Abstract

Abstract Registries have been widely utilized to track clinical results in observational cohorts for quality improvement. They are successful in orthopaedics, particularly in the context of arthroplasties where they have optimized implant selection, improved patient safety and identified underperforming implants. However, equivalent systems to monitor outcomes in soft-tissue disorders are lacking. This protocol described the design, ethics and implementation of a regional registry focusing on upper limb soft tissue orthopaedic conditions. Patient Registry of Upper Limb pathology Outcomes (PRULO) is a multi-cohort, prospective observational, clinical quality registry collating clinical data and patient-reported outcomes for patients presenting to a specialist orthopaedic clinic with upper limb pathology. PRULO is currently a single-centre study involving three clinician investigators, which aims to determine what patient characteristics, pathology factors and treatment strategies are associated with treatment success within 2 years of surgical or non-surgical treatment of pathology. PRULO captures patient-reported outcomes (VAS, EQ5D-5 L, QuickDASH, MODEMS-Expectations and Satisfaction, WORC, WOSI), clinical and radiological data. Data points are recorded at practice registration, after initial consultation, intraoperatively and at 3, 6, 12 and 24 months. Inclusion criteria are patients aged 16 and above offered treatment by the surgeons for upper limb orthopaedic pathology. Patient cohorts will include shoulder conditions affecting the rotator cuff (tear, tendinopathy), conditions associated with glenohumeral instability, as well as all other conditions presenting in the shoulder elbow, hand and wrist, according to the surgeon-generated diagnosis. Ethical approval was obtained by the Barwon Health Research Ethics Committee (19/70).

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