Postpartum Hemorrhage, Twin; Complicating Pregnancy
Conditions
Brief summary
Obstetrical hemorrhage (excessive bleeding related to pregnancy) is a leading cause of maternal morbidity (disease or symptom of disease) and mortality (death) worldwide with a significantly higher frequency and severity following cesarean delivery. Twin gestations (twin pregnancy) are at particularly higher risk for postpartum hemorrhage, yet the management of obstetrical bleeding following twin delivery remains identical to singleton delivery. The purpose of this study is to understand the effect of prophylactic methylergonovine on blood loss in scheduled twin pregnancy cesarean deliveries. Participants will be randomized (like tossing a coin) to Methylergonovine (investigational drug) or water with salt (saline) (placebo). Methylergonovine or saline will be given as an injection immediately after delivery.
Detailed description
Obstetrical hemorrhage is a leading cause of maternal morbidity and mortality worldwide with a significantly higher frequency and severity following cesarean delivery. In 2020, 31.9 percent of pregnant women in the United States underwent cesarean delivery, making it the second most common operation performed. Though multiple complications can occur following cesarean delivery, hemorrhage morbidities are among the most common with significant cardiovascular implications. Twin gestations are at particularly higher risk for postpartum hemorrhage due to impaired myometrial contractility and atony following overdistention; increased maternal blood volume; and increased uterine blood flow compared to singletons, yet the management of obstetrical bleeding following twin delivery remains identical to singleton delivery. Current strategies to address intrapartum hemorrhage have relied on pharmacological and mechanical treatments after intraoperative identification. However, there is extensive work on prophylactic therapies administered intraoperatively to prevent obstetrical hemorrhage. Recent evidence has emerged about the utility of prophylactic Methylergonovine for the prevention of obstetrical hemorrhage. Methylergonovine, a semisynthetic ergot alkaloid, acts primarily on alpha adrenergic receptors of uterine and vascular smooth muscle, increasing uterine tone and promoting vasoconstriction. In a randomized trial of 80 women undergoing intrapartum cesarean delivery found that fewer patients who were allocated to the methylergonovine group received additional uterotonic agents (20% vs 55%, relative risk (RR) 0.4, 95% confidence interval (CI) 0.2-0.6). Participants receiving methylergonovine were more likely to have satisfactory uterine tone (80% vs 41%, RR 1.9, 95% CI 1.5-2.6), lower incidence of postpartum hemorrhage (35% vs 59%, RR 0.6, 95% CI 0.4-0.9), lower mean quantitative blood loss (967 mL vs 1,315 mL; mean difference 348, 95% CI 124-572), and a lower frequency of blood transfusion (5% vs 23%, RR 0.2, 95% CI 0.1-0.6). Investigators concluded that the administration of prophylactic methylergonovine in addition to oxytocin in patients undergoing intrapartum cesarean birth reduces the need for additional uterotonic agents. In a prospective study of 1210 participants found that intraoperative, prophylactic methylergonovine decreased post-operative blood loss with no adverse side effects. Randomized trials of Methylergonovine as prophylaxis to prevent hemorrhage in cesarean delivery have exclude twin gestations. Currently, there remains a paucity of research regarding prophylactic procedures for twin cesarean delivery. There is an opportunity to prophylactically address hemorrhage in high-risk groups. Therefore, the investigators propose a prospective randomized controlled trial which will compare maternal blood loss associated with prophylactic methylergonovine during cesarean delivery among patients with twin.
