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Short and long term outcomes of total knee arthroplasty patients surgically exposed with patellar eversion are compared to those patients exposed by laterally retracting the patella. It was hypothesized that there would be no difference.
Background:
Patellar mobilization during total knee arthroplasty (TKA) has been debated, with some proponents of minimally invasive TKA suggesting that laterally retracting, rather than everting the patella may be beneficial. It was our hypothesis that by using randomized, prospective, blinded study methods, there would be no significant difference in clinical outcome measures based solely on eversion of the patella during total knee arthroplasty.
Methods:
After an a priori power analysis was done, 120 primary total knee replacements indicated for degenerative joint disease were included in the study and randomized to one of two patella exposure techniques: lateral retraction or eversion. Collaborating investigators and patients were blinded to randomization.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patellar Eversion | Experimental | Patients randomized to the Patellar Eversion arm of the study were surgically exposed by everting the patella during their Primary Total Knee Replacement Surgery. |
|
| Patellar Lateral Retraction | Active Comparator | Patients randomized to the Patellar Lateral Retraction arm of the study were surgically exposed by laterally retracting the patella during their Primary Total Knee Replacement Surgery. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Primary Total Knee Replacement Surgery | Procedure | Patients randomized to the eversion group had patellas everted during the flexion portions of the surgery. Patients randomized to the retraction group had patellas everted only for the patellar resurfacing portions of the surgery. Both groups were mobilized with anterior tibial translation. All other aspects of surgery including postoperative care, anticoagulation, pain control, and physical therapy were done as per standard arthroplasty protocols at our institution. |
| Measure | Description | Time Frame |
|---|---|---|
| change in quadriceps strength | Quadriceps strength was measured isometrically using a Biodex dynamometer with the patient's knee in 60 degrees of flexion. | preop, 6 weeks, 3 months, 1 year postop |
| Measure | Description | Time Frame |
|---|---|---|
| change in ability to perform straight leg raise | For the purposes of this study, we defined the ability to straight leg raise as a patient independently raising their heel 6 inches off of the bed with foot dorsiflexed and knee fully extended without extension lag. | up to three days postop |
| change in Visual Analog Scale of Pain |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jose A Rodriguez, MD | Lenox Hill Hospital | Principal Investigator |
| Derek R Jenkins, MD | Mayo Clinic | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lenox Hill Hospital | New York | New York | 10021 | United States |
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| ID | Term |
|---|---|
| D000092462 | Patella Fracture |
| ID | Term |
|---|---|
| D000092443 | Knee Fractures |
| D050723 | Fractures, Bone |
| D014947 | Wounds and Injuries |
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|
Patient reported pain using standardized VAS diagram |
| preop, up to 3 days postop, 6 weeks, 3 months, and 1 year postop |
| change in Ambulation Distance | up to 3 days postop |
| Length of Hospital Stay | expected average 2 to 3 days |
| change in SF-36 score | preop, 6 weeks, 3 months, 1 year postop |
| change in Range of knee motion | goniometer used to standardize measurements | preop, 6 weeks, 3months, 1 year |