Prediction of Maternal Arterial Hypotension After Spinal Anesthesia by Passive Leg Raise Test.

Spinal Anesthesia Clinical Trial

— EDLIDL  

Official title:

Assessment of the Value of Passive Leg Raising (PLR) in Predicting the Onset of Maternal Arterial Hypotension and Norepinephrine Requirements After Spinal Anesthesia for Scheduled Cesarean Section.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05133271
• Other study ID #: APHP210937
• Secondary ID: 2021-A01099-32
• Status: Recruiting
• Phase: N/A
• Start date: February 3, 2021
• Est. completion date: June 3, 2024

Study information

• Verified date: January 2024
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Xavier Repessé, MD
• Phone: 1 71 39 68 89
• Email: xavier.repesse[@]aphp.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Spinal anesthesia for cesarean section is associated with a high incidence of low blood pressure. However, the pathophysiology of this arterial hypotension is not unequivocal and could involve, in addition to drug vasoplegia, a mechanical cause linked to lower caval compression or even true or relative hypovolemia. Passive leg raise test has been proposed in an attempt to identify parturients who are more likely to develop low blood pressure after spinal anesthesia. Nevertheless, the data available on this volume expansion test to predict hemodynamic variations after performing spinal anesthesia are still limited and few objective criteria have been described to predict this arterial hypotension. The objective of the research is to study the hypothesis according to which the presence of hypovolaemia (true or relative) objectified by a positive passive leg raise test would cause hypotension more frequent and more marked in intensity.

Description:

Spinal anesthesia for cesarean section is associated with a high incidence of low blood pressure. However, the pathophysiology of this arterial hypotension is not unequivocal and could involve, in addition to drug vasoplegia, a mechanical cause linked to lower caval compression or even true or relative hypovolemia. Passive leg raise test has been proposed in an attempt to identify parturients who are more likely to develop low blood pressure after spinal anesthesia. Nevertheless, the data available on this volume expansion test to predict hemodynamic variations after performing spinal anesthesia are still limited and few objective criteria have been described to predict this arterial hypotension. The objective of the research is to study the hypothesis according to which the presence of hypovolaemia (true or relative) objectified by a positive passive leg raise test would cause hypotension more frequent and more marked in intensity. Patients will have a clinical hemodynamic and echocardiographic evaluation, before performing the spinal anesthesia, before and after the passive leg raise test. Then, the patients will benefit from a clinical hemodynamic evaluation during the preparation of the parturient in the operating room and finally after the completion of the spinal anesthesia and until the clamping of the umbilical cord.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 63
• Est. completion date: June 3, 2024
• Est. primary completion date: June 3, 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult women admitted to Necker Enfants Malades hospital for scheduled cesarean section under spinal anesthesia
• Written informed consent

Exclusion Criteria:

• No health insurance
• Urgent cesarean
• Failure of spinal anesthesia
• Free and informed consent impossible to obtain (especially due to a language barrier)
• Severe cardiovascular or neurovascular comorbidities
• Contraindication to the PLR (intracranial hypertension, fractures of the pelvis and / or lower limbs, ...)
• Background of preeclampsia or eclampsia
• Severe fetal pathology

Related Conditions & MeSH terms

• Cesarean
• Hypotension
• Spinal Anesthesia

Intervention

Other:
• Clinical hemodynamic and echocardiographic evaluation
Clinical hemodynamic and echocardiographic evaluation in two stages T1 and T2, before performing the spinal anesthesia, carried out by a doctor different from the doctor in charge of the parturient in the operating room to ensure the blind hemodynamic results before the spinal anesthesia, in particular those of the passive leg raise test (PLR) : T1: clinico-echographic evaluation in dorsal decubitus position (45 °) with cushion under the right buttock. T2: clinico-ultrasound evaluation after performing the PLR. Then, clinical hemodynamic evaluation during two periods T3 and T4: T3: conditioning time of the parturient in the operating room during which clinical hemodynamic monitoring is set up and the basic values of arterial pressures (systolic, diastolic and mean) and heart rate are defined. T4: period after performing spinal anesthesia until clamping of the umbilical cord.

