Saint Luke's College Of: Nursing
Saint Luke's College Of: Nursing
Saint Luke's College Of: Nursing
“Blood Disorders”
(Assignment #4)
Submitted by:
APRIL MAE M. LABRADOR
Batch Savere Vita
4NU01- GROUP #4
Submitted to:
EDNA U. ROBLES, RN, MAN
Clinical Instructor
Sickle cell anemia is an inherited disorder of the hemoglobin in blood. Sickle cell
anemia requires the inheritance of two sickle cell genes. The major symptoms of sickle
cell anemia are the direct result of the abnormally shaped sickled red blood cells
blocking the flow of blood.
Causes of Anemia:
A mutation in the gene that tells your body to make the red, iron-rich compound
that gives blood its red color (hemoglobin). In sickle cell anemia, the abnormal
hemoglobin causes red blood cells to become rigid, sticky and misshapen.
The sickle cell gene is passed from generation to generation in a pattern of
inheritance called autosomal recessive inheritance. This means that both the
mother and the father must pass on the defective form of the gene for a child to
be affected.
Diagnostic Laboratories:
Blood test can check for hemoglobin S (screening test)
Mother's womb (amniotic fluid) sampling test
Treatment Blood transfusion, Nitric Oxide,
Bone marrow transplant, also Gene therapy
known as stem cell transplant
Hydroxyurea (Droxia, Hydrea) Nursing Problems
Antibiotic and Pain relief Organ damage
medication Acute chest syndrome
Pneumococcal vaccine and Stroke
annual Flu vaccine Pulmonary hypertension
Blindness
Nursing Interventions
Advise client to avoid temperature extremes.
Encourage client to take folic acid supplements daily, and choose a healthy diet.
Advise client to take an early screening test as possible.
Teach client in exploring ways to cope with the pain. Work with your doctor to
find ways to control your pain.
B. THALASSEMIA
Thalassemia is a blood disorder that is caused by DNA mutations in cells that are
responsible for producing hemoglobin. Thalassemia is inherited, meaning that at least
one of your parents must be a carrier of the disorder. It’s caused by either a genetic
mutation or a deletion of certain key gene fragments.
Thalassemia minor is a less serious form of the disorder. There are two main forms
of thalassemia that are more serious. In alpha thalassemia, at least one of the alpha
globin genes has a mutation or abnormality. In beta thalassemia, the beta globin genes
are affected.
Causes of Anemia
Occurs when there’s an abnormality or mutation in one of the genes involved in
hemoglobin production.
If only one or both of your parents is a carrier for thalassemia.
Diagnostic Laboratories:
Test for hemoglobin electrophoresis
Physical examination
Pathophysiology:
Nursing Interventions:
Evaluate client’s hemoglobin level and assist client personal information, major
stress and conditions.
Encourage client to avoid excess intake of iron.
Advise client to avoid infections, cuts and encourage client to eat a healthy diet.
Causes of Anemia:
A change in a gene, called a mutation, causes your body to make abnormal red
blood cells. These cells don’t have proteins that shield them from your immune
system. People with a certain type of anemia, called aplastic anemia, are more
likely to get PNH.
People who have cardiovascular problem (congestive heart failure), and
edematous patient.
Pathophysiology
Usually caused by congestive heart failure, most commonly (but not always) in
people who also have had episodes of dyspnea with exertion, or of orthopnea
(shortness of breath when lying down). In early left ventricular failure, the cardiac
output does not increase sufficiently in response to moderate exercise; tissue
and cerebral acidosis occurs, and the patient experiences dyspnea on exertion.
The shortness of breath may be accompanied by fatigue or a sensation of
smothering or sternal compression. In the later stages of left ventricular failure,
the pulmonary circulation remains congested, and dyspnea occurs with mild
exertion.
Diagnostic Laboratories:
CBC test Urine test BMA
Treatment:
Folic acid to help your bone marrow make more normal blood cells
Iron supplements to make more red blood cells
Blood transfusion, Bone marrow stem cell transplant.
Blood thinners
Eculizumab (Soliris) This drug prevents the breakdown of red blood cells.
Nursing Problems:
Sleep apnea Diastolic heart failure
Asthma Acute cardiac ischemia
Pulmonary embolus.
Nursing Interventions:
The most important dietary change that people suffering from congestive heart
failure and paroxysmal nocturnal dyspnea need is to reduce their salt intake.
Suggestions for altering the way the client sleep; she/he might suggest to sleep
propped up with several pillows to help alleviate lung congestion at night.
Encourage client to avoid processed food, canned or frozen food, and fast food.
Iso Antibody
An antibody that occurs only in some individuals of a species and reacts specifically with
a particular foreign isoantigen. For specific isoantibodies of blood groups, also known as
alloantibody. Isoantibodies are produced against an epitope that is expressed by all
normal individuals and is not polymorphic. In the area of human platelet immunology, a
classic example of isoimmunization occurs when a patient with an inherited deficiency of
a membrane glycoprotein has been subjected to multiple platelet transfusions to correct
a bleeding diathesis.
Auto Antibody
Autoantibodies are the result of a failure of the immune system to discriminate between
“self” and “nonself,” which target a person’s own antigen.
Changes in antibody quantity may be used to monitor successful therapy or disease
exacerbation. They may be used as indicators of individuals at risk for future diseases in
disorders that are familial. Autoantibody tests are never used by themselves for
diagnosis of disease.