Interventions
Methylergonovine 200mcg Intramuscular (IM)
Matching saline placebo
Sponsors
Study design
Eligibility
Inclusion criteria
* Twin gestation * Scheduled cesarean delivery (\>=34 weeks)
Exclusion criteria
* Patients with known hypertensive disease: history of chronic hypertension, gestational hypertension or preeclampsia with or without severe features * Use of protease inhibitors given known vasoconstrictive side effects with concomitant methylergonovine administration * Hypersensitivity to methylergonovine or any of the ingredients * Participating in another intervention study where the primary outcome includes postpartum bleeding or thromboembolism, or the study intervention directly affects postpartum bleeding or thromboembolism * Receipt of uterotonics, other than oxytocin, or planned or expected use of uterotonic prophylaxis * Non-elective cesarean delivery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Maternal Hemoglobin Level | Baseline and Postoperative Day 1 (Approximately 48 hours) | The change in maternal hemoglobin level as taken from blood samples. The change will be calculated from preoperative day 1 (baseline) to postoperative day 1. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Estimated Blood Loss | Intraoperative (Approximately 24 hours) | At the end of the surgery, the primary surgeon will estimate the blood loss throughout the case. |
| Quantitative Blood Loss | Intraoperative (Approximately 24 hours) | Quantitative blood loss is calculated by weighing the used towels during the operation. The number is calculated by the circulating nurse in the operating room. |
| Number of Participants With Postpartum Hemorrhage | Intraoperative (Approximately 24 hours) | The number of participants with postpartum hemorrhage (defined as estimated blood loss \>1000 cc) |
| Number of Participants Requiring Use of Uterotonics | Intraoperative (Approximately 24 hours) | Number of participants given uterotonics, such as prostaglandins |
| Number of Participants Requiring Use of Tranexamic Acid | Intraoperative (Approximately 24 hours) | Number of participants given Tranexamic acid |
| Number of Participants Requiring Use of Open-Label Methylergonovine | Intraoperative (Approximately 24 hours) | Number of participants requiring the use of any amount of open-label methylergonovine (not blinded study drug) |
| Number of Participants Requiring Transfusion (Intraoperative) | Intraoperative (Approximately 24 hours) | Number of participants requiring transfusion of 1 or more units of packed red blood cells, including whole blood or cell saver. |
| Number of Participants With Surgical or Radiological Interventions | Intraoperative (Approximately 24 hours) | Composite number of surgical or radiological interventions (such as: laparotomy, evacuation of hematoma, hysterectomy, uterine packing, intrauterine balloon tamponade, interventional radiology) to control bleeding and related complications or maternal death. |
| Surgical Time | Intraoperative (Approximately 24 hours) | Surgical time measured from the time of incision to closure |
| Number of Participants Requiring Transfusion (6 Weeks) | 6 weeks | Number of participants requiring transfusion of 1 or more units of fresh frozen plasma, cryoprecipitate, or platelets or administration of any factor concentrates. |
| Number of Participants With Acute Elevation of Serum Creatinine | 48 hours | Number of participants with acute elevation of serum creatinine of ≥ 0.3 mg/dL |
| Number of Postpartum Infectious Complications | 6 weeks | Number of Postpartum infectious complications such as: endometritis, surgical site infection, pelvic abscess |
| Number of Participants With Admission to the Intensive Care Unit | 6 weeks | Number of participants with admission to the intensive care unit for more than 24 hours |
| Length of Stay | Up to 6 weeks | Length of stay measured from the time of hospital admission to hospital discharge. |
| Number of Participants Re-Admitted to the Hospital | 6 weeks | The number of participants who experienced hospital re-admission |
| Apgar Scores | 1 and 5 minutes post-delivery (approximately 24 hours post-baseline) | Apgar score is a measure of the physical condition of a newborn infant. Scores range from 0-10 with a higher score indicating a better outcome; Apgar score of 0-3 is low, 4-6 is moderately abnormal, and 7-10 is reassuring. |
| Neonatal Intensive Care Unit (NICU) Admission | Time of delivery (Approximately 24 hours) | Number of newborns admitted to the neonatal intensive care unit (NICU). |
| Number of Participants With Transfusion Related Acute Lung Injury (TRALI) | 6 weeks | Number of participants with transfusion related acute lung injury (TRALI) |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Prophylactic Methylergonovine Prophylactic methylergonovine 200mcg IM | 33 |
| Placebo Normal Saline 1mL | 33 |
| Total | 66 |
Baseline characteristics
| Characteristic | Prophylactic Methylergonovine | Placebo | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 33 Participants | 33 Participants | 66 Participants |
