PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study

Author:

Branchi Federica,Klingenberg-Noftz Rolf,Friedrich Kristina,Bürgel Nataly,Daum Severin,Buchkremer Juliane,Sonnenberg Elena,Schumann Michael,Treese Christoph,Tröger Hanno,Lissner Donata,Epple Hans-Jörg,Siegmund Britta,Stroux Andrea,Adler Andreas,Veltzke-Schlieker Winfried,Autenrieth Daniel,Leonhardt Silke,Fischer Andreas,Jürgensen Christian,Pape Ulrich-Frank,Wiedenmann Bertram,Möschler Oliver,Schreiner Maximilian,Strowski Mathias Z.,Hempel Volkmar,Huber Yvonne,Neumann Helmut,Bojarski ChristianORCID

Abstract

Abstract Background A recently developed haemostatic peptide gel for endoscopic application has been introduced to improve the management of gastrointestinal bleeding. The aim of this pilot study was to evaluate the feasibility, safety, efficacy and indication profiles of PuraStat in a clinical setting. Methods In this prospective observational multicentre pilot study, patients with acute non-variceal gastrointestinal bleeding (upper and lower) were included. Primary and secondary application of PuraStat was evaluated. Haemoglobin, prothrombin time, platelets and transfusion behaviour were documented before and after haemostasis. The efficacy of PuraStat was assessed during the procedure, at 3 days and 1 week after application. Results 111 patients with acute gastrointestinal bleeding were recruited into the study. 70 percent (78/111) of the patients had upper gastrointestinal bleeding and 30% (33/111) had lower gastrointestinal bleeding. After primary application of PuraStat, initial haemostatic success was achieved in 94% of patients (74/79, 95% CI 88–99%), and in 75% of the patients when used as a secondary haemostatic product, following failure of established techniques (24/32, 95% CI 59–91%). The therapeutic success rates (absence of rebleeding) after 3 and 7 days were 91% and 87% after primary use, and 87% and 81% in all study patients. Overall rebleeding rate at 30 day follow-up was 16% (18/111). In the 5 patients who finally required surgery (4.5%), PuraStat allowed temporary haemostasis and stabilisation. Conclusions PuraStat expanded the therapeutic toolbox available for an effective treatment of gastrointestinal bleeding sources. It could be safely applied and administered without complications as a primary or secondary therapy. PuraStat may additionally serve as a bridge to surgery in order to achieve temporary haemostasis in case of refractory severe bleeding, possibly playing a role in preventing immediate emergency surgery.

Funder

Charité - Universitätsmedizin Berlin

Publisher

Springer Science and Business Media LLC

Subject

Surgery

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