Thromboembolic Disorders: Treatments

Thromboembolic Disorders: Treatments
Thromboembolic Disorders: Treatments
Generic Brand Form Indication Adult Dose*
ANTICOAGULANTS
Anticoagulant Proteins
protein C concentrate [human] Ceprotin inj Venous thrombosis and purpura fulminans in severe congenital Protein C deficiency Give by IV infusion only. <10kg: max rate 0.2mL/kg/min; ≥10kg: max rate 2mL/min. Individualize. Acute episodes/short term prophylaxis: initially 100–120 IU/kg, then 60–80 IU/kg every 6hrs for 3 doses (adjust dose to maintain target peak protein C activity of 100%); maintenance: 45–60 IU/kg every 6 or every 12hrs (maintain trough protein C level above 25% for duration of therapy); continue until desired anticoagulation achieved. Long-term prophylaxis: 45–60 IU/kg every 12hrs (maintain trough protein C level above 25%).
Antithrombins
antithrombin III [human] Thrombate III inj Hereditary antithrombin III (AT-III) deficiency in surgical or obstetrical procedures and thromboembolism Infuse over 10–20mins. Dose (units required) = [desired (% of normal) – baseline (% of normal) AT-III level] × weight (kg)/1.4. Loading dose: increase AT-III to 120% of normal. Subsequent dose should be based on AT-III levels obtained 20min post-infusion, every 12hrs, and before the next dose. Maintain AT-III levels at 80–120% of normal for 2–8 days. See full labeling.
Coumarins
warfarin tabs DVT/PE prophylaxis or treatment Initially 2–5mg daily. Usual maintenance: 2–10mg once daily. CYP2C9 or VKORC1 enzyme variations, elderly, debilitated, Asians: use lower initial and maintenance doses. Closely monitor INR; adjust dose based on response and clinical condition.
Atrial fibrillation and/or cardiac valve replacement; post-MI
Direct Thrombin Inhibitors
argatroban inj Prophylaxis and treatment of thrombosis in HIT Discontinue heparin and obtain baseline aPTT before initiation. Initially 2mcg/kg/min by IV infusion; check aPTT 2hrs after starting. Titrate to 1.5–3x baseline aPTT (max 100sec); max 10mcg/kg/min.
PCI with or at risk of HIT 350mcg/kg bolus by large bore IV line over 3–5mins, then infuse at 25mcg/kg/min. Check ACT 5–10mins after bolus; titrate based on ACT to therapeutic ACT of 300–450secs (see full labeling).
bivalirudin Angiomax inj PCI with HIT/HITTS Give with aspirin. Initiate 0.75mg/kg IV bolus (may give additional bolus of 0.3mg/kg after 5mins, if needed based on ACT value), followed by an infusion of 1.75mg/kg/hr for the duration of procedure. May continue infusion at 1.75mg/kg/hr for up to 4hrs post-procedure in patients with STEMI. Renal impairment (CrCl <30mL/min): reduce infusion rate to 1mg/kg/hr; (hemodialysis): 0.25mg/kg/hr.
dabigatran Pradaxa caps DVT/PE treatment; reduce DVT/PE recurrence CrCl>30mL/min: 150mg twice daily (if treatment, give after 5–10 days of parenteral anticoagulation). CrCl ≤30mL/min or on dialysis: not recommended. CrCl <50mL/min with concomitant P-gp inhibitors: avoid.
DVT/PE prophylaxis post hip replacement CrCl>30mL/min: 110mg for first day (given 1–4hrs post surgery and after hemostasis achieved), then 220mg daily for 28–35 days. CrCl ≤30mL/min or on dialysis: not recommended. CrCl <50mL/min with concomitant P-gp inhibitors: avoid.
Reduce risk of stroke and systemic embolism in non-valvular AF CrCl>30mL/min: 150mg twice daily. Renal impairment (CrCl 15–30mL/min): 75mg twice daily; CrCl<15mL/min or on dialysis: not recommended. Moderate renal impairment (CrCl 30–50mL/min) with concomitant dronedarone or systemic ketoconazole: 75mg twice daily. CrCl <30mL/min with concomitant P-gp inhibitors: avoid.
Factor Xa Inhibitors
apixaban Eliquis tabs DVT/PE treatment 10mg twice daily for 7 days, then 5mg twice daily. Concomitant with combined P-gp and strong CYP3A4 inhibitors: reduce dose by 50%.
