antithrombotic therapies Flashcards
(35 cards)
3 groups of antithrombotic therapy
-original drugs like heparin, coumadin, and aspirin
-drugs entered clinical use like heparin derivatives
-newest drugs which are direct-acting oral and intravenous anticoad
venous thromboembolism (VTE) includes
superficial and deep vein thrombosis
pulmonary embolism
therapy for VTE
IV standard UFH (unfractionated heparin)
-low molecular weight heparin
-DOAC
-oral vitamin K antagonist-coumadin
ALL arterial thrombosis treated with
blah blah
-many people take aspirin to reduce mortality when taken within minutes of acute onset of stroke or cardiac symptoms
fibrinolytics or thrombolytic therapy used to resolve
DVT
PE
PAO
AMI
Stroke
these drugs are recombinant forms of tissue plasminogen activator
dosage of drugs depends if given
prophylactically (lower dose)
established thrombotic issue (higher dose)
why are antithrombotics dangerous
effective dose range narrow
-must be monitored regularly
what is coumadin
vitamin K antagonist
-suppresses gamma-carboxylation of glutamic acid by slowing activity of vitamin K epoxide reductase
uses of coumadin
-prophylactically or as therapy
-prevent TIAs and stroke in pts with non-valvular A-fib
-prevent VTE after trauma
-prevent DVT and PE
-given after AMI
-mechanical heart valves
how long does coumadin take to reach therapeutic level
5 days
since protein C is vit K dependent and it has 6 hr half-life
activity decreases and for first 2-3 days of therapy pts at risk for thrombosis
UFH, LFWH given for 5 days to cover this
issues with coumadin therapy
1- crosses the placenta
2-excreted in breast milk
3- needs monthly monitoring
INR
international normalized ratio
-first sample is collected and performed 24 hrs after coumadin therapy is initiated
INR =
Pt(patient) / PT (normal) ^Is1
-closer the ISI to 1 the better it is
routine prophylaxis INR range
2-3
INR range with prosthetic heart valve
2.5-3.5
action of heparin
treats venous thrombosis
-mixture of sulfated glycosaminoglycans extracted from porcine mucosa which potentiates the action of anti-thrombin by 1000x
heparin is metabolized by the liver half life
60-90 min
APTT is commonly used but the
chromogenic anti-Xa heparin assay also used
APTT reference range
old method: 1.5-2.5 x patient’s baseline
current method: ex vivo or brill-edwards method
establishing reference range for UFH
20-30 plasma samples are collected from patients being infused with UFH at all levels of anticoag
pt can’t be on coumadin
APTT is checked after 4-6 hours from the start of therapy this result should
fall in therapeutic range adjustments are made and APTT checked every 24 hrs and dose is continuously adjusted
indication of HIT
> 40% reduction in plt count
heparin can be reversed immediately by giving pt
protamine sulfate