Can we validate a clinical score to predict the risk of severe infection in patients with systemic lupus erythematosus? A longitudinal retrospective study in a British Cohort

ObjectiveSevere infections are a major cause of morbidity and mortality in patients with systemic lupus erythematosus (SLE). Our primary objective was to use data from a large Spanish cohort to develop a risk score for severe infection in SLE, the SLE Severe Infection Score (SLESIS) and to validate...

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Veröffentlicht in:BMJ open 2019-06, Vol.9 (6), p.e028697-e028697
Hauptverfasser: Tejera Segura, Beatriz, Rua-Figueroa, Iñigo, Pego-Reigosa, Jose Maria, del Campo, Victor, Wincup, Chris, Isenberg, David, Rahman, Anisur
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Sprache:eng
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Zusammenfassung:ObjectiveSevere infections are a major cause of morbidity and mortality in patients with systemic lupus erythematosus (SLE). Our primary objective was to use data from a large Spanish cohort to develop a risk score for severe infection in SLE, the SLE Severe Infection Score (SLESIS) and to validate SLESIS in a separate cohort of 699 British patients.Design and settingRetrospective longitudinal study in a specialist tertiary care clinic in London, UK.ParticipantsPatients fulfilling international classification criteria for SLE (n=209). This included 98 patients who had suffered severe infections (defined as infection leading to hospitalisation and/or death) and 111 randomly selected patients who had never suffered severe infections.OutcomesWe retrospectively calculated SLESIS at diagnosis for all 209 patients. For the infection cases we also calculated SLESIS just prior to infection and compared it to SLESIS in 98 controls matched for disease duration. We carried out receiver operator characteristic (ROC) analysis to quantify predictive value of SLESIS for severe infection.ResultsMedian SLESIS (IQR) at diagnosis was higher in the infection group than in the control group (4.27 (3.18) vs 2.55 (3.79), p=0.0008). Median SLESIS prior to infection was higher than at diagnosis (6.64 vs 4.27, p
ISSN:2044-6055
2044-6055
DOI:10.1136/bmjopen-2018-028697