Exposición compleja de placa craneal / Complex exposure of cranial plate

Es recomendable que los pacientes con antecedentes de trauma craneal moderado o grave, con pérdida de fragmentos de calota, que deben reparar con posterior craneoplastia, la realicen luego de 3 a 6 meses, reduciendo el riesgo de infección y de hipertensión endocraneana. Los materiales a utilizar son diversos; y para evitar la reapertura es fundamental un cierre sin tensión, en dos planos y sin tejido desvitalizado. Las infecciones son raras; son más frecuentes cuando la craneopatía se realizó dentro del 1er año del trauma. Otra complicación es la úlcera crónica, de manejo muy complejo. Material y métodos. Paciente de 58 años, sufrió un traumatismo encefalocraneano con pérdida de conocimiento en el año 2011, por accidente de tránsito; craneoplastia realizada a 8 meses del trauma, posterior ulceración sobre líneas de incisión en dos oportunidades, reparado en ambas con colgajos locales, conservando la placa craneal. La paciente consultó presentando nueva ulceración parietal izquierda y adelgazamiento del cuero cabelludo y translucencia del material frontoparietal izquierdos; sin infección local; y múltiples cicatrices remanentes. Se retiró la placa craneal, y a dos años se realizó expansión con insuflados lentos controlados con la signosintomatología que presentaba la paciente. Al 3er mes se recolocó nueva placa de titanio y cobertura con colgajos del cuero cabelludo. Discusión. La expansión tisular del cuero cabelludo es un método simple, con baja frecuencia de complicaciones si la técnica es delicada y atendemos la signosintomatología del paciente. Conclusión. El trabajo conjunto multidisciplinario, es la piedra angular para obtener resultados óptimos en la reconstrucción de lesiones complejas.

Patients with a history of moderate or severe skull trauma, with loss of shell fragments, which must be repaired with subsequent cranioplasty, it is recommended to perform it after 3 to 6 months, reducing the risk of infection and endocranial hypertension. The materials to use are diverse; and to avoid reopening, a tension-free closure is essential, in two planes and without devitalized tissue. Infections are rare, being more frequent when the craniopathy took place within 1 year of the trauma. Another complication is the chronic ulcer, very complex to handle. Material and methods. Fifty eight year-old patient, suffered a traumatic brain injury with loss of consciousness in 2011, due to a traffic accident; craneoplasty performed 8 months after trauma, subsequent ulceration on incision lines on two occasions, both repaired with local flaps, preserving the cranial plate. The patient consulted presenting a new left parietal ulceration, and thinning of the scalp and translucency of the left fronto-parietal material; no local infection; and multiple remaining scars. The cranial plate was removed, and two years later, expansion was performed with slow insufflants controlled with the patient's symptom sign. At the 3rd month, a new titanium plate was replaced and covered with flaps of the scalp. Discussion. Tissue expansion of the scalp is a simple method, with little frequency of complications if the technique is delicate, and we attend to the patient's sign-symptomatology. Conclusion. Multidisciplinary joint work is the cornerstone for obtaining optimal results in the reconstruction of complex injuries.

Desempenho do Stent Recoberto por Titânio-Óxido Nítrico em Pacientes com Doença Coronária Multiarterial / Performance of the Titanium-Nitride-Oxide Coated Stent in Patients with Multivessel Coronary Artery Disease

Introdução: Até o momento, nenhum estudo avaliou o stent recoberto por titânio-óxido nítrico em pacientes com doença arterial coronariana multiarterial. Comparamos o desempenho do stent Titan-2® ao stents farmacológicos de segunda geração nesse cenário. Métodos: No período de 2011 a 2012, 284 pacientes foram tratados com o stent Titan-2®, dos quais 100 (35,2%) eram portadores de doença arterial coronariana multiarterial. Esse grupo foi comparado a 100 pacientes, de um grupo de 304 (38,9%), com doença arterial coronariana multiarterial, tratados com o stent farmacológico de segunda geração com polímeros duráveis ou biodegradáveis. O desfecho primário foi a ocorrência de eventos cardíacos adversos maiores em 1 ano. Resultados: Características clínicas, angiográficas e do procedimento não apresentaram diferenças entre os grupos. A maioria dos pacientes do grupo Titan-2® era do sexo masculino (70%), com idade de 68,4 ± 12,9 anos e 25% eram diabéticos. Predominaram os quadros clínicos estáveis (68%), 51% tinham acometimento triarterial e a função ventricular estava preservada. A incidência de eventos cardiovasculares adversos maiores em 1 ano no grupo Titan-2® foi de 21% (vs. 17%; p = 0,59), óbito ocorreu em 3% (vs. 2%; p > 0,99) dos pacientes, infarto do miocárdio em 5% (vs. 4%; p > 0,99) e nova revascularização miocárdica em 13% (vs. 11%; p = 0,83). Não foram constatadas tromboses de stent definitivas em nenhum grupo. Conclusões: O uso do Titan-2® apresentou resultados similares aos do stent farmacológico de segunda geração, o que o torna atrativo para ser utilizado no complexo cenário de pacientes portadores de doença arterial coronariana multiarterial...

