Block 2-Reymann (Coag) Flashcards

1
Q

Hemostatis

A
  • Is cessation of blood loss from a DAMAGED vessel
  1. Vascular spasm
  2. Platelet plug formation (primary)
  3. Blood coag (secondary)
  4. Dissolution of fibrin clot (tertiary)
  • _2 major systems down reg coag _
  • Firbrin inhibition (limit coag)
  • Plasma has protease inhibitors that inactivate coag proteins
  • Fibrinolysis (antagonize coag)
  • Inactive plasminogen is converted to proteolytic plasmin <u><strong>(DIGESTS fibrin)</strong></u>
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2
Q

Drugs for disorders in Coag

A
  • Inhibit coag (-):
  • Platelet aggregation inhibitors
  • Anticoag
  • Thrombolytics
  • Restore or promote coag (+):
  • Plasminogen activation inhibitors
  • Protamine sulfate
  • VIt k
  • serine protease inhibitors
  • Plasma fractions
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3
Q

Platelet aggregation inhibitors (Aspirin)

A
  • Decrease synthesis/action of mols that promote aggregation
  • Cyclooxigenase inhibitor
  • Thromboxane A2=Platelet degranulate & aggregate
  • Aspirin antagonize <u><strong>(inhibits)</strong></u> this pathway=PROLONGED BLEEDING TIME
  • Mech-Inhibits TXA2 synthesis by irrever acetylation of enzyme COX
  • Takes 10 days for new COX synthesize
  • 81Mg = Anti-platelet (no SEs)
  • Preventive treatment-cerebral ischemia & POST MI (ischemic coronary)
  • 600-1000Mg-Analgesic/anti-inflammatory/Anti-fever
  • CI: before surgery due to <u><strong>INCREASE BLEEDING TIME</strong></u>
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4
Q

Platelet aggregation inhibitors (ADP receptor blockers)

A
  • 1st gen=Ticlopidine
  • 2nd gen=Clopidogrel
  • 3rd gen=Prausgral
  • PK:
  • All above are PRODRUGS
  • Slow onset of action - LOADING dose may be required
  • PD:
  • Irreversible inhibitors of P2Y12 (ADP receptor on platelet surface)
  • Use:
  • Pts intolerant to aspirin
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5
Q

Platelet aggregation inhibitors (Phosphodiesterase inhibitors)

A
  • Dipyridamole
  • PD:
  • Elevation of cAMP lvls by inhibition of phosphodiesterase
  • Blockade of adenosine uptake-ACTS on A2 receptors ACTIVATES platelet adenylyl cyclase
  • Use:
  • Preventive combo antiplatelet w/aspirin or warfarin
  • “prosthetic heart valve”
  • Test coronary reserve (opens coronary arteries)
  • NO USE as anti-anginal drug - can PROVOKE coronary steal
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6
Q

Platelet aggregation inhibitors (Phosphodiesterase inhibitors)

A
  • Cilostazol
  • Newer drug
  • Promotes vasodialation & inhibition of platelet aggregation
  • Use:
  • Primarily in treatment of <u><strong>INTERMITTENT CLAUDICATION </strong></u>or “window shopping disease”
  • Signs of artheroscelrosis in lower extermities
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7
Q

Platelet aggregation inhibitors (Block G2B/3A)

A
  • Use in pts w/acute coronary syndromes
  • The 2B/3A complex receptor for fibronogen, vitronectin, firbonectin, & VWF
  • Activation of this receptor is Final part of Common pathway <u><strong>(Factor 7)</strong></u>
  • AbcixMAB: monoclonal Ab against human G2b/3a receptor. Reversible w/thrombo-infusion ONLY = Restore coag cascade
  • Eptifibatide: Peptide reversible antagonist of GP2B/3A receptor
  • Tirofiban: Non-peptide reversible antagonist of GP2B/3A receptor
  • Uses:
  • Unstable angina
  • High-risk percutaneous coronary interventions <u><strong>(Treating stenosis)</strong></u>
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8
Q

Anticoags (Heparin)

A
  • Water sol Injectible RAPID acting anti-coag & <u><strong>SAFE IN PREGERS</strong></u>
  • Used to acutely interfere w/formation of THROMBI
  • Mixture of straight chain anionic glycosaminoglycans w/a MEAN MW=15,000
  • PD:
  • Anti-throm 3 is Alpha-glob that inhibits <u><strong>(serine proteases &amp; several clotting factors-thrombin)</strong></u>
  • Absence of heparin=Anti-throm 3 interacts w/thrombin VERY SLOWLY
  • Heparin allows Antithrombin 3 to RAPIDLY inhibit thrombin <u><strong>(DOES NOT EFFECT ALREADY BOUND FIBRIN)</strong></u>
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9
Q

Anticoags (LMWH)

A
  • Low-Mol weight Heparin
  • Heterogeneous compounds produced by chemical or enzymatic depolymerization of unfractionated heparin <u><strong>(UFH)</strong></u>
  • LWMH inhibit activated factor 10 BUT has less effect on thrombin than regular Heparin
  • Has LITTLE acceleration & less likely to <u><strong>INDUCE HYPERSENSITIVITY</strong></u>
  • Danaparoid: LMWP from pork gut
  • Contains Hep sulfate, dermatan sulfate, chondroitin sulfate
  • Mainly inhibits Factor 10 w/LESS EFFECT on thrombin
  • Use:
  • For DVTs in hip replacement surgeries
  • Treatment of HIT <u>(Type 2 Hypersen)</u>
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10
Q

Anticoags (Heparin)

