Sickle Cell Anemia: Understanding the Signs, Symptoms, and Advances in Treatment

Today, we’re going to discuss the symptoms, the diagnosis, and the treatment of sickle cell anemia. Keep reading.

What is sickle cell anemia?

Well, sickle cell anemia, also known as sickle cell disease, is an inherited disorder that affects the red blood cells. Your red blood cells are normally shaped like round donuts. They are very pliable and very bendy, and they are able to make it through blood vessels very easily in order to carry oxygen to your body’s tissues and your body’s organs. In patients with sickle cell anemia, instead of having nice round blood vessels, their blood vessels are shaped like crescents or like sickles.

They are not able to carry oxygen adequately to tissues, and because of their odd shape, they don’t always fit nicely and easily through blood vessels, and they often get stuck in blood vessels and capillaries. When they get stuck in these blood vessels and capillaries, it’s like causing a traffic jam to your circulatory system. So in patients who are having sickle cell crises, they are not able to oxygenate the tissue as well, and they can have very severe pain in these areas, and they can also have multiple other medical problems.

What causes sickle cell anemia?

Sickle cell anemia is an inherited disorder; it is genetic. So if you have two parents who each carry the sickle cell trait, if each parent passes one sickle cell gene to a child, that child has sickle-cell anemia. If one parent passes a sickle cell gene to the child while the other parent passes a normal hemoglobin gene to the child, then that child has sickle cell trait. The child will not actually have sickle cell disease, but the child is now a carrier and can pass the sickle cell gene down to his or her child.

What are the signs and symptoms of sickle cell anemia?

Patients with sickle cell anemia can present as babies just a few months old.

– Babies with sickle cell anemia often present with painful, red, swollen hands and feet.

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– Children with sickle cell often have delayed puberty and delayed growth. They often look much younger than their actual age.

– Other signs and symptoms of sickle cell disease include severe anemia, difficulty breathing, chest pain, acute chest syndrome, and poor oxygenation.

– Sickle cell patients frequently get severe, debilitating bone pain. They can get myocardial infarctions or heart attacks, strokes, kidney infarctions, and splenic infarctions. They can be prone to more infections than a typical patient.

– Patients with sickle cell can get severe hip pain, and avascular necrosis. They can also get venous thrombosis or DVT.

– Men with sickle-cell anemia can get something called priapism, which is an unwanted, often painful erection in the absence of sexual desire. It can last for hours and can lead to permanent damage if not treated promptly.

Priapism is a medical emergency to get sickle cell anemia in the United States, sickle cell anemia is most prevalent among African Americans and people of African descent. Worldwide, sickle cell anemia is prevalent in regions such as sub-Saharan Africa, and the Mediterranean, especially in Greece, in certain parts of India, and in the Caribbean. It is believed that the sickle cell gene is actually protective against malaria, which is an infection that can be prevalent in these regions.

How is sickle cell anemia diagnosed?

There is a blood test that can test if you have sickle cell anemia or if you carry the traits. In the United States, all newborns are tested for sickle cell anemia before they even leave the hospital.

What is the treatment for sickle cell anemia?

Well, there are a variety of treatments for sickle cell. Some are aimed at preventing the symptoms and complications of sickle cell anemia, while other treatments are aimed at relieving the symptoms. The treatments include:

1. Hydroxyurea

Hydroxyurea is a medication that causes the production of more normal hemoglobin in a patient.

2. Folic acid treatment

Vaccinations prevent certain infections that patients with sickle cell are predisposed to, such as the pneumococcal vaccination and the flu vaccination.

3. Antibiotics

Both to prevent infections and to treat infections as well.

4. Blood transfusion

Blood transfusions are part of the treatment regimens.

The only curative option for sickle cell anemia at this time is a hematopoietic stem cell transplantation. Though the stem cell transplant is the only curative option, it has very significant risks.

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So, it is very important for a patient with sickle cell anemia to weigh the pros and cons of getting this transplantation with their hematologist. A major part of the treatment for sickle cell anemia includes pain management because these patients can be in severe, debilitating, uncompromising pain.

According to Dr. Tina’s experience;

When I did my med-peds residency at Georgetown University Hospital, during my pediatric hematology/oncology rotation, I had the pleasure of taking care of many, many patients with sickle cell anemia. Let me tell you, the children with sickle cell anemia are some of the most resilient, most precocious, most wonderful people I have ever encountered. They would have to come into the hospital, miss school, miss social activities, and have to deal with pain which I can only imagine, and they would do it with such bravery.

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I had patients who had stem cell transplants; some did well, but some really did have major complications, such as graft-versus-host disease. One of the most difficult parts for me as a physician taking care of patients with sickle cell anemia would be the way that they’re often judged by clinicians. These patients have been dealing with pains that some of us can’t even imagine, and narcotics are a big part of that treatment.

So, oftentimes when sickle cell patients present to the emergency department, they already know what works for them and what doesn’t work, and they do require high amounts of narcotics. It’s difficult for me when I see them being judged or when a sickle cell anemia patient comes in true crisis and true pain, and all of a sudden, people look at them like, “Hmm, they just want some drugs.” Well, of course, they want narcotics because they are in pain. We just need to really be more empathetic and learn more and educate ourselves about sickle cell anemia.

In conclusion

If you are a patient with sickle cell anemia or if you are living and loving a patient with sickle cell, please comment down below. I want to know your experiences. I want to know what treatment regimens have worked for you or some things you do to cope with this very real, very heavy disease.

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