Esophageal stenting is a well-established treatment modality for managing various esophageal pathologies. However, despite its benefits, stent-related complications can occur. We present a rare case of hemorrhage following the placement of a fully covered esophageal stent. The prompt identification and management of this complication resulted in a favorable outcome.
We present a case of a 73-year-old man with a complex medical history of esophageal stenosis secondary to esophageal perforation caused by a dental foreign body. Additionally, the patient was under full anticoagulation due to chronic atrial fibrillation. The patient underwent regular follow-up, receiving hydrostatic dilations. Despite partial response to treatment after five dilations, the patient continued to experience dysphagia. A contrast study revealed a stenosis affecting the distal 15 cm of the esophagus. Subsequently, a fully covered esophageal stent measuring 24 × 120 mm was successfully placed without complications. However, on the 8th day post-stent placement, the patient presented with hematemesis, melena, and hemorrhagic shock.
Esophagogastroduodenoscopy revealed entrapment of the stent in the esophageal mucosa and the presence of multiple clots in the esophageal lumen, without active bleeding ( Fig. 1 ). Prompt removal of the stent exposed diffuse and active mucosal bleeding ( Fig. 2 ), which was effectively managed using Nexpowder hemostatic powder (Medtronic, Minneapolis, Minnesota, USA) ( Fig. 3 , Video 1 ). Fluoroscopy confirmed the absence of strictures post-hemostasis. The patient had an uneventful recovery and remained free from further bleeding episodes and dysphagia.
Esophageal stents can be used for the treatment of refractory benign esophageal strictures for a maximum period of 3 months following insertion. The use of self-expanding metal stents as a first-line therapy is not recommended due to the potential for adverse events, the availability of alternative therapies, and the associated cost 1 .
Hemorrhage is a rare but potentially life-threatening complication following esophageal stent placement. Timely recognition and intervention are crucial to ensure optimal patient outcomes. This case highlights the importance of close monitoring post-stenting and the need for prompt endoscopic evaluation in the presence of bleeding symptoms. The Nexpowder endoscopic hemostatic system is a powder used for hemostasis, delivered through a catheter. It is made of a hydrophilic and biocompatible adhesive material that contains succinic anhydride and oxidized dextran. When it comes into contact with water or blood, the system forms an adhesive gel by reversible bonding. This crosslinked gel helps prevent upper gastrointestinal bleeding, fluid loss, and contamination of ulcer sites by adhering to the bleeding site in the upper gastrointestinal tract. Over time, the gel naturally degrades within a period of 1 to 3 days. In our patient's case, the use of hemostatic powder proved to be effective in achieving hemostasis.
Endoscopy_UCTN_Code_CPL_1AH_2AC
Footnotes
Conflict of Interest Romain Leenhardt is cofounder and shareholder of Augmented Endoscopy and has given a lecture for Abbvie. Marine Camus is a consultant for Cook Medical, Ambu and Medtronic. Xavier Dray is a founder of and shareholder of Augmented Endoscopy and has acted as a consultant for Boston Scientific and Norgine and has given lectures for Fujifilm, Medtronic, MSD, and Pentax. Ulriikka Chaput is a consultant for Boston Scientific. The others authors have no discosures.
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Reference
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