Hypotension
Conditions
Keywords
vasopressor, blood pressure, Cesarean section, spinal anesthesia
Brief summary
Spinal anesthesia is the most common anesthetic technique for elective Cesarean delivery (CD), but the most frequent unwanted side effect is hypotension, which can cause nausea and vomiting, as well as effects on the fetus. Prevention and treatment of maternal hypotension includes intravenous fluids and vasopressors. Phenylephrine is the most common vasopressor used for this purpose. However, it has been shown to reduce maternal heart rate and cardiac output, which may be a concern in an already compromised fetus. Norepinephrine is commonly used in high concentrations in intensive care and recent studies have suggested that in low concentrations it may be a better alternative to phenylephrine in elective CD, as it does not reduce the maternal heart rate or cardiac output. The optimum bolus dose of norepinephrine to prevent hypotension after spinal anesthesia in elective CD has not been elucidated. The investigators propose this study to determine the dose that would be effective in 90% of patients (ED90). A previous study by Ngan Kee et al, using continuous infusion of norepinephrine to prevent hypotension in elective CD, suggested a potency ratio for norepinephrine to phenylephrine of approximately 16:1. Hence, the investigators hypothesise that the ED90 will be approximately 6 µg, given that the current phenylephrine bolus dose at the investigators' institution is approximately 100 µg.
Detailed description
The use of norepinephrine to prevent and treat hypotension during cesarean delivery (CD) is new and data in the literature are scarce. A recent randomised controlled trial by Ngan Kee et al compared continuous infusions of norepinephrine and phenylephrine to prevent hypotension during CD. They showed that norepinephrine was effective at maintaining blood pressure, with a greater cardiac output and heart rate compared to phenylephrine. However, the effective bolus dose of norepinephrine needed to prevent maternal hypotension was not determined, and since this is a relatively new arena, no dose-response studies are available in the literature either. Therefore, it would be logical to establish the effective bolus dose of norepinephrine TO PREVENT HYPOTENSION during elective CD.
Interventions
DRUGNorepinephrine
DRUGNormal Saline
0.9% sodium chloride solution, used as a diluent.
Sponsors
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* Elective CD under spinal anesthesia * Normal singleton pregnancy beyond 36 weeks gestation * ASA physical status II/III * Weight 50-100 kg, height 150-180 cm * Age over 18 years * Informed consent
Exclusion criteria
* Patient refusal * Allergy or hypersensitivity to norepinephrine or sulfite * Preexisting or pregnancy-induced hypertension * Cardiovascular or cerebrovascular disease * Fetal abnormalities * History of diabetes, excluding gestational diabetes * Use of monoamine oxidase inhibitors, triptyline or imipramine antidepressants
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Systolic blood pressure | 30 minutes | The primary outcome of this study will be the success/response of the norepinephrine dose to maintain the systolic blood pressure at or above 80% of baseline, from induction of spinal anesthesia to delivery of the fetus. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Presence of Vomiting | 30 minutes | Presence of vomiting in patients from induction of spinal anesthesia to delivery of the fetus. |
| Hypertension: Systolic blood pressure at or above 120% of baseline | 30 minutes | Systolic blood pressure at or above 120% of baseline, from induction of spinal anesthesia to delivery of the fetus. |
| Bradycardia: Heart rate less than 50 bpm | 30 minutes | Heart rate less than 50 bpm, from induction of spinal anesthesia |
| Upper sensory level of anesthetic block, assessed by pinprick upon delivery | 30 minutes | Upper sensory level of anesthesia, assessed by pinprick upon delivery |
| Umbilical artery pH | 24 hours | Umbilical artery pH |
| Umbilical artery partial pressure of carbon dioxide | 24 hours | Umbilical artery partial pressure of carbon dioxide |
| Umbilical artery partial pressure of oxygen | 24 hours | Umbilical artery partial pressure of oxygen |
| Presence of Nausea | 30 minutes | Presence of nausea in patients from induction of spinal anesthesia to delivery of the fetus. |
| Umbilical artery base excess | 24 hours | Umbilical artery base excess |
| Umbilical vein pH | 24 hours | Umbilical vein pH |
| Umbilical vein partial pressure of carbon dioxide | 24 hours | Umbilical vein partial pressure of carbon dioxide |
| Umbilical vein partial pressure of oxygen | 24 hours | Umbilical vein partial pressure of oxygen |
| Umbilical vein bicarbonate | 24 hours | Umbilical vein bicarbonate |
| Umbilical vein base excess | 24 hours | Umbilical vein base excess |
| Umbilical artery bicarbonate | 24 hours | Umbilical artery bicarbonate |
Countries
Canada
Outcome results
None listed