Dopaminergic agonists in Parkinson's disease

被引:47
作者
Alonso Canovas, A. [1 ]
Luquin Piudo, R. [2 ]
Garcia Ruiz-Espiga, P. [3 ]
Burguera, J. A. [4 ]
Campos Arillo, V. [5 ]
Castro, A. [6 ]
Linazasoro, G. [7 ]
Lopez del Val, J. [8 ]
Vela, L. [9 ]
Martinez Castrillo, J. C. [1 ]
机构
[1] Hosp Univ Ramon y Cajal, Serv Neurol, Madrid, Spain
[2] Univ Navarra Clin, Serv Neurol, Pamplona, Spain
[3] Fdn Jimenez Diaz, Serv Neurol, E-28040 Madrid, Spain
[4] Hosp La Fe, Serv Neurol, E-46009 Valencia, Spain
[5] Hosp Quiron, Serv Neurol, Malaga, Spain
[6] Hosp Xeral Galicia, Serv Neurol, La Coruna, Spain
[7] Policlin Guipuzcoa, Ctr Invest Parkinson, San Sebastian, Spain
[8] Hosp Clin Univ, Serv Neurol, Zaragoza, Spain
[9] Fdn Hosp Alcorcon, Serv Neurol, Madrid, Spain
来源
NEUROLOGIA | 2014年 / 29卷 / 04期
关键词
Dopamine agonists; Pramipexole; Ropinirole; Rotigotine; Prolonged release; Equivalence; ROPINIROLE PROLONGED-RELEASE; PRAMIPEXOLE EXTENDED-RELEASE; IMPULSE CONTROL DISORDERS; ROTIGOTINE TRANSDERMAL SYSTEM; DOUBLE-BLIND; DROPPED HEAD; LEVODOPA; PLACEBO; EFFICACY; SAFETY;
D O I
10.1016/j.nrl.2011.04.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background: Non-ergoline dopamine agonists (DA) are effective treatments for Parkinson's disease (PD). This review presents the pharmacology, evidence of efficacy and safety profile of pramipexole, ropinirole, and rotigotine, and practical recommendations are given regarding their use in clinical practice. Results: Extended-release formulations of pramipexole and ropinirole and transdermal continuous delivery rotigotine patches are currently available; these may contribute to stabilising of plasma levels. In early PD, the three drugs significantly improve disability scales, delay time to dyskinesia and allow a later introduction of levodopa. In late PD they reduced total 'off'-time, improved Unified Parkinson's Disease Rating Scale (UPDRS) in both 'on' and 'off' state and allowed a reduction in total levodopa dosage. A significant improvement in quality of life scales has also been demonstrated. Extended-release formulations have proved to be non-inferior to the immediate release formulations and are better tolerated (ropinirole). Despite a generally good safety profile, serious adverse events, such as impulse control disorder and sleep attacks, need to be routinely monitored. Although combination therapy has not been addressed in scientific literature, certain combinations, such as apomorphine and another DA, may be helpful. Switching from one DA to another is feasible and safe, although in the first days an overlap of dopaminergic side effects may occur. When treatment with DA is stopped abruptly, dopamine withdrawal syndrome may present. Suspending any DA, especially pramipexole, has been linked to onset of apathy, which may be severe. Conclusions: New non-ergotine DAs are a valuable option for the treatment of both early and late PD. Despite their good safety profile, serious adverse effects may appear; these effects may have a pathoplastic effect on the course of PD and need to be monitored. (C) 2011 Sociedad Espana de Neurologia. Published by Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:230 / 241
页数:12
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