Mamoplastia secundária com ressecção em monobloco e neoposicionamento do implante no espaço retropeitoral parcial / Secondary mammaplasty with monobloc resection and implant repositioning in the partial retropectoral pocket

Introdução: As cirurgias de aumento de mamas com implantes de silicone estão entre os procedimentos de cirurgia plástica mais realizados. O objetivo desse estudo é avaliar os casos de pacientes com prótese de silicone, submetidas à mamoplastia secundária, apresentando uma alternativa de abordagem com ressecção em monobloco do tecido mamário, cápsula fibrosa e prótese de silicone; e o neoposicionamento do implante em loja retromuscular peitoral parcial. Métodos: Foram analisados 24 casos de mamoplastia secundária com neoposicionamento da prótese, apresentando os motivos da indicação da cirurgia e o detalhamento da abordagem cirúrgica para maior facilidade na execução do procedimento e a obtenção de resultados mais satisfatórios. Resultados: Todos os casos operados apresentavam alterações no exame físico das mamas, como: ptose mamária contratura capsular, posicionamento inadequado dos implantes e assimetrias mamárias. Nos casos estudados, as próteses com revestimento de poliuretano e sua completa adesão à cápsula fibrosa permitiram a ressecção mais prática, mesmo com variáveis graus de contratura capsular. As cápsulas fibrosas que envolviam implantes texturizados tinham características mais finas e a instabilidade das próteses, pela presença de seroma residual ou pelo excessivo tamanho da loja da prótese, desencadearam maior dificuldade na ressecção. Conclusão: A realização de mamoplastia secundária com troca de prótese, empregando a ressecção em monobloco e neoposicionamento do implante no espaço retromuscular peitoral parcial com suturas do músculo ao tecido mamário, oferece uma alternativa para otimizar o procedimento, maior estabilidade do músculo até completa cicatrização e a formação de nova cápsula fibrosa.

Introduction: Breast augmentation with silicone implants is one of the most common plastic surgery procedures. The objective of this study was to evaluate patients with previous silicone implantations undergoing secondary mammaplasty, presenting an alternative approach with en block resection of breast tissue, fibrous capsule, and silicone implant, followed by implant repositioning in the partial retropectoral pocket. Methods: This study included 24 cases of secondary mammaplasty with implant repositioning. It presents the indications for surgery and details the surgical approach for easier procedures and more satisfactory results. Results: All the included cases presented breast changes on physical examination, such as breast ptosis, capsular contracture, improper implant position, and breast asymmetry. In the studied cases, the use of polyurethane-coated implants and their complete adherence to the fibrous capsule resulted in a more practical resection even with varying degrees of capsular contracture. Fibrous capsules of textured implants were thinner, and implant instability due to the presence of residual seroma or pockets bigger than necessary resulted in more difficult resection. Conclusion: Secondary mammaplasty with en bloc resection, along with implant replacement and repositioning in the partial retropectoral pocket with sutures involving muscle and breast tissue is an alternative to optimize the procedure, providing greater muscle stability until complete healing and new fibrous capsule formation.

Implante submuscular em duplo bolso para mastopexias de aumento / Submuscular implant in double pocket for augmentation mastopexy

Introdução: A utilização de implantes mamários vem aumentando. O posicionamento do implante na literatura é relatado como subglandular, subfascial, submuscular total e parcial, cada qual com suas indicações, limitações e complicações. Métodos: Este trabalho mostra uma manobra para cobertura do implante e sua sustentação utilizando dois retalhos musculares. Entre novembro de 2009 e abril de 2012, foram analisados 80 casos de pacientes submetidas à inclusão de implantes em posição submuscular em duplo bolso, independentemente da via de acesso, do grau de flacidez e ptose. Resultados: A versatilidade desta manobra permite que seja utilizada em uma ampla variedade de mamas, desde aumento sem flacidez a mamopexia com implante, podendo ser realizada por via periareolar, inframamária ou aberta. Foi utilizada em cirurgias primárias e secundárias, com ou sem uso de retalho de tecido mamário e retirada de pele. Conclusões: A cobertura do implante com o músculo peitoral pela técnica de duplo bolso demonstrou ótimos resultados, com baixo índice de complicações e reintervenções. Esta técnica está sendo utilizada em uma maior casuística e um seguimento mais longo tem sido feito para confirmar os resultados obtidos até o momento.

