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patho/pharm exam 3
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hematopoietic system
the body’s blood forming system with the function to produce, mature, and regulate blood cells that carry O2, fight infection, and control clotting
bone marrow
soft spongy tissue inside bones and source of all blood cells (RBCs especially) except lymphocytes
red bone marrow
vascular (found in pelvis, sternum, and vertebrae)
RBC count, WBC count, platelet count
most important things in CBC?
hemoglobin (Hgb)
responsible for carrying O2 to tissues
hematocrit (Hct)
measure volume of blood (thickness)
anemia
the loss of RBCs, decreased production of RBCs, and the increased destruction of RBCs which causes less O2 to be carried to tissues
treatment for Iron deficiency anemia
ferrous sulfate (which can cause black stool, nausea, vomiting, and constipation)
megaloblastic anemia
B12 deficiency which causes impaired DNA synthesis and leads to large immature RBC made in the bone marrow.
these pts will be malnourished
sources of B12
dairy, eggs, poultry, meat, fish
sickle cell anemia
crescent shaped RBCs which cause blood to sludge. Crescent shaped RBCs will catch/ get stuck on blood vessels causing blood to get thicker since blood clotting and not receiving O2
pts will be SOB and in agony
African Americans
what type of pts are predisposed to sickle cell anemia?
treatment for sickle cell anemia
HYDRATION (if not then clots will form in joint areas), pain management (always fist), blood transfusion + O2
symptoms of anemia
pale, SOB, weakness + fatigue, dizziness, tachycardia, smooth red tongue (B12), GI symptoms
hemorrhage
excessive/uncontrolled bleeding, happens in the kidneys (kidneys produce erythropoietin which helps make RBCs, so if kidneys dont work then pt will be anemic)
causes of anemia
leukemia, bone marrow, hemorrhage
WBC normal range
4,000 - 10,000
platelet normal range
150,000 - 450,000
hemoglobin (hgb) normal range
11 - 17
hematocrit (hct) normal range
W: 39% - 48%
M: 42% - 50%
reticulocyte count
immature red blood cells
an increase indicates that the body senses a issue (blood loss or anemia) and is overproducing RBCs, but these cells are underdeveloped and don’t work yet
example of reticulocyte count increase
pt with breathing issues → low O2 → increase in erythropoietin → increase in RBCs → increase in X
polycythemia vera
proliferative disorder (cells multiply too quickly) where bone marrow makes RBCs without normal control, so body will make way too many RBC’s causing blood to turn into sludge and further causing circulation issues
secondary polycythemia
responds to low O2 (like with COPD or heart disease)
symptoms of polycythemia
SOB, fatigue, pulmonary issues, enlarged spleen
treatment for polycythemia
splenectomy, therapeutic aphaeresis (removes certain cells from blood), therapeutic phlebotomy
whole blood
contains all natural components of blood (RBCs, platelets, plasma, WBCs)
packed RBCs
concentrated RBCs made by removing plasma from the blood. Must get type and cross test before giving to pts to determine their blood type. Protein Source.
anemic pts, hemorrhage pts, post-op
what pts are given packed RBCs?
platelets blood component
pooled platelets separated from blood
thrombocytopenia pts, chemotherapy pts, mylosupression pts, leukemia pts
what pts get platelets blood component?
fresh frozen plasma
liquid portion of whole blood (plasma) that is frozen after donation to preserve clotting factors
contains Factor 8, Factor 9, albumin, immune globulin, factor 7
Factor VII (7)
natural (liver) and man made clotting factor which allows body to stop bleeding for a set amount time. Very expensive and will cause no active bleeding within 3-4 hrs. Used during surgery.
pts who dont have enough clotting factors (coagulopathy), used to help stop or prevent bleeding
what pts get fresh frozen plasma?
washed RBCs
removes every antigen possible. Removes most of plasma, proteins, and antibodies in blood. FOR EXTREME ALLERGIES. Must be used within 24 hrs.
immunocompromised pts
what pts get washed RBCs?
