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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.
Afiliação
  • Fuller A; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham, UK.
  • Hancox J; School of Health Sciences, Loughborough University, Loughborough, UK.
  • Williams HC; Lifespan and Population Health, University of Nottingham, Nottingham, UK.
  • Card T; Lifespan and Population Health, University of Nottingham, Nottingham, UK.
  • Taal MW; Lifespan and Population Health, University of Nottingham, Nottingham, UK.
  • Aithal GP; Centre for Kidney Research and Innovation, Translational Medical Sciences, University of Nottingham, Derby, UK.
  • Fox CP; Nottingham Digestive Diseases Centre, Translational Medical Sciences, University of Nottingham, Nottingham, UK.
  • Mallen CD; NIHR Nottingham Biomedical Research Centre (BRC), Nottingham University Hospitals NHS Trust and The University of Nottingham, Nottingham, UK.
  • Maxwell JR; School of Medicine, University of Nottingham, Nottingham, UK.
  • Bingham S; Primary Care Centre Versus Arthritis, Keele University, Keele, UK.
  • Vedhara K; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Abhishek A; Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, UK.
Article em En | MEDLINE | ID: mdl-38483276
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article