Apraclonidine for the pharmacologic confirmation of acute Horner syndrome.
Anisocoria
Apraclonidine
Horner syndrome
Neuro-ophthalmology
Pharmacological testing
Journal
Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403
Informations de publication
Date de publication:
15 Dec 2020
15 Dec 2020
Historique:
received:
03
08
2020
revised:
22
09
2020
accepted:
12
10
2020
pubmed:
20
10
2020
medline:
15
5
2021
entrez:
19
10
2020
Statut:
ppublish
Résumé
Apraclonidine is the most widely used pharmacologic agent to confirm Horner syndrome. It is a strong α-2 and a weak α-1 adrenergic agonist and reversal of anisocoria is considered a positive test. The utility of apraclonidine in acute Horner syndrome remains controversial as the exact timing for denervation sensitivity to develop remains unknown. The goal of this study was to describe the use of apraclonidine in the diagnosis of acute Horner syndrome in patients with an unequivocal onset within 7 days. We identified 3 patients who were referred to ophthalmology/neuro-ophthalmology service and had reversal of anisocoria within 7 days. Two cases of second-order Horner syndrome after cardiac surgery and a case of a third-order Horner syndrome from a carotid cavernous sinus fistula resulted in reversal of anisocoria 72 h, 48 h, and 5 days after onset. Photographic documentation was provided for all cases. Our results suggest that apraclonidine has utility in the acute period and positive results can be seen as early as 48 h after onset. Apraclonidine should therefore still be considered to confirm the presence of acute Horner syndrome before extensive neuroimaging is performed.
Identifiants
pubmed: 33075593
pii: S0022-510X(20)30526-8
doi: 10.1016/j.jns.2020.117190
pii:
doi:
Substances chimiques
Adrenergic alpha-Agonists
0
apraclonidine
843CEN85DI
Clonidine
MN3L5RMN02
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
117190Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.