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S6A:4 A population-based study on mortality and the influence of medication use in 4356 patients with systemic lupus erythematosus and 21845 matched controls from the united kingdom
  1. IE Bultink1,
  2. F de Vries2,3,
  3. RF van Vollenhoven1 and
  4. A Lalmohamed2,4
  1. 1Amsterdam Rheumatology and immunology Centre, location VUmc, Department of Rheumatology, Amsterdam, The Netherlands
  2. 2Utrecht University, Department of Pharmacoepidemiology and Clinical Pharmacy, Utrecht, The Netherlands
  3. 3Maastricht University Medical Centre, Department of Clinical Pharmacy and Toxicology, Maastricht, The Netherlands
  4. 4University Medical Centre Utrecht, Department of Clinical Pharmacy, Utrecht, The Netherlands


Purpose To estimate the magnitude of the risk from all-cause, age-specific, sex-specific, and cause-specific mortality in patients with SLE and relative risks compared with matched controls, and to evaluate the influence of medication exposure on mortality risk in SLE.

Methods We conducted a population-based cohort study using the Clinical Practice Research Datalink, Hospital Episode Statistics, and national death certificates (from 1987 to 2012). Each SLE patient (n=4356) was matched with up to 6 controls (n=21845) by age and sex. Multivariate Cox regression analysis estimated adjusted relative rates (RR) of mortality, and time interaction terms to evaluate mortality timing patterns. Time-dependent Cox models were used to evaluate the association of glucocorticoid use and hydroxychloroquine use on mortality and were adjusted for age, sex, lifestyle parameters, comorbidities and comedication.

Results A total of 442 out of 4356 SLE patients died during the study period. Patients with SLE had an increased mortality rate for all-cause mortality compared with age- and sex-matched subjects, after adjustment for confounders (adjusted RR 1.80, 95% CI: 1.57 to 2.08). The RR was highest in patients aged 18–39 years (adjusted RR 4.87, 95% CI: 1.93 to 12.3). Moratlity rates were not defferent between male and female patients. Glucocorticoid use in the previous six months raised the mortality rate while the adjusted RR was 45% decreased with low dose hydroxychloroquine use. SLE patients had increased cause-specific mortality rates for cardiovascular disease, infectious disease, noninfectious respiratory disease and for death due to accidents or suicide, while mortality rate for cancer was reduced, compared to age- and sex-matched subjects.The mortality rate was significantly increased for patients with a history of dementia, seizures, diabetes, cancer, and renal disease (table 1).

Conclusions Patients with SLE have a 1.8-fold increased mortality rate compared with the general population. Gluococorticoid use, female sex and young age are associated with an increased mortality risk while low dose hydroxychloroquine use significantly reduces the mortality rate. In addition, special attention should be paid to lupus patients with neuropsychiatric complications, diabetes, malignancy or renal disease since these subgroups of patients are at high risk of death.

Abstract S6A:4 Table 1

Risk of all-cause monthly within SLE patients (n=4356), stratified according to organ damage (reference = no risk factor)

  • mortality
  • cause of death
  • systemic lupus erythematosus

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