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Real-world evidence of long-term survival and healthcare resource use in patients with hepatic encephalopathy receiving rifaximin-α treatment: a retrospective observational extension study with long-term follow-up (IMPRESS II)

Real-world evidence of long-term survival and healthcare resource use in patients with hepatic encephalopathy receiving rifaximin-α treatment: a retrospective observational extension study with long-term follow-up (IMPRESS II)
Real-world evidence of long-term survival and healthcare resource use in patients with hepatic encephalopathy receiving rifaximin-α treatment: a retrospective observational extension study with long-term follow-up (IMPRESS II)
Objective: To describe survival of patients with hepatic encephalopathy (HE), up to 5 years after initiation of rifaximin-α (RFX) treatment.
Design/Method: A retrospective, observational extension study within 9 National Health Service secondary/tertiary UK care centres. All patients had a clinical diagnosis of HE, were being treated with RFX and were included in the previous IMPRESS study which reported the 1-year experience. Demographics, clinical outcomes, selected cirrhosis-related complications, hospital admissions and attendances up to 5 years from RFX initiation were extracted from patient medical records and hospital electronic databases. The primary outcome measure was survival at 5 years post-initiation of RFX treatment.
Results: The study included 138 patients. The survival rate at 5 years post-initiation of RFX was 35% (95% CI 28.2% to 44.4%) overall and 36% (95% CI 26.1% to 45.4%) for patients with alcohol-related liver disease. Median survival from RFX initiation was 2.8 years (95% CI 2.0 to 3.8; n=136). Among 48 patients alive at 5 years, 69% remained on RFX treatment at the end of the observation period, 74% reported no cirrhosis-related complications and 24% (9/37) had received a liver transplant. Between 1 and 5 years post-initiation, total numbers of liver-related emergency department visits, inpatient admissions, intensive care unit admissions and outpatient visits were 84, 194, 3 and 709, respectively; the liver-related 30-day readmission rate was 37%.
Conclusion: Within UK clinical practice, RFX use in HE was associated with a 35% survival rate with high treatment adherence, 76% transplant-free survival rate, minimal healthcare resource and low rates of complications at 5 years post-initiation.
antibiotic therapy, hepatic encephalopathy, liver cirrhosis
2041-4137
228-235
Aspinall, Richard J
acd5e5ee-f4a7-443d-a73c-edaac9f209c7
Hudson, Mark
0e9865f4-d845-4f88-8030-d717baf5f7eb
Ryder, Stephen D
a6492b44-27e1-4aa3-82d0-86da8278bf21
Richardson, Paul
8b08e854-841d-419d-86fa-c371b0a9b1a9
Farrington, Elizabeth
f437bb73-c71d-476b-90a2-ef91f1eab4f7
Wright, Mark
43325ef9-3459-4c75-b3bf-cf8d8dac2a21
Przemioslo, Robert T
4a4f84d0-bddc-4bb8-bb99-7ea07e7cd04d
Perez, Francisco
adedee67-10ec-42af-89d8-1d93d8399bf8
Kent, Melanie
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Henrar, Roland
b310d494-ea0b-454d-837d-09491f5a4584
Hickey, Joe
8eeed625-caf0-4511-a701-518670e63ceb
Shawcross, Debbie L
0c99f187-b53e-40db-b8b9-731cbdbcf587
et al.
Aspinall, Richard J
acd5e5ee-f4a7-443d-a73c-edaac9f209c7
Hudson, Mark
0e9865f4-d845-4f88-8030-d717baf5f7eb
Ryder, Stephen D
a6492b44-27e1-4aa3-82d0-86da8278bf21
Richardson, Paul
8b08e854-841d-419d-86fa-c371b0a9b1a9
Farrington, Elizabeth
f437bb73-c71d-476b-90a2-ef91f1eab4f7
Wright, Mark
43325ef9-3459-4c75-b3bf-cf8d8dac2a21
Przemioslo, Robert T
4a4f84d0-bddc-4bb8-bb99-7ea07e7cd04d
Perez, Francisco
adedee67-10ec-42af-89d8-1d93d8399bf8
Kent, Melanie
b528c663-19d4-4c74-91c1-689e073fdeae
Henrar, Roland
b310d494-ea0b-454d-837d-09491f5a4584
Hickey, Joe
8eeed625-caf0-4511-a701-518670e63ceb
Shawcross, Debbie L
0c99f187-b53e-40db-b8b9-731cbdbcf587

Aspinall, Richard J, Hudson, Mark, Ryder, Stephen D and Wright, Mark , et al. (2023) Real-world evidence of long-term survival and healthcare resource use in patients with hepatic encephalopathy receiving rifaximin-α treatment: a retrospective observational extension study with long-term follow-up (IMPRESS II). Frontline Gastroenterology, 14 (3), 228-235. (doi:10.1136/flgastro-2022-102221).

