How is hemophilia treated

Hemophilia is treated by infusing a replacement therapy into the veins of a person. Once infused this contains a clotting factor missing in the persons blood that will help in stopping the bleeding. Look here for more information: https:/…

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The main treatment for hemophilia is called replacement therapy. Concentrates of clotting factor VIII (for hemophilia A) or clotting factor IX (for hemophilia B) are slowly dripped in or injected into a vein. These infusions help replace th…

http://www.nhlbi.nih.gov/health/dci/Diseases/hemophilia/hemophilia_treatments.html

National Hemophilia Foundation: Hemophilia Treatment Centers

http://ghr.nlm.nih.gov/condition%3Dhemophilia

Related Questions Answered on Y!Answers

hemophilia?

Q: how is hemophilia treated???

A: The patient is given blood transfusions.

how were people with hemophilia treated in the past?

Q:

A: They weren’t. The only treatment for hemophilia is infusion with human clotting factor which hemoophiliacs can’t produce themselves (factor replacement therapy). There are two ways to get the clotting factors, from human plasma (a component of blood) or from a genetically engineered (artificial) cell line made by DNA technology. Unfortunately, the half life of the clotting factor only 24 hours, so after only 3 days almost none is left. So, treatment is an ongoing thing.These treatment options weren’t available in the past – so you had to be very carful and lucky, but still you would not die of old age.Well, there are a few other drugs, but they are not useful with severe hemophilia and they weren’t available 100 years ago, either (Desmopressin, Cyklokapron and Amicar)

Has anyone had replacement therapy for blood/hemophilia?

Q: Could you please explain to me what replacement therapy is, how it’s done and anything else you know about this if you have experienced or know someone who has? Thank you. Are there other options or is this the only method of treating hemophilia?

A: By replacement therapy I assume you mean factor replacement. For example I am a factor 9 hemophiliac. This means I lack factor 9 thus to have my blood clot like a normal person I need factor 9 added to me.This is done with me with a simple IV and the factor 9 (in my case) is added to my body. After this has been added sometimes a blood test will be done to see what your new clotting level is. If more is needed more can be added. Once at the right level my blood clotting level stays normal for about 24 hours. Around 1994 drugs came out that in short are man-made factor 8/9. Before this the factor one would get came from human blood. This led many people with hemophilia to acquire HIV/AIDS and Hepatitis B/C. Treatment plans for those with hemophilia really depends mostly on the following factors:1) Access to said factor ( either by location or money )2) How much of the clotting factor is the person lacking. 3) Is there an issue with the person having inhibitors. This means when the factor is added to the person the body attacks it thus making less effective. With all that in mind. The two main ways of treating hemophilia are:1) Treatment on demand. This is just a way of saying the person only gets factor when they need it.2). Proactive treatment. This means a person get factor lets say 3 times a week regardless if they are having a bleed or not. The thinking behind this is the person will have a better quality of life as they should have less bleeds thus less joint damage over time.Its important to remember the cost of the safer man-made factor is through the roof. By that I mean without insurance $ 50,000 hospital bills are not uncommon. I know of one person with hemophilia in one year racked up over 700,000 in factor costs. Not much he could do about. Better to have an insane hospital bill than bleed to death.Other treatments: There can be some treatments that can be done without factor or in turn used with factor. For dental or mouth bleeds a drug such as Amicar or Cyklokapron can be used to help clots in the mouth and gums. Awhile back there was a nasal spray that was undergoing testing for those with factor 8. As a person with factor 9 I have no idea whatever happened with this. Might be something to ask about.That’s all I can think of off hand. If you have any other questions feel free to send me a message.