Current Status of Pain Management in Parkinson's Disease

被引:23
作者
Karnik, Vikram [1 ]
Farcy, Nicole [2 ]
Zamorano, Carolina [2 ]
Bruno, Veronica [1 ]
机构
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[2] Univ Buenos Aires, Buenos Aires, DF, Argentina
关键词
Parkinson's disease; Pain management; Clinical trials; PROLONGED-RELEASE OXYCODONE; RANDOMIZED CONTROLLED-TRIAL; BOTULINUM TOXIN; EXERCISE; THRESHOLD; SYMPTOMS; STIMULATION; LEVODOPA; NALOXONE; MOTOR;
D O I
10.1017/cjn.2020.13
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Pain is a non-motor symptom in Parkinson's disease (PD) which commonly goes underreported. Adequate treatment for pain in PD remains challenging, and to date, no clear guidelines for management are available. Methods: With the goal of understanding and organizing the current status of pain management in PD, we conducted a review of pharmacological and non-pharmacological treatments for pain in patients with PD. Suitable studies cataloged in PubMed and the Cochrane database up to October 31, 2019, were included prioritizing randomized controlled trials. Post-hoc analyses and open-label studies were also included. Results: Treatment with levodopa increases pain thresholds in patients with PD. Apomorphine did not have similar efficacy. Duloxetine provided benefit in an open-label trial. Oxycodone-naloxone PR did not have a significant improvement in pain, but per-protocol analysis showed a reduction in pain when adherence was strong. Rotigotine patch had numerical improvement on pain scales with no statistical significance. Safinamide significantly improved the "bodily discomfort" domain in the PDQ-39 questionnaire. Botulinum toxin A had a non-significant signal toward improving dystonic limb pain in PD. DBS to the subthalamic nucleus may modulate central pain thresholds, and a pilot study of cranioelectric therapy warrants future research in the area. Conclusion: After optimizing dopaminergic therapy, understanding the type of pain a patient is experiencing is essential to optimizing pain control in PD. While recommendations can be made regarding the treatment options in each domain, evidence remains weak and future randomized controlled studies are needed.
引用
收藏
页码:336 / 343
页数:8
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