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Sunflower Syndrome: A Survey of Provider Awareness and Management Preferences.
Baumer, Fiona M; Julich, Kristina; Friedman, Jennifer; Nespeca, Mark; Thiele, Elizabeth A; Bhatia, Sonal; Joshi, Charuta.
Afiliación
  • Baumer FM; Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, California. Electronic address: fbaumer@stanford.edu.
  • Julich K; Department of Neurology, The University of Texas at Austin Dell Medical School, Austin, Texas.
  • Friedman J; Department of Neurosciences, University of California San Diego, San Diego, California.
  • Nespeca M; Department of Neurosciences, University of California San Diego, San Diego, California.
  • Thiele EA; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts.
  • Bhatia S; Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
  • Joshi C; Department of Pediatrics, Children's Medical Center Dallas, University of Texas Southwestern, Dallas, Texas.
Pediatr Neurol ; 152: 177-183, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38295719
ABSTRACT

BACKGROUND:

Sunflower syndrome is a rare photosensitive pediatric epilepsy characterized by stereotyped hand-waving in response to bright lights. These stereotyped movements with maintained awareness can be mistaken for a movement disorder. This study assessed neurology providers' diagnostic reasoning, evaluation, and treatment of Sunflower syndrome.

METHODS:

A 32-question anonymized electronic survey, including a clinical vignette and video of hand-waving in sunlight, was distributed to child neurology providers to assess (1) initial diagnosis and evaluation based on clinical information, (2) updated diagnosis and management after electroencephalography (EEG), and (3) prior experience with Sunflower syndrome.

RESULTS:

Among 277 viewed surveys, 211 respondents provided information about initial diagnosis and evaluation, 200 about updated diagnosis, 191 about management, and 189 about prior clinical experience. Most providers (135, 64%) suspected seizure, whereas fewer suspected movement disorders (29, 14%) or were unsure of the diagnosis (37, 22%). EEG was recommended by 180 (85%). After EEG, 189 (95%) diagnosed epilepsy, 111 of whom specifically diagnosed Sunflower syndrome. The majority (149, 78%) recommended antiseizure medications (ASMs) and sun avoidance (181, 95%). Only 103 (55%) had managed Sunflower syndrome. Epileptologists and those with prior clinical experience were more likely to suspect a seizure, order an EEG, and offer ASMs than those without prior experience.

CONCLUSIONS:

Although many providers had not managed Sunflower syndrome, the majority recognized this presentation as concerning for epilepsy. Epilepsy training and prior clinical experience are associated with improved recognition and appropriate treatment. Educational initiatives that increase awareness of Sunflower syndrome may improve patient care.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epilepsia Refleja / Helianthus / Trastornos del Movimiento Límite: Child / Humans Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epilepsia Refleja / Helianthus / Trastornos del Movimiento Límite: Child / Humans Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article
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