The way in which an individual is told they have serious eye disease has an effect on their psychological health and ability to cope with the eye condition in the long-term, stated a new study. A research team led by Dr Jasleen Jolly, of Anglia Ruskin University (ARU) interviewed patients across a range of ages who had been diagnosed with eye disease in England over the course of several decades, and assessed the psychological impact of the way their diagnosis was communicated.
‘This is one of the first studies to examine how the communication of a diagnosis impacts psychologically on a patient in the long-term, and we found that the words and demeanor of medical professionals affected a patient’s ability to come to terms with their condition.’
Tweet it Now
Interviewees had been diagnosed with a variety of conditions, including diabetic retinopathy, macular degeneration, Stargardt disease and retinitis pigmentosa, all of which can cause significant vision loss. The interviews showed four themes; the convoluted process of being diagnosed; the impact of clinicians’ words; the search for information; and reflections on what could be improved.
Researchers found that patients often vividly remembered the way they were told they had their condition, and the manner of the medical professional that delivered the news. This impacted on how they saw their vision loss and themselves, as well as their interactions with other people.
Eye Diseases Diagnosis
One patient described the news as “like being hit with a brick”. Another said: “It was very brief, very clinical. They literally told me that I had this and in time was slowly going blind. There was no cure.”Some had waited months or years for diagnosis from initially being aware of a problem, creating a sense of frustration and anxiety. One younger patient said: “You’re told ‘something is wrong, you’re going to have an appointment in 14 weeks to have this test done, you need to wait five or six months for the results.’ Five or six months is a long time when you’re waking up every day, worried, and you’re not sleeping well. And it’s affecting relationships with other people, potentially your job.”
Some patients felt the need to trawl the internet to find out more, coming across misinformation and “scare stories” online and increasing their anxiety about their condition.
Advertisement
“Clinicians should carefully consider how they communicate a diagnosis to patients, how and when they offer information about diagnosis or prognosis, and signpost them to appropriate charities, support systems or counselling services as soon as possible. Hospitals need to put in place better support mechanisms, such as more Eye Care Liaison Officers, to provide information and support to patients, as well as more training on empathetic communication.”
Advertisement