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      Management of the Exposed and/or Infected Breast Prosthesis: A Proposal for a Standardized Approach

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          Abstract

          BACKGROUND Implant infection and exposure are the main complications related to breast reconstructive and aesthetic surgery. 1,2 In the past, treatment was immediate device removal with implant repositioning no earlier than 6 months. Recently, numerous successful attempts of device salvage have been reported. 3,4 There is still disagreement about the indications and the procedures. 5 We propose the protocol adopted at Bellaria Hospital of Bologna for device salvage. METHOD Complications were classified as follows: local implant infection responsive to oral antibiotics, persistent infection (more than 7 days), and partial exposure with or without infection. The severity of infection was an important factor in deciding whether or not to attempt to salvage. Oral antibiotics (amoxicillin + clavulanate and trimetoprim + sulfametoxazol/clindamycin) were given in case of initial infection for 7 days. In case of persistent infection or in case of partial implant exposure, intravenous antibiotics (piperacillin + tazobactam/ampicillin + sulbactam and vancomycin/teicoplanin) were administered for at least 10 days and immediate surgical operation was performed. Operative steps included wound cultures collection; implant removal; pulse lavage; capsulectomy; and device exchange for the same type of implant in augmentation mammoplasty or for a smaller and less projected prosthesis in reconstructive surgery, primary closure, or capsular flaps in case of exposure. Inflammatory markers were evaluated at admission and in postoperative days 1, 3, 5, and 7. Targeted IV antibiotics were continued after surgery. RESULTS We report 2 cases of successful device salvage following this protocol. The first case, a 54-year-old woman, underwent right mastectomy and prosthetic breast reconstruction; 3 years after surgery, she presented with implant infection. The second case, a 32-year-old woman, underwent periareolar augmentation mammoplasty. After 2 years, she presented with a right implant exposure (Figs. 1, 2). Both patients were treated following our protocol (Fig. 3). No complications were observed after 6 and 12 months, respectively. Fig. 1. Implant exposure 2 years after periareolar augmentation mammoplasty. Fig. 2. Details of the implant exposure. Fig. 3. Result 12 months after the application of our protocol. CONCLUSION In our experience, device salvage is a possible option in selected cases, adopting a well-defined approach. Our purpose is to apply this protocol to a further prospective study, expanding the cohort of patients and providing long-term results of this method.

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          Infection following implant-based reconstruction in 1952 consecutive breast reconstructions: salvage rates and predictors of success.

          Few studies address salvage rates for infection in implant-based breast reconstruction. An understanding of success rates and clinical predictors of failure may help guide management.
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            The infected or exposed breast implant: management and treatment strategies.

            Among the potential complications associated with the use of breast implants are the risks of periprosthetic infection and device extrusion. There is little published information about the effective management of these situations. Conservative recommendations include antibiotic therapy and removal of the implant until resolution of the infection or until the wound has healed. A retrospective review identified patients with periprosthetic infection or threatened or actual device exposure treated by the senior author. Twenty-four patients encompassing 26 affected prostheses were available for review and were classified into seven groups based on initial presentation as follows: group 1, mild infection (n = 8); group 2, severe infection (n = 4); group 3, threatened exposure without infection (n = 3); group 4, threatened exposure with mild infection (n = 3); group 5, threatened exposure with severe infection (n = 1); group 6, actual exposure without clinical infection (n = 5); and group 7, actual exposure with infection (n = 2). To salvage the prosthesis in these patients, various treatment strategies were utilized. All patients with a suspected infection or device exposure were started immediately on appropriate antibiotic therapy (oral antibiotics for mild infections and parenteral antibiotics for severe infections). Salvage methods included one or more of the following: antibiotic therapy, débridement, curettage, pulse lavage, capsulectomy, device exchange, primary closure, and/or flap coverage. Twenty (76.9 percent) of 26 threatened implants with infection or threatened or actual prosthesis exposure were salvaged after aggressive intervention. The presence of severe infection adversely affected the salvage rate in this series. A statistically significant difference exists among those patients without infection or with mild infection only (groups 1, 3, 4, and 6); successful salvage was achieved in 18 (94.7 percent) of 19 patients, whereas only two of seven of those implants with severe infection (groups 2, 5, and 7) were salvaged (p = 0.0017). Ten (90.9 percent) of 11 devices with threatened or actual exposure, not complicated by severe infection (groups 3, 4, and 6), were salvaged. Several treatment strategies were developed for periprosthetic infection and for threatened or actual implant exposure. Patients with infection were placed on oral or intravenous antibiotics; those who responded completely required no further treatment. For persistent mild infection or threatened or actual exposure, operative intervention was required, including some or all of the following steps: implant removal, pocket curettage, partial or total capsulectomy, débridement, site change, placement of a new implant, and/or flap coverage; the menu of options varied with the precise circumstances. No immediate salvage was attempted in five cases, due to either severe infection, nonresponding infection with gross purulence, marginal tissues, or lack of options for healthy tissue coverage. Based on the authors' experience, salvage attempts for periprosthetic infection and prosthesis exposure may be successful, except in cases of overwhelming infection or deficient soft-tissue coverage. Although an attempt at implant salvage may be offered to a patient, device removal and delayed reinsertion will always remain a more conservative and predictable option.
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              Management of the infected or exposed breast prosthesis: a single surgeon's 15-year experience with 69 patients.

