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Different Approaches to Maternal Hypotension During Cesarean Section

Pharmacological or Non-Pharmacological Management of Maternal Hypotension During Elective Cesarean Section Under Subarachnoid Anesthesia: a Randomized, Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00991627
Enrollment
36
Registered
2009-10-08
Start date
2009-09-30
Completion date
2010-08-31
Last updated
2010-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Cesarean Section, Anesthesia,Spinal, Hypotension

Keywords

Ephedrine, Adrenergic Agents, Central Nervous System Stimulants, Sympathomimetics, Vasoconstrictor Agents, Bupivacaine, Anesthetics, Local, Atropine, Adjuvants, Anesthesia, Anti-Arrhythmia Agents, Bronchodilator Agents, Muscarinic Antagonists, Mydriatics, Parasympatholytics, Morphine, Analgesics, Opioid, Narcotics, Ringer's Lactate, Isotonic Solutions, Hypotension, Blood pressure, Signs and Symptoms, Pregnancy, Anesthesia, Obstetrical, Inferior Vena Cava

Brief summary

The aim of this study is to compare two different therapeutic approaches to blood pressure reduction: pharmacological vs. non-pharmacological. The setting is that of patients undergoing scheduled Cesarean section under spinal anesthesia and suffering from aorta-caval compression syndrome, which causes a sudden drop in blood pressure.

Detailed description

The supine hypotensive syndrome of pregnancy is induced by compression of the inferior caval vein by the enlarged uterus. It occurs in approximately 8% of pregnant women at term. More patients may develop an asymptomatic variety of this syndrome in the supine position. The hypotensive effect of spinal anesthesia per se may thus be aggravated in a significant number of term parturients. A preoperative supine stress test (SST) before elective cesarean section under spinal anesthesia has been shown to predict severe systolic hypotension with reasonable accuracy. Different strategies have been proposed for the management of this complication; they can be divided into pharmacological and non-pharmacological ones. According to pharmacological strategies, vasoactive drugs are used to treat hypotension induced by sympathetic efferent blockade following spinal anesthesia. To this end, α-agonist ephedrine is commonly considered the best choice because of its minimal impact on the fetoplacental circulation. However, excessive use of ephedrine may be detrimental to neonatal well-being because of its vasoconstrictor effect on fetoplacental circulation. Non-pharmacological treatments may represent a valuable, safer alternative. According to many authors non-pharmacological treatments aimed at removing the cause of aorta-caval compression syndrome are to be preferred because more appropriate from an etiopathogenetic point of view. The use of a wedge-shaped cushion placed under the right hip is a well-known non-pharmacological strategy which allows the uterine left lateral displacement and, consequently, the removing of the compression from the inferior vena cava. The aim of the present study is to compare, through the evaluation of neonatal well-being, the efficacy of these approaches to hypotension after spinal anesthesia for elective Caesarean section in parturients affected by aorto-caval compression.

Interventions

DRUGBupivacaine

10 mg of a 5 mg/ml hyperbaric solution, intrathecally

DRUGMorphine

200 µg of a 100 µg/ml solution, intrathecally

25 ml/min intravenously

DRUGEphedrine, continuous infusion

37.5 mg/h intravenously

DRUGEphedrine, bolus

6.25 mg IV bolus prn. Hypotension defined according to study protocol for each arm.

DRUGAtropine

0.1 mg/kg iv bolus prn Bradycardia defined as 50% drop in heart rate from baseline values.

Sponsors

Azienda Ospedaliero-Universitaria di Parma
CollaboratorOTHER
University of Parma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing spinal anesthesia for elective Cesarean section * Patients in ASA Physical Status Class I or II * Informed written consent to participation * Positive Supine Stress Test

Exclusion criteria

* Any known fetal pathology * Indication to general anesthesia * Known allergy to any of the study drugs

Design outcomes

Primary

MeasureTime frame
Neonatal arterial base excess<5 min from birth

Secondary

MeasureTime frame
Apgar score1 and 5 minutes from birth
Maternal serum levels of cardiac troponin (baseline, immediate postsurgery, 6 and 12 hours after surgery)Baseline and up to 12 h postoperatively
Incidence of maternal hypotension ( <20% baseline or mean arterial pressure <60 mmHg).q5min from anesthesia to end of surgery
Incidence of maternal bradycardia (heart rate <30% of baseline or <60 beats per minute)q5min from anesthesia to end of surgery
Neonatal arterial and venous pH, venous base excess<5 min from birth
Administered atropinefrom anesthesia to end of surgery
Amount of ephedrine administered (mg)from anesthesia to end of surgery
Time between induction of anesthesia and skin incision
Time between skin incision and delivery
Peripheral arterial oxygen saturation: incidence of desaturation (SpO2 <92%) and mean values for each arm.q5min from anesthesia to end of surgery

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026