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Thalassemia Treatment

Learn about the treatment options for Thalassemia Minor and Major, including blood transfusions, splenectomy, and bone marrow transplant.

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Questions and Answers

What is the primary goal of treatment for Thalassemia major?

To normalize Hgb

What is the purpose of deferoxamine in treating Hemosiderosis?

To bind excess iron for excretion by the kidney

What is the main purpose of splenectomy in Thalassemia major treatment?

To remove the site of hemolysis

What is the treatment approach for Thalassemia minor?

<p>No intervention or monitoring</p> Signup and view all the answers

What is the purpose of blood transfusions in Thalassemia major treatment?

<p>To maintain a normal Hgb level</p> Signup and view all the answers

In Thalassemia major, what is the primary site of hemolysis that is targeted by splenectomy?

<p>Spleen</p> Signup and view all the answers

What is the mechanism of action of deferoxamine in treating Hemosiderosis?

<p>It binds excess iron for excretion by the kidney</p> Signup and view all the answers

Which of the following is a potential long-term complication of frequent blood transfusions in Thalassemia major?

<p>Hemosiderosis</p> Signup and view all the answers

Which of the following is a definitive treatment for Thalassemia major?

<p>Bone marrow transplant</p> Signup and view all the answers

What is the main purpose of monitoring Hgb levels in Thalassemia major?

<p>To adjust the frequency of blood transfusions</p> Signup and view all the answers

Study Notes

Treatment of Thalassemia

Thalassemia Minor

  • No intervention or monitoring is required

Thalassemia Major

  • The goal of treatment is to normalize Hemoglobin (Hgb) levels
  • Frequent blood transfusions are necessary to maintain normal Hgb levels
  • Splenectomy is performed to eliminate the site of hemolysis
  • Bone marrow transplant is a possible treatment option
  • Hemosiderosis is a complication that can occur due to iron overload
  • Hemosiderosis can be treated with iron-chelating drugs such as deferoxamine (Desferal)
  • Deferoxamine binds excess iron for excretion by the kidney

Treatment of Thalassemia

Thalassemia Minor

  • No intervention or monitoring is required

Thalassemia Major

  • The goal of treatment is to normalize Hemoglobin (Hgb) levels
  • Frequent blood transfusions are necessary to maintain normal Hgb levels
  • Splenectomy is performed to eliminate the site of hemolysis
  • Bone marrow transplant is a possible treatment option
  • Hemosiderosis is a complication that can occur due to iron overload
  • Hemosiderosis can be treated with iron-chelating drugs such as deferoxamine (Desferal)
  • Deferoxamine binds excess iron for excretion by the kidney

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