Choi Gi Won, Park Kwang Hwan, Yoon Yeo Kwon, Lee Jin Woo, Shim Dong Woo
Department of Orthopedic Surgery, Korea University Ansan Hospital, Ansan, 15355, Korea.
Department of Orthopedic Surgery, Yonsei University College of Medicine, Seoul, 03722, Korea.
J Orthop Surg Res. 2024 Dec 26;19(1):882. doi: 10.1186/s13018-024-05321-7.
To compare the analgesic efficacy, adverse effects, and long-term functional outcomes of perioperative naproxen alone versus naproxen with pregabalin for treating pain in ankle fractures.
This study included 70 patients who underwent operative fixation of rotatory ankle fractures. Group A received naproxen 500 mg only, and Group B received naproxen 500 mg with pregabalin 75 mg 2-hour before surgery and 12 hourly for 14 days thereafter. The minimal clinically important difference of the visual analog scale (VAS) for pain was set at 1.8 out of 10. VAS for pain, opioid consumption, and any adverse effects were recorded for 3 days postoperatively. VAS for pain was checked at 2- and 6-weeks and 3- and 6-months, and functional outcomes were measured at 3- and 6-months postoperatively.
Sixty-three patients (33 and 30 in groups A and B, respectively) completed the 6-month follow-up. Demographic data were similar between groups. VAS for pain did not significantly differ between the groups at any timepoint up to 6 months (P ≥ 0.520), with 95% confidence intervals consistently within 1.8. No significant differences were observed between groups in opioid consumption and functional outcomes (P ≥ 0.211). In group B, dizziness at 48-hour and somnolence at 72-hour were significantly predominant (P ≤ 0.05).
Our study demonstrated comparable pain reduction between two groups following operative fixation of rotatory ankle fractures. However, side effects, including dizziness and somnolence, were predominant in Group B between 48 and 72 h.
比较围手术期单独使用萘普生与萘普生联合普瑞巴林治疗踝关节骨折疼痛的镇痛效果、不良反应及长期功能结局。
本研究纳入70例行旋转型踝关节骨折手术固定的患者。A组仅接受500 mg萘普生治疗,B组在术前2小时接受500 mg萘普生与75 mg普瑞巴林治疗,术后每12小时给药1次,共14天。疼痛视觉模拟量表(VAS)的最小临床重要差异设定为10分制中的1.8分。术后3天记录疼痛VAS、阿片类药物消耗量及任何不良反应。在术后2周和6周、3个月和6个月检查疼痛VAS,并在术后3个月和6个月测量功能结局。
63例患者(A组33例,B组30例)完成了6个月的随访。两组间人口统计学数据相似。在长达6个月的任何时间点,两组间疼痛VAS均无显著差异(P≥0.520),95%置信区间始终在1.8以内。两组间阿片类药物消耗量及功能结局无显著差异(P≥0.211)。在B组中,48小时时的头晕和72小时时的嗜睡显著更常见(P≤0.05)。
我们的研究表明,旋转型踝关节骨折手术固定后两组的疼痛减轻程度相当。然而,B组在48至72小时之间出现的副作用,包括头晕和嗜睡更为常见。