he global burden of gout continues to grow. 1 Amid concerns regarding possible cardiovascular adverse effects with febuxostat, 2 the number of patients with gout prescribed allopurinol may increase. Furthermore, as clinical trials 3 investigate allopurinol's purported cardiorenal benefits, 4,5 use of allopurinol among those without gout may also increase. Although generally safe and well-tolerated, allopurinol has been associated with severe cutaneous adverse reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis, which are collectively referred to as allopurinol-associated severe cutaneous adverse reactions. A Taiwanese population-based study found that heart disease was independently associated with increased risk of hospital admission for allopurinol-associated severe cutaneous adverse reactions. 6 However, this finding has not been replicated in a non-Asian cohort. We sought to fill this knowledge gap by investigating the association in a Canadian general population cohort. Moreover, we investigated the potential joint impact of heart disease and other risk factors, including chronic kidney disease, 6-8 higher starting allopurinol dosage 6,8,9 and demographic factors. 6,8,10,11 Methods Population and study design We conducted a cohort study using Population Data BC, an administrative database with de-identified patient-level data on hospital discharge records, 12 outpatient dispensed prescriptions 13 and vital statistics for nearly all of British Columbia's 4.7 million residents. 14 We used hospital admission and RESEARCH Heart disease and the risk of allopurinolassociated severe cutaneous adverse reactions: a general population-based cohort study