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NRSG_2350_Study_Guide_Exam_2

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STUDY Guide for NRSG 2350 Exam 2 Exam will cover Modules 4 – 6 (Heme/Onc, Neuro and Cardiac) For Patho: Please be sure you understand the A&P. Always know what is normal so you can understand when something is abnormal. For all patho, review risk factors, signs and symptoms, diagnostics, assessment data / labs. All disorders / diseases will be listed in the vocab list below. For all Pharm: Please know the class and prototype given. I may list additional meds in a class below, so be familiar with those as well. Know the MOA, the reason for giving, what are the intended / therapeutic effects, what are the side effects, are there any contraindications, are there any drug-drug interactions, and what is the nursing management? Be familiar with the trade and generic name of a med. VOCAB LIST: These are concepts, diseases, medications, etc., that you may or will see on the exam. Please see above for details regarding patho and pharm specifics. PATHO Hematopoiesis – the formation of RBCs Anemia – disorder with too few or ineffective RBCs (result of aleration of erythropoiesis or hemolysis of cells) Classified based on size of RBCs or underlying etiology Cytic – classification – refers to cell size Chromic – classification – refers to cell Hgb content Microcytic – abnormally small RBCs [ex. = iron deficiency and thalassemia (lacks one of the 2 proteins that make up hemoglobin)] Also usually hypochromic – Not enough hemoglobin to carry the oxygen Macrocytic – Large, thick RBCs, AKA Megaloblastic, normal amount of Hgb – vitamin B12 or folate deficient Pernicious – subtype of Vitamin B12 deficiency Normocytic – insufficient number of RBCs – normal in size and Hgb content Anemia of chronic disease – inflammation Aplastic – failure to produce all types of blood cells Hemolytic – result from excessive destruction or hemolysis of RBCs [ex. Sickle cell, thalassemia] Sickle cell – RBCs have an abnormal crescent shape Key factors of making healthy RBCs = enough iron (form hemoglobin rings to carry oxygen), B12 and Folic Acid (form supporting structure), Amino acids and carbohydrates (complete hemoglobin rings, cell membrane, and basic structure) White Blood Cells = Neutrophil, eosinophil, basophil, monocyte, lymphocyte WBC disorders: (normal range is 5k-10k cells/mL) Leukocytosis: a state of increased WBC, usually indicates infectious process Leukocytopenia: a state of decreased WBC, indicate immune deficiency, bone marrow suppression Neutropenia: decreased neutrophil count, makes body poorly equipped to fight infection WBC diseases: Lymphomas – Proliferation of lymphocytes in lymphoid tissue Hodgkin’s lymphoma = T-cell Non-Hodgkins lymphoma (NHL) – 40 types – B or T cells (80/20%) Leukemias (myeloid or lymphoid) – risk factors = exposure to chemicals, viral, radiation mutagens, smoking, immunodeficiency disorders Acute: Immature cells, Onset abrupt and rapid, Short survival time of patients, but improving Chronic: Mature in appearance but does not function normally, Gradual onset, Good survival Multiple Myeloma - excessive number of abnormal plasma cells in the bone marrow, crowds blood forming cells. Bleeding disorders: Hemophilia A – Deficiency or abnormality of clotting factor 8 (VIII) Aplastic Anemia (Pancytopenia) – Does not produce WBCs, RBCs, or Thrombocytecs (may be caused by cancer, autoimmune, tonxins, genetics, etc.) Cancer – causes many bleeding disorders Hemoglobin – protein contained in red blood cells that is responsible for delivery of oxygen to the tissues Normal ranges = men 14 to 18 g/dl, women 12 to 16 g/dl. Hematocrit - measures the volume of red blood cells compared to the total blood volume (red blood cells and plasma). Normal hematocrit ranges = men 40 to 54%, women 36 to 48%. Erythropoiesis – production of RBCs, stimulated by erythropoeitin, stimulating agents = Epoetin Alfa (Epogen or Procrit), Darbepoetin Alfa (Aranesp) Made in kidney in response to hypoxia Colony stimulating factors: Filgr

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STUDY Guide for NRSG 2350 Exam 2
Exam will cover Modules 4 – 6 (Heme/Onc, Neuro and Cardiac)

For Patho: Please be sure you understand the A&P. Always know what is normal so you can understand
when something is abnormal. For all patho, review risk factors, signs and symptoms, diagnostics,
assessment data / labs. All disorders / diseases will be listed in the vocab list below.

