100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached 4.6 TrustPilot
logo-home
Summary

Summary Patho Pharm Exam 1

Rating
-
Sold
-
Pages
31
Uploaded on
06-05-2025
Written in
2024/2025

This study guide provides a comprehensive and organized overview of anemia and gastrointestinal (GI) disorders, serving as a valuable resource for nursing students and healthcare professionals. It covers the key features, causes, and clinical manifestations of various anemia conditions, with a focus on both acute and long-term implications. The guide also details commonly used medications, including their therapeutic roles and potential side effects. Emphasis is placed on essential nursing considerations such as patient assessment, safety precautions, and effective communication strategies to support patient care and recovery.

Show more Read less











Whoops! We can’t load your doc right now. Try again or contact support.

Document information

Uploaded on
May 6, 2025
Number of pages
31
Written in
2024/2025
Type
Summary

Subjects

Content preview

ANEMIAS
Red Blood cells:
Structure
- 1 heme = 1 iron
- 1 hemoglobin = 4 iron
- 4 heme = 1 globin
- No nuclei, mitochondria or ribosomes
What do they do?
- Transport O2 to tissues, bring CO2 back
- Male: 4.5 – 6.3 million
- Female: 4.2 – 5.5 million
Lifespan
- 120 days (3 months)
- Reticulocyte à erythrocyte
- 24-36hrs à 36hrs – 120 days
Hemoglobin
- Red pigment that gives whole blood its color
- Male: 14-18 g/dL
- Female: 12-16 g/dL
- Oxyhemoglobin/deoxyhemoglobin
Hematocrit
- Percentage of RBCs in centrifuged whole blood
- Male: 40-54%
- Female: 37-47%
- (1:3 à hemoglobin: hematocrit)

,Anemia:
Causes
- Reduction in # of erythrocytes
- Impaired production (BMS, kidney problems)
- Blood loss (MVA, GSW, birth)
- Increase erythrocyte production (mismatched blood, end stage renal disease,
hemodialysis = destroyed RBCs
Definition
- Decreased erythrocytes
- Decreased hemoglobin
- Decreased hematocrit
Size Issues
- Microcytic hypochromic = small RBCs and decreased hematocrit
- Macrocytic = large RBCs (B12 and folic acid deficiency)
- Normocytic normochromic = normal size and hemoglobin… problem with
shape (sickle cell)
Iron Deficiency Anemia:
What is it?
- Microcytic hypochromic
Etiology
- Inadequate dietary intake, decrease absorption, increased demand
(pregnancy), increase loss)
Clinical Manifestations
- Pallor
- Glossitis
- Cheilitis
Evaluation
- Measurement of ferritin levels (Iron stores)
Treatment
- Identify source, iron replacement (PO, IV, IM), sodium gluconate

, - Usually continues 6-12 months AFTER bleeding stop s but may continue as
long as 24 months
- Diet!!!
Drug Therapy
à Oral iron (Ferrous sulfate) - Best absorbed on empty stomach (2 hrs before
meals, NO milk, drink with orange juice)
à Iron adverse effects - Constipation, N/V, cramps, black/ tarry stools
(expected), liquid iron can stain teeth! (Drink with straw)
à Parental Iron - Test dose 1st time then give if no reaction, may cause
orthostatic hypotension
1.) Ferric gluconate (safe for renal)
2.) Iron sucrose (venefor): hypotension, give large doses over 2.5-3.5
hours, sit upright for 15-30 min after oral iron to avoid esophageal
corrosion
Megaloblastic Anemia :
What is it?
- Large RBCs
- Results from deficiency on Vitamin B 12 (Cobalamin) and Folic acid
Pernicious Anemia (Vitamin B12 deficiency)***
- Most common megaloblastic anemia
- Lacks intrinsic factor (protein secreted by parietal cells in gastric mucosa (in
stomach)
- CANNOT absorb B12 without intrinsic factor
- Can give B12 shot to bypass the stomach
Clinical manifestations
- Weakness / fatigue
- Paresthesia’s of feet and fingers, difficulty walking (specific to B12
deficiency)
- NEUROLOGIC SYMPTOMS FROM NERVE DEMYELINATION B/C
VITAMIN B12 IS NEEDED FOR MYELINATION OF NERVES!!!
Diagnostics
- Blood tests
- Bone marrow aspiration, gastric biopsy (intrinsic factor)
Treatment

, - Weekly/monthly injections or high oral doses of vitamin B12 are
administered
- Teach to eat red meats, liver and eggs
Folic Acid Deficiency ***
- Megaloblastic anemia
Causes
- Dietary deficiencies (leafy greens, fish, veggies)
- Malabsorption syndromes (chrons, ulcerative colitis)
- Alcohol abuse
Treatment
• Folic acid with food
• Dosages decrease serum phenytoin levels by speeding up metabolism
of this drug (need to increase dose of phenytoin)
Hematopoietic Drugs
Contraindications
- Allergy
- >10% myeloid blasts
ADEs
- Fever
- Muscle aches
- Bone pain
- Flushing
- Interactions
• Antineoplastics that cause BMS
Treatment
à Filgrastim (Neupogen) – increases WBC count, given for non-myeloid
cancers when drugs will cause BMS, injection, discontinues if neutrophil
count is >10,000
à Sargramostim (Leukine) – given after bone marrow transplant, injection
à Oprelvekin (Neumega) – stimulates platelets in severe chemotherapy to
avoid platelet transfusion
$31.99
Get access to the full document:

100% satisfaction guarantee
Immediately available after payment
Both online and in PDF
No strings attached

Get to know the seller
Seller avatar
nwessie

Also available in package deal

Thumbnail
Package deal
Patho Pharm II Study Guides
-
5 2025
$ 173.95 More info

Get to know the seller

Seller avatar
nwessie Monroe Community College (Rochester)
View profile
Follow You need to be logged in order to follow users or courses
Sold
3
Member since
2 year
Number of followers
0
Documents
43
Last sold
1 year ago

0.0

0 reviews

5
0
4
0
3
0
2
0
1
0

Recently viewed by you

Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Frequently asked questions