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Parkinson's disease (PD) is a complex neurodegenerative disorder, leading to impairment of various neurological faculties, including motor, planning, cognitivity, and executive functions. Motor- and non-motor symptoms of the disease may intensify a patient's restrictions to performing usual tasks of daily living, including driving. Deep Brain Stimulation (DBS) associated with optimized clinical treatment has been shown to improve quality of life, motor, and non-motor symptoms in PD. In most countries, there are no specific guidelines concerning minimum safety requirements and the timing of return to driving following DBS, leaving to the medical staff of individual DBS centres the responsibility to draw recommendations individually regarding patients' ability to drive after surgery. The aim of this study was to evaluate factors that might influence the ability to drive following DBS in the management of PD. A total of 125 patients were included. Clinical, epidemiological, neuropsychological, and surgical factors were evaluated. The mean follow-up time was 129.9 months. DBS improved motor and non-motor symptoms of PD. However, in general, patients were 2.8-fold less likely to drive in the postoperative period than prior to surgery. Among the PD characteristics, patients with the akinetic subtype presented a higher risk to lose their driving licence postoperatively. Furthermore, the presence of an abnormal postoperative neuropsychological evaluation was also associated with driving restriction following surgery. Our data indicate that restriction to drive following surgery seems to be multifactorial rather than a direct consequence of DBS itself. Our study sheds light on the urgent need for a standardised multidisciplinary postoperative evaluation to assess patients' ability to drive following DBS.
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http://dx.doi.org/10.3390/jcm12010166 | DOI Listing |
Parkinsonism Relat Disord
September 2025
Federal University of São Paulo, Department of Neurology and Neurosurgery, São Paulo, SP, Brazil.
Background: Huntington disease-like 2 (HDL2) is an autosomal dominant disorder caused by an abnormal CAG/CTG repeat in exon 2A of junctophilin-3. This is the most common Huntington's Disease phenocopy and is characterized by psychiatric, cognitive, and movement disorders. This study aimed to describe the clinical phenotype of HDL2 patients in Brazil and compare the findings with those in the literature.
View Article and Find Full Text PDFJ Neurol Neurosurg Psychiatry
September 2025
Department of Management, University of Verona, Verona, Italy.
Background: Functional motor disorders (FMD) cause long-term disability and economic burden. There is a need for multidisciplinary interventions to manage both motor and non-motor symptoms. We aim to evaluate the clinical and economic effects of integrating digital telemedicine into multidisciplinary FMD management.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, County Clinic Hospital, Calea Bucuresti 25-27 Street, 500037 Brasov; Faculty of Medicine, Transilvania University, Balcescu Street 56, 500040 Brasov, Romania.
Shifting away from the traditional perspective on parkisonism, which focused only on the motor state of the patients, recent research proves the importance of early recognition and treatment of non-motor symptoms. Patients with parkinsonism, who suffer from various sleep disturbances, such as excessive daytime sleepiness (EDS), experience lower quality of life, a negative impact on activities of daily living, and possible exposure to life-threatening situations. Implementing the routine use of subjective and objective means of diagnosing EDS, into clinical practice, allows for a personalised management plan, in scope of efficiently decreasing disease burden for both the patient and the caregiver.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, National Institute of Mental Health & Neuro Sciences (NIMHANS), Hosur Road, Bengaluru 560029, Karnataka, India. Electronic address:
Sleep dysfunction is a significant component of the non-motor symptom profile in Parkinson's disease (PD). Patients with early onset PD (EOPD) are a unique challenge and may present with specific patterns of sleep disturbances, which tend to be related to the underlying genetic causes. Furthermore, owing to the younger age of patients with EOPD, sleep disturbances significantly impact multiple domains including employment, ability to drive, social interactions, caregiver burden, and so forth.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Dementech Neuroscience Academic Centre, London, UK. Electronic address:
Parkinson's disease is a syndrome with many clinical presentations. It is often dominated by visible motor symptoms; however, specific nonmotor features, such as cognitive dysfunction, sleep dysfunction, pain, apathy, dysautonomia, depression, and anxiety, enrich the clinical picture significantly. Proposed non-motor phenotypes segregate to central cholinergic, serotonergic, or noradrenergic dysfunctions, and clinical and biomarker-driven studies support these subtypes.
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