Predictors of the experience of a Cytosponge test: analysis of patient survey data from the BEST3 trial.
Barrett’s oesophagus
Cytosponge
Inventory to assess patient satisfaction
Patient experience
Journal
BMC gastroenterology
ISSN: 1471-230X
Titre abrégé: BMC Gastroenterol
Pays: England
ID NLM: 100968547
Informations de publication
Date de publication:
10 Jan 2023
10 Jan 2023
Historique:
received:
14
07
2022
accepted:
20
12
2022
entrez:
10
1
2023
pubmed:
11
1
2023
medline:
13
1
2023
Statut:
epublish
Résumé
The Cytosponge is a cell-collection device, which, coupled with a test for trefoil factor 3 (TFF3), can be used to diagnose Barrett's oesophagus, a precursor condition to oesophageal adenocarcinoma. BEST3, a large pragmatic, randomised, controlled trial, investigated whether offering the Cytosponge-TFF3 test would increase detection of Barrett's. Overall, participants reported mostly positive experiences. This study reports the factors associated with the least positive experience. Patient experience was assessed using the Inventory to Assess Patient Satisfaction (IAPS), a 22-item questionnaire, completed 7-14 days after the Cytosponge test. All BEST3 participants who answered ≥ 15 items of the IAPS (N = 1458). A mean IAPS score between 1 and 5 (5 indicates most negative experience) was calculated for each individual. 'Least positive' experience was defined according to the 90th percentile. 167 (11.4%) individuals with a mean IAPS score of ≥ 2.32 were included in the 'least positive' category and compared with the rest of the cohort. Eleven patient characteristics and one procedure-specific factor were assessed as potential predictors of the least positive experience. Multivariable logistic regression analysis using backwards selection was conducted to identify factors independently associated with the least positive experience and with failed swallow at first attempt, one of the strongest predictors of least positive experience. The majority of responders had a positive experience, with an overall median IAPS score of 1.7 (IQR 1.5-2.1). High (OR = 3.01, 95% CI 2.03-4.46, p < 0.001) or very high (OR = 4.56, 95% CI 2.71-7.66, p < 0.001) anxiety (relative to low/normal anxiety) and a failed swallow at the first attempt (OR = 3.37, 95% CI 2.14-5.30, p < 0.001) were highly significant predictors of the least positive patient experience in multivariable analyses. Additionally, sex (p = 0.036), height (p = 0.032), alcohol intake (p = 0.011) and education level (p = 0.036) were identified as statistically significant predictors. We have identified factors which predict patient experience. Identifying anxiety ahead of the procedure and discussing particular concerns with patients or giving them tips to help with swallowing the capsule might help improve their experience. Trial registration ISRCTN68382401.
Sections du résumé
BACKGROUND
BACKGROUND
The Cytosponge is a cell-collection device, which, coupled with a test for trefoil factor 3 (TFF3), can be used to diagnose Barrett's oesophagus, a precursor condition to oesophageal adenocarcinoma. BEST3, a large pragmatic, randomised, controlled trial, investigated whether offering the Cytosponge-TFF3 test would increase detection of Barrett's. Overall, participants reported mostly positive experiences. This study reports the factors associated with the least positive experience.
METHODS
METHODS
Patient experience was assessed using the Inventory to Assess Patient Satisfaction (IAPS), a 22-item questionnaire, completed 7-14 days after the Cytosponge test.
STUDY COHORT
UNASSIGNED
All BEST3 participants who answered ≥ 15 items of the IAPS (N = 1458).
STATISTICAL ANALYSIS
METHODS
A mean IAPS score between 1 and 5 (5 indicates most negative experience) was calculated for each individual. 'Least positive' experience was defined according to the 90th percentile. 167 (11.4%) individuals with a mean IAPS score of ≥ 2.32 were included in the 'least positive' category and compared with the rest of the cohort. Eleven patient characteristics and one procedure-specific factor were assessed as potential predictors of the least positive experience. Multivariable logistic regression analysis using backwards selection was conducted to identify factors independently associated with the least positive experience and with failed swallow at first attempt, one of the strongest predictors of least positive experience.
RESULTS
RESULTS
The majority of responders had a positive experience, with an overall median IAPS score of 1.7 (IQR 1.5-2.1). High (OR = 3.01, 95% CI 2.03-4.46, p < 0.001) or very high (OR = 4.56, 95% CI 2.71-7.66, p < 0.001) anxiety (relative to low/normal anxiety) and a failed swallow at the first attempt (OR = 3.37, 95% CI 2.14-5.30, p < 0.001) were highly significant predictors of the least positive patient experience in multivariable analyses. Additionally, sex (p = 0.036), height (p = 0.032), alcohol intake (p = 0.011) and education level (p = 0.036) were identified as statistically significant predictors.
CONCLUSION
CONCLUSIONS
We have identified factors which predict patient experience. Identifying anxiety ahead of the procedure and discussing particular concerns with patients or giving them tips to help with swallowing the capsule might help improve their experience. Trial registration ISRCTN68382401.
Identifiants
pubmed: 36627580
doi: 10.1186/s12876-022-02630-1
pii: 10.1186/s12876-022-02630-1
pmc: PMC9832657
doi:
Banques de données
ISRCTN
['ISRCTN68382401']
Types de publication
Randomized Controlled Trial
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
7Subventions
Organisme : Innovate UK
ID : 105857
Organisme : Innovate UK
ID : 105857
Organisme : Innovate UK
ID : 105857
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14478/A21047, C8162/A16892, C8162/A25356, C7492/A17219, C8640/A23385
Pays : United Kingdom
Organisme : Medical Research Council
ID : RG84369
Pays : United Kingdom
Investigateurs
Stephen Attwood
(S)
Max Parmar
(M)
Brendan Delaney
(B)
John de Caestecker
(J)
Wendy Atkin
(W)
Allan Hackshaw
(A)
Charles van Heyningen
(C)
Tim Underwood
(T)
Alberto Stella
(A)
Charlotte Saxby
(C)
Attila Lorincz
(A)
Naomi Turnbull
(N)
Jamie Doorbar
(J)
Georgia Mannion-Krase
(G)
Irene Kaimi
(I)
Mary Kasanicki
(M)
Stephen Kelleher
(S)
Louise Stockley
(L)
Tracy Assari
(T)
Sonakshi Kadyan
(S)
Victoria Hollamby
(V)
Katie Edwards
(K)
Helen MacDonald
(H)
Viv Shaw
(V)
Heather Leishman
(H)
Holly Roper
(H)
Kate McCloskey
(K)
Helen Jung
(H)
Alex Phillips
(A)
Gosia Masjak-Newman
(G)
Kim Fell
(K)
Helen Collins
(H)
Olga Zolle
(O)
Pauline McGlone
(P)
Tania Crabb
(T)
Lauren Merrin
(L)
Martine Cross
(M)
Alex Jones
(A)
Tom Simpson
(T)
Emma Murray
(E)
Andrew Perugia
(A)
Marie Thompson
(M)
Jen Dumbleton
(J)
Monique Morar
(M)
Nadia Frowd
(N)
Antonia Hardcastle
(A)
Debbie Carmichael
(D)
Fiona Maxton
(F)
Frances Farnworth
(F)
Elaine Baddeley
(E)
Informations de copyright
© 2023. The Author(s).
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