Hamza Kassimi, Alaoui Hassane, Youssef Halhoul, Ahmed Fakri, Khalil Abouelalaa, Abderrahmane ELwali, Abdelilah Radi, Hicham Balkhi, Mustapha Bensghir
Journal: Medpeer Publisher
ISSN: 3066-2737
Volume: 2
Issue: 10
Date of Publication: 2025/10/24
Glanzmann’s thrombasthenia (GT) is a rare inherited platelet disorder causing defective aggregation and severe bleeding risk. We report a seven-year-old boy with GT who underwent circumcision and dental extraction under sevoflurane sedation. A single intravenous dose of recombinant activated factor VII (rFVIIa) 90 µg/kg was given preoperatively. The procedure and recovery were uneventful, with no bleeding or transfusion required. rFVIIa proved effective in achieving hemostasis by bypassing the platelet defect and promoting thrombin generation. Anesthetic management should avoid invasive or bleeding-prone techniques, emphasizing multidisciplinary coordination to ensure patient safety.
Glanzmann’s thrombasthenia, rFVIIa, anesthesia, pediatric, bleeding disorder
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