Arnold Lesley M, McCarberg Bill H, Clair Andrew G, Whalen Ed, Thomas Neal, Jorga Anamaria, Pauer Lynne, Vissing Richard, Park Peter W
a Department of Psychiatry and Behavioral Neuroscience, Women's Health Research Program , University of Cincinnati College of Medicine , Cincinnati , OH , USA.
b Department of Family Medicine , University of California at San Diego School of Medicine , San Diego , CA , USA.
Postgrad Med. 2017 Nov;129(8):921-933. doi: 10.1080/00325481.2017.1384691. Epub 2017 Oct 16.
The pregabalin dose-response for pain, Patient Global Impression of Change (PGIC), and sleep quality measures in painful diabetic peripheral neuropathy (pDPN), postherpetic neuralgia (PHN), and fibromyalgia (FM) is relevant for physicians treating these patients. This analysis aimed to demonstrate the dose-response of pregabalin for each indication and describe the onset (incidence), onset/continuation (prevalence), and resolution of adverse events (AEs) occurring during treatment.
Data from 14 placebo-controlled, fixed-dose pregabalin trials in pDPN, PHN, and FM were pooled within each indication. Patients had mean baseline pain scores ≥6 on an 11-point numeric rating scale. A hyperbolic E dose-response model examined the dose-response of pregabalin for pain, PGIC, and sleep quality. Safety assessments included onset and prevalence of common AEs each week, and resolution in the first 2 months of treatment.
In all indications, the likelihood of patients experiencing pain relief and improvements in PGIC and sleep quality increased in a dose-dependent manner with increasing doses. In all indications, new incidences of dizziness and somnolence were highest after 1 week of treatment, with few subsequent new reports at a given dose. Prevalence rates decreased steadily after 1 week of treatment. In FM, new onset weight gain emerged 6-8 weeks following treatment; prevalence rates generally increased then remained steady over time. With the exception of weight gain, many AEs resolved in month 1.
The dose-response of pregabalin for pain, PGIC, and sleep quality was demonstrated, highlighting the benefit of achieving the maximum recommended dose of 300 mg/day for pDPN, 300-600 mg/day for PHN, and 300-450 mg/day for FM. Common AEs are generally seen within 1 week of starting treatment, with few subsequent new reports at a given dose. New onset weight gain occurs after 6 weeks of treatment, reinforcing the need for regular monitoring of weight.
普瑞巴林在疼痛性糖尿病周围神经病变(pDPN)、带状疱疹后神经痛(PHN)和纤维肌痛(FM)患者中对疼痛、患者总体印象改善(PGIC)及睡眠质量指标的剂量反应,对治疗这些患者的医生而言具有重要意义。本分析旨在证明普瑞巴林在每种适应症中的剂量反应,并描述治疗期间发生的不良事件(AE)的发生情况(发病率)、发生/持续情况(患病率)及缓解情况。
在每种适应症范围内,汇总来自14项针对pDPN、PHN和FM的安慰剂对照、固定剂量普瑞巴林试验的数据。患者在11点数字评分量表上的平均基线疼痛评分≥6分。采用双曲线E剂量反应模型研究普瑞巴林对疼痛、PGIC和睡眠质量的剂量反应。安全性评估包括每周常见AE的发生情况和患病率,以及治疗前2个月内的缓解情况。
在所有适应症中,随着剂量增加,患者疼痛缓解、PGIC改善及睡眠质量提高的可能性呈剂量依赖性增加。在所有适应症中,头晕和嗜睡的新发病率在治疗1周后最高,在给定剂量下随后新报告很少。治疗1周后患病率稳步下降。在FM中,治疗6 - 8周后出现新的体重增加;患病率通常先增加,然后随时间保持稳定。除体重增加外,许多AE在第1个月内缓解。
证明了普瑞巴林对疼痛、PGIC和睡眠质量的剂量反应,突出了对于pDPN达到最大推荐剂量300mg/天(PHN为300 - 600mg/天,FM为300 - 450mg/天)的益处。常见AE通常在开始治疗1周内出现,在给定剂量下随后新报告很少。治疗6周后出现新的体重增加,强化了定期监测体重的必要性。