首页> 外文期刊>Clinical drug investigation >Impact of pregabalin treatment on pain, pain-related sleep interference and general well-being in patients with neuropathic pain: a non-interventional, multicentre, post-marketing study.
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Impact of pregabalin treatment on pain, pain-related sleep interference and general well-being in patients with neuropathic pain: a non-interventional, multicentre, post-marketing study.

机译:普瑞巴林治疗对神经性疼痛患者的疼痛,与疼痛相关的睡眠干扰和总体健康的影响:一项非干预,多中心,上市后研究。

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Background and Objectives: Numerous controlled clinical trials have demonstrated the safety and efficacy of pregabalin in the treatment of neuropathic pain. The objectives of the present study were to assess the impact of pregabalin under real-world conditions on pain, pain-related sleep interference and general well-being, and to assess the tolerability and safety of pregabalin in patients diagnosed with neuropathic pain of central or peripheral origin. Methods: This was a non-interventional, multicentre study in which pregabalin was administered for 8 weeks, at the therapeutic dosages of 150-600 mg/day, to patients with a diagnosis of neuropathic pain. Pain intensity and pain-related sleep interference were measured using 11-point numerical rating scales, while well-being was assessed by documenting how often emotions associated with anxiety or depression were felt over the past week. Patient and Clinician Global Impression of Change (PGIC and CGIC) were assessed at the final visit. Results: In the 668 patients included in the full analysis set, there were significant (p < 0.0001) reductions in mean pain and pain-related sleep interference scores of 4.16 and 4.02, respectively. Indicators of general well-being showed improvement from baseline to final visit. The majority of patients were rated as 'much improved' (43.7% and 36.7%) or 'very much improved' (24.0% and 26.2%) on CGIC and PGIC scores, respectively. Discontinuation because of lack of efficacy occurred in 0.7% of 691 patients in the safety analysis set while discontinuation because of adverse events occurred in 5.1% of this population; 76.4% continued treatment after the study ended. Conclusion: Significant reductions in pain and pain-related sleep interference, combined with reductions in feelings of anxiety and depression, suggest that pregabalin under real-world conditions improves the overall health and well-being of patients with neuropathic pain.
机译:背景与目的:大量对照临床试验证明普瑞巴林治疗神经性疼痛的安全性和有效性。本研究的目的是评估普瑞巴林在现实世界条件下对疼痛,与疼痛相关的睡眠干扰和总体健康的影响,并评估普瑞巴林在诊断为中枢性或神经性神经痛的患者中的耐受性和安全性。外围起源。方法:这是一项非干预性的多中心研究,其中以诊断剂量为150-600 mg / day的普瑞巴林(pregabalin)给药8周,用于诊断为神经性疼痛的患者。使用11点数字评分量表测量疼痛强度和与疼痛相关的睡眠干扰,同时通过记录过去一周内与焦虑或抑郁相关的情绪记录的频率来评估幸福感。在最终访问时评估患者和临床医生的整体变化印象(PGIC和CGIC)。结果:包括在完整分析集中的668例患者中,平均疼痛和与疼痛相关的睡眠干扰评分分别显着(p <0.0001)降低了4.16和4.02。总体幸福感指标显示从基线到最终就诊均改善。大多数患者的CGIC和PGIC评分分别为“好转”(43.7%和36.7%)或“好转”(24.0%和26.2%)。在安全性分析中,由于691名患者中0.7%的患者因缺乏疗效而停药,而因不良事件而停药的人群中有5.1%发生了停药。研究结束后,有76.4%的患者继续接受治疗。结论:疼痛和与疼痛相关的睡眠干扰的显着减少,以及焦虑和抑郁感的减少,表明在现实条件下的普瑞巴林可改善神经性疼痛患者的整体健康和幸福感。

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