Learning outcomes
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Identify and differentiate between common causes of bleeding
- Describe ht main components of the haemostatic system and outline how each is activated to control bleeding
- Describe the pattern of blooding following injury to large blood vessels and to the microvasculature, and the mechanisms needed to establish good haemostasis in each
- Identify the main tests used to screen for haemostatic abnormalities and the main factors that effect each
- outline how the haemostatic system is controlled and thrombosis avoided
- Identify the main principles involved in treating inherited or acquired bleeding disorders caused by reduced levels of coagulation factors
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Be able to diagnose haemophilia, identify the role of the therapeutic team and discuss the main issues involved in managing long term treatment.
- Interpret laboratory coagulation test results to diagnose haemphilia and distinguish it from other common bleeding disorders
- describe the respective roles of individuals who make up a therapeutic team for managing a condition such as Haemophilia A (patient, immediate family, - parent, haemophilia nurse, physiotherapist, haematologist, and GP) and other specialist staff from time to time, eg paediatrician geneticist orthopaedic surgeon
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Identify the reproductive and generic choices related to serious inherited diseases.
- Outline the risks and benefits of genetic testing and screening
- identidy ethical issues associated with prebirth and familial genetic testing
- understnad th efactors in reproductive decision making in families with haemophilia
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Identify and apply knowledge of core ethical concepts to clinical cases.
- apply a framework of values/principles to the desire of a person with haemophilia to engage in normal but ""risky” activities
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Identify and apply knowledge os the psychological and social support important in the management of the aging adult with haemophilia.