Emergency (Red Code) Cesarean Section : Maternal and Fetal Prognosis Depending on Anesthetic Modalities in a Level 3 Maternity Ward
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 150
- Locations
- 1
- Primary Endpoint
- To evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome
Study Overview
Brief Summary
We try to evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome on emergency (Red Code) Cesarean Section.
This study occurred in a Level 3 Maternity Ward.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Retrospective
Eligibility Criteria
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Pregnant women
- •emergency "code red" cesarean section
Exclusion Criteria
- •Any other intervention
- •Planned cesarean section
Outcomes
Primary Outcomes
To evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome
Time Frame: From July 19, 2018 to July 19, 2023.
Identify all pregnant women who received an emergency "code red" cesarean section Confront epidural anesthesia and general anesthesia on maternal complications (low blood pressure, anesthetic failure) and neonatal outcomes (Apgar scores, arterial pH at the umbilical cord, arterial lactate, need for tracheal intubation at birth, admission of the newborn to intensive care/intensive care, death)
Secondary Outcomes
No secondary outcomes reported
Investigators
STANOWSKI Mattieu
MD
Central Hospital, Nancy, France