Management of gestational hypertension - The impact of HYPITAT

Aims: The objective of this study was to examine the impact of one trial (the HYPITAT trial) on management of gestational hypertension. Study design: This is a retrospective cohort study of 5077 patients delivered at our institution from 7/1/2008 to 6/15/2011. " Pre-HYPITAT " was defined as 7/1/2008 - 9/30/2009 and " Post-HYPITAT " as 10/1/2009- 6/15/2011. The primary outcome is the rate of delivery intervention for gestational hypertension. Secondary maternal and neonatal outcomes were analyzed in patients with gestational hypertension only. Statistical analyses included the χ₂ -test, Fisher ' s exact test, and the two-sample t -test. Results: The rate of delivery intervention Pre-HYPITAT was 1.9 % , compared to 4 % Post-HYPITAT (P<0.001). There was no significant change in secondary outcomes. Conclusion: There was a statistically significant increase in delivery intervention for gestational hypertension at our institution after the publication of the HYPITAT trial. There was no significant change in immediate maternal or neonatal outcomes for patients with gestational hypertension.