Postpartum Hemorrhage
Conditions
Keywords
pregnancy, postpartum hemorrhage, cesarean delivery, carbetocin, duratocin, oxytocin
Brief summary
The study investigators are comparing 2 drugs (oxytocin and carbetocin) at 2 different dosages, to help prevent serious bleeding (hemorrhage) after cesarean deliveries. These drugs are used routinely to help contract the uterus and keep it contracted after the delivery of the baby and placenta; this reduces the amount of blood you might lose. At Mount Sinai Hospital, currently oxytocin is used, but its effect on the uterus is much shorter than that of carbetocin. Internationally, there is no consensus as to what the most effective drug to use is and at which dose. The Society of Obstetricians and Gynaecologists of Canada has recently revised its guidelines to suggest 100 micrograms (mcg) of carbetocin as the drug of choice at elective cesarean section. Guidelines from the United Kingdom and the United States currently suggest oxytocin at various doses as the drug of choice at elective cesarean sections. Previous studies at Mount Sinai Hospital have shown that lower doses of oxytocin, 0.35 International Units (IU), and carbetocin, 20 mcg, may be as effective as the higher recommended doses. The investigators plan to conduct a large study to confirm these findings so that they can use the most appropriate dose in the future. Furthermore, the investigators hope to demonstrate that side effects are lower with the lower dose regimens.
Detailed description
Postpartum hemorrhage (PPH) is a major cause of maternal death worldwide. Oxytocin is the most commonly used uterotonic drug to prevent and treat PPH in the world. However, oxytocin has a very short duration of action, requiring a continuous infusion to achieve sustained uterotonic activity. Moreover, large doses are associated with adverse effects like hypotension, nausea, vomiting, dysrhythmias and ST changes. The Society of Obstetricians and Gynecologists of Canada (SOGC) has recommended a single dose of 100 mcg of the longer acting carbetocin at elective cesarean section to promote uterine contraction. In multiple studies performed at Mount Sinai Hospital, we have shown that smaller doses of oxytocin (ED 90 0.35 IU) and carbetocin (ED 90 14.8 mcg) are effective in achieving adequate uterine tone at elective cesarean section. No study has directly compared the high dose regimens with the low dose regimens; therefore a large double-blind randomized controlled trial is necessary to show the non-inferiority of the lower doses of both drugs. There is a lack of consensus as to what the optimal uterotonic regime is globally. Furthermore, variability in the international guidelines regarding the choice of first line uterotonic in prevention of PPH adds to the confusion. With the widespread availability of carbetocin in some of the developed countries, including Canada, the question of which uterotonic to adopt and at which dose becomes even more difficult to ascertain. Studies that have currently been published suggest the ED90 doses of carbetocin and oxytocin provide adequate uterine contraction with possibly fewer side effects associated with the lower dosed regimens. These advantages may provide a better safety profile and patient satisfaction. To the best of our knowledge, no studies have compared the low doses (ED90) of oxytocin vs. carbetocin, or low (ED90) vs high (conventional) doses of the two drugs in the setting of elective cesarean section. The results of this study will provide evidence on the efficacy and safety of the ED90 dosing compared directly to the higher dosing of both drugs. Our hypothesis is that the ED90 doses of carbetocin and oxytocin will not be inferior to the higher dosing as determined by the intensity of uterine contraction using a VNRS in women undergoing elective cesarean section. We anticipate that the intensity of uterine contraction using the VNRS at 2 minutes post administration of all drugs will fall within the predetermined margin to signify non-inferiority of all regimens.
Interventions
DRUGCarbetocin
Patient is given carbetocin (20 or 100 mcg) intravenously over 1 minute, immediately upon delivery of the anterior shoulder of the baby.
DRUGOxytocin
Patient is given oxytocin (0.5 or 5 IU) intravenously over 1 minute, immediately upon delivery of the anterior shoulder of the baby.
Sponsors
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* Elective cesarean section under spinal anesthesia. * Written informed consent to participate in this study. * Full-term pregnancy * Non labouring patients
Exclusion criteria
* Refusal to give written informed consent. * Allergy or hypersensitivity to carbetocin or oxytocin. * Labouring patients * Need for general anesthesia * Conditions that predispose to uterine atony and postpartum hemorrhage such as placenta previa, multiple gestation, preeclampsia, eclampsia, macrosomia, polyhydramnios, uterine fibroids, previous history of uterine atony and postpartum bleeding, or bleeding diathesis. * Hepatic, renal, and cardiovascular disease.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Uterine Tone 2 minutes | 2 minutes | Intensity of uterine tone on a VNRS scale of 0-10 as evaluated by the obstetrician at 2 minutes after completion of injection of the bolus study drug. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Uterine Tone 10 minutes | 10 minutes | Intensity of uterine tone on a VNRS scale of 0-10 as evaluated by the obstetrician at 10 minutes after completion of injection of the bolus study drug. |
| Additional uterotonics - operating room | 1 hour | The use of additional uterotonic agents in the operating room |
| Additional uterotonics - 24 hours | 24 hours | The use of additional uterotonic agents at any time after admission to the recovery room and up to 24 hours post delivery |
| Estimated blood loss | 24 hours | Blood loss will be calculated through the difference in hematocrit values assessed prior to and at the end of 24 hours after the cesarean section. |
| Hypotension: systolic blood pressure less than 80% of baseline | 2 hours | Systolic blood pressure \< 80% of baseline, from drug administration until end of surgery |
| Hypertension: systolic blood pressure greater than 120% of baseline | 2 hours | Systolic blood pressure \> 120% of baseline, from drug administration until end of surgery |
| Tachycardia: heart rate greater than 130% of baseline | 2 hours | Heart rate \> 130% of baseline, from drug administration until end of surgery |
| Bradycardia: heart rate less than 70% of baseline | 2 hours | Heart rate \< 70% of baseline, from drug administration until end of surgery |
| Uterine Tone 5 minutes | 5 minutes | Intensity of uterine tone on a VNRS scale of 0-10 as evaluated by the obstetrician at 5 minutes after completion of injection of the bolus study drug. |
| Presence of atrial fibrillation: ECG | 2 hours | Presence of atrial fibrillation as recorded by ECG, from drug administration until end of surgery |
| Presence of atrial flutter: ECG | 2 hours | Presence of atrial flutter as recorded by ECG, from drug administration until end of surgery |
| Presence of nausea: questionnaire | 2 hours | The presence of nausea and number of episodes, from drug administration until end of surgery, as reported by the patient |
| Presence of vomiting: questionnaire | 2 hours | The presence of vomiting and number of episodes, from drug administration until end of surgery |
| Presence of chest pain: questionnaire | 2 hours | Any presence of chest pain, from drug administration until end of surgery, as reported by the patient |
| Presence of shortness of breath: questionnaire | 2 hours | Any presence of shortness of breath, from drug administration until end of surgery, as reported by the patient |
| Presence of headache: questionnaire | 2 hours | Any presence of headache, from drug administration until end of surgery, as reported by the patient |
| Presence of flushing: questionnaire | 2 hours | Any presence of flushing, from drug administration until end of surgery |
| Presence of ventricular tachycardia: ECG | 2 hours | Presence of ventricular tachycardia as recorded by ECG, from drug administration until end of surgery |
Countries
Canada
Outcome results
None listed