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Perineural dexamethasone with subsartorial saphenous nerve blocks in ACL reconstruction.
Chisholm, Mary F; Cheng, Jennifer; Fields, Kara G; Marx, Robert G; Maalouf, Daniel B; Liguori, Gregory A; Gordon, Michael A; Zayas, Victor M; Yadeau, Jacques T.
Afiliação
  • Chisholm MF; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA. ChisholmM@hss.edu.
  • Cheng J; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
  • Fields KG; Healthcare Research Institute, Hospital for Special Surgery, New York, NY, USA.
  • Marx RG; Department of Orthopedic Surgery, Hospital for Special Surgery, New York, NY, USA.
  • Maalouf DB; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
  • Liguori GA; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
  • Gordon MA; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
  • Zayas VM; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
  • Yadeau JT; Department of Anesthesiology, Hospital for Special Surgery, New York, NY, USA.
Knee Surg Sports Traumatol Arthrosc ; 25(4): 1298-1306, 2017 Apr.
Article em En | MEDLINE | ID: mdl-27075893
ABSTRACT

PURPOSE:

Subsartorial saphenous nerve blockade (SSNB) is an effective analgesic alternative to femoral nerve blockade after anterior cruciate ligament (ACL) reconstruction with bone-tendon-bone (BTB) autograft. It was hypothesized that dexamethasone in a SSNB will prolong analgesia, improve pain and satisfaction, and reduce postoperative opioid requirements and side effects.

METHODS:

One hundred ninety-five patients undergoing ACL reconstruction with BTB autograft (ages 16-65) were enrolled. Subjects received SSNB with 13 ml of 0.5 % bupivacaine (control group), 1 mg preservative-free dexamethasone +0.5 % bupivacaine (treatment group I), or 4 mg preservative-free dexamethasone +0.5 % bupivacaine (treatment group II). Subjects received identical perioperative management. On postoperative days 1 and 2, subjects reported perceived block duration, pain scores, satisfaction, opioid use, and side effects. Cox-proportional hazards modelling was used to compare block duration, adjusting for body mass index, age, sex, tourniquet time, American Society of Anesthesiologists classification, and intravenous dexamethasone dose.

RESULTS:

Patient-perceived block duration was significantly increased in treatment group I [hazard ratio (95 % confidence interval [CI]) 0.48 (0.31-0.75); P = 0.001] and treatment group II (hazard ratio (95 % CI) 0.52 (0.33-0.81); P = 0.004) compared to control. The block was extended from a median (95 % CI) of 33.1 (28.4-37.3) to 41.2 (32.4-50.9) and 46.5 (35.8-48.9) hours, respectively. Additionally, patients in treatment group II reported increased time that block provided pain relief, higher patient satisfaction, lower pain scores at rest, and decreased drowsiness and confusion.

CONCLUSION:

The addition of 1 and 4 mg of dexamethasone to the block injectate significantly increased SSNB duration by 8-13 h compared to control. LEVEL OF EVIDENCE Therapeutic study, level 1.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Pós-Operatória / Dexametasona / Enxerto Osso-Tendão Patelar-Osso / Bloqueio Nervoso Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Pós-Operatória / Dexametasona / Enxerto Osso-Tendão Patelar-Osso / Bloqueio Nervoso Idioma: En Ano de publicação: 2017 Tipo de documento: Article