Your browser doesn't support javascript.
loading
Single-Injection Adductor Canal Block With Multiple Adjuvants Provides Equivalent Analgesia When Compared With Continuous Adductor Canal Blockade for Primary Total Knee Arthroplasty: A Double-Blinded, Randomized, Controlled, Equivalency Trial.
Turner, James D; Dobson, Sean W; Henshaw, Daryl S; Edwards, Christopher J; Weller, Robert S; Reynolds, Jon W; Russell, Gregory B; Jaffe, Jonathan D.
Afiliação
  • Turner JD; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Dobson SW; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Henshaw DS; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Edwards CJ; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Weller RS; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Reynolds JW; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Russell GB; Department of Biostatistical Sciences, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Jaffe JD; Department of Anesthesiology, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
J Arthroplasty ; 33(10): 3160-3166.e1, 2018 10.
Article em En | MEDLINE | ID: mdl-29903459
BACKGROUND: Peripheral nerve blockade is used to provide analgesia for patients undergoing total knee arthroplasty. This study compared a single-injection adductor canal block (SACB) with adjuvants to continuous adductor canal blockade (CACB). The hypothesis was that the 2 groups would have equivalent analgesia at 30 hours after neural blockade. METHODS: This was a double-blinded, randomized, controlled, equivalency trial. Sixty patients were randomized to either the SACB group (20 mL of 0.25% bupivacaine, 1.67 mcg/mL of clonidine, 2 mg of dexamethasone, 150 mcg of buprenorphine, and 2.5 mcg/mL of epinephrine) or the CACB group (20 mL 0.25% of bupivacaine injection with 2.5 mcg/mL of epinephrine followed by an 8 mL/h infusion of 0.125% bupivacaine continued through postoperative day 2). The primary outcome was movement pain scores at 30 hours using the numeric rating scale (NRS). The secondary outcomes included serial postoperative NRS pain scores (rest and movement every 6 hours), opioid consumption, time to first opioid administration, ability to straight leg raise, patient satisfaction, length of stay, and the incidence of nausea/vomiting. RESULTS: An intention-to-treat analysis included 59 patients. The NRS pain scores with movement were equivalent at 30 hours (SACB 5.5 ± 2.8 vs CACB 5.7 ± 2.9 [mean NRS ± standard deviation]; mean difference 0.2 [-1.5 to 1.0 {90% confidence interval}]). All NRS pain scores were equivalent until 42 hours (rest) and 48 hours (rest and movement) with the CACB group having lower pain scores. Other secondary outcomes were not statistically different. CONCLUSION: An SACB provides equivalent analgesia for up to 36 hours after block placement when compared with a CACB for patients undergoing total knee arthroplasty, though a CACB was favored at 42 hours and beyond.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Pós-Operatória / Artroplastia do Joelho / Anestésicos Locais / Bloqueio Nervoso Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Pós-Operatória / Artroplastia do Joelho / Anestésicos Locais / Bloqueio Nervoso Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article