CompletedNot Applicable

The Patient AS EDUcator in Anesthesia: Exploring the Patients' Experience During and After Unexpected Cesarean Delivery Under Neuraxial Anesthesia to Inform Anesthetic Practice

Canada25 participantsStarted 2025-01-07

Plain-language summary

This study aims to explore the patients' and providers' perspectives and inform future anesthetic practice for patients undergoing unexpected cesarean delivery (CD) under neuraxial anesthesia (NA). The consideration of patients' concerns, preferences, expectations, and suggestions may lead to enhanced patient satisfaction, compliance, and quality of care that future patients receive during unexpected CD under NA. The investigators will possibly be able to identify gaps in procedural performance that warrant further investigation during the second phase of this study which will contribute to improvement of overall patient care. During the third phase, educational material will be generated from patient insights and will be distributed to the Department of Anesthesia, Department of Obstetrics and Gynaecology, Labour and Delivery Nurses and team of Anesthesia Assistants and Respiratory Therapists.

Who can participate

Age range18 Years – 50 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * aged 18 years or older * English language proficiency (as interviews will be performed in English) * ASA Physical Classification Score 2-5 +/- E * Emergency or Urgent CD that can be done with the existing or newly applied neuraxial anesthesia (specifically, without the need for general anesthesia) due to fetal or maternal emergencies (e.g., fetal bradycardia, pre-eclampsia, chorioamnionitis, etc.) * uCD is defined as Level 1 (Emergency - Immediate threat to life of woman or fetus) and Level 2 (Urgent - Maternal or fetal compromise which is not immediately life-threatening) CD 16 * Patients will be included if they undergo preterm delivery (under 37 weeks of gestation, or are having a multiple gestation pregnancy, also, if there is a significant fetal anomaly present Exclusion criteria: * Under 18 years of age * Unable to answer questions due to a language barrier or because of their mental or physical state (e.g., intubated patients) * BMI at the time of delivery that falls in the super-morbidly obese category (BMI \> 55 kg/m2) * Patients who underwent preterm delivery (under 32 weeks gestation) * Patients will be excluded if neonatal death has occurred. * Patients who were scheduled for an elective CD will be excluded.

What they're measuring

Patient questionnaire

Timeframe: Following cesarean delivery, and prior to hospital discharge (at approximately 48 hours postpartum).

Patient interview

Timeframe: Following cesarean delivery, and prior to hospital discharge (at approximately 48 hours postpartum).

Trial details

NCT IDNCT06589687

SponsorSamuel Lunenfeld Research Institute, Mount Sinai Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-06-19