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37 Cards in this Set
- Front
- Back
RBC count for women and men
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female 4-5
males 4.5-6 |
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HBG count for females and males
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female 12-16
male 13.5-18 |
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hct count
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female 38-47
male 40-54 |
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iron def anemia symptoms
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burning tongue, pallor, inflammation of lips, sore tongue, headache, parenthesis
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Thalassemia
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iron def r/t inadequate production of hgb
problem with globin synthesis |
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Thalassemia major
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blood transfusion to keep hgb at 10, even w/tx still risk for growth failure, hemochromatosis and cardiac failure
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cobalamin def anemia symptoms
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sore tongue, anorexia, n/v, abd pain, wkness, paresthesia feet/hands, reduced vibratory and position sensations, ataxia, muscle wkness, impaired thought processes
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cobalamin tx
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administer parentally daily for 2 weeks, then weeky until normal, then monthly for life
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folic acid deficiency
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symptoms same as cobalamin except neuro, dypepsia, beefy tongue
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aplastic anemia
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reduced RBC production, all marrow elements are decreased. tx w/bone marrow transplant and immunosuppressive therapy
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blood loss sx
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20-no sx at rest, tachycardia w/activity adn slight postural hypotension
30-normal supine bp and p @ rest, postural hypotension and tachycardic w/exercise 40-loss bp, cvp, and co below normal at rest, rapid thready pulse, cold clammy skin |
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sickle cell sx
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delayed growth and development, failure to thrive, pain
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complications of sickle cell
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foot/hand syndrome, ischemic heart leads to CHF, pulmonary hypertension, heart failure, retinal detachment leads to blindness, kidney injury from increased viscosity
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glucose 6 phosphate dehyrogenase deficiency
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reduction in glucose used by rbcs leading to damage of old rbcs and destruction by hemolysis
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hemochromatosis
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increased iron absorption resulting in increased tissue iron deposits
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hemachromatosis sx
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liver enlargement (cirrhosis), diabetes, skin pigmentation, cardiac changes, arthritis, testicular atrophy
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polycythemia
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production and presence of increased RBCs impairing blood circulation---viscosity
secondary is compensation |
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polycythemia sx
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htn, headache, vertigo, tinnitus, dizzines, vertigo, angina, CHF,
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polycythemia complications
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CVA, hemorrhage, pneumonia, heptomegay/cplenomegaly
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platelet count
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should be 150,000-400,000
<20,000 spontaneous bleeding |
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idiopathic, immune thrombocytopenia
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platelet covered with antibody that is identified as foreign in spleen and destroyed. chronic form is 20-40 yo
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thrombotic thrombocytopenia
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enhanced agglutination of platelets forming micro-thrombi in arterioles and capillaries---may be from use of estrogen or pregnancy. 20-50 yo
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Willebrand Disease
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hereditary bleeding disorder more in males, defective coagulation factor
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willebrand disease sx
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slow persistent bleeding, delayed bleeding from minor wounds, gi bleeding, gastritis, hematuria, subq hematoma, neuro sx, can lead to early death, primarily in children.
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willebrand disease tx
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administrate clotting factors, rest joint if bleeding in joint
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disseminated intravascular coagulation DIC
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abnormally initiated and accelerated clotting leading to decrease in clotting factors and platelets-bleeding with no cause
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neutropenia
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wbc norm 4000-11000 (50-70%), this is 1000-1500-suspicious for bone marrow suppression and reduced immunity
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neutropenia tx
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identify cause, identify organism causing infection, heatopoietic growth factors administered (neupogen); protective isolation, precautions, monitor for infection
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acute mylolytic leukemia
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60-70yo, fatigue, wkness, mouth sores, bleeding, fever, infection, sternal tenderness (CBC, hypercellular bone marrow w/myeloblasts)
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chronic mylolytic leukemia
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25-60yo, no early sx, fatigue, wkness, joint and bone pain, massive splenomegaly, increased sweating (CBC, philadelphia chromosome, low leukocyte count, low alkalin phosphatase)
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acute lymphocytic leukemia
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hepatosplenomegaly, lymphadenopathy, incrased ICP, headache, fever, pallor, bleeding mouth sores(CBC, hypercellular bone marrow w/lymphoblasts)
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chronic lymphocytic leukemia
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no usual sx, found on routine exam, chronic fatigue, anorexia, spleno, hepto,megaly, lymphadenopathy. (mild anemia, thrombocytopenia, increased peripheral and bone marrow lymphoblasts
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hodgkins lymphoma
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15% of all lymphomas, proliferation of abnormal giant multinucleated celss 15-30 and above 50 yos,
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hodgkins sx
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enlargement of cervical,axillary, or inguinal lymph nodes, nodes are painless and movable except when drink alcohol, wt loss, fatigue, wkness, fever, chills, tachy, night sweats
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non hodgkins
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variety of malignant neoplasms of the immune system affecting all ages
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non hodgkins sx
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painless lymph node enlargement, fever, night sweats, wt loss, depends on location
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multiple myeloma
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plasma cell myeloma, neoplastic plasma cells infiltrate bone marrow and destroy bone
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