Introduction: The use of implants is steadily increasing. Reports have been published of implants in the subglandular, subfascial, total, and partial submuscular positions each with its indications, limitations, and complications. Methods: This study presents a technique to cover the implant and support it using two muscle flaps. Between November 2009 and April 2012, 80 patients who submitted to inclusion of implants in the submuscular position in double pocket were analyzed, regardless of the access route, the degree of flaccidity, and ptosis. Results: The versatility of this maneuver allows it to be used in a wide variety of breasts, from breast augmentation without flaccidity to mastopexy with implant, and may be carried out via the periareolar, inframammary, or open access routes. It was used in primary and secondary surgeries, with or without the use of breast tissue flap and removal of skin. Conclusions: The coverage of the implant with the pectoral muscle by the double pocket technique displayed excellent results, with a low rate of complications and reinterventions. This technique is being studied in a larger sample with a longer follow-up to confirm the results obtained so far.

Huge Abscess due to Mycobacterium Abscessus Infection after Breast Augmentation

Periprosthetic capsular contracture, implant rupture, and deflation are well-known delayed complications of augmentation mammaplasty. However, infection remains the most common cause of reoperation after breast implant surgery. We report the case of a nontuberculous mycobacterial infection with huge abscess formation after augmentation mammaplasty. A 29-year-old woman visited our clinic with enlarged breasts after undergoing breast augmentation at a local clinic 4 years ago. She had no pain and tenderness, except some hardness around the breast margin. Nine months after surgery, her breasts began to grow larger, but showed no other typical symptoms, which led the patient to neglect the enlargement. After exploring through an inframammary approach, a large amount of serous fluid leaked out on both sides and we identified a huge abscess in a pocket localized in the submuscular plane. During exploration, the infected implants, which contained a pus-like fluid with a foul odor, were completely drained. The specimen culture revealed growth of Mycobacterium abscessus, which is a rare cause of infections after breast augmentation. While the overall incidence of mycobacterial infections after breast augmentation is low, our case demonstrates that huge abscess and granuloma formation should be considered as a potential complication of breast surgery.

Treatment of Capsular Contracture after Breast Augmentation with Serial Fat Grafting and Implantation

BACKGROUND: Capsular contracture is the most common complication after breast augmentation using implants. In case of severe capsular contracture, surgical correction is inevitable. We introduce a treatment for severe capsular contracture with serial fat grafting before augmentation using implants. METHODS: In severe cases of capsular contracture, we removed the implants and performed partial capsulectomy. We harvested fat from the flanks or thighs using liposuction. The first fat graft was performed in the subdermal, subcutaneous, and subglandular layers of the breast. The harvested fat was frozen and stored. One month after implant removal and the first graft, a second fat graft was performed. One month later, a third fat graft was performed. Six months after implant removal, we augmented the breasts with implants. RESULTS: The cases of severe breast contracture were treated without any complications. The volume and contour of the breasts were satisfactory. CONCLUSIONS: After implant removal in cases of severe capsular contracture, breast augmentation may be needed. Serial fat grafting before augmentation using implants prevents scarring of the breast envelope and provides sufficient volume with a secure breast envelope.

