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Anne Lübbeke Division of Orthopaedic Surgery and Traumatology, Geneva University Hospitals, Switzerland; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, UK

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the more and more widespread use of patient-reported outcomes (PRO). 4 , 5 Another reason is the increasing ability to routinely collect large amounts of diverse data in clinical and administrative databases and in electronic health records (e

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Christian Smith Guys and St Thomas NHS Foundation Trust, London, UK

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Razi Zaidi Guys and St Thomas NHS Foundation Trust, London, UK

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Jagmeet Bhamra Guys and St Thomas NHS Foundation Trust, London, UK

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Anna Bridgens Evelina Children’s Hospital, Westminster Bridge Road, London, UK

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Caesar Wek Guys and St Thomas NHS Foundation Trust, London, UK

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Michail Kokkinakis Evelina Children’s Hospital, Westminster Bridge Road, London, UK

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adults where data for paediatric patients was not readily separable - Pathology other than flexible pes planus (e.g. tarsal coalition, neurogenic pes planus) - Lack of reported meaningful radiological, kinematic or clinical outcomes

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Marco Gupton MountainView Regional Medical Center, Orthopaedic Surgery Residency, Las Cruces, New Mexico, USA

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Jordan E Johnson MountainView Regional Medical Center, Orthopaedic Surgery Residency, Las Cruces, New Mexico, USA

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G Robert Cummings MountainView Regional Medical Center, Orthopaedic Surgery Residency, Las Cruces, New Mexico, USA

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Chenthuran Deivaraju Department of Orthopaedic Surgery, University of Minnesota, St Cloud, Minnesota, USA

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- and postoperative x-rays or advanced imaging; (iii) TKA performed for osteoarthritis; (iv) reported subjective and/or objective patient outcomes in relation to PFJ overstuffing; (v) patient follow-up of at least 1 year; (vi) prosthetic implant that is

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Kwaku Baryeh The Academic Surgical Unit, South West London Elective Orthopaedic Centre, UK

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Jeewaka Mendis Surrey Clinical Trials Unit, University of Surrey, UK

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David H. Sochart The Academic Surgical Unit, South West London Elective Orthopaedic Centre, UK

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, cohort or case-control studies and case series. If there was more than one paper reporting on the same patient cohort, the earlier one was removed, but the subsidence result retained to calculate average annual subsidence rates. Where there was

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Mark Anthony Roussot Department of Trauma and Orthopaedics, University College London Hospitals, London, UK
Department of Orthopaedic Surgery, University of Cape Town, South Africa

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Georges Frederic Vles Department of Trauma and Orthopaedics, University College London Hospitals, London, UK

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Sam Oussedik Department of Trauma and Orthopaedics, University College London Hospitals, London, UK

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outcomes or have an impact on survivorship of the TKA remains unknown. In this systematic review, we will present and critique the current clinical evidence to determine whether, compared to MA, KA (1) translates to improvement in subjective patient-reported

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Reinier Feitz Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Plastic, Reconstructive and Hand Surgery, Nijmegen, The Netherlands

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Yara E. van Kooij Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Department of Plastic, Reconstructive, and Hand Surgery, Rotterdam, The Netherlands
Department of Rehabilitation Medicine, Rotterdam, The Netherlands

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Marloes H. P. ter Stege Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands

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Mark J. W. van der Oest Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Department of Plastic, Reconstructive, and Hand Surgery, Rotterdam, The Netherlands
Department of Rehabilitation Medicine, Rotterdam, The Netherlands

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J. Sebastiaan Souer Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands

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Robbert M. Wouters Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Department of Plastic, Reconstructive, and Hand Surgery, Rotterdam, The Netherlands
Department of Rehabilitation Medicine, Rotterdam, The Netherlands

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Harm P. Slijper Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Department of Plastic, Reconstructive, and Hand Surgery, Rotterdam, The Netherlands
Department of Rehabilitation Medicine, Rotterdam, The Netherlands

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Ruud W. Selles Department of Plastic, Reconstructive, and Hand Surgery, Rotterdam, The Netherlands
Department of Rehabilitation Medicine, Rotterdam, The Netherlands

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Steven E. R. Hovius Hand and Wrist Center, Xpert Clinics, Amsterdam, The Netherlands
Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Plastic, Reconstructive and Hand Surgery, Nijmegen, The Netherlands

