Tapentadol vs oxycodone for postoperative pain treatment the first 7 days after total knee arthroplasty: a randomized clinical trial

被引:7
|
作者
Rian, Torbjorn [1 ,2 ]
Skogvoll, Eirik [1 ,3 ]
Hofstad, Janne [2 ,4 ]
Hovik, Lise [1 ,3 ]
Winther, Siri B. [4 ]
Husby, Vigdis Schnell [3 ,4 ,5 ]
Klaksvik, Jomar [4 ]
Egeberg, Tarjei [4 ]
Sand, Kari [6 ]
Klepstad, Pal [1 ,3 ]
Wik, Tina Stromdal [2 ,4 ]
机构
[1] Trondheim Reg & Univ Hosp, Dept Anaesthesiol & Intens Care Med, St Olavs Hosp, Trondheim, Norway
[2] Norwegian Univ Sci & Technol NTNU, Dept Neuromed & Movement Sci, Trondheim, Norway
[3] Norwegian Univ Sci & Technol NTNU, Fac Med & Hlth Sci, Dept Circulat & Med Imaging, Trondheim, Norway
[4] Trondheim Reg & Univ Hosp, Dept Orthopaed Surg, St Olavs Hosp, Trondheim, Norway
[5] OsloMet Oslo Metropolitan Univ, Fac Hlth Sci, Inst Nursing, Oslo, Norway
[6] SINTEF Digital, Dept Hlth Res, Trondheim, Norway
关键词
Randomized controlled trial; Placebo control; Tapentadol Depot; Oxycodone Depot; Analgesia; Postoperative pain; Postoperative pain treatment; Total knee arthroplasty; FAST-TRACK HIP; DOUBLE-BLIND; HOSPITAL DISCHARGE; EFFICACY; PLACEBO; RELEASE; TOLERABILITY; MANAGEMENT; SURGERY; IR;
D O I
10.1097/j.pain.0000000000002026
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Pain after total knee arthroplasty is a prevalent condition. This study compared the effectiveness of tapentadol extended-release (ER) 50 mg x 2, oxycodone controlled-release (CR) 10 mg x 2, and placebo, as added to a multimodal analgesic regime both in-hospital and at home the first week after total knee arthroplasty. The study was randomized and blinded for investigators, staff, outcome assessors, and patients. Follow-up included pain intensity on mobilization, pain at rest, worst pain in the previous 24 hours, and adverse effects measured on 0 to 10 numerical rating scales. A total of 134 patients in 3 study groups received their allocated intervention and were included in the analysis. The primary outcome pain on mobilization the 7 first postoperative days reported as area under the curve was 528.1 (SD 267.5, interquartile range (IQR) 356.6-665.4) for placebo, 427.2 (SD 203.9, IQR 303.6-544.3) for tapentadol ER, and 507.9 (SD 243.7, IQR 292.4-686.8) for oxycodone CR (P = 0.12). With the exception of constipation being less prevalent in the tapentadol ER group (P = 0.02), we found no significant differences between treatment groups for the secondary outcomes. Tapentadol ER as an add-on to multimodal analgesia did not significantly improve pain relief when compared to oxycodone CR or placebo. Constipation was lowest in the tapentadol ER group.
引用
收藏
页码:396 / 404
页数:9
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