The objective of this research project is to conduct a single-site pilot trial within our
institution's clinical remote blood pressures (BP) management program to assess the
feasibility and effect of tight blood pressure control versus usual care in the immediate
postpartum period after a hypertensive disorder of pregnancy (HDP).
The investigators' central hypothesis is that tight blood pressure control will be feasible
and acceptable to postpartum individuals and will result in lower BP at six months postpartum
and a reduction in postpartum hospital readmissions. Subjects will undergo 3 study visits (1
in-person and 2 remote) involving BP measurements, blood draws, and/or questionnaires. Up to
60 adult subjects will be enrolled at Magee-Women's Hospital.