Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. The objective of this trial is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).
Hypertensive disorders are frequent during the course of pregnancy-puerperal cycle and an important cause of maternal morbidity and mortality, fetal and perinatal. The high frequency of maternal death can be explained by the presence of numerous complications such as eclampsia. Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. Currently, allows the use of either 1 g / h to 2 g / h of magnesium sulphate during the maintenance phase to prevent eclamptic convulsions. However, there is no report in the literature of randomized controlled trials comparing different doses of magnesium sulfate in the maintenance phase to prevent eclampsia. The objective of this study is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).There will be a trial randomized and triple blind in the Integrative Medicine Institute Prof. Fernando Figueira (IMIP) from March 2015 to April 2017, and will be included 2000 women randomized into two groups: MgSO4 maintenance dose of 1 g / h or 2 g / h. Patients who had eclampsia before loading dose, with use of other medications or illicit drugs that may interfere with maternal hemodynamics or with contraindications to the use of magnesium sulfate will be excluded. The primary endpoint will be the incidence of eclampsia. Other complications such as oliguria, bleeding, recurrence of seizures, disseminated intravascular coagulation, maternal death, presence of side effects related to the use of MgSO, neonatal outcome and other variables will be considered secondary outcomes. Randomization for preventive treatment of eclamptic seizures with MgSO4 1g / h or MgSO4 2g / h will be held according to a table of sequential numbers from one to 2000, using the letters A and B and not knowing its meaning. The analysis will be performed with the groups identified as A or B, breaking the secrecy only after the results obtained and prepared the tables, or by resolution of the External Monitoring Committee.
Patients will receive after the loading dose os magnesium sulfate, the maintenance dose of 1g/hour of intravenous of magnesium sulfate for 24 hours after loading dose
Patients will receive after the loading dose os magnesium sulfate, the maintenance dose of 1g/hour of intravenous of magnesium sulfate for 24 hours after loading dose
Instituto Materno Infantil Prof. Fernando Figueira
Recife, Pernambuco, Brazil
ECLAMPSIA
Seizures that occur after the loading dose, during magnesium sulfate, until 24 hours after the delivery of the baby
Time frame: From end of loading dose, until 24 hours after delivery
Placental abruption
Occurence of placental abruption
Time frame: From end of loading dose, until delivery of the child
postpartum hemorrhage
Occurence of postpartum hemorrhage, diagnosed clinically by the attending phisician
Time frame: From end of loading dose, until 48 hours after delivery
COMPLICATIONS
Occurence of a retained placenta
Time frame: From end of loading dose, until 3 hours after delivery
thromboembolic complications
Diagnosis of thromboembolic complications bay doppler compression ultrasound or CT
Time frame: From end of loading dose, until 15 days after delivery
liver failure
Occurence of liver failure according to laboratorial exams
Time frame: From end of loading dose, until 15 days after delivery
OLIGURIA
Oliguria diagnosed as the presence of urine output under 0.5 (mililiters per kilogram) mL/kg for six hours,
Time frame: From end of loading dose, until 15 days after delivery
RENAL FAILURE
Occurence of renal failure diagnosed as the presence of oliguria for more than 24 hours or elevation serum creatinine (3X )
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Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
62
Time frame: From end of loading dose, until 15 days after delivery
Disseminated intravascular coagulation (DIC)
Presence of disseminated intravascular coagulation
Time frame: From end of loading dose, until 15 days after delivery
acute pulmonary edema
Presence of clinically diagnosis of acute pulmonary edema
Time frame: From end of loading dose, until 15 days after delivery
Maternal death
Maternal death occuring for direct obstetric causes
Time frame: From end of loading dose, until 42 days after delivery
Composite maternal morbidity
Presence of one of the investigated complications
Time frame: From end of loading dose, until 42 days after delivery
RECURRENCE
Recurrence of seizures after loading dose of magnesium sulfate
Time frame: From end of loading dose, until 24 hours after delivery
additional anticonvulsant
Need for additional anticonvulsant after the use of magnesium sulfate
Time frame: From end of loading dose, until 24 hours after delivery
SIDE EFFECTS
Presence of side effects of magnesium sulfate use
Time frame: From end of loading dose, until 24 hours after delivery
DISCONTINUATION OF MAGNESIUM SULFATE
Occurence of discontinuation of treatment due to side effects
Time frame: From end of loading dose, until 24 hours after delivery
GLUCONATE USE
Need for the use of calcium gluconate
Time frame: From end of loading dose, until 24 hours after delivery
MAGNESIUM LEVELS
Serum magnesium levels evaluated at the beginning of maintenance dose and after 30. minutes, every 2 hours for six hours and after every six hours until 24 hous after loading dose. This outcome will be evaluated in the first 62 patients
Time frame: From end of loading dose, until 24 hours after delivery
Hypertensive crises
Presence of hypertensive crises and need for antihypertensive drugs and need to continue therapy for more than 24 hours.
Time frame: From end of loading dose, until 24 hours after delivery