-
The production of blood
Hematopoiesis
-
Blood performs 3 makor functions
Transportation, regulation, and protection
-
composed primarily of water, contains proteins, electrolytes, gases, nutrients and waste
Plasma
-
Three types of Blood cells
- Erythrocytes (RBC)
- Leukocytes (WBC)
- Thrombocytes (Platelets)
-
Primary function is phagocytosis(a process by which WBCs engulf any unwanted organisms and kill them)
Granulocytosis
-
Most common type of granulocytes
Neutrophil
-
Primary function is to initiate the clotting process by producing a platelet plug
Thrombocytes
-
Blood clotting process
Hemostasis
-
A large component of the hematologic system
Classified into 4 components: hematopoietic, filtration, immunologic and storage
Spleen
-
Conists of Lymph fluid, lymphatic capillaries, ducts, and lymph nodes
Carries fluid from the interstitial space to the blood
Lymph system
-
Involves several lab tests, assessing the three major blood cells formed in the bone marrow
CBC
-
measures the sedementation or settling of RBCs and is used to measure many diseases, especially inflammatory conditions
ESR (Sed rate)
-
Serum Iron
Total iron-binding capacity (TIBC)
serum ferritin
transferrin saturation
Tests to evaluate iron metabolism
-
CT
MRI
Radiologic studies for the hemotologic system, kidneys, spleen, liver and lymph nodes
-
A deficiency in the # and or volume of RBCs, and the quantity of hemoglobin
Anemia
-
used to determine the severity of anemia
Hemoglobin
-
Ultimate goal of anemia therapy
Correct the cause
-
may include blood transfusion, drug therapy, volume replacement, O2 therapy, diet/lifestyle changes,
Interventions for correcting anemia
-
may develop from inadequate dietary intake, malabsorption, blood loss, or hemolysis
Iron- deficiency anemia
-
A group of diseases that has an autosomal-recessive genetic basis that involves inadequate production of normal hemoglobin
Thalassemia
-
-requires no treatment bc the body addapts (jaundice and enlarged spleen)
-managed with blood trasfusions(life threatning, sympts develop in childhood, pale, enlarged spleen, hepatomegly, bone marrow hyperplasia)
- -Thalassemia minor
- -Thalassemia major
-
A group of disorders caused by impaired DNA sythesis and characterized by the presence of large RBCs
Megaloblastic anemias
-
common form of Megaloblastic(large RBCs) Anemia
results in poor absorption through the GI tract
symptoms; sore tongue, anorexia, N/V, abd pain
parenteral or intranasal administration is the Tx of choice
Cobalamin (Vit B12) deficiency Anemia
-
another common form of Megaloblastic anemia
required for DNA synthesis leading to RBC formation and maturation
treated by replacement therapy
Folic Acid deficiency anemia
-
-a disease in which the patient has a decrease of all blood cell types and hypocellular bone marrow
-Tx includes finding and removing the causitive agent and providing support ; reverse isolation
Aplastic anemia
-
-A group of inherited, autosomal recessive disorders characterized by abnormally shaped (sickle shaped) RBCs; incurable and often fatal
-episodes are most commonly triggered by low O2 tension in the blood
-S/S; anemia, jaundice, pain, fever, swelling, HTN, N/V
-Tx includes alleviating the symptoms and minimizing end target organ damage
-
Sickle cell disease
-
Low MCV (82-96)
Microcytic size
-
Low MCHC (31%-36%)
hypochromic (pale) color of cell
-
High MCV (82-96)
Macrocytic (large and weak)
-
-non differentiated immature blood cell found in bone marrow
-all three types of blood cells develop from this
-responds to increased demand for the dif types of cells
Stem Cells
-
-Transports O2, nutrients, hormones, and waste products
-Assists in regulation of fluid, electrolyte and acid/base balance
-Composed of plasma and blood cells
Blood
-
-Arrives first to the site of infection
-Primary function is phagocytosis
Neutrophils
-
-Found in large numbers in the GI tract and lungs
-Contains histamine
-Defends against parasites
Eosinophils
-
-Ignites immune response
-Limited role in phagocytosis
-Contains heparin, serotonin, and histamine
Basophils
-
Monocytes that have migrated into tissue
-Called Kupffer cells
-Called ostoclasts
-Called Alveolar macrophages
- Macrophages
- -in Liver
- -in bone
- -in lungs
-
-stored as ferritin and hemosiderin in bone marrow,spleen, liver and macrophages
-recycled after macrophages ingest and destroy old,damaged RBCs
Iron
-
-Initate clots
-Life span of 5-7 days
-Participate in clot shrinkage and reaction
Thrombocyte
-
1. Vascular response
2. Platelet plug formation
3. Development of fibrin clot of platelet plug by plasma clotting factors
4. Lysis of clot
4 components of normal hemostasis
-
-Stores excess Iron
-produces hepcidin
Liver
-
-Able to produce RBCs during fetal development
-Filters RBCs
-Contains rich supply of Lymphocytes, monocytes, and immunoglobin
-Stores RBCs and 30% of mass platelets
Spleen
-
Hgb, Hct, Differential, Platelet ct, ESR, Blood typing, RH factor, Bilirubin, Serum iron, TIBC, Ferritin
Lab tests of the hematological system
-
CT,MRI,Bone scan, Biopsies of bone marrow and lymph nodes, gene analysis
Diagnostic studies of the hematological system
-
-May exsist w/o symptoms
-Possible symptoms
- Palpations/dyspnea/diaphoresis
Mild anemia (10-12)
-
-symptoms of increased cardio symptoms at rest or on exertion
Moderate anemia (6-10)
-
symptoms of multiple body systems; skin(pallor, jaundice),eyes(pale),mouth(pale,dry),cardio(palpitations)
Severe anemia (<6)
-
-common symptoms of anemia; pallor being the most common
-Swollen tongue is the second most common
Iron Deficiency
-
-Heartburn, constipation and diarrhea
-Black stools
side effects of Iron supplementation
-
severe prolonged bleeding due to defective clotting
Hemophilia
-
-A reduction in the # of neutrophils
-clients normal flora most common source of infection
-S/S; diarrhea, sore throat, lesions, vaginal itching, SOB
-pt usually in reverse isolation
Neutropenia
|
|