| アブストラクト | BACKGROUND: Patients established on thiopurines (e.g., azathioprine) are recommended to undergo three-monthly blood tests for the early detection of blood, liver, or kidney toxicity. These side-effects are uncommon during long-term treatment. We developed a prognostic model that could be used to inform risk-stratified decisions on frequency of monitoring blood-tests during long-term thiopurine treatment, and, performed health-economic evaluation of alternate monitoring intervals. METHODS: This was a retrospective cohort study set in the UK primary-care. Data from the Clinical Practice Research Datalink Aurum and Gold formed development and validation cohorts, respectively. People age >/=18 years, diagnosed with an immune mediated inflammatory disease, prescribed thiopurine by their general practitioner for at-least six-months between January 1, 2007 and December 31, 2019 were eligible. The outcome was thiopurine discontinuation with abnormal blood-test results. Patients were followed up from six-months after first primary-care thiopurine prescription to up to five-years. Penalised Cox regression developed the risk equation. Multiple imputation handled missing predictor data. Calibration and discrimination assessed model performance. A mathematical model evaluated costs and quality-adjusted life years associated with lengthening the interval between blood-tests. FINDINGS: Data from 5982 (405 events over 16,117 person-years) and 3573 (269 events over 9075 person-years) participants were included in the development and validation cohorts, respectively. Fourteen candidate predictors (21 parameters) were included. The optimism adjusted R(2) and Royston D statistic in development data were 0.11 and 0.76, respectively. The calibration slope and Royston D statistic (95% Confidence Interval) in the validation data were 1.10 (0.84-1.36) and 0.72 (0.52-0.92), respectively. A 2-year period between monitoring blood-test was most cost-effective in all deciles of predicted risk but the gain between monitoring annually or biennially reduced in higher risk deciles. INTERPRETATION: This prognostic model requires information that is readily available during routine clinical care and may be used to risk-stratify blood-test monitoring for thiopurine toxicity. These findings should be considered by specialist societies when recommending blood monitoring during thiopurine prescription to bring about sustainable and equitable change in clinical practice. FUNDING: National Institute for Health and Care Research. |
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| 投稿者 | Nakafero, Georgina; Card, Tim; Grainge, Matthew J; Williams, Hywel C; Taal, Maarten W; Aithal, Guruprasad P; Fox, Christopher P; Mallen, Christian D; van der Windt, Danielle A; Stevenson, Matthew D; Riley, Richard D; Abhishek, Abhishek |
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| 組織名 | Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham;NG5 1PB, UK.;Lifespan and Population Health, School of Medicine, University of Nottingham,;Nottingham NG5 1PB, UK.;Centre for Kidney Research and Innovation, School of Medicine, Translational;Medical Sciences, University of Nottingham, Derby DE22 3NE, UK.;Nottingham Digestive Diseases Centre, Translational Medical Sciences, School of;Medicine, University of Nottingham, Nottingham NG7 2UH, UK.;Translational Medical Sciences, School of Medicine, University of Nottingham,;Nottingham, UK.;Primary Care Centre Versus Arthritis, School of Medicine, Keele University, Keele;ST5 5BJ, UK.;School of Health and Related Research, University of Sheffield, Sheffield S1 4DA,;UK.;Institute of Applied Health Research, College of Medical and Dental Sciences,;University of Birmingham, Birmingham B15 2TT, UK. |
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