Normotensive Postpartum Cesarean Section Patients Clinical Trial
Official title:
Ambulatory Blood Pressure and the Normal Increase in Maternal Blood Pressure Postpartum
Investigators plan to study blood pressure trends on days 3 to 6 of the postpartum period. Investigators will use a home blood pressure monitor that stays on the arm, and takes blood pressures hourly. Participants will record any symptoms that they feel are attributed to high blood pressure and pain medication use.
Participants will be screened postpartum for inclusion. Only women with cesarean deliveries
will be included as they are kept for 3 days in the hospital as opposed to 2 days for
vaginal deliveries. If they meet inclusion criteria they will be asked to participate in the
study, and consented. Each patient will receive routine postpartum care. The ambulatory
blood pressure cuff will be introduced and validated on the particpant prior to discharge.
Particpants will then be given specific instructions on when to place the cuff on their am
and when to remove it. The ambulatory cuff will take blood pressure measurements every hour.
The Particpant will be asked to keep a log of actives, symptoms, and pain medication use for
the 72 hour period that her blood pressures are being recorded. The BP device will be
returned to the department of OB/GYN at St. Mary's after completion of her 72 hours of
monitoring. This will occur at her first post op visit. Particpants will be asked to
complete a survey about comfort of device and return with the device. Information pertaining
to their pregnancy and delivery will be collected while the patient is in the hospital.
Particpants are not responsible for damage or loss of equipment.
All of these procedures are part of the study.
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