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petechiae
small, pinpoint red or purple spots, less than 3mm and dont fade when pressed
petechiae are caused by
tiny blood vessels brekaing under skin
purpura
large red or purple spots, several mm, may appear in clusters and look like bruises
purpura are caused by
blood vessel rupture
hypochromic cells
rbc that have a pale color due to lower amount of hemoglobin
hypochromic cells can be a sign of
anemia
microcytic cells
red blood cells that are smaller than normal
microcytic cells indicate
problem with hemoglobin production
oncotic pressure
pressure exerted by proteins that pulls water into bloodstream
oncotic pressure is also called
colloid osmotic pressure
oncotic pressure is dependent on the protein
albumin
the pressure at the arterial end of capillaries is
vascular pressure that is higher than oncotic pressure xausing fluid to move out of blood
the pressure at the venous end of capillaries is
decreased hydrostatic pressure to pull fluid back to blood
when pressures are off balance this can lead to
edema
anemia can lead to
microcytic hypochromic cells
microcytic hypochromic cells
small, pale rbc due to insufficient hemoglobin caused by low iron
iron is required for
hemoglobin synthesis
the most common anemia is
iron deficiency anemia
causes of iron deficiency anemia
dietary, blood loss, impaired absorption
telling symptom of iron deficicency anemia
spoon shaped nails
general symptoms of anemias
pallor, dry skin and membranes, SOB
chronic signs of iron deficiency anemia
spoon shaped nails, pica, malnurished
labs for iron deficiency anemia
hemoglobin, hematocrit, minerals (iron)
hemoglobin
protein within rbc that carries oxygen
hematocrit
measures rbcs in blood
those with iron deficiency anemia wants to include more
meats and leafy greens in their diet
pernicious anemia is due to
vitamin b12 deficit
cause of pernicious anemia
malabsorption, chronic gastritis, vegetarian diet
telling sign of pernicious anemia
pin and needles, tingling limbs
labs for pernicious anemia
B12, hemoglobin, hematocrit
intrinsic factor
protein produced in the stomach that allows B12 intestinal absorption
aplastic anemia
bone marrow fails to produce sufficient blood cells
a cause of aplastic anemia can be
pancytopenia
pancytopenia
small cells leading to low bone marrow function leading to low blood cells- anemia
symptoms of aplastic anemia
low blood cells, bleeding, infection, pancytopenia
autoimmune cause of aplastic anemia
75%- HIV, eptein barr, hepatitis
environmental cause of aplastic anemia
15%- chemicals, radiation
megaloblastic anemia
charcterized by large blood cells
causes of megaloblastic anemia
B12 deficiency, folic deficiency
symptoms of megaloblastic anemia
general anemia symptooms
sickle cell anemia
rbcs change shape and cannot carry oxygen- clog up
sickle cell pathophysiology
genetic both parents, african and medditerranean, male manifested
triggers of a sickle cell crisis
hypoxemia, dehydration, stress, high altittude, surgery
hypoxemia
low oxygen in blood
acute symptoms of sickle cell
pain from clots
chronic symptoms of sickle cell
delayed growth, priapism- sustained erection
managment of sickle cell
PAIN MANAGEMENT, hydration, immunizations, constricting clothing, oxygen
acute leukemia
bone marrow cancer
sumptoms of acute leukemia
bone pain, enlarged lymphnoids, anemia, purpura, wounds, weight loss
labs for acute leukemia
peripheral blood smear, bone marrow biopsy, cbc- wbc
acute lymphoblastic leukemia ALL is common in
children
acute myeloid leukemia AML is common in
adults
pathophysiology of acute leukemia
high immature wbc, low rbc and platelets
chronic leukemia is linked to
radiation and genetics
chronic leukemia has a slow progression which leads to
late discovery
with leukemia monitor for
infection and bleeding
with leukemia wash hands and use
electric razor to avoid bleeding
thrombocytopenia
low platelets in blood
casues of thrombocytopenia
chemotherapy, autoimmune, heparin, infection
symptoms of thrombocytopenia
petechiae, purpura, general bleeding
polycythemia vera
overproduction of rbc, blood gets thick- thrombus forms
thrombus
clot in blood vessel
primary cause of polycythemia vera
genetics
secondary cause of polycythemia vera
tumor
disseminated intravascular coagulation DIC
blood clotting is activated systemically, leading to excessive clotting and bleeding, MEDICAL EMERGENCY
leukopenia
low wbcs
leukopenia wbc count
less than <4,000
heparin is an
anticoagulant, prevent and treats clots
herparin is fast acting and administered
IV/SQ
heparin is monitored by
PTT
partial thromboplastin time PTT
measures how long it takes for blood to clot
heparin antidote
protamine sulfate
wafarin is an
anticoagulant
warfarin is oral and has
delayed onset
IV heparin is given as bridge until
warfarin is effective
warfarin is monitored by
PT and INR
prothrombin time PT
measures how quickly blood is clotting
international normalized ratio INR
measures how long for blood to clot
warfarin antidote
phytonadione- vitamin K
avoid while taking warfarin
alcohol, excess vitamin K
enoxaparin is an
anticoagulant- low molecular weight heparin
there is no routine coagulation monitoring for
enoxaparin
administer enoxaparin SQ with
air bubble
black box enoxaparin
spinal hematoma
thrombolytics
breakdown existing clots
alteplase is a
thrombolytic
alteplase is used for
stroke, pulmonary embolis, MI, occlusion of shunts and catheters
what does alteplase do
digests fibrin- stops all clotting and reestablishes blood flow
major risk with alteplase
internal bleeding
antithrombolytics
prevent clot formation
after administering antithrombolytics monitor for
unusual/excessive bleeding
clotting drugs are
systemic drugs, must educate and monitor bleeding
antifibrinolytics
prevent and treat excessive bleeding, promote clot formation
desmopressin is an
antifibrinolytic
hematopoiesis
production of blood cells
hematopoiesis fetal site
spleen/liver
hematopoiesis adult site
bone marrow
erythropoiesis
production of rbc
erythropoiesis is triggered by
hypoxia
hypoxia
low oxygen levels in tissues