spinal anesthesia-induced hypotension during cesarean delivery
Conditions
Interventions
low weight group(body weight 50-70 kg):Each patient received a prophylactic infusion of 5µg/ml norepinephrine delivered using a syringe pump and started at the time of intrathecal injection.For the fi
high weight group(body weight 70-90 kg):Each patient received a prophylactic infusion of 5µg/ml norepinephrine delivered using a syringe pump and started at the time of intrathecal injection.For the f
Sponsors
Obstetrics and Genecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: American Society of Anesthesiologists (ASA) physical status I/II and full-term women with singleton pregnancy scheduled for elective cesarean delivery under regional anesthesia
Exclusion criteria
Exclusion criteria: Height 170 cm, allergy to norepinephrine, preexisting or pregnancy-induced hypertension, cardiovascular or cerebrovascular disease, diabetes mellitus, fetal abnormalities, obstetric complication (ruptured membranes, placenta praevia, placental abruption),and any contraindication to spinal or epidural anaesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence of hypotension; | — |
Secondary
| Measure | Time frame |
|---|---|
| the incidence of hypertension;the incidence of bradycardia;the incidence of nausea;the incidence of vomiting;the incidence of shivering;Apgar scores 1 and 5 min after delivery;measurement of umbilical arterial blood gases; | — |
Countries
China
Contacts
Public ContactShaoqiang Huang
Obstetrics and Genecology Hospital of Fudan University
Outcome results
None listed