Contracted Nose after Silicone Implantation: A New Classification System and Treatment Algorithm

BACKGROUND: Silicone implants are frequently used in augmentation rhinoplasty in Asians. A common complication of silicone augmentation rhinoplasty is capsular contracture. This is similar to the capsular contracture after augmentation mammoplasty, but a classification for secondary contracture after augmentation rhinoplasty with silicone implants has not yet been established, and treatment algorithms by grade or severity have yet to be developed. METHODS: Photographs of 695 patients who underwent augmentation rhinoplasty with a silicone implant from May 2001 to May 2015 were analyzed. The mean observation period was 11.4 months. Of the patients, 81 were male and 614 were female, with a mean age of 35.9 years. Grades were assigned according to postoperative appearance. Grade I was a natural appearance, as if an implant had not been inserted. Grade II was an unnatural lateral margin of the implant. Clearly identifiable implant deviation was classified as grade III, and short nose deformation was grade IV. RESULTS: Grade I outcomes were found in 498 patients (71.7%), grade II outcomes in 101 (14.5%), grade III outcomes in 75 (10.8%), and grade IV outcomes in 21 patients (3.0%). Revision surgery was indicated for the 13.8% of all patients who had grade III or IV outcomes. CONCLUSIONS: It is important to clinically classify the deformations due to secondary contracture after surgery and to establish treatment algorithms to improve scientific communication among rhinoplasty surgeons. In this study, we suggest guidelines for the clinical classification of secondary capsular contracture after augmentation rhinoplasty, and also propose a treatment algorithm.

Histological evaluation of capsules formed by silicon implants coated with polyurethane foam and with a textured surface in rats

ABSTRACT PURPOSE: To assess the capsules formed by silicone implants coated with polyurethane foam and with a textured surface. METHODS: Sixty-four Wistar albinus rats were divided into two groups of 32 each using polyurethane foam and textured surface. The capsules around the implants were analyzed for 30, 50, 70 and 90 days. Were analyzed the following parameters: foreign body reaction, granulation tissue, presence of myofibroblasts, neoangiogenesis, presence of synovial metaplasia, capsular thickness, total area and collagen percentage of type I and III, in capsules formed around silicone implants in both groups. RESULTS: The foreign body reaction was only present in the four polyurethane subgroups. The formation of granulation tissue and the presence of myofibroblasts were higher in the four polyurethane subgroups. Regarding to neoangiogenesis and synovial metaplasia, there was no statistical difference between the groups. Polyurethane group presented (all subgroups) a greater capsule thickness, a smaller total area and collagen percentage of type I and a higher percentage area of type III, with statistical difference. CONCLUSION: The use of polyurethane-coated implants should be stimulated by the long-term results in a more stable capsule and a lower incidence of capsular contracture, despite developing a more intense and delayed inflammatory reaction in relation to implants with textured surface.

Implantes mamarios, eventos adversos y complicaciones poco frecuentes: hallazgos por mamografía, ecografía y resonancia magnética / Breast Implants, Adverse Events and Rare Complications: Findings by Mammography, US and MR Imaging

Introducción: En la actualidad, la mamoplastia de aumento con implantes es un procedimiento cada vez más común, con fines exclusivamente cosméticos o reconstructivos después de una mastectomía. Existen complicaciones locales ampliamente conocidas, como la ruptura y contracturas capsulares, pero también se le han atribuido otras complicaciones menos frecuentes, como el linfoma anaplásico y el síndrome autoinmune/inflamatorio inducido por adyuvantes (ASIA). Objetivo: Revisar las características por imagen de las complicaciones frecuentes e infrecuentes asociadas al aumento mamario con prótesis. Metodología: Recolección retrospectiva de casos con complicaciones relacionadas con implantes mamarios; revisión y edición de las diferentes modalidades de imágenes en pacientes de la clínica Fundación Valle del Lili de Cali durante los dos últimos años. Resultados: Es frecuente encontrar cambios postquirúrgicos por mamoplastia de aumento con implantes. Aunque la mamografía tiene un papel limitado en la valoración de las complicaciones del implante, continúa siendo la herramienta de tamizaje de cáncer en la mama aumentada. La ecografía es un instrumento muy útil y costo-efectivo en la evaluación de los implantes. La RM con secuencias de silicona es la modalidad con más alta sensibilidad y especificidad si se quiere valorar la integridad del implante y el tejido mamario en su conjunto.

