There are limited data on contemporary outcomes for women with sickle cell disease (SCD) in pregnancy. We conducted a single-site matched cohort study, comparing 131 pregnancies to women with SCD between 2007 and 2017 to a comparison group of 1310 pregnancies unaffected by SCD. Restricting our analysis to singleton pregnancies that reached 24 weeks of gestation, we used conditional Poisson regression to estimate adjusted risk ratios (aRRs) for perinatal outcomes. Infants born to mothers with SCD were more likely to be small for gestational age [aRR 1Á69, 95% confidence interval (CI) 1Á13-2Á48], preterm (aRR 2Á62, 95% CI 1Á82-3Á78) and require Neonatal Unit (NNU) admission (aRR 3Á59, 95% CI 2Á18-5Á90). Pregnant women with SCD were at higher risk of pre-eclampsia/ eclampsia (aRR 3Á53, 95% CI 2Á00-6Á24), more likely to receive induction of labour (aRR 2Á50, 95% CI 1Á82-1Á76) and caesarean birth (aRR 1Á44, 95% CI 1Á18-1Á76). In analysis stratified by genotype, the risk of adverse outcomes was highest in haemoglobin SS (HbSS) pregnancies (n = 80). There was no strong evidence that haemoglobin SC (HbSC) pregnancies (n = 46) were at higher risk of preterm birth, caesarean delivery, or NNU admission. Pre-eclampsia/eclampsia was more frequently observed in HbSC pregnancies. Despite improvements in the care of pregnant women with SCD, the increased risk of adverse perinatal outcomes remains.