cryoprecipitate
blood product made from fresh frozen plasma and contains factor VIII (8)
pts who dont have Factor VIII (8), pts who have low fibrinogen levels
what pts get cryprecipitate?
febrile, non-hemolytic reactioin
most common transfusion reaction caused when pts are sensitive to blood even w/ closest match, pts are sensitive to doner’s WBCs + cytokins), no RBC destruction
no pain, FEVER may occur
acute hemolytic reaction
life-threatening reaction where transfused RBC’s are destroyed (hemolyzed) by pts immune system, usually due to wrong blood type being given
happens within minutes of transfusion
kidney pain and hypotension
MUST STOP IMMEDIATELY
4 hrs
how long are transfusions given over?
blood transmitted diseases
AIDS/HIV, hepatitis
circulatory overload
when pt gets too much blood or fluid too quickly leading to overload and pulmonary edema
long-term transfusion therapy
citrate is put in so blood or fluid wont clump, citrate love Ca+ and can take Ca_ out of commission
white blood cells
leukocytes, body’s infection fighting cells in the blood and immune system
hemostasis
body’s process of stopping bleeding with platelets and fibrin/clotting factors
platelets (thrombocytes)
in blood and help form clots to stop bleeding, they will adhere to damaged vessel wall and change shape further exposing surface receptors and clumping together to from a plug, first responders
lifespan= 10 days
thrombocytosis
increase in circulating platelets ( > 450,000)
makes platelets harder to stick together further preventing clotting factors which are needed
why must patients stop taking aspirin before surgery?
antibiotics (piptazo), aspirin, anticoagulants
medications that impact platelets (eat platelets)?
thrombocytopenia
decrease in circulating platelets (< 150,000) which causes increase risk of bleeding and bruising (ecchymosis)
heparin-induced thrombocytopenia (HIT)
allergic reaction to heparin that causes low platelets and increased clotting (due to increased bleeding) since platelets get used up
bad for pts with dialysis
clotting cascade
extrinsic (damage to tissues) and intrinsic (damage to blood vessels) factors meet at common pathway where Factor X (10) is activated into Factor Xa (10a)
Factor Xa (10a) converts prothrombin into thrombin
thrombin converts fibrinogen into fibrin which forms a stable clot
clot dissolves
3- stages of hemostasis
vessel spasm (vasoconstriction)- after injury to limit blood flow and reduce blood loss
platelet plug formation (first responders)- platelets stick to exposed collagen at the injury site
coagulation- clotting factors are activate in a chain reaction w/ intrinsic and extrinsic pathways
disseminated intravascular coagulopathy (DIC)
mother-load of all clotting problems, will release all clotting factors at once and cause many small clots to form until depletion
second phase is bleeding out (hemorrhage) since all clotting factors are depleted
shock, sepsis, childbirth, trauma, tumors
what causes disseminated intravascular coagulopathy (DIC)?
will give fluid and try to stop bleeding but can cause multiple organ system failure quickly!
what do we do to help DIC?
anticoagulants
prevent clot formation and extension. Prevents new clots from forming and stops existing clots from getting bigger. Interferes w/ clotting cascade. DOES NOT DESTROY EXISTING CLOTS!
warfarin, heparin
antiplatelet drugs
prevent platelets from sticking together, stops platelet plug formation.
Clopidogrel (plavix), aspirin
thrombolytic agents
dissolves existing clots, converts plasminogen to plasmin which digests fibrin clots, cannot give if pt is on anticoagulants or has stokes
streptokinase, alteplase (tPA)
heparin
rapid acting anticoagulant that helps prevent new blood clots and stops existing ones from growing (will see effects within 1 hr)
works by activating antithrombin III, which blocks conversion of prothrombin to thrombin and fibrinogen to fibrin overall stopping the clotting cascade.
