OBS-QoR-10 in Patients With and Without Postpartum Hemorrhage
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Obstetric Quality of Recovery-10 (ObsQoR-10©) Scoring Tool.
- Who it may be relevant to
- Registry conditions: Postpartum Hemorrhage (Primary). Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Comparing the Obstetric Quality of Recovery-10 (OBS-QoR-10) in Patients With and Without Postpartum Hemorrhage: A Matched Case-control Study
Overview
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).
Interventions
- Other Obstetric Quality of Recovery-10 (ObsQoR-10©) Scoring Tool
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.
Primary outcome measures
- Obstetric Quality of Recovery-10 (ObsQoR-10) score 24-48 hours [Time frame: 24 hours]
Secondary outcome measures (5)
- Semi-quantitative blood loss total (ml) [Time frame: 1 hour]
- Length of hospital stay (hours) [Time frame: 4 days]
- Additional uterotonic medication administered - questionnaire [Time frame: 24 hours]
- Blood transfusion [Time frame: 48 hours]
- Surgical interventions for PPH - questionnaire [Time frame: 2 hours]
Eligibility criteria
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
- Quantitative Blood Loss (QBL) ≥ 1000 mL or,
- Transfusion of blood due to PPH or,
- Transfer to ICU level care due to PPH
- Significant PPH intervention, i.e. hysterectomy or arterial embolization Non-PPH
- QBL < 500 mL and,
- No transfusion of blood products, and
- No need for elevated care environment, i.e. HAU or ICU
Exclusion criteria
- Patients with pre-existing psychiatric disorders affecting recovery assessment.
- Patients who experience severe obstetric complications other than PPH (e.g., eclampsia, uterine rupture).
- Overdistended uterus due to; Polyhydramnios (amniotic fluid index >24 cm) or multiple gestation
- History of previous PPH (documented with blood loss of >1000 ml, blood transfusion, use surgical methods such as Bakri balloon, B-Lynch sutures, uterine artery ligation or embolization)
- BMI > 50
- Language barrier (English)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-control
Study locations
Canada · 1 center
- Mount Sinai Hospital — Toronto
Identifiers
NCT: NCT07199803 · 25-03