Effect of adductor canal block on pain in patients with severe pain after total knee arthroplasty: a randomized study with individual patient analysis

被引:52
作者
Grevstad, U. [1 ]
Mathiesen, O. [3 ]
Lind, T. [2 ]
Dahl, J. B. [4 ]
机构
[1] Copenhagen Univ Hosp, Gentofte Hosp, Dept Anaesthesia & Intens Care Med, DK-2900 Hellerup, Denmark
[2] Copenhagen Univ Hosp, Gentofte Hosp, Dept Orthopaed Surg, DK-2900 Hellerup, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Ctr Head & Orthopaed, Sect Acute Pain Management, DK-2900 Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Ctr Head & Orthopaed, Dept Anaesthesia, DK-2900 Copenhagen, Denmark
关键词
acute pain; arthroplasty; replacement; knee; nerve block; pain; postoperative; PERIPHERAL-NERVE BLOCKS; CLINICALLY SIGNIFICANT DIFFERENCE; LOCAL INFILTRATION ANALGESIA; ANALOG SCALE PAIN; POSTOPERATIVE PAIN; ORTHOPEDIC-SURGERY; TRIALS; HIP; COMPLICATIONS; METAANALYSIS;
D O I
10.1093/bja/aet441
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. Total knee arthroplasty (TKA) is associated with varying degrees of pain. A considerable proportion (25-40%) of patients experience severe pain, despite a comprehensive multimodal analgesic regimen. We hypothesized that adductor canal block (ACB) would reduce pain in this patient category compared with placebo. Methods. Fifty patients with severe pain, defined as having a visual analogue scale (VAS) pain score of >60 during active flexion of the knee on the first or the second postoperative day after TKA, were included in this randomized, double-blind, placebo-controlled trial. All the patients had received a comprehensive multimodal analgesic regimen. Group A received an ACB with ropivacaine 0.75%, 30 ml at time 0 and isotonic saline after 45 min. Group B received an ACB with isotonic saline at time 0 and ropivacaine 0.75%, 30 ml after 45 min. Results. A 32-mm difference in VAS pain score, during active flexion of the knee (primary endpoint), was observed in favour of Group A, 95% confidence interval (CI): 23-42, P<0.0001. At rest, the difference in VAS pain score was 15 mm in favour of Group A, 95% CI: 8-23 mm, P=0.0001. Individual patient analysis revealed that 25% of the patients had no effect during active flexion. At rest, however, only 8% had more than mild pain after ACB compared with 57% at inclusion. Conclusions. ACB reduced VAS with 32 mm, during active flexion of the knee, in patients with severe pain after TKA, but a large proportion (78%) still had at least moderate, movement-related pain.
引用
收藏
页码:912 / 919
页数:8
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