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92 Cards in this Set
- Front
- Back
BLOOD
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THICK RED FLUID CONTAINING RBC'S, WBC'S & PLATELETS IN A FLUID CALLED PLASMA
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NORMAL PH
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7.35 - 7.45
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FUNCTIONS OF BLOOD
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TRANSPORT O2, REGULATE PH, PROTECT AGAINST INFECTION AND BLOOD LOSS
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ERYTHROCYTES
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RED BLOOD CELLS (RBC'S)
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HEMOGLOBIN
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COMPOUND IN RBC THAT CARRIES O2 & CO2
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NORMAL Hgb IN MALES & FEMALES
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14-18 g/dl MALES, 12-16g/dl IN FEMALES
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RBC LIFESPAN
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120 DAYS
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ARE RBC'S NUCLEATED?
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NO
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WHERE ARE RBC'S PRODUCED
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BONE MARROW
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PRODUCTION IS STIMUTATED BY _____ PRODUCED IN THE ________
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ERYTHROPOIETIN / KIDNEYS
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ERYTHROPOIETIN MEASURES
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LOW OXYGEN LEVELS IN THE BLOOD
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HEMATOCRIT
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MEASURE OF PACKED CELL VOLUME OF RBC'S
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HEMATOCRIT SHOULD BE ______ THE HEMOGLOBIN
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3 TIMES
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NORMAL HEMATOCRIT IN MALES/FEMALES
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42-52% IN MALES 37-47% IN FEMALES
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LEUKOCYTES
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WHITE BLOOD CELLS
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# OF WBC'S
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5,000 - 10,000
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LIFESPAN OF WBC'S
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FEW DAYS TO SEVERAL YEARS
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ARE WBC'S NEUCLEATED?
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YES
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WBC'S PRODUCED?
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BONE MARROW
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DIFFERENTIAL
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DIFFERENT KINDS OF WBC'S ARE REPORTED AS PERCENTAGES OF THE TOTAL
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2 CATAGORIES OF WBC'S
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GRANULOCYTES AND AGRANULOCYTES
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3 GRANULOCYTES
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NEUTROPHILS, EOSINOPHILS, BASOPHILS
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2 AGRANULOCYTES
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LYMPHOCYTES, MONOCYTES
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IF WBC'S < 3000
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MONITOR FOR & PREVENT INFECTION (FEVER CLOUDY URINE)
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GRANULOCYTES
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FROM RED BONE MARROW, CONTAIN GRANULES IN THEIR CYTOPLASM
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NEUTROPHILS
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PHAGOCYTOSIS, LYSOZYME
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POLYMORPHONUCLEAR LEUKOCYTES
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"POLYS" OR BANDS RELEASED INTO THE BLOOD STREAM WHEN NEUTROPHILS ARE DEPLETED
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EOSINOPHILS
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ALLERGIC REACTION & FIGHT AGAINST CERTAIN PARASITIC WORMS
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BASOPHILS
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NONSPECIFIC RESPONSE TO INFLAMMATION, RELEASE HISTAMINE CAUSING VASODILATION
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AGRANULOCYTE - MONOCYTE
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FUNTION SIMILAR TO NEUTROPHILS THROUGH PHAGOCYTOSIS
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AGRANULOCYTE - LYMPHOCYTES
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ANTIBODY FORMATION B CELLS AND T CELLS
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B-CELLS
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BIND TO SPECIFIC ANTIGEN
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T-CELLS
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MUTIPLY AND DIVIDE IN RESPONSE TO ANTIGEN
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THROMBOCYTES
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PLATELETS
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ARE PLATELES NUCLEATED OR NON-NUCLEATED
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NON NUCLEATED
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PLATELETS PRODUCED
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RED BONE MARROW (SMALLEST CELLS)
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PLATELETS LIFE SPAN
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5-9 DAYS
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# OF PLATELETS
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150,000 - 400,000
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PLATELET FUNCTION
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HEMOSTASIS AND CLOT FORMATION
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DESCIBE HEMOSTASIS
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PREVENTION OF BLOOD LOSS, VESSEL SPAM, PLATELET PLUG FORMATION, CLOT FORMATION
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(PT)
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PROTHOMBIN TIME 11 - 12.5 SECONDS (RAPIDITY OF BLOOD CLOTTING)
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(INR)
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INTERNATIONAL NORMALIZED RATION 0.7 - 1.8
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(PTT)
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PARTIAL THROMBOPLASTIN TIME 60 - 70 SECONDS FIBRIN CLOT FORMATION
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BLEEDING TIME
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1 - 9MINUTES (SMALL STAB WOUND)
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CLOTTING TIME
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3 - 9MINUTES AMT OF TIME FOR BLOOD TO CLOT IN A TUBE
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4 BLOOD TYPES
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A, B, AB, & O
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TYPE O
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UNIVERSAL DONOR
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TYPE AB
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UNIVERSAL RECIPIENT
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Rh FACTOR
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85% (+) IF Rh(-) PERSON RECIEVES Rh (+) THE PERSON DEVELOPS ANTIBODIES
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RhoGAM
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SHOT GIVEN TO (-)MOTHER WITH (+)FETUS TO AVOID HEMOLYSIS
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LYMPHATIC SYSTEM
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VESSELS, FLUID, TISSUE, NODES, TONSILS, SPLEEN, THYMUS
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FUNCTIONS OF LYMPH SYSTEM
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FLUID BALANCE, PRODUCTION OF LYMPHOCYTES, APSORBTION OF LIPIDS FROM INTESTINE TO BLOOD
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LYMPH NODES
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FILTER IMPURITIES & PRODUCE LYMPHOCYTES
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TONSILS
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LYMPHOID TISSUE IN THE OOROPHARANX
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SPLEEN
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LUQ STORES 500ML OF BLOOD
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THYMUS
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UPPER THORAX DEVELOPS T LYMPHOCYTES
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CBC
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COMPLETE BLOOD COUNT INCLUDES RBC, WBC, HCT, HGB, ERYTHROCYTE INDICES & DIFFERENTIAL
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MCV
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SIZE OF CELL
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MCH
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AMOUNT OF HGB AND COLOR OF CELL
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MCHC
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CONCENTRATION OF HGB
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RDW
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RED CELL DISTRIBUTION
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PERIPHERAL BLOOD SMEAR
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EXAMS SIZE, SHAPE & STRUCTURE OF RBC & PLATELETS
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SERUM MEGOBLASTIC ANEMIA PROFILE
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DX PERNICIOUS ANEMIA, REPLACES SCHILLING TEST, MEASURES VIT B12
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SCHILLING TEST
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MEASURES ABSORPTION OF RADIO ACTIVE VIT B12 AS IS EXCRETED IN URINE.
