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92 Cards in this Set

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