Eight-Year Follow-Up Outcome Of Subthalamic Deep Brain Stimulation For Parkinson'S Disease: Maintenance Of Therapeutic Efficacy With A Relatively Low Levodopa Dosage And Stimulation Intensity

CNS NEUROSCIENCE & THERAPEUTICS(2021)

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摘要
Aims This follow-up study aimed to examine the 8-year efficacy and safety of subthalamic nucleus (STN) deep brain stimulation (DBS) for patients with Parkinson's disease (PD) in southern China. Methods The follow-up data of 10 patients with PD undergoing STN-DBS were analyzed. Motor symptoms were assessed before and 1, 3, 5, and 8 years after the surgery with stimulation-on in both off-medication (off-med) and on-medication (on-med) status using the Unified Parkinson's disease Rating Scale Part III. The quality of life was assessed using the 39-item Parkinson's Disease Questionnaire. The sleep, cognition, and emotion were evaluated using a series of nonmotor scales. Levodopa equivalent daily dose (LEDD) and stimulation parameters were recorded at each follow-up. Results The motor symptoms were improved by 50.9%, 37.7%, 36.7%, and 37.3% in 1, 3, 5, and 8 years, respectively, in the off-med / stimulation-on status compared with the baseline. The quality of life improved by 39.7% and 56.1% in 1 and 3 years, respectively, but declined to the preoperative level thereafter. The sleep, cognition, and emotion were mostly unchanged. LEDD reduced from 708.1 +/- 172.5 mg to 330 +/- 207.8 mg in 8 years. The stimulation parameters, including amplitude, pulse width, and frequency, were 2.77 +/- 0.49 V, 71.3 +/- 12.8 mu s, and 121.5 +/- 21 Hz, respectively, in 8 years. Conclusion Long-term therapeutic efficacy of STN-DBS could be achieved even with relatively low stimulation intensity and medication dosage for PD patients in southern China. Motor improvement and medication reduction were maintained through the 8-year follow-up, but improvement in quality of life lasted for only 3 years. No definite changes was found in nonmotor symptoms after STN-DBS.
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关键词
deep brain stimulation, follow-up Studies, Parkinson's disease, subthalamic nucleus
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