| Chorionicity, n (%) Dichorionic | 21 Participants | 21 Participants | 42 Participants |
| Chorionicity, n (%) Monochorionic-Diamniotic | 12 Participants | 12 Participants | 24 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 15 Participants | 14 Participants | 29 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 18 Participants | 19 Participants | 37 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Gestational diabetes mellitus, n (%) | 5 Participants | 6 Participants | 11 Participants |
| Maternal BMI (kg/m2), mean, SD | 30.0 kg/m^2 STANDARD_DEVIATION 5.7 | 30.5 kg/m^2 STANDARD_DEVIATION 7.3 | 30.25 kg/m^2 STANDARD_DEVIATION 6.5 |
| Number of Prior Cesarean Deliveries, n (%) 0 | 23 Participants | 24 Participants | 47 Participants |
| Number of Prior Cesarean Deliveries, n (%) 1 | 7 Participants | 7 Participants | 14 Participants |
| Number of Prior Cesarean Deliveries, n (%) >=2 | 3 Participants | 2 Participants | 5 Participants |
| Preoperative maternal hemoglobin level (g/dL), mean (SD) | 11.6 g/dL STANDARD_DEVIATION 1.2 | 12.0 g/dL STANDARD_DEVIATION 1.3 | 11.8 g/dL STANDARD_DEVIATION 1.25 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 2 Participants | 2 Participants |
| Race (NIH/OMB) Black or African American | 11 Participants | 9 Participants | 20 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 22 Participants | 22 Participants | 44 Participants |
| Sex: Female, Male Female | 33 Participants | 33 Participants | 66 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
| Tobacco use in pregnancy, n (%) | 1 Participants | 0 Participants | 1 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 33 | 0 / 33 |
| other Total, other adverse events | 0 / 33 | 0 / 33 |
| serious Total, serious adverse events | 0 / 33 | 0 / 33 |
Outcome results
Change in Maternal Hemoglobin Level
The change in maternal hemoglobin level as taken from blood samples. The change will be calculated from preoperative day 1 (baseline) to postoperative day 1.
Time frame: Baseline and Postoperative Day 1 (Approximately 48 hours)
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Prophylactic Methylergonovine | Change in Maternal Hemoglobin Level | 1.1 g/dL | Standard Deviation 0.7 |
| Placebo Group | Change in Maternal Hemoglobin Level | 2.1 g/dL | Standard Deviation 0.9 |
Apgar Scores
Apgar score is a measure of the physical condition of a newborn infant. Scores range from 0-10 with a higher score indicating a better outcome; Apgar score of 0-3 is low, 4-6 is moderately abnormal, and 7-10 is reassuring.
Time frame: 1 and 5 minutes post-delivery (approximately 24 hours post-baseline)
Population: Newborns were assessed rather than the mothers (i.e. enrolled participants). Each participant gave birth to twins (66 newborns total). Newborns were not considered enrolled but did contribute to this assessment.
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Prophylactic Methylergonovine | Apgar Scores | Apgar 1 minute | 8 score on a scale |
| Prophylactic Methylergonovine | Apgar Scores | Apgar 5 minutes | 9 score on a scale |
| Placebo Group | Apgar Scores | Apgar 1 minute | 8 score on a scale |
| Placebo Group | Apgar Scores | Apgar 5 minutes | 9 score on a scale |
Estimated Blood Loss
At the end of the surgery, the primary surgeon will estimate the blood loss throughout the case.
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Prophylactic Methylergonovine | Estimated Blood Loss | 800 cc |
| Placebo Group | Estimated Blood Loss | 1000 cc |
Length of Stay
Length of stay measured from the time of hospital admission to hospital discharge.
Time frame: Up to 6 weeks
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Prophylactic Methylergonovine | Length of Stay | 4 days |
| Placebo Group | Length of Stay | 4 days |
Neonatal Intensive Care Unit (NICU) Admission
Number of newborns admitted to the neonatal intensive care unit (NICU).
Time frame: Time of delivery (Approximately 24 hours)
Population: Newborns were assessed rather than the mothers (i.e. enrolled participants). Each participant gave birth to twins (66 newborns total). Newborns were not considered enrolled but did contribute to this assessment.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Prophylactic Methylergonovine | Neonatal Intensive Care Unit (NICU) Admission | 19 newborns |
| Placebo Group | Neonatal Intensive Care Unit (NICU) Admission | 20 newborns |
Number of Participants Re-Admitted to the Hospital
The number of participants who experienced hospital re-admission
Time frame: 6 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Re-Admitted to the Hospital | 1 Participants |
| Placebo Group | Number of Participants Re-Admitted to the Hospital | 3 Participants |
Number of Participants Requiring Transfusion (6 Weeks)
Number of participants requiring transfusion of 1 or more units of fresh frozen plasma, cryoprecipitate, or platelets or administration of any factor concentrates.
