Linazasoro Gurutz
Centro de Investigación Parkinson. Policlínica Gipuzkoa, San Sebastián, Spain.
Clin Neuropharmacol. 2008 Jan-Feb;31(1):19-24. doi: 10.1097/wnf.0b013e318067bcc4.
Cabergoline is an ergotic dopamine agonist with D2 receptor activity and a very long half-life. This pharmacological profile may result in clinically different effects. Small clinical trials indicate that overnight switching from 1 agonist to another can be performed safely.
To determine safety and efficacy of overnight switching from dopamine agonists to cabergoline in patients with advanced Parkinson disease (PD).
Patients with advanced PD and motor complications not optimally controlled by levodopa and a stable dose of bromocriptine, pergolide, pramipexole, and ropinirole were converted to cabergoline overnight. Patients were assessed by using an on-off diary, Unified Parkinson Disease Rating Scale (subscales I-IV), Parkinson's Disease Quality of Life 8 (PDQ-8), an ad hoc sleep questionnaire and an ad hoc off-period severity questionnaire. All rating scales were administered just before conversion and after 2, 6, and 12 weeks of treatment, when patients were on an optimal dose of cabergoline. Adverse effects were assessed at every visit following a check list.
One hundred twenty-eight patients were included in the trial. Forty were on pergolide (mean dose, 2.8 mg/d), 38 on pramipexole (mean dose, 2.1 mg/d), and 32 on ropinirole (mean dose, 8.1 mg/d). Patients on bromocriptine (n = 18) were excluded from the analysis because of the small sample size. Three patients reported serious side effects (respiratory arrest, dyskinesias, and face edema and abdominal pain). Twenty-eight patients reported 41 adverse events. Twelve patients were withdrawn due to adverse effects (hallucinations [n = 5], dyspnea [n = 1], dizziness [n = 4], and vascular problems [n = 2]). A significant improvement in assessed parameters was obtained (P < 0.0001). Mean levodopa dose remained unchanged. After 12 weeks, the mean dose of cabergoline was 3.2 mg, and 25% of patients were taking the drug twice a day.
Switching from pergolide, ropinirole, and pramipexole to cabergoline in an overnight schedule is safe. The observed clinical improvement may be related to a placebo effect, to the use of low doses of dopamine agonists, or to a direct effect of cabergoline.
卡麦角林是一种具有D2受体活性且半衰期很长的麦角多巴胺激动剂。这种药理学特性可能导致临床上不同的效果。小型临床试验表明,从一种激动剂夜间转换为另一种激动剂可以安全进行。
确定晚期帕金森病(PD)患者从多巴胺激动剂夜间转换为卡麦角林的安全性和有效性。
晚期PD且运动并发症未通过左旋多巴和稳定剂量的溴隐亭、培高利特、普拉克索及罗匹尼罗得到最佳控制的患者,夜间转换为卡麦角林。使用开-关日记、统一帕金森病评定量表(I-IV分量表)、帕金森病生活质量8项问卷(PDQ-8)、一份特设睡眠问卷和一份特设关期严重程度问卷对患者进行评估。所有评定量表均在转换前以及治疗2、6和12周后(此时患者服用最佳剂量的卡麦角林)进行施测。按照检查表在每次就诊时评估不良反应。
128例患者纳入试验。40例服用培高利特(平均剂量2.8mg/d),38例服用普拉克索(平均剂量2.1mg/d),32例服用罗匹尼罗(平均剂量8.1mg/d)。服用溴隐亭的患者(n = 18)因样本量小被排除在分析之外。3例患者报告了严重副作用(呼吸骤停、运动障碍、面部水肿和腹痛)。28例患者报告了41次不良事件。12例患者因不良反应退出(幻觉[n = 5]、呼吸困难[n = 1]、头晕[n = 4]和血管问题[n = 2])。评估参数有显著改善(P < 0.0001)。左旋多巴平均剂量保持不变。12周后,卡麦角林平均剂量为3.2mg,25%的患者每日服用该药两次。
夜间从培高利特、罗匹尼罗和普拉克索转换为卡麦角林是安全的。观察到的临床改善可能与安慰剂效应、低剂量多巴胺激动剂的使用或卡麦角林的直接作用有关。