pharm and transfusion (idk if ill finish this so chill yall) Flashcards

1
Q

what do you give someone with anemia

A

packed red blood cells

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2
Q

what do you give someone with clotting factor deficiency

A

fresh frozen plasma (coagulation factors)

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3
Q

what do you give someone with a platelet deficiency

A

platelets

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4
Q

what is contained in the “buffy coat” portion of the blood?

A

platelets and immune cells

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5
Q

what is the difference between homologous and autologous transfusions?

A

homologous transfusions are collecting blood from a compatable donor

autologous transfusions is refusing a patients own blood back into themselves. (used during surgery sometimes)

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6
Q

Be sure to go over the blood groups, antigens, antibodies ect cuz im too lazy to type that out

A

k cool

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7
Q

what is the pre transfusion testing that you want to complete before a transfusion

A

tying
antibody screen
crossmatch

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8
Q

what does type and screen test for

A

determines ABO and Rh phenotype of the RECIPIENTs blood (type)
identifies antibodies directed against other antigens (screen)

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9
Q

what does “cross matching” test

A

takes donor blood and mixes it with recipient blood to assure it is a match.

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10
Q

hen is cross and match ordered

A

only when there is a high likelyhood that the recipient will be recieving packed RBCs (not used in emergencies cuz not enough time.

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11
Q

What are the three reasons someone may need a transfusion

A
  1. to replace acute blood loss
  2. oxygen delivery
  3. morbidity and mortality
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12
Q

what indicates the need for a transfusion?

A
  1. Hgb <6 g/dL – Transfusion recommended except in exceptional circumstances
  2. Hgb 6 to 7 g/dL – Transfusion generally likely to be indicated
  3. Hgb 7 to 8 g/dL – Transfusion should be considered in postoperative surgical patients, including those with stable cardiovascular disease, after evaluating the patient’s clinical status
  4. Hgb 8 to 10 g/dL – Transfusion generally not indicated, but should be considered for some populations (eg, those with symptomatic anemia, ongoing bleeding, acute coronary syndrome with ischemia)
  5. Hgb >10 g/dL – Transfusion generally not indicated except in exceptional circumstances
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13
Q

How do we transfuse?

Optimal transfusion practice should provide……….. but should avoid………

A

Optimal transfusion practice should provide enough RBCs to maximize clinical outcomes while avoiding unnecessary transfusions

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14
Q

How do we transfuse?

how soon after transfusion can Hgb be reassessed

A

as early as 15 minutes as long as the patient is not actively bleeding

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15
Q

How do we transfuse?

what is the ratio of PRBC to increase in Hgb?

A

i unit of PRBCs shoul increase Hgb by 1g/dL in average sized adults… this is usually given over 1-2 hours.

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16
Q

How do we transfuse?

prior to NON EMERGENT blood transfusions what must be completed?

A

signed informed consent

probs also a cross match

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17
Q

What is the main risk of transfusion?

A

transfusion reactions.

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18
Q

When do transfusion reactions typically occur? What are the symptoms? what should be done if one occurs?

A

within 24 hours of the transfusion. symptoms include: fever, chills, pruritus or urticaria. stop transfusion immediately and report it to the blood bank

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19
Q

What are the risks for transfusion

A

PEACHING HAI (like youre getting high off peaches:) i dont make the rules here im sorry)

Post transfusion Purpura
Electrolyte toxicity such as hyperkalemia
Allergic reactions
Circulatory Overload
Hypothermia
Iron overload
Non hemolytic reactions (febrile)
Graft versus host disease (transfusion acquired)

Hemolytic transfusion reaction
Acute lung injury related to trasnfusion
Infectious complications (viral or sepsis)

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20
Q

What are the 5 types of transfusions

A

Whole blood
packed red blood cells
fresh frozen plasma
cryoprecipitate
platelets

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21
Q

in what setting would you use whole blood transfusion. why is it rarely used?

A

in the setting of a massive hemorrhage, very rarely used.

stored at a temperature where RBCs are maintained but platelets become dysfunctional and clotting factors become degraded.

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22
Q

what is the main effect that PRBC transfusion has on a patient and what is the volume of each PRBC unit

A

increases oxygen carrying capacity of patients with anemia.
each unit is 200ml

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23
Q

what are the modifications that can be done to PRBCs

A
  1. leukocyte reduced - used to reduce risk of immunologically mediated effects, infectious disease transmission or reperfusion injury
  2. irradiated - used to avoid graft versus host disease in patients who are immune deficient.
  3. washed - to prevent or eliminate complications associated with infusion of proteins present in the small amount of residual plasma in red cell concentrates.
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24
Q

what is contained in plasma? how is it given?

