• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/146

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

146 Cards in this Set

  • Front
  • Back
Fluid part of the blood:
Plasma
What does plasma consist of:
Albumin
Globulin
Fibrinogen (clotting)
Primary site of blood formation:
Bone Marrow
Types of Blood Cells:
WBC
RBC
Platletes
Complex formation and maturation of blood cells:
Hematopoiesis
Normal amount of blood in the human body:
5-6 Liters
What does blood carry:(5)
O2
Nutrients
Hormones
Antibodies
Waste Products
What are the function of Erythrocytes:
Carry O2
Rid CO2
What % is hemaglobin;
95%
Immature form of RBCs
Reticulocytes
What are 2 examples of Reticulocytes:
Anemia
Sickle Cell
What is the term for production of Blood cells:i
Erythropoiesis
Hormone that is produced by the kidneys in response to low O2 levels:
(chronic kidney disease)
Erythropoietin
What can cause stem cells to differentiate:
Erythropoietin
What does production of blood require:(5)
Iron
B12
Folic Acid
B6
Protein
What is the lifespan of a RBC
120 days
What can happen when erythrocytes are less elastic:
CO2 can get trapped in blood vessels
Where are erythrocytes broken down:
Spleen
What cells break down erythrocytes :
Phagocytes
What is an enlarged spleen a sign of:
Abnormal Cell Depletion
Pigment portion of blood:
Bilirubin
Where is Bilirubin excreted:
in bile and through the urine
What can elevated levels of Bilirubin indicate:
Certain Diseases
What type of cells, if you do not have enough, will you bleed:
Thrombocytes
Proteins in the blood consist of :
Albumin
Globulin
Globulins made in the liver are:
Clotting factors (fribrinogen)
Transporters (carry materials to make Fe)
Where is albumin Produced:
Liver
Blood protein that is important for maintenance of fluid balance within the vascular system
(cannot pass through capillary walls which holds fluid inside vessels)
Albumin
The process of prevention of blood loss and stoppage of bleeding:
Homeostasis
Clotting Factors and Materials: (3)
Thrombin,
Prothrombin
Fibrin
Term used for a consideration of the bone's marrows ability to respond is decreased, may result in leukopenia or anemia
Gerontologic Considerations
A Hematologic Disorder where the cells are produced defective:
Qualitative
A Hematologic Disorder where the cell numbers are either increased or decreased:
Quantitative
What is the best way to find Hematologic Disorders:
Lab Work
(few symptoms so lab work must be thoroughly analyzed)
What does Differential Hematologic Study Measure:
Shows numbers of specific cells
A smear that shows the appearance of the cells: (Shapes, sizes, and appearances)
Peripheral Blood Smear
What blood test shows an index rate of production of immature cells:
Reticulocytes
Blood test that shows the % of red cells as compared to the blood:
Hematocrit
If a person is dehydrated, they're Hematocrit % will
Increase
Blood test that shows The amount of O2 content in the blood:
Hemaglobin
An elevated WBC count is an indicator of:
Infection
What does Mean Corpuscular Volume mean: (MCV)
Volume or Size of Red Cells
What does Mean Corpuscular Hemoglobin Concentration (MCHC) mean:
Color of RBC; if not enough Fe, color will decrease
2 tests that can assess the quality and quantity of the marrow and how cells are being formed, can also see infections or tumors:
Biopsy and
Bone Marrow Aspiration
Where can Biopsy and Bone Marrow Aspiration be performed:
Iliac Crest (hip bone)
What are the steps of Biopsy and Bone Marrow Aspiration: (3)
Local Anestheic
Nurse Positions Pt + Administers Med.