Introduction: At present, breast augmentation with implants is an increasingly common procedure, be it solely for cosmetic reasons or for reconstructive purposes after mastectomy. There are widely known local complications associated with this intervention, such as implant rupture and encapsulation, but there are other less common complications too, such as anaplastic lymphoma and autoimmune/inflammatory syndrome induced by adjuvants (ASIA). Objective: To review the imaging characteristics of frequent and infrequent complications associated with breast augmentation with implants. Methodology: Cases of different complications were retrospectively collected, in order to review mammography, ultrasound, CT and MRI images of patients with such complications at the Fundación Valle del Lili Clinic (Cali, Colombia) over the past two years. Conclusions: It is common to find post-surgical changes due to breast augmentation with implants. The study concludes that although mammography has a limited role in the assessment of implant complications, it remains the main screening tool for cancer in augmented breasts. Ultrasound is a very useful and cost-effective tool in evaluating implants. MRI with silicone sequences has the highest sensitivity and specificity when assessing the integrity of the implant and breast tissue as a whole. Key words (MeSH) Breast implants Implant capsular contracture Seroma Adjuvants, immunologic

Comparação entre implantes anatômicos e redondos por via periareolar em aumentos mamários primários / Comparison of anatomic and round implants using periareolar access in primary breast augmentation

INTRODUÇÃO: Aumentos mamários exigem planejamento com critérios objetivos e rigorosos, que foram padronizados pelo sistema High Five, de Tebbetts. Existe um grande número de combinações possíveis, entre via de acesso, plano e tipo de implante, o que permite proporcionar o melhor resultado para cada paciente. MÉTODO: 100 pacientes operadas, 30 com implantes anatômicos e 70 com redondos, por via retromuscular ou subglandular, com a realização de roundblock ou não. Todos os casos foram operados pela via periareolar. A avaliação pré-operatória foi realizada conforme a sistematização High Five. RESULTADOS: Roundblock foi mais utilizado no grupo de implantes anatômicos, representando 43% da amostra neste caso. O plano subglandular foi o mais utilizado, representando 76,6% da amostra total. Com relação ao implante anatômico, 86,7% dos implantes foram colocados no plano subglandular. Dos anatômicos, 71,4% foram colocados no plano subglandular. Ocorreram quatro casos de contratura capsular graus III e IV, mais comum com o uso de implante redondo. O índice de rotação do implante anatômico foi de 10%, com três casos no total. CONCLUSÃO: Ocorreu baixo índice de complicações, em conformidade com a incidência da literatura. O acesso periareolar proporcionou bons resultados em todos os casos. O paciente deve ser informado sobre a possibilidade da rotação do implante anatômico.

INTRODUCTION: Breast augmentation requires planning with objective and rigorous criteria, which were standardized by the High Five system of Tebbetts. There are a many possible combinations based on access route, implant plane, and type of implant, enabling the best outcome for each patient. METHOD: Of 100 patients studied, 30 received anatomic implants and 70 received round implants in the retromuscular or subglandular position, with or without round block technique. All cases used periareolar access. Preoperative evaluation was performed according to the High Five system. RESULTS: The round block technique was used more often with anatomic implants (43%). The subglandular plane was most commonly used (76.6%). Of 30 anatomic implants, 86.7% were placed in the subglandular plane. Of 70 round implants, 71.4% were placed in the subglandular plane. There were 4 cases of grade III and IV capsular contracture, which is more common with the use of round implants. The rate of rotation among anatomic implants was 10%, with 3 cases. CONCLUSION: There was a low complication rate, in accordance with published data. Periareolar access provided good results in all cases. The patient should be informed about the possibility of rotation with use of anatomic implants.

