“…18 Although controversial, special circumstances that may warrant anti-Xa activity monitoring include renal or hepatic insufficiency, extremes of body weight (< 40 kg, > 150 kg), newborns and children, pregnancy, prolonged therapy (> 7-10 days), and the presence of other factors that may increase the risk of bleeding complications such as recent trauma or surgery. 5,10,[22][23][24] Although appropriate timing, frequency, and desired therapeutic range of anti-Xa activity are not clearly defined and remain controversial, peak anti-Xa activity (4 hrs after subcutaneous injection) generally is considered a more useful predictor of LMWH safety and efficacy than trough (just before dose) activity. 18 For prevention of venous thromboembolism (VTE), a peak anti-Xa level of 0.1-0.2 U/ml 4 hours after subcutaneous injection of an LMWH is recommended.…”