Case Study Sickle Cell Crisis

“In the United States, it's estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans” (NHLBI, NIH, Who is at risk for sickle cell anemia). SCD is a disease that is a serious disorder in which the body can make normal blood cells and sickle shape cells. Sickle shape cells can block the blood flow in your vessels and cause pain or organ damage also put you in risk for infections. SCD has no cure available but there are many treatments out there to deal with the complications of it. From over years treatments did get better from way back in the day doctors have learned. Sickle cell disease has lack of attention and funding because it’s only affecting

Sickle Cell Disease is an illness that affects people all across the globe. This paper will give a description of the sickness through the discussion of the causes, symptoms, and possible cures. Sickle Cell Disease (SCD) is a "group of inherited red blood cell disorders."(1) These disorders can have various afflictions, such as pain, damage and a low blood count--Sickle Cell Anemia.

Sickle cell crisis is an acute form of sickle cell disease where pain and sickling are extensive (Byar, 2013). SCD is a genetic disease that predominantly affects black people of African decent (Gersten, 2016). Abnormal hemoglobin chains are the main issue with SCD (Byar, 2013). Normal hemoglobin chains are comprised of 99% hemoglobin A (HbA) however, in SCD an abnormal form of the gene, hemoglobin S (HbS) is present in approximately 40% of total hemoglobin (Byar, 2013). In order for a person to be born with SCD, both parents must carry the abnormal gene, HbS (Byar, 2013). HbS is extremely sensitive to the changes in oxygen amount of the RBC and when exposed to decreased oxygen the HbS cause the RBC to distort and become sickle-shaped,

Sickle cell disease usually reveals itself early in a child’s life. Sickle cell disease brands a set of genetic red blood cell disorders. People with SCD have irregular hemoglobin called sickle hemoglobin, inside of their red blood cells. Hemoglobin is a protein located in red blood cells that transfers oxygen through the body. SCD is inherited which means that genes pass the disease from parents to their offspring. SCD is not infectious. A person cannot catch SCD, like a cold or STD. Alzheimer’s disease also runs in my family. My Great-Grand Mother is currently showing signs of dementia. Alzheimer’s is a disease that destroys remembrance and other key psychological functions used to preform everyday routines. Alzheimer’s is non-preventable and

Thank you for sharing your post regarding the Interprofessional and collaborative practice in managing sickle cell disease. You have highlighted the core competencies of Interprofessional collaboration, illustrated the communication forms applied in your capstone project and indicated the most relevant domain as understanding the role and responsibility of each member. I absolutely agreed with you that sickle cell patients require care coordination approach to effectively manage pain and complications associated with sickle cell episode.

According to Centers for Disease Control and Prevention “Sickle cell Trait is people who inherit one sickle cell gene and one normal gene have sickle cell trait (SCT). People with SCT usually do not have any of the symptoms of sickle cell disease (SCD), but they can pass the trait on to their children.” (sickle cell trait)

The term sickle cell infection (SCD) depicts a gathering of acquired red platelet issue." Normal red blood cells are shaped like discs or donuts. They are soft and flexible so they can easily move through very small blood vessels"(anonymous, 2015).Individuals with SCD have anomalous hemoglobin, called hemoglobin S or sickle hemoglobin, in their red platelets. Hemoglobin is a protein in red platelets that conveys oxygen all through the body. The most well-known sort is known as, sickle-cell frailty (SCA) and there is A few Types of Sickle Cell Sickness: Hemoglobin SS, Hemoglobin SC, Hemoglobin SD. In the Unified States, a great many people with sickle cell illness (SCD) are of African family line or recognize themselves as dark. About1 out of 13 African American children is

Sickle cell disease is an inherited form of anemia. This means both parents must pass on the defective gene for a child to be affected. The gene is more common in families that come from Saudi Arabia, Africa, Mediterranean countries, India, the Caribbean islands, and North, South, and Central America of African descent.

Sickle cell disease (SCD) is a destructive abnormality in red blood cells that results in circulatory impairment. Sickle cell disease can cause pain, infection, organ damage and strokes. SCD is inherited through the infants’ parental genes (James, 2014). For instance, if an infant inherits the gene from one parent that infant will automatically have the sickle cell trait. As a result, the infant will be a carrier of the disease but won’t actually have the SCD. It is very rare for a carrier to have any symptoms. Women who have SCD are considered high risk if they become pregnant. SCD poses complication for both mother and fetus during

Sickle cell anemia has been a huge or major controversy in the united states ever since 1973 until today. It is an inherited disease that affects the red blood cells.

Sickle Cell disease also known as SCD is a genetic disease of a person’s red blood cells. The shape of a normal person’s RBC is shaped like a disk. This shape of the red blood cells allows for the flexibility that helps the cells move through blood vessels.

Sickle cell disease is a chronic condition that a person can inherit from their parents in which it effects the globular structure of the patients red blood cells. A more sickle shaped structure, which can alter a person’s blood flow, replaces the more common globular structure. This impairment in blood flow can lead to blood clots, severe debilitating pain and damage to vital organs such as the liver, kidney and spleen. This disease currently affects over 90,000 people in the United States, with the majority of them being African American and

Sickle cell disease (SCD) is an autosomal recessive disease that is common in African Americans. This disease arises from a single base-pair substitution of thymine for adenine and this makes valine in its place of glutamine in the sixth position of the Beta-globin molecule. When this swap occurs in a homozygous state and this is the sickle cell disease. Clinical signs result from polymerization of the abnormal haemoglobin and the sickling of cells. (Thompson, 2010)

Individuals that have inherited Sickle Cell Disease (SCD) may experience symptoms of acute and/or chronic pain. SCD is a disease in which the red blood cells are deformed and form a sickle cell shape. This causes the sickle shaped red blood cells to not perform as a normal red blood cell would through the blood vessels and capillaries. Due to the sickle shape of the red blood cells, the oxygen delivery to the tissues significantly decreases and the blood flow is restricted causing occlusion. Due to the lack of performance of the sickle red blood cells, tissue damage is a result, which in turn, causes pain.

consequently had more of a prevalence of SCD while they were compared to those who did not undergo a hemodialysis (Derebail et al, 2014). Concluding from this one study that dealt mainly with African-Americans, the results show how prevalent sickle-cell disease can be in black people. The higher rate of the trait can again be linked back to the monetary elements but it may not be limited only be limited to that as family ties are an important genetic factor of this disease.