Outcomes from an international multicenter registry of patients with acute gastrointestinal bleeding undergoing endoscopic treatment with Hemospray.


Journal

Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society
ISSN: 1443-1661
Titre abrégé: Dig Endosc
Pays: Australia
ID NLM: 9101419

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 26 04 2019
accepted: 28 07 2019
pubmed: 1 8 2019
medline: 6 11 2020
entrez: 1 8 2019
Statut: ppublish

Résumé

Acute gastrointestinal bleeding carries poor outcomes unless prompt endoscopic hemostasis is achieved. Mortality in these patients remains significant. Hemospray is a novel intervention that creates a mechanical barrier over bleeding sites. We report the largest dataset of patient outcomes after treatment with Hemospray from an international multicenter registry. Prospective data (Jan 2016-May 2018) from 12 centers across Europe were collected. Immediate hemostasis was defined as endoscopic cessation of bleeding within 5 min after application of Hemospray. Rebleeding was defined as subsequent drop in hemoglobin, hematemesis, persistent melena with hemodynamic compromise post-therapy. Three hundred and fourteen cases were recruited worldwide (231 males, 83 females). Median pretreatment Blatchford score was 11 (IQR: 8-14) and median complete Rockall score (RS) was 7 (IQR: 6-8) for all patients. Peptic ulcer disease (PUD) was the most common pathology (167/314 = 53%) and Forrest Ib the most common bleed type in PUD (100/167 = 60%). 281 patients (89.5%) achieved immediate hemostasis after successful endoscopic therapy with Hemospray. Rebleeding occurred in 29 (10.3%) of the 281 patients who achieved immediate hemostasis. Seven-day and 30-day all-cause mortality were 11.5% (36/314) and 20.1% (63/314), respectively (lower than the predicted rates as per the RS). Similar hemostasis rates were noted in the Hemospray monotherapy (92.4%), combination therapy (88.7%) and rescue therapy (85.5%) groups. These data show high rates of immediate hemostasis overall and in all subgroups. Rebleeding and mortality rates were in keeping/lower than predicted rates.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Acute gastrointestinal bleeding carries poor outcomes unless prompt endoscopic hemostasis is achieved. Mortality in these patients remains significant. Hemospray is a novel intervention that creates a mechanical barrier over bleeding sites. We report the largest dataset of patient outcomes after treatment with Hemospray from an international multicenter registry.
PATIENTS AND METHODS METHODS
Prospective data (Jan 2016-May 2018) from 12 centers across Europe were collected. Immediate hemostasis was defined as endoscopic cessation of bleeding within 5 min after application of Hemospray. Rebleeding was defined as subsequent drop in hemoglobin, hematemesis, persistent melena with hemodynamic compromise post-therapy.
RESULTS RESULTS
Three hundred and fourteen cases were recruited worldwide (231 males, 83 females). Median pretreatment Blatchford score was 11 (IQR: 8-14) and median complete Rockall score (RS) was 7 (IQR: 6-8) for all patients. Peptic ulcer disease (PUD) was the most common pathology (167/314 = 53%) and Forrest Ib the most common bleed type in PUD (100/167 = 60%). 281 patients (89.5%) achieved immediate hemostasis after successful endoscopic therapy with Hemospray. Rebleeding occurred in 29 (10.3%) of the 281 patients who achieved immediate hemostasis. Seven-day and 30-day all-cause mortality were 11.5% (36/314) and 20.1% (63/314), respectively (lower than the predicted rates as per the RS). Similar hemostasis rates were noted in the Hemospray monotherapy (92.4%), combination therapy (88.7%) and rescue therapy (85.5%) groups.
CONCLUSIONS CONCLUSIONS
These data show high rates of immediate hemostasis overall and in all subgroups. Rebleeding and mortality rates were in keeping/lower than predicted rates.

Identifiants

pubmed: 31365756
doi: 10.1111/den.13502
doi:

Substances chimiques

Hemostatics 0
Minerals 0
hemospray 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

96-105

Subventions

Organisme : Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS) at UCL
ID : 203145Z/16/Z

Informations de copyright

© 2019 Japan Gastroenterological Endoscopy Society.

Références

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Auteurs

Durayd Alzoubaidi (D)

Division of Surgery and Interventional Science, University College London (UCL), London, UK.

Mohamed Hussein (M)

Division of Surgery and Interventional Science, University College London (UCL), London, UK.

Radu Rusu (R)

Department of Gastroenterology, Guy's and St Thomas' Foundation Trust Hospitals, London, UK.

Duncan Napier (D)

Department of Gastroenterology, Gloucestershire Hospitals NHS Foundation Trust - Cheltenham General Hospital, Cheltenham, UK.

Selena Dixon (S)

Department of Gastroenterology, Bradford Teaching Hospitals Foundation Trust, Bradford, UK.

Johannes W Rey (JW)

Department of Gastroenterology, Clinic Osnabruck, Osnabruck, Germany.

Cora Steinheber (C)

Department of Gastroenterology, Tubingen University Hospital, Tubingen, Germany.

Sina Jameie-Oskooei (S)

Department of Gastroenterology, The Royal Free Hospital, London, UK.

Martin Dahan (M)

Department of Gastroenterology, University Hospital Centre, Nantes, France.

Bu Hayee (B)

Department of Gastroenterology, Kings College London, London, UK.

Shraddha Gulati (S)

Department of Gastroenterology, Kings College London, London, UK.

Edward Despott (E)

Department of Gastroenterology, The Royal Free Hospital, London, UK.

Alberto Murino (A)

Department of Gastroenterology, The Royal Free Hospital, London, UK.

Sharmila Subramaniam (S)

Department of Gastroenterology, Portsmouth Hospitals NHS Trust, Portsmouth, UK.

Sulleman Moreea (S)

Department of Gastroenterology, Bradford Teaching Hospitals Foundation Trust, Bradford, UK.

Phil Boger (P)

Department of Gastroenterology, University Hospital Southampton, Southampton, UK.

Maxworth Hu (M)

Department of Gastroenterology, University Hospital Southampton, Southampton, UK.

Patricia Duarte (P)

Department of Gastroenterology, University Hospital Southampton, Southampton, UK.

Jason Dunn (J)

Department of Gastroenterology, Guy's and St Thomas' Foundation Trust Hospitals, London, UK.

Inder Mainie (I)

Department of Gastroenterology, Belfast Trust, Belfast, UK.

John McGoran (J)

Department of Gastroenterology, Belfast Trust, Belfast, UK.

David Graham (D)

Department of Gastroenterology, University College London Hospital (UCLH), London, UK.

John Anderson (J)

Department of Gastroenterology, Gloucestershire Hospitals NHS Foundation Trust - Cheltenham General Hospital, Cheltenham, UK.

Pradeep Bhandari (P)

Department of Gastroenterology, Portsmouth Hospitals NHS Trust, Portsmouth, UK.

Martin Goetz (M)

Department of Gastroenterology, Tubingen University Hospital, Tubingen, Germany.

Ralf Kiesslich (R)

Horst Schmidt Clinic, Wiesbaden, Germany.

Emmanuel Coron (E)

Department of Gastroenterology, University Hospital Centre, Nantes, France.

Laurence Lovat (L)

Division of Surgery and Interventional Science, University College London (UCL), London, UK.

Rehan Haidry (R)

Division of Surgery and Interventional Science, University College London (UCL), London, UK.
Department of Gastroenterology, University College London Hospital (UCLH), London, UK.

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