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Nystagmus

Evaluating the impact of information and support for people with nystagmus in the digital age: A patient and carer questionnaire study

, , , ORCID Icon, , & ORCID Icon show all
Pages 713-717 | Received 05 Aug 2019, Accepted 16 Nov 2019, Published online: 26 Dec 2019
 

ABSTRACT

Background: Nystagmus is a disorder of rhythmic, involuntary oscillations of the eyes and can be classified as either infantile or acquired. Whether it occurs in isolation or as a part of other visual or neurological disorders, it causes significant visual dysfunction and problems with social functioning. In this study, we seek to understand ways in which people with nystagmus are currently supported across the UK and identify any geographical variations or disconnects between current practice and best practice, as judged by patients and their carers.

Methods: A nationwide, qualitative, cross-sectional, questionnaire study of people with nystagmus and their carers. Recruitment was achieved through specialist clinics, charity events, online advertisements and social media calls. Data was gathered using five, age-appropriate questionnaires which were completed and returned to the research team between November 2016 and August 2018.

Results: 184 respondents were included (89 carers, 47 patients aged 4–10 years, 5 aged 11–14 years, 4 aged 15–17 years and 39 > 18 years). Notably, respondents rated social media as the best source of information they have received, even compared with face-to-face consultation with medical professionals. Additionally, only 33% of the respondents had been offered visual impairment support. Notably, patterns of clinical practice and patient experience emerged according to geographical location, particularly provision of initial information and ongoing VI support.

Conclusions: This study highlights a significant variation in the support and information received by people in the UK with nystagmus. It also supports the role of charities and increasingly, social media in the provision of patient information. The study also highlights the need for standardized guidelines for the management of patients with nystagmus, particularly with regard to support and information.

Acknowledgments

The authors would like to thank all the participants in the study and the listed charities for their support, in particular, the UK Nystagmus Network and Albinism Fellowship charities.

Declaration of interests

None of the authors have any financial interest in the work completed in this study.

Supplementary Material

Supplemental data for this article can be accessed here.

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