• Foot Ankle Int · Oct 2019

    Randomized Controlled Trial Comparative Study

    Comparison of Single-Agent Versus 3-Additive Regional Anesthesia for Foot and Ankle Surgery.

    • Debbie Y Dang, Sean M McGarry, Eric J Melbihess, Craig T Haytmanek, Andrew T Stith, Matthew J Griffin, Katherine J Ackerman, and Christopher B Hirose.
    • Saint Alphonsus Regional Medical Center Coughlin Clinic, Boise, ID, USA.
    • Foot Ankle Int. 2019 Oct 1; 40 (10): 1195-1202.

    BackgroundThis study compared the results of regional blocks containing a single anesthetic, bupivacaine, with those containing bupivacaine and 3 additives (buprenorphine, clonidine, and dexamethasone) in patients undergoing foot and ankle surgery.MethodsEighty patients undergoing foot and ankle surgery over a 9-month period were prospectively enrolled and randomized to receive a peripheral nerve block containing either a single anesthetic (SA) or one with 3 additives (TA). Patients, surgeons, and anesthesiologists were blinded to the groups. Patients maintained pain diaries and were evaluated at 1 and 12 weeks postoperatively. Fifty-six patients completed the study.ResultsThe TA group had a longer duration of analgesic effect than the SA group (average 82 vs 34 hours, P < .05). Forty-eight hours after surgery, 93% of SA blocks, compared with 34% of TA blocks, had completely worn off. The TA group had a longer duration of sensory effects. At 3 months, 10 of 26 (38.5%) TA patients, compared with 3 of 30 (10%) SA patients, reported postoperative neurologic symptoms. Pain scores in both groups were not statistically different at 1 week or 3 months after surgery. Patients in both groups were similarly satisfied with their blocks.ConclusionBoth types of nerve blocks provided equivalent pain control and patient satisfaction in patients undergoing foot and ankle surgery. The 3-additive agent blocks were associated with a longer duration of pain relief and a longer duration of numbness, as well as higher rates of postoperative neurologic symptoms. Longer pain relief may be obtained at the cost of prolonged sensory deficits.Level Of EvidenceLevel II, prospective comparative study.

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