Pectus excavatum ­ Correção cirúrgica utilizando tala externa de poliuretano fabricada com tecnologia de impressão 3D / Pectus excavatum ­ Surgical correction, using polyurethane external splint made with 3D printing technology

Objetivou-se relatar o emprego de uma tala externa confeccionada com material de poliuretano e cobertura interna de neopreme na reparação cirúrgica do pectus excavatum em um felino jovem. O felino apresentava deformidade anatômica congênita na região do externo e sinais clínicos respiratórios. Imagens avançadas de tomografia foram utilizadas para moldar a tala impressa com tecnologia tridimensional. Esta alternativa possibilitou melhor planejamento cirúrgico e, com isso, conforto para o paciente, além da qualidade própria do material de poliuretano que é levemente maleável, o que permitiu melhor moldagem e expansão torácica durante a respiração. A tala se provou resistente o suficiente para suportar a tração ocasionada pelos fios de sutura e possibilitou o reposicionamento adequado do osso esterno ao mesmo tempo que se mostrou confortável e acarretou mínimas lesões ao paciente.

The aim of this paper was to report the use of an external splint made of polyurethane material and internal neopreme covering in the surgical repair of a pectus excavatum in a young feline. The feline exhibited a congenital anatomical deformity in the external region and clinical respiratory signs. Advanced CT images were used to shape the 3D-printed splint. This alternative allowed better surgical planning and, therefore, comfort for the patient, this because to the quality of the polyurethane material, which is slightly malleable, and allowed for better molding and chest expansion during breathing. The splint proved to be strong enough to withstand the traction caused by the suture threads and allowed the proper repositioning of the sternum, at the same time it was comfortable and caused minimal injuries to the patient.

Survival of sealants in molars affected by molar-incisor hypomineralization: 18-month follow-up

Abstract The objective of this study was to evaluate the clinical survival of sealants applied in first permanent molars (FPMs) affected by molar-incisor hypomineralization (MIH), at 18 months of follow-up. Forty-one first permanent molars were selected from 21 children, 6–8 years of age. MIH was classified by one calibrated examiner (kappa = 0.80) according to EAPD criteria. The inclusion criteria were fully erupted FPMs with MIH or sound FPMs (without MIH) for which sealant treatment was indicated. The FPMs were assigned to two groups: CG (control group) and HG (MIH group). Both groups were treated with sealant (FluroShield). Clinical follow-up was performed from baseline to 18 months to assess anatomical form, marginal adaptation, retention and presence of caries, according to criteria set by the United States Public Health Service-Modified, and was conducted by a blinded examiner (kappa = 0.80). The actuarial method was used to evaluate the survival of the sealants. The survival rates for the groups were compared using Fisher’s exact test (α = 5%). The cumulative survival rates were 81% at 1 month, 68.8% at 6 months, 68.8% at 12 months, and 62.6% at 18 months for CG, and 88% at 1 month, 84% at 6 months, 76% at 12 months, and 72% at 18 months for HG. No significant difference was found between the groups. The sealants in molars affected by MIH presented a survival rate similar to the sealants in the control, suggesting that sealants may be an adequate approach for preventing carious lesions in MIH-affected molars.

A wet dressing for male genital surgery: A phase II clinical trial

ABSTRACT Purpose: This study was to confirm the safety and efficacy of BC dressing when used in surgical male wound healing at the urogenital area. Methods: Open, non-controlled clinical study of phase II. A total of 141 patients, among those children, adolescents and adults with hypospadias (112), epispadias (04), phymosis (13) and Peyronie's disease (12) that had a BC dressing applied over the operated area after surgery. A written informed consent was obtained from all participants. Study exclusion criteria were patients with other alternative treatment indications due to the severity, extent of the injury or the underlying disease. The outcomes evaluated were efficacy, safe and complete healing. The costs were discussed. Results: In 68% patients, the BC dressing fell off spontaneously. The BC was removed without complications in 13% of patients at the outpatient clinic during the follow-up visit and 17% not reported the time of removal. In 3% of the cases, the dressing fell off early. Complete healing was observed between 8th and 10th days after surgery. The BC dressings have shown a good tolerance by all the patients and there were no reports of serious adverse events. Conclusion: The bacterial cellulose dressings have shown efficacy, safety and that can be considered as a satisfactory alternative for postoperative wound healing in urogenital area and with low cost.

