Cesarean Section Complications
Conditions
Brief summary
Independent form anesthetic methods, during C/S, considering both maternal and fetal conditions, some crucial hemodynamic changes can appear and can be claimed non invasively with the whole body bioimpedance. In this research, any kind of hemodynamic difference between this method and urgent or elective C/S case will be detected and the clinic pursuit can be developed creating an advantage in favor of both maternal and fetal conditions.
Detailed description
Independent form anesthetic methods, during C/S, considering both maternal and fetal conditions, some crucial hemodynamic changes can appear and can be claimed non invasively with the whole body bioimpedance. In this research, any kind of hemodynamic difference between this method and urgent or elective C/S case will be detected and the clinic pursuit can be developed creating an advantage in favor of both maternal and fetal conditions. Under general anesthesia, measuring the hemodynamic changes with the method of non-invasive whole-body bioimpedance system during C/S. Detection of in which phase of operations the potential changes densify and differences between urgent and elective conditions non invasively.
Interventions
DIAGNOSTIC_TESTnon invasive whole body bioimpedence system
Noninvasive hemodynamic changes will be observed by using whole-body impedance method urgent or elective cesarian section patients under general anesthesia. The whole-body bioimpedance method will be used to monitör the hemodynamic changes non invasively. This method can evaluate such as cardiac output, cardiac index, stroke volüme, stroke index, stroke volüme variations, cardiac reserve, etc. Parameters with a completely noninvasive method by using only electrots. The device consists of a laptop, a software which calculates cardiac parameters and two electrodes. The measurement is done by the following process: one of these electrodes, which looks like ECG electrodes, is stuck to the wrist and the other one to the opposite ankle or each one to two wrists.
Sponsors
Gaziosmanpasa Research and Education Hospital
Study design
Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 49 Years
Inclusion criteria
* Must be scheduled for elective or emergency cesarean section
Exclusion criteria
* History of cardiac surgery, and advanced cardiac valvular disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| MAP | 1, 5, 15, and 30 minutes following the induction of the anesthesia | The difference in mean arterial pressure during the cesarean section between elective and emergency ceasreansection subjects |
Countries
Turkey (Türkiye)
Contacts
Primary ContactZuhal Cavus, MD
Backup ContactZuhal Cavus, Cavus
Outcome results
None listed