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Assessment of bleeding risk in low-weight patients receiving prophylactic subcutaneous unfractionated heparin
Andrew J Jatis1, Scott D Nei1, Joseph J Zieminski1
1Department of Pharmacy, Mayo Clinic, Rochester, MN, USA.
Insights
Bleeding risk in low-weight patients receiving unfractionated heparin for VTE prophylaxis is low. However, ICU admission at the start of treatment may increase bleeding risk, warranting further investigation.
Area of Science:
- Internal Medicine
- Pharmacology
- Critical Care Medicine
Background:
- Underweight patients may face higher bleeding risks during venous thromboembolism (VTE) prophylaxis.
- Identifying patient-specific bleeding risk factors in this population is crucial.
- This study focuses on low-weight patients receiving subcutaneous unfractionated heparin (SQH) for VTE prophylaxis.
Purpose of the Study:
- To determine the incidence of bleeding in low-weight patients receiving SQH for VTE prophylaxis.
- To identify risk factors associated with bleeding in this patient group.
- To inform clinical practice regarding VTE prophylaxis in underweight individuals.
Main Methods:
- A single-center, retrospective, nested case-control study was conducted.
- Low-weight patients (<= 60 kg) receiving SQH for VTE prophylaxis for at least 48 hours were included.
- Cases (bleeding events) and controls (no bleeding) were matched 1:3 for age, sex, service, and time at risk.
Main Results:
- A total of 3761 patients were analyzed, with 38 cases of clinically relevant bleeding.
- The bleeding incidence was 1% by hospital day 6 and 2.8% by hospital day 14.
- Intensive Care Unit (ICU) admission at SQH initiation was associated with increased bleeding risk (OR 2.97).
Conclusions:
- Clinically relevant bleeding is uncommon in low-weight patients on prophylactic SQH.
- ICU admission at the start of SQH therapy may be a risk factor for bleeding.
- Further research is needed to identify additional risk factors and explore dose adjustments in this population.
Background:
Underweight patients may be at an increased risk of bleeding while receiving venous thromboembolism (VTE) prophylaxis. Additional evidence is needed to identify patient-specific factors associated with bleeding. The objective of the study was to describe the incidence and identify risk factors associated with bleeding in low-weight (⩽ 60 kg) adult patients receiving subcutaneous unfractionated heparin (SQH) for VTE prophylaxis.
Methods:
This was a single-center, retrospective, nested case-control study of low-weight patients receiving SQH for VTE prophylaxis for ⩾ 48 hours. Cases, patients with clinically relevant bleeding while receiving SQH, and controls, patients without a bleeding event, were matched in a 1:3 ratio for age, sex, primary service (surgical or medical), and time at risk of bleeding on SQH to determine factors associated with bleeding.
Results:
A total of 3761 patients met the inclusion criteria, of which 38 cases of clinically relevant bleeding were identified. The bleeding incidence was 1% at hospital day 6 and 2.8% at hospital day 14. Most patients in this study (69%) received SQH 5000 units three times daily. ICU admission at SQH start was associated with bleeding, OR 2.97 (95% CI 1.21-7.29).
Conclusion:
Bleeding in low-weight patients on prophylactic SQH was uncommon. Patients admitted to the ICU at time of SQH start may be at a higher risk of bleeding. Further studies are needed to detect additional risk factors associated with bleeding and investigate the effects of reduced dosing in this population.
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