Ankle arthritis is associated with debilitating pain and chronic disability. For the treatment of severe ankle arthritis, total ankle arthroplasty (TAA) is one treatment option. Postoperative pain management in joint arthroplasty is an ongoing and relevant issue. The purpose of this study is to examine if differences exist in postoperative pain control, overall patient satisfaction, and use of narcotics using an intra-articular injection in the operating room compared with a peripheral nerve block in patients undergoing TAA.
This is a two-arm, prospective, randomized, controlled clinical study. Use of intra-articular injections in TAA are not widely reported in literature; however, they are commonly used during total knee arthroplasty's (TKAs). The purpose of this study is to examine if differences exist in postoperative pain control, overall patient satisfaction, and use of narcotics using the intra-articular injection compared with a peripheral nerve block in patients undergoing TAA. Results will contribute to the literature for the best surgical practice for pain management following a TAA for ankle arthritis. Patients will be randomized to receive one of the following interventions for pain control in the operating room: 1. Intra-articular Injection 2. Preoperative Peripheral Nerve Block: The study aims are: * Aim 1: Determine if intra-articular injection as source of pain control for TAA lowers postoperative pain as measured by self-reported narcotic use and pain vs. the peripheral nerve block. * Aim 2: Evaluate differences in functional outcomes and health related quality of life between intra-articular injections and peripheral nerve block as reported by pre- and post-operative patient questionnaires Patients who consent to participate will complete study activities pre-operatively, and at 2 weeks, 6 weeks, and 3 months post-operatively.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Intra-articular injection at the completion of TAA procedure.
Pre-operative peripheral nerve block.
Slocum Research & Education Foundation
Eugene, Oregon, United States
RECRUITINGTotal narcotic use in morphine equivalents
Narcotic dose and frequency captured through patient diary; used to calculate morphine equivalents.
Time frame: Up to 3 months post-operatively
Self-reported pain captured with a visual analog pain scale
Measures self-reported pain between 0 (no pain) and 100 (extreme pain)
Time frame: Up to 3 months post-operatively
Foot and Ankle Ability Measure (FAAM)
Measures self-reported outcomes accessing physical function for individuals with foot and ankle related impairments.
Time frame: Up to 3 months post-operatively
American Orthopaedic Foot and Ankle Society (AOFAS) Ankle Hindfoot Score
Grades ankle, subtalar, talonavicular, and calcaneocuboid joint levels in terms of pain (40 points), function (50 points), and alignment (10 points); 100 points possible sub-scores are summed, higher indicates better outcome.
Time frame: Up to 3 months post-operatively
Veterans Rand (VR) 36 item Health Survey
VR-36 Consists of select items from eight concepts of health in the VR-36, measuring health-related quality of life, and differences in disease burden.
Time frame: Up to 3 months post-operatively
Time to narcotic discontinuation
Number of days narcotics were taken for post-operative pain control
Time frame: Up to 3 months post-operatively
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