Reduce DVT/PE recurrence 2.5mg twice daily after at least 6mos of DVT/PE treatment. Concomitant with combined P-gp and strong CYP3A4 inhibitors: avoid.
DVT prophylaxis post hip or knee replacement 2.5mg twice daily; initially give 12–24hrs after surgery. Hip: treat for 35 days. Knee: treat for 12 days. Concomitant with combined P-gp and strong CYP3A4 inhibitors: avoid.
Reduce risk of stroke and systemic embolism in non-valvular AF 5mg twice daily; 2.5mg twice daily if patient has any 2 of the following: age ≥80yrs, ≤60kg, or creatinine ≥1.5mg/dL. Concomitant with combined P-gp and strong CYP3A4 inhibitors: reduce dose by 50%; if already on 2.5mg twice daily, avoid.
edoxaban Savaysa tabs Reduce risk of stroke and systemic embolism in non-valvular AF CrCl >50mL/min: 60mg once daily; CrCl 15–50mL/min: 30mg once daily.
DVT/PE Treatment CrCl >50mL/min: 60mg once daily after 5-10 days of initial parenteral anticoagulant; CrCl 15–50mL/min, ≤60kg, or concomitant P-gp inhibitors: 30mg once daily.
fondaparinux Arixtra inj DVT/PE treatment (with warfarin) <50kg: 5mg; 50–100kg: 7.5mg; >100kg: 10mg.Give SC once daily for at least 5 days and until INR 2–3 (usually 5–9 days; max 26 days); start warfarin within 72hrs.
DVT prophylaxis post surgery 2.5mg SC once daily (after hemostasis is established, no earlier than 6–8hrs post-op) for 5–9 days. Hip or knee replacement: max 11 days. Hip fracture: give for up to 24 more days (max 32 days total). Abdominal: max 10 days.
rivaroxaban Xarelto tabs DVT/PE treatment 15mg twice daily with food for first 21 days, then 20mg once daily for the remaining treatment. CrCl<15mL/min: avoid.
Reduce DVT/PE recurrence 10mg once daily (after ≥6mos of standard anticoagulant therapy). CrCl<15mL/min: avoid.
DVT prophylaxis post hip or knee replacement 10mg once daily (6–10hrs after surgery once hemostasis established) for 35 days (hip) or 12 days (knee). CrCl<15mL/min: avoid.
VTE prophylaxis in acutely ill medical patients (in hospital and after discharge) 10mg once daily for 31–39 days. CrCl<15mL/min: avoid.
Reduce risk of stroke and systemic embolism in non-valvular AF CrCl>50mL/min: 20mg once daily with PM meal; CrCl ≤50mL/min: 15mg once daily with PM meal.
Reduce risk of major CV events in chronic CAD or PAD (with aspirin) 2.5mg twice daily with aspirin
Heparins
heparin sodium inj VTE, peripheral arterial embolism, coagulopathy treatment See full labeling. Individualize based on lab results and disease.
VTE, peripheral arterial embolism prophylaxis
AF with embolization
Anticoagulant in surgery, transfusions, extracorporeal circulation, dialysis
Low Molecular Weight Heparins
dalteparin Fragmin inj Extended VTE treatment (cancer patients) 200 IU/kg SC once daily for 30 days, then 150 IU/kg SC once daily for 2–6mos; max 18,000 IU/day.
DVT prophylaxis Hip replacement: post-op start: 2500 IU 4–8hrs after surgery, then 5000 IU once daily (≥6hrs after 1st dose); pre-op start day of surgery: 2500 IU within 2hrs before surgery, then 2500 IU 4–8hrs after surgery, then 5000 IU once daily (≥6hrs after previous dose); pre-op evening before surgery: 5000 IU 10–14hrs before surgery, then 5000 IU 4–8hrs after surgery, then 5000 IU once daily (allow 24hrs between doses); for all hip replacement regimens: usually treat for 5–10 days; max up to 14 days post-op. Abdominal surgery: 2500 IU once daily (usually for 5–10 days) starting 1–2hrs pre-op; for high risk of thromboembolism (eg, malignancy): see full labeling. Severely restricted mobility: 5000 IU once daily (usually for 12–14 days).
