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1.
Acta Orthop Belg ; 89(3): 515-524, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37935237

RESUMO

Diminutive data is available on the outcome of several previously used total ankle replacement implants. The purpose of this study was to investigate the medium-term functional and radiological outcome and implant survival of the CCI Evolution implant. Consecutive series of 40 ankles operated in our hospital with primary TAR using the CCI Evolution implant in 2010-2013 were available for follow-up. The prospective clinical and radiographic data including the Kofoed score, subjective satisfaction and standard radiographs were collected preoperatively and at fixed time-points postoperatively. A CT was obtained in cases where osteolysis or loosening were suspected. The improvement of the Kofoed score and subjective satisfaction were statistically significant (p<0.0001). The implant survival was 97% (95% confidence interval (CI) 81%-100 %) at 5 years, and 81 % (95% confidence interval (CI) 60 %-92%) at 8 years. There were altogether 25 (64%) complications. Overall revision rate was 28% and failure rate 13%. The CCI implant outcome was not acceptable. The malposition of prosthetic components, subsidence, and peri-implant osteolysis were recorded often. Although the patient reported outcome measures improved, mostly due to positive changes in pain severity, overall revision and failure rates were high and comparable with previous findings of the CCI implant.


Assuntos
Artroplastia de Substituição do Tornozelo , Prótese Articular , Osteólise , Humanos , Artroplastia de Substituição do Tornozelo/efeitos adversos , Tornozelo , Seguimentos , Prótese Articular/efeitos adversos , Estudos Retrospectivos , Osteólise/diagnóstico por imagem , Osteólise/epidemiologia , Osteólise/etiologia , Estudos Prospectivos , Desenho de Prótese , Articulação do Tornozelo/diagnóstico por imagem , Articulação do Tornozelo/cirurgia , Reoperação/efeitos adversos , Resultado do Tratamento , Falha de Prótese
2.
Scand J Surg ; 107(1): 76-81, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28950789

RESUMO

BACKGROUND AND AIMS: Aneurysmal bone cysts represent about 1% of primary bone tumors. The standard treatment is curettage, followed by local adjuvant treatments and bone grafting. The problem is the high recurrence rate. The purpose of this study was to evaluate retrospectively the use of bioactive glass as a filling material in the treatment of aneurysmatic bone cysts in children. MATERIAL AND METHODS: A total of 18 consecutive children (mean 11.3 years at surgery; 10 males; 11 lower, 6 upper limb, 1 pelvis; 15 with primary surgery) with histologically proven primary aneurysmal bone cysts operated with curettage and bioactive glass filling between 2008 and 2013 were evaluated after a mean follow-up of 2.0 years (range, 0.7-5.1 years). RESULTS: Two (11%) patients showed evidence of aneurysmal bone cyst recurrence and both have been re-operated for recurrence. Bone remodeling was noted in all patients with remaining growth and no growth plate disturbances were recorded. Two patients needed allogeneic blood transfusion. No intraoperative or postoperative complications were recorded. CONCLUSION: We conclude that bioactive glass is a suitable filling material for children with primary aneurysmal bone cyst. Bioactive glass did not affect bone growth and no side effects were reported.


Assuntos
Materiais Biocompatíveis/uso terapêutico , Cistos Ósseos Aneurismáticos/diagnóstico por imagem , Cistos Ósseos Aneurismáticos/cirurgia , Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/cirurgia , Cerâmica/uso terapêutico , Adolescente , Remodelação Óssea/fisiologia , Criança , Pré-Escolar , Estudos de Coortes , Bases de Dados Factuais , Feminino , Seguimentos , Humanos , Masculino , Cuidados Pré-Operatórios , Radiografia/métodos , Estudos Retrospectivos , Medição de Risco , Resultado do Tratamento
3.
J Bone Joint Surg Br ; 91(7): 907-14, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19567855

RESUMO

Between 2002 and 2008, 130 consecutive ankles were replaced with an hydroxyapatite (HA) and titanium-HA-coated Ankle Evolutive System total ankle prosthesis. Plain radiographs were analysed by two independent observers. Osteolytic lesions were classified by their size and location, with cavities > 10 mm in diameter considered to be 'marked'. CT scanning was undertaken in all patients with marked osteolysis seen on the plain radiographs. Osteolytic lesions were seen on the plain films in 48 (37%) and marked lesions in 27 (21%) ankles. The risk for osteolysis was found to be 3.1 (95% confidence interval 1.6 to 5.9) times higher with implants with Ti-HA porous coating. Care should be taken with ankle arthroplasty until more is known about the reasons for these severe osteolyses.


Assuntos
Articulação do Tornozelo/diagnóstico por imagem , Prótese Articular/efeitos adversos , Osteólise/diagnóstico por imagem , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Articulação do Tornozelo/cirurgia , Artroplastia de Substituição/métodos , Durapatita , Feminino , Humanos , Interpretação de Imagem Assistida por Computador , Masculino , Pessoa de Meia-Idade , Osteólise/prevenção & controle , Osteólise/cirurgia , Radiografia , Titânio , Adulto Jovem
4.
Scand J Surg ; 96(3): 243-51, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17966751

RESUMO

BACKGROUND AND AIMS: Ceramic bone graft substitutes have a potential to be used as replacement of allogeneic bone grafting and, under optimal distribution of particle size, they may even provide mechanical support. The current study examined the efficacy of bioactive glass granules as an extender of autogenous bone grafting in a segmental bone replacement model of the canine femur. MATERIAL AND METHOD: A 16 mm long segment of the femur shaft was bilaterally replaced with an intercalary titanium implant in eight animals. The implant had cementless grooved proximal and distal stems. In one leg, the peri-implant space was packed with composite graft consisting of a mixture of bioactive glass granules and autogenous bone graft in proportion of 50:50. In the opposite leg, the peri-implant space was treated with autogenous bone graft alone. After surgery, unlimited functional loading was allowed. The outcome was evaluated at three months. RESULTS: Eight out of sixteen autografted implants and seven out of sixteen composite-grafted implants were radiographically incorporated and clinically stable at three months. In the paired comparison, the proximal components of composite-grafted implants showed lower maximum load under torsional testing (p = 0.068), less new bone in the longitudinal grooves of the stems (p = 0.036) and lower affinity of new bone to implant surface (p = 0.046). The distal components of the two sides showed a similar trend for less new bone in the grooves and lower bone affinity of new bone in the distal composite-grafted components. CONCLUSIONS: The current study suggests that supplementation of periprosthetic bone graft with bioactive ceramic particles may not help to promote healing of cementless implants under high dynamic loading conditions.


Assuntos
Materiais Biocompatíveis , Transplante Ósseo/métodos , Cerâmica/farmacologia , Fêmur/cirurgia , Animais , Fenômenos Biomecânicos , Modelos Animais de Doenças , Cães , Fêmur/diagnóstico por imagem , Fêmur/fisiopatologia , Sobrevivência de Enxerto , Desenho de Prótese , Tomografia Computadorizada por Raios X , Transplante Autólogo , Resultado do Tratamento
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