Table 2.

Low-molecular-weight heparin in patients with antiphospholipid syndrome

Clinical indications for consideration of LMWH in patients with APS:
• Anticoagulant-refractory thrombotic APS (anticoagulant is warfarin/VKA)
• CAPS
• Pregnancy
• Warfarin/VKA intolerance
• Bleeding concerns with warfarin/VKA
Dosing:
Weight-based dosing, without anti-Xa monitoring, is generally appropriate
Careful review of LMWH dose during periods of thrombocytopenia 
Monitoring:
Monitor platelets for HIT:
• during LMWH use after major surgery or major trauma (intermediate risk, 0.1%-1.0%)
• not required in medical or obstetric patients or after minor surgery or trauma (low risk, <0.1%)45
ASH VTE guidance suggests (with low/very low certainty) against anti-Xa monitoring in:
• pregnancy
• renal impairment (creatinine clearance <30mL/min), favoring fixed dose reduction per manufacturer's recommendations
• obesity, favoring dosing by actual body weight (uncapped)
Limitations of chromogenic anti-Xa assays for monitoring LMWH include:
• clinical utility uncertain
• not universally available
• suboptimal reproducibility and interlaboratory variation 
Clinical indications for consideration of LMWH in patients with APS:
• Anticoagulant-refractory thrombotic APS (anticoagulant is warfarin/VKA)
• CAPS
• Pregnancy
• Warfarin/VKA intolerance
• Bleeding concerns with warfarin/VKA
Dosing:
Weight-based dosing, without anti-Xa monitoring, is generally appropriate
Careful review of LMWH dose during periods of thrombocytopenia 
Monitoring:
Monitor platelets for HIT:
• during LMWH use after major surgery or major trauma (intermediate risk, 0.1%-1.0%)
• not required in medical or obstetric patients or after minor surgery or trauma (low risk, <0.1%)45
ASH VTE guidance suggests (with low/very low certainty) against anti-Xa monitoring in:
• pregnancy
• renal impairment (creatinine clearance <30mL/min), favoring fixed dose reduction per manufacturer's recommendations
• obesity, favoring dosing by actual body weight (uncapped)
Limitations of chromogenic anti-Xa assays for monitoring LMWH include:
• clinical utility uncertain
• not universally available
• suboptimal reproducibility and interlaboratory variation 

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