Custos de coberturas para a prevenção de úlcera por pressão sacral / Costo de apósitos para la prevención de la úlcera por presión sacra / Cost of dressings for prevention of sacral pressure ulcers

RESUMO Objetivo: identificar os custos com coberturas na prevenção de úlcera por pressão sacral em uma Unidade de Terapia Intensiva para Adultos do Paraná, Brasil. Métodos: pesquisa de análise secundária com 25 pacientes internados entre outubro/2013 e março/2014, que utilizaram filme transparente de poliuretano (n=15) ou placa hidrocoloide (n=10) na região do sacro. O custo de cada intervenção se baseou na quantidade unitária utilizada, em cada tipo de cobertura e seu preço de aquisição (filme transparente = R$15,80, hidrocoloide = R$68,00). Resultados: O custo médio/paciente foi de R$23,17 para uso do filme transparente e de R$190,40 para uso de hidrocoloide. O principal motivo para a troca de cobertura foi o descolamento. Conclusão: O filme transparente consistiu na alternativa economicamente mais vantajosa para a prevenção de úlcera por pressão sacral em pacientes críticos; mas são necessários estudos adicionais que incluam a avaliação da efetividade de ambas as coberturas.

RESUMEN Objetivo: identificar los costos de apósitos para la prevención de úlcera por presión sacra en una Unidad de Terapia Intensiva de Adultos en Paraná, Brasil. Métodos: investigación de análisis secundario con 25 pacientes internados entre octubre de 2013 y marzo de 2014, que utilizaron film transparente de poliuretano (n=15) o placa hidrocoloide (n=10) en la región sacra. El costo de cada intervención se basó en la cantidad unitaria utilizada, en cada tipo de cobertura y su costo de adquisición (film transparente = R$15,80, hidrocoloide = R$68,00). Resultados: el costo promedio/paciente fue de R$23,17 usando film transparente y R$190,40 usando hidrocoloide. El principal motivo de cambio fue la mala adhesión. Conclusión: el film tranparente constituyó la alternativa económica más ventajosa para la prevención de la úlcera por presión sacra en pacientes críticos, pero se necesita de estudios adicionales que incluyan la evaluación de la efectividad de ambos apósitos.

ABSTRACT Objective: to identify costs of dressings to prevent sacral pressure ulcers in an adult intensive care unit in Paraná, Brazil. Methods: secondary analysis study with 25 patients admitted between October 2013 and March 2014, using transparent polyurethane film (n=15) or hydrocolloid dressing (n=10) on the sacral region. The cost of each intervention was based on the unit amount used in each type of dressing, and its purchase price (transparent film = R$15.80, hydrocolloid dressing = R$68.00). Results: the mean cost/patient was R$23.17 for use of transparent film and R$190.40 for use of hydrocolloid dressing. The main reason for changing the dressing was detachment. Conclusion: the transparent film was the most economically advantageous alternative to prevent sacral pressure ulcers in critical care patients. However, additional studies should be carried out including assessment of the effectiveness of both dressings.

Apresentação aguda da doença de Mondor em pós-operatório de mamoplastia de aumento com implantes de silicone / Acute presentation of Mondor's disease after breast augmentation with silicone implants

Há 50 anos, no Jefferson Davis Hospital, em Houston (EUA), realizou-se a primeira cirurgia de mamoplastia de aumento com implantes de silicone. Atualmente, o avanço da tecnologia médica disponibilizou no mercado implantes de diversas formas e texturas, assim como permitiu o desenvolvimento de inúmeras técnicas para a realização desta cirurgia. Este procedimento cirúrgico pode apresentar algumas complicações locais imediatas e tardias no pós-operatório. Por se tratar de um implante constituído de material biocompatível ao organismo, mesmo com 50 anos de evolução, deve-se sempre estudar e, se possível, relatar as possíveis complicações que possam ocorrer. O objetivo deste artigo é revisar as complicações mais frequentes que ocorrem no pós-operatório das mamoplastias de aumento com implante de silicone, bem como relatar o caso de uma complicação atípica, doença de Mondor, no pós-operatório desta cirurgia.

The first breast augmentation surgery with silicone implants was performed at the Jefferson Davis Hospital in Houston (USA) about 50 years ago. Recent advances in medical technology have made implants of various shapes and textures commercially available and led to the development of numerous techniques for performing this surgery. However, this surgical procedure may have some immediate and long-term local complications . Since the implant is made of biocompatible material , it is important to investigate and report complications that occur despite the 50 years of research. The purpose of this study was to review the most frequent complications occurring after breast augmentation surgery with silicone implants and to report a case of an unusual complication, Mondor's disease.