Locations

Country	Name	City	State
France	Hôpital Necker-Enfants Malades	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maternal arterial hypotension	Maternal arterial hypotension following spinal anesthesia. Maternal hypotension is defined as a drop in systolic blood pressure (SBP)> 20% of baseline.	Day 0
Primary	Positivity of passive leg raise test	A positive passive leg raise test is defined as an increase in the Subaortic Flow Velocity Time Integral of 10% or more. The increase in cardiac output is measured by a cardiac ultrasound.	Day 0
Primary	Positive passive leg raise test performance	Performance of a positive passive leg raise test in predicting the onset of maternal arterial hypotension after spinal anesthesia. Significant performance will be defined by sensitivity and specificity > 90%.	Day 0
Secondary	Total dose of norepinephrine	Total dose of norepinephrine received during the procedure from the beginning of the spinal anesthesia injection up to umbilical cord clamping measured in micrograms.	Day 0
Secondary	Onset of severe arterial hypotension	Onset of severe arterial hypotension defined as a drop in systolic blood pressure greater than 30% of baseline.	Day 0
Secondary	Onset of nausea and vomiting	Onset of nausea and vomiting from the spinal anesthesia injection up to the end of the c-section.	Day 0
Secondary	Occurrence of disturbances of consciousness	Occurrence of consciousness alteration assessed by the Glasgow Coma Scale (from Teasdale G & Jennett B. Lancet 1974).; Three aspects of behavior are measured independently: motor response, verbal response and eye opening.; Each component has a number of grades starting with the most severe. The best ocular response has 4 grades; the best verbal response has 5 grades; the best motor response has 6 grades.; Rating: the score of each component as well as the sum of the components are considered. The total score is out of 15 points; lower scores indicating more severe impairment. The lowest possible score is 3, indicating deep coma or death, and the highest possible score is 15, indicating a fully awake individual.	Day 0
Secondary	Occurrence of sedation and agitation	Occurrence of sedation and agitation during the c-section assessed by the Richmond Agitation-Sedation scale (RASS).; This score is based on the observation of the patient It has 10 stages ranging from +4 (combative patient) to -5 (patient who cannot be woken up).	Day 0
Secondary	Assessment of fetal well-being	Evaluation of fetal well-being by fetal heartbeat, by the Apgar score at 1, 3 and 5 minutes of life, and study of the pH in the umbilical cord, a pH value <7.2 defines fetal distress.	Day 0
Secondary	Quality of ultrasound images	Assessment of obtaining views (parasternal long-axis view, parasternal short-axis view, apical 4-chamber view, subcostal).; Interpretability of the measurements obtained.	Day 0
Secondary	Relative or absolute hypovolemia	Describe the echocardiographic parameters reflecting the different physiopathological mechanisms at the origin of arterial hypotension secondary to spinal anesthesia of the parturient at the end of pregnancy.; To note the parameters suggestive of relative or absolute hypovolaemia: inferior vena cava diameter < 8 mm; "kissing sign" of the left ventricle, defined as à end-systolic collapse of the left ventricle; E/A ratio < 1.	Day 0
Secondary	Right ventricle systolic or diastolic dysfunction	Describe the echocardiographic parameters reflecting the different physiopathological mechanisms at the origin of arterial hypotension secondary to spinal anesthesia of the parturient at the end of pregnancy.; Right ventricle systolic function: measurement of the TAPSE (tricuspid annular plane systolic excursion; presence of a paradoxical septal motion (yes/no).; Right ventricle diastolic function: presence of right ventricle dilation defined as end-diastolic right ventricle area (EDRVA) / end-diastolic left ventricle area (EDLVA) > 0.6; "severe" dilatation is defined as a ratio > 1.	Day 0
Secondary	Left ventricle systolic and diastolic dysfunction	Describe the echocardiographic parameters reflecting the different physiopathological mechanisms at the origin of arterial hypotension secondary to spinal anesthesia of the parturient at the end of pregnancy.; Left ventricle systolic function: left ventricle ejection fraction (LVEF) - apical-4-chamber view - defined as LVEF = (EDLVA-ESLVA)/EDLVA Left ventricle shortening fraction (LVSF) - parasternal short-axis view - defined as LVSF = (EDLVA-ESLVA)/EDLVA MAPSE (mitral annular plane systolic excursion; Left ventricle diastolic function: Mitral flow profile: E wave / A wave ratio Left atrium area (cm²)	Day 0
Secondary	Pericardial effusion	Describe the echocardiographic parameters reflecting the different physiopathological mechanisms at the origin of arterial hypotension secondary to spinal anesthesia of the parturient at the end of pregnancy.; Measurement of the size (in mm) of the pericardial effusion (left and right ventricles lateral walls).	Day 0
Secondary	Maternal comfort during the passive leg raising	Assessment of the maternal comfort during the passive leg raising test with a numerical scale (from 0: maximal discomfort to 10: maximal comfort).	Day 0
Secondary	Heart rate	Association of increased up heart rate and total dose of neosynephrine at the end of the c-section.	Day 0