AMY FULLER Amy.Fuller@nottingham.ac.uk
Research Fellow
Patient and health professional views on risk-stratified monitoring of immune-suppressing treatment in adults with inflammatory diseases
Fuller, Amy; Hancox, Jennie; Williams, Hywel C; Card, Tim; Taal, Maarten W; Aithal, Guruprasad P; Fox, Christopher P; Mallen, Christian D; Maxwell, James R; Bingham, Sarah; Vedhara, Kavita; Abhishek, Abhishek
Authors
Jennie Hancox
HYWEL WILLIAMS HYWEL.WILLIAMS@NOTTINGHAM.AC.UK
Professor of Dermato-Epidemiology
Dr TIM CARD tim.card@nottingham.ac.uk
Clinical Associate Professor
MAARTEN TAAL M.TAAL@NOTTINGHAM.AC.UK
Professor of Medicine
GURUPRASAD AITHAL Guru.Aithal@nottingham.ac.uk
Professor of Hepatology
Professor CHRIS FOX Christopher.Fox@nottingham.ac.uk
Clinical Professor in Haematology
Christian D Mallen
James R Maxwell
Sarah Bingham
Kavita Vedhara
ABHISHEK ABHISHEK ABHISHEK.ABHISHEK@NOTTINGHAM.AC.UK
Clinical Professor
Abstract
Objective
To explore the acceptability of an individualised risk-stratified approach to monitoring for target-organ toxicity in adult patients with immune-mediated inflammatory diseases established on immune-suppressing treatment(s).
Methods
Adults (≥18 years) taking immune-suppressing treatment(s) for at-least six months, and healthcare professionals (HCPs) with experience of either prescribing and/or monitoring immune-suppressing drugs were invited to participate in a single, remote, one-to-one, semi-structured interview. Interviews were conducted by a trained qualitative researcher and explored their views and experiences of current monitoring and acceptability of a proposed risk-stratified monitoring plan. Interviews were transcribed verbatim and inductively analysed using thematic analysis in NVivo.
Results
Eighteen patients and 13 HCPs were interviewed. While participants found monitoring of immune-suppressing drugs with frequent blood-tests reassuring, the current frequency of these was considered burdensome by patients and HCPs alike, and to be a superfluous use of healthcare resources. Given abnormalities rarely arose during long-term treatment, most felt that monitoring blood-tests were not needed as often. Patients and HCPs found it acceptable to increase the interval between monitoring blood-tests from three-monthly to six-monthly or annually depending on the patients’ risk profiles. Conditions of accepting such a change included: allowing for clinician and patient autonomy in determining an individuals’ frequency of monitoring blood-tests, the flexibility to change monitoring frequency if someone’s risk profile changed, and endorsement from specialist societies and healthcare providers such as the National Health Service.
Conclusion
A risk-stratified approach to monitoring was acceptable to patients and HCPs. Guideline groups should consider these findings when recommending blood-test monitoring intervals.
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 12, 2024 |
Online Publication Date | Mar 14, 2024 |
Deposit Date | Mar 21, 2024 |
Journal | Rheumatology |
Print ISSN | 1462-0324 |
Electronic ISSN | 1462-0332 |
Publisher | Oxford University Press (OUP) |
Peer Reviewed | Peer Reviewed |
Article Number | keae175 |
DOI | https://doi.org/10.1093/rheumatology/keae175 |
Keywords | Pharmacology (medical); Rheumatology |
Public URL | https://nottingham-repository.worktribe.com/output/32749610 |
Publisher URL | https://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/keae175/7628623? |
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