Mastopexia periareolar (circum-areolar) com implante mamário cônico: tratamento de ptose, hipomastia e alterações de posição e tamanho do complexo aréolo-papilar / Periareolar (circumareolar) mastopexy with conical breast implants: treatment of ptosis, hypomastia, and changes in position and size of the nipple-areola complex

INTRODUÇÃO: A cirurgia de mastopexia associada ao aumento mamário vem sendo cada vez mais solicitada. Ao mesmo tempo, pacientes com graus menores de ptose aceitam menos as correções por meio de cicatrizes verticais. Nesse contexto, a mastopexia periareolar (circum-areolar) com implante cônico é uma opção que resulta em cicatriz limitada ao perímetro areolar e possibilita o tratamento das alterações de posição e tamanho do complexo aréolo-papilar. MÉTODO: Foram avaliadas 22 pacientes, submetidas à mastopexia periareolar com utilização de próteses cônicas, revestidas com poliuretano, colocadas em posição subglandular e operadas pelo mesmo cirurgião. RESULTADOS: Dados observados: 45% das pacientes apresentavam ptose grau I; 32%, grau II, e 23%, grau III; 86% das pacientes apresentavam assimetria do complexo aréolo-papilar; 27%, lateralização, e 18%, aréolas grandes, havendo associações na mesma paciente. O volume das próteses variou de 215 mL a 380 ml. Houve dois casos de alargamento da cicatriz, mas não houve casos de alargamento de aréola ou cicatriz hipertrófica. Não houve, no período pesquisado, complicações relacionadas à colocação do implante. No questionário de satisfação, a maioria das pacientes considerou o aspecto da mama natural, conferindo boas notas aos aspectos: formato, simetria e altura das mamas, qualidade da cicatriz e posição, formato e tamanho das aréolas. CONCLUSÕES: A técnica permite resultados satisfatórios nos casos indicados, como ptoses leves a moderadas, aréolas grandes, lateralização e assimetria do complexo aréolo-papilar. São aspectos técnicos importantes: a retirada conservadora de pele periareolar, o uso de implantes de tamanhos moderados e a confecção da sutura de contenção em round-block.

INTRODUCTION: Mastopexy surgery associated with breast augmentation is increasingly being requested. At the same time, patients with lower degrees of ptosis are less receptive to any correction through vertical scars. In this context, periareolar (circumareolar) mastopexy with a conical implant is an option that results in a scar that is limited to the areolar perimeter, and enables the treatment of changes in the position and size of the nipple-areola complex. METHOD: We evaluated 22 patients submitted to periareolar mastopexy with use of conical prostheses coated with polyurethane and placed in a subglandular position. All patients were operated on by the same surgeon. RESULTS: Among the patients, 45% presented with grade I ptosis, 32% grade II, and 23% grade III, and 86% exhibited asymmetry of the nipple-areola complex, 27% lateralization, and 18% large areolas, with some combination in the same patient. The volume of the prostheses ranged from 215 to 380 mL. There were two cases of scar enlargement; however, there were no cases of enlargement of the areola or hypertrophic scar. During the period studied, there were no complications related to the placement of the implant. In the satisfaction questionnaire, most of the patients considered the aspect of the breast to be natural in appearance, giving good grades to the size, symmetry, and height of the breasts; the quality of the scar; and the position, shape, and size of the areolas. CONCLUSIONS: This technique produces satisfactory results in cases of mild to moderate ptoses, large areolas, lateralization, and asymmetry of the nipple-areola complex. Important technical aspects include the conservative removal of periareolar skin, use of implants of moderate sizes, and the use of the round-block containment suture.

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.

Uso de espumas em áreas doadoras de enxertos / Use of polyurethane foam dressings on skin graft donor sites

Introdução: O sucesso de um enxerto de pele é avaliado não apenas pela integração do enxerto em si, mas também pela qualidade da recuperação da área doadora. A despeito de as áreas doadoras de enxertos representarem o melhor local para estudo de cicatrização de feridas, regimes de tratamento, de áreas doadoras, tem sido incompletamente estudados. Objetivo: Avaliação da eficácia de espumas de poliuretano como curativo de áreas doadoras de enxertos. Método: Estudo prospectivo no qual áreas doadoras de enxertos foram tratadas com espumas de poliuretano como alternativa a filmes de acetato de celulose. Resultados: Foram tratados 11 pacientes e catorze áreas doadoras de enxerto. Aderência prolongada (73%) e odor desagradável (45%) foram os problemas encontrados. Os resultados foram considerados insatisfatórios na grande maioria dos casos (73%). Conclusões: O uso de espumas de poliuretano mostrou-se ineficaz, nesse grupo de pacientes, devido à ocorrência de alto índice de complicações.

Introduction: The success of a skin graft is evaluated by not only the integration of the graft itself, but also the quality of the recovery of the donor site. Despite the fact that graft donor sites represent the best place to study wound healing, treatment regimens for donor sites have not been studied extensively. Method: To evaluate the efficiency of polyurethane foam as a dressing for graft donor sites. Methods: We conducted a prospective study in which graft donor sites were treated with polyurethane foam dressing, as an alternative to a cellulose acetate film. Results: We treated 11 patients and 14 donor graft sites. Problems associated with the use of polyurethane foam included prolonged adherence (73%) and an unpleasant odor (45%). The majority of patients reported that they found the dressing to be unsatisfactory (73%). Conclusions: The use of a polyurethane foam was shown to be ineffective as a graft donor site dressing, due to the high rate of associated complications.