Time frame: 6 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Requiring Transfusion (6 Weeks) | 2 Participants |
| Placebo Group | Number of Participants Requiring Transfusion (6 Weeks) | 4 Participants |
Number of Participants Requiring Transfusion (Intraoperative)
Number of participants requiring transfusion of 1 or more units of packed red blood cells, including whole blood or cell saver.
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Requiring Transfusion (Intraoperative) | 0 Participants |
| Placebo Group | Number of Participants Requiring Transfusion (Intraoperative) | 0 Participants |
Number of Participants Requiring Use of Open-Label Methylergonovine
Number of participants requiring the use of any amount of open-label methylergonovine (not blinded study drug)
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Requiring Use of Open-Label Methylergonovine | 0 Participants |
| Placebo Group | Number of Participants Requiring Use of Open-Label Methylergonovine | 7 Participants |
Number of Participants Requiring Use of Tranexamic Acid
Number of participants given Tranexamic acid
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Requiring Use of Tranexamic Acid | 2 Participants |
| Placebo Group | Number of Participants Requiring Use of Tranexamic Acid | 7 Participants |
Number of Participants Requiring Use of Uterotonics
Number of participants given uterotonics, such as prostaglandins
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants Requiring Use of Uterotonics | 0 Participants |
| Placebo Group | Number of Participants Requiring Use of Uterotonics | 6 Participants |
Number of Participants With Acute Elevation of Serum Creatinine
Number of participants with acute elevation of serum creatinine of ≥ 0.3 mg/dL
Time frame: 48 hours
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants With Acute Elevation of Serum Creatinine | 0 Participants |
| Placebo Group | Number of Participants With Acute Elevation of Serum Creatinine | 0 Participants |
Number of Participants With Admission to the Intensive Care Unit
Number of participants with admission to the intensive care unit for more than 24 hours
Time frame: 6 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants With Admission to the Intensive Care Unit | 0 Participants |
| Placebo Group | Number of Participants With Admission to the Intensive Care Unit | 0 Participants |
Number of Participants With Postpartum Hemorrhage
The number of participants with postpartum hemorrhage (defined as estimated blood loss \>1000 cc)
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants With Postpartum Hemorrhage | 6 Participants |
| Placebo Group | Number of Participants With Postpartum Hemorrhage | 18 Participants |
Number of Participants With Surgical or Radiological Interventions
Composite number of surgical or radiological interventions (such as: laparotomy, evacuation of hematoma, hysterectomy, uterine packing, intrauterine balloon tamponade, interventional radiology) to control bleeding and related complications or maternal death.
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants With Surgical or Radiological Interventions | 0 Participants |
| Placebo Group | Number of Participants With Surgical or Radiological Interventions | 0 Participants |
Number of Participants With Transfusion Related Acute Lung Injury (TRALI)
Number of participants with transfusion related acute lung injury (TRALI)
Time frame: 6 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Participants With Transfusion Related Acute Lung Injury (TRALI) | 0 Participants |
| Placebo Group | Number of Participants With Transfusion Related Acute Lung Injury (TRALI) | 0 Participants |
Number of Postpartum Infectious Complications
Number of Postpartum infectious complications such as: endometritis, surgical site infection, pelvic abscess
Time frame: 6 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Prophylactic Methylergonovine | Number of Postpartum Infectious Complications | 0 Participants |
| Placebo Group | Number of Postpartum Infectious Complications | 2 Participants |
Quantitative Blood Loss
Quantitative blood loss is calculated by weighing the used towels during the operation. The number is calculated by the circulating nurse in the operating room.
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Prophylactic Methylergonovine | Quantitative Blood Loss | 891 cc |
| Placebo Group | Quantitative Blood Loss | 1017 cc |
Surgical Time
Surgical time measured from the time of incision to closure
Time frame: Intraoperative (Approximately 24 hours)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Prophylactic Methylergonovine | Surgical Time | 62.0 Minutes |
| Placebo Group | Surgical Time | 61.0 Minutes |