Atony, Uterine, Cesarean Section Complications, Uterine Bleeding
Conditions
Brief summary
The research was planned as a face-to-face survey evaluation. The questionnaire will be applied to obstetricians and anesthesiologists working in public and private hospitals. The universe of the research will be selected by simple random sampling method, and the total number of people who will participate is planned to be 200, approximately 100 from each of the two branches. Our survey consists of 5 parts structurally. Demographic data, rate of cesarean section and postpartum hemorrhage, uterotonic agent preferences in low/high risk cesarean section surgeries, the preference for second-line uterotonic agents, and the dose preferences of uterotonic agents.
Interventions
None listed
Sponsors
Gazi University
Study design
Observational model
OTHER
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
obstetricians and anesthesiologists who want to participate in the survey
Exclusion criteria
the ones who do not want to participate \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Uterotonic usage habits in postpartum hemorrhage | 3 months | to learn the uterotonic use preferences of both obstetricians and anesthesiologists in postpartum |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Uterotonic usage habits in elective cesearean section | 3 months | to learn the uterotonic use preferences of both obstetricians and anesthesiologists in elective cesarean section |
Countries
Turkey (Türkiye)
Outcome results
None listed