Deep brain stimulation for Parkinson's disease: Prevalence of adverse events and need for standardized reporting

2008 ◽  
Vol 23 (3) ◽  
pp. 343-349 ◽  
Author(s):  
Aleksandar Videnovic ◽  
Leo Verhagen Metman
2007 ◽  
Vol 23 (3) ◽  
pp. 416-421 ◽  
Author(s):  
Marwan I. Hariz ◽  
Stig Rehncrona ◽  
Niall P. Quinn ◽  
Johannes D. Speelman ◽  
Carin Wensing

2014 ◽  
Vol 156 (8) ◽  
pp. 1505-1512 ◽  
Author(s):  
Fernando Seijo ◽  
Sayoa Alvarez de Eulate Beramendi ◽  
Elena Santamarta Liébana ◽  
Beatriz Lozano Aragoneses ◽  
Antonio Saiz Ayala ◽  
...  

2021 ◽  
Vol 10 (8) ◽  
pp. 1557
Author(s):  
Michael J. Bos ◽  
Dianne de Korte-de Boer ◽  
Ana Maria Alzate Sanchez ◽  
Annelien Duits ◽  
Linda Ackermans ◽  
...  

Background: Subthalamic nucleus (STN) deep brain stimulation (DBS) has become a routine treatment of advanced Parkinson's disease (PD). DBS surgery is commonly performed under local anesthesia (LA) to obtain reliable microelectrode recordings. However, procedural sedation and/or analgesia (PSA) is often desirable to improve patient comfort. The impact of PSA in addition to LA on outcome is largely unknown. Therefore, we performed an observational study to assess the effect of PSA compared to LA alone during STN DBS surgery on outcome in PD patients. Methods: Seventy PD patients (22 under LA, 48 under LA + PSA) scheduled for STN DBS implantation were included. Dexmedetomidine, clonidine or remifentanil were used for PSA. The primary outcome was the change in Movement Disorders Society Unified Parkinson’s Disease Rating Score III (MDS-UPDRS III) and levodopa equivalent daily dosage (LEDD) between baseline, one month before surgery, and twelve months postoperatively. Secondary outcome measures were motor function during activities of daily living (MDS-UPDRS II), cognitive alterations and surgical adverse events. Postoperative assessment was conducted in “on” stimulation and “on” medication conditions. Results: At twelve months follow-up, UPDRS III and UPDRS II scores in “on” medication conditions were similar between the LA and PSA groups. The two groups showed a similar LEDD reduction and an equivalent decline in executive function measured by the Stroop Color-Word Test, Trail Making Test-B, and verbal fluency. The incidence of perioperative and postoperative adverse events was similar between groups. Conclusion: This study demonstrates that PSA during STN DBS implantation surgery in PD patients was not associated with differences in motor and non-motor outcome after twelve months compared with LA only.


2011 ◽  
Vol 23 (1) ◽  
pp. 56-62 ◽  
Author(s):  
L. B. Zahodne ◽  
F. Susatia ◽  
D. Bowers ◽  
T. L. Ong ◽  
C. E. Jacobson ◽  
...  

Neurosurgery ◽  
2007 ◽  
Vol 61 (2) ◽  
pp. 297-305 ◽  
Author(s):  
Melissa Tir ◽  
David Devos ◽  
Serge Blond ◽  
Gustavo Touzet ◽  
Nicolas Reyns ◽  
...  

Abstract OBJECTIVE To prospectively assess the impact of subthalamic nucleus (STN) deep brain stimulation (DBS) at 12 months after surgery in a series of 100 consecutive patients treated in a single center. The primary objective was to describe the clinical outcome in terms of efficacy and tolerance in STN-DBS patients. A secondary objective was to discuss presurgery clinical characteristics a posteriori as a function of outcome. METHODS One hundred and three consecutive patients with severe Parkinson's disease received bilateral STN-DBS in our clinic between May 1998 and March 2003. Clinical assessment was performed before and 12 months after surgery and was based on the Unified Parkinson's Disease Rating Scale, Parts II, III, and IV A; the Schwab and England Scale; and cognitive evaluation. Patient-rated overall improvement was also evaluated. RESULTS Twelve months after surgery, the Unified Parkinson's Disease Rating Scale Part III score decreased by 43%, the Unified Parkinson's Disease Rating Scale Part II score (activities of daily living) fell by 34%, and the severity of dyskinesia-related disability decreased by 61%. The main surgical complications after STN-DBS were as follows: infection (n = 7), intracerebral hematoma (n = 5), electrode fracture (n = 4), and incorrect lead placement (n = 8). We observed cognitive decline and depression in 7.7 and 18% of the patients, respectively. The mean patient-rated overall improvement score was 70.7%. CONCLUSION The efficacy and safety of STN-DBS in our center's large cohort of Parkinsonian patients are generally similar to the results obtained by other groups, albeit at the lower limit of the range of reported values. In contrast to efficacy, the occurrence of adverse events cannot be predicted. Younger patients with Parkinson's disease (i.e., those younger than 60 yr) often show an excellent response to levodopa. However, in view of our data on overall patient satisfaction and the occurrence of adverse events, we suggest that older patients (but not those older than 70 yr) and less dopa-sensitive patients (but not those with a response <50%) should still be offered the option of STN-DBS.


2009 ◽  
Vol 36 (S 02) ◽  
Author(s):  
J Gierthmühlen ◽  
P Arning ◽  
G Wasner ◽  
A Binder ◽  
J Herzog ◽  
...  

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