A wet dressing for hypospadias surgery

Introduction One of the main problems faced by surgeons involved in male genitalia surgeries, in particular in children with hypospadias, is the type of dressing and its use during the post-operatory period. Materials and Methods From a multidisciplinary project involving the use of sugarcane biopolymer membrane developed in the last 10 years, produced by bacterial action over sugarcane molasses, we developed a multiperforated pellicle that, when applied around the penis, protects the surgical field. It is a proven inert material that does not induce any reaction on the surgical field and can be left in situ maintaining the same characteristics during a long period of time without the need of replacement. This multiperforated tape can involve several times the penis shaft and due to its adhesiveness it hardly loosens. We compared the use of this dressing with a commercial one (made by polyurethane). Thirty patients with hypospadias were randomly selected for the use of this new type of dressing in the last 18 months. A similar group of patients used a similar commercial dressing made of polyurethane (Tegaderm©) according to the same criteria of use. For safety reasons, we applied one or two sutures without the inclusion of the skin using an absorbable suture in order to prevent early detachment. A small gauze was left for 24 hours in order to absorb any possible bleeding. We recommended the irrigation of the dressing with water or saline at least three or four times a day and the patient was allowed to bath. The dressing did not need any special care and if not removed it usually detached spontaneously after 10 to 14 days. Results The tolerance to the material was satisfactory and there were no adverse reactions on the penile surface. In two cases of the biopolymer group the dressing detached spontaneously on the first and third days, respectively. In two cases of the polyurethane ...

In vitro evaluation of three different biomaterials as scaffolds for canine mesenchymal stem cells

PURPOSE: To evaluate in vitro ability the of three different biomaterials - purified hydroxyapatite, demineralized bone matrix and castor oil-based polyurethane - as biocompatible 3D scaffolds for canine bone marrow mesenchymal stem cell (MSC) intending bone tissue engineering. METHODS: MSCs were isolated from canine bone marrow, characterized and cultivated for seven days with the biomaterials. Cell proliferation and adhesion to the biomaterial surface were evaluated by scanning electron microscopy while differentiation into osteogenic lineage was evaluated by Alizarin Red staining and Sp7/Osterix surface antibody marker. RESULTS: The biomaterials allowed cellular growth, attachment and proliferation. Osteogenic differentiation occurred in the presence of hydroxyapatite, and matrix deposition commenced in the presence of the castor oil-based polyurethane. CONCLUSION: All the tested biomaterials may be used as mesenchymal stem cell scaffolds in cell-based orthopedic reconstructive therapy.

Biocompatibility of a new device of self-expandable covered and non-covered tracheal stent: comparative study in rats

PURPOSE: To investigate the compatibility of a new model of self-expandable tracheal stent in rats. METHODS: A new device of polyurethane covered and non - covered stent was placed in the trachea of Wistar rats. Animals were distributed in two groups: the polyurethane covered and non-covered group. Macroscopic parameters included position within the tracheal lumen, adherence to the mucosa, degree of dilatation, permeability and internal diameter. Microscopic findings evaluated were: incorporation, inflammatory activity, granulation tissue and epithelial revetment injuries. The observation follow-up was six weeks. All parameters were quantified based on determined score values. Incorporation of the stents was evaluated based on the observation if the stent was fixed into the trachea or if it could be removed. Degree of dilatation was performed by external diameter measurements. Granulation tissue was evaluated by measurements of height of the tissue growing into the tracheal lumen. RESULTS: 100% of non-covered stents had total attachment to mucosa and 100% of polyurethane covered type had adherence only. Regarding dilatation, granulation tissue, inflammatory activity and internal diameter measurements, there were no significant differences between the groups. Pathological tracheal wall injuries were present in both groups. CONCLUSION: Both models of stent demonstrated biocompatibility with the trachea. Rats are suitable for an experimental model of tracheal stent study.

