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. 2010 May 12;30(19):6667–6677. doi: 10.1523/JNEUROSCI.5459-09.2010

Table 1.

Clinical characteristics of the PD patients

Patient Age Gender Disease duration (years) UPDRS off UPDRS on l-DOPA dose per day Contacts R/L Motor states studied
P1 45 M 3 33 21 a 0–1 Both
0–2
P2 65 M 18 33 8 1725 2 Off
1
P3 62 F 20 52 23 1570 2 Off
2
P4 58 M 17 62 24 1430 1–2 Both
0–3
P5 58 M 19 27 3 900 1–3 Both
2
P6 55 M 10 42 19 1600 1 Both
1–3
P7 60 M 11 30 10 1925 2 Both
3
P8 59 M 11 34 15 875 1–2 Both
1–2
P9 54 M 10 55 23 1605 2–3 Both
1–3
P10 67 F 10 45 15 1275 2–1 Both
2–1
P11 67 M 13 27 13 500 3 Both
3
P12 67 M 10 33 10 1000 1 On
1
P13 47 M 12 44 17 875b 2–0 Both
1–3
P14 59 M 11 34 21 525b 1–3 Both
1
P15 55 F 7 27 14 1615 2–3 Both
3

The UPDRS scores are the motor subscale scores (UPDRS-III) before surgery. The l-DOPA dose includes the equivalent dose of all dopaminergic drugs taken by each patient in milligrams per day (100 mg of standard levodopa = 130 mg of controlled-released levodopa = 10 mg of bromocriptine = 1 mg of pergolide = 1 mg of lisuride = 1 mg of pramipexole = 5 mg of ropinirole). The contacts used for final programming in each patient are indicated in the last column.

aSustained dopaminergic treatment was suppressed at the time of surgery because of gastrointestinal intolerance.

bThe patient was also given continuous apomorphine infusion of a total dose of ∼100 mg/d.