Across rheumatic diseases

Cost-effectiveness of risk-stratified blood test monitoring strategies for adults with inflammatory conditions

Rheumatology (Oxford)Published Cost-effectiveness analysis

Authors' conclusion

Extending the interval between monitoring blood tests appears to be cost-effective with annual monitoring producing consistently good results regardless of assumptions related to risks of AEs, risk decile or treatment.

Study context

Population
Adults with inflammatory conditions on established treatment with low-dose weekly MTX (≤25 mg/week), LEF or SSZ
Comparison
6-, 12- and 24-monthly monitoring blood tests vs 3-monthly monitoring
Outcome
iNMB of 6-, 12- and 24-monthly vs 3-monthly monitoring, for each drug by risk decile
Follow-up
5 years of established treatment
Methodological detailsmodel-based, prognostic models incorporated, risk-decile stratified, pessimistic sensitivity analysis, Risk of 1 of 11 avoidable adverse events (AEs) estimated by clinicians, who erred towards overestimating the risks, AE costs and QALY loss sourced from recent NICE appraisals or targeted searches
  • Model-based
  • Prognostic models incorporated
  • Risk-decile stratified
  • Pessimistic sensitivity analysis
  • Risk of 1 of 11 avoidable AEs estimated by clinicians, who erred towards overestimating the risks
  • AE costs and QALY loss sourced from recent NICE appraisals or targeted searches

Performance

As reported in the abstract

Cost-effectiveness (iNMB) of extended monitoring intervals
  • Extending the duration between monitoring appointments is cost-effective in all scenarios, including a pessimistic analysis (risks of all AEs tripled, costs of some AEs increased)
  • Base case: biennial monitoring often most cost-effective, although incremental net monetary benefit (iNMB) between annual and biennial monitoring often small

Original publication

Cost-effectiveness of risk-stratified blood test monitoring strategies for adults with inflammatory conditions. Rheumatology (Oxford). Published 21 November 2025. doi:10.1093/rheumatology/keaf623

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