Osteoarthritis
Conditions
Keywords
Shoulder
Brief summary
To collect medium to long-term survivorship implant outcomes on the DePuy Global Unite Shoulder System
Interventions
PROCEDURETotal Shoulder Arthroplasty
Sponsors
Rothman Institute Orthopaedics
Study design
Observational model
COHORT
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
* Patient greater than 18 years of age and skeletally mature * Patient qualifies for primary or revision total or reverse shoulder arthroplasty based on diagnosis of investigator of osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, un-united humeral head fractures, irreducible 3- and 4- part proximal humeral fracture, avascular necrosis, or gross rotator cuff deficiency. * Patient is willing and able to provide written informed consent and to complete scheduled follow up visits/evaluations/questionnaires
Exclusion criteria
* Patient has one of the following compromise the affected limb; a significant injury to the upper brachial plexus, paralysis of the axillary nerve, or a neuromuscular disease compromising the affected limb * Patient has a known or suspected infection * Patient is known to be pregnant * Patient has a sensitivity or allergic reaction to one or more of the implanted materials * Patient is unwilling or unable to provide consent or comply with follow up visits
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Implant Survivorship | 10 years post-operative |
Outcome results
None listed