Inage Kazuhide, Sainoh Takeshi, Okuyama Kohei, Yamashita Masaomi, Ohyama Shuhei, Fujimoto Kazuki, Chikubu Hiroto, Abe Koki, Ohtori Seiji, Orita Sumihisa
Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, JPN.
Orthopaedic Surgery, Sainou Hospital, Toyama, JPN.
Cureus. 2024 Oct 22;16(10):e72124. doi: 10.7759/cureus.72124. eCollection 2024 Oct.
There are no established treatments for low back pain. Conventional treatments include physiotherapy and pharmacological treatments, such as non-steroidal anti-inflammatory drugs (NSAIDs). Recently, analgesics with mechanisms of action different from those of NSAIDs have emerged. Tramadol formulations have especially attracted attention for being effective among patients in whom NSAIDs are not entirely effective. However, they are associated with side effects that can disrupt treatment. Tramadol hydrochloride immediate-release and extended-release tablets have been recently launched. Herein, we report our experience with these formulations in chronic low back pain patients.
To investigate the incidence of side effects and the analgesic effect of tramadol hydrochloride immediate-release and extended-release tablets in patients with chronic low back pain.
This was a multicenter retrospective observational study. The study included patients prescribed tramadol hydrochloride immediate-release and extended-release tablets for chronic low back pain at 13 facilities in Japan between January 2021 and December 2023. The primary outcome was the incidence of side effects observed during the study period. The secondary outcomes were changes in the visual analog scale (VAS) score.
The incidence of side effects was 37.7% (40/106 cases), which included constipation, nausea, drowsiness, and dizziness in 23 (21.7%), 13 (12.3%), 4 (3.8%), and 2 (1.9%) cases, respectively. The rate of treatment discontinuation owing to side effects was relatively low (16/106 cases, 15.1%). Furthermore, after four weeks of treatment, we found a significant reduction in the VAS scores for low back pain from baseline.
This study shows the incidence of side effects following the administration of tramadol hydrochloride immediate-release and extended-release tablets. Regarding the breakdown of side effects, constipation, nausea, drowsiness, and dizziness were noted. Regarding pain evaluation, we found a significant reduction in the VAS scores for low back pain from baseline after four weeks of treatment, suggesting that tramadol hydrochloride immediate-release and extended-release tablets may provide excellent analgesic effects owing to their pharmacokinetic properties that ensure stable tramadol concentrations in the bloodstream.
目前尚无针对腰痛的既定治疗方法。传统治疗方法包括物理治疗和药物治疗,如非甾体抗炎药(NSAIDs)。近年来,出现了作用机制与NSAIDs不同的镇痛药。曲马多制剂因其在NSAIDs不完全有效的患者中具有疗效而备受关注。然而,它们会产生可能干扰治疗的副作用。盐酸曲马多速释片和缓释片最近已上市。在此,我们报告我们在慢性腰痛患者中使用这些制剂的经验。
研究盐酸曲马多速释片和缓释片在慢性腰痛患者中的副作用发生率和镇痛效果。
这是一项多中心回顾性观察研究。该研究纳入了2021年1月至2023年12月期间在日本13家医疗机构因慢性腰痛而开具盐酸曲马多速释片和缓释片的患者。主要结局是研究期间观察到的副作用发生率。次要结局是视觉模拟量表(VAS)评分的变化。
副作用发生率为37.7%(40/106例),其中便秘、恶心、嗜睡和头晕分别有23例(21.7%)、13例(12.3%)、4例(3.8%)和2例(1.9%)。因副作用停药的比例相对较低(16/106例,15.1%)。此外,治疗四周后,我们发现腰痛的VAS评分较基线有显著降低。
本研究显示了服用盐酸曲马多速释片和缓释片后的副作用发生率。在副作用分类方面,注意到了便秘、恶心、嗜睡和头晕。在疼痛评估方面,我们发现治疗四周后腰痛的VAS评分较基线有显著降低,这表明盐酸曲马多速释片和缓释片因其药代动力学特性可确保曲马多在血液中浓度稳定,可能具有出色的镇痛效果。