A

plasma contains platelets and proteins (procoagulant and anticoagulant factors)

it is given by giving 1 unit of platelets with 1 unit of FFP

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25
what is the universal donor and universal recipient for plasma?
universal plasma donor - AB universal recipient - O
26
what is FFP. what does it contain. what is it separated from. and how is it used?
fresh frozen plasma. this contains all the coagulation factors. it does not contain RBCs, WBCs, or platelets after obtained, it is frozen and then thawed when needed.
27
once thawed, why must FFP be used within 24 hours
because the factor V and factor VIII will start to decline.
28
what is cryoprecipitate
collected by thwaing FFP at 4 degrees C and collecting the white precipitate. this is rich in von willebrand factor, factor XIII, factor VIII, and fibrinogen.
29
what is the advantage of cryoprecipitate
it allows von willebrand factor, factor VIII, XIII adn fibrinogen to be replaced using a much smaller volume than if those factors were replaced by transfusing FFP.
30
a factor concentrate contains what? and what is the major indication for this?
Basically highly concentrated clotting factor major indication is to replace specific factor deficiencies such as in hemophilia A and B with minimal volume and without supplying extraneous proteins.
31
what are platelets used to manage when are platelets indicated?
thrombocytopenia or platelet dysfunction when platelet count = <10,000 when platelet count = <50,000 and pt is actively bleeding when latelet count is = <100,000 and have central nervous system injury or are undergoing neurosurgery
32
each unit of transfused platelets should increase the platelet count by
5,000-10,000
33
what are the 4 hemostasis promoting agents
1. protamine sulfate 2. Vitamin K 3. desmopressin 4. thrombin Things that PROMOTE CLOTTING
34
Protamine Sulfate Indications dosage (determined by what) black box warning
Indications: Neutralizes Heparin (Heparin Reversal Agent) Dosage is determined by the dosage of heparin May result in severe hypotensive or anaphylactoid-like reactions (black-box warning)
35
Vitamin K Indications Dosage and route is dependent on what metabolism and excretion
Mephyton Indications: Reversal Agent for warfarin (Coumadin) Dosage/Administration/MOA: PO, IM, IV, or SubQ Dosage and route varies depending on severity of bleeding, INR level, procedure planned, etc. Metabolism: Rapidly hepatic Excretion: Urine and feces
36
Desmopressin (vasopressin) MOA Route caution
MOA: Increases plasma levels of von Willebrand factor, factor VIII, and t-PA contributing to a shortened aPTT and bleeding time Route: Administered IV or Intranasal may rarely lead to hyponatremia and extreme decreases in plasma osmolality, resulting in seizures, coma, and death Restrict fluid intake Monitor sodium levels
37
Topical Thrombin MOA Uses Contraindications
MOA: converts fibrinogen to fibrin directly at the site of bleeding. Uses: In various types of surgery to aid in hemostasis whenever oozing blood and minor bleeding from capillaries and small venules is accessible. Contraindications: patients with a known sensitivity to components of bovine origin, not for use in massive bleeding. Must not be injected or allowed to enter large vessels.
38
What are the antithrombotic drugs
antiplatelet drugs anticoagulants fibrinolytic agents
39
anticoagulants General indication General Contraindications
General indication for all is to prevent or treat CLOT/THROMBUS Most commonly for venous thrombosis General contraindications for all: Bleeding – current or past (not an absolute contraindication) Most are cleared by kidneys so renal function is important to assess (Not Unfrac Heparin) Allergic reaction to the drug
40
To check kidney functions what do you order
BMP, GFR, CrCl
41
what are the parenteral anticoagulants
Unfractionated) Heparin Low-molecular-weight heparin (LMWH) (Enoxaparin/Lovenox) Bivalirudin (Angiomax) Argatroban (Acova)
42
Unfractionated heparin MOA route metabolism CI Monitoring adverse effects
USED INPATIENT ONLY MOA: combines to anithrombin III and enhances its activation of factor Xa and thrombin route: must be parenteral (SC or IV) Metabolism: hepatic CI - pregnancy category C (does not cross placenta), Heparin induced thrombocytopenia, active bleeding, hemophilia monitor: daily pTT Adverse effect: bleeding, thrombocytopenia, osteoporosis, elevated LFTs
43
what is HIT
Heparin induced thrombocytopenia heparin combines with PF4 to make your IgG attatch to platelets. this causes the platelet to activate and cause clotting it also causes the spleen to destroy the platelets (thrombocytopenia)
44
what are the four areas to assess when you are concerned about HIT
Thrombocytopenia (how much did platelet count drop) Timing of platalet count drop (how fast) thrombosis or other squeal (skin necrosis) Other causes of thrombocytopenia
45
what is the management for HIT
stop heparin begin anticoagulation with a non heparin coagulent long term oral anticoagulation will need to be given (warfarin) for 2-3 months if no thrombotic event or 3-6 months if thrombotic event occurred list heparin allergy in chart
46
Low molecular weight heparin dosing depends on metabolism adverse effects CI
