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酒石酸布托啡诺透皮贴剂治疗中重度慢性非癌痛的临床疗效观察

Efficacy of tapentadol prolonged release for pre- and post-operative low back pain: a prospective observational study.

机构信息

Section of Anesthesia, Intensive Care and Pain medicine, Department of Emergency and Urgency, Città di Castello Hospital, Città di Castello, Perugia, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Nov;23(4 Suppl):14-20. doi: 10.26355/eurrev_201911_19377.

Abstract

OBJECTIVE

Low back pain (LBP) is a highly prevalent chronic pain condition with a neuropathic component of pain that limits the benefits of classical opioids. Tapentadol is an innovative drug for the treatment of chronic severe pain, with a dual mechanism of action combining µ-opioid receptors agonism and noradrenaline re-uptake inhibition (NRI). Its efficacy is equal to that of strong opioids, with a better tolerability profile and a consequently lower risk of treatment discontinuation. The aim of this study was to evaluate the analgesic efficacy and tolerability of tapentadol prolonged release (PR) vs. other analgesics in patients with moderate-to-severe neuropathic low back pain, before and after back surgery.

PATIENTS AND METHODS

The primary endpoints of the study were the rate of response to treatment, measured as ≥30% reduction in pain intensity on the Numeric Rating Scale (NRS), and tapentadol PR efficacy for pain relief. The secondary endpoints were the improvements of the neuropathic component of pain and of sleep quality.

RESULTS

A total of 40 patients were enrolled in the study, receiving either tapentadol PR (n=21, 52.5%) or other analgesics (n=19, 47.5%), both before and after surgery. The rate of response to treatment was statistically in favor of tapentadol PR (p<0.01). The reduction in pain intensity was statistically significant in the group treated with tapentadol PR, both before and after surgery (p<0.01), with a complete resolution of pain 90 days after surgery. The quality of sleep after surgery improved more in patients treated with tapentadol PR than in the comparator group (p<0.01), with 100% of the patients reporting a "good" sleep quality 2 months after surgery.

CONCLUSIONS

Tapentadol PR was well tolerated by all patients, and its efficacy for pain relief was also confirmed in our small group of "real-life" patients with chronic, severe low back pain. Overall, the tolerability of this treatment may help to improve patients' quality of life, which is frequently compromised because of pain and its related comorbidities.

摘要

目的

腰痛(LBP)是一种常见的慢性疼痛疾病,具有疼痛的神经病理性成分,限制了经典阿片类药物的疗效。盐酸他喷他多是一种治疗慢性重度疼痛的创新药物,具有双重作用机制,即阿片μ受体激动作用和去甲肾上腺素再摄取抑制(NRI)。其疗效与强阿片类药物相当,但具有更好的耐受性,因此停药风险较低。本研究旨在评估盐酸他喷他多缓释片(PR)与其他镇痛药在中重度神经病理性腰痛患者手术前后的镇痛疗效和耐受性。

患者和方法

研究的主要终点是治疗反应率,以数字评分量表(NRS)上疼痛强度降低≥30%来衡量;以及盐酸他喷他多 PR 的止痛效果。次要终点是改善疼痛的神经病理性成分和睡眠质量。

结果

共有 40 例患者入组本研究,分别接受盐酸他喷他多 PR(n=21,52.5%)或其他镇痛药(n=19,47.5%)治疗,包括手术前后。治疗反应率统计学上有利于盐酸他喷他多 PR(p<0.01)。手术前后,接受盐酸他喷他多 PR 治疗的患者疼痛强度降低具有统计学意义(p<0.01),手术后 90 天疼痛完全缓解。手术后,接受盐酸他喷他多 PR 治疗的患者睡眠质量改善较对照组更明显(p<0.01),手术后 2 个月,100%的患者报告“良好”的睡眠质量。

结论

所有患者均耐受良好,且在我们的小样本“真实世界”慢性重度腰痛患者中,也证实了盐酸他喷他多 PR 的止痛疗效。总体而言,这种治疗方法的耐受性可能有助于改善患者的生活质量,因为疼痛及其相关并发症经常会降低患者的生活质量。

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