Background: To date, there are no studies evaluating the use of the titanium-nitride-oxide coated stent in patients with multivessel coronary artery disease. We have compared the performance of the Titan-2® stent to that of the second generation drug-eluting stents in this scenario. Methods: From 2011 to 2012, 284 patients were treated with the Titan-2® stent, of which 100 (35.2%) had multivessel coronary artery disease. This group was compared to 100 patients, of a group of 304 (38.9%) patients with multivessel coronary artery disease treated with second generation drug-eluting stents with durable or biodegradable polymers. The primary endpoint was the occurrence of major adverse cardiovascular events at 1 year. Results: Clinical, angiographic and procedure-related characteristics of the patients did not show differences between groups. Most patients in the Titan-2® group were male (70%), mean age was 68.4 ± 12.9 years and 25% were diabetic. Stable symptomatic patients were prevalent (68%), 51% had three-vessel disease and ventricular function was preserved (55.6 ± 12.7%). The incidence of major adverse cardiovascular events at 1 year in the Titan-2® group was 21% (vs. 17%; p = 0.59), death was observed in 3% (vs. 2%; p > 0.99) of the patients, acute myocardial infarction in 5% (vs. 4%; p > 0.99) and a new revascularization procedure in 13% (vs. 11%; p = 0.83). Definitive stent thrombosis was not observed in either group. Conclusions: The Titan-2® stent showed similar results to those of the second-generation drug-eluting stents, which makes it attractive for use in the complex scenario of patients with multivessel coronary artery disease...

Assessment of sternal closure using titanium plate / Avaliação do fechamento esternal com placa de titânio

INTRODUCTION: The use of plates and screws for more rigid fixation of the sternum, without maintaining contact between the upper portion of the sternum and mediastinum. The present study seeks new choice of plate with a significant difference, the same does not need to be removed in order to proceed to open when necessary sternal emerging opening of the bone. OBJECTIVE: The current study aims to evaluate the efficacy and safety of this procedure. METHODS: To this end, we selected ten patients with coronary artery disease have shown no significant risk factors for mediastinitis. The surgery was thus performed in the usual way that all patients with coronary artery disease surgeries are done at the institution. Only at the time of sternal closure is that there was a change, with the combination of steel wires and plates. RESULTS: All cases had sternal closure properly with good outcome in the medium term. CONCLUSION: The use of plates ENGIMPLAN proved safe and effective for sternal closure.

INTRODUÇÃO: A utilização de placas e parafuso para a mais rígida fixação do esterno, sem manter contato entre a porção superior do esterno e o mediastino. O estudo atual busca nova opção de placa, com um diferencial importante; a mesma não precisa ser retirada para que se proceda à abertura esternal em caso de necessidade emergente de abertura do osso. OBJETIVO: O presente estudo tem por objetivo avaliar a eficácia e a segurança de tal procedimento. MÉTODOS: Para tal, foram selecionados dez pacientes portadores de doença arterial coronária que não apresentassem importantes fatores de risco para mediastinite. As cirurgias foram, portanto, realizadas da maneira habitual, a todas os procedimentos em portadores de coronariopatias são feitas na Instituição. Somente no momento do fechamento esternal é que houve uma modificação, com a associação de fios de aço e placas. RESULTADOS: Todos os casos apresentaram fechamento esternal de forma adequada com boa evolução a médio prazo. CONCLUSÃO: O emprego das placas ENGIMPLAN se mostrou seguro e eficaz no fechamento esternal.

