Anticoagulation I Flashcards
Signs and Sx of DVT and PE
DVT
-Unilateral leg swelling (warmth, tender, discoloration)
-Pain behind knee/calf when flexing foot (+ Homan’s)
-Palpable cord
PE
-Dyspnea
-Tachycardia/tachypnea
-Chest pain/tightness
Diagnosis of DVT and PE
DVT
-US (+ dopple/b mode)
-Dimer 240+ (elevated)
-Wells score 2+
PE
-V/Q scan (+)
-Spiral CT
-Dimer 240+
-Wells PE score >4
Wells Score: DVT and PE
DVT
-Low: =< 0
-Mod: 1-2
-High: >= 3
PE
-Likely: > 4
-Unlikely: =< 4
General Approach: Treatment of VTE
- Cardiopulmonary compromise or high risk of limb loss = FIBrinolytic + UFH/LMWH
- Active bleeding or CI and lower extremity = IVC filter, initiate AC when cleared
- Poor prognosis/can’t tx output = hospitalize
-CrCl < 30 = UFH x 5 overlap warfarin
-CrCl 30+ = UFH x 5 overlap warfarin or UFH with DOAC transition OR vvv - Outpt tx = Riva/Apix/LMWH with fonda x 5 then dab/edox or LMWH x 5 overlap warfarin (RALF DWEL)
Risk Factors for Major Bleeding While Taking Anticoagulation Therapy
-65+
-NSAID use
-Hx of GI bleed
-Recent surgery/trauma
-Heavy alcohol use
-Renal failure
-Malignancy
-Initiation of tx
Fibrinolytic Drugs Potential
-Alteplase (t-PA)
-Tenecteplase (TNK)
-Streptokinase
-Urokinase
Potential to dissolve not only pathologic thrombi but physiologically appropriate fibrin clots
– could lead to hemorrhage of varying severity
*bc not site specific
Fibrinolytic Drugs: Indications/CI
Indications
1) Massive ileo-femoral DVT at risk for limb gangrene due to venous occlusion
2) Hemodynamically unstable PE patients (ie. SBP < 90, shock)
CI
-Active bleeding, hemorrhage hx
-Ischemic stroke within 3 months
-Cancer/vascular lesion
-Aortic dissection
-Trauma/surgery (head)
-Severe uncon HTN
(BIHH VCAT)
Fibrinolytic Drugs: Dosing
Before fibrinolytic therapy begins, administer IV heparin in full therapeutic doses (then suspend during fib tx)
Altepase
-PE: 100 mg IV infusion over 2 hours x 1 dose
-Cardiac arrest: 50 mg IV bolus x 1 dose
Initial Acute Phase Treatment
Rapid-acting (FULAR)
-UFH (IV/SC)
-SC LMWH
-SC Fondaparinux
-Oral rivaroxaban or apixaban
-Dab/edox not used bc need 5-10 days of parenteral tx first
Transition from parenteral therapy to orals:
–5 days and until INR 2-3 for at least 24 hr, then continue on PO warfarin alone = BEST PRACTICE
– No overlap is necessary if switching from parenteral therapy to rapid acting DOAC (rivaroxaban or apixaban)
Heparin: Monitoring
PREFERRED IN RENALLY IMPAIRED PTS = not renally excreted
Baseline Labs
* CBC with platelets
* PT/INR
* aPTT
* BUN
* Serum creatinine
Ongoing Labs
* aPTT or anti-Xa
– 6 hours after initial bolus
– every 6 hours until 2 consecutive aPTT / anti-Xa values are therapeutic, then daily
* CBC with platelets
– Daily if pretx < 100,000
– Every 72 hours if > 100,000
Heparin: Dosing
IV: 80 u/kg (max 10,000) followed by 18 u/k/hr (max rate 2,150 u/hr)
- goal aPTT 50-77 seconds
- goal anti-Xa 0.3-0.7 IU/mL
Heparin: Precautions and Side Effects
-Narrow therapeutic window
-Heparin induced thrombocytopenia
-Hemorrhage
-Hypersensitivity rxn
-Hyperkalemia
-Osteoporosis
(HHHHON)
LMWH: Enoxaparin/Dalteparin
Dosing/Monitoring
Enoxaparin
1mg/kg SC BID or 1.5-2.0 mg/kg SC daily
*renal adj req for both
Higher risk patients that may require monitoring: CCEO at 30
– obese pts
– renal, CrCl <30
– elderly/children
– cancer
Use anti-factor Xa
- labs: hemoglobin, hematocrit, platelet count
Heparin Induced Thrombocytopenia
- Platelet count drop of 50% from baseline
- Venous or arterial thrombosis
- Skin lesions at heparin injection sites
- Acute systemic reactions that occur after a bolus of IV heparin
*Prompt DC of ALL heparin products
-Initiation of argatroban/bivalirudin (ICU) or fondaparinux (= if stable) as alt
-Platelet count usually recovers in 4-7 days
4 Ts (thrombocyto/time/thrombosis/other)
- ≤3: low for HIT
– 4-5: intermediate
– 6-8: high for HIT
Fondaparinux (Arixtra®)
- < 50 kg: 5 mg SC daily
- 50-100 kg: 7.5 mg SC daily
- > 100 kg: 10 mg SC daily
CLcr < 30 mL/min: CONTRAINDICATED