Norepinephrine Addition in Spinal Anesthesia of Caesarean Section

NCT ID: NCT03626454

Last Updated: 2024-11-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 300 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-10-16
• Study Completion Date: 2024-02-01

Brief Summary

The objective is to compare efficacy of prophylactic norepinephrine bolus versus Infusion in prevention of hypotension which occurs frequently after spinal anesthesia for caesarean section. The authors hypothesize that prophylactic norepinephrine bolus is as effective as infusion in Prevention of hypotension after spinal anesthesia in caesarean section

Detailed Description

Introduction Spinal anesthesia is the technique of choice for elective cesarean delivery. During spinal anesthesia for cesarean delivery, maternal hypotension is a major complication with the incidence up to 60-70%. Prolonged hypotension leads to decreased utero-placental blood flow and fetal acidosis. Vasopressors such as ephedrine, phenylephrine, and norepinephrine are therefore commonly recommended to reduce the incidence of hypotension.Phenylephrine is currently the first-choice vasopressor for prevention and treatment of maternal hypotension during spinal anesthesia for cesarean delivery (CD).

phenylephrine in this context has been questioned, owing to its propensity to increase afterload, reduce maternal heart rate, and reduce cardiac output. A recent studies indicated that norepinephrine infusion or bolus during spinal anesthesia for cesarean delivery was associated with greater heart rate and cardiac output compared with phenylephrine. Other studies also showed that norepinephrine could act as an alternative to phenylephrine without adverse outcomes.Because it is a potent α-adrenergic agonist with some β-adrenergic effect and, therefore, should not have a tendency to reduce heart rate and cardiac output as much as phenylephrine.

The use of norepinephrine to prevent and treat hypotension during CD is new and data in the literature are scarce. Although treatment of hypotension during spinal anesthesia is listed by the manufacturer as an indication for the use of norepinephrine, there is limited information available for its use for this purpose in the literature and few reports of its use in obstetric patients.

Carvalho and Dyer suggested that more investigations of norepinephrine using simpler methods of delivery than computer-controlled systems are required. Such studies are now emerging.

Anesthetic technique:

Patients will fast overnight and no premedication will be administered. On the day of surgery in the operating room, intravenous (IV) access will be obtained with an 18 gauge IV cannula in an upper limb vein and an infusion of lactated Ringer's (LR) solution of 10 ml/kg will be started as a bolus immediately preceding and with the intrathecal injection, followed by a maintenance rate of 15-30 ml/minute to keep the vein open until delivery of the fetus. Infusion bags will be suspended approximately 1.5 meter above the mid-point of the top surface of the operating table, and the fluid will be administered through a wide-bore administration set with the clamp fully opened.

All patients will be monitored by standard routine monitoring which includes a 5-lead electrocardiography, a non-invasive blood pressure, pulse oximetry. A baseline systolic blood pressure (SBP), mean arterial pressure (MAP) and heart rate (HR) will be measured and recorded in the sitting position by averaging 3 readings taken 1 minute apart using an automated device for noninvasive blood pressure assessment and pulse oximetry (or electrocardiography). All measurements will be continuously recorded until the end of surgery and to avoid possible influence on the measurements, the monitoring module will be placed on the other arm of IV cannula. Spinal anesthesia will be performed with the patient in the sitting position, using a 25-gauge Quincke needle after full aseptic precautions. After skin infiltration with lidocaine 2% (w/v), spinal needle will be inserted at what will be estimated to be the L3 to L4 or L4 to L5 vertebral interspace. After confirmation of free flow of cerebrospinal fluid, intrathecal injection using 0.5% hyperbaric bupivacaine 2.2-2.5 ml mixed with preservative-free fentanyl 15 µg will be injected over 15 seconds, as per our standard practice to achieve surgical anesthesia. The patient will be then positioned supine, with left uterine displacement using a wedge under the right hip. Oxygen 3 L/min via nasal prongs or 5 L/min via mask, if the oxygen saturation fell below 95%. Block level will be assessed by pinprick with a 23 G needle and controlled within T4-6.

Immediately after intrathecal injection, the study medications will be started at 1 ml/kg/h using an infusion pump and injected for 30 seconds for bolus. A rescue bolus of 10 µg norepinephrine or 15 mg ephedrine will be used to treat hypotension. The study protocol will be continued until the end of surgery. After delivery, intravenous oxytocin of 15 U will be administered by slow infusion.

