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Publications

Activity outcomes after hip arthroplasty: an information tool based on patients' experience captured in a hospital registry.

Cole S. et al, (2025), BMC Musculoskelet Disord, 26

Inequality in COVID-19 vaccine acceptance and uptake: A repeated cross-sectional analysis of COVID vaccine acceptance and uptake in 13 countries.

Abel ZD. et al, (2025), Health Policy, 153

Development of a patient-centred tool for use in total hip arthroplasty

Lubbeke A. et al, (2024), PLoS ONE

Reverse total shoulder replacement versus anatomical total shoulder replacement for osteoarthritis: population based cohort study using data from the National Joint Registry and Hospital Episode Statistics for England

Valsamis E. et al, (2024), The BMJ

Patients' experience on pain outcomes after hip arthroplasty: insights from an information tool based on registry data.

Fabiano G. et al, (2024), BMC Musculoskelet Disord, 25

Modelled cost-effectiveness analysis of the Support and Treatment After Replacement (STAR) care pathway for chronic pain after total knee replacement compared with usual care

Cole S. et al, (2024), Cost Effectiveness and Resource Allocation

Patients’ experience to inform decision-making and clinical follow-up: The example of total hip arthroplasty

Lübbeke A. et al, (2023)

LEVERAGING REGISTRY DATA TO IMPROVE PATIENT-CLINICIAN COMMUNICATION ABOUT TOTAL HIP ARTHROPLASTY: THE CASE OF 'PATIENTS LIKE ME' INFORMATION TOOL

PINEDO VILLANUEVA R. et al, (2023)

Finding an appropriate instrument for data collection about burden on carers of people with X-Linked Hypophosphataemia: a carer-centred selection process

PINEDO VILLANUEVA R. et al, (2023)

VALUATION OF LOST PRODUCTIVITY OF ADULTS WITH X-LINKED HYPOPHOSPHATAEMIA AND OSTEOGENESIS IMPERFECTA

Cole S. et al, (2023)

Patient-reported outcomes measures of X-linked hypophosphataemia participants: findings from a prospective cohort study in the UK.

Cole S. et al, (2023), Orphanet J Rare Dis, 18

LEVERAGING REGISTRY DATA TO IMPROVE PATIENT-CLINICIAN COMMUNICATION ABOUT TOTAL HIP ARTHROPLASTY: THE CASE OF ''PATIENTS LIKE ME'' INFORMATION TOOL

Pinedo-Villanueva R. et al, (2023), AGING CLINICAL AND EXPERIMENTAL RESEARCH, 35, S315 - S316

Patient-reported outcomes measures of X-linked hypophosphataemia participants: findings from a prospective cohort study in the UK

Cole S. et al, (2022)

Valuation of Lost Productivity for Individuals Diagnosed with Osteogenesis Imperfecta: Follow-up Findingsfrom the Rudy Cohort Study in the UK

Cole S. et al, (2022)

Valuation of lost productivity for people with osteogenesis imperfecta: preliminary results from the RUDY cohort

Cole S. et al, (2022)

Progression of chronic pain and associated health-related quality of life and healthcare resource use over 5 years after total knee replacement: evidence from a cohort study

Cole S. et al, (2022), BMJ Open

Have People Like Me Experienced A Complication After Primary THA?: Insights From An Information Tool Based On Registry Data

Lübbeke A. et al, (2022)

''Will I Have To Get My Other Hip Replaced As Well?'' Contralateral Outcomes After Hip Arthroplasty From An Information Tool Based On Registry Data

Pinedo-Villanueva R. et al, (2022)

Function Outcomes Of 'Patients Like Me' After Hip Replacement? Insights From DEdiCADE, An Information Tool Based On Registry Data

Cole S. et al, (2022)

Have People Like Me Experienced Pain After Their Hip Arthroplasty? Insights From DEdiCADE, An Information Tool Based On Registry Data

Fabiano G. et al, (2022)

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