dosing amount depends on indication but its always SC metabolized by kidney, contraindicated in ESRD adverse effects include bleeding, HIT, osteoporosis (all lest common with LMWH than with heparin) CI - HIT, active bleeding preg cat B (reccomended over heparin)
47
in what circumstances before and after elective surgery or invasive procedures would "bridging" want to be done? what drug is often used as a bridging drug?
Lovenox is often used. in the circumstances of: emoblic stroke w/i the past 3 months previous embolic stroke or VTE during interuption of chronic anticoagulation mechanical heart valve atrial fibrillation in pt with high stroke risk
48
argatroban (acova) MOA metabolism indications SE CI
MOA: direct thrombin inhibitor Metabolism: hepatic (measure PTT to adjust dose) indications: HIT percutaneous coronary intervention SE: bleeding CI - none really, but preg category B
49
Bivalirudin MOA Metabolism Indications SE
MOA: non-heparin thrombin inhibitor Metabolism: renally cleared Indications: Alternative to heparin in patient undergoing percutaneous coronary intervention especially if they have hx of HIT SE: bleeding (duh)
50
what are the oral forms of anticoagulants
warfarin DOACs
51
warfarin (coumadin) Class MOA monitor CI Indications adverse reactions
class:vitamin K antagonists MOA: inhibits activation of vitamin K Monitor: PT/INR CI: in pregnant women! class D or X indications: prophylactic treatment of thromboembolic disorders (DVT/PE) adverse reactions: bleeding, rarely tissue necrosis or gangrene
52
what are the drug and dietary interactions for coumadin (warfarin)
drug - literally so many, just know theres alot food - alcohol, vitamin E (increases effect), cranberry juice (increases), foods rich in vitamin K (decreases)
53
what drugs are included in DOACs why are these used?
pradaxa, xarelto, eliquis, savaysa they are safer than warfarin and given in a fixed dose. therefore you dont have to monitor their levels! (PT/INR)
54
Pradaxa MOA Indications metabolism major averse event Drug interactions
MOA: direct thrombin inhibitor indications: stroke prevention, Afib, DVT/PE, prophylaxis metabolism: renally, therefore decrease dose in renal impairment. CI in ESRD or HD major adverse event is GI bleeding: reversal agent is Praxbind (only used in emergent situations) Drug interactions: Ketoconazole, cyclosporine, tacrolimus
55
Xarelto MOA monitor CI
MOA oral factor Xa inhibitor indications:stroke prevention, Afib, DVT/PE, prophylaxis monitor for kidney and liver disease, avoid taking grapefruit juice w it, no CYP3a4 inhibitors (CCB, flourquinolones)
56
eliquis MOA monitor CI
oral factor Xa inhibitor superior to warfarin in inhibiting clots. indications: stroke prevention, Afib, DVT/PE, prophylaxis no grapefruit juice, watch for hepatic or renal impairement
57
Savaysa MOA monitor CI
MOA: oral factor Xa inhibitor indications: stroke prevention, Afib, DVT/PE, prophylaxis avoid in patients with renal impairment, hepatic impairment or in patients who have great kidneys and clear things renally very quickly CI if pathologically bleeding
58
just as a review, how do you monitor heparin. what is the reversal agent?
with aPTT for dosing adjusments with a CBC daily to monitor for signs of bleeidng does NOT require dose reduction in renal impairment reveral = protamine
59
just as a review, how do you monitor warfarin. what is the reversal agent?
monitor with PT/INR for dosage adjustments does not require reduced dose in renal impairment reversal = vitamin K
60
just as a review, how do you monitor DOACs.
no monitoring required keep an eye on kidney function esp if hx of kidney disease. may require reduced dose
61
what are the platelet aggregation inhibitors that we learn about
Aspirin plavix Effient Ticlid Brilinta Kengreal
62
aspirin MOA uses adverse events
MOA : inhibits COX 1 production which is critical for forming thromboxane irreversabley!! uses: prophylaxis of MI, secondary prevention in vascular events adverse events: bleeding, dyspepsia
63
plavix MOA uses avoid with what
MOA: irreversibly blocks ADP receptor uses: primary prophylaxis of MI, standard precention in patients with hx of vascular events avoid drugs: omeprazole, esomeprazole (pralosec)
64
Effient MOA CI
irreversibly blocks P2Y12 CI with hx of stroke or TIA
65
Ticlid MOA SE
MOA: irreversibly blocks P2Y12 SE: not used as much because it has alot of blood side effects such as neutropenia, agranulocytosis, thrombotic thrombocytopenia purpura, and aplastic anemia THEREFORE must do routine monitoring with a CBC every 2 weeks
66
Brilinta MOA SE
MOA: reversibly binds to P2Y12 BBW: aspirin reduces effects if aspirin is taken above 100mg daily.
67
Kenreal MOA route
MOA reversably binds to P2Y12 only reversable one available in IV
68
Integrilin and Reopro routes
MOA: Gp IIB/IIA receptor inhibitor IV only Given in cath lab
69
fibrinolytics
used to break down thrombi in the setting of a life threatening or massive thrombus. can be given IV or catheter to the actual clot itself. MOA: converts plasminogen to plasmin which then degrades the fibrin matrix of thrombi and produces soluble fibrin degredation products.
70
Tpa
given IV for PE, acute ST elevation, heart attack, DVT approved fro ischemic stroke but must be given within 3 hours. MOA: preferentially activates plasminogen that is bound to fibrin which in theory confines fibrinolysis to the formed thrombus.
71
streptokinase
converts plasminogen into plasma given IV for PE ,stemi or severe DVT.