Effect of propranolol on capsular reaction around silicone implants in guinea pigs

PURPOSE: To evaluate the effect of propranolol on capsular architecture around silicone implants by measuring the inflammation, capsular thickness, and collagen fiber density, using a guinea pig experimental model. METHODS: Thirty six adult male guinea pigs randomly divided into two groups (n=18) were used. Each one received a silicone implant with textured-surface. The capsular tissue around implants from untreated or treated animals with the beta-adrenoceptor antagonist propranolol (10 mg/kg, dissolved in daily water) were analyzed for inflammation by histological scoring, capsular thickness by computerized histometry, and collagen fibers type I and Type III density by picrosirius polarization at different time points (7, 14 or 21 days after silicone implantation). RESULTS: Propranolol treatment reduced inflammation and impaired capsular thickness and delayed collagen maturation around the textured implant. CONCLUSION: Propranolol reduces the risk of developing capsular contracture around silicone implants with textured surface. .

Opções a capsulotomia e capsulectomia no tratamento da contratura capsular: existem alternativas medicamentosas ao tratamento cirúrgico? Revisão de literatura / Options for capsulotomy and capsulectomy in the treatment of capsular contracture: are there clinical treatment alternatives to surgery? A literature review

INTRODUÇÃO: A contratura capsular é uma das principais complicações em cirurgias envolvendo implantes mamários. A classificação mais usada para avaliar o grau de contratura é a de Baker, que a divide em graus I, II, III e IV, sendo as de grau III e IV consideradas significativas. Apesar de existirem diversas teorias, a etiologia da contratura capsular permanece incerta. O tratamento convencional para os casos de contratura é a abordagem cirúrgica com realização de capsulotomia ou capsulectomia. Estes procedimentos, no entanto, não estão isentos de morbidades, com complicações como deiscências, hematomas, seromas, pneumotórax, assimetrias e recidiva da contratura. Este estudo faz uma revisão sobre as alternativas ao tratamento cirúrgico convencional, descritas na literatura. MÉTODOS: Foi realizada pesquisa nas bibliotecas da Pubmed e da Cochrane, utilizando-se os termos: 'capsular contracture', 'capsular contracture treatment' e 'capsular contracture breast treatment'. Foram identificados 991 artigos e selecionados os que discutiam opções medicamentosas para o tratamento de contratura, diferentes de capsulectomia e capsulotomia. RESULTADOS: Foram encontrados vårios estudos utilizando drogas com o fim de reduzir a contratura capsular, das quais o Zafirlucaste é apresentado em maior número de trabalhos. CONCLUSÃO: Dentre as várias drogas utilizadas, o Zafirlucaste apresentou boa eficácia, com baixos índices de complicação; a Triancinolona parece ser também uma boa opção, no entanto precisa de profissional habilitado para realizar as infiltrações. As demais drogas necessitam de maiores estudos.

INTRODUCTION: Capsular contracture is among the main complications of surgeries involving breast implants. The most commonly used classification to assess the degree of contracture is the Baker grading system, which divides contractures into grades I, II, III, and IV. Of these, grade III and IV contractures are considered significant. Although several causes have been postulated, the etiology of capsular contracture remains uncertain. Conventional treatment for contracture is based on a surgical approach, specifically capsulotomy or capsulectomy. These procedures, however, are not exempt from morbidity, and patients may develop complications such as dehiscence, hematoma, seroma, pneumothorax, asymmetry, and contracture recurrence. This study provides a review of alternatives to conventional surgery described in the literature. METHODS: We researched the PubMed and Cochrane Library databases using the following keywords: "capsular contracture", "capsular contracture treatment", and "capsular contracture breast treatment". We identified 991 articles from which we selected those discussing medication options for contracture treatment other than capsulectomy and capsulotomy. RESULTS: We identified several studies in which drugs, most commonly zafirlukast, were used to reduce capsular contracture. CONCLUSION: Among the various reported drugs, zafirlukast exhibited good efficacy and a low rate of complication. Triamcinolone also appears to be a good option, although professional assistance would be needed for drug administration via infiltration. The other drugs described would require further investigation.

