Initiating therapy for Parkinson's disease

被引:17
作者
Silver, DE
Ruggieri, S
机构
[1] Scripps Mem Hosp, La Jolla, CA USA
[2] Univ Roma La Sapienza, Dipartimento Sci Neurol, I-00185 Rome, Italy
[3] IRCCS Neuromed, Pozzilli, Italy
关键词
D O I
10.1212/WNL.50.6_Suppl_6.S18
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Accurate diagnosis and individualized assessment of the risks and benefits of available antiparkinsonian medications should guide initiation of treatment for patients with early Parkinson's disease (PD). In general, the goals of treatment for younger patients (less than age 60 years) are control of impairing symptoms, sparing of levodopa to minimize long-term complications, and consideration of neuroprotection. The primary initial medication choices for patients under age 50 years include selegiline, amantadine, and anticholinergic agents. Patients in their fifties may require a dopamine agonist in addition to or instead of selegiline to achieve adequate symptom control. If the desired response is still not achieved, sustained-release carbidopa-levodopa should be added, followed by adjunctive amantadine or anticholinergic therapy. For older patients (60 years and over), improvement of functional impairment is the primary goal. For these patients, a special concern is to avoid inducing or exacerbating cognitive impairment. Sustained-release carbidopa-levodopa is considered first-line treatment for these patients. Inadequate response can be handled by a trial of immediate-release carbidopa-levodopa and then addition of a dopamine agonist when maximum levodopa doses are reached. Anticholinergic agents, amantadine, and selegiline should be avoided because of their CNS effects.
引用
收藏
页码:S18 / S22
页数:5
相关论文
共 22 条
  • [1] Comparison of immediate-release and controlled release carbidopa/levodopa in Parkinson's disease - A multicenter 5-year study
    Block, G
    Liss, C
    Reines, S
    Irr, J
    Nibbelink, D
    Aarli, J
    Aguilar, M
    Ahrens, S
    Bakheit, A
    Baumel, B
    Bertoni, J
    Capildeo, R
    CastroCaldas, A
    Deza, L
    Donaldson, I
    Franck, G
    Fusillo, J
    Gauthier, S
    Gershanik, O
    Granerus, AK
    Hauser, RA
    Hennessey, K
    Hutton, JT
    Joffe, R
    Koller, W
    Last, B
    LeWitt, P
    Mamoli, B
    Manyam, B
    Mark, M
    Nakano, K
    Nausieda, P
    Otero, E
    Paulson, G
    Pinter, M
    Reich, S
    Rodnitzky, R
    Sage, J
    Sampaio, C
    Smith, B
    Teravainen, H
    Tetrud, J
    Tolosa, E
    Ulm, G
    Valesco, F
    [J]. EUROPEAN NEUROLOGY, 1997, 37 (01) : 23 - 27
  • [2] Bravi D, 1996, EUR J NEUROL, V3, P13
  • [3] CALNE DB, 1993, NEW ENGL J MED, V329, P1021
  • [4] CALNE DB, 1994, NEUROLOGY, V44, P8
  • [5] VARIABLE EXPRESSION OF PARKINSONS-DISEASE - A BASE-LINE ANALYSIS OF THE DATATOP COHORT
    JANKOVIC, J
    MCDERMOTT, M
    CARTER, J
    GAUTHIER, S
    GOETZ, C
    GOLBE, L
    HUBER, S
    KOLLER, W
    OLANOW, C
    SHOULSON, I
    STERN, M
    TANNER, C
    WEINER, W
    [J]. NEUROLOGY, 1990, 40 (10) : 1529 - 1534
  • [6] JENNER P, 1995, NEUROLOGY S3, V45, pS6
  • [7] PHARMACOLOGICAL TREATMENT OF PARKINSONIAN TREMOR
    KOLLER, WC
    [J]. ARCHIVES OF NEUROLOGY, 1986, 43 (02) : 126 - 127
  • [8] KOLLER WC, 1992, NEUROLOGY, V42, P6
  • [9] KOLLER WC, 1994, NEUROLOGY S1, V44, pS10
  • [10] DEPRENYLS EFFECT AT SLOWING PROGRESSION OF PARKINSONIAN DISABILITY - THE DATATOP STUDY
    LEWITT, PA
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 1991, 84 : 79 - 86