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Hand–Wrist Study Group RAM Blomme, BJR Sluijter, DJJC van der Avoort, A Kroeze, J Smit, J Debeij, ET Walbeehm, GM van Couwelaar, Guus M Vermeulen, JP de Schipper, JFM Temming, JH van Uchelen, HL de Boer, KP de Haas, K Harmsen, OT Zöphel, R Koch, TM Moojen, X Smit, GJ Halbesma, R van Huis, PY Pennehouat, K Schoneveld, YE van Kooij, RM Wouters, JJ Veltkamp, A Fink, WA de Ridder, J Tsehaie, R Poelstra, MC Janssen, PO Sun, VJMM Schrier, L Hoogendam, JS Teunissen, Jak Dekker, M Jansen-Landheer

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distributed via email. Patients were asked to complete validated Dutch versions of hand-specific patient-reported outcome measurements (PROMs) at baseline and after surgery depending on the type of treatment. 7 Amongst other PROMs, we use the Boston

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Ian Wilson Concordia Joint Replacement Group, Winnipeg, Manitoba, Canada

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Eric Bohm Canadian Joint Replacement Registry, University of Manitoba, Concordia Joint Replacement Group, Winnipeg, Manitoba, Canada

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Anne Lübbeke Geneva Arthroplasty Registry, Division of Orthopaedic Surgery, Geneva University Hospitals, Geneva, Switzerland

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Stephen Lyman Hospital for Special Surgery and Weill Cornell Medical College, New York, New York, USA

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Søren Overgaard Danish Hip Arthroplasty Register, University of Southern Denmark, Odense, Denmark

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Ola Rolfson Swedish Hip Arthroplasty Register and Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

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Annette W-Dahl Swedish Knee Arthroplasty Register, Skåne University Hospital, Lund, Sweden

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Mark Wilkinson University of Sheffield, Sheffield, United Kingdom

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Michael Dunbar Canadian Joint Replacement Registry, Dalhousie University, Halifax, Nova Scotia, Canada

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Patient-Reported Outcome Measurement Information System Global 10 PROMIS-10 Global 2004 No No > 40 10 2 to 3 Specific Oxford Knee Score OKS 1998 Knee Yes 19 12 3 to 4 Oxford Hip Score OHS

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Daniel Murphy St George’s University Hospitals NHS Foundation Trust, London, UK
St George’s, University of London, London, UK

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Mohsen Raza St George’s University Hospitals NHS Foundation Trust, London, UK

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Hiba Khan St George’s University Hospitals NHS Foundation Trust, London, UK

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Deborah M. Eastwood Great Ormond Street Hospital, London, UK
University College London (UCL), London, UK

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Yael Gelfer St George’s University Hospitals NHS Foundation Trust, London, UK
St George’s, University of London, London, UK

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; patient-reported outcome measures (PROMs); and complications ( Table 1 ). Articles were categorized by trial intervention. Data were extracted into a standardized collection form using Microsoft Excel (Microsoft Corporation, Redmond, WA, USA). Bias

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R J M Morrison Northumbria Healthcare NHS Foundation Trust, Ashington, UK
Newcastle University, Newcastle upon Tyne, UK

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W G Fishley Northumbria Healthcare NHS Foundation Trust, Ashington, UK
University of York, York, UK

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K S Rankin Newcastle University, Newcastle upon Tyne, UK
The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK

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M R Reed Northumbria Healthcare NHS Foundation Trust, Ashington, UK
University of York, York, UK

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been associated with a range of adverse post-operative outcomes ( 3 ), and there is a high incidence of deficiency reported in patients undergoing total hip (THR) or knee (TKR) arthroplasty ( 4 ). Previous systematic reviews ( 4 , 5 , 6 , 7 ) have

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Yvet Mooiweer Department of Health Services Research, Carl von Ossietzky University, Oldenburg, Germany
Department of Orthopedics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

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Lina Roling School of Medicine and Health Sciences, Carl von Ossietzky University, Oldenburg, Germany

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Margaret Vugrin Preston Smith Library, Texas Tech University Health Sciences Center, Lobbock, Texas, USA

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Lena Ansmann Department of Health Services Research, Carl von Ossietzky University, Oldenburg, Germany
Chair of Medical Sociology, Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR) Faculty of Medicine, University of Cologne, Oldenburg, Germany

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Martin Stevens Department of Orthopedics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

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Gesine H Seeber Department of Orthopedics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
University Hospital of Orthopedics and Trauma Surgery Pius-Hospital, Medical Campus University of Oldenburg, Oldenburg, Germany

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measurement’, ‘outcome measurement’, ‘study confounding’, and ‘statistical analysis and reporting’. The QUIPS tool is presented in appendix 2. Study quality assessment was performed using Covidence, therefore all QUIPS-tool items were transformed into a

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