ID.1
Item
patient has received an aequalis® resurfacing head implant as per the manufacturer's instructions (including the recommended indication): degenerative indication such as primary osteoarthritis, secondary osteoarthritis (post-traumatic post instability), avascular osteonecrosis of the humeral head ;
boolean
ID.2
Item
with a functional rotator cuff ;
boolean
ID.3
Item
has clinical and radiographic follow-up data available ;
boolean
ID.4
Item
is informed about the study and has provided informed consent as applicable.
boolean
ID.5
Item
patient with proximal humeral fracture,
boolean
ID.6
Item
previous history of infection,
boolean
ID.7
Item
rotator cuff tear, cuff tear arthropathy,
boolean
ID.8
Item
significant bone loss of the glenoid (more than 25% of the articular surface),
boolean
ID.9
Item
nerve palsy,
boolean
ID.10
Item
revision arthroplasty.
boolean