The Preventive Effect of Topical Zafirlukast Instillation for Peri-Implant Capsule Formation in Rabbits

BACKGROUND: Capsular contracture is the most troublesome complication in breast implant surgery. Although capsule formation can be seen as a normal reaction to a foreign body, it can induce pain, hardness, deformity, and other pathologic problems. Surgical intervention is required in severe cases, but even surgery cannot guarantee a successful outcome without recurrence. This experimental study confirms that single topical administration of leukotriene antagonist zafirlukast (Accolate, Astrazeneca) reduces peri-implant capsule formation and prevents capsular contracture. METHODS: Twelve smooth-surfaced cohesive gel implants were implanted in New Zealand White rabbits. These miniature implants were designed to be identical to currently used products for breast augmentation. The rabbits were divided into 2 groups. In the experimental group (n=6), the implant and normal saline with zafirlukast were inserted in the submuscular pocket. In the control group (n=6), the implant and normal saline alone were used. Two months later, the implants with peri-implant capsule were excised. We evaluated capsule thickness and collagen pattern and performed immunohistochemical staining of myofibroblasts, transforming growth factor (TGF)-beta1, 2. RESULTS: The thickness of the capsules in the experimental group was reduced in both dorsal and ventral directions. The collagen pattern showed parallel alignment with low density, and the number of myofibroblasts as well as the amounts of TGF-beta1 and TGF-beta2 were reduced in the experimental group. CONCLUSIONS: We suggest that single topical administration of leukotriene antagonist zafirlukast can be helpful in reducing capsule formation and preventing capsular contracture via myofibroblast suppression, modulation of fibroblastic cytokines, and anti-inflammatory effect.

Polyurethane-Coated Breast Implants Revisited: A 30-Year Follow-Up

BACKGROUND: Polyurethane coating of breast implants has been shown to reduce capsular contracture in short-term follow-up studies. This 30-year study is the longest examination of the use of polyurethane-coated implants and their correlation with capsular contracture. METHODS: This study evaluates the senior surgeon's (F.D.P.) experience with the use of polyurethane-coated implants in aesthetic breast augmentation in 382 patients over 30 years. Follow-up evaluations were conducted for six months after surgery. After the six-month follow-up period, 76 patients returned for reoperation. The gross findings, histology, and associated capsular contracture were noted at the time of explantation. RESULTS: No patient during the six-month follow-up period demonstrated capsular contracture. For those who underwent reoperation for capsular contracture, Baker II/III contractures were noted nine to 10 years after surgery and Baker IV contractures were noted 12 to 21 years after surgery. None of the explanted implants had macroscopic evidence of polyurethane, which was only found during the first five years after surgery. The microscopic presence of polyurethane was noted in all capsules up to 30 years after the original operation. CONCLUSIONS: An inverse correlation was found between the amount of polyurethane coating on the implant and the occurrence of capsular contracture. Increasingly severe capsular contracture was associated with a decreased amount of polyurethane coating on the surface of the implants. No contracture occurred in patients whose implants showed incomplete biodegradation of polyurethane, as indicated by the visible presence of polyurethane coating. We recommend research to find a non-toxic, non-biodegradable synthetic material as an alternative to polyurethane.

Estudo de complicações em próteses mamárias: avaliação de 546 casos em oito anos / A report on complications of breast implantation: evaluation of 546 cases in 8 years

