Centre for Big Data Research in Health, University of New South Wales, Sydney, Australia.
Menzies Centre for Health Policy, The University of Sydney, Sydney, Australia.
Br J Clin Pharmacol. 2020 Sep;86(9):1882-1887. doi: 10.1111/bcp.14276. Epub 2020 Mar 22.
Following the 2013 public subsidy of pregabalin in Australia for neuropathic pain not responding to other medicines, use and misuse increased substantially. We used pharmaceutical dispensing claims for a 10% sample of Australians to quantify initiation, discontinuation and dispensing of other analgesics before and after initiation. We identified 130 770 people initiating pregabalin between 2013/14 and 2017/18 (median age: 61 years; 56.8% female). Discontinuation rates at 1-year increased from 77.0% in 2013/14 to 85.9% in 2017/18; 38% only had 1 dispensing. Approximately 1/3 (37.5%) initiated on the lowest strength capsule (25 mg) with only 31.2% later up-titrating to a higher strength. 47.4% and 53.0% were dispensed opioids within 180 days before and after pregabalin initiation, respectively. Many individuals are using pregabalin for short treatment durations and low dose ranges not consistent with treatment of neuropathic pain, which is generally a chronic condition. This may suggest poorer tolerability than observed in clinical trials, or use for other conditions, some of which may be for indications where the balance of benefits and risk is less clear.
在澳大利亚于 2013 年对其他药物治疗无效的神经病理性疼痛进行公共补贴后, pregabalin 的使用和滥用大幅增加。我们利用澳大利亚 10%的药品配给数据样本,在 pregabalin 起始治疗前后,对其他镇痛药的起始、停止和配给情况进行了量化。我们确定了 2013/14 年至 2017/18 年间共有 130770 人开始使用 pregabalin(中位年龄:61 岁;56.8%为女性)。1 年内停药率从 2013/14 年的 77.0%增加到 2017/18 年的 85.9%;38%的患者仅配给 1 次。约有 1/3(37.5%)患者起始使用最低剂量胶囊(25 毫克),仅有 31.2%的患者随后增加到较高剂量。在 pregabalin 起始治疗前后的 180 天内,分别有 47.4%和 53.0%的患者配给了阿片类药物。许多患者的治疗持续时间和剂量范围较短,与治疗神经病理性疼痛不一致,而神经病理性疼痛通常是一种慢性疾病。这可能表明其耐受性比临床试验中观察到的要差,或者用于其他疾病,其中一些疾病可能用于获益和风险平衡不太明确的适应证。