Stent aórtico pulsátil: uma nova alternativa na assistência ventricular crônica / Pulsatile stent graft: a new alternative in chronic ventricular assistance

OBJETIVO: A insuficiência cardíaca é uma das causas mais comuns de internação. Dispositivos para assistência circulatória crônica foram testados e, em sua maioria, são de alta complexidade. O objetivo deste estudo é a descrição de uma endoprótese contrátil com capacidade de pulsação crônica no interior da aorta descendente, de maneira semelhante à produzida pelo balão intra-aórtico. MÉTODOS: Endopróteses pulsáteis compostas de níquel-titânio foram posicionadas de forma a envolver tubos de látex, simulando a aorta. Diferentes correntes elétricas foram aplicadas a unidades ligadas em série, de modo a causar contração da estrutura e deslocamento de uma coluna líquida. Foram realizadas duas sequências de testes: a primeira com duas gaiolas metálicas e a segunda com cinco gaiolas. Na primeira sequência de testes, aplicou-se tensão de 16,3 volts e corrente de 5 amperes e, na segunda sequência, tensão de 15 volts e corrente de 7 amperes. RESULTADOS: Na primeira sequência de testes, obteve-se o efeito pulsátil dos 2 stents, havendo contração do tubo e deslocamento da coluna d'água suficientes para validar o efeito pulsátil da endoprótese. As duas estruturas ejetaram um volume de 2,6 mL por ciclo, com uma variação de 29 mm na altura da coluna de água, equivalente a 8% de contração durante a pulsação. Na segunda sequência, conseguiu-se uma variação de 7,4 mL por ciclo. CONCLUSÃO: Os resultados obtidos comprovam a contratilidade da endoprótese pulsátil ativada pela aplicação de corrente elétrica. Continuidade do estudo e aperfeiçoamento do material se fazem necessários para obtenção de modelo mais eficiente do ponto de vista energético e com maior pulsação, para permitir volumes de ejeção comparáveis aos de balões intra-aórticos.

OBJECTIVE: Heart failure is currently one of the most common hospitalization causes. Several chronic circulatory assist devices have been tested and are highly complex. The objective is the description of a pulsatile endoprosthesis capable of applying a chronic pulse within the descending aorta, similar to that produced by intra-aortic balloon. METHODS: Pulsatile stents composed of nickel-titanium were built and positioned to engage latex tubes simulating the aorta. Different electric currents were applied to units connected in series in order to cause structure contraction and displacement of a liquid column. There were two sequence tests: first composed of two metallic cages and the second composed of five cages. At first sequence tests was applied a voltage of 16.3 volts and a current of 5 amperes. In the second, voltage of 15 volts and current of 07 amperes. RESULTS: In the first sequence was obtained the pulsatile effect of stent, with contraction of the tube and displacement of the water column sufficient to validate the pulsating effect of the endoprosthesis. The two structures ejected a volume of 2.6 ml per cycle, with a range of 29 mm in height of the column of water equivalent to 8% shrinkage during the pulse. In the second sequence, it reachead a variation of 7.4 mL per cycle. CONCLUSION: The results obtained confirm the stent pulsatile contractility activated by electrical current. The continuity of the study and material improvement are necessary to obtain more efficient model from the point of view of energy and pulse, to allow ejection volumes comparable with the intra-aortic balloons.

Radical cystectomy with W-shaped orthotopic ileal neobladder constructed with non-absorbable titanium staples-long term follow-up

Purposes We retrospectively assessed our experience with the W-shaped orthotopic ileal pouch, which was constructed with non –absorbable titanium staples. For these purpose, we discuss the results of bladder capacity, urinary continence and early and long-term postoperative complications. Materials and Methods We included in the study 17 patients who underwent radical cystoprostatectomy followed by construction of an orthotopic W-shaped ileal pouch between October 2000 and November 2009. A 65-70 cm segment of ileum was isolated and prearranged into a W- configuration, leaving two 10 cm intact segments on both sides of the ileal fragment. In our technique we entirely anatomized all adjacent limbs in order to create a sphere-shaped pouch. The ureters were directly anastomized to both intact segments of the ileal division. All our patients underwent pouchscopy 6 months after operation and annually. Results Mean operative time for neobladder reconstruction and ureteral anastomoses was 87 ± 7.67 minutes. In one patient a leak from the ileo-ileal anastomosis was confirmed on the 3rd day after operation. In 2 cases unilateral stricture of the ureteral-neobladder anastomosis was documented. Staple lines were mostly covered with ileal mucosa after 6 months. The mean functional bladder capacity was 340 ± 27.6 mL and 375 ± 43.4 mL at 6 and 12 months, respectively. First-year daytime and nighttime continence was good and acceptable in 90% and 78% of patients, while it increased to 95% during the 2nd year. Conclusions The long term follow-up shows that non-absorbable titanium staples can be safely used for creation of an orthotopic ileal neobladder. However, these data should be further validated in a larger series of patients. .

