Effect of high-dose preoperative methylprednisolone on recovery after total hip arthroplasty: a randomized, double-blind, placebo-controlled trial

被引:99
作者
Lunn, T. H. [1 ,2 ]
Andersen, L. O. [1 ,2 ]
Kristensen, B. B. [1 ,2 ]
Husted, H. [2 ,3 ]
Gaarn-Larsen, L. [2 ]
Bandholm, T. [3 ,4 ,5 ]
Ladelund, S. [4 ]
Kehlet, H. [2 ,6 ]
机构
[1] Hvidovre Univ Hosp, Dept Anaesthesiol, DK-2650 Hvidovre, Denmark
[2] Hvidovre Univ Hosp, Lundbeck Ctr Fast Track Hip & Knee Arthroplasty, DK-2650 Hvidovre, Denmark
[3] Hvidovre Univ Hosp, Dept Orthopaed Surg, DK-2650 Hvidovre, Denmark
[4] Hvidovre Univ Hosp, Clin Res Ctr, DK-2650 Hvidovre, Denmark
[5] Hvidovre Univ Hosp, Dept Phys Therapy, DK-2650 Hvidovre, Denmark
[6] Univ Copenhagen Hosp, Rigshosp, Sect Surg Pathophysiol, DK-2100 Copenhagen, Denmark
关键词
arthroplasty; replacement; hip; glucocorticoids; methylprednisolone; pain; postoperative; KNEE ARTHROPLASTY; STEROID USE; DEXAMETHASONE; PAIN; SURGERY; ANALGESIA; RECOMMENDATIONS; INFLAMMATION; QUALITY; BENEFIT;
D O I
10.1093/bja/aes345
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. High-dose glucocorticoid may reduce postsurgical pain and improve recovery. We hypothesized that 125 mg methylprednisolone (MP) would reduce time to meet functional discharge criteria after total hip arthroplasty (THA). Methods. Forty-eight patients undergoing unilateral THA under spinal anaesthesia were consecutively included in this randomized, double-blind, placebo-controlled trial receiving preoperative i.v. MP or saline. All patients received a standardized, multimodal analgesic regime with paracetamol, celecoxib, and gabapentin. The primary outcome was time to meet well-defined functional discharge criteria. Secondary outcomes were handgrip strength and endurance, pain, nausea, vomiting, fatigue, sleep quality, and rescue analgesic-, antiemetic-, and hypnotic medicine requirements. The inflammatory response measured by C-reactive protein (CRP) and actual length of stay were also registered. Discharge criteria were assessed twice daily (at 09: 00 and 14: 00 h) until discharge. Other outcomes were assessed at 2, 4, 6, 8, and 24 h after operation, and also in a questionnaire from postoperative day (POD) 1-4. Results. Time to meet discharge criteria was [median (IQR) (95% CI), MP vs placebo]: 23.5 (23.3-23.7) (17.8-43.8) vs 23.5 (23.0-23.8) (20.0-46.8) h, the mean difference (95% CI) being 21.3 (24.7 to 2.2) h, P=0.65. Overall pain for the first 24 h after surgery was significantly reduced in the MP vs the placebo group (P<0.01), as was CRP at 24 h (P<0.0001). No other between-group differences were observed. No drug-related complications were observed at follow-up on POD30. Conclusions. MP 125 mg i.v. before surgery added to a multimodal oral analgesic regime did not reduce time to meet functional discharge criteria after THA, but improved analgesia for the first 24 h.
引用
收藏
页码:66 / 73
页数:8
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