Two-year longitudinal follow-up of visual illusions and hallucinations in Parkinson's disease.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 16 12 2021
accepted: 08 03 2022
revised: 07 03 2022
pubmed: 18 3 2022
medline: 22 7 2022
entrez: 17 3 2022
Statut: ppublish

Résumé

Previous longitudinal studies assessing visual hallucinations in Parkinson's disease (PD) have not specifically considered the respective evolution of visual illusions (VI) and visual hallucinations (VH), neither did they assess the role of ocular pathology on the evolution of those manifestations. We aimed to determine whether VI evolve towards VH along the time in PD, and whether ophthalmological treatment may have a positive effect on the prognosis of those visuo-perceptive manifestations. PD patients from a previous cohort [PD with VI (n = 26), PD with VH (n = 28), and PD without VI or VH (n = 28)] were contacted by phone 2 years later and questioned regarding the current presence of VI or VH, any current visual complaints, and the occurrence of any ophthalmological or antipsychotic treatment during the 2-year period, as well as any dopatherapy adjustment. Among PD-VI patients, 43% normalized, 48% remained PD-VI, 9% evolved towards coexisting VI and VH, and none converted to pure VH. Among PD-VH patients, 42% normalized, 32% remained PD-VH, 21% evolved towards coexisting VI and VH, and only 5% converted to pure VI. At follow-up, visual complaints remained greater among PD-VI and PD-VH compared to controls (p = 0.005). Among PD-VI and PD-VH who became control at follow-up, 35% received ophthalmologic treatment, 29% antipsychotic treatment, and 23% a dopatherapy reduction. PD Patients with VI do not necessarily evolve towards VH over time, and ophthalmological treatment may have a positive effect on the prognosis of those visuo-perceptive manifestations in PD similar to antipsychotic treatment and dopatherapy adjustment. clinicaltrials.gov number NCT01114321.

Sections du résumé

BACKGROUND BACKGROUND
Previous longitudinal studies assessing visual hallucinations in Parkinson's disease (PD) have not specifically considered the respective evolution of visual illusions (VI) and visual hallucinations (VH), neither did they assess the role of ocular pathology on the evolution of those manifestations.
OBJECTIVE OBJECTIVE
We aimed to determine whether VI evolve towards VH along the time in PD, and whether ophthalmological treatment may have a positive effect on the prognosis of those visuo-perceptive manifestations.
METHODS METHODS
PD patients from a previous cohort [PD with VI (n = 26), PD with VH (n = 28), and PD without VI or VH (n = 28)] were contacted by phone 2 years later and questioned regarding the current presence of VI or VH, any current visual complaints, and the occurrence of any ophthalmological or antipsychotic treatment during the 2-year period, as well as any dopatherapy adjustment.
RESULTS RESULTS
Among PD-VI patients, 43% normalized, 48% remained PD-VI, 9% evolved towards coexisting VI and VH, and none converted to pure VH. Among PD-VH patients, 42% normalized, 32% remained PD-VH, 21% evolved towards coexisting VI and VH, and only 5% converted to pure VI. At follow-up, visual complaints remained greater among PD-VI and PD-VH compared to controls (p = 0.005). Among PD-VI and PD-VH who became control at follow-up, 35% received ophthalmologic treatment, 29% antipsychotic treatment, and 23% a dopatherapy reduction.
CONCLUSION CONCLUSIONS
PD Patients with VI do not necessarily evolve towards VH over time, and ophthalmological treatment may have a positive effect on the prognosis of those visuo-perceptive manifestations in PD similar to antipsychotic treatment and dopatherapy adjustment.
TRIAL REGISTRATION BACKGROUND
clinicaltrials.gov number NCT01114321.

Identifiants

pubmed: 35296961
doi: 10.1007/s00415-022-11074-2
pii: 10.1007/s00415-022-11074-2
doi:

Substances chimiques

Antipsychotic Agents 0

Banques de données

ClinicalTrials.gov
['NCT01114321']

Types de publication

Letter

Langues

eng

Sous-ensembles de citation

IM

Pagination

4546-4554

Subventions

Organisme : Fondation de France
ID : 76354

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

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Auteurs

Steven Beze (S)

Neurology Department, Clermont-Ferrand University Hospital, Institut Pascal, Clermont Auvergne INP, CNRS, Université Clermont Auvergne, 63000, Clermont-Ferrand, France.
Ophthalmology Department, Clermont-Ferrand University Hospital, 63000, Clermont-Ferrand, France.

Lucia Castellani (L)

Neurology Department, Clermont-Ferrand University Hospital, Institut Pascal, Clermont Auvergne INP, CNRS, Université Clermont Auvergne, 63000, Clermont-Ferrand, France.

Bruno Pereira (B)

Biostatistics Department, Clermont-Ferrand University Hospital, 63000, Clermont-Ferrand, France.

Frédéric Chiambaretta (F)

Ophthalmology Department, Clermont-Ferrand University Hospital, 63000, Clermont-Ferrand, France.

Franck Durif (F)

Neurology Department, Clermont-Ferrand University Hospital, Institut Pascal, Clermont Auvergne INP, CNRS, Université Clermont Auvergne, 63000, Clermont-Ferrand, France.

Ana Marques (A)

Neurology Department, Clermont-Ferrand University Hospital, Institut Pascal, Clermont Auvergne INP, CNRS, Université Clermont Auvergne, 63000, Clermont-Ferrand, France. ar_marques@chu-clermontferrand.fr.

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