Flexible intramedullary nails with traction versus plaster cast for treating femoral shaft fractures in children: comparative retrospective study / Hastes intramedulares flexíveis com tração versus aparelho gessado para o tratamento de fraturas diafisárias do fêmur em crianças: estudo comparativo retrospectivo

Femoral fractures are common in children between 2 and 12 years of age, and 75% of the lesions affect the femoral shaft. Traction followed by a plaster cast is universally accepted as conservative treatment. However, in some situations, a surgical approach is recommended. The objective here was to compare treatments for femoral shaft fractures using intramedullary nails (titanium elastic nails, TEN) versus traction and plaster casts in children. The hypothesis was that TEN might provide better treatment, with good clinical results in comparison with plaster casts.

This retrospective comparative study was conducted in a public university hospital.

Sixty children with femoral fractures were evaluated; 30 of them underwent surgical treatment with TEN and 30 were treated conservatively using plaster casts. The patients' ages ranged from 5 to 13 years (mean of 9 years).

The mean duration of hospitalization was nine days for the surgical group and 20 days for the conservative group. The incidence of overgrowth in the patients treated with TEN was 60.0% and, for those treated conservatively, 13.3%. Partial weight-bearing was allowed after 3.5 weeks in the surgical group and after 9.6 weeks in the conservative group. New hospitalization was required for 90.0% in the surgical group and 16.7% in the conservative group. Patients treated with plaster casts presented higher incidence of complications, such as loss of reduction.

The surgical method presented better results for children. .

Fraturas femorais são comuns em crianças entre 2 e 12 anos de idade, e 75% das lesões acometem a diáfise. Tração seguida de aparelho gessado (“gesso”) é universalmente aceita como tratamento conservador. Entretanto, em algumas situações o tratamento cirúrgico é recomendado. O objetivo foi comparar o tratamento de fraturas diafisárias do fêmur com hastes intramedulares (titanium elastic nails, TEN) com tração e gesso em crianças. A hipótese era de que TEN pode ser melhor tratamento, com bons resultados clínicos em comparação com o gesso.

Este estudo retrospectivo e comparativo foi conduzido num hospital público universitário.

Sessenta crianças com fraturas de fêmur foram avaliadas, 30 delas foram submetidas a tratamento cirúrgico com TEN e 30 foram tratadas de forma conservadora usando gesso. A idade dos pacientes variou de 5 a 13 anos (média de 9 anos).

O tempo médio de internação foi de 9 dias para o grupo cirúrgico e 20 dias para o grupo conservador. A incidência de crescimento excessivo nos pacientes tratados com TEN foi de 60,0% e, para aqueles tratados de forma conservadora, 13,3%. Sustentação parcial de peso foi permitida após 3,5 semanas no grupo cirúrgico e após 9,6 semanas no grupo conservador. Houve 90,0% de novas internações no grupo cirúrgico e 16,7% no grupo conservador. Pacientes tratados com gesso apresentaram maior incidência de complicações, tais como perda de redução.

