Hello all forum's member...
i am new in this forum and this is my first post.
This forum is very complete all about thalassemia but sometimes I am still confused so please help...
i live in indonesia and i have 2 YO child.
The First time he diagnosed with alpha thalassemia ( HbH Disease ) is when he was 13 Month. At that time, he has fever, diarrhea , cold and flu for 10 days. So I decide to do blood examination worrying about high incidence of dengue fever in Indonesia.
He is very active child, No Splenomegali, Body weight= 11.2 KG, Height = 85 cm, still can not talk ( 10 words), sweat easier than others.
The latest haemoglobin level 8.8 g/dl ( May 18).
DNA Analysis : Double Heterozygot Deletional 2 gen globin Alpha type SEA and One Deletional Globin alpha type 3,7 kb ( -- SEA / α-3,7kb).
Hb Electrophoresis / Hb Analysis / HPLC:
HbA2 : < 1.7%
HbF : < 1%
Other Fraction : NEgatives
Here is the history of blood exam in my child.
Until Now He never been get any transfusion.
We give supplementation folic acid 2.5mg + Vit E 100mg daily
My Question is:
1. Do you think transfusion is required ?
some of the local pediatric haematologic suggest to do blood transfusion base on the Hb level…no matter the type of thalassemia…but some also suggest to monitor the growth with CDC chart growth before transfusing...but I postpone it because no symptomps...
2. are we in the correct management?
2. What is the blood examination should we monitored in my childrdren?