Norepinephrine to Prevent Hypotension in Ceasrean Delivery
Hypotension, Cesarean Section Complications
About this trial
This is an interventional prevention trial for Hypotension focused on measuring hypotension, norepinephrine
Eligibility Criteria
Inclusion Criteria:
- ASA I & II
- Non laboring
- Normotensive
- Elective cesarean delivery under spinal anesthesia.
- Baseline systolic blood pressure 90-140 mm Hg
Exclusion Criteria:
- Known fetal abnormality.
- Preexisting or pregnancy-induced hypertension.
- Known cardiovascular or cerebrovascular disease.
- Thrombocytopenia, coagulopathy or any contraindication to spinal anesthesia.
- Weight <50 or >100 kg, height <140 or >180 cm.
- Inability or refusal to give informed consent
Sites / Locations
- Faculty of Medicine, University Hospitals
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
infusion
bolus
patients will receive an infusion of norepinephrine that will be started at 2.5μg/min immediately after intrathecal injection and then manually adjusted according to monitoring of blood pressure (bp), heart rate, fluid responsiveness (thoracic volume variations and stroke volume variations), cardiac index and systemic vascular resistance by using cardiometry, with the objective of maintaining values near baseline
patient with no prophylactic vasopressor and a bolus of 5 μg norepinephrine will be given whenever systolic BP decreases to <80% of the baseline value.