Patient journey in erosive oesophagitis: real-world perspectives from US physicians and patients.


Journal

BMJ open gastroenterology
ISSN: 2054-4774
Titre abrégé: BMJ Open Gastroenterol
Pays: England
ID NLM: 101660690

Informations de publication

Date de publication:
07 2022
Historique:
received: 25 04 2022
accepted: 07 07 2022
entrez: 22 7 2022
pubmed: 23 7 2022
medline: 27 7 2022
Statut: ppublish

Résumé

Management of erosive oesophagitis (EE) remains suboptimal, with many patients experiencing incomplete healing, ongoing symptoms, and relapse despite proton pump inhibitor (PPI) treatment. The Study of Acid-Related Disorders investigated patient burden of individuals with EE in a real-world setting. US gastroenterologists (GIs) or family physicians (FPs)/general practitioners (GPs) treating patients with EE completed a physician survey and enrolled up to four patients with EE for a patient survey, with prespecified data extracted from medical records. 102 GIs and 149 FPs/GPs completed the survey; data were available for 73 patients (mean age at diagnosis, 45.4 years). Omeprazole was healthcare professional (HCP)-preferred first-line treatment (60.8% GIs; 56.4% FPs/GPs), and pantoprazole preferred second line (29.4% and 32.9%, respectively). Price and insurance coverage (both 55.5% HCPs) and familiarity (47.9%) key drivers for omeprazole; insurance coverage (52.0%), price (50.0%), familiarity (48.0%), initial symptom relief (46.0%), and safety (44.0%) key drivers for pantoprazole. Only 49.3% patients took medication as instructed all the time; 56.8% independently increased medication frequency some of the time. Despite treatment, 57.5% patients experienced heartburn and 30.1% regurgitation; heartburn was the most bothersome symptom. 58.9% patients believed that their symptoms could be better controlled; only 28.3% HCPs were very satisfied with current treatment options. 83.6% patients wanted long-lasting treatment options. Fast symptom relief for patients was a top priority for 66.1% HCPs, while 56.6% would welcome alternatives to PPIs. This real-world multicentre study highlights the need for new, rapidly acting treatments in EE that reduce symptom burden, offer durable healing and provide symptom control.

Identifiants

pubmed: 35868653
pii: bmjgast-2022-000941
doi: 10.1136/bmjgast-2022-000941
pmc: PMC9316025
pii:
doi:

Substances chimiques

2-Pyridinylmethylsulfinylbenzimidazoles 0
Anti-Ulcer Agents 0
Benzimidazoles 0
Proton Pump Inhibitors 0
Pantoprazole D8TST4O562
Omeprazole KG60484QX9

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: CP and RJ are employees of Phathom Pharmaceuticals. All other authors are consultants to Phathom Pharmaceuticals.

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Auteurs

Michael F Vaezi (MF)

Gastroenterology, Hepatology, and Nutrition, Vanderbilt University Medical Center, Nashville, Tennessee, USA michael.vaezi@vumc.org.

Stephen Brunton (S)

Primary Care Education Consortium, Winnsboro, Texas, USA.

A Mark Fendrick (A)

Department of Internal Medicine, University of Michigan Department of Internal Medicine, Ann Arbor, Michigan, USA.

Colin W Howden (CW)

University of Tennessee, Tennessee, Nashville, USA.

Christian Atkinson (C)

Adelphi Real World, Bollington, Cheshire, UK.

Corey Pelletier (C)

Phathom Pharmaceuticals, New Jersey, New Jersey, USA.

Rinu Jacob (R)

Phathom Pharmaceuticals, New Jersey, New Jersey, USA.

Stuart J Spechler (SJ)

Division of Gastroenterology, Baylor University Medical Center at Dallas, Dallas, Texas, USA.

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Classifications MeSH