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Response of non-motor symptoms to levodopa in late-stage Parkinson's disease: results of a levodopa challenge test

dc.contributor.authorFabbri, Margherita
dc.contributor.authorCoelho, Miguel
dc.contributor.authorGuedes, Leonor Correia
dc.contributor.authorChendo, Inês
dc.contributor.authorSousa, Catarina
dc.contributor.authorRosa, Mario M.
dc.contributor.authorAbreu, Daisy
dc.contributor.authorCosta, Nilza
dc.contributor.authorGodinho, Catarina
dc.contributor.authorAntonini, Angelo
dc.contributor.authorFerreira, Joaquim J.
dc.date.accessioned2019-10-11T11:19:01Z
dc.date.available2019-10-11T11:19:01Z
dc.date.issued2017-06
dc.descriptionArticle under a CC-BY-NC-ND license - https://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.description.abstract"BACKGROUND: Non-motor symptoms (NMS) are extremely common among late-stage Parkinson's disease (LSPD) patients. Levodopa (L-dopa) responsiveness seems to decrease with disease progression but its effect on NMS in LSPD still needs to be investigated. OBJECTIVE: To assess the response of blood pressure (BP), pain, fatigue and anxiety to L-dopa in LSPD patients. METHODS: 20 LSPD patients, defined as Schwab and England ADL Scale <50 or Hoehn Yahr Stage >3 (MED ON) and 22 PD patients treated with subthalamic deep brain stimulation (advanced PD group) underwent an L-dopa challenge. BP and orthostatic hypotension (OH) assessment, a visual analogue scale (VAS) for pain and fatigue and the Strait Trait Anxiety (STAI) were evaluated before and after the L-dopa challenge. RESULTS: Systolic BP dropped significantly after L-dopa intake (p < 0.05) in LSPD patients, while there was no change in pain, fatigue or anxiety. L-dopa significantly improved (p < 0.05) pain and anxiety in the advanced PD group, whereas it had no effect on BP or fatigue. L-dopa-related adverse effects (AEs), namely OH and sleepiness, were more common among LSPD patients. 40% and 65% of LSPD patients were not able to fill out the VAS and the STAI, respectively, while measurement of orthostatic BP was not possible in four LSPD patients. CONCLUSIONS: This exploratory study concludes that some non-motor variables in LSPD do not benefit from the acute action of L-dopa while it can still induce disabling AEs. There is a need for assessment tools of NMS adapted to these disabled LSPD patients."pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationParkinsonism Relat Disord. 2017 Jun;39:37-43. doi: 10.1016/j.parkreldis.2017.02.007pt_PT
dc.identifier.doi10.1016/j.parkrelis.2017.02.007pt_PT
dc.identifier.issn1353-8020
dc.identifier.urihttp://hdl.handle.net/10400.26/29941
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://doi.org/10.1016/j.parkreldis.2017.02.007pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectParkinson's diseasept_PT
dc.subjectLate-stagept_PT
dc.subjectLevodopapt_PT
dc.subjectNon-motor symptomspt_PT
dc.titleResponse of non-motor symptoms to levodopa in late-stage Parkinson's disease: results of a levodopa challenge testpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage43pt_PT
oaire.citation.startPage37pt_PT
oaire.citation.titleParkinsonism and Related Disorderspt_PT
oaire.citation.volume39pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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