A
  • Monitoring effects:
  • Preformed by **PTT of activated factors **
  • aPTT test integrity of <u><strong>INTRINSIC &amp; COMMON </strong></u>pathways
  • LMW Hep:
  • Has higher therapeutic index that its Big brother - in Prevention care
  • NOT necessary to monitor LMW Hep
  • SE:
  • Bleeding-USE of protamine sulphate acts as antagonism of Hep
  • Hypersensivity Rxn <u><strong>(HIT type 2)</strong></u>
  • Thrombosis-w/long term admin of hep=reduction of Anti-thrombin 3 activity
  • This decrease of coag factors=<u><strong>HIGHER risk of thrombosis</strong></u>
  • Minimize risk w/Low doses
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11
Q

Heparin-induced Thrombocytopenia (HIT)

A
  • Ab recognize complexes of heparin & platelet factor 4 on platelet membrane
  • through IgG binds to PF4/Hep complex = <u><strong>IMMUNE COMPLEX</strong></u>
  • Leads to to platelet aggregation & release of platelet contents
  • Result is thrombocytopenia & thrombosis
  • Treatment: Sub Hep w/a DTI or Fondaparinux (LMW HeP)
  • DTIs=exert anticoag effect by direct binding to active site of thrombin
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12
Q

Anticoags (Factor X active inhibitors)

A
  • Fondaparinux-Synthetic pentasaccharide
  • Sequence of 5 carbs necessary for BINDING to anti-thrombin 3
  • Binding induces conformational change in anti-thrombin required for Factor 10
  • SPECIFIC inhibitor of 10A
  • Negligible ANTI-thrombin activity
  • Approved for prevention treatment of DVTs
  • Use as INJECTION once a day
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13
Q

Anticoags (DTIs)

A
  • Exert anti-coag effect directly binding to active site on thrombin
  • Lepirudin, Desirudin, Bivalrudin, Argatroban
  • Hirudin powerful & specific thrombin inhibitor from leech
  • Recombinant form peptide =<u><strong> LEPIRUDIN</strong></u>
  • Action independent from Anti-thrombin 3=reach inactivate fibrin bound thrombin in <u><strong>THROMBI</strong></u>
  • Given parenterally
  • Monitor by aPTT
  • Bivalirdin=Thrombotic Anticoag
  • Argatroban=Small mol thrombin activator
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14
Q

Anticoag (Coumarin)

A
  • Warfarin & Dicumarol
  • Unlike Hep they are Lipid sol and given <u><strong>ORAL</strong></u>
  • _PD: _
  • Inhibit VIT K **epoxide reductase **
  • Use:
  • Treating inactive clotting factors DUE to LACK of gamma-carboxyglutamyl side chains
  • Take 8-12 hours for onset
  • Anticoag effects can be overcome with VitK <u><strong>TAKES 24 HRS</strong></u>
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15
Q

Anticoag (warfarin)

A
  • Monitoring LVLS:
  • Has narrow TI & participates in MANY drug to drug interactions
  • Effects must be monitored <u><strong>every 2-4 weeks</strong></u>
  • Preformed by PT <u><strong>(extrinsic &amp; common)</strong></u>
  • Prolongs PT decreases amount of functional Factor 7
  • SE:
  • Hemmorrhage
  • Skin necrosis related w/reduced activity of protein C <u><strong>(Occurs 1st weeks of therapy)</strong></u>
  • Crosses placenta <u><strong>(lipid sol)</strong></u> can cause <u><strong>hemorrhagic disorder in fetus (ANACEPHALY)</strong></u>
  • Antibiotics mess w/flora = LOW VIT K
  • Anti-bile reabsorb-Mess with Vit K
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16
Q

Anticoag (Fibrinolytics)

A
  • Lyse thrombi by catalyzing conversion of plasminogen into PLASMIN
  • Reduce mortality of ACUTE MI <u><strong>(dissolve thrombus to save Myocaridal tissue)</strong></u>
  • Used in situations where angoplasty(balloon catheter) <u><strong>NOT AVAILABLE</strong></u>
  • Streptokinase
  • Urokinase
  • Anistrepeplase
  • Alteplase
17
Q

Drugs for bleeding disorders

A
  1. Plasminogen activation inhibitors <u><strong>(OPPOSITE of THROMBOLYSIS)</strong></u>
  2. Protamine sulfate
  3. VIT K
  4. Plasma factors
18
Q

Drugs for bleeding disorders (Plasminogen A Inhibitors)

A
  • Aminocaporic acid & tranexamic acid
  • Inhibit plasminogen activation
  • Decrease plasmin LVLS
  • Down-reg of fibrinolysis
  • Down Reg of fibronogen breakdown
19
Q

Drugs for bleeding disorders (Protamine sulfate)

A
  • Antagonizes <u><strong>(inhibits)</strong></u> Heparin
  • HIGH in arginine-Cationic protein interacts w/anionic Hep
  • Forms complex w/<u><strong>NO ANTICOAG activity</strong></u>
  • Dose dep has immediate effect
20
Q

Drugs for bleeding disorders (VIT K)

A
  • Stop bleeding due to oral-anticoag <u><strong>(warfarin)</strong></u>
  • Effect delayed 6-12 hours w/complete penetrance by 24hours
  • NOT for use in ACUTE bleeds <u><strong>(USE FROZEN FRESH PLASMA or BLOOD TRANSFUSION)</strong></u>
21
Q

Plasma Fractions Def.

A
  • Def in plasma coag factors can cause bleeding
  • Spont bleeding occurs when factor activity is less 5-10% of normal
  • Factor 8 (Hemo A)
  • Factor 9 (Hemo B or Christmas)