The Abduction Wedge maintains the leg abduction position after total hip replacement surgery to prevent prosthetic joint dislocation, with a compact 240 x 160 x 180mm profile suitable for both bed and chair use during recovery. High-resiliency foam with no sharp edges at contact zones. Bi-stretch PU cover with a soft adjustable attachment system, eliminating the friction and skin irritation of traditional belt-based systems. MDR 2017/745 Class I medical device. Post-operative use requires surgeon's abduction prescription. NCL-P911L1HW.
| Specification | Detail |
|---|---|
| Construction | High-resiliency foam - no sharp edges |
| Dimensions | 240 x 160 x 180mm |
| Cover | Bi-stretch polyurethane - friction-reducing |
| Fixation | Soft adjustable attachment system |
| Clinical Use | Post-hip replacement abduction maintenance - bed and chair |
| Chair Compatibility | Low-profile design fits under tables and bedside trays |
| Reference | NCL-P911L1HW |
| Regulatory Status | MDR 2017/745 Class I medical device |
The Abduction Wedge is a Class I medical device under MDR 2017/745. Post-operative use must be prescribed by the operating surgeon or physiotherapist with the specific abduction requirement, duration, and applicable positions documented. For care home settings receiving post-hip replacement residents, the discharge documentation must include the abduction prescription before the wedge is deployed. Equipment register records and MDR conformity documentation must be maintained for CQC Regulation 12 compliance.
What movements must post-hip replacement patients avoid, and how does the Abduction Wedge prevent each?
After a posterior approach total hip replacement, three movement combinations are classically restricted in the early post-operative period to prevent dislocation: flexion beyond 90 degrees (bending the hip acutely, such as sitting in a low chair or bending forward to reach the floor); adduction past the midline (crossing the legs or bringing the knees together); and internal rotation (turning the foot and lower leg inward). The Abduction Wedge specifically prevents adduction by maintaining a physical separation between the thighs that cannot be closed without removing the wedge; it does not address the flexion or rotation restrictions, which are managed through patient education, the height of seating, and movement restrictions enforced through activity modification. The wedge is most effective at preventing inadvertent nocturnal adduction during sleep, when the patient cannot consciously monitor their leg position, which is when the dislocation risk from adduction is highest. The flexion restriction (not bending the hip past 90 degrees) is particularly relevant for chair use - the chair height must be appropriate to avoid acute hip flexion when sitting down.
How does this Abduction Wedge compare to the micro-bead Hip Abduction Wedge (ID 236) for post-hip replacement use?
The two products share the same clinical indication in part but have different material properties and design priorities. The micro-bead Hip Abduction Wedge (ID 236) is filled with conformable micro-beads that adapt to the inner thigh contours, providing a very low-friction, highly conforming surface that is clinically appropriate for residents requiring prolonged abduction positioning for both pressure care and postural maintenance. The foam Abduction Wedge (this product, ID 249) uses high-resiliency foam to provide a more structurally firm and dimensionally stable abduction barrier, which some surgical protocols prefer for the specific post-replacement application because the firm profile provides more definitive separation resistance; the attachment system is also specifically designed for the post-operative patient's ability to manage fixation independently or with minimal assistance during progressive rehabilitation. The compact 240 x 160 x 180mm size is also calibrated for the specific thigh separation distance prescribed after hip replacement rather than as a general abduction aid. For the prescribing clinician, the selection between the two products depends on the surgical team's preference, the patient's comfort and compliance with each device, and any specific protocol the physiotherapy team has established for the post-operative abduction management.