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Development and validation of a multivariable risk prediction model for serious infection in patients with psoriasis receiving systemic therapy

Authors :
Yiu, Z. Z. N.
Sorbe, C.
Lunt, M.
Rustenbach, S. J.
Kuehl, L.
Augustin, M.
Mason, K. J.
Ashcroft, D. M.
Griffiths, C. E. M.
Warren, R. B.
Ormerod, Anthony D.
Barker, Jonathan N. W. N.
Evans, Lan
McElhone, Kathleen
Smith, Catherine H.
Reynolds, Nick J.
Murphy, Ruth
Benham, Marilyn
Burden, A. David
Hussain, Sagair
Kirby, Brims
Lawson, Linda
Owen, Caroline M.
Source :
Yiu, Z Z N, Sorbe, C, Lunt, M, Rustenbach, S J, Kuehl, L, Augustin, M, Mason, K J, Ashcroft, D M, Griffiths, C E M, Warren, R B, Ormerod, A D, Barker, J N W N, Evans, L, McElhone, K, Smith, C H, Reynolds, N J, Murphy, R, Benham, M, Burden, A D, Hussain, S, Kirby, B, Lawson, L & Owen, C M 2019, ' Development and validation of a multivariable risk prediction model for serious infection in patients with psoriasis receiving systemic therapy ', British Journal of Dermatology, vol. 180, no. 4, pp. 894-901 . https://doi.org/10.1111/bjd.17421
Publication Year :
2019

Abstract

BackgroundPatients with psoriasis are often concerned about the risk of serious infection associated with systemic psoriasis treatments.ObjectivesTo develop and externally validate a prediction model for serious infection in patients with psoriasis within 1 year of starting systemic therapies.MethodsThe risk prediction model was developed using the British Association of Dermatologists Biologic Interventions Register (BADBIR), and the German Psoriasis Registry PsoBest was used as the validation dataset. Model discrimination and calibration were assessed internally and externally using the C‐statistic, the calibration slope and the calibration in the large.ResultsOverall 175 (1·7%) out of 10 033 participants from BADBIR and 41 (1·7%) out of 2423 participants from PsoBest developed a serious infection within 1 year of therapy initiation. Selected predictors in a multiple logistic regression model included nine baseline covariates, and starting infliximab was the strongest predictor. Evaluation of model performance showed a bootstrap optimism‐corrected C‐statistic of 0·64 [95% confidence interval (CI) 0·60–0·69], calibration in the large of 0·02 (95% CI −0·14 to 0·17) and a calibration slope of 0·88 (95% CI 0·70–1·07), while external validation performance was poor, with C‐statistic 0·52 (95% CI 0·42–0·62), calibration in the large 0·06 (95% CI −0·25 to 0·37) and calibration slope 0·36 (95% CI −0·24 to 0·97).ConclusionsWe present the first results of the development of a multivariable prediction model. This model may help patients and dermatologists in the U.K. and the Republic of Ireland to identify modifiable risk factors and inform therapy choice in a shared decision‐making process.

Details

Language :
English
Database :
OpenAIRE
Journal :
Yiu, Z Z N, Sorbe, C, Lunt, M, Rustenbach, S J, Kuehl, L, Augustin, M, Mason, K J, Ashcroft, D M, Griffiths, C E M, Warren, R B, Ormerod, A D, Barker, J N W N, Evans, L, McElhone, K, Smith, C H, Reynolds, N J, Murphy, R, Benham, M, Burden, A D, Hussain, S, Kirby, B, Lawson, L & Owen, C M 2019, ' Development and validation of a multivariable risk prediction model for serious infection in patients with psoriasis receiving systemic therapy ', British Journal of Dermatology, vol. 180, no. 4, pp. 894-901 . https://doi.org/10.1111/bjd.17421
Accession number :
edsair.od......2761..d16523f43cbaeb4d0b0ab83b8c1f964d