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Haroon Majeed Manchester University Foundation NHS Trust, Manchester, United Kingdom

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’ familiarity with the procedure. 7 The options for replacement include a silastic (silicone) or a metallic implant. It follows the basic principles of any joint-replacement surgery aiming to reduce pain, restore joint kinematics, be long lasting and not be

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Maurizio Calcagni University Hospital Zürich, Switzerland

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Thomas Giesen University Hospital Zürich, Switzerland

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s by means of ulna head replacement with silastic implants. We define these implants as Type 1 implants, aimed at creating an interposition between the bone ends. Since the failed silicone arthroplasty was abandoned, until recently few reports could

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Massimo Ceruso Hand Surgery Unit, Centro Traumatologico Ortopedico, Azienda Ospedliero-Universitaria Careggi, Florence, Italy

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Sandra Pfanner Hand Surgery Unit, Centro Traumatologico Ortopedico, Azienda Ospedliero-Universitaria Careggi, Florence, Italy

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Christian Carulli Orthopaedic Clinic, University of Florence, Florence, Italy

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Introduction Until the late 1980s, finger joint prosthetic reconstruction had been almost exclusively performed by using monobloc silicone spacers as developed by Swanson et al more than 20 years previously. 1 Such implants are not fixed

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Bryant Ho Hinsdale Orthopaedics, Hinsdale, Illinois, USA

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Judith Baumhauer University of Rochester, Department of Orthopaedics, Rochester, New York, USA

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arthroplasty began historically with silastic implants and progressed to all-metal implants and, more recently, synthetic cartilage implants. Both first and second generation silastic implants have been found to be associated with high rates of osteolysis with

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Jetske Viveen Department of Trauma and Orthopedic Surgery, Flinders Medical Centre and University, Adelaide, Australia
Upper Limb Unit, Department of Orthopedic Surgery, Amphia Hospital, Breda, The Netherlands

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Izaak F. Kodde Department of Orthopedic Surgery, Amsterdam University Medical Centers, Amsterdam, The Netherlands

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Andras Heijink Department of Orthopedic Surgery, Catharina Hospital, Eindhoven, The Netherlands

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Koen L. M. Koenraadt Foundation for Orthopedic Research, Care & Education, Amphia Hospital, Breda, The Netherlands

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Michel P. J. van den Bekerom Shoulder and Elbow Unit, Department of Orthopedic Surgery, Amsterdam, The Netherlands

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Denise Eygendaal Upper Limb Unit, Department of Orthopedic Surgery, Amphia Hospital, Breda, The Netherlands
Department of Orthopedic Surgery, Amsterdam University Medical Centers, Amsterdam, The Netherlands

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to good results have been reported for both primary 4 , 5 and revision surgery of RHA. 6 Implant revision and removal rates up to 8% at four years have been described. 4 More recent studies showed conflicting 10-year survival numbers

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E. Carlos Rodríguez-Merchán Department of Orthopaedic Surgery, “La Paz” University Hospital-IdiPaz, Madrid, Spain

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Noiles rotating hinge knee prosthesis 46 The Finn rotating hinge 47 Indications for hinged implants in primary total knee arthroplasty In 2014, Gerhke et al analysed the role of hinges in primary total knee arthroplasty (TKA

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Alessio Bernasconi Orthopaedic and Traumatology Unit, Department of Public Health, “Federico II” Naples University, Naples, Italy

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François Lintz Clinique de l’Union, Saint-Jean, France

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Francesco Sadile Orthopaedic and Traumatology Unit, Department of Public Health, “Federico II” Naples University, Naples, Italy

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’ to describe a similar procedure, that is to say, the insertion of a bone graft in the sinus tarsi fixed by a temporary staple. 52 Very soon the idea of placing an external synthetic implant in the sinus tarsi to support the talus on the calcaneus

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Kinner Davda Department of Foot & Ankle Surgery, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, HA7 4LP, UK

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Karan Malhotra Department of Radiology, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, HA7 4LP, UK

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Paul O’Donnell Department of Foot & Ankle Surgery, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, HA7 4LP, UK

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Dishan Singh Department of Foot & Ankle Surgery, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, HA7 4LP, UK

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Nicholas Cullen Department of Foot & Ankle Surgery, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, HA7 4LP, UK

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fibrotic, a staged approach can be used: the first stage involves excising the scarred tissue and implanting a 6 mm silastic rod in the peroneal muscle bed, suturing it to the distal tendon. The second stage is performed six to 12 weeks later when a

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