Advanced liver fibrosis and care continuum in emergency department patients with chronic hepatitis C.


Journal

The American journal of emergency medicine
ISSN: 1532-8171
Titre abrégé: Am J Emerg Med
Pays: United States
ID NLM: 8309942

Informations de publication

Date de publication:
02 2019
Historique:
received: 23 05 2018
revised: 25 08 2018
accepted: 27 08 2018
pubmed: 10 11 2018
medline: 28 10 2019
entrez: 10 11 2018
Statut: ppublish

Résumé

FIB-4, a non-invasive serum fibrosis index (which includes age, ALT, AST, and platelet count), is frequently available during ED visits. Our objective was to define 1-year HCV-related care outcomes of ED patients with known HCV, for the overall group, and both those with and without advanced fibrosis. As part of an ongoing HCV linkage-to-care (LTC) program, HCV-infected ED patients were identified retrospectively via medical record review. Components of FIB-4 were abstracted, and patients with an FIB-4 > 3.25 were classified with advanced fibrosis and characterized with regards to downstream HCV care continuum outcomes at one-year after enrollment. Of the 113 patients with known HCV, 38 (33.6%) had advanced fibrosis. One-year outcomes along the HCV care continuum after ED encounter for 'all' 113, 75 'without advanced fibrosis', and 38 'advanced fibrosis' patients, respectively, were as follows: agreeing to be linked to care [106 (93.8%), 72 (96.0%), 34 (89.5%)]; LTC [38 (33.6%), 21 (28.0%), 17 (44.7%)]; treatment initiation among those linked [16 (42.1%), 9 (42.9%), 7 (41.2%)]; sustained virologic response 4 weeks post-treatment among those treated [15 (93.8%), 9 (100.0%), 6 (85.7%)]; documented all-cause mortality [10 (8.8%), 3 (4.0%), 7 (18.4%)]. Notably, 70% of those who died had advanced fibrosis. For those with advanced liver fibrosis, all-cause mortality was significantly higher, than those without (18.4% versus 4.0%, p = 0.030). Over one-third of HCV-infected ED patients have advanced liver fibrosis, incomplete LTC, and higher mortality, suggesting this readily-available FIB-4 might be used to prioritize LTC services for those with advanced fibrosis.

Sections du résumé

BACKGROUND
FIB-4, a non-invasive serum fibrosis index (which includes age, ALT, AST, and platelet count), is frequently available during ED visits. Our objective was to define 1-year HCV-related care outcomes of ED patients with known HCV, for the overall group, and both those with and without advanced fibrosis.
METHODS
As part of an ongoing HCV linkage-to-care (LTC) program, HCV-infected ED patients were identified retrospectively via medical record review. Components of FIB-4 were abstracted, and patients with an FIB-4 > 3.25 were classified with advanced fibrosis and characterized with regards to downstream HCV care continuum outcomes at one-year after enrollment.
RESULTS
Of the 113 patients with known HCV, 38 (33.6%) had advanced fibrosis. One-year outcomes along the HCV care continuum after ED encounter for 'all' 113, 75 'without advanced fibrosis', and 38 'advanced fibrosis' patients, respectively, were as follows: agreeing to be linked to care [106 (93.8%), 72 (96.0%), 34 (89.5%)]; LTC [38 (33.6%), 21 (28.0%), 17 (44.7%)]; treatment initiation among those linked [16 (42.1%), 9 (42.9%), 7 (41.2%)]; sustained virologic response 4 weeks post-treatment among those treated [15 (93.8%), 9 (100.0%), 6 (85.7%)]; documented all-cause mortality [10 (8.8%), 3 (4.0%), 7 (18.4%)]. Notably, 70% of those who died had advanced fibrosis. For those with advanced liver fibrosis, all-cause mortality was significantly higher, than those without (18.4% versus 4.0%, p = 0.030).
CONCLUSIONS
Over one-third of HCV-infected ED patients have advanced liver fibrosis, incomplete LTC, and higher mortality, suggesting this readily-available FIB-4 might be used to prioritize LTC services for those with advanced fibrosis.

Identifiants

pubmed: 30409463
pii: S0735-6757(18)30718-6
doi: 10.1016/j.ajem.2018.08.067
pmc: PMC6348121
mid: NIHMS1511747
pii:
doi:

Substances chimiques

Biomarkers 0
RNA, Viral 0
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

286-290

Subventions

Organisme : NIAID NIH HHS
ID : K01 AI100681
Pays : United States
Organisme : NIDA NIH HHS
ID : K24 DA034621
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA016065
Pays : United States
Organisme : NIDA NIH HHS
ID : R37 DA013806
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

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Auteurs

Yu-Hsiang Hsieh (YH)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States. Electronic address: yhsieh1@jhmi.edu.

Danielle Signer (D)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Anuj V Patel (AV)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Valentina Viertel (V)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Mustapha Saheed (M)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Risha Irvin (R)

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Mark S Sulkowski (MS)

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

David L Thomas (DL)

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Richard E Rothman (RE)

Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

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