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PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study
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. MET...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001238/ https://www.ncbi.nlm.nih.gov/pubmed/34129089 http://dx.doi.org/10.1007/s00464-021-08589-6 |
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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, Christian |
author_facet | 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, Christian |
author_sort | Branchi, Federica |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00464-021-08589-6. |
format | Online Article Text |
id | pubmed-9001238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-90012382022-04-27 PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study 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, Christian Surg Endosc Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00464-021-08589-6. Springer US 2021-06-15 2022 /pmc/articles/PMC9001238/ /pubmed/34129089 http://dx.doi.org/10.1007/s00464-021-08589-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article 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, Christian PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title | PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title_full | PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title_fullStr | PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title_full_unstemmed | PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title_short | PuraStat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
title_sort | purastat in gastrointestinal bleeding: results of a prospective multicentre observational pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001238/ https://www.ncbi.nlm.nih.gov/pubmed/34129089 http://dx.doi.org/10.1007/s00464-021-08589-6 |
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