Análise microbiológica comparativa da ação de diferentes agentes descontaminantes sobre superfícies de titânio / Microbiological comparison of different decontaminant agents on rough and smooth titanium surfaces: microbiological analysis

Os implantes de titânio estabeleceram-se, ao longo do tempo, como uma opção de tratamento com grande índice de sucesso. Entretanto, falhas são passíveis de ocorrer, devido à exposição de suas superfícies ao meio bucal, imediatamente ou até muito tempo passado de sua implantação. Estas superfícies de titânio podem se infectar por bactérias e seus produtos, de forma semelhante à que ocorre na superfície de raízes dentais. Tais contaminantes intensificam a resposta inflamatória, além de alterar a estrutura superficial do implante podendo dar origem às doenças peri-implantares, como a mucosite peri-implantar e a peri-implantite. Para o tratamento destas doenças, diversos métodos de descontaminação de superfícies de implantes têm sido propostos, incluindo o uso substâncias anti-sépticas, jatos abrasivos, ácidos, antibióticos e lasers. O objetivo foi avaliar comparativamente a capacidade de descontaminação do peróxido de hidrogênio a 1,5 % (H2O2), do gluconato de clorexidina a 0,12% (CLX) e do soro fisiológico (SF) já que, até o momento, nenhuma metodologia está estabelecida como padrão ouro para a limpeza superficial. Placa bacteriana foi colhida de sítios de doença periodontal crônica para contaminação de discos de titânio de superfícies lisas e rugosas. Posteriormente, os discos foram submersos em 10 mL das substâncias estudadas por 1 minuto, friccionados com swab e enxaguados em solução fisiológica. Discos controle (C) foram somente enxaguados em soro fisiológico. Desta forma resultaram os seguintes grupos de estudo, constituídos de 5 discos de cada tipo de superfície lisa (L) e rugosa (R): H2O2 R , CLXR, SFR, CR, H2O2L, CLXL , SFL e CL. A avaliação do potencial descontaminante das substâncias foi realizada através da quantificação do crescimento bacteriano pela contagem das unidades formadoras de colônia (UFCs) após semeadura em Agar-brucella e incubação em jarra de CO2 a 37oC por 24 horas. Os resultados após descontaminação foram comparados através da...

Actually, the titanium implants are a successful option of treatment in Dentistry. However, failures are possible to occur due to surface exposition to oral environment immediately or lately after its implantation. The titanium implants surfaces can be infected by bacteria and its products similarly to dental roots surfaces. The contaminants turn the inflammatory response tissues more intensive and them alter the surface structure of the implant and cause periimplant diseases like mucositis and peri-implantitis. Several methods of treatment for those diseases have been proposed in the literature, including antiseptics rinses, abrasives air powder, acids, antibiotics and lasers. The aim of this work was to comparatively evaluate the potential for decontamination of the hydrogen peroxide at 1,5% (H2O2), the 0,12% chlorhexidine gluconate (CLX) and the saline solution (SF) as cleaning methods, once until this moment there is not a gold standard method established for this purpose. Bacterial plaque harvested from sites of chronic periodontal disease was used to contaminate smooth and rough surfaces of titanium. Subsequently, decontamination procedures were realized by submerging the discs in 10 ml of the studied substances for 1 minute, cleaned by rubbing with swab and washed on saline solution. Control discs (C) were only washed in saline solution. The following test groups composed by 5 discs of each surface, smooth (L) and rough (R):, were then originated: H2O2 R , CLXR, SFR, CR, H2O2L, CLXL , SFL and CL. The decontaminant potential of studied substances was realized by counting the colony forming units after seeding in Agar-brucella, under anaerobiosis condition for 24 hours under 37oC. The data analysis was made by Variance Analysis (ANOVA) at 5% of significance level. The results lead to the following conclusions: the chronic periodontal biofilm adhesion was possible on smooth and rough titanium surfaces; the surface characteristic had no significant...

Cirugía mínimamente invasiva: promontofijación laparoscópica con malla y anclaje de titanio para prolapso de cúpula vaginal / Minimally invasive surgery: laparoscopic promontofixation with mesh and titanium anchor for vaginal vault prolapse

OBJETIVO: Analizar y evaluar la factibilidad técnica, eficacia y seguridad de la promontofijación laparoscópica con malla y anclajes helicoidales de titanio para el tratamiento del prolapso de cúpula vaginal. MÉTODO: Entre noviembre de 2005 y julio de 2006, en el Servicio de Ginecología del Hospital Clínico de la Universidad Católica, se efectuaron 5 promontofijaciones laparoscópicas, utilizando técnica consistente en malla unida al promontorio del sacro con anclajes helicoidales de titanio. El rango de edad de las pacientes fue entre 46 y 65 años, con paridad vaginal entre 2 y 3. RESULTADOS: La técnica quirúrgica logró corregir el defecto en las 5 pacientes. No hubo complicaciones intraoperatorias, ni post operatorias, con rápida recuperación y reintegración a las actividades habituales. CONCLUSIONES: Nos enfrentamos a una novedosa técnica, segura y reproducible, con las ventajas de la laparoscopia, alta precoz y estéticamente óptima.

