Across rheumatic diseases

The development of a risk threshold to aid risk stratified approach to monitoring for haematological, hepatic and/or renal adverse drug reactions during established cs DMARD treatment for systemic autoimmune rheumatic diseases: a RAND/UCLA Appropriateness Method consensus study

Rheumatology (Oxford)Published Consensus study

Authors' conclusion

A threshold to aid risk-stratified monitoring during established csDMARD treatment was agreed for adults with SARD.

Study context

Population
Members of the BSR csDMARD guideline working group who manage adults with systemic autoimmune rheumatic diseases (SARD); scenarios of adults prescribed csDMARDs for ≥1 year for SARDof 27 invitees
Participants
21 members
Outcome
Appropriateness of intervals between monitoring blood tests by 5-year predicted risk of discontinuing treatment due to abnormal monitoring blood tests (5% to 25%); consensus = median panel score ≥7 and up to six experts rating <7
Methodological detailsRAND/UCLA Appropriateness Method, two rounds (scenarios without agreement recirculated), 9-point Likert-type scales, nine scenarios, Panel: 11 consultants/GPs, 5 specialist nurses, 3 pharmacists, 2 rheumatology specialty trainees, Results discussed with patient and public involvement members and experts
  • RAND/UCLA Appropriateness Method
  • Two rounds (scenarios without agreement recirculated)
  • 9-point Likert-type scales
  • Nine scenarios
  • Panel: 11 consultants/GPs, 5 specialist nurses, 3 pharmacists, 2 rheumatology specialty trainees
  • Results discussed with patient and public involvement members and experts

Recommendations

As reported in the abstract

Appropriate monitoring interval by 5-year predicted risk
  • Consensus reached for all scenarios
  • 6-monthly blood tests appropriate when predicted 5-year risk ≤10%
  • 3-monthly blood tests appropriate when predicted 5-year risk >10%

Original publication

The development of a risk threshold to aid risk stratified approach to monitoring for haematological, hepatic and/or renal adverse drug reactions during established cs DMARD treatment for systemic autoimmune rheumatic diseases: a RAND/UCLA Appropriateness Method consensus study. Rheumatology (Oxford). Published 3 February 2026. doi:10.1093/rheumatology/keag031

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