Thromboembolic Disorders: Treatments | ||||
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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. 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) |
Thromboembolic Disorders: Treatments