Sickle Cell Disease Test Diagnosis and Treatments

What is Sickle Cell Disease: Symptoms, Causes and Risk Factors

Test And Diagnosis

A blood test can verify for hemoglobin S – the defective form of hemoglobin that underlines sickle cell anemia . In the United States, the Blood test is part of routine newborn screening done at the optical. However, older children and adults can be examined, too.
In adults, a blood sample is drawn a vein in the arm, In young children and babies, the blood sample is usually obtained from a finger or heel. The sample is then sent to a laboratory where it’s screened from hemoglobin S.
If the screening test is negative, there is no sickle cell gene in the body. If young children and babies, a blood sample is usually collected from a finger a heel. The sample is then sent to a laborer where it is screened for hemoglobin S.

Additional test
To confirm any diagnosis, a sample of blood is examed under a microscope to check for significant numbers of sickle cells – a marker of the disease. If ou or your children as the disease, a blood test to monitor for anemia, a low red blood cell count will be conducted. And your physician suggests an additional test check for likely complications of the disease.

If you or your child displays the sickle cell gene, you may be referred to agentic counselor – an expert in genetic diseases.

Test to detect sickle cell genes before birth

Sickle cells disease can be diagnosed in an unborn baby by sampling some of the fluid surrounding the baby in the month’s womb (amniotic fluid) to look for the sickle cell gene. If you or your partner have been diagnosed with sickle cell anemia or sickle cell trait, you can ask your doctor about where you should consider this screening. Ask for a referral to genetic councilor who can help your understand the risk of your baby.

Treatments and Medications from Sickle Cell Anemia
Bone marrow transplant gives the only potential cure for sickle cell anemia. But finding a donor is challenging, and the procedure has serious risk linked with it, including death.
As a result, treatment for sickle cell anemia is ordinarily aimed at circumventing crises, resolving symptoms and stopping complications if you have sickle cell symptoms and preventing complications. If you have sickle cell anemia, you’ll need to have regular visits to your doctor to review your red blood cell count and monitor your health. Treatment may include medications to reduce pain and prevent complications blood transfusions and supplemental oxygen, as well as bone marrow transplant.

Medications Used to treat sickle cell Anemia Included:
Antibiotics – Children with sickle cell an email may being taking the antibiotic penicillin when they are about two months of age and continue taking it until they are at leat five years old. Do so helps prevent infections, such as pneumonia, which can be life stretching to an infant or child with sickle cell anemia. Antiboitics may also assist helping adults with sickle cell anemia fight certain infections.
Pain-relieving medications – To relieve pain during a sickle crisis, your doctor may advise over -the counter pain relievers and application of heat to the affected area you may also need stronger prescription pain medication.
Hydroxyurea (Droxia, Hydrea). When hydroxyurea is taken, it exceeds the frequencies of painful crises and may help reduce the need for blood transfusions. Hydroxyurea seems to work by stimulating production fo fetal hemoglobin, a type of hemoglobin found in newborns that assist in stopping the formation of sickle cells. Hydroxyurea increases your risk of infections, and there is some concern that long-term use of this drug can cause tumors or leukemia in certain people. However, this has not yet been seen in studies of the drug.

Hydroxyurea was initially used in only adults with severe sickle cell anemia. Studies on children has shown that the drug may prevent some of the serious complications associated with sickle cell anmeia. But the long-term consequences of the drug on children is still unknown. Your doctor can help you determine if this drug may be beneficial for your or your child.

Assessing Stroke Risk
Utilizing a special ultrasound device (transcranial) doctors can learn which children have a higher risk of stroke. This treatment can be used on children as young as two years old, and those who are discovered to have a high risk of stroke are then treated with regular blood transfusions.

Vaccinations to Prevent Infections

Childhood vaccinations are crucial for preventing diseases in all children. However, these vaccinations are even more essential for children with sickle cell anemia. Due to infections being served in children with sickle cell anemia. Your physician will ensure you child receives all of the prescribed childhood vaccinations. Vaccinations, such as the pneumococcal vaccine and the yearly flu shot, are also critical fro adults with sickle cell anemia.

Blood transfusions
In a red blood cell transfusions, red blood cells are withdrawn from a supply of donated blood. These donated cells are then provided intravenously to an individual with sickle cell anemia
Blood transfusions increase the number of healthy red blood cells in circulation in the body, helping to relieve an email. In children the sickle cell anemia at high risk of stroke, a regular blood transfusion can decrease their risk fo stroke.
Blood transfusion carries some risk. Blood contains iron. regular blood transfusion causes an excess amount of iron to build up in your body. Because excess iron and damage your heart, liver and other organs, people who undergo regular transfusions may require treatment to decrease iron levels. Deferasirox (Exjade) is an oral drug that can reduce excess iron levels.
Supplemental oxygen
Breathing additional oxygen through a breathing mask adds oxygen to your bod and helps your breath easier. It may be beneficial if you have acute chest syndrome or a sickle cell crisis.

Stem cell transplant
A stem cell transplant, also designated to as bone marrow transplant involves substituting bone marrow attacked by sickle cell anemia with healthy bone marrow from a doctor. Because of the risk related to a stem cell transplant and procure is recommended only for people who have signal at symptoms and problems from sickle cell anemia.
If a donor is found, disease bone marrow in the person with sickle cell anemia is first depleted with radiation of chemotherapy. A healthy stem cell from the donor is filtered from the blood. The healthy stem cells from the donor are filtered from the blood. The health stems cells are injected intravenously into the bloodstream of the person with sickle cells anemia. Where in they migrate to the bone marrow cavities and begin generating new blood cells. The procure requires the lengthy hospital stay. After the transplant, you will remove drugs to prevent rejection of the donated stem cells.
A stem cell transplant carries risk. There is a chance your body may reject the transplant, leading to a life threatening complications. Also, not everyone is a candidate for transplantation or can find a suitable donor.

Treating complications
Doctor treat most complications of sickle cell-cell anemia as they occur. Treatment may include antibiotics, vitamins, blood transfusions, pain relieving medicines, other medications and possibly surgery, such as to correct vision problems to remove a damaged spleen.

Health Life Media Team