The main characteristics and treatment of sickle cell anemia

He died of pneumonia in and is buried in the Catholic cemetery at Sauteurs in the north of Grenada. Your doctor may recommend further testing to assess the potential for wound healing.

The obstetrician should work with a hematologist or primary medical doctor who is well informed about sickle cell disease and its complications.


Transfusion increased Hb 9. They should also receive additional vaccines to prevent other infections. The transition to more independent self-management may be difficult, and following treatment plans may become less likely.

These people should also be referred as soon as possible for special care. Prevention People with sickle cell disease should have their eyes checked every year to look for damage to the retina.

Prior to her current role, Kemi previously worked as a High Risk Midwife with a special interest in caring for women with haemoglobinopathies.

Complications and Treatments of Sickle Cell Disease

Adults should have the flu vaccine every year, as well as the pneumococcal vaccine and any others recommended by a doctor.

The treatment of foot ulcers varies depending on the cause of the ulcer. Research on the circumstances surrounding the death of children with SCD in Minas Gerais State, points to the difficulty in providing transportation to the health treatment center as a contributing factor to premature deaths Although a greater percentage of participants with Hb SC reported home treatment, they claimed a more intense need for medical treatment, compared to Hb SS, the more serious variation of the disease.

The pain crises, the blood transfusions, occurrence of other diseases and hospitalizations, in addition to the social aspects such as unemployment, low income, and difficulties to access the health service, negatively impacted the QOL of this population.

Painful crises are treated symptomatically with pain medications ; pain management requires opioid administration at regular intervals until the crisis has settled.

The patient with suspected acute chest syndrome should be admitted to the hospital with worsening A-a gradient an indication for ICU admission. A number of different treatments are available for SCD: Mass media education and public events were also done, supported by the Ministries of Health and Education using publicity drive: Blood and urine testing People who have sickle cell disease need to have frequent lab tests.

Dr Gupta is also a recipient of the Excellence in Hemoglobinopathies Research Award from NHLBI to examine the potential of cannabinoids to treat pain and develop methods to quantify pain objectively.

Infants need to take liquid penicillin. Delayed growth Delayed growth often occurs in people with SCD. He has co-authored national guidelines for management of children and adults with sickle cell disease, and thalassaemia. This breaking apart of RBCs is called chronic hemolysis.

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During the physical examination, your doctor will look for signs of infection, such as redness and warmth. Supplemental oxygen is given through a mask.The causes of anemia may be classified as impaired red blood cell (RBC) production, increased RBC destruction (hemolytic anemias), blood loss and fluid overload (hypervolemia).Several of these may interplay to cause anemia eventually.

Sickle cell disease is the name for a group of inherited conditions that affect the red blood cells.

Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders

The most serious type is called sickle cell anaemia. Sickle cell disease mainly affects people of African, Caribbean, Middle Eastern, Eastern Mediterranean and Asian origin. In the UK, it's.

The alpha (HBA1, ; HBA2, ) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, beta globin that sickles causes sickle cell anemia ().Absence of beta chain causes beta-zero-thalassemia.

Reduced amounts of detectable beta globin causes beta-plus-thalassemia. 1. A. m J Hematol. Dec doi: /ajh [Epub ahead of print] Sleep disordered breathing does not predict acute severe pain episodes in children with sickle cell anemia.


American Society of Hematology

Visiting Professor, Nanyang Technological University, Mar. - present Adjunct Professor, CAMP-Nano, Xi'an Jiaotong University, Oct.

- present Principal Research Scientist, Dept of Materials Sci & Eng, MIT, Feb. - present Principal Investigator & Director, Nanomechanics Lab, MIT, Oct. - present. Sickle cell anemia (sickle cell disease) is a disorder of the blood caused by an inherited abnormal hemoglobin (the oxygen-carrying protein within the red blood cells).

The abnormal hemoglobin causes distorted (sickled appearing under a microscope) red blood cells.

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The main characteristics and treatment of sickle cell anemia
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