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NR507 Final Exam Study Guide – Normocytic Anemias & Hemoglobinopathies (Advanced Pathophysiology Review)

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This final exam study guide provides a focused review of normocytic anemias and hemoglobinopathies commonly tested in NR507 Advanced Pathophysiology. Content includes the pathophysiology, causes, and clinical manifestations of anemia of chronic disease, acute blood loss anemia, aplastic anemia, and hemolytic anemias, as well as major hemoglobin disorders such as sickle cell disease and thalassemia. Key diagnostic findings, laboratory patterns, and clinical correlations are emphasized to support exam readiness and advanced clinical reasoning.

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NR 507 ADVANCED PATHOPHYSIOLOGY
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NR 507 ADVANCED PATHOPHYSIOLOGY
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NR 507 ADVANCED PATHOPHYSIOLOGY

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Uploaded on
December 17, 2025
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Nr507 hemoglobinopathies edapt

Advanced Pathophysiology (Chamberlain University)

,Introduction to Normocytic Anemias
Normocytic anemias are a group of blood disorders characterized
by a norma l mean corpuscular volume (MCV). The most common
types of normocytic an emias include anemia of chronic disease
and hemolytic anemia.
This learning module focuses on the disease process of
normocytic anemias and enables you to meet the following
course outcomes:
• CO 1: Analyze pathophysiologic mechanisms associated
with selected disease states across the lifespan.
• CO 2: Examine the way in which homeostatic, adaptive, and
compensa tory physiological mechanisms can be supported
and/or altered throug h specific therapeutic interventions
across the lifespan.
• CO 3: Distinguish risk factors associated with selected
disease states a cross the lifespan.
• CO 4: Integrate advanced pathophysiological concepts in the
diagnosis and treatment of health problems in selected
populations.


Anemia of Chronic Disease Pathophysiology A nurse practitioner
(NP) evaluates a 45-year-old client who presents with fatigue and
weakness. The NP diagnoses the client with anemia of chronic
disease. What is the primary pathophysiological mechanism
causing this normocytic anemia? Excessive blood loss
Impaired iron absorption

,Delayed maturation of erythrocyte precursors
Defective erythropoiesis
The primary pathophysiological mechanism underlying normocytic
anemias such as anemia of chronic disease is defective
erythropoiesis. Chronic inflammation affects the bone marrow,
leading to impaired production of red blood cells despite adequate
iron availability.
Impaired iron absorption is more relevant to microcytic anemias,
where the size of red blood cells is reduced due to insufficient iron
for hemoglobin synthesis. Excessive blood loss typically results in
hypovolemic anemia and can lead to microcytic or normocytic
anemia, depending on the rate of blood loss. However, normocytic
anemias are not primarily characterized by excessive blood loss.
Delayed maturation of erythrocyte precursors is a characteristic
feature of macrocytic anemias, not normocytic anemias.
A nurse practitioner (NP) evaluates a 28-year-old client who
presents with fatigue, jaundice, and dark-colored urine. The NP
diagnoses the client with hemolytic anemia. What is the most
likely pathophysiological mechanism causing this normocytic
anemia?



Impaired iron absorption
Increased red blood cell
destruction Excessive blood
loss
Defective erythropoiesis
Hemolytic anemia is characterized by the premature destruction
of red blood cells, leading to the release of hemoglobin. The
symptoms of fatigue, jaundice, and dark-colored urine are classic
manifestations of hemolysis.
Impaired iron absorption is more relevant to microcytic anemias,
where the size of red blood cells is reduced due to insufficient iron
for hemoglobin synthesis.
Defective erythropoiesis involves abnormalities in the production
of red blood cells. While it can contribute to certain types of
anemias, hemolytic anemia is primarily characterized by the
accelerated destruction of mature red blood cells.

, Excessive blood loss, while a cause of anemia, typically leads to
hypovolemic anemia rather than hemolytic anemia.
Risk for Hemolytic Anemia
Which client should the nurse practitioner (NP) recognize as most
at risk for developing hemolytic anemia?



60-year-old with a history of iron-deficiency anemia
35-year-old who recently underwent surgery for a
bleeding ulcer 28-year-old with a family history of
thalassemia
50-year-old who experienced a transfusion reaction after a blood transfusion

A client who experienced a transfusion reaction after a blood transfusion is
at significant risk for developing hemolytic anemia. Transfusion reactions
can involve the destruction of donor red blood cells, leading to hemolysis
and associated symptoms such as fever, chills, and jaundice.

Iron-deficiency anemia is characterized by a lack of iron to produce
hemoglobin. It does not inherently predispose individuals to hemolytic
anemia.

Thalassemia is a genetic disorder affecting the production of hemoglobin but
does not directly lead to hemolysis of red blood cells, a key feature of
hemolytic anemia.

Excessive blood loss from surgery can lead to hypovolemic anemia but does
not inherently cause hemolysis.

Pathophysiology of Normocytic Anemias

Normocytic anemias are characterized by the presence of normal-sized red
blood cells. The red blood cells of normocytic anemias have a mean
corpuscular volume (MCV) of 80-99 dL. When a client presents with
normocytic anemia, a reticulocyte count should be performed to assess the
number of immature red blood cells in the bone marrow.
Hemolytic anemia and anemia due to blood loss will cause elevated
reticulocyte counts because the bone marrow is compensating for
a loss.

The pathophysiology of normocytic anemia can be attributed to various
underlying causes, and it often involves disruptions in the production,
maturation, or survival of red blood cells. Some common causes of
normocytic anemias include chronic inflammatory diseases, chronic kidney
disease, hemolytic anemias, chronic blood loss, endocrine

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