Outcomes of Hemospray therapy in the treatment of intraprocedural upper gastrointestinal bleeding post-endoscopic therapy
Hussein, Mohamed ; Alzoubaidi, Durayd ; de la Serna, Alvaro ; Weaver, Michael ; Fernandez-Sordo, Jacobo ; Rey, Johannes ; Hayee, Bu'Hussain ; Despott, Edward ; Murino, Alberto ; Moreea, Sulleman ... show 10 more
Hussein, Mohamed
Alzoubaidi, Durayd
de la Serna, Alvaro
Weaver, Michael
Fernandez-Sordo, Jacobo
Rey, Johannes
Hayee, Bu'Hussain
Despott, Edward
Murino, Alberto
Moreea, Sulleman
Glos Author
Date
2020-01-12
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Journal Article
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Abstract
Introduction: With increasing advances in minimally invasive endoscopic therapies and endoscopic resection techniques for luminal disease, there is an increased risk of post-procedure bleeding. This can contribute to significant burden on patient's quality of life and health resources when reintervention is required. Hemospray (Cook Medical, North Carolina, USA) is a novel haemostatic powder licensed for gastrointestinal bleeding. The aim of this single-arm, prospective, non-randomised multicentre international study is to look at outcomes in patients with upper gastrointestinal bleeds following elective endoscopic therapy treated with Hemospray to achieve haemostasis.
Methods: Data was prospectively collected on the use of Hemospray from 16 centres (January 2016-November 2019). Hemospray was used during the presence of progressive intraprocedural bleeding post-endoscopic therapy as a monotherapy, dual therapy with standard haemostatic techniques or rescue therapy once standard methods had failed. Haemostasis was defined as the cessation of bleeding within 5 min of the application of Hemospray. Re-bleeding was defined as a sustained drop in haemoglobin (>2 g/l), haematemesis or melaena with haemodynamic instability after the index endoscopy.
Results: A total of 73 patients were analysed with bleeding post-endoscopic therapy. The median Blatchford score at baseline was five (interquartile range 0-9). The median Rockall score was six (interquartile range 5-7). Immediate haemostasis following the application of Hemospray was achieved in 73/73 (100%) of patients. Two out of 57 (4%) had a re-bleed post-Hemospray, one was following oesophageal endoscopic mucosal resection and the other post-duodenal endoscopic mucosal resection. Both patients had a repeat endoscopy and therapy within 24 h. Re-bleeding data was missing for 16 patients, and mortality data was missing for 14 patients. There were no adverse events recorded in association with the use of Hemospray.
Conclusion: Hemospray is safe and effective in achieving immediate haemostasis following uncontrolled and progressive intraprocedural blood loss post-endoscopic therapy, with a low re-bleed rate.
Citation
Hussein, M., Alzoubaidi, D., Serna, A., Weaver, M., Fernandez-Sordo, J. O., Rey, J. W., Hayee, B., Despott, E., Murino, A., Moreea, S., Boger, P., Dunn, J., Mainie, I., Graham, D., Mullady, D., Early, D., Ragunath, K., Anderson, J., Bhandari, P., Goetz, M., … Haidry, R. (2020). Outcomes of Hemospray therapy in the treatment of intraprocedural upper gastrointestinal bleeding post-endoscopic therapy. United European gastroenterology journal, 8(10), 1155–1162. https://doi.org/10.1177/2050640620938549
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