The time interval between blood pressure readings will be 1 minute, therefore the maximum frequency of administration of norepinephrine will be every minute. Hypotension will be defined as a SBP < 80% of the baseline value, in which case the treatment will be deemed a failure, and the anesthesiologist in charge will revert to the standard practice ephedrine 5 mg/mL. Hypertension will be defined as a SBP > 120% of the baseline value, in which case the study solution will be held until the SBP will be less than baseline and a vasodilator (nitroglycerin) can be given if necessary. Bradycardia will be defined as a heart rate < 50 bpm and can be treated with anticholinergics (0.6 mg atropine) if necessary. Decision to treat will be at the discretion of the anesthesiologist. All patients with sensory block levels lower than T6 at 20 minutes were to be considered a dropout.

Use of norepinephrine after completion of the study period will be at the discretion of the attending anesthesiologist, otherwise ephedrine 5 mg/mL will be used, as per standard practice. Upon delivery, a segment of the umbilical cord will be collected for assessment of blood gases in both the umbilical artery and umbilical vein. Hemodynamic values including SBP, MBP, DBP and HR will be recorded at the following timepoints: baseline, after 3 minutes, 5 minutes, 10 minutes, 15 minutes, 20 minutes (± 30 minutes), delivery of fetus, oxytocin administration and end of surgery. Norepinephrine consumption before delivery and during the surgery will be recorded. Adverse effects including shivering, headache, restlessness, pruritus, and peripheral vascular constriction will be recorded. In addition, neonatal outcomes including umbilical venous blood gases and Apgar scores at 1 and 5 min will be recorded by the attending pediatrician, who will be unaware of the vasopressor used

Statistical analysis:

For Sample size calculation MedCalc Statistical Software version 18 (MedCalc Software bvba, Ostend, Belgium; http://www.medcalc.org; 2018) is used. According to previous studies showing that incidence of hypotension among norepinephrine bolus 15% is while it is 31% among norepinephrine infusion. So, a sample size of 144 patients per group will be required to detect a difference of 16% with allocation ratio 1, two-sided α error of 0.05 and 90% power. To compensate for possible dropouts or excluded cases, the authors will include 150 patients in each group with total sample size of 300 patients. Statistical analysis will be performed using SPSS version 24.0 (IBM, Armonk, NY, USA). Data will be tested for normality using the Kolmogorov-Smirnov test. Continuous variables are presented as mean ± standard deviation (SD) or median (interquartile range) as appropriate and categorical variables are presented as number of patients (%). Parametric continuous variables will be analyzed by unpaired t-test and non-parametric continuous variables will be analyzed by Mann-Whitney U test. For categorical variables, the Chi-square (X2) test or Fisher's exact test will be used as appropriate. Two-tailed p values of 0.05 will be considered statistically significant.For Sample size calculation MedCalc Statistical Software version 18 (MedCalc Software bvba, Ostend, Belgium; http://www.medcalc.org; 2018) is used. Previous studies show that the incidence of hypotension among norepinephrine bolus 15% is while it is 31% among norepinephrine infusions. So, a sample size of 105 patients per group will be required to detect a difference of 16% with allocation ratio 1, two-sided α error of 0.05, and 80% power. To compensate for possible dropouts or excluded cases, the authors will include 110 patients in each group with a total sample size of 220 patients. Statistical analysis will be performed using SPSS version 24.0 (IBM, Armonk, NY, USA). Data will be tested for normality using the Kolmogorov-Smirnov test. Continuous variables are presented as mean ± standard deviation (SD) or median (interquartile range) as appropriate and categorical variables are presented as number of patients (%). Parametric continuous variables will be analyzed by unpaired t-test and non-parametric continuous variables by Mann-Whitney U test. The Chi-square (X2) test or Fisher's exact test will be used as appropriate for categorical variables. Two-tailed p-values of 0.05 will be considered statistically significant.

Conditions

Hypotension Drug-Induced

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: TRIPLE

Study Groups

group B

'Norepinephrine bolus' of 6 µg plus Normal Saline 0.9% Infusion Solution

Group Type: ACTIVE_COMPARATOR

Norepinephrine Bolus

Intervention Type: DRUG

'Norepinephrine Bitartarte' bolus of 6 µg/mL for 30 seconds immediately after intrathecal injection

Normal Saline 0.9% Infusion Solution

Intervention Type: DRUG

50 ml syringe with normal saline infuse at a rate 1ml/kg/h immediately after intrathecal injection

group I

'Norepinephrine infusion' 6 µg/kg/h plus 'Normal Saline Flush, 0.9% Injectable Solution

Group Type: ACTIVE_COMPARATOR

Norepinephrine infusion

Intervention Type: DRUG

an infusion of 6 µg/mL norepinephrine that was started at 6 µg/kg/h immediately after intrathecal injection

