Genetic haemochromatosis (GH) is a relatively common but under-diagnosed condition. Due to the generic nature of early symptoms, diagnosis can be missed, misdiagnosed, or diagnosed late. Late diagnosis increases the risk of the development of serious complications.
Increasing primary care healthcare practitioners' knowledge of this condition can lead to earlier diagnosis, allowing for timely treatment and possible reduction in GH related complications.
This video also gives an overview regarding the genetic/psychological aspects of being diagnosed with a hereditary condition, which can require lifelong treatment.
Learning objectives :
The aim of this video is to provide an overview of GH, exploring the signs, symptoms, diagnosis, treatment, and management of this condition. The possible complications of treatment will be examined to allow healthcare practitioners to consider the physical and psychological aspects that should be addressed when managing those diagnosed with this condition.
After completing the module and reflection activities primary healthcare practitioners should be able to:
• Describe the signs and symptoms that might indicate GH
• Identify the blood tests required to diagnose GH and be able to interpret the results
• Discuss the implications of GH on those diagnosed with the condition and their family and/or carers
Based upon the RCGP-accredited eLearning module authored by : Dr Susan Hancock FRCGP and Dr Doug Jenkinson FRCGP, in collaboration with Haemochromatosis UK (registered charity 1001307 and SCO41701)
Presenter : Diogo Gomes PGCert (ANP), NMP, RGN Advanced Nurse Practitioner - Information & Advisory, Haemochromatosis UK
For further details & resources : www.haemochrom...
Негізгі бет An Introduction to Genetic Haemochromatosis for Primary Care Practitioners
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