Prophylaxis of ischemic complications in unstable angina and non-Q-wave MI 120 IU/kg SC (max 10,000 IU) every 12hrs until stabilized (usually 5–8 days), with aspirin 75–165mg once daily.
enoxaparin Lovenox inj DVT treatment: with or without PE (inpatient); without PE (outpatient) Inpatient: 1mg/kg SC every 12hrs or 1.5mg/kg SC once daily with warfarin. Outpatient: 1mg/kg SC every 12hrs with warfarin. Both: start warfarin usually within 72hrs, continue enoxaparin at least 5 days and until INR 2–3 (usually 7 days; usual max 17 days). CrCl <30mL/min: 1mg/kg SC once daily.
DVT prophylaxis Knee replacement: 30mg SC every 12hrs for 7–10 days; max 14 days (1st dose 12–24hrs post-op). Hip replacement: 30mg SC every 12hrs (1st dose 12–24hrs post-op), or 40mg SC once daily (1st dose 9–15hrs pre-op), for 7–10 days, then 40mg SC once daily for 3wks. Abdominal surgery: 40mg SC once daily (1st dose 2hrs pre-op) for 7–10 days; max 12 days. Severely restricted mobility due to acute illness: 40mg SC once daily for 6–11 days, max 14 days. CrCl <30mL/min: 30mg SC once daily.
Prophylaxis of ischemic complications in unstable angina and non-Q-wave MI 1mg/kg SC every 12hrs for at least 2 days, with aspirin 100–325mg once daily, until stable (usually 2–8 days; usual max 12.5 days). CrCl <30mL/min: 1mg/kg SC once daily.
Acute STEMI <75yrs: 30mg IV bolus + 1mg/kg SC, then 1mg/kg SC every 12hrs (max 100mg for 1st 2 doses only, then 1mg/kg dosing for remaining doses). ≥75yrs: 0.75mg/kg SC every 12hrs (no bolus; max 75mg for 1st 2 doses only, then 0.75mg/kg dose for remaining doses). Both: give with aspirin 75–325mg once daily; treat usually for 8 days or until hospital discharge. CrCl <30mL/min: see full labeling.
ANTIPLATELETS
anagrelide Agrylin caps Thrombocythemia due to myeloproliferative disorders Initially 0.5mg 4 times daily or 1mg twice daily for ≥1wk. May increase dose by 0.5mg/day weekly to maintain normal platelet count; max 10mg/day or 2.5mg/dose. Moderate hepatic impairment: initially 0.5mg/day.
dipyridamole + aspirin caps Reduce risk of stroke in TIA or ischemic stroke 1 cap twice daily (AM and PM). Alternative if intolerable headaches: switch to 1 cap at bedtime and low-dose aspirin in AM; return to usual regimen within 1wk.
Glycoprotein IIb/IIIa (GP IIb/IIIa) Inhibitors
eptifibatide inj ACS 180mcg/kg IV bolus, then continuous IV infusion of 2mcg/kg/min until discharge or CABG surgery, up to 72hrs. If PCI planned, continue infusion until discharge, or for up to 18−24hrs after procedure, whichever comes first, allowing up to 96hrs of therapy. CrCl <50mL/min: reduce rate to 1mcg/kg/min. Concomitant use with aspirin and heparin.
PCI, including those undergoing intracoronary stenting 180mcg/kg IV bolus, then 2mcg/kg/min infusion; repeat 180mcg/kg IV bolus 10mins after 1st bolus; continue infusion until discharge, or for up to 18–24hrs, whichever comes first, minimum 12-hr infusion recommended. CrCl <50mL/min: reduce rate to 1mcg/kg/min. Concomitant use with aspirin and heparin.
tirofiban Aggrastat inj Reduce thrombotic CV events in non-ST elevation ACS 25mcg/kg IV within 5mins, then 0.15mcg/kg/min for up to 18hrs. Renal impairment (CrCl ≤60mL/min): 25mcg/kg IV within 5mins, then 0.075mcg/kg/min for up to 18hrs.
