None listed
Conditions
Interventions
Drug, Medical Device : This study was designed as a prospective cohort study. HemoSphere monitor is connected after inserting an arterial catheter before anesthesia in 106 patients (53 patients in eac
baseline, 5 minute after spinal anesthesia, baby out time, 5 minute after baby out, 15 minute after baby out, end of surgery.
Sponsors
Ewha Womans University Seoul Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women in term pregnancy for elective cesarean section via spinal anesthesia
Exclusion criteria
Exclusion criteria: (1) patient refuse (2) emergent surgery (3) minor under 18 years of age (4) fetal abnormality (congenital) (5) contraindication for spinal anesthesia (6) abnormal placenta such as previa, accreta, etc (7) other patients eliminated by the researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of hypotensive event after spinal anesthesia and dose of vasopressors used, Performance of HPI index during delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in cardiac output (CO), systemic vascular resistance (SVR), stroke volume (SV), and stroke volume variability (SVV) measured before and after anesthesia, before and after delivery, and at the end of surgery | — |
Countries
Korea, Republic of
Contacts
Public ContactSang-Mee An
Ewha Womans University Seoul Hospital
Outcome results
None listed