NEVER GIVE IM, WILL CAUSE BLEEDING
pulmonary embolism (clots traveling to lungs), stoke, DVT (overall so pt wont clot as fast)
what is heparin used for?
adverse effects of heparin
HEMORRHAGE, thrombocytopenia, hypersensitivity reactions (like HIT)
aPTT
platelets, Hgb, Hct (will cause these to decrease)
what to monitor for pts taking Heparin?
aPTT
measures how long it takes blood to clot
therapeutic range for aPTT
60-70 s
anything higher than 70 is bad and means blood is too thin
anti-Factor Xa
lab test that measures effectiveness of heparin by checking how well factor Xa is being inhibited
high → blood is too thin and increase risk of bleeding which means dose of heparin will need to be decreased
low → blood is too thick which means more clotting is happening still and dose of heparin will need to be increased
low molecular weight heparin
a modified from of heparin that’s smaller and more predictable and longer acting. ONLY INACTIVATES FACTOR Xa
normal range for aPTT
30-40 s
protamine sulfate
reverses heparin by binding to heparin and neutralizing its anticoagulation effects
max does = 50 mg delivered at 5 mg per min (10 mins total)
CAUTION WITH FISH ALLERGIES (has iodine base)
anaphylaxis, circulatory collapse, pulmonary edema
adverse effects of protamine sulfate
side effects of protamine sulfate
hypotension, bradycardia, dyspnea, flushing, nausea + vomiting
lovenox (enoxaparin)
a low molecular weight heparin used for joint (joint replacement) and abdominal cases
risk for HIT
no lab surveillance needed
warfarin
oral anticoagulant that helps prevent blood clots from forming and growing. Works by blocking Vitamin K from making clotting factors VII (7), IX (9), X (10), and prothrombin
HEART VALVE REPLACEMENTS!, atrial fibrillation, post MI, stoke, cardiac embolism
what is warfarin used for?
adverse effects of warfarin
unusual bleeding, excessive menstrual bleeding, blood in stool or urine, bruising, excessive nose bleeds, bleeding gums
PREGNANT, uncontrolled alcohol/drug use, unsupervised dementia/psychosis
what pts should not use heparin?
international normalized ratio (INR)
used to monitor warfarin levels, allows for comparison of results between labs and standardizes reporting of prothrombin time (transferable from hospital to hospital)
normal range for INR
2.0-3.0
warfarin drug interactions
ibuprofen (acetamin), steroids, aspirin, clopedagril, antifungals → increase warfarin levels
oral contraceptives, vitamin K → decrease warfarin levels
conversion from heparin to warfarin
start warfarin while pt is still on heparin
heparin should be continued for minimum of 4 days bc even if INR rises, the antithrombotic (clot prevention) effect of warfarin takes about 96 hrs/4 days. SO MUST CONTINUE BOTH DRUGS FOR 4 DAYS!
monitor INR until therapeutic range is met (2.0-3.0)
when INR reaches desired therapeutic range, STOP heparin (after a min of 4 days) and continue warfarin only
Eliquis (Apixaban)
oral anticoagulant that is a direct Factor Xa inhibitor. Decreases stroke risk more than warfarin.
Used for non-valve Afib, pulmonary embolism
must have frequent lab surveillance
what must pt on warfarin do regularly?
aspirin
causes inhibition of cyclooxygenase, an antiplatelet drug used for pain relief, inflammation, fever, and clot prevention (stop EARLY clot formation)
encotrin= coating on drug that allows it to break down in the bowl instead of the gut
clopidogrel (plavix)
an antiplatelet drug that works by blocking platelet surface receptors and helps to prevent blood clots in arteries
major use in vascular stent maintenance
thrombolytic drugs
“clot busters”, drugs that dissolve existing blood clots quickly. Cause conversion of plasminogen to plasmin.
streptokinase, reteplase, alteplase
DVT, MI, massive pulmonary embolism
what are thrombolytic drugs used for?
HYPOTENSION, bleeding, fever
adverse effects of thrombolytic drugs
what must you monitor before and after with thrombolytic drugs
aPTT, INR, Hgb/Hct
deep vein thrombosis (DVT)
a blood clot in a deep vein, often in one of the legs
S+S → unilateral swelling, pain + tenderness, warmth, redness
treatment for DVT
compression stockings, warfarin, heparin