We studied the effectiveness of cabergoline as an adjunct
in patients with early Parkinson’s disease receiving another
dopamine agonist (pramipexole or ropinirole), at the maximal
permitted dose. The study enrolled 47 patients: 35 had motor
fluctuations and were receiving a dopamine agonist with
levodopa; and 12, without motor fluctuations, were receiving a
dopamine agonist without levodopa. These medications had in all
cases failed to achieve adequate symptom control. In the 35
patients with motor fluctuations, when cabergoline was added to
therapy, the time spent in the OFF period decreased by 65.6%
(from 3.14±1.11 to 1.08±1.07 hours p<0.0001); and the Unified
Parkinson’s Disease Rating Scale (UPDRS) motor score decreased
by 19.24% (from 41.68±12.6 to 33.66±10.22; (p<0.0001) during
the OFF condition, and by 7.11% (from 17.01±6.63 to 15.8±7.22;
p<0.001) during the ON condition. Nocturnal akinesia improved
in all the patients except one. In the 12 patients without motor
fluctuations, when cabergoline was added, the UPDRS score
improved by 34.4% (from 23.5±5.3 to 15.5±4.7).