Hematology/Oncology & Infectious Disease Flashcards
(317 cards)
Heparin
MOA
Lab
Activated antithrombin
Then inactivates factor Xa, Thrombin (IIa)
Increases PTT
Warfarin
MOA
Lab
Inhibits synthesis of Vit K- dependent coagulation factors (II, VII, IX, X and to a lesser extent proteins C and S) by blocking vitamin K epoxide reductase
Increases PT
Rapid reversal give FFP (or Vit K)
Teratogenic
Tissue plasminogen activators (tPAs)
- name
- MOA
- Lab (3)
Alteplase
Reteplase
Tenecteplase
Aid conversion of plasminogen to plasmin which breaks down fibrin
Increase PT
Increase PTT
No change in platelet count
Factor Xa inhibitors
- Name
- MOA
- Lab
- Reversal agent
ApiXAban
RivaroXAban
Directly inhibit factor Xa
New/noval oral anticoagulant (NOAC)
PT/PTT not monitored
Reversal agent: Andexanet alfa
LMWH
- Name
- MOA
- Administered
Enoxaparin
Dalteparin
Mainly inhibits factor Xa
Can be administered SQ
Direct thrombin inhibitors
- Name
- MOA
- Antidote
Dabigatran
Argatroban
Directly inhibit factor II (thrombin)
NOAC
Antidote: idarucizumab
Glycoprotein IIb/IIa inhibitors
- Name
- MOA
Abciximab
Eptifibatide
Tirofiban
Reversibly binds to the glycoprotein receptor IIb/IIIa on activated platelet, preventing aggregation
Hemophilia A
Hemophilia B
Hemophilia C
Hemophilia A
- Factor VIII
Hemophilia B
- Factor IX
Hemophilia C
- Factor XI
- Ashkenazi Jews
- AR
X linked recessive for males
Hemophilia Lab
Tx
PTT prolonged
PT and bleeding time normal
Tx: Transfuse missing factor
- If unavailable: Cryoprecipitate
If bleeding not severe: Desmopressin
Cryoprecipitate
Consists of factor VIII and fibrinogen with smaller concentrations of factor XIII, vWF, and fibronectin
Von Willebrand disease
- Inheritence
- MOA
Autosomal dominant
Deficiency in vWF with decreased levels of factor VIII
Epistaxis
Gum and gingival bleeding
Menorrhagia
Dx
Lab
Tx
Von Willebrand
Dx: Ristocetin cofactor assay (decreased agglutination )
Lab:
Increased bleeding time
Increased PTT
Normal PT and platelet
Tx: Desmopressin
Activated protein C (APC) resistance/ Factor V Leiden
Inherited thrombophilia
Single point mutation in factor V, rendering it resistant to inactivation/ breakdown by activated protein C
Heparin-induced thrombocytopenia (HIT)
- Caused by
- MOA
- Timeline
- Also seen
- NOT seen
- Tx
More common w/ Heparin
Can happen w/ Heparin or enoxaparin
Immunologic reaction to heparin which creates platelet activating antibodies which leads to blood clots and rapid drop in platelet count
5-10 days after starting heparin
Skin necrosis at injection site
[No bleeding]
Tx: Stop heparin immediately
Start a direct thrombin inhibitor (fondaparinux, argatroban, bivalirudin)
Antiphospholipid syndrome (APS)
- Associated with
- Antibodies
- Two features
- Lab
- Tx
Associated with SLE and rheumatoid arthritis
APS antibodies
- Lupus anticoagulatn
- Anticardiolipin
Spontaneous abortion
Arterial and venous thrombi formation
Prolonged PTT
Tx: Heparin and warfarin
Recurrent miscarriages and stroke
PE
Antiphospholipid syndrome
Disseminated Intravascular Coagulation
Acquired coagulopathy caused by deposition of fibrin in small blood vessels leading to thrombosis and end-organ damage
Depletion of clotting factors and platelets leading to bleeding diathesis
Bleeding for venipuncture sites
Lab
Tx
Disseminated intravascular coagulation (DIC)
Increased PT and PTT
Decreased platelets
Increased D-dimer and fibrin
Decreased fibrinogen
Factor VIII depressed
Tx: Transfuse RBC, platelets and FFP
Thrombotic Thrombocytopenic purpura
- what is it
- MOA
- Addition result
- Features (5)
- Lab
- Tx
TTP is a deficiency of the vWF-cleaving enzyme (ADAMTS-13) resulting in abnormally large vWF multimers that aggregate platelets and create platelet microthrombi
Block small blood vessels —> end organ damage
RBC are fragmented by contact w/ microthrombi —> hemolysis
Microangiopathic hemolytic anemia
TTP = adults HUS= children associated with E.coli
Low platelet count Neurologic changes (delirium, seizure, stroke, decreased vision) Pyrexia (fever) Schistocytes Acute kidney injury
Decreased platelets
Decreased hemoglobin
Increased creatinine
Normal clotting cascade
Tx: Plasma exchange
Hemolytic uremic syndrome
- Causes
- Features (6)
- Lab (4)
- Tx
Children more often
Similar to TTP but no neurologic features
Ecoli diarrhea preceedes Shiga toxin (atypical HUS)
Renal failure Microangiopathic hemolytic anemia Low platelets Abdominal pain Bloody diarrhea Schistocytes
Decreased platelets
Decreased hemoglobin
Increased creatinine
Normal clotting cascade
Tx: Dialysis for AKI
Plasma exchange
Idiopathic thrombocytopenic purpura
- MOA (3)
- Lab
- Affects who
- Feature (5)
- Antibody
- Tx
IgG antibodies (antiplatelet antibodies) are formed against the patients platelets
Platelet antibodies complexes are destroyed in the spleen
Bone marrow production of platelets is increased
Increased Megakaryocytes
Women of child bearing age
Mucocutaneous bleeding Easy bruising Petechiae Hematuria Melena
If Acute: following viral infection, children 2-6, self limiting purpura
Antiplatelet Ab
Tx: if platelet <30,000 then Corticosteriods and IVIG
Basophilic stippling
Lead poisoning (low iron) Sideroblastic anemia (high iron)
B12 deficiency
Folate deficiency
B12 deficiency
- Increased MMA (methylmalonic acid)
- Increased homocysteine
Folate deficiency
- Normal MMA
- Increased homocysteine
African american male
Fatigue
Dark urine
SOB
Jaundice
Taking TMP-SMX for cold
- Inheritence?
G6PD deficiency
X linked