture, which tends to occur when the implant is close to the skin (2,15).

In performing breast reconstruction using an LD muscle onlay patch, there are some limitations. Breast reconstruction using an LD muscle needs an additional surgery which takes a relatively long time, and it can cause donor site morbidity (18). And flap necrosis can occur when the anchoring suture to fix as patch type. However, the surgical technique is quite easy and provides excellent cosmetic outcomes (19). In a recent study, we verified that using the LD muscle onlay patch method is not inferior to the ADM method. Although the surgical time and hospital stay for the LD muscle onlay patch group were both significantly longer than that of the ADM group, this method was not harmful to the patients. Additionally, the incidence of postoperative complications was lower in the LD muscle onlay patch group, even if this decrease did not show statistical significance. Furthermore, satisfaction with regard to breast symmetry and shape was significantly higher in the LD muscle onlay patch group.

The surgeons should strive to achieve satisfactory cosmetic outcomes with regard to breast volume, breast symmetry, and breast shape. Implant-based breast reconstruction using a concurrent autologous tissue flap would achieve some of these outcomes. In conclusion, the implant-based breast reconstruction using an LD muscle onlay patch is a feasible surgical technique achieving good cosmetic outcomes as well as fewer postoperative complications compared to the using ADM method.

Acknowledgements

This work was supported by a 2-Year Research Grant of Pusan National University. And the authors thank to Dongkyun Kang, illustrator, for his art work and advice.

Disclosure: The authors declare no conflict of interest.

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