Kupsch Andreas, Trottenberg Thomas, Bremen Dirk
Department of Neurology, Homboldt University of Berlin, Charité, Augustenburger Platz 1, 13353 Berlin, Germany.
Curr Med Res Opin. 2004 Jan;20(1):115-20. doi: 10.1185/030079903125002775.
The catechol-O-methyl transferase inhibitor entacapone is given in combination with levodopa/dopa decarboxylase inhibitor for Parkinson's disease (PD) patients experiencing end-of-dose wearing-off. This 4-week post-marketing surveillance study was undertaken to assess patients' responses to levodopa combined with entacapone in a real clinical practice setting. Overall, 466 patients with idiopathic PD treated with levodopa and experiencing symptoms of wearing-off were recruited. Both physicians and patients recorded the response to therapy, including improvements and side-effects. Following initiation of entacapone treatment, the average daily levodopa dose was reduced from 510 to 453 mg. Physician assessment of entacapone efficacy was judged to be "very good" or "good" in 77.6% of the patients, and tolerability was considered to be "very good" or "good" in 92.4% of patients, with only 12 patients (2.6%) withdrawing from the study. Compared with baseline, there was a decrease in the mean duration of daily 'off' time from 3.0 to 1.3 h per day during the treatment period. Adverse events were in line with those previously reported, with diarrhoea being the most frequent event. The percentage of patients suffering from dyskinesia decreased from 46 to 34%, and of those patients still suffering from dyskinesia, the average daily duration of dyskinesia was reduced from 2.2 to 1.7 h. The use of adjunct dopamine agonists decreased from 67 to 59%. At study end, the percentage of patients who rated their quality of life (QoL) as "very good" or "good" increased from 12.1 to 51.7% and the percentage of patients who rated their QoL as "bad" or "very bad" decreased from 40 to 10.7%. In summary, the results of this survey conducted in real clinical practice support the findings of previous clinical trials demonstrating the efficacy and tolerability of entacapone, as well as the benefits of improved QoL, for patients achieved with entacapone.
儿茶酚-O-甲基转移酶抑制剂恩他卡朋与左旋多巴/多巴脱羧酶抑制剂联合用于治疗出现剂末疗效减退的帕金森病(PD)患者。这项为期4周的上市后监测研究旨在评估在实际临床实践中患者对左旋多巴联合恩他卡朋的反应。总体而言,招募了466例接受左旋多巴治疗且出现疗效减退症状的特发性PD患者。医生和患者均记录了治疗反应,包括改善情况和副作用。恩他卡朋治疗开始后,左旋多巴的平均日剂量从510毫克降至453毫克。医生对恩他卡朋疗效的评估在77.6%的患者中被判定为“非常好”或“好”,92.4%的患者认为耐受性“非常好”或“好”,仅有12例患者(2.6%)退出研究。与基线相比,治疗期间每日“关”期的平均时长从3.0小时降至1.3小时。不良事件与先前报道的一致,腹泻是最常见的事件。患运动障碍的患者比例从46%降至34%,在仍患有运动障碍的患者中,运动障碍的平均每日时长从2.2小时降至1.7小时。辅助使用多巴胺激动剂的比例从67%降至59%。在研究结束时,将生活质量(QoL)评为“非常好”或“好”的患者比例从12.1%增至51.7%,将QoL评为“差”或“非常差”的患者比例从40%降至10.7%。总之,在实际临床实践中进行的这项调查结果支持了先前临床试验的结果,表明恩他卡朋对患者具有疗效和耐受性,以及改善QoL的益处。