OBJECTIVE: To analyze and evaluate the technical feasibility, effectiveness and security of the laparoscopic sacrocolpopexy with mesh and helical titanium anchorages for the treatment of vaginal vault prolapse. METHOD: Between November 2005 and July 2006, five laparoscopic sacrocolpopexies, using this technique, took place in the Gynecology Service of the Clinical Hospital of Pontificia Universidad Católica de Chile, consisting of mesh joined to the sacro promontory with helical titanium anchorages. The age of the patients was between 46 and 65 years, with vaginal parity between 2 and 3. RESULTS: In all patients the surgical technique corrects the defect. There were no interoperating or postoperating complications, with a prompt recovery and reintegration to usual activities. CONCLUSIONS: We face a novel, safe and reproducible technique, with the advantages of the laparoscopy, early leave hospital and esthetically optimum.

The use of a modular titanium endoprosthesis in skeletal reconstructions after bone tumor resections: method presentation and analysis of 37 cases

We analyzed 37 patients who underwent segmental wide resection of bone tumors and reconstruction with a modular titanium endoprosthesis at the Orthopaedic Oncology Group, between 1992 and 1998. Twelve patients were male and 25 were female, with a mean age of 30 years (9 - 81). The mean follow-up was 14 months (2 - 48). The diagnoses were: steosarcoma (14 cases), metastatic carcinoma (10), Ewing's sarcoma (4), giant cell tumor (4), malignant fibrous histiocytoma (3), chondrosarcoma (1), and aneurysmal bone cyst (1). Eleven articulated total knee, 8 partial proximal femur with bipolar acetabulum, 8 partial proximal humerus, 3 total femur, 2 partial proximal tibia, 2 diaphyseal femur, 2 diaphyseal humerus, and 1 total proximal femur with cementless acetabulum endoprosthesis implant procedures were done. The complications related to the procedure included: infection (5 cases), dislocation (3), module loosening (1), and ulnar nerve paresthesia (1). We used the following criteria for the clinical evaluation: presence of pain, range of motion, reconstruction stability, surgical and oncologic complications, and patient acceptance. The results were good in 56.8 per cent of the cases, regular in 32.4 per cent and poor in 10.8 per cent.

Reservorio subcutáneo venoso como acceso vascular en el paciente oncológico / Venous subcutaneous reservoir as a vascular acces in the oncological patient

Presentamos cuatro años de experiencia con el manejo de 135 pacientes oncológicos a quienes de les colocó catéter Port-A-Cath. Los padecimientos oncológicos asociados más frecuentes fueron: cáncer de mama (34.81 por ciento), cáncer broncopulmonar (14 por ciento) y linfoma (9.62 por ciento). El 97.7 por ciento de los catéteres se colocaron en la vena cava superior y el 2.2 por ciento en la vena cava inferior. No hubo mortalidad operatoria. Se observó morbilidad operatoria en el 2.2 por ciento de los pacientes: en dos casos hubo malposición del catéter hacia la vena yugular interna y en uno se presentó infección de la herida quirúrgica. Se obtuvo un seguimiento completo en el 80 por ciento de los casos que varió de 0.3 a 47 meses, durante el cual el 50 por ciento de los pacientes fallecieron, en promedio, a los 8.14 meses por progresión de su enfermedad oncológica. La mortalidad no operatoria se registro sólo en cinco enfermos (4.62 por ciento): uno con necrosis cutánea por infusión subcutánea de adriamicina, otro con fractura parcial del catéter, uno más con trombosis venosa profunda axilo-subclavia, otro con trombosis del reservorio y el último con migración espontánea del catéter. En el 95.37 por ciento de los pacientes restantes, sus catéteres funcionaron sin problemas y fueron utilizados en promedio cada 28 días. Con base a los resultados de este estudio, podemos concluir que el empleo del catéter port-A-Cath como reservorio subcutáneo venoso para acceso vascular central en el paciente oncológico tiene nula mortalidad operatoria, mínima morbilidad y fue de gran ayuda y confort en le manejo quimioterapéutico de estos enfermos