Anti-coagulant therapy with dabigatran for cystic fibrosis patients

Manvi Bansal1, Clement L Ren1

  • 1Division of Pediatric Pulmonology, Golisano Children's Hospital, University of Rochester, Rochester, New York.

Pediatric Pulmonology
|April 30, 2016
PubMed

Insights

Cystic fibrosis (CF) patients face higher risks of blood clots, particularly with central venous catheters. This study suggests dabigatran is a viable oral anticoagulant option for CF patients, offering an alternative to traditional therapies.

Area of Science:

  • Pulmonology
  • Hematology
  • Pharmacology

Background:

  • Patients with cystic fibrosis (CF) have an elevated risk of venous thromboembolism (VTE), often linked to central venous catheter use.
  • Traditional anticoagulants like coumarins and low molecular weight heparin present administration challenges in CF patients.

Observation:

  • This case series reports the successful long-term anticoagulation therapy using dabigatran in two CF patients.
  • Dabigatran, an oral direct thrombin inhibitor, was used as an alternative anticoagulant medication.

Findings:

  • Dabigatran was successfully administered for long-term anticoagulation in CF patients.
  • The study demonstrates the feasibility of using dabigatran in this specific patient population.

Implications:

  • Dabigatran represents a potential alternative oral anticoagulant for managing VTE in cystic fibrosis patients.
  • Further research is warranted to confirm the safety and efficacy of dabigatran in a larger CF cohort.

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