Manejo de defectos óseos complejos por la técnica de inducción de membrana / Membrane induced technique in the management of complex osseous defects

El manejo de pseudoartrosis infectadas, osteomielitis y defectos óseos representa un reto enorme para el cirujano ortopedista. Hace diez años, Masquelet presentó la técnica de inducción de membrana como alternativa al manejo de las complicaciones mencionadas arriba con excelentes tasas de consolidación y erradicación del proceso infeccioso. Estudiamos una de serie de 14 casos, prospectiva, con seguimiento clínico y radiológico mínimo de 2 años (enero 2015-diciembre 2018), donde evaluamos múltiples variables en pacientes a quienes se les realizó el protocolo de Masquelet. Obtuvimos una tasa de consolidación de 85,7% (12/14). Con un tiempo promedio para alcanzarla de 6,1 meses (3-9m). Todos los pacientes que lograron la consolidación se encontraban libres de infección al final del seguimiento. Por su reproducibilidad y alta tasa de consolidación, consideramos la técnica de inducción de membrana, como una excelente opción en el manejo de pseudoartrosis infectadas complejas(AU)

The management of infected nonunions, osteomyelitis, and bone defects represents an enormous challenge for the orthopedic surgeon. Ten years ago, Masquelet presented the membrane induction technique as an alternative to the management of the complications afore mentioned with excellent rates of consolidation and eradication of the infectious process. We prospectively studied a series of 14 cases, with a clinical and radiological follow-up of at least 2 years (january 2015-december 2018). Where we evaluated multiple variables in patients who underwent the Masquelet protocol. We obtained a consolidation rate of 85.7% (12/14). With an average time to reach it of 6.1 months (3-9m). All patients who achieved union were free of infection at the end of follow-up. Due to its reproducibility and high consolidation rate, we consider the membrane induction technique an excellent option in the management of complex infected nonunions(AU)

Virtual planning and construction of prototyped surgical guide in implant surgery with maxillary sinus bone graft

PURPOSE: To evaluate the efficacy of associating techniques of bone grafting in the maxillary sinus with the use of a prototyped surgical guide for planning and positioning dental implants in total edentulous maxillae, rehabilitated after six months. METHODS: Eight patients consecutives with totally edentulous maxilla presenting few remaining bone in the posterior alveolar ridge, associated with pneumatization of the maxillary sinus were selected. Twenty eight Brånemark RP 10mm implants were installed in 14 maxillary sinuses. The surgical planning for the implant installation was performed with the DentalSlice software by means of a computerized tomography. The obtained images were used for building a surgical guide that, placed over the maxilla, showed the exact position for the implants installation (prototyped surgical guide). The portion of the implants that went into the maxillary sinus was covered by an autogenous bone graft. RESULTS: The patients were re-evaluated six months after the surgery and a 100% success rate was achieved. All of the implants presented no mobility or symptoms, permitting an oral rehabilitation with total fixed screw-retained prosthesis over the implants. CONCLUSION: The technique of associating implants and bone graft in the maxillary sinus aided by a prototyped guide planned on DentalSlice has showed itself efficient for positioning implants and for quantifying and locating the bone graft.

Particularities in the surgical technique of calvaria graft / Particularidades en la técnica quirúrgica de injerto de calota

Calvaria grafts provide good bone quantity for the reconstruction of the atrophic maxilla, and have lower morbidity and resorption rates when compared to iliac crest. The aim of this paper is to present the technique for obtaining a graft of the skull. Initially, the depth of the osteotomy is determined by a manually conducted bur, which establishes the limits of the structures of the skull (outer table, diploe and inner table), making the removal of bone blocks easier and safer. Thus, osteotomies of the blocks are made with greater security, avoiding the complications inherent to surgical technique. The case that will be presented it is from a male patient of 65 years who refused to submit to the iliac crest graft, opting for the calvaria, despite being bald, that is a contraindication for this treatment modality. A delicate suture associated with placement of titanium mesh to maintain the conformation of the patient's skull in the region of the bone defect, created after removal of the graft, provided a good cosmetic result at the donor site. The use of titanium mesh for re-anatomization of bone defects created in the grafts is well indicated for bald patients...

Los injertos de calvaria proporcionan una buena cantidad de hueso para la reconstrucción del maxilar atrófico, y tienen menores tasas de morbilidad y reabsorción en comparación con la cresta ilíaca. El objetivo de este trabajo es presentar la técnica para la obtención de un injerto del cráneo. Inicialmente, la profundidad de la osteotomía se determina mediante una fresa manualmente, lo que establece los límites de las estructuras del cráneo (tabla externa, diploe y tabla interna), lo que hace la eliminación de bloques óseos más fácil y segura. Por lo tanto, las osteotomías de los bloques se hacen con mayor seguridad, evitando las complicaciones inherentes a la técnica quirúrgica. Se presenta el caso de un paciente hombre de 65 años que se negó a ser sometido a injerto de cresta ilíaca, optando por la bóveda craneal, a pesar de ser calvo, que es una contraindicación para esta modalidad de tratamiento. Una sutura cuidadosa asociada con la colocación de malla de titanio para mantener la conformación del cráneo del paciente en la región del defecto óseo creado después de obtención del injerto, deja un buen resultado cosmético en el sitio donante. El uso de malla de titanio para la re-anatomización de defectos óseos creados en los injertos está bien indicada para pacientes calvos...