Record type: Article

Abstract

Objective: To describe survival of patients with hepatic encephalopathy (HE), up to 5 years after initiation of rifaximin-α (RFX) treatment.
Design/Method: A retrospective, observational extension study within 9 National Health Service secondary/tertiary UK care centres. All patients had a clinical diagnosis of HE, were being treated with RFX and were included in the previous IMPRESS study which reported the 1-year experience. Demographics, clinical outcomes, selected cirrhosis-related complications, hospital admissions and attendances up to 5 years from RFX initiation were extracted from patient medical records and hospital electronic databases. The primary outcome measure was survival at 5 years post-initiation of RFX treatment.
Results: The study included 138 patients. The survival rate at 5 years post-initiation of RFX was 35% (95% CI 28.2% to 44.4%) overall and 36% (95% CI 26.1% to 45.4%) for patients with alcohol-related liver disease. Median survival from RFX initiation was 2.8 years (95% CI 2.0 to 3.8; n=136). Among 48 patients alive at 5 years, 69% remained on RFX treatment at the end of the observation period, 74% reported no cirrhosis-related complications and 24% (9/37) had received a liver transplant. Between 1 and 5 years post-initiation, total numbers of liver-related emergency department visits, inpatient admissions, intensive care unit admissions and outpatient visits were 84, 194, 3 and 709, respectively; the liver-related 30-day readmission rate was 37%.
Conclusion: Within UK clinical practice, RFX use in HE was associated with a 35% survival rate with high treatment adherence, 76% transplant-free survival rate, minimal healthcare resource and low rates of complications at 5 years post-initiation.

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More information

Published date: May 2023
Additional Information: Funding Information: The authors thank the following for their contribution to study data collection: Ms Alison Dimmer and Ms Beverley Longhurst at Portsmouth Hospitals University NHS Trust, Portsmouth. Mr David Tyrer and Ms Giovanna Bretland at Royal Liverpool & Broadgreen University Hospitals NHS Trust, Liverpool. Mr Andrew Ayers at King’s College Hospital, London. Ms Eleanor King at Royal Cornwall Hospital, Cornwall. Mr Varinder Kaur Ryan at Nottingham University Hospitals NHS Trust. Ms Charlotte Cranfield, Ms Louise Jennings and Ms Danielle Gervaise-Brazier at Southmead Hospital, Bristol. Ms Stefanie Hobson at University Hospital of North Durham, Durham. Ms Gabriella Campos and Ms Loredana-Julieta Gergely at The Freeman Hospital, Newcastle Upon Tyne. Ms Mariya Shaji and Ms Sanchia Triggs at University Hospital Southampton, Southampton. We would like to thank the patients whose data were included in the study. The authors also thank Will Cottam PhD of OPEN Health, Marlow, who provided medical writing support (funded by Norgine). Funding Information: This study was sponsored and funded by Norgine. Publisher Copyright: © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Keywords: antibiotic therapy, hepatic encephalopathy, liver cirrhosis

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Local EPrints ID: 477939
URI: http://eprints.soton.ac.uk/id/eprint/477939
ISSN: 2041-4137
PURE UUID: afb02326-a1aa-44f6-a8eb-b1f23a254bb4

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Date deposited: 16 Jun 2023 16:46
Last modified: 17 Mar 2024 02:14

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Contributors

Author: Richard J Aspinall
Author: Mark Hudson
Author: Stephen D Ryder
Author: Paul Richardson
Author: Elizabeth Farrington
Author: Mark Wright
Author: Robert T Przemioslo
Author: Francisco Perez
Author: Melanie Kent
Author: Roland Henrar
Author: Joe Hickey
Author: Debbie L Shawcross
Corporate Author: et al.

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