Clear PD dx by movement disorder neurologist crucial (other conditions like progressive supranuclear palsy & multiple system atrophy can mimic PD but don't respond to Qx)
Off-med & on-supratherapeutic oral levodopa ("on-off" testing) strongly predicts quantitative improvement in UPDRS III post-DBS
Two Qx indications: motor complications from long-term Rx (commonly dyskinesias & motor fluctuations) ± Rx intractable tremor
DBS can ↓ severity, duration, & frequency of "off" periods and ↓ medication-induced complications → ↑ QOL
Investigation ongoing into DBS for early motor complications of PD
Deep Brain Stimulation (DBS) for confirmed idiopathic Parkinson's Disease (PD) pts
Idiopathic PD: bradykinesia ± rigidity, resting tremor, postural instability
Postural instability early in disease → potential atypical parkinsonism, relative DBS CI
Atypical parkinsonian syndromes (PSP, MSA, Lewy body dementia, corticobasal ganglionic degeneration) can mimic idiopathic PD → avoid DBS, ↓ response to stimulation
Atypical parkinsonism: early onset, rapid progress, early dysautonomia, bulbar dysfunction, respiratory compromise, spasticity, ataxia, apraxia
PD severity & duration ≠ DBS outcome predictors, but rule out atypical parkinsonism
Advanced Sx < 5 yrs after onset → further ✓ for atypical parkinsonism
DBS CI if severe motor complications → ↓ QOL
Average PD duration b/w 11-14 yrs at DBS, but earlier DBS (7 yrs) shows promising results
Severe PD disability typically aligns w/ UPDRS motor scores ~30 or MDS-UPDRS scores ~50
Ideal DBS candidate: severe disability off levodopa, manages well on Rx ± dyskinesias
Sustained preoperative levodopa response: ↑ diagnostic support for PD, best predictor of DBS outcome
Levodopa response defined as ≥ 30% ↑ in UPDRS motor scores over "off" state
Levodopa response beneficial even in levodopa intolerant PD pts or w/ dopa-refractory tremor
Advanced age (especially >70 yrs) can negatively influence DBS outcome (↑ cognitive decline, gait instability), but no specific age cutoff
DBS decisions in elderly individualized considering disability level, Qx risks, life expectancy, motivation
Preoperative dementia is a risk factor for cognitive decline post-DBS, especially in older pts and severe preoperative cognitive impairment
PD cognitive decline: impaired executive fnx, visuospatial abnormalities, impaired memory, language deficits
Preoperative psychiatric evaluation may assess untreated depression, anxiety, dopaminergic dysregulation syndrome, medication-induced hypomania/mania, psychotic symptoms, suicide risk
Postoperative depression reported in 1% to 25% pts, but preoperative depression assessment not always conducted
Psychosis in PD usually visual hallucinations, delusions
Postoperative suicide attempts and suicides reported in 0.5% to 2.9% of PD pts after DBS, but further study required
Severe cognitive impairment (detectable w/ neuropsychological ✓) is DBS CI as it can worsen post-Qx & override motor impairment as main disability driver
Marked cognitive dysfnx on MMSE or low score on Mattis Dementia Rating Scale diminishes DBS QOL benefit → relative CI to DBS in PD
↑ motor fnx in severely demented pts can be dangerous due to ↑ risk of falls, potentially worsened by ↑ impulsivity caused by STN-DBS
Age is a prognostic factor (DBS benefit ↓ in pts >65 yrs)
Comorbidities (HTN, DM, need for anticoagulation) ↑ Qx risk;
Age & HTN ↑ intraoperative hemorrhage rates in DBS
Pts w/ poor axial scores on UPDRS III & severe postural instability unlikely to benefit from DBS
Hypophonia, a levodopa-nonresponsive Sx, unlikely to improve with DBS; pts & families should be warned of potential worsening in voice strength post-Qx.
Mood & cognition: ↑ risk of decline post STN-DBS
Borderline cognitive fnx pts: better fnx maintenance, QOL ↑ w/ GPi-DBS.
STN-DBS: can alter decision making under stress → ↑ impulsive behavior, judgment errors.
Swallowing fnx: ↓ in PD → aspiration pneumonia, death. STN stim: worsen swallowing unlike GPi-DBS.
Weight gain: observed w/ STN-DBS, inconclusive w/ GPi stim.
STN-DBS long term benefits: possible ↑ battery life, greater dopaminergic Rx ↓
STN-DBS vs GPi-DBS: only one study shows better motor fnx in "off" state post STN-DBS.
GPi: considered more challenging target due to greater anatomic variability.
Vim: 1st target for PD, only ↓ tremor, valuable in tremor-dominant PD.
STN & GPi: preferred over VIM as they alleviate tremor + other motor Sx.
Unilateral implant: consider if sig. asymmetry in Sx, advanced age or preoperative cognitive deficits.
Unilateral Qx: faster recovery, ↓ postoperative edema (limited to one hemisphere).
Severe Sx side: treat first w/ unilateral implant, then other side if necessary.
Unilateral STN-DBS: sig. ↑ motor fnx, ↓ cognitive performance aspects, less than bilateral DBS.
Early (up to 6 mos.)
7.5% had early (90 days) complications in a large review
Wound infx (3.6%), pneumonia (2.3%), hemorrhage (1.4%), PE (0.6%)
No ↑ in complications for pts >75 yrs old
Symptomatic hemorrhage risk during MER-guided DBS: 0.5% - 2.2%
↑ risk w/ HTN, MER
↓ risk strategies: maintain BP < 90 mm Hg, proper hydration, trajectories avoiding blood vessels
Hardware infx requiring additional Qx (up to 10% cases)
Abrupt cessation of stimulation, prolonged antibiotic Rx, emotional & economic strain on pt and team
Late complications:
hardware erosion, lead frx, lead migration
Erosion prevention: countersinking bur hole technique, ↑ IPG pocket size rostrally-caudally, multilayered closure
Early erosion Dx → possible partial hardware explantation
Lead frx: ~2% of PD pts
Stress relief loops, securing lead extension above occipital ridge w/ extra fascial stitch may ↓ frx risk
Deep subcutaneous tunneling in the neck may ↓ "bowstringing" and scarring → ↓ frx risk
Malpositioned electrodes requiring Qx revision: 0.8% - 1.7% per lead
Small repositioning (~2 mm) towards motor territory center can ↑ efficacy of marginally placed lead.