Management and Follow-up of Thalassemia
I have thalassemia, and my hemoglobin levels are around 8-9 g/dL, with no specific symptoms on a daily basis.
When I visited the doctor, in addition to blood tests, I was prescribed folic acid to take 5 mg daily.
1.
I checked the recommended daily intake of folic acid, which is 0.4 mg.
Is it okay for me to take such a high dose of folic acid every day? Can I take it long-term? Is it necessary for me to take it?
2.
I previously tested my ferritin levels, which were around 700 ng/mL.
This seems to be below the threshold for insurance coverage for oral iron chelators.
Should I consider paying out of pocket for iron chelation therapy? Currently, I am trying to limit my iron intake through diet.
3.
How often should I have follow-up appointments for this condition? What indicators should I monitor to assess my anemia status during these follow-ups?
Mr. Chen, 60~69 year old female. Ask Date: 2022/05/12
Dr. Chen Yunfang reply Oncology
Hello: 1.
You do not need to take folic acid; it is unnecessary and not beneficial.
2.
Currently, there is no need to take iron chelators.
For patients with similar conditions, I only prescribe iron chelators covered by insurance if their ferritin levels exceed 2000.
3.
In principle, if you have no symptoms, there is no need to see a doctor.
This is not a disease; it is a hereditary condition that cannot be treated.
I would recommend that you just have regular adult health check-ups every two years.
Unless your levels drop too low, then you can come back to me for a blood transfusion.
Thank you.
Reply Date: 2022/05/12
More Info
Managing Mediterranean Anemia, also known as Thalassemia, requires a comprehensive approach that includes treatment, dietary supplements, and regular monitoring. Given your situation, where your hemoglobin levels are around 8-9 g/dL and you are currently taking 5 mg of folic acid daily, let’s address your questions one by one.
1. Folic Acid Intake: The recommended daily allowance (RDA) for folic acid for adults is indeed around 0.4 mg (400 mcg). However, in the context of thalassemia or Mediterranean anemia, higher doses of folic acid are often prescribed to support red blood cell production. The 5 mg dose you are taking is significantly higher than the RDA, but it is generally considered safe for most individuals, especially under medical supervision. Long-term use of high-dose folic acid is typically acceptable, but it’s essential to have regular follow-ups with your healthcare provider to monitor your levels and ensure that you are not experiencing any adverse effects. Folic acid is crucial for DNA synthesis and red blood cell formation, so continuing it is usually necessary in your case.
2. Iron Levels and Chelation Therapy: Your ferritin level of over 700 ng/ml indicates that you have a high iron load, which is common in patients with thalassemia due to increased intestinal absorption of iron and repeated blood transfusions. While the threshold for starting chelation therapy may vary, it is essential to manage iron overload to prevent complications such as liver damage, heart problems, and diabetes. Since you are not yet at the threshold for insurance coverage for oral iron chelators, you should discuss with your doctor the potential benefits of starting chelation therapy even if it is self-paid. Dietary management is also important; continue to limit iron-rich foods and avoid vitamin C supplements, which can increase iron absorption.
3. Monitoring and Follow-Up: Regular monitoring is crucial in managing Mediterranean anemia. Typically, patients should have their hemoglobin levels checked every 3-6 months, but this can vary based on individual circumstances. Key indicators to monitor include hemoglobin levels, ferritin levels, and complete blood counts (CBC). Additionally, liver function tests and cardiac evaluations may be necessary to assess the impact of iron overload. Your healthcare provider may also recommend periodic assessments of your folate and vitamin B12 levels, as these can affect your overall health and anemia status.
In summary, managing Mediterranean anemia involves a tailored approach that includes appropriate supplementation, monitoring of iron levels, and regular follow-ups with your healthcare provider. It is essential to maintain open communication with your doctor about your treatment plan, any side effects you may experience, and any changes in your symptoms. By doing so, you can ensure that you are receiving the best possible care for your condition.
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