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Anesthetic and Obstetric Outcomes in Morbidly Obese Pregnancy and Cesarean Delivery

Anesthetic and Obstetric Outcomes in Morbidly Obese Pregnant Patients Undergoing Cesarean Delivery: Retrospective Analysis of a Single Center Experience

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03590951
Enrollment
771
Registered
2018-07-18
Start date
2017-05-03
Completion date
2018-02-13
Last updated
2018-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Morbid Obesity, Cesarean Section Complications, Pregnancy Related

Brief summary

Given that morbid obesity has been strongly associated with obstetric, neonatal and anesthetic complications, and that scarce reports have evaluated anesthetic and obstetric outcomes after cesarean delivery in morbidly obese patients; This study retrospectively analyzed anesthetic, obstetric and neonatal outcomes in morbidly obese pregnant patients who underwent cesarean delivery at Augusta University Medical Center, during a 2-year period (2015-2016).

Detailed description

This study compared non-obese, obese and morbidly obese patients with respect to maternal, perinatal and anesthetic outcomes. Obstetric aspects included emergent procedure, estimated blood loss, obstetric complications, maternal disposition, length of stay and in-hospital mortality. Neonatal aspects included Apgar scores. Anesthetic aspects included anesthetic technique, intraoperative hemodynamic instability, failed regional anesthesia and anesthetic complications.

Interventions

A retrospective chart review was conducted to evaluate the effect of body mass index on obstetric, anesthetic and neonatal complications in patients who underwent cesarean section at our institution

Sponsors

Augusta University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pregnant patients who underwent cesarean section at Augusta University Medical Center. * Patients older than 18 years.

Exclusion criteria

* Gestational age \<37 weeks. * Patients with chronic pain conditions

Design outcomes

Primary

MeasureTime frameDescription
Obstetric complicationsFrom beginning to end of cesarean section (2