Effects of Nasopore Packing on Dacryocystorhinostomy

PURPOSE: To investigate the effects of placement of the absorbable packing material Nasopore at the anastomosis site of newly formed mucosal flaps on postoperative re-bleeding, discomfort, and on the success rate of dacryocystorhinostomy (DCR). METHODS: A review of the medical records of patients with primary acquired nasolacrimal duct obstruction that underwent external or endonasal DCR by a single surgeon was performed. The degree of re-bleeding, discomfort, and postoperative results, including anatomical success, functional success and postoperative nasal findings such as granulation, synechiae, and membrane formation were compared in patients whose anastomosis site was packed with either Nasopore or Merocel, a non-absorbable packing material. RESULTS: A total of 77 patients (101 eyes) were included. Of the 101 eyes, 30 were packed with Nasopore, while 71 were packed with Merocel. The Nasopore group showed significantly better results than the Merocel group in the degree of re-bleeding and the level of patient discomfort (p = 0.000, 0.039, respectively; Pearson's chi-square test), whereas there were no statistically significant differences between the two groups in postoperative anatomical and functional success (p > 0.05). CONCLUSIONS: Nasopore significantly reduced postoperative nasal re-bleeding and patient discomfort during the early post-surgical period, but failed to show an effect on the postoperative anatomical and functional success of DCR.

Effects of Nasopore Packing on Dacryocystorhinostomy

PURPOSE: To investigate the effects of placement of the absorbable packing material Nasopore at the anastomosis site of newly formed mucosal flaps on postoperative re-bleeding, discomfort, and on the success rate of dacryocystorhinostomy (DCR). METHODS: A review of the medical records of patients with primary acquired nasolacrimal duct obstruction that underwent external or endonasal DCR by a single surgeon was performed. The degree of re-bleeding, discomfort, and postoperative results, including anatomical success, functional success and postoperative nasal findings such as granulation, synechiae, and membrane formation were compared in patients whose anastomosis site was packed with either Nasopore or Merocel, a non-absorbable packing material. RESULTS: A total of 77 patients (101 eyes) were included. Of the 101 eyes, 30 were packed with Nasopore, while 71 were packed with Merocel. The Nasopore group showed significantly better results than the Merocel group in the degree of re-bleeding and the level of patient discomfort (p = 0.000, 0.039, respectively; Pearson's chi-square test), whereas there were no statistically significant differences between the two groups in postoperative anatomical and functional success (p > 0.05). CONCLUSIONS: Nasopore significantly reduced postoperative nasal re-bleeding and patient discomfort during the early post-surgical period, but failed to show an effect on the postoperative anatomical and functional success of DCR.

A validação do uso de filme transparente de poliuretano nas úlceras por pressão de estágio I na região de calcâneos / Validation of the use of transparent polyurethane film of pressure ulcers in the region of stage I of the heel

Resumo: A úlcera por pressão (UP) se caracteriza por áreas de danos localizado na pele e tecidos subjacentes causado por pressão, cisalhamento, fricção e ou uma combinação destes. Este agravo causa ao paciente dor, desconforto, interfere na qualidade de vida, favorece o aumento no tempo de permanência hospitalar, aumento de custos e desqualificação do cuidado prestado. OBJETIVO: Descrever a evolução das úlceras por pressão de estágio I (UPI) para úlcera por pressão estágio II (UPII) utilizando o filme transparente de poliuretano (FTP) na região dos calcâneos de pacientes hospitalizados em unidades críticas. MATERIAIS E MÉTODO: Trata-se de um estudo de validação. O período de coleta de dados foi de 6,5 meses com uma amostra final composta por 27 pacientes. Os pacientes com úlcera por pressão em estágio I receberam o filme transparente de poliuretano, diariamente foram realizados exames físicos dos sítios corpóreos selecionados e avaliados quanto à presença de úlceras por pressão e seus estágios, permanência do filme transparente de poliuretano e sinais de reação adversa, estes foram acompanhados até o agravo ou regressão da lesão, alta hospitalar ou óbito. RESULTADOS: O tempo de acompanhamento dos pacientes variou de 3 a 41 dias de avaliações diárias, média de 10 dias. Entre os 27 pacientes avaliados 63% (17) do sexo masculino e 37% (10) do sexo feminino. A média de idade foi de 63 anos. As patologias causadoras da hospitalização foram diversas, destacando-se insuficiência cardíaca congestiva e acidente vascular cerebral. Quanto à variável de desfecho, 26% apresentaram a regressão da ÚP l da região dos calcâneos, 33% evoluíram para UP II e 41% dos participantes do estudo foram censurados por alta hospitalar ou óbito durante as avaliações. Entre os pacientes que tiveram agravo da UP, o tempo mediano livre de agravo da UP (evolução para UPII), com o uso do filme transparente de poliuretano (FTP), foi igual a 6 dias, sendo o mínimo de 3 dias e o máximo de 25 dias. O tempo médio de permanência do filme foi igual a 3,1 dias com desvio padrão de 1,8 dia, sendo o mínimo igual a 1 e o máximo igual a 8 dias. CONCLUSÕES:A úlcera por pressão estágio I na região dos calcâneos não permaneceu estável com o uso do filme transparente de poliuretano. Não se observou significância estatística nos testes efetuados. Sugere-se dar continuidade a esta pesquisa para comprovar ou refutar os resultados apresentados com estudos comparativos.

