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Postpartum hemorrhage (PPH) remains a leading cause of maternal death and morbidity. Moreover, it also contributes to psychological trauma such as depression and post-traumatic stress disorder. The American College of Obstetrics and Gynecology (ACOG) and the Society for Maternal Fetal Medicine (SMFM) defines this morbidity as an unintended outcome in the birthing process that may have significant short-term and long-term consequences to an individual's health. A recent study in 2018 developed core outcomes set for PPH through Delphi consensus encompassing elements of prevention and management of PPH.
Patient-reported outcomes, breastfeeding, and overall sense of wellbeing were not included in the final outcome set. Nevertheless, investigators felt strongly that they should be included, but further work was needed to assess the factors influencing the quality of recovery in the context of PPH. This is aligned with increasing recognition that patient experiences are important to improving the quality of care and quality of recovery after Cesarean delivery. The most effective, i.e. validated tool for assessing postpartum recovery is the Obstetric Quality of Recovery-10 (Obs-QoR-10). However its application in patients with PPH remains unexplored. It would appear logical that patient experiencing PPH experience a potentially more challenging recovery process which may include more surgical complications, depressive symptoms, sleep deprivation, physical exhaustion and stress due to unexpected and undesired delivery events. This study aims to compare Obs-QoR-10 scores in patients with and without PPH to evaluate the impact of severe postpartum bleeding on recovery outcomes using a matched case-control design.
The investigators plan to determine the differences in Obs-QoR-10 scores between patients who experience PPH during childbirth and those deliver without PPH, and to evaluate the impact of PPH on specific recovery domains (physical comfort, emotional well-being, and functional recovery).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Vaginal delivery with PPH | Patients who deliver vaginally with a quantitative blood loss greater than or equal to 1000ml. |
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| Vaginal delivery without PPH | Patients who deliver vaginally with a quantitative blood loss less than 1000ml. |
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| Cesarean delivery with PPH | Patients who deliver vaginally with a quantitative blood loss greater than or equal to 1000ml. |
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| Cesarean delivery without PPH | Patients who deliver vaginally with a quantitative blood loss less than 1000ml. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Obstetric Quality of Recovery-10 (ObsQoR-10©) Scoring Tool | Other | The ObsQoR-10 tool aims to quantitatively measure functional recovery at 24 hours postpartum. It includes 10 questions on a 0 to 10 scale, aimed at pain management, the adverse effects of narcotics and the perception of recovery by the patient. |
| Measure | Description | Time Frame |
|---|---|---|
| Obstetric Quality of Recovery-10 (ObsQoR-10) score 24-48 hours | ObsQoR-10 score between 24 and 48 hours postpartum. There are 10 questions, and the results are tabulated out of 100. The higher the overall score out of 100, the better quality of recovery a patient is experiencing. | 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Semi-quantitative blood loss total (ml) | Semi-quantitative blood loss total (ml) as measured postpartum | 1 hour |
| Length of hospital stay (hours) | Time from admission to discharge from hospital in hours |
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Inclusion Criteria:
Patients aged 18 years or older who have delivered at Mount Sinai Hospital.
Delivery via vaginal or cesarean delivery with neuraxial analgesia or anesthesia
Ability to communicate in English (to answer OBSQoR-10 survey) PPH Cohort
Exclusion Criteria:
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Patients that deliver at Mount Sinai Hospital with measured blood loss greater than or equal to 1000ml, and a set of controls matching the following criteria with measured blood loss less than 1000ml:
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ronald George, MD | Contact | 416-586-4800 | 2681 | ron.george@uhn.ca |
| Kristi Downey, MSc | Contact | 416-586-4800 | 2366 | kristi.downey@uhn.ca |
| Name | Affiliation | Role |
|---|---|---|
| Ronald George, MD | MOUNT SINAI HOSPITAL | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mount Sinai Hospital | Recruiting | Toronto | Ontario | M5G1X5 | Canada |
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| ID | Term |
|---|---|
| D006473 | Postpartum Hemorrhage |
| ID | Term |
|---|---|
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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|
| 4 days |
| Additional uterotonic medication administered - questionnaire | Presence of administration and dosing of any additional uterotonic medication. | 24 hours |
| Blood transfusion | Administration of any blood product and amount given. | 48 hours |
| Surgical interventions for PPH - questionnaire | Use of any surgical interventions for PPH as documented by the surgical team. | 2 hours |
| D011644 | Puerperal Disorders |
| D014592 | Uterine Hemorrhage |
| D006470 | Hemorrhage |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |