Table 1.
PD/ET DBS Adverse Events (AE) | Frequency |
---|---|
DBS Tremor study n = 424 | |
Patient with ≥1 device/surgery AE (i.e. 7% postoperative pain) | 28% |
Patients ≥ 1 stimulation AE (i.e. paresthesia 33%) | 40% |
Death , DBS-related | 0.7% * |
DBS PD study n = 160 | |
Patients ≥ 1 device AE | 96.3% |
Stimulation adverse events | 51.9% |
Device adverse events | 36.9% |
Ongoing stimulation adverse events | 22.5% |
Ongoing device adverse events | 10.0% |
Stimulation serious adverse events | 9.4% |
Device serious adverse events | 17.5% |
Serious ongoing stimulation AE | 3.1% |
Serious ongoing device AE | 6.3% |
Infection | 10.6%* |
Paresis/asthenia | 10.0% |
Hemiplegia/hemiparesis | 8.1% |
Intracranial hemorrhage | 7.5%* |
Death , DBS-related | 0.6% * |
Life threatening; (Medtronic 2015).