For all Pharm: Please know the class and prototype given. I may list additional meds in a class below, so
be familiar with those as well. Know the MOA, the reason for giving, what are the intended /
therapeutic effects, what are the side effects, are there any contraindications, are there any drug-drug
interactions, and what is the nursing management? Be familiar with the trade and generic name of a
med.

VOCAB LIST: These are concepts, diseases, medications, etc., that you may or will see on the
exam. Please see above for details regarding patho and pharm specifics.
PATHO

Hematopoiesis – the formation of RBCs

Anemia – disorder with too few or ineffective RBCs (result of aleration of erythropoiesis or hemolysis of
cells) Classified based on size of RBCs or underlying etiology

Cytic – classification – refers to cell size

Chromic – classification – refers to cell Hgb content

Microcytic – abnormally small RBCs [ex. = iron deficiency and thalassemia (lacks one of the 2
proteins that make up hemoglobin)]

Also usually hypochromic – Not enough hemoglobin to carry the oxygen

Macrocytic – Large, thick RBCs, AKA Megaloblastic, normal amount of Hgb – vitamin B12 or
folate deficient

Pernicious – subtype of Vitamin B12 deficiency

Normocytic – insufficient number of RBCs – normal in size and Hgb content

Anemia of chronic disease – inflammation

Aplastic – failure to produce all types of blood cells

Hemolytic – result from excessive destruction or hemolysis of RBCs [ex. Sickle cell, thalassemia]

Sickle cell – RBCs have an abnormal crescent shape

Key factors of making healthy RBCs = enough iron (form hemoglobin rings to carry oxygen), B12 and Folic
Acid (form supporting structure), Amino acids and carbohydrates (complete hemoglobin rings, cell
membrane, and basic structure)

White Blood Cells = Neutrophil, eosinophil, basophil, monocyte, lymphocyte

, WBC disorders: (normal range is 5k-10k cells/mL)

Leukocytosis: a state of increased WBC, usually indicates infectious process

Leukocytopenia: a state of decreased WBC, indicate immune deficiency, bone marrow
suppression

Neutropenia: decreased neutrophil count, makes body poorly equipped to fight infection

WBC diseases:

Lymphomas – Proliferation of lymphocytes in lymphoid tissue

Hodgkin’s lymphoma = T-cell

Non-Hodgkins lymphoma (NHL) – 40 types – B or T cells (80/20%)

Leukemias (myeloid or lymphoid) – risk factors = exposure to chemicals, viral, radiation
mutagens, smoking, immunodeficiency disorders

Acute: Immature cells, Onset abrupt and rapid, Short survival time of patients, but
improving

Chronic: Mature in appearance but does not function normally, Gradual onset, Good
survival

Multiple Myeloma - excessive number of abnormal plasma cells in the bone marrow, crowds
blood forming cells.

Bleeding disorders:

Hemophilia A – Deficiency or abnormality of clotting factor 8 (VIII)

Aplastic Anemia (Pancytopenia) – Does not produce WBCs, RBCs, or Thrombocytecs (may be
caused by cancer, autoimmune, tonxins, genetics, etc.)

Cancer – causes many bleeding disorders

Hemoglobin – protein contained in red blood cells that is responsible for delivery of oxygen to the
tissues

Normal ranges = men 14 to 18 g/dl, women 12 to 16 g/dl.

Hematocrit - measures the volume of red blood cells compared to the total blood volume (red blood
cells and plasma).

Normal hematocrit ranges = men 40 to 54%, women 36 to 48%.

Erythropoiesis – production of RBCs, stimulated by erythropoeitin, stimulating agents = Epoetin Alfa
(Epogen or Procrit), Darbepoetin Alfa (Aranesp)

Made in kidney in response to hypoxia

Colony stimulating factors:

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