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Re: DBS Adverse Events: Results from 1154 PD Patients


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I feel lucky I was helped by DBS. I feel like mentally I am sharper, no more ocular
migraines, am never depressed , no more shaking, speaking is a real problem though. My other PD symptoms seem to have plateaued - no meds.


Ray
Rayilyn Brown
Board Member AZNPF
Arizona Chapter National Parkinson's Foundation
rbrown@xxxxxxxxx
----- Original Message ----- From: "M.Schild" <mmoo@xxxxxxxxxxxxxxxx>
To: <PARKINSN@xxxxxxxxxxxxxxxxxxxx>
Sent: Friday, March 28, 2008 12:23 PM
Subject: DBS Adverse Events: Results from 1154 PD Patients



Deep brain stimulation for Parkinson's disease: Prevalence of adverse events
and need for standardized reporting
A Videnovic, L Verhagen Metman
Movement Disorders 2008;23:343-349



Adverse events related to deep brain stimulation are common, but their true
prevalence cannot be accurately determined with current reporting methods,
according to this study.


The authors analyzed reports of adverse events from 47 studies of STN and GPi
DBS in PD published from 1996 to 2007, representing 1,154 patients (928 STN,
226 GPi) and 2,205 electrode placements. They grouped AEs into three classes:
procedure-related, hardware-related, and stimulation- or disease
progression-related events.


The most common events were:

Procedure-related events:
STN (%) GPi (%)
Mental status/behavioral 18.4 9.3
Infection 2 2.6
ICH-symptomatic 2 4
Misplaced electrode 1.7 2
Speech disturbance 1.5 3.9
Infarction 0.2 2.2

Among mental status changes, confusion was by far the most common.

Hardware-related events (combined GPi and STN, %):
Infection 2.4
Malfunctioning 1
Lack of benefit 0.9

A total of 8.7% of patients experienced one or more hardware-related AE.

Stimulation- or progression-related events, which did not disappear with
adjustment (%):
STN (%) GPi (%)
Weight gain 37.5 17.6
Dysarthria 12.8 11.8
Eyelid opening apraxia 11.3 0
Gait ignition failure 0 17.6

Because of the variation in classification of AE reporting among the included
studies, the authors note that "a retrospective review of the available
literature cannot provide accurate data on the prevalence of AEs associated
with DBS in PD." They recommend the adoption of a standardized system for AE
reporting in DBS trials, in which all AEs are classified along the lines they
employed in this study, plus the temporal characteristics of the AE and its
response to programming adjustments.



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