Frontiers in Surgery (Apr 2024)

Recurrent gastric antral vascular ectasia: a single center experience

  • Andrea Cavallaro,
  • Antonio Zanghì,
  • Maria Di Vita,
  • Vito Emanuele Catania,
  • Giovanni Longo,
  • Emanuele Lo Menzo,
  • Roberta Granata,
  • Maria Rosaria Valenti,
  • Alessandro Cappellani,
  • Simone Di Majo

DOI
https://doi.org/10.3389/fsurg.2024.1356409
Journal volume & issue
Vol. 11

Abstract

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IntroductionGastric antral vascular ectasia (GAVE) is a rare cause of chronic or acute gastrointestinal bleeding. This condition accounts for ∼4% of upper gastrointestinal bleeding cases. This disease is often associated with systemic diseases, such as liver cirrhosis, chronic kidney failure, autoimmune conditions, diabetes mellitus, hypothyroidism, and cardiovascular diseases. However, its etiopathogenesis remains controversial.Materials and methodWe retrospectively reviewed the cases of GAVE treated at our digestive surgery unit. A total of nine patients were identified with a male/female ratio of 1.25:1 and an average age of 75.51 years (SD ± 9.85). All patients underwent endoscopic argon plasma coagulation (APC) treatment. At the time of the review, data on eight patients were available after 36 months of follow-up.ResultsAPC appears to be safe and effective for hemostasis of bleeding vascular ectasia. Only one (11.1%) patient required surgical intervention due to hemodynamic instability after multiple unsuccessful endoscopic treatments. No intraoperative and postoperative complication or bleeding relapse was experienced.DiscussionBased on our findings, we concluded that endoscopic APC is technically simple, but requires multiple re-interventions due to the incidence of relapses. Furthermore, larger randomized studies should be conducted to assess the role of elective surgery as the first intervention in stable patients with severe pathology and the timing of surgery after failed endoscopic treatment.

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