INTRODUÇÃO: O implante de próteses mamárias é uma das cirurgias mais frequentes e desafiadoras da cirurgia plástica, devido às complicações associadas. MÉTODO: Foi realizado um estudo retrospectivo de 546 pacientes operadas em oito anos (maio de 2004 a maio de 2012), sendo estudadas todas as pacientes submetidas à inclusão de próteses mamárias, isoladamente ou associadas à mastopexia ou mamoplastia redutora. RESULTADOS: Foram utilizadas próteses texturizadas em 84,8% e poliuretano, em 15,2%, com plano de implantação subglandular em 91,7% e submuscular, em 8,24%. Foram estudados: contratura (3,3%), seroma (2,7%), ptose (2,7%) e infecção (0,6%). A maioria das contraturas surgiu cinco anos após a cirurgia e apenas nas próteses texturizadas, que tiveram tempo de seguimento maior (4,2 anos, nas próteses texturizadas versus 1,7 ano nas de poliuretano). Houve maior frequencia de ptose nas texturizadas e de infecção, nas de poliuretano. Somente apresentaram contraturas pacientes com próteses texturizadas no período observado. Comparando-se o plano de implantação, o seroma foi mais frequente nas submusculares. Considerando-se a complexidade do procedimento, houve aumento do índice de complicações: nas implantadas com poliuretano, aumentou o índice de infecção; nas texturizadas, de ptose e seroma, mas não houve diferenças quanto à contratura. Todos os casos de infecção ocorreram em mamoplastias redutoras com próteses de poliuretano e foram causados por germes comuns, sem casos de micobactérias. CONCLUSÕES: Contraturas e ptose foram exclusivas em próteses texturizadas, no tempo de seguimento mais curto. Infecção apenas ocorreu em próteses de poliuretano. As mastopexias e mamoplastias redutoras apresentaram um índice progressivamente mais alto de complicações.

INTRODUCTION: Breast augmentation implant surgery is one of the most frequently performed plastic surgery procedures; however, it can be challenging because of its associated complications. METHOD: We conducted a retrospective study of 546 patients operated on in eight years (May 2004 to May 2012). These patients underwent breast augmentation, alone or in association with mastopexy or breast reduction. RESULTS: In this study, 84.8% textured and 15.2% polyurethane prostheses, with 91.7% deployed in the subglandular plane and 8.24% in the submuscular plane, were used. We investigated the occurrence of contracture (3.3%), seroma (2.7%), ptosis (2.7%), and infection (0.6%). Most contractures occurred 5 years after surgery and only in textured prostheses, which had a longer follow-up (4.2 years for textured implants vs. 1.7 years for polyurethane implants). There was a higher frequency of ptosis in textured implants and of infection in polyurethane implants. Only patients with textured prostheses showed contractures in the observed period. Concerning the deployment plane, seroma was more frequently observed in submuscular implants. More complex procedures showed a higher rate of complications. Polyurethane implants were associated with increased infection rates, whereas textured implants resulted in ptosis and seroma; however, there were no differences in contracture rates. All cases of infection occurred in patients who received reduction mammoplasty with polyurethane prostheses and were caused by common germs, with no cases of mycobacterial infection. CONCLUSIONS: Contractures and ptosis uniquely occurred in textured prostheses in the shortest follow-up time. Infection occurred only in polyurethane prostheses. Mastopexies and reduction mammoplasties showed a progressively higher rate of complications.

Tratamento das contraturas nas mamoplastias de aumento retroglandulares: implante retropeitoral com retalho capsular / Treatment of contractures in retroglandular mammary augmentation using retropectoral implants and capsular flaps

Capsular contracture is one of the most common causes of surgical revision in the mammary augmentation procedure. This phenomenon can happen with any kind of implant, or layer of the pocket. The literature shows that there is an increased prevalence in the implant in the retro mammary position, and for this reason the majority of patients whom operate for treating contracture are in this situation. In these patients we observe a significant thinning of the gland and the subcutaneous tissue, then, we create a rectropectoralis pocket to insert the new implant making use of a capsular flap, to involve it completely. This allows larger implants house with great security, nice cosmetic results and high satisfaction...

Este trabalho propõe, nos casos de contratura capsular em mamoplastias de aumento retroglandulares, a inclusão de novos implantes no plano retropeitoral, empregando retalhos de cápsula para sua fixação. Método: Foram avaliadas, retrospectivamente, 27 pacientes portadoras de contratura capsular tratadas desta forma entre maio de 2007 e junho de 2012. Resultados: A técnica utilizada permitiu abrigar implantes maiores com bom aspecto de contorno mamário, assegurados pela cobertura muscular, estabilizada pelo retalho capsular. Conclusões: A técnica apresentada é um método seguro, reprodutível, tecnicamente simples, de resultados satisfatórios e baixa prevalência de intercorrências...

