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Modified: Friday, July 20, 2007

GUIDELINES FOR DOSING AND MONITORING ENOXAPARIN

Table of Contents

  1. General Dosing Guidelines
  2. Dosing Adjustments in Obesity
  3. Dosing in Renal Impairment
  4. Short Term Monitoring
  5. Long Term Monitoring
  6. Use in Pregnancy

===================================================

I. General Dosing Guidelines

A. Initial treatment of acute thrombosis:

  • Enoxaparin 1mg/kg SQ q12h until minimum course of 5 days has been completed and INR is greater than 2.0 (1.5mg/kg q24h may also be used in pts who are not obese [BMI > 27] and who do not have malignancy).

    B. Initial anticoagulation in patients with atrial fibrillation, heart valve replacement, LV thrombus, or other cardiovascular indications for anticoagulation:

    • Enoxaparin 1mg/kg SQ q12h.

    C. Bridge therapy during prolonged periods of under anticoagulation:

    • Enoxaparin 1mg/kg SQ q12h until INR > lower limit of therapeutic range (1.5mg/kg q24h may also be used in patients whose indication for anticoagulation is DVT/PE or other non-cardiovascular indication for anticoagulation, including patients with malignancy).

    D. Bridge therapy before and after invasive or dental procedures:

    • Enoxaparin 1mg/kg SQ q12h initiated when INR < lower limit of therapeutic range and discontinued when INR > lower limit of therapeutic range (1.5mg/kg q24h may also be used in patients whose indication for anticoagulation is DVT/PE or other non-cardiovascular indication for anticoagulation, including patients with malignancy).

    E. Long term use in place of warfarin:

    • Enoxaparin 1mg/kg q12h (1.5mg/kg q24h may also be used in patients whose indication for anticoagulation is DVT/PE or other acute non-cardiovascular indication for warfarin, including patients with malignancy).

    II. Dosage Adjustments in Obesity

    A. Use Total Body Weight (TBW) up to 190kg.

    B. If > 190kg:

      1. AntiXa level monitoring available:
        • Use TBW and adjust dose downward if necessary based on antiXa levels
      2. AntiXa level monitoring NOT available
        • Use TBW and adjust dose downward if necessary if bleeding occurs

    III. Dosing in Renal Impairment

    A. If no antiXa monitoring available: Avoid use if Clcr < 30

    B. If antiXa monitoring is available, consider the following initial dosing and adjust as necessary based on peak antiXa activity levels:

    • Clcr > 60: 1mg/kg q12h
    • Clcr 30-60: 0.85mg/kg q12h
    • Clcr < 30: 1mg/kg q24h

    C. Trough antiXa monitoring may be indicated to evaluate accumulation at the end of the dosing interval. If peak antiXa levels suggest the need for dosing adjustment, consider the following nomogram:

    ANTIXa LEVEL
    (U/mL)
    HOLD NEXT DOSE
    DOSAGE CHANGE
    NEXT ANTIXa LEVEL
    < 0.35

    NO

    Increase 25%
    4hrs after next dose
    0.35-0.49
    NO
    Increase 10%
    4hrs after next dose
    0.5-1.0
    NO
    NO
    Next day, then within 1 week
    1.1-1.5
    NO
    Decrease 20%
    Before next dose
    1.6-2.0
    For 3 hrs
    Decrease 30%
    Before next dose and 4hrs after next dose
    > 2.0
    Until antiXa level
    < 0.5 U/mL
    Decrease 40%
    Before next dose and q12h until antiXa level < 0.5 U/mL

    IV. Short Term Monitoring Guidelines

    A. Baseline labs:

    • PT/aPTT
    • HCT
    • Plt and q2-3 days during the first 2 weeks of LMWH therapy
    • Scr

    B. Peak antiXa activity:

    • 3 to 4 hrs after dose in patients with:
      • renal impairment (Clcr< 60)
      • obesity (wt > 190kg)
      • unexpected hemorrhage.
    • Check after 3rd dose and again if adjustment required.
    • Goal:
      • 0.5-1.0 U/mL for bid dosing
      • 1.0-2.0 U/mL for qd dosing

    C. Trough antiXa activity:

    • At end of dosing interval
    • Check before 4th dose and again if adjustment required
    • Goal: < 0.5 U/mL

    V. Long Term Monitoring Guidelines

    Although LMWHs typically do not require therapeutic monitoring, under certain circumstances (changing weight, changing renal function, changing health status, etc), patients undergoing long-term therapy may require therapeutic monitoring. Suggests for long-term monitoring under these and other circumstances are described below.

    A. Peak and/or trough antiXa activity: Check at 7-14 days, then q 1-3 months.

    B. Scr: Check q 1-3 months.

    D. Clcr: Calculate q 1-3 months (adjust dose as necessary).
    E. Patient weight: Check q 1-3 months (adjust dose as necessary)
    F. Platelets: Check q 1-3 months (routine labs acceptable)

    G: Hct: Check q 1-3 months (routine labs acceptable)

    VI. Use in Pregnancy

    A. 1st and 2nd trimester

    • Peak/trough antiXa activity: Check q month.
    • Scr/Clcr: Check/calculate q month.
    • Patient weight: Check q month.
    • Hct: Periodic evaluation.
    • Platelets: Periodic evaluation.

    B. 3rd trimester

    • Peak/trough antiXa activity: Check q 2 weeks.
    • Scr/Clcr: Check/calculate q 2 weeks.
    • Patient weight: Check q 2 weeks.
    • Hct: Periodic evaluation.
    • Platelets: Periodic evaluation.
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