Abstract: The pressure ulcer (PU) is characterized by localized injury to the skin and underlying tissue as a result of pressure, shear, friction or a combination of these factors. This harm causes the patient pain, iscomfort, affects the life quality, leads to an extended length of hospital stay, increasing costs and favoring disqualification of the care provided. OBJECTIVE: Describing the evolution of pressure ulcer from Stage I to Stage II using transparent polyurethane film in the calcaneus region in critical units of a University Hospital in Curitiba. MATERIALS AND METHOD: This is a Validation Studies. The data collection took 6.5 onths and the final sample consisted of 27 patients. The patients with pressure ulcer Stage I received the transparent polyurethane film. Physical examinations were performed daily in the selected body sites and they were evaluated according to the presence of pressure ulcers and their respective stages; the transparent polyurethane film fixedness; and adverse reaction signs. The patients were followed until the injury aggravation or regression, their discharge or death. RESULTS: Follow-up time of patien s ranged from 3 to 41 days of daily evaluation, average of 10 days. Among the 27 patients studied, 63% (17) were male and 37% (10) were female. An average of 63 years old. The pathologies that caused hospitalization were diverse, especially congestive heart failure and stroke. Regarding the outcome variable, 26% showed regression of the pressure ulcer Stage I in the calcaneus region, 33% evolved to PU Stage II and 41% of the study participants were censored due to discharge or death during the evaluation period. Among the patients who had worsening of PU, the median time free of aggravation of PU (evolution to PU Stage II) was equal to 6 days, with a minimum of 3 days and a maximum of 25 days. The mean time of fixedness of the transparent polyurethane film was equal to 3.1 days with standard deviation of 1.8 day, the minimum being equal to 1 and the maximum equal to 8 days. CONCLUSIONS: Pressure ulcer Stage I in the calcaneus region did not emain stable with use of transparent polyurethane film. There was no statistical significance in the tests performed due to small number of cases studied. The sample size did not allow pointing out secure inferences that would justify the regression or aggravation of pressure ulcers. Other researches must be conducted to confront these results.

Propriedades mecânicas do cimento ósseo e da poliuretana de mamona com e sem catalisador / Mechanical properties of bone cement and castor oil-based polyurethane with and without a catalyst

Avaliou-se o comportamento mecânico do polímero de mamona, tendo por variáveis o tempo de produção e a presença de catalisador, e utilizando como padrão comparativo o cimento ósseo (polimetilmetacrilato). Foram estabelecidos três grupos experimentais, de acordo com o tipo de corpo de prova (cilindro ou barra) e polímero utilizado, que foram posteriormente subdivididos em subgrupos conforme o tempo após produção, ou seja, 24, 48 e 72 horas. O ensaio de compressão analisou a carga máxima e a tensão e o ensaio de dobramento estudou o módulo de dobramento e a resistência. Estatisticamente não houve diferenças nos valores de resistência à compressão ou ao dobramento às 24, 48 e 72 horas após a produção do polimetilmetacrilato e da poliuretana, com ou sem catalisador. A poliuretana com catalisador foi a mais resistente nos ensaios de compressão, apresentando módulo de dobramento semelhante ao do polimetilmetacrilato e resistência ao dobramento superior à da poliuretana sem catalisador. Conclui-se que: o tempo não alterou as propriedades mecânicas dos compósitos avaliados; o catalisador melhorou o desempenho mecânico da poliuretana de mamona; na resistência mecânica à compressão, a poliuretana com catalisador suportou mais carga que o polimetilmetacrilato.

The mechanical properties of castor oil-based polyurethane was evaluated considering post-production time and the presence of a catalyst as variables and using bone cement (polymethylmetacrylate) as a comparative pattern. According to proof body type (cylinders or bars) and the used polymer, three experimental groups were established. Such groups were later subdivided according to post-production time, namely, 24, 48, and 72 hours. A compression assay analyzed maximum load and tension, and a folding assay evaluated the folding module and resistance. There were no statistical differences in the values for resistance to compression or folding at 24, 48, and 72 hours after the production of polymethylmetacrylate and polyurethane with or without a catalyst. Castor oil-based polyurethane with a catalyst showed to be the most resistant during the compression assays as its folding module was similar to that of polymethylmetacrylate, and its folding resistance was higher than that of polyurethane without a catalyst. In conclusion, time did not change the mechanical properties of the evaluated composites; the catalyst improved the mechanical performance of castor oil-based polyurethane; castor oil-based polyurethane with a catalyst supported more load during the assay for mechanical resistance to compression than did polymethylmetacrylate.