Effect of zafirlukast on capsular contracture around silicone implants in rats / Efeito do zafirlukast na contratura capsular ao redor de implantes de silicone em ratos

PURPOSE: To evaluate the effect of zafirlukast on capsular contracture around silicone implants by measuring the pressure within the implant, using a rat experimental model. METHODS: Forty adult female Wistar rats were used. Each one received two silicone implants, one with smooth-surface and the other with textured-surface. They were randomly divided into four groups (n=10). The rats of control group I were sacrificed after the implants. The remaining animals were subjected to a daily regimen of intra-peritoneal injection for a period of 90 days and they were distributed as follows: control group II received 0.9 percent physiological saline solution; experimental group I received zafirlukast 1.25 mg/kg; and experimental group II received zafirlukast 5 mg/kg. The measurement of intra-implant pressure of control group I was determined on the surgery day and in other groups on the ninetieth day, after being sacrificed. RESULTS: In the evaluation of textured implants there was an increase of internal pressure in the control group II, and there was no increase in the experimental groups. Compared to the controls there were not significant differences in smooth implants. CONCLUSION: Zafirlukast reduced the risk of developing capsular contracture around silicone implants with textured surface.

OBJETIVO: Avaliar o efeito do zafirlukast na contratura capsular ao redor de implantes de silicone, através da aferição da pressão intra-implante, utilizando-se um modelo experimental de ratos. MÉTODOS: Quarenta ratos fêmeas Wistar foram utilizados. Cada um recebeu dois implantes de silicone, sendo um com superfície lisa e outro texturizada. Foram divididos aleatoriamente em quatro grupos (n=10). Os ratos do grupo controle I foram sacrificados após o implante. O restante dos animais foi submetido a um regime diário de injeção intraperitoneal por um período de 90 dias e foram distribuídos: grupo controle II recebeu solução salina fisiológica 0,9 por cento, grupo experimental I recebeu zafirlukast 1,25 mg/kg, e grupo experimental II recebeu zafirlukast 5 mg/kg. O grupo controle II recebeu solução salina; grupo experimental I, 1,25 mg/kg/dia de zafirlukast; grupo experimental II, 5mg/kg/dia de zafirlukast. A aferição da pressão intra-implante do grupo controle I foi averiguada no dia do ato operatório, e nos outros grupos no nonagésimo dia, após serem sacrificados. RESULTADOS: Na avaliação dos implantes texturizados houve aumento da pressão interna no grupo controle II e, não se observou aumento nos grupos experimentais. Na comparação com os controles não foram observadas diferenças significativas nos implantes lisos. CONCLUSÃO: O Zafirlukast reduziu o risco de desenvolver contratura capsular em torno de implantes de silicone com superfície texturizada.

Breast Augmentation using Expandable Implants

Ideal results of augmentation mammaplasty consist of symmetry, natural shape, soft feeling and inconspicuous scar. In addition, patient's preferences about size and shape should be included. Static implants could not perfectly satisfy patients' desires for size and shape, but expandable implants enable to change the volume after the operation. From September 2001 to September 2004, 76 patients(150 breasts) underwent breast augmentation using permanent expandable implant. The procedure was unilateral in 2 women and bilateral in 74 women. Age ranged from 19 to 50 years(mean, 29 years). Fifty nine patients underwent simple augmentation mammaplasty, 7 patients were corrected of their severe asymmetry, 2 patients with the congenital breast deformity underwent mammaplasty using this, and 2 patients who had undergone unilateral mastectomy were reconstructed of their breasts using expandable implant. There were no definite complications such as capsular contracture, implant rupture, asymmetry. And there reported little dissatisfaction about the size. The permanent expandable implants might be good alternatives in cases of ordinary breast augmentation as well as tissue deficient patients, asymmetry, congenital anomaly, and breast reconstruction.