Hemophilia Disease Presentation: Healthcare, Symptoms, and Treatment

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Added on  2022/08/18

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Hemophilia Disease
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Hemophilia Disease
It is a rare disease where the blood of
consumers does not clot as it lacks enough
blood-clotting proteins.
It is a genetic disease that can damage the
organs and tissues of the individuals.
Consumers with hemophilia produce a lesser
amount of factor VIII and IX (Ferraris, Boral,
Cohen, Smyth, & White, 2015).
This presentation highlights the problem of
hemophilia.
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Signs and Symptoms
There are various signs and symptoms of
hemophilia including:
Unexplained and excessive bleeding from cuts
Deep bruises
Rare bleeding after vaccinations
In children, mysterious irritability
Spontaneous nosebleeds (Swystun, & James, 2017).
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Treatment
There are various treatment methods that
can be used for addressing hemophilia
disease such as:
Replacement therapy (Example- To stop bleeding
episodes)
Replace the lost blood clotting aspect (Example- treat
hemophilia A includes Advate and Xyntha.)
Apply Desmopressin therapy (Example- manage
hemophilia in patients)
Clot-preserving medications (Example- plasma-
derived factor VIII treatments).
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Compilation
It is important for the care providers to find
risk factors associated with hemophilia.
Health care providers may provide
intervention programs for handling risks that
lead to hemophilia.
After applying replacement therapy on
individuals suffering from hemophilia nurses
should compile and check the effect of
applied therapy (Hartmann, & Croteau,
2016).
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Nursing’s care
Nurses play a crucial character in the
reduction of hemophilia disease (Angelini,
Konkle, & Sood, 2016).
It is important for the nurses to provide
complete information about the disease and
helps patients for addressing the disease.
Nursing care can help patients to effectively
solve the problem of hemophilia disease and
manage risk factors linked with hemophilia.
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References
Ferraris, V. A., Boral, L. I., Cohen, A. J., Smyth, S. S., &
White, G. C. (2015). Consensus review of the treatment
of cardiovascular disease in people with hemophilia A and
B. Cardiology in review, 23(2), 53.
Swystun, L. L., & James, P. D. (2017). Genetic diagnosis in
hemophilia and von Willebrand disease. Blood
reviews, 31(1), 47-56.
Hartmann, J., & Croteau, S. E. (2016). 2017 Clinical trials
update: Innovations in hemophilia therapy. American
journal of hematology, 91(12), 1252-1260.
Angelini, D., Konkle, B. A., & Sood, S. L. (2016). Aging
among persons with hemophilia: contemporary concerns.
In Seminars in hematology, 53(1), 35-39.
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