The mornings after-periarticular liposomal bupivacaine infiltration does not improve analgesic outcomes beyond 24 hours following total knee arthroplasty: a systematic review and meta-analysis

被引:27
|
作者
Hussain, Nasir [1 ]
Brull, Richard [2 ]
Sheehy, Brendan T. [1 ]
Kushelev, Michael [1 ]
Essandoh, Michael K. [1 ]
Abdallah, Faraj W. [3 ,4 ]
机构
[1] Ohio State Univ, Wexner Med Ctr, Anesthesiol, Columbus, OH USA
[2] Toronto Western Hosp, Anesthesiol, Toronto, ON, Canada
[3] Univ Toronto, Anesthesiol & Pain Med, Ottawa, ON, Canada
[4] Univ Ottawa, Ottawa, ON, Canada
关键词
PAIN-CONTROL; POSTSURGICAL ANALGESIA; INJECTABLE SUSPENSION; STANDARD BUPIVACAINE; DOUBLE-BLIND; INJECTION; EFFICACY; QUALITY; BENEFIT; BLOCKS;
D O I
10.1136/rapm-2020-101995
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Periarticular local infiltration analgesia (LIA) is integral to multimodal analgesia following total knee arthroplasty (TKA); however, the duration of analgesia using traditional long-acting local anesthetics is often insufficient. LIA with slow-release liposomal bupivacaine may provide extended analgesia, but evidence of efficacy beyond the first 24 hours is conflicting. This meta-analysis compares the effects of periarticular liposomal and plain bupivacaine LIA on day 2 analgesic outcomes post-TKA. Trials comparing liposomal and plain bupivacaine LIA for TKA were sought. The two coprimary outcomes were (1) cumulative oral morphine equivalent consumption and (2) difference in area under the curve (AUC) of pooled rest pain scores on day 2 (24-48 hours) post-TKA. We also evaluated pain and analgesic consumption on day 3 (48-72 hours), functional recovery, length of hospital stay, patient satisfaction; and opioid-related side effects. Data were pooled using random-effects modeling. Seventeen trials (1836 patients) were analyzed. Comparing liposomal versus plain bupivacaine LIA for TKA failed to detect differences in morphine consumption and pain AUC on day 2 postoperatively, with mean differences of 0.54 mg (95% CI -5.09 to 6.18) and 0.08 cm/hour (95% CI -0.19 to 0.35), respectively (high-quality evidence). Secondary outcome analysis did not uncover any additional analgesic, functional or safety advantages to liposomal bupivacaine on postoperative day 2 or 3. Results indicate that liposomal and plain bupivacaine LIAs are not different for extended postoperative analgesic outcomes, including pain control, opioid consumption, as well as functional and safety outcomes on days 2 and 3 post-TKA. High-quality evidence does not support using liposomal bupivacaine LIA for TKA.
引用
收藏
页码:61 / 72
页数:12
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