Normal Saline Flush, 0.9% Injectable Solution

Intervention Type: DRUG

10 ml normal saline in syringe for bolus for 30 seconds immediately after intrathecal injection

Interventions

Norepinephrine Bolus

'Norepinephrine Bitartarte' bolus of 6 µg/mL for 30 seconds immediately after intrathecal injection

Intervention Type: DRUG

Norepinephrine infusion

an infusion of 6 µg/mL norepinephrine that was started at 6 µg/kg/h immediately after intrathecal injection

Intervention Type: DRUG

Normal Saline Flush, 0.9% Injectable Solution

10 ml normal saline in syringe for bolus for 30 seconds immediately after intrathecal injection

Intervention Type: DRUG

Normal Saline 0.9% Infusion Solution

50 ml syringe with normal saline infuse at a rate 1ml/kg/h immediately after intrathecal injection

Intervention Type: DRUG

Other Intervention Names

NORB; NORI; NORSB; NORSI

Eligibility Criteria

Inclusion Criteria

• 18 - 45 years
• American Society of Anesthesiologists physical status classification II or III
• Elective caesarean section under spinal anesthesia
• Normal singleton pregnancy beyond 36 weeks gestation
• Weight 50-100 kg, height 150-180 cm

Exclusion Criteria

• Patient refusal
• Allergy or hypersensitivity to norepinephrine
• Diabetes, excluding gestational diabetes
• Preexisting or pregnancy-induced hypertension
• Arrhythmia
• Cerebrovascular disease
• Known fetal abnormality or fetal distress
• Any contraindication to spinal anesthesia
• Use of monoamine oxidase inhibitors, triptyline or imipramine antidepressants

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Fayoum University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Yasser S Mostafa, MD

Lecturer of anesthesia

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hany M Yassin, M.D.

Role: STUDY_CHAIR

Fayoum University

Locations

Fayoum University hospital

El Fayoum Qesm, Faiyum Governorate, Egypt

Countries

Egypt

References

Ngan Kee WD, Lee SWY, Ng FF, Khaw KS. Prophylactic Norepinephrine Infusion for Preventing Hypotension During Spinal Anesthesia for Cesarean Delivery. Anesth Analg. 2018 Jun;126(6):1989-1994. doi: 10.1213/ANE.0000000000002243.

Reference Type: BACKGROUND

PMID: 28678073 (View on PubMed)

Onwochei DN, Ngan Kee WD, Fung L, Downey K, Ye XY, Carvalho JCA. Norepinephrine Intermittent Intravenous Boluses to Prevent Hypotension During Spinal Anesthesia for Cesarean Delivery: A Sequential Allocation Dose-Finding Study. Anesth Analg. 2017 Jul;125(1):212-218. doi: 10.1213/ANE.0000000000001846.

Reference Type: BACKGROUND

PMID: 28248702 (View on PubMed)

Ngan Kee WD, Khaw KS, Tan PE, Ng FF, Karmakar MK. Placental transfer and fetal metabolic effects of phenylephrine and ephedrine during spinal anesthesia for cesarean delivery. Anesthesiology. 2009 Sep;111(3):506-12. doi: 10.1097/ALN.0b013e3181b160a3.

Reference Type: BACKGROUND

PMID: 19672175 (View on PubMed)

Ngan Kee WD, Lee SW, Ng FF, Tan PE, Khaw KS. Randomized double-blinded comparison of norepinephrine and phenylephrine for maintenance of blood pressure during spinal anesthesia for cesarean delivery. Anesthesiology. 2015 Apr;122(4):736-45. doi: 10.1097/ALN.0000000000000601.

Reference Type: BACKGROUND

PMID: 25635593 (View on PubMed)

Chen D, Qi X, Huang X, Xu Y, Qiu F, Yan Y, Li Y. Efficacy and Safety of Different Norepinephrine Regimens for Prevention of Spinal Hypotension in Cesarean Section: A Randomized Trial. Biomed Res Int. 2018 May 23;2018:2708175. doi: 10.1155/2018/2708175. eCollection 2018.

Reference Type: BACKGROUND

PMID: 29951531 (View on PubMed)

Carvalho B, Dyer RA. Norepinephrine for Spinal Hypotension during Cesarean Delivery: Another Paradigm Shift? Anesthesiology. 2015 Apr;122(4):728-30. doi: 10.1097/ALN.0000000000000602. No abstract available.

Reference Type: BACKGROUND

PMID: 25654435 (View on PubMed)

Other Identifiers

NASA2018

Identifier Type: -

Identifier Source: org_study_id