Orthopedics. 2021 Mar-Apr;44(2):105-110. doi: 10.3928/01477447-20201216-04. Epub 2020 Dec 30.
Nonsteroidal anti-inflammatory drugs can delay bone healing. This knowledge is mainly derived from retrospective and animal studies. The authors therefore conducted a human study to investigate whether ibuprofen affects radiological, functional, densitometrical, and biochemical outcomes following a Colles' fracture, as well as the analgesic effect of ibuprofen. This was a single-center, triple-blinded, randomized, placebo-controlled clinical trial with a total of 96 patients. All of the patients received basic treatment with 1000 mg of acetaminophen 4 times daily. The placebo group received a placebo for 7 days. The 3-day ibuprofen group received 600 mg of ibuprofen 3 times daily for the first 3 days and a placebo for the following 4 days. The 7-day ibuprofen group received ibuprofen 3 times daily for 7 days. The primary outcome was the fragment migration for a period of 5 weeks. The secondary outcomes were changes in the wrist's range of motion; Disabilities of the Arm, Shoulder and Hand score; bone mineral density of the injured wrist; changes in serum CrossLaps (Roche Diagnostics) and osteocalcin; and analgesic effects. Analyses were performed according to an intention-to-treat approach. No significant differences in radiological migration or functional, densitometrical, and biochemical effects were established among the treatment groups (.06≤≤.9). During the first 3 days, the pain score was lower (=.02) in the ibuprofen groups than in the placebo group. The findings of this study offer an indication for ibuprofen as a bone-safe analgesic treatment after Colles' fracture and may be translated into other fields of cancellous bone fracture treatment. [. 2021;44(2):105-110.].
非甾体抗炎药会延迟骨骼愈合。这一知识主要源自回顾性和动物研究。因此,作者进行了一项人类研究,以调查布洛芬是否会影响科雷氏骨折后的影像学、功能、骨密度和生化结果,以及布洛芬的镇痛效果。这是一项单中心、三盲、随机、安慰剂对照的临床试验,共有 96 名患者。所有患者均接受了基础治疗,即每日 4 次服用 1000 毫克对乙酰氨基酚。安慰剂组在第 7 天服用安慰剂。3 天布洛芬组前 3 天每日 3 次服用 600 毫克布洛芬,接下来 4 天服用安慰剂。7 天布洛芬组连续 7 天每日 3 次服用布洛芬。主要结果是 5 周内的断端移位。次要结果是腕关节活动范围的变化;手臂、肩部和手部残疾评分;受伤腕部的骨密度;血清 CrossLaps(罗氏诊断)和骨钙素的变化;以及镇痛效果。分析按照意向治疗方法进行。在影像学迁移或功能、骨密度和生化作用方面,各治疗组之间未发现显著差异(0.06≤≤0.9)。在前 3 天,布洛芬组的疼痛评分低于安慰剂组(=0.02)。本研究的结果表明,布洛芬可用作科雷氏骨折后的骨安全镇痛治疗,且可能推广至其他松质骨骨折治疗领域。[. 2021;44(2):105-110.].