              In 2004, the senior author (S.L.S.) published an algorithm for the management of breast device infection and/or exposure. The purpose of this study was to build on the authors' prior experience by expanding the cohort of patients and to identify risk factors for failed breast device salvage and recurrent infection/exposure. A retrospective study was carried out on a single plastic surgeon's experience between 1993 and 2008. Patients with infected and/or exposed breast devices were classified into one of seven groups and salvage rates were calculated. Patient demographics and wound culture pathogens were analyzed as possible risk factors for device loss and recurrent infection/exposure. Over a 15-year period, the senior author managed 69 patients with 87 events of breast device infection and/or exposure. The overall salvage rate was 64.4 percent. Failed device salvage was significantly associated with the presence of atypical pathogens, such as gram-negative rods, methicillin-resistant Staphylococcus aureus, and Candida parapsilosis. Recurrent device infection and/or exposure was significantly associated with a history of radiotherapy or the presence of S. aureus on wound culture. Salvage of the infected and/or exposed breast prosthesis remains a challenging yet viable option for a subset of patients. Relative contraindications include atypical pathogens on wound culture, such as gram-negative rods, methicillin-resistant S. aureus, and C. parapsilosis. Patients with a prior device infection and/or exposure and a history of either radiotherapy or S. aureus on wound culture should be monitored closely for signs of recurrence and managed cautiously in the setting of elective breast surgery.
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                Author and article information

                Journal
                Plast Reconstr Surg Glob Open
                Plast Reconstr Surg Glob Open
                GOX
                Plastic and Reconstructive Surgery Global Open
                Wolters Kluwer Health
                2169-7574
                March 2016
                18 March 2016
                : 4
                : 3
                : e658
                Affiliations
                From the [* ]Plastic Surgery Department, School of Plastic and Reconstructive Surgery, S.Orsola–Malpighi Hospital, University of Bologna, Bologna, Italy; and []Plastic Surgery Department, Bellaria Hospital, Bologna, Italy.
                Author notes
                Elisa Antoniazzi, MD, Plastic Surgery Department, School of Plastic and Reconstructive Surgery, S.Orsola–Malpighi Hospital, University of Bologna, via Massarenti 9, Bologna 40138, Italy, E-mail: eliantoniazzi@ 123456hotmail.it
                Daniele Fasano, MD, Plastic Surgery Department, Bellaria Hospital, via Brugnoli 5, Bologna, 40122, Italy, E-mail: daniele.fasano@ 123456fastwebnet.it
                Article
                00028
                10.1097/GOX.0000000000000637
                4874302
                27257588
                06b1296a-5c93-4818-bf44-8957918077a6
                Copyright © 2016 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. All rights reserved.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.

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