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1.
Acta Med Okayama ; 75(6): 751-754, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34955545

RESUMO

The improved cemented cup technique has attained excellent long-term results in primary total hip arthroplasty. When cup revision surgery was performed, the cemented cup, which was loosened at the bone-cement interface, was easily removed. However, with a well-fixed bone-cement interface, it remains difficult to remove the cemented cup for a revision in the event of a recurring dislocation. In addition, protrusions in the cement can cause unpredictable bone defects. A new removal device was created and used successfully to remove a well-fixed cemented cup safely and efficiently. This report introduces the device and the technique used in cemented cup removal.


Assuntos
Artroplastia de Quadril , Cimentos Ósseos , Remoção de Dispositivo/instrumentação , Reoperação/instrumentação , Idoso , Feminino , Humanos
2.
Acta Med Okayama ; 60(6): 311-8, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17189974

RESUMO

The present retrospective study assessed radiographs to determine socket wear in total hip arthroplasty (THA) with 22-mm zirconia or COP (Cobalt-Chrome alloy rich in Cobalt and Phosphorous) heads, and in cemented stems at more than 10 years after operation. Sockets of ultra high molecular weight polyethylene were used in each of two THA groups (13 hips each) in a clinical trial in our hospital between 1989 and 1990. Three observers carried out masked assessments of the radiographs. Upon final examination, there was no remarkable loosening in the zirconia or COP group, and no case had required revision surgery as of 2005. There was a statistically significant difference between the 2 groups in average annual linear wear, at 0.093 mm/year and 0.046 mm/year in the zirconia and COP groups, respectively. Volume wear and average annual volume wear were also significantly greater in the zirconia group despite its superior mechanical strength and toughness in vitro. Our present findings do not confirm early expectations of lower wear in long-term results of 22-mm zirconia femoral heads used in THA.


Assuntos
Artroplastia de Quadril , Ligas de Cromo , Prótese de Quadril , Zircônio , Adulto , Idoso , Cobalto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fósforo , Polietileno , Fatores de Tempo , Resultado do Tratamento
3.
Tissue Eng Part A ; 14(6): 1089-98, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19230129

RESUMO

CCN family protein 2/connective tissue growth factor (CCN2/CTGF) is a unique molecule that promotes the entire endochondral ossification process and regeneration of damaged articular cartilage. Also, CCN2 has been shown to enhance the adhesion and migration of bone marrow stromal cells as well as the growth and differentiation of osteoblasts; hence, its utility in bone regeneration has been suggested. Here, we evaluated the effect of CCN2 on the regeneration of an intractable bone defect in a rat model. First, we prepared two recombinant CCN2s of different origins, and the one showing the stronger effect on osteoblasts in vitro was selected for further evaluation, based on the result of an in vitro bioassay. Next, to obtain a sustained effect, the recombinant CCN2 was incorporated into gelatin hydrogel that enabled the gradual release of the factor. Evaluation in vivo indicated that CCN2 continued to be released at least for up to 14 days after its incorporation. Application of the gelatin hydrogel-CCN2 complex, together with a collagen scaffold to the bone defect prepared in a rat femur resulted in remarkable induction of osteoblastic mineralization markers within 2 weeks. Finally, distinct enhancement of bone regeneration was observed 3 weeks after the application of the complex. These results confirm the utility of CCN2 in the regeneration of intractable bone defects in vivo when the factor is incorporated into gelatin hydrogel.


Assuntos
Regeneração Óssea/efeitos dos fármacos , Fator de Crescimento do Tecido Conjuntivo/farmacologia , Gelatina/metabolismo , Hidrogel de Polietilenoglicol-Dimetacrilato/metabolismo , Absorção/efeitos dos fármacos , Animais , Osso e Ossos/efeitos dos fármacos , Osso e Ossos/patologia , Cartilagem/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Colágeno/metabolismo , Preparações de Ação Retardada/farmacologia , Escherichia coli , Células HeLa , Humanos , Camundongos , Osteoblastos/citologia , Osteoblastos/efeitos dos fármacos , Osteoblastos/metabolismo , Ratos , Ratos Wistar , Proteínas Recombinantes/farmacologia , Alicerces Teciduais
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