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WHAT CAUSES B12 TO NOT EXCRETE
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NO INSTRINSIC FACTOR (GASTRIC BYPASS)
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GASTRIC ANALYSIS
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USEFUL IN DETERMINING PERNICIOUS ANEMIA, GASTRIC SECRETIONS LOW, PH ELEVATED
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LYMPHANGIOGRAPHY
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DETECTS METASTATIC CANCER INVOLVEMENT OF LYMPH NODES ASSESS FOR ALLERGIES TO IODINE & SHELL FISH
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BONE MARROW ASPIRATION
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ILLIAC CREST, USED FOR PROFOUND ANEMIA, NEUTROPENIA, ACUTE LEUKEMIA, & THROMBOCYTOPENIA
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NAME 4 DIAGNOSTIC BLOOD TESTS
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GASTRIC ANALYSIS, LYMPHANGIOGRAPHY, CT OR MRI & BONE MARROW ASPIRATION
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ANEMIA
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LOW RBC'S, LOW Hgb, LOW Hct, & RBC DESTRUCTION
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4 DIVISIONS OF ANEMIA
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HEMORRHAGE, BONE MARROW DEPRESSION, HEMOLYSIS, IRON DEFICIENCY
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APLASTIC ANEMIA
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FAILURE OF RED BONE MARROW TO PRODUCE RBC'S, CAN BE CONGENITAL OR CAUSED BY VIRUS
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PANCYTOPENIA
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DECREASED RBC'S WBC'S AND PLATELETS
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(IDA) IRON DEFICIENCY ANEMIA
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RBC'S CONTAIN DECREASED AMOUNTS OF Hgb
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SICKEL CELL ANEMIA
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ABNORMAL CRESENT SHAPE RBC CONTAINING DEFECTIVE HEMOGLOBIN MOLECULE
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POLYCYTHEMIA
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AKA ERYTHROCYTOSIS ABNORMAL INCREASE IN RBC'S
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AGRANULOCYTOSIS
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SEVERE REDUCTION IN GRANULOCYTOSIS, B.E.N.
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LEUKOPENIA
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EXTREMLY LOW WBC'S
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LEUKEMIA
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EXCESS OF DEFECTIVE IMMATURE WBC'S IN BONE MARROW, LYMPH NODEAND BLOOD
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HEPATOMAGALY
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ENLARGED LIVER
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SPLEENOMEGALY
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ENLARGED SPLEEN
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COAGUALTION
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ANY MANIFESTATION THAT INTERFERES WITH THE CLOTTING MECHANISMS
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PETECHIAE
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BLEEDING UNDER THE SKIN
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THROMBOCYTOPENIA
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PLATELET DISORDER PLATES UNDER 100,000, SERIOUS RISK IF UNDER 20,000, UNDER 5,000 HEMMORAGE
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HEMOPHILLIA
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CLOTTING DISORDER
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DIC
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DISEMMINATED INTRAVASCULAR COAGULATION
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DX OF DIC
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PROLONGED CLOTTING TIME FACTOR V AND FACTOR VIII BLEEDING & CLOTTING OCCUR SIMULTANEOUSLY
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MULTIPLE MYELOMA
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PLASMA CELL DISORDER
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LYMPHANGITIS
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INFLAMMATION OF ONE OR MORE LYMPH VESSELS FROM INFECTION OF AN EXTREMITY
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LYMPHEDEMA
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ACCUMULATION OF LYMPH IN SOFT TISSUE
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HODGKINS LYMPHOMA
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T CELL DISORDER, LYMPHOID TISSUE ENLARGEMENT EPSTEIN BARR VIRUS & REED STERNBERG CELLS
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NON HODGKINS LYMPHOMA
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LYMPHOID TISSUE ENLARGEMENT, VIRAL SOURCE & NO REED STERNBERG CELLS
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