Tirzepatide and reduced risk of pulmonary embolism and deep vein thrombosis: a multicenter U.S. cohort study - Scorecard - MDSpire

Tirzepatide and reduced risk of pulmonary embolism and deep vein thrombosis: a multicenter U.S. cohort study

  • By

  • Fredy Kahkedjian

  • Jaffer Shah

  • Firas Kreidieh

  • July 1, 2026

  • 0 min

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Clinical Scorecard: Tirzepatide's Impact on the Incidence of Pulmonary Embolism and Deep Vein Thrombosis: Findings from a Multicenter Cohort Study in the U.S.

At a Glance

CategoryDetail
ConditionVenous thromboembolism (VTE)
Key MechanismsTirzepatide is a dual glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist.
Target PopulationAdults with type 2 diabetes and overweight or obesity.
Care SettingPopulation-based retrospective cohort study.

Key Highlights

  • Tirzepatide use was associated with a significantly lower 12-month risk of pulmonary embolism compared to lifestyle intervention alone.
  • The risk of deep vein thrombosis was also significantly lower with tirzepatide use.
  • No significant difference was observed for superficial vein thrombosis.
  • Findings remained significant in a 90-day landmark analysis.
  • Tirzepatide showed a lower risk of deep vein thrombosis compared to semaglutide.

Guideline-Based Recommendations

Diagnosis

  • Monitor for signs and symptoms of venous thromboembolism in patients with type 2 diabetes and obesity.

Management

  • Consider tirzepatide as a treatment option for patients with type 2 diabetes and obesity, weighing thromboembolic risks.

Monitoring & Follow-up

  • Regularly assess patients for thromboembolic events during and after treatment initiation.

Risks

  • Be aware of the potential for thromboembolic events, particularly in patients with risk factors.

Patient & Prescribing Data

Adults with type 2 diabetes and overweight or obesity.

Tirzepatide may reduce the risk of pulmonary embolism and deep vein thrombosis in this population.

Clinical Best Practices

  • Utilize propensity score matching to control for confounding variables in observational studies.
  • Conduct regular follow-ups to monitor for adverse events in patients starting new therapies.

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