Spot needs sterile dressing + pressure afterwards may ache for 2 days
Term used when hemoglobin concentration is lower than normal, or fewer erythrocytes, decreased amount of O2 delivered to tissue:
Anemia
Types of Anemia: (3)
Hypoproliferative
Hemolytic
Loss
Anemia that not enough blood is being produced, either not enough bone marrow, or not enough nutrients:
Hypoproliferative
What Causes hyproproliferative Anemia: (3)
Marrow Damage
Lack of factors for production
Chronic Illness
3 Types of Hypoproliferative Anemia:
Fe Deficient
Megaloblastic
Decreased Erythropoietin
Type of of Hypoproliferative Anemia that has a decrease in Iron
Fe Deficient
Type of of Hypoproliferative Anemia that is Folate or B12 deficient and causes large RBCs
Megaloblastic
Type of of Hypoproliferative Anemia that has a lighter color and may be smaller
Decreased Erythopoietin
Anemia that is classified as a destruction of cells, can be inherited:
Hemolytic Anemia
4 Types of Hemolytic Anemia
Sickle Cell
Thalassemia
Hyperspleenism
Liver Disease, Infection, Autoimmune, Drug Induced, Mechanical Heart Valve
Type of Hemolytic Anemia that is genetic and hemoglobin defective, and has a sickle shape
Sickle Cell Anemia
What is a good way to find out if a pt has Anemia:
Labs
Which labs will show Anemia
H&H
Reticulocyte Count (immature rbc)
MCV
RDW
MCHC
Iron Studies
B12
Folate
Erythropoietin
CBC
What Are you Looking for with Anemia
Weakness, Fatigue
Appearance
Hx
Nutritional Status
Cardiac Status
Respiratory Status
GI System
Menstration
Neurological Assessment
What can happen to circulatory system with a pt with anemia:
Heart pumps more due to less O2
Decreased Viscosity, more blood back to heart can cause murmur and cardiac failure
What can happen to children with anemia:
Growth Retardation
Delayed Sexual Maturation
How does dairy and antacid effect hyproliferative iron deficiency anemia:
Decreases Iron Absorption
What are the primary symptoms of hyproliferative iron deficiency:
Fatigue Palor Malaise
What can happen if hyproliferative iron deficiency is prolonged:
Smooth sore tongue
Brittle Ridges Nails
Angular Cheilosis (cracked lip edges)
Pica (craving abnormal stuff)
Diagnostics of hyproliferative iron deficiency: Hemoglobin
low
Diagnostics of hyproliferative iron deficiency:Ferritin (iron stores)
low
Diagnostics of hyproliferative iron deficiency:MCV
(Mean Corpuscular Volume)
low (size of RBC become smaller)
Diagnostics of hyproliferative iron deficiency:MCHC
(Mean Corpuscular Hemaglobin Concentration
Low (refelcts color)
Diagnostics of hyproliferative iron deficiency: TIBC
high
(represents the protein that carries the iron, also referred as transferrin
Which vitamin helps with iron absorption
Vit C
How long will it take for HGB to increase:
Few Weeks
Foods High In Iron:
Organ Meat (beef , liver)
Beans
Leafy Greens
Raisins
Vit C to help absorption (citrus, juice, strawberries)
hypoproliferative Anemia which is b12 and folic acid deficiency:
Megaloblastic
How do you find out if someone has hypoproliferative megaloblastic anemia:
High MCV levels
(Mean Corpuscular Volume)
(RBC abnormally large
wbc and platelets also abnormal
how does bone marrow show signs of hypoproliferative megaloblastic anemia:
Shows increased amounts of abnormal cells
term used for decrease in RBC, WBC, and Platelets
Pancytopenia
The fastest depleating Hypoproliferative megaloblastic anemia:
Folic
What foods can be eating for Hypoproliferative megaloblastic folic anemia:
Green vegetables and liver
what can increase folic acid requirements
Alcohol
A type of B12 deficiency anemia where the body lacks intrinsic factor
Pernicious Anemia
Intrinsic Factor is secreted by:
Gastic Cells
B12 is absorbed in the
Ileum
Hypoproliferative Anemia that may or may not show symptoms:
B12
what kind of test would you give someone who you expect to have Pernicious Anemia
Schilling Test
Hypoproliferative Anemia where WBC attack bone marrow and is replaced with fat:
Aplastic Anemia
how would you find out pt has Aplastic Anemia
Bone Marrow Aspirate will show aplastic marrow (no cells) replaced with fat.
