Sickle ce Study guides, Class notes & Summaries
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Davis Advantage Sickle Cell Disease latest questions and answers all are correct graded A+
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The patient who has sickle cell anemia developed the condition of hand-foot syndrome because of what 
physiological process? 
Repeat crisis and infarction of the bones leading to uneven development of fingers and toes 
Damage to the liver related to repeat sickle cell crisis 
Repeat crisis and infarction involving the circulatory system of the arms and legs 
Damage to the kidneys related to repeat sickle cell crisis - Answer-C 
A patient is admitted to the nurse's unit with sickle cell crisis. ...
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Sickle Cell Disease questions with correct answers
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Get Regular Checkups 
 
-Regular health checkups with a primary care doctor can help prevent some serious problems. - Answer Babies from birth to 1 year of age should see a doctor every 2 to 3 months. 
 
Children from 1 to 2 years of age should see a doctor at least every 3 months. 
 
Children and adults from 2 years of age or older 
should see a doctor at least once every year. 
 
Prevent Infections - Answer -Common illnesses, like the flu, can quickly become dangerous for a child with sic...
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Sickle Cell Anemia - ATI: Nursing Care of Children Exam Questions and Answers
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Sickle Cell Anemia - ATI: Nursing Care of Children 
Exam Questions and Answers 
Sickle Cell Disease - Answer- a group of diseases (autosomal recessive genetic 
disorder) in which abnormal sickle hemoglobin S (HbS) replaces normal adult 
hemoglobin (Hgb A). 
Sickle Cell Anemia - Answer- the homozygous and most common form of SCD. 
Increased destruction of RBCs occurs. 
manifestations of SCA (resultl of RBC sickling) - Answer- increased blood viscosity, 
obstruction of blood flow, and tissue hypox...
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HEMATOLOGY NURSING III SICKLE CELL ANEMIA, ANEMIA, THROMBOCYTOPENIA, IVS QUESTIONS WITH ANSWERS 100% CORRECT
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HEMATOLOGY NURSING III SICKLE CELL ANEMIA, ANEMIA, THROMBOCYTOPENIA, IVS QUESTIONS WITH ANSWERS 100% CORRECT
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Sickle Cell Anemia questions with correct answers
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What is sickle cell anemia? - Answer An autosomal recessive disorder resulting in a mutated form of hemoglobin (HbS) 
 
What causes sickle cell TRAIT? - Answer ONE allele on the beta globin gene carries the sickle mutation, one normal allele for HbA (heterozygous) 
 
What causes sickle cell DISEASE? - Answer TWO alleles on the beta globin gene carries mutation for sickle mutation (homozygous) 
 
What does the sickle cell mutation cause resistance to? - Answer Plasmodium falciparum (malar...
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Sickle Cell Disease questions with correct answers
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Sickle Cell Disease - Answer Is a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. 
 
Risk Factors for Sickle Cell Disease Include - Answer 1-Genetics: Having parents heterozygous for hemoglobin S 
 
2-Ethnicity: Been of African American descent 
 
Other races that can be affected are people from Mediterranean , Caribbean, Arabian, and east Indian descent. 
 
Hemoglobin S is Sensitive t...
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NUR MISC FINAL ANSWER KEY UNFOLDING Reasoning Sickle Cell Anemia Anthony Perkins, 15 years old
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NUR MISC FINAL ANSWER KEY UNFOLDING Reasoning Sickle Cell Anemia Anthony Perkins, 15 years old 
 
© 2016 Keith Rischer/www.KeithRN.com 
Sickle Cell Anemia 
Anthony Perkins, 15 years old 
Primary Concept 
Perfusion 
Interrelated Concepts (In order of emphasis) 
1. Pain 
2. Clotting 
3. Fluid and Electrolyte Balance 
4. Clinical Judgment 
5. Patient Education 
6. Communication© 2016 Keith Rischer/www.KeithRN.com 
UNFOLDING Reasoning: ANSWER KEY 
Sickle Cell Crisis 
History of Present Problem: 
A...
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NURSING 5327 mod 5 case study sickle cell crisis.
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NURSING 5327 mod 5 case study sickle cell crisis.
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Lecture Notes Diagnostic Biochemistry and Haematology - Sickle Cell Anaemia and the Thalassaemias
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These lecture notes focus on Diagnostic Biochemistry and Hematology, particularly discussing Sickle Cell Anemia and Thalassemias. It delves into the structure of hemoglobin, the synthesis of various types of hemoglobin, and how genetic defects impact the production of normal hemoglobin chains. 
 
The lecture covers the different forms of hemoglobin (Hb A, Hb F, Hb A2) present in adult blood and explains their composition. It also discusses the sequence of hemoglobin synthesis in early life, from...
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Sickle Cell Disease questions with correct answers
- Exam (elaborations) • 10 pages • 2023
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Sickle Cell Disease - Answer Is a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. 
 
Risk Factors for Sickle Cell Disease Include - Answer 1-Genetics: Having parents heterozygous for hemoglobin S 
 
2-Ethnicity: Been of African American descent 
 
Other races that can be affected are people from Mediterranean , Caribbean, Arabian, and east Indian descent. 
 
Hemoglobin S is Sensitive t...
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