Hospital Prophylaxis for Adult Inpatients
DVT Prophylaxis
For acutely ill hospitalized medical patients at increased risk of thrombosis, pharmacologic prophylaxis with LMWH, low-dose unfractionated heparin (LDUH), or fondaparinux should be administered throughout hospitalization. 1
Standard Prophylactic Regimens
Recommended first-line options include:
- Enoxaparin 40 mg subcutaneously once daily 1, 2
- Unfractionated heparin 5000 units subcutaneously every 8 hours (preferred in cancer patients and provides more consistent anticoagulant effect than twice-daily dosing) 1, 2, 3
- Dalteparin 5000 IU subcutaneously once daily 1, 2
- Fondaparinux 2.5 mg subcutaneously once daily 1
Special Population Adjustments
Renal impairment (CrCl <30 mL/min):
- Reduce enoxaparin to 30 mg subcutaneously once daily 2, 4
- Unfractionated heparin is preferred as it's primarily metabolized by the liver 2, 5
- Fondaparinux is contraindicated in severe renal insufficiency 5
Obesity (BMI >30 kg/m²):
- Consider enoxaparin 40 mg subcutaneously every 12 hours or weight-based dosing at 0.5 mg/kg every 12 hours 2, 5, 4
Cancer patients:
Critically ill patients:
- LMWH or LDUH is recommended over no prophylaxis 1
Duration of Prophylaxis
Continue DVT prophylaxis until the patient is fully ambulatory or hospital discharge, with a minimum duration of 7-10 days for surgical patients. 1, 2, 4, 6
- Do not extend prophylaxis beyond the period of immobilization or acute hospital stay for most medical patients 1
- Selected high-risk patients may benefit from extended prophylaxis of 14-30 days post-discharge, particularly those with multiple VTE risk factors or elevated D-dimer 4
Contraindications and High Bleeding Risk
For patients who are actively bleeding or at high risk for major bleeding, anticoagulant thromboprophylaxis is contraindicated. 1
- Use mechanical prophylaxis with graduated compression stockings or intermittent pneumatic compression instead 1
- When bleeding risk decreases and VTE risk persists, substitute pharmacologic for mechanical prophylaxis 1
Do not use prophylaxis in low-risk hospitalized medical patients. 1
GI Prophylaxis (Stress Ulcer Prophylaxis)
While the provided evidence focuses primarily on DVT prophylaxis, limited guidance on GI prophylaxis is available from the FDA drug label for ranitidine. 7
For hospitalized patients requiring stress ulcer prophylaxis:
- Ranitidine 50 mg IV every 6-8 hours can be administered via intermittent bolus (diluted to ≤2.5 mg/mL, injected over 5 minutes) or intermittent infusion (diluted to ≤0.5 mg/mL, infused over 15-20 minutes) 7
- Continuous IV infusion at 6.25 mg/hour is an alternative for maintenance therapy 7
Dose adjustment for renal impairment (CrCl <50 mL/min):
- Reduce to 50 mg every 18-24 hours, with frequency potentially increased to every 12 hours if clinically required 7
Critical Clinical Pitfalls
Timing considerations:
- Do not administer anticoagulants too close to neuraxial anesthesia due to increased risk of spinal hematoma 2
- For surgical patients, enoxaparin should be started 2-4 hours preoperatively or 10-12 hours preoperatively 2
Monitoring:
- Routine anti-Xa monitoring is not required for prophylactic doses in most patients 2
- Monitor platelet counts every 2-3 days from day 4 to day 14 for patients at risk of heparin-induced thrombocytopenia (HIT), particularly with UFH where risk may be as high as 5% in orthopedic surgery patients 5
Common errors to avoid:
- Do not discontinue DVT prophylaxis prematurely before mobility is restored, even if the primary condition improves 4
- Do not use standard LMWH dosing in severe renal impairment without dose reduction 2, 4
- Do not forget to assess bleeding risk before initiating prophylaxis, particularly in patients with active gastroduodenal ulcer, recent bleeding, or platelet count <50 × 10⁹/L 4