Low WBC RBC Platlets
How can aplastic anemia be treated:
Marrow Transplant especially in children
term used for a binding protein for hemoglobin
Haptoglobin
Term used for sickle cell anemia to where an area is clogged
Sickle Cell Crisis
Why does cold aggravate sickle cell anemia
Vasoconstriction
A new born sickle cell screening which is mandatory:
Hemoglobin Electrophoresis
chemo drug used to decrease permanent formation of sickled cells
Hydroxyurea
Antistickling properties and enhances nitric oxide (vasodialator)
Arginine
How will Sickle cell anemia increase risk for ulcers?
circulation is decreased
term used for decreased amount of hemoglobin
hypochromia
what type of anemia is hypochromia really noticed in
Thalassemia
Anemia that has abnormally high levels of RBCs
Polycythemia
What are pts with polycythemia at risk for
Heart attack, Bleeding Stroke
What are S/S of polycythemia (inc blood volume)
Dizzyness, fatigue, blurred vision
What are S/S of polycythemia (inc viscosity)
Angina(chest pain)
Claudiction (cramp in leg)
what can the RBC counts be in polycythemia:
>60%
blood disordered where there is a decreaed number of leukocytes (WBCs)
Leukopenia
blood disordered where there is a decreaed number of neutrophils
Neutropenia
What do you look for when they have neutropenia
Infection
CBC w different changes
Look for Temp Changes >= 100.5*** call md****
What intervention would you give to neutropenia:
Antibiotics
If fever spikes, call md could be a new infection get new antibiotic
What are some neutropenic precautions:
No Fresh: fruits, flowers, vegetables.
Private Room
No invasive prodecudres (rectal)
Pulmonary Hygiene (pneumonia)
a stem cell disorder in the bone marrow where increased platelet production:
Thrombocythemia
a stem cell disorder in the bone marrow where decreased platelet production:
Thrombocytopenia
what platelet level can bleeding occur
below 50,000
what platelet level can spontaneous bleeding occur (GI, Brain)
<5000
S/S of Thrombocytopenia
Bleeding Burising
Headache- Brain Bleeding
Bleeding from Mucosa
Interventions for Thrombocytopenia
Goal to inc Platlet Count (30,000-50,000)
Temp Immunosupressant therapy (bring to macrophages before destroying platlets)
a group of bleeding disorders in which it takes a long time for the blood to clot.
Hemophilia
Treatments for Hemophilia
Factor 8 + 9 available for infusion
Hemophilia that is a genetic deficit in factor 8
Hemophilia A
Hemophilia A with a deficit in factor 9
Hemophilia B
What do you do during a bleeding episode with Hemophilia
RICE
Rest Ice Compression Elevation
What are Acquired Coagulation Disorders
Liver Disease
Vit K Deficient
Acquired Coagulation Disorders that is a hepatic dysfunction resulting in Deminisehed amounts of blood coagulant factors
Liver Disease
Acquired Coagulation Disorders common in malnourishment sometimes from antibiotics will be reflected on PT levels
Vit K Deficiency
how do you treat Acquired Coagulation Disorders
Anticoagulant Therapy
Heparin and Coumadin
Vit K
What INR number is too thin of blood
>3.5
Why is the spleen important to clotting?
Where RBC are destroyed and Fe recycling
Holds Platlets
Helps fight infections
Therapy for blood disorders where you can filter out what is not functioning correctly
Apheresis
Therapy where you remove excess blood usualy with Polycythemia:
Phlebotomy
What blood type do you only transfuse only in an emergency
Type O
Antigen present on 85% of population blood
Rh Antigen +
(no antigen -)
What are the majority of reations due to in transfusions:
WBCs (leukeocytes)
What can do you to reduce the reactions in blood transfusions:
Filtration to remove leukocytes
What is the time window for transfusions:
2-4 Hours
(will develop bacteria)
3 types of reactions in transfusions:
Acute Hemolytic
Febrile Nonhemolytic Reaction
Allergic Reation (plasma proteins)
most dangerous reaction to blood transfusion:
Acute Hemolytic
(blood cells are destroyed)
transfusion complication where antibodies attack donor leukocytes:
Febrile Nonhemolytic Reations (2 hr after infusion)
transfusion complication where there is a sensitivity to plasma proteins:
Allergic Reaction
2 other transfusion complications:
Circulatory Overload
Bacterial Contamination
transfusion complication where blood is transfused too fast:
Circulatory Overload
transfusion complication where blood products are contaminated:
Bacterial Contamination
*** Steps in Managing Transfusion
(7)
Stop Blood IV Saline
Assess
Call MD
Notify Bank
Send Blood to Bank
Samples
Document
Hemoglobin Levels Male
13-18
Hemoglobin Levels Female
12-16
HTC levels Male
37-49
HTC levels Female
36-46
WBC Levels
4.5-11k
Platlet Levels
150-300k
Coumadin (clotting Time
PT
PTT
INR