21 Therapeutic Modalities in Hematology Flashcards

(48 cards)

1
Q

Irreversibly binds COX-1 and COX-2

A

Aspirin

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2
Q

Antiplatelet drugs

A

Aspirin
Thienopyridines
Dipyridamole
Abeiximab, eptifibatide, tirofiban

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3
Q

Inhibit ADP-induced platelet aggregation

SE: bleeding

A

Thienopyridines

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4
Q

Prodrugs that require metabolic activation by the hepatic cytochrome P450 enzyme system

A

Clopidogrel

Prasugrel

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5
Q

Indication of thienopyridines

A

Oral, Prasugrel for patients undergoing stenting

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6
Q

Inhibits PDE, increases cAMP, reduce Ca ions leading to inhibition of activation
SE: vasodilation

A

Dipyridamole

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7
Q

GpIIb/IIIa inhibitor

SE thrombocytopenia, bleeding

A

Abeiximab, eptifibatide, tirofiban

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8
Q

Administration of Abeiximab, eptifibatide, tirofiban

A

IV bolus then infusion

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9
Q

Fab fragment of a humanized murine monoclonal AB directed against the activated form of GpIIb/IIIa
Binds to the activated receptor with high affinity and blocks the binding of adhesive molecules

A

Abciximab

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10
Q

Cyclic heptatide that bind GpIIb/IIIa because it incorporates the KGD motif

A

Eptifibatide

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11
Q

Anonpeptidic tyrosine derivative that acts as an RGD mimetic

A

Tirofiban

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12
Q

Anticoagulant drugs

A
Heparin
Low molecular weight heparin
Fondaparinux
Lepirudin, argatroban, bivalrudin
Vitamin K antagonist (warfarin)
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13
Q

Activates antithrombin III
IV or SC, monitored via PTT
SE: Bleeding, thrombocytopenia

A

Heparin

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14
Q

Activates antithrombin III
SC or IV, high bioavailability, monitored by anti FXa levels
SE: bleeding
Low risk of thrombocytopenia

A

Low molecular weight heparin (enoxaparin)

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15
Q
Synthetic analogue of ATIII activating sequence
Binds and activates antithrombin III
SC, high bioavailability
SE: bleeding
Does not cause HIT
A

Fondaparinux

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16
Q

Direct thrombin inhibitor
IV infusion, monitored via PTT
SE: bleeding

A

Lepirudin
Argatroban
Bivalirudin

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17
Q

Inhibits carboxylation of vitamin K dependent clotting factors
Oral, metabolized by CYP450 system, narrow therapeutic window, monitored by INR and PT
SE: Bleeding, skin necrosis, embryopathy

A

Warfarin

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18
Q

Drugs that attack diseases more precisely via specific unique pathways and cell surface markers

A

Targeted therapy

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19
Q

Targeted therapy drugs

A

Gemtuzumab + ozogamicin
Denileukin + diptheria toxin
Ibritumomab + 90Y

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20
Q

Anti CD33 + calicheamicin

For AML

A

Gemtuzumab + ozogamicin

21
Q

Anti-IL2 + protein synthesis inhibitor

For cutaneous T-cell lymphoma

A

Denileukin + Diptheria toxin

22
Q

Anti-CD20 + ionizing radiation

Refractory B-cell lymphoma

A

Ibritumomab + 90Y

23
Q

Replace an abnormal but non-malignant lymphohematopoietic with one from a normal donor
Replace a malignant hematopoietic system with one from a normal donor

A

Hematopoietic stem cell transplant

24
Q

2 types of hematopoietic stem cell transplant

A

Allogeneic bone marrow transplant

Autologous bone marrow transplant

25
From another member of the same species
Allogeneic bone marrow transplant
26
Type of transplant that makes use of a person's own stem cells for treatment Can be used for lymphoma-related diseases Can't be used for aplastic anemia or thalassemia
Autologous bone marrow transplant
27
Large needle is connected to a large machine and centrifuges the blood that comes in the machine and it just gets the stem cells The other components of blood are returned to the patient
Apheresis
28
Frequent complication of allogeneic stem cell transplantation, in which lymphocytes from the donor attack and cannot be eliminated by an immunodeficient host
Graft-versus-host disease
29
Provides immediate correction of deficient cellular and soluble blood components
Transfusion therapy
30
To treat fibrinogen deficiencies
Cryoprecipitate
31
To treat or prevent bleeding due to low platelet levels | To correct functional platelet problems
Concentrate of platet
32
To correct a deficiency in coagulation factors or to treat shock due to plasma loss from burns or massive bleeding
Fresh frozen plams
33
To increase the amount of RBC after trauma or surgery or to treat severe anemia
RBC
34
``` Storage period; RBC FFP Plasma concentrate Cryoprecipitate ```
42 days (ref) or 10y (freezer) 1y (freezer) 5 days (RT) 1y (freezer)
35
Never requested unless for emergencies
Fresh whole blood
36
Oxygen carrying capacity + volume expansion No viable platelets, degraded coagulation factors Immunogenic due to presence of plasma For exchange transfusion in neonates
Whole Blood
37
Fibrinogen and FVII and vWF
Cryoprecipitate
38
Decreased fibrinogen, FII, FVII, FIX, X No large multimers of vWF Plasma exchange in thrombotic thrombocytopenic purpura
Cryosupernatant
39
This is performed before the transfusion of red cells | Donor red cells are mixed mixed with the patient serum
Cross matching
40
Usually due to ABO incompatibility | Hypotension, tachycardia, fever, chills, hemoglobinuria
Acute hemolytic transfusion reaction
41
Due to sensitization from previous reaction
Delayed hemolytic transfusion reaction
42
Most frequent reaction to transfusion Chilled, rigors, increase in temperature by 1 deg Antibodies against donor leukocytes
Febrile nonhemolytic transfusion reaction
43
Treatment for FNHTR
Use of leukodepleted products
44
Due to presence of plasma proteins
Allergic transfusion reactions
45
Treatment for allergic transfusion reactions
Premedicate with antihistamines
46
T-lymphocytes from donor attack the immunodeficient host
Graft versus host disease
47
Most common cause of transfusion related mortalities | Signs of acute lung injury after transfusion of plasma
Transfusion related acute lung injury
48
Volume expansion due to transfusion
Transfusion associated circulatory overload