Pain in Parkinson's disease: new concepts in pathogenesis and treatment.


Journal

Current opinion in neurology
ISSN: 1473-6551
Titre abrégé: Curr Opin Neurol
Pays: England
ID NLM: 9319162

Informations de publication

Date de publication:
08 2019
Historique:
entrez: 2 7 2019
pubmed: 2 7 2019
medline: 21 4 2020
Statut: ppublish

Résumé

In this review, we discuss the most recent evidence on mechanisms underlying pathological nociceptive processing in Parkinson's disease patients, as well as novel treatment strategies. In Parkinson's disease, specific neurodegenerative changes may cause alterations in nociceptive processing at multiple levels. Optimization of dopaminergic therapies should always be the first step in the management of Parkinson's disease pain. Reportedly, rotigotine transdermal patch, a monoamine oxidase type B inhibitor safinamide (as an add-on therapy to levodopa), subcutaneous apomorphine and intrajejunal levodopa infusion therapy may have a beneficial effect on pain sensations in Parkinson's disease patients. Among the nondopaminergic pharmacological therapies, prolonged-release oxycodone/naloxone and duloxetine may be effective in the treatment of chronic pain in Parkinson's disease. Botulinum toxin (BTX) injections should be considered for the treatment of dystonic Parkinson's disease pain. Deep brain stimulation (DBS) may lead to pain relief with a long-lasting effect in Parkinson's disease patients. Physiotherapy and physical activity in general are essential for Parkinson's disease patients suffering from pain. Pain in Parkinson's disease is not simply a consequence of motor complainants. The management of Parkinson's disease-related pain implicates maintenance of stable levels of dopaminergic drugs. Nondopaminergic pharmacological therapies (prolonged-release oxycodone/naloxone, duloxetine, BTX) and nonpharmacological interventions (DBS, physiotherapie) may also be beneficial in treatment of Parkinson's disease pain.

Identifiants

pubmed: 31260418
doi: 10.1097/WCO.0000000000000711
pii: 00019052-201908000-00011
doi:

Substances chimiques

Analgesics 0
Naloxone 36B82AMQ7N
Duloxetine Hydrochloride 9044SC542W
Oxycodone CD35PMG570
Botulinum Toxins EC 3.4.24.69

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

579-588

Subventions

Organisme : Department of Health
Pays : United Kingdom

Auteurs

Katarina Rukavina (K)

Institute of Psychiatry, Psychology & Neuroscience at King's College and King's College Hospital NHS Foundation Trust.
Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.
Klinik für Gerontopsychiatrie, Asklepios Klinik Nord - Ochsenzoll, Hamburg, Germany.

Valentina Leta (V)

Institute of Psychiatry, Psychology & Neuroscience at King's College and King's College Hospital NHS Foundation Trust.
Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.

Carolina Sportelli (C)

Institute of Psychiatry, Psychology & Neuroscience at King's College and King's College Hospital NHS Foundation Trust.
Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.

Yazead Buhidma (Y)

Institute of Psychiatry, Psychology & Neuroscience, Wolfson Centre for Age-Related Diseases, King's College London, London, UK.

Susan Duty (S)

Institute of Psychiatry, Psychology & Neuroscience, Wolfson Centre for Age-Related Diseases, King's College London, London, UK.

Marzia Malcangio (M)

Institute of Psychiatry, Psychology & Neuroscience, Wolfson Centre for Age-Related Diseases, King's College London, London, UK.

Kallol Ray Chaudhuri (K)

Institute of Psychiatry, Psychology & Neuroscience at King's College and King's College Hospital NHS Foundation Trust.
Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.

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Classifications MeSH