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Midterm outcomes of high-flexion total knee arthroplasty on Japanese lifestyle

OBJECTIVE: To evaluate the clinical outcomes after total knee arthroplasty (TKA) using the Genesis II posterior stabilized prosthesis with a high-flex insert during the mid-term follow-up and to assess its effect on the Japanese lifestyle. MATERIALS AND METHODS: Fifty-three consecutive patients (8 m...

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Detalles Bibliográficos
Autores principales: Ohno, Hiroshi, Murata, Minoru, Ozu, Satoshi, Matsuoka, Nariyasu, Kawamura, Hiroshi, Iida, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Association of Orthopaedics and Traumatology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197585/
https://www.ncbi.nlm.nih.gov/pubmed/27681375
http://dx.doi.org/10.1016/j.aott.2016.08.005
Descripción
Sumario:OBJECTIVE: To evaluate the clinical outcomes after total knee arthroplasty (TKA) using the Genesis II posterior stabilized prosthesis with a high-flex insert during the mid-term follow-up and to assess its effect on the Japanese lifestyle. MATERIALS AND METHODS: Fifty-three consecutive patients (8 men and 45 women) underwent primary TKA. The mean follow-up time was 76 months (5–9 years). Clinical results were assessed with the Japanese Orthopedic Association osteoarthritis knee rating score (JOA knee score), range of motion, and lifestyle changes. RESULTS: The postoperative JOA knee score improved significantly compared to the preoperative JOA knee score. The mean preoperative flexion range improved from 112° to 123° postoperatively (p < 0.05). Additionally, our findings showed that 39% of patients enjoyed a floor-sitting life preoperatively, but only 30% of patients enjoyed floor-sitting life postoperatively. CONCLUSION: The postoperative range of knee motion and JOA knee score improved after TKA using the Genesis II posterior stabilized prosthesis with a high-flex insert, but the number of patients who enjoyed floor-sitting life decreased from 39% to 30% because of feelings of fear and discomfort. Level of Evidence: Level IV, Therapeutic study