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Subthalamic deep brain stimulation in advanced Parkinson’s disease using the STarFix system
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Abstract
Background
Deep brain stimulation (DBS) is a well-established and highly effective treatment for patients with medically uncontrolled Parkinson’s disease (PD). This study presents the outcome of patients with PD after subthalamic deep brain stimulation (STN DBS) using the microtargeting the platform (MTP) stereotactic system (the STarFixSystem, FHC Inc., Bowdoin, Me., USA) for accurate localization of the target and precise placement of DBs electrodes. Patients were evaluated preoperatively and the follow up period was 1 year utilizing the Unified Parkinson’s Disease Rating Scale (UPDRS II and III) in on and off medication-stimulation conditions. It included 18 STN DBS procedures in 10 patients over a 2-year period. The technical features and the practical application of the STarFix system and the clinical outcome are reported. Also lead location analysis is done by doing postoperative CT to evaluate the clinical accuracy of the stereotactic system.
Results
The mean age of PD patients was 67.7 years. Six patients were males (60%) and 4 patients were females (40%). The mean postoperative improvement in ADL was 83.47 ± 2.39 over Dopa therapy alone. The mean postoperative improvement in UPDRs motor score was 78.96 ± 7.74 over Dopa therapy alone. The STarFix system showed high accuracy with target error 1.89 mm (SD 0.8) without accounting for brain shift.
Conclusion
Deep brain stimulation (DBS) targeting the subthalamic nucleus (STN) offers fundamental benefits for patients with advanced Parkinson’s disease (PD). The usage of the STarFix system for implanting DBS electrodes in the STN provides an accurate, safe, and effective alternative to traditional stereotactic techniques. This approach simplifies the surgical procedure, boosts patient comfort, and minimizes the duration of the operation.
Clinical trial registration ClinicalTrials.gov identifier: NCT03562403. Registered 19 June 2018, https://classic.clinicaltrials.gov/ct2/show/NCT03562403.
Springer Science and Business Media LLC
Title: Subthalamic deep brain stimulation in advanced Parkinson’s disease using the STarFix system
Description:
Abstract
Background
Deep brain stimulation (DBS) is a well-established and highly effective treatment for patients with medically uncontrolled Parkinson’s disease (PD).
This study presents the outcome of patients with PD after subthalamic deep brain stimulation (STN DBS) using the microtargeting the platform (MTP) stereotactic system (the STarFixSystem, FHC Inc.
, Bowdoin, Me.
, USA) for accurate localization of the target and precise placement of DBs electrodes.
Patients were evaluated preoperatively and the follow up period was 1 year utilizing the Unified Parkinson’s Disease Rating Scale (UPDRS II and III) in on and off medication-stimulation conditions.
It included 18 STN DBS procedures in 10 patients over a 2-year period.
The technical features and the practical application of the STarFix system and the clinical outcome are reported.
Also lead location analysis is done by doing postoperative CT to evaluate the clinical accuracy of the stereotactic system.
Results
The mean age of PD patients was 67.
7 years.
Six patients were males (60%) and 4 patients were females (40%).
The mean postoperative improvement in ADL was 83.
47 ± 2.
39 over Dopa therapy alone.
The mean postoperative improvement in UPDRs motor score was 78.
96 ± 7.
74 over Dopa therapy alone.
The STarFix system showed high accuracy with target error 1.
89 mm (SD 0.
8) without accounting for brain shift.
Conclusion
Deep brain stimulation (DBS) targeting the subthalamic nucleus (STN) offers fundamental benefits for patients with advanced Parkinson’s disease (PD).
The usage of the STarFix system for implanting DBS electrodes in the STN provides an accurate, safe, and effective alternative to traditional stereotactic techniques.
This approach simplifies the surgical procedure, boosts patient comfort, and minimizes the duration of the operation.
Clinical trial registration ClinicalTrials.
gov identifier: NCT03562403.
Registered 19 June 2018, https://classic.
clinicaltrials.
gov/ct2/show/NCT03562403.
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