Bone regeneration after demineralized bone matrix and castor oil (Ricinus communis) polyurethane implantation

Innocuous biocompatible materials have been searched to repair or reconstruct bone defects. Their goal is to restore the function of live or dead tissues. This study compared connective tissue and bone reaction when exposed to demineralized bovine bone matrix and a polyurethane resin derived from castor bean (Ricinus communis). Forty-five rats were assigned to 3 groups of 15 animals (control, bovine bone and polyurethane). A cylindrical defect was created on mandible base and filled with bovine bone matrix and the polyurethane. Control group received no treatment. Analyses were performed after 15, 45 and 60 days (5 animals each). Histological analysis revealed connective tissue tolerance to bovine bone with local inflammatory response similar to that of the control group. After 15 days, all groups demonstrated similar outcomes, with mild inflammatory reaction, probably due to the surgical procedure rather than to the material. In the polymer group, after 60 days, scarce multinucleated cells could still be observed. In general, all groups showed good stability and osteogenic connective tissue with blood vessels into the surgical area. The results suggest biocompatibility of both materials, seen by their integration into rat mandible. Moreover, the polyurethane seems to be an alternative in bone reconstruction and it is an inexhaustible source of biomaterial.

Morphology of autogenous bone graft and castor oil polyurethane in the infraorbital rim of rabbits: a comparative study / Estudo morfológico comparativo do enxerto ósseo autógeno e polímero de mamona em rebordo infra-orbitário de coelhos

PURPOSE: Morphological study comparing castor oil polyurethane and autogenous bone graft to repair bone defect in zygomatic bone of rabbits. METHODS: Twenty-four adult, male New Zealand rabbits were randomly distributed between two groups of twelve. Bone defects of 5mm in diameter were cut through the zygomatic bone and filled with polyurethane discs in the experimental group or autogenous bone harvested from the tibia in the control group. Animals were sacrificed after 30, 60 or 90 days, and the zygomatic bones were macro- and microscopically analyzed. Student's, Fisher's, chi-squared and McNemar's tests were used for statistical analysis. RESULTS: Both the castor oil polyurethane and the autograft adapted well to the defect, with no need for fixation. Fibrous connective tissue encapsulated the polyurethane, but no inflammation or giant cell reaction was observed. Acidophilic and basophilic areas were observed inside the micropores of the polyurethane, suggesting cell nuclei. After 90 days, bone repair with a lamellar pattern of organization was observed in the control group. CONCLUSION: The castor oil polyurethane was biocompatible and did not cause inflammation. It may be considered an alternative to fill bone defects.

OBJETIVO: Estudo morfológico comparativo do implante de poliuretana de mamona e enxerto ósseo autógeno em defeito ósseo padrão em osso zigomático de coelhos. MÉTODOS: Vinte e quatro coelhos Nova Zelândia, machos, adultos, foram distribuídos aleatoriamente em dois grupos de 12. Defeitos de 5mm de diâmetro, perenes, foram confeccionados em osso zigomático e preenchidos com discos pré-fabricados de poliuretana no grupo experimento ou osso autógeno extraído da tíbia no grupo controle. Os animais foram sacrificados após 30, 60 e 90 dias e as peças anatômicas foram avaliadas macro e microscopicamente. Foram utilizados os testes de Student, Fisher,qui-quadrado e McNemar para a análise estatística dos resultados. RESULTADOS: A poliuretana e o osso autógeno se adaptaram ao defeito sem necessidade de fixação. Houve formação de tecido conjuntivo fibroso envolvendo a poliuretana, sem reação inflamatória ou presença de células gigantes. Verificaram-se áreas acidófilas e basófilas nos poros do material implantado, sugestivas de núcleos celulares. No grupo controle, observou-se aos 90 dias o reparo ósseo de padrão lamelar clássico. CONCLUSÃO: A poliuretana de mamona foi biocompatível e não causou reação inflamatória deletéria. Pode ser uma alternativa para o preenchimento de defeitos ósseos.

Use of castor oil polyurethane in an alternative technique for medial patella surgical correction in dogs

PURPOSE: Comparative morphologic study of utilization of castor oil polymer in dogs joints, as an alternative technique to autogenous graft, in surgical correction of medial patella luxation. METHODS:Twelve adult dogs, of both sexes, were randomly allocated to two different groups of six animals each. Group I (biopolymer) consisted of the deepening of the right femoral troclea, with the implantation of the biopolymer prothesis, and compared to group II (control) which consisted of the conventional trocleoplastia technique with wedged cut of the left femoral troclea. The dogs were sacrified after 30 or 90 days and the anathomic peaces were analyzed macro and microscopically. Qui square and Wilcoxon tests were used for the statistic analyses of the results, considering probability of 5 percent. RESULTS: It was not observed bony integration on the castor oil polymer group. There was resorption of the graft along experimental period and absence of inflammatory cells in the studied periods. CONCLUSION: Castor oil polymer assisted cicatrisation process, was biocompatible without inflammation, and it can be used in joints as an alternative for bony filling.