P2Y12 Platelet Inhibitors
cangrelor Kengreal inj Reduce risk of periprocedural MI, repeat coronary revascularization, and stent thrombosis Patients not treated with other P2Y12 platelet inhibitor and glycoprotein IIb/IIIa inhibitor: 30mcg/kg IV bolus prior to PCI, immediately followed by 4mcg/kg/min IV infusion; continue infusion for ≥2hrs or for duration of PCI, whichever is longer.
clopidogrel Plavix tabs Reduce risk of MI and stroke in ACS Initially 300mg loading dose, then 75mg once daily. Take with aspirin.
Reduce risk of MI and stroke in recent MI, stroke or PAD 75mg once daily.
prasugrel Effient tabs Reduce thrombotic CV events in ACS 60mg loading dose, then 10mg once daily. <60kg: consider 5mg once daily. Take with aspirin 75mg–325mg daily.
ticagrelor Brilinta tabs Reduce risk of CV death, MI and stroke in ACS or history of MI Initially 180mg loading dose, followed by 90mg twice daily for 1st yr, then 60mg twice daily thereafter. Take with aspirin 75–100mg daily.
Stent thrombosis prophylaxis
Reduce risk of a first MI or stroke in CAD 60mg twice daily. Take with aspirin 75–100mg daily.
Reduce risk of stroke in acute ischemic stroke or high-risk TIA Initially 180mg loading dose, followed by 90mg twice daily for up to 30 days. Take with aspirin 300–325mg loading dose, then aspirin 75–100mg daily.
ticlopidine tabs Reduce risk of thrombotic stroke (aspirin-intolerant) 250mg twice daily with food.
Protease-Activated Receptor-1 (PAR-1) Antagonist
vorapaxar Zontivity tabs Reduce thrombotic CV events in MI or PAD 2.08mg once daily. Take with aspirin and/or clopidogrel based on indications.
THROMBOLYTICS
Tissue Plasminogen Activators (tPA)
alteplase Activase inj Acute MI Max 100mg total dose. Accelerated infusion (≤67kg): 15mg IV bolus, then 0.75mg/kg (max 50mg) infused over 30mins, then 0.5mg/kg (max 35mg) over 60mins; (>67kg): 15mg IV bolus, then 50mg infused over 30mins, then 35mg infused over 60mins; 3-hour infusion (≥65kg): 60mg infused in the 1st hr (of which 6–10mg is given as bolus), then 20mg/hr for 2hrs; (<65kg): 1.25mg/kg over 3hrs (of which 0.075mg/kg as bolus, 0.675mg/kg for the rest of the 1st hr, then 0.25mg/kg/hr for 2hrs).
Acute ischemic stroke Initiate within 3hrs of symptom onset. 0.9mg/kg (max 90mg total dose) infused over 60min with 10% of total dose given as initial IV bolus over 1min.
Acute massive PE 100mg IV infusion over 2hrs. Initiate parenteral anticoagulation near the end of or immediately after Activase infusion when PTT or thrombin time returns to twice normal or less.
reteplase Retavase inj Acute STEMI Start as soon as possible after onset of STEMI. 10 units IV over 2mins; repeat with 10 units 30mins after the first dose.
tenecteplase TNKase inj Acute MI Start treatment soon after onset of AMI. Give as single IV bolus over 5sec. <60kg: 30mg; ≥60–<70kg: 35mg; ≥70–<80kg: 40mg; ≥80–<90kg: 45mg; ≥90kg: 50mg. Max: 50mg.
NOTES

Key: ACS = acute coronary syndrome; ACT = activated clotting time; AF = atrial fibrillation; AMI = acute myocardial infarction; CAD = coronary artery disease; CV = cardiovascular; DVT = deep vein thrombosis; GPI = glycoprotein IIb/IIIa inhibitors; HIT = heparin-induced thrombocytopenia; HITTS = HIT and thrombosis syndrome; MI = myocardial infarction; NSTEMI = non-ST-elevation MI; PAD = peripheral artery disease; PCI = percutaneous coronary intervention; PE = pulmonary embolism; PM = evening; PTCA = percutaneous transluminal coronary angioplasty; SC = subcutaneous; STEMI = ST-elevation MI; TIA = transient ischemic attack; VTE = venous thromboembolism

*For children’s dosing, see drug monograph or full labeling.
Associated with a Black Box Warning. Please see full drug labeling.

Not an inclusive list of medications, official indications, and/or dosing details. Please see drug monograph at www.eMPR.com and/or contact company for full drug labeling.

(Rev. 6/2023)