Perineural dexamethasone with subsartorial saphenous nerve blocks in ACL reconstruction

被引:9
作者
Chisholm, Mary F. [1 ]
Cheng, Jennifer [1 ]
Fields, Kara G. [2 ]
Marx, Robert G. [3 ]
Maalouf, Daniel B. [1 ]
Liguori, Gregory A. [1 ]
Gordon, Michael A. [1 ]
Zayas, Victor M. [1 ]
Yadeau, Jacques T. [1 ]
机构
[1] Hosp Special Surg, Dept Anesthesiol, 535 E 70th St, New York, NY 10021 USA
[2] Hosp Special Surg, Inst Healthcare Res, 535 E 70th St, New York, NY 10021 USA
[3] Hosp Special Surg, Dept Orthoped Surg, 535 E 70th St, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
ACL reconstruction; Patellar tendon autograft; Subsartorial saphenous nerve block; Postoperative pain; BRACHIAL-PLEXUS BLOCK; INTRAVENOUS DEXAMETHASONE; SYSTEMIC DEXAMETHASONE; STATISTICAL-METHODS; LONGITUDINAL-DATA; SHOULDER SURGERY; CONTROLLED-TRIAL; DOUBLE-BLIND; DURATION; ROPIVACAINE;
D O I
10.1007/s00167-016-4120-3
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
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. 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. 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. The addition of 1 and 4 mg of dexamethasone to the block injectate significantly increased SSNB duration by 8-13 h compared to control. Therapeutic study, level 1.
引用
收藏
页码:1298 / 1306
页数:9
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