img
What is Sickle Cell Anemia?

Sickle Cell Anemia is a genetic blood disorder that affects the shape of red blood cells, causing them to become rigid and take on a crescent or "sickle" shape. These abnormal cells can block blood flow, leading to pain, organ damage, and other complications.

What is the cost of Sickle Cell Anemia treatment?

The cost of Sickle Cell Anemia treatment can vary depending on the type of treatment required, the duration of treatment, and the location of the hospital. 

USD 8039 TO 10719

Who is the right doctor to consult for Sickle Cell Anemia?

A hematologist, who specializes in the treatment of blood disorders, is the right doctor to consult for Sickle Cell Anemia.

What technology is used during Sickle Cell Anemia treatment?

Hemoglobin electrophoresis: a laboratory technique used to analyze the type of hemoglobin present in the blood and diagnose Sickle Cell Anemia.

Transcranial Doppler ultrasound: a noninvasive test that uses ultrasound waves to measure the blood flow in the brain and detect the risk of stroke.

Pulse oximetry: a noninvasive test that measures the amount of oxygen in the blood.

What precautions should be taken during Sickle Cell Anemia treatment?
  • Stay hydrated and drink plenty of fluids.
  • Avoid exposure to extreme temperatures, which can trigger a pain crisis.
  • Get plenty of rest and maintain a healthy diet.
  • Avoid smoking and limit alcohol consumption.
What are the key tests during Sickle Cell Anemia treatment?
  • Complete blood count to monitor the patient's overall blood counts.
  • Blood oxygen level tests to monitor the amount of oxygen in the blood.
  • Kidney and liver function tests to monitor the health of these organs, which can be affected by Sickle Cell Anemia.
  • Imaging tests such as X-rays, CT scans, or MRIs may be used to monitor the progression of the disease.

Share your reports for review with our doctors

Get a second opinion
img

Frequently Asked Questions

Yes, congenital heart disease can be passed down from a parent to a child. If one or both parents have a congenital heart defect, there is an increased risk of their child having the condition as well. However, it is important to note that not all congenital heart defects are inherited and some can occur due to other factors such as infections during pregnancy or exposure to certain medications or substances.

The initial treatment process for a child with congenital heart disorder depends on the type and severity of the condition. This could include medications for visible symptoms and monitoring with regular checkups.

The tests for congenital heart disorders do not always require hospitalization. Many of the tests can be performed on an outpatient basis, which means the patient can leave the hospital or clinic on the same day. However, some tests may require a short hospital stay, particularly if the patient is an infant or young child.

The treatment options for congenital heart disease may depend on the type and severity of the condition. These options may include medications or procedures like cardiac catheterization.