Four dopamine-agonists, two calechol-o-methyltransferase-inhibitors, budipi
ne, a dispersible levodopa preparation and deep brain stimulation enriched
the armamentarium for Parkinson's disease treatment between the years 1995-
1998 in Germany. Amantadine goes through a renaissance as it was shown to b
e effective in levodopa induced dyskinesias. Deep brain stimulation in the
subthalamic nucleus and internal globus pallidus is emerging as a new treat
ment strategy for patients with severe on-off fluctuations and levodopa dys
kinesias while the original target for tremor-suppression, VIM thalamic nuc
leus, is used less frequently in Parkinson's disease. The introduction of t
hese new therapeutic options has widened the scope and increased the comple
xities of Parkinson's disease treatment.