FisiograftTM as a bone material in the treatment of periodontal vertical defects and its clinical and radiological evaluation: clinical study / FisiograftTM como material de enxerto ósseo no tratamento de defeitos periodontais verticais e sua avaliação clínica e radiográfica: um estudo clínico

Objectives: The purpose of this clinical study is to determine the efficacy of Fisiograft™ as a bone graft materialin the treatment of three wall vertical defects in generalized chronic periodontitis patients and theirclinical and radiological evaluation. Materials and methods: Twenty patients (with 30 defects) diagnosedwith generalized chronic periodontitis having two or more three wall vertical defects were selected for thisstudy. Clinical parameters like plaque index, gingival index, probing pocket depth and clinical attachmentlevels were recorded at different points of time over six months. Radiographic evaluation included the depthof the bone defect and the percentage of bone defect fill, and was carried out for both the groups at baseline,three months and six months. After recording clinical parameters and administering phase-1 therapy, thesites were randomly treated either with Fisiograft™ or open flap debridement only. Results: At the end of sixmonths there was a significant reduction in the plaque and gingival scores in both test and control groups.There was 64% decrease in probing pocket depth for the test site as compared to 55% decrease seen for thecontrol group. Similarly there was an 85% gain in clinical attachment level from the baseline to six monthspost operatively for the experimental group in comparison to 69% gain for the control group. Furthermore,44% bone fill was observed for the experimental site whereas only 18% of bone fill was evident in the controlsite. Conclusion: Fisiograft™ improves healing outcomes, leads to a reduction of probing depth, a resolutionof osseous defects and a gain in clinical attachment, compared with open flap debridement by itself.

Objetivo: O objetivo do presente estudo clínico foi determinar a eficácia do Fisiograft®, como material de enxerto ósseo, no tratamento de defeitos ósseos verticais de três paredes em pacientes com periodontite crônica,bem como avaliações clínica e radiográfica. Materiais e métodos: Vinte pacientes (com 30 defeitos)diagnosticados com periodontite crônica generalizada, portando dois ou mais defeitos ósseos verticais detrês paredes foram selecionados para o estudo. Parâmetros clínicos como índice de placa, índice gengival,profundidade de bolsa à sondagem e níveis clínicos de inserção foram registrados em diferentes intervalos de tempo até seis meses. Avaliações radiográficas incluíram a profundidade do defeito ósseo e a porcentagem de preenchimento do defeito ósseo, sendo realizadas em ambos os grupos imediatamente (baseline),em três meses e seis meses. Após registrar os parâmetros clínicos e administrar a terapia de fase-1, os locais foram tratados aleatoriamente com Fisiograft® ou retalho de espessura total somente. Resultados: Ao fim do período de seis meses houve redução significativa nos índices de placa e gengival em ambos os grupos,controle e experimental. Houve redução de 64% na profundidade de bolsa à sondagem para os locais de teste comparado, 55% de redução no grupo controle. Similarmente, houve ganho de 85% no nível clínico de inserção do baseline para o período de seis meses de pós-operatório para o grupo experimental em comparação ao ganho de 69% para o grupo controle. Adicionalmente, um preenchimento ósseo de 44% foi observado para os locais experimentais, enquanto somente 18% de preenchimento foi evidente nos locais de controle.Conclusão: O Fisiograft® melhora os resultados de cicatrização, promove redução na profundidade de sondagem,constitui uma resolução para os defeitos ósseos e aumento na inserção clínica, comparado ao retalho de espessura total somente.

Reconstruccion acetabular con injerto oseo molido e impactado / Acetabular reconstruction with impacted morselized bone graft

Introducción: Evaluación retrospectiva de una serie consecutiva de reconstrucciones acetabulares con técnica de injerto óseo molido e impactado, intentando determinar su utilidad en distintos defectos acetabulares. Materiales y métodos: El grupo de estudio comprendió 61 revisiones acetabulares en 60 pacientes. El tiempo de seguimiento promedio fue de 68 meses (60 a 120 meses). La media de edad de los pacientes fue de 66 años (rango 39 a 88 años); 17 (28,33 por ciento) fueron varones y 43 (81,66 por ciento), mujeres. Los defectos acetabulares se evaluaron mediante la clasificación de Paprosky. En todos los casos se utilizó injerto óseo molido criopreservado no irradiado con copa acetabular cementada y aletada sin anillo de refuerzo, según la técnica original de Slooff. Se realizó la evaluación radiológica, determinándose la migración horizontal y vertical del cotilo con respecto a la imagen en lágrima. Se consideró incorporación ósea del injerto al observar su remodelación trabecular y cuando la densidad y la arquitectura eran semejantes a las del hueso nativo. La falla radiológica se determinó cuando se demostró migración acetabular igual o mayor de 4 mm o angulación de 5°. Resultados: De 61 cotilos evaluados en 60 pacientes, 48 (78,6 por ciento) pertenecieron a defectos de tipo II; se observó incorporación y trabeculado del injerto en 46 (96 por ciento) cotilos entre el tercero y el sexto mes posoperatorio. La evaluación clínica preoperatoria fue, en promedio, de 9,2 ± 0,6 y la posoperatoria, de 16,1 ± 0,9. Trece casos (21 por ciento) fueron defectos de tipo III. En 10 de ellos se determinó falla radiológica. La evaluación clínica preoperatoria fue, en promedio, de 5,3 ± 0,4 y la posoperatoria, de 9,3 ± 1,17. Conclusiones: En la clasificación de Paprosky la diferencia entre los defectos de tipos II y III se basa, fundamentalmente, en la migración acetabular mayor de 2 cm. El injerto molido e impactado sin utilizar anillo de refuerzo en defectos de tipo II d...