Use of ROTEM Intraoperatively in Women With Placenta Accreta (ROTEM)
Placenta Accreta
About this trial
This is an interventional diagnostic trial for Placenta Accreta focused on measuring thromboelastography
Eligibility Criteria
Inclusion Criteria:
- Women diagnosed with placenta accreta during pregnancy who are scheduled to have delivery by cesarean section with hysterectomy to follow.
Exclusion Criteria:
- Non-English speaking
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
ROTEM
Standard treatment
Participants randomized to this arm will have rapid testing of hematocrit and clotting function every 30 minutes during the hysterectomy portion of their surgery for placenta accreta, with transfusion of blood products based on defined abnormalities in these tests.
Participants randomized to this arm will have standard visual assessment of blood loss and standard laboratory studies to assess blood count and clotting function when indicated during the hysterectomy portion of their surgery for placenta accreta. Transfusion of blood products will be based on abnormalities of these test results.