Patient and health professional views on risk-stratified monitoring of immune-suppressing treatment in adults with inflammatory diseases

Author:

Fuller Amy1ORCID,Hancox Jennie23,Williams Hywel C3,Card Tim3,Taal Maarten W4ORCID,Aithal Guruprasad P56,Fox Christopher P7,Mallen Christian D8ORCID,Maxwell James R9,Bingham Sarah10,Vedhara Kavita311,Abhishek Abhishek16

Affiliation:

1. Academic Rheumatology, School of Medicine, University of Nottingham , Nottingham, UK

2. School of Health Sciences, Loughborough University , Loughborough, UK

3. Lifespan and Population Health, University of Nottingham , Nottingham, UK

4. Centre for Kidney Research and Innovation, Translational Medical Sciences, University of Nottingham , Derby, UK

5. Nottingham Digestive Diseases Centre, Translational Medical Sciences, University of Nottingham , Nottingham, UK

6. NIHR Nottingham Biomedical Research Centre (BRC), Nottingham University Hospitals NHS Trust and The University of Nottingham , Nottingham, UK

7. School of Medicine, University of Nottingham , Nottingham, UK

8. Primary Care Centre Versus Arthritis, Keele University , Keele, UK

9. Department of Rheumatology, Sheffield Teaching Hospitals NHS Foundation Trust , Sheffield, UK

10. Department of Rheumatology, Norfolk and Norwich University Hospitals NHS Foundation Trust , Norwich, UK

11. School of Psychology, Cardiff University , Cardiff, UK

Abstract

Abstract Objective To explore the acceptability of an individualized 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 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 health care professionals. Guideline groups should consider these findings when recommending blood-test monitoring intervals.

Funder

National Institute for Health and Care Research—Health Technology Assessment programme

Publisher

Oxford University Press (OUP)

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