OBJETIVO: Estudo morfológico do implante da prótese de polímero de mamona em articulações de cães, como técnica alternativa ao enxerto ósseo autógeno na correção cirúrgica da luxação medial de patela. MÉTODOS: Doze cães adultos, de ambos os sexos, foram distribuídos aleatoriamente em dois grupos de 6 animais. No grupo I (poliuretano) foi feito o aprofundamento da tróclea femoral direita com prótese de polímero de mamona, que foi comparado com o grupo II (controle) sendo feita a trocleoplastia por ressecção em cunha da tróclea femoral esquerda. Os animais foram sacrificados após 30 e 90 dias e as peças anatômicas foram avaliadas macro e microscopicamente. O teste do quiquadrado e o teste não-paramétrico de Wilcoxon foram utilizados para a análise estatística dos resultados. Fixou-se em 5 por cento, o nível de rejeição da hipótese de nulidade. RESULTADOS: Não foi observada interação óssea (osteointegração) no grupo polímero de mamona. Houve reabsorção do enxerto ao longo do período experimental e ausência de células inflamatórias nos períodos analisados. CONCLUSÃO: O polímero de mamona auxiliou no processo cicatricial, foi biocompatível sem presença de inflamação, podendo ser usado em articulações como uma alternativa para o preenchimento ósseo.

Utilização de película de poliuretano na síntese cutânea de gatas após celiotomia / Use of polyurethane film in skin closure of cats after celiotomy

Introdução - A película de poliuretano é um filme transparante, semipermeável e autoadesivo, primeiramente utilizada em queimaduras e na proteção de cateteres venosos centrais em unidades de terapia intensiva. Sua principal propriedade é a constituição de uma barreira capaz de proteger a pele lesada contra colonização bacteriana, sem impedir trocas gasosas entre tecido e ambiente. O presente estudo, objetivou avaliar as vantagens do emprego deste adesivo como técnica alternativa na síntese cutânea de felinos domésticos submetidos a laparotomia. Métodos - Foram utilizadas 25 gatas, nas quais realizou-se celiotomia mediana para ovariosalpingohisterectomia eletiva. Os procedimentos pré e trans-cirúrgicos foram habituais com preparo de rotina e do campo operatório, seguido por celiotomia pré-retroumbical, ligaduras dos pedículos e corpo uterino com fio de nylon 2-0 e sutura da linha alba com o mesmo material em pontos simples separados. Após aproximação do tecido subcutâneo com fio categute 4-0, foi empregada bandagem porosa adesiva hipoalergênica para cooptação das margens da ferida cirúrgica cutânea, seguida pela aplicação de película de poliuretano. Resultados - Todos animais foram reexaminados sete dias após o ato operatório, momento no qual a película foi removida. Não houve deiscência ou sinais de infecção em nenhum dos animais. No entanto, quatro gatas apresentaram eritema localizado na região de aplicação do material, o qual foi tratado com iodo povidine durante três dias consecutivos. Conclusão - Por meio dos resultados obtidos, conclue-se que o uso da película de poliuretano na pele em substituição às suturas convencionais após a realização de celiotomia representa procedimento mais rápido e prático que as técnicas usualmente utilizadas com este fim.

Comparison among Op-site, polyvinyl chloride film and tulle gauze in the treatment of skin graft donor sitet.

A prospective analytic study was performed at the Division of Plastic and Reconstructive Surgery, Department of Surgery, King Chulalongkorn Memorial University Hospital and the Department of Surgery, Chiang Mai University Hospital to compare among Polyvinyl chloride film (PVC film), Op-site and tulle gauze in the treatment of skin graft donor site. From October 1998 to January 2000, 81 donor sites in the same number of patients were treated by three different methods; tulle gauze (26 patients), Op-site (27 patients) and PVC film (28 patients). Each wound was followed until it was completely healed and visual analogue scale was used for pain evaluation. Donor site dressed with PVC film had a healing time of 10.44 days which was not different from Op-site (10.54 days) but significantly faster (p<0.001) than tulle gauze (17.84 days). Pain as measured with visual analogue scale in the group of PVC film (1.48) was not different from Op-site (1.34) but significantly less than (p<0.001) tulle gauze (5.45). There was no difference in the rate of infection between each group. In conclusion, the authors found no difference between Op-site and PVC film in healing time and pain. Both of them were better than tulle gauze. The results demonstrate the usefulness of PVC film as a donor site dressing as it promises relatively rapid healing, less pain and is inexpensive.