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NUR171-Hemato-2

Hematology - Ch 30 - File 2

QuestionAnswer
Smoking __ platelet reactivity increases – also hematocrit and blood viscosity
Hematemesis bright red, brown, or black vomitus
__ problems should be anticipated in cases of known alcohol abuse bleeding
Iron and folic acid deficiencies are associated with inadequate intake of liver, meat, eggs, whole grain, breads/cereals, potatoes, citrus fruits, legumes
Folic acid deficiencies may be offset by a diet including foods high in iron
A nontender swollen lymph node may be a sign of Hodgkin’s lymphoma or non-Hodgkin’s lymphoma
Cardiovascular disorders such as valvular disease or hypertension may predispose pts to hemolysis
Meds used to treat cardio disease can cause abnormalities in hematopoietic cell production or coagulation
Pulmonary disorders that lead to hypoxemia may cause chronic stim of erythropoietin and result in polycythemia
Arthralgia joint pain
Aching bones may result from pressure of expanding bone marrow with diseases Diuretics interfere with
H2 blocking agents affect hematologic function how? interfere with platelet production
Hemarthrosis blood in joint – with bleeding disorders – painful
Agent Orange is associated with? leukemia and lymphoma
Epistaxis may occur with low platelet counts, especially if they strain
Smooth tongue sign of pernicious anemia, iron-deficiency anemia
Purpura can be sign of decreased platelets or clotting factors
Flusing of the palms of the hands or soles of the feet may indicate anemia
Paresthesias of feet and hands; ataxia could be sign of Cobalamin (B12) deficiency or folate deficiency.
Superficial lymph nodes can be evaluated by light palpation
Deep lymph nodes should be evaluated by radiologic exam – cannot be palpated
Lymph nodes should be assess for? symmetry, size, fixation, tenderness, and texture
Tender nodes are usually sign of inflammation, while hard/fixed nodes suggest malignancy
Erythrocytosis often produces sm. Vessel occlusions causing a purple, mottled appearance of face, nose, fingers or toes.
Clubbing of fingers send with chronic anemia as in pt with sickle cell disease.
Telangiectasia dilation of a group of small blood vessels – like a spider nevus
What skin signs can indicate bleeding disorders? petechiae, ecchymoses, spider nevus
Pancytopenia marked decreases in number of ALL blood cells – RBCs, WBCs, and platelets
Hb value is reduced in cases of? anemia, hemorrhage, hemodilution (FVE).
Hb value increases in polycthemia, hemoconcentration (dehydration FVD).
Hct values reduced in anemia, hemorrhage, hemodilution (FVE).
Hct values increased in polycthemia, hemoconcentration (dehydration FVD).
Hct is usually __ times that of Hb. 3
Hb measurement of gas-carrying capacity of RBC – 12-16 woman, 13.5-18 man
Hct measure of packed cell volume of RBCs
Red cell indices Indicators of RBC volume, color, hemoglobin saturation – can provide insight into cause of anemia – marcro vs microcytosis
RBC morphologies Dohl bodies, Heinz bodies, anisocytes, schistocytes, and sickled cells
Dohl bodies usually associated with burns, systemic infections, cytotoxic agents, and neoplastic diseases – leukocyte includsion in neutrophils
Heinz bodies Granules in RBCs – seen in thalassemias and after splenectomy
Anisocytes various sized RBCs
Schistocytes Fragmented RBC – hemolytic anemias, severe burns
WBC counts over 11,000 indicates infection, inflammation, tissue injury or death, and malignancies (leukemia, lymphoma)
WBC less than 4000 is associated with leukopenia – bone marrow depression, severe or chronic illness, leukemia
WBC differential is significant because WBC count main be normal, despite marked change in 1 type of leukocyte
Neutropenia absolute neutrophils count less than 1000 cells
Severe neutropenia less than 500 cells
Thrombocytopenia platelet count below 100,000
Spontaneous bleeding can occur once platelet count falls below 20,000
Thrombocytosis excessive platelets – inflammation and some malignant disorders
Complications from a splenectomy Increase in RBCs, WBCs, platelets, immunologic deficiencies – infection
Medications that can cause petechiae heparin, thiazide diuretics, digoxin, ibuprofen, antibiotics, H2 antagonists, quinine
Nursing care for patient w/post bone marrow aspiration sterile pressure dressing – lie on site for 30-60 mins to maintain pressure
Assessment of lymph nodes on patient lt palpation for superficial, radiologic for deep – assessed symmetrically for location, fixation, tenderness (inflame), and texture
What the term shift to the left means increase in immature forms of WBCs (bands) being released before they have matured
Expected lab findings in pt with iron deficiency anemia lower hb/hct, low iron, low MCV, flow ferritin, yet increase in TIB (tot. iron-bind capacity)
Foods nurse would recommend for pt w/iron def. anemia liver, muscle meat, eggs, dk green leaf veg, whole-grain, enriched breads
Lab finding in CBC of pt w/folic acid def r/t chronic alcohol abuse dec. hct/hb, increase in iron, bili, transferring & ferritin
Pt teaching r/t pernicious anemia need to take cobalamin to absorb intrinsic factor, protect from falls, burns, & trauma due to neuro impair, incr. GI cancer
Care of pt w/sickle cell crisis bed rest, oxy ther, pain mngt, fluids & ele, infection cntr, folic acid
Complications of thrombocytopenia bleeding – petechiae, ecchymosis, epistaxis
Care of pt rec. blood trans Baseline vitals, slow infus for 15 mins, then vital 15 min, watch for trans rxn, fluid bal ass
Care of pt w/heparin-induced thrombocytopenia and thrombosis syndrome watch for bleed, DVTs, vascular ischemiaw/stroke, seizure, discontinue hep flush, use soft toothbrush
Care of pt w/acute polycythemia vera reduce blood volume, hydration, adequate oxy, I/O, med, dietary, DVT avoidance, monitor hct/hb, anemia
Care of pt w/immune thrombocytopenia purpura (ITP) avoid asparin, cntr bleed, use soft toothbrush, avoid inject, avoid causative agents
Care of pt w/type A hemophilia prevent & treat bleed, preventative care, avoid accidents, health pro, daily oral care
Care of pt w/von Willebrand’s disease prevent & treat bleed, preventative care, avoid accidents, health pro, daily oral care
Causes of disseminated intravascular coagulation (DIC) abnormally initiated & accelerated clotting, tumors, gram neg bact, leukemia, blood transfusion rxn
Lab value in pt w/myelodysplastic dyndrome (MDS) periperial blood cytopenias & hypercellular bone marrow w/dysplastic changes
Neupogen/Filgrastim management of servere chronic neutropenia – stims immature neutrophils to divide and diverentiate – activates mature neutrophils
How is Neupogen beneficial for bone marrow transpalantation? Improves harvest of progenitor cells
Complications of neutropenia infection from norm flora, pathogens, impaired inflame., masks signs of infection, sepsis, systemic infections
Complications in pt w/non-Hodgkin’s lymphoma can involve CNS, spleen, liver, GI tract, & bone marrow – raidiation therapy causes skin issues
Nursing interventions for pt w/multiple myeloma ambulation & hydration to deal w/hypercal, weight-bearing, pain, monitor ele & I/O, fracture prevent, infect cntrl
Coumadin Warfarin - anticoagulant – evaluate INR or PT and watch for intracranial bleeding
Heparin anticoagulant – antithrombin, anemic thrombocytopenia can result after long use, bleeding
Lovenox Enoxaparin – prevent DVT and PE, anticoag, bleeding, anemia, thrombocytopenia
Myodyplastic syndrome (MDS) can turn into acute leukemia
Created by: Ladystorm
 

 



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