100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
NSG 533 Exam 4 | Questions & Answers (100 %Score) Latest Updated 2024/2025 Comprehensive Questions A+ Graded Answers | With Expert Solutions $13.48   Add to cart

Exam (elaborations)

NSG 533 Exam 4 | Questions & Answers (100 %Score) Latest Updated 2024/2025 Comprehensive Questions A+ Graded Answers | With Expert Solutions

 7 views  0 purchase
  • Course
  • NSG 533
  • Institution
  • NSG 533

NSG 533 Exam 4 | Questions & Answers (100 %Score) Latest Updated 2024/2025 Comprehensive Questions A+ Graded Answers | With Expert Solutions

Preview 2 out of 10  pages

  • August 7, 2024
  • 10
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • NSG 533
  • NSG 533
avatar-seller
VasilyKichigin
NSG 533 Exam 4 | Questions & Answers (100 %Score) Latest Updated 2024/2025
Comprehensive Questions A+ Graded Answers | With Expert Solutions




Anemia can contribute to: - coronary ischemia

Composition of blood - 5.5L total. 50-55% = plasma; 90% water

Erythropoesis is stimulated by... - erythropoetin

Hemoglobin A - the majority of adult hemoglobin. 97% of circulating hemoglobin. 2
alpha and 2 beta chains.

HbA2 - minor adult hemoglobin. 2-3% of circulating hemoglobin. 2 alpha and 2 delta
chains.

Hemoglobin F - Fetal hemoglobin. 2 alpha and 2 gamma chains. Has a greater affinity
for and more regularly binds O2.

Anemia - a decrease in circulating red blood cells in the body, as reflected by a
reduction in hemoglobin, hematocrit, and/or RBCs. Less than 14 in men and less than
12 in women.

Normal RBC - 4.5-6

Normal Hemoglobin - >13 in men, >12 in women.

Normal HCT - 40-50in men; 35-45 in women. usually 3x the hemoglobin count.

Reticulocyte count - Low (<0.5%) High (>2%) if high, bone marrow is trying to
compensate for loss in hgb or red cells. problem exists outside of the bome marrow

MCV (mean corpuscular volume) - description of the volume of an RBC. NOT
DIAGNOSTIC

RDW (red cell distribution width) - 11.5-15 %; index of variation in RBC size and shape.
Indicates evolving macro/microcytic anemia.

MCH (mean corpuscular hemoglobin) - commonly used: 27 - 31 pg/ cell
Amount of hemoglobin per RBC

Microcytic anemia - Iron deficiency, thalassemia, inflammation. low MCV <80. Low
reticulocyte count. Underproduction.

, macrocytic anemia - Underproduction. B12 deficiency, Folic Acid Deficiency,
Antimetabolite drugs. MCV > 100; low reticulocyte count

Normocytic Anemia - MCV 80-100; low reticulocyte count; ex: dilutional/iatrogenic
secondary to phlebotomy.

Folate Deficiency Anemia - Macrocytic anemia; poor intake; low retic, elevate
MCV/MCH, thrombocytopenia ad neutropenia, elevated homocysteine; low RBC folate.
Eat orange fruits! Never treat folate deficiency without testing for B12 deficiency - can
worsen neurological symptoms specific to B12 deficiency

Vitamin B12 Deficiency - Macrocytic; malabsorption; occurs when B12 is not released
from food proteins due to impaired digestion; Elevated MCV/Macrocytic;

Pernicious Anemia - lack of mature erythrocytes caused by inability to absorb vitamin
B12 into the bloodstream

Destruction (Hemolytic anemia) - anemia with elevated reticulocytes; intrinsic and
extrinsic

intrinsic hemolytic anemia (hereditary) - - Abnormal hemoglobin
- Enzyme deficiencies (pyruvate kinase, G6PD)
- RBC membrane abnormalities: sickle cell anemia, thalassemia

extrinsic hemolytic anemia (acquired) - (+) Coomb's
DIC: abnormal coags (prolonged PT/PTT)
TTP
HUS
paroxysmal nocturnal hemoglobinuria: dark urine worse in AM
hypersplenism
Traumatic 2/2 prosthetic valve;
elevated LDH, low haptoglobin; elevated indirect bilirubin

Sickle Cell Anemia - Hemolytic/hereditary. Identified at birth - 6 months when HbSS
replaces fetal hemoglobin. hereditary disorder of abnormal hemoglobin producing
sickle-shaped erythrocytes and hemolysis

Thalassemia Major - Hemolytic/microcytic; defective production of either alpha or beta
globin. leads to damage of the RBC membrane, resulting in ineffective erythropoesis
and hemolysis

Alpha Thalassemia - 4 genes determine synthesis of alpha chain. Silent carrier = 1
abnormal allele; 2 abnormal alleles = alpha thalassemia minor; 3 abnormal alleles =
Alpha Thalassemia Intermedia: chronic anemia; 4 abnormal alleles not compatible with
life, Hydrops Fetalis

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller VasilyKichigin. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $13.48. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

81531 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$13.48
  • (0)
  Add to cart