Evaluation of the Efficacy of the Addition of Magnesium Sulfate to Morphine on the Occurrence of Acute Urinary Retention Following Epidural Anesthesia for Cesarean Section.

The main objective of this study is to evaluate the efficacy of the addition of epidural magnesium sulfate in reducing the occurrence of acute post-Caesarean urine retention.

In fact, the incidence of acute urine retention after epidural anaesthesia for Caesarean section is around 33%. Two encouraging studies suggest that adding magnesium sulfate to epidurals could reduce the incidence of acute urine retention by 15%.

This study will be carried out on the obstetric population of the REIMS maternity hospital, starting in summer 2024. It is a randomized, double-blind, placebo-controlled clinical trial. The number of subjects required is calculated at 290 patients, with a power of 80% and an alpha risk of 5%. The statistical hypothesis is that magnesium sulfate reduces the incidence of acute urine retention by 15% compared with placebo (isotonic saline).

Parturients will be informed of the study during a pre-anaesthetic consultation in the 6th month of pregnancy.

Some of these patients will be scheduled for delivery by caesarean section. The remaining patients will be scheduled for a vaginal delivery, which may end up being an emergency caesarean section (10-15% of patients).

After the Caesarean section, patients are taken to the post-procedure monitoring room, where they are monitored for 2 hours.

It is at this point that patients are examined to verify the inclusion and non-inclusion criteria of the protocol. If the inclusion and non-inclusion criteria are met, our teams will provide patients with explanatory documents on our protocol, as well as a consent form for their signature.

When the patient agrees to enter the protocol, the investigators randomize her to one of the following groups:

• Group A: injection of morphine 2 mg into the epidural catheter + magnesium sulfate 500 mg
• Group B: injection of morphine 2 mg into the epidural catheter + isotonic saline.

Group B is the control group. This is the protocol we use in daily practice for parturients who have undergone Caesarean section, in line with the French recommendations of anesthesia societies.

This reduces the parturient's postoperative pain for 20-24 hours. Group A will be the experimental group. Patients will be monitored in the post-natal care unit for 72 hours. The investigators will carry out the same monitoring and care as a parturient outside the protocol. Various data on diuresis, the quantity of urine in the bladder visualized by ultrasound, and the need for urinary catheterization will be recorded.

Statistical analyses will determine whether the incidence of acute urine retention differs between each group.

Inclusion criteria

• Patients who have undergone scheduled or emergency Caesarean section surgery under extended epidural anesthesia or combined epidural and spinal anesthesia at the Reims University Hospital.
• Patients who have just undergone caesarean section and have the epidural catheter in place in the post-interventional monitoring room (SSPI).
• Patients who agree to take part in the research and have signed the informed consent form
• Patients of legal age
• Patients affiliated to a social security scheme

Exclusion criteria

• Minor patients
• Patients protected by law
• Patients allergic to local anesthetics, morphine or magnesium sulfate
• Patients with severe renal insufficiency (GFR < 30 ml/min)
• Patients with pre-pregnancy mictional disorders
• Patients with an American Society of Anesthesiologists (ASA) score of 4
• Patients undergoing caesarean section under general anaesthesia, after failure of perimedullary anaesthesia
• Patients with accidental intraoperative injury to the urinary tract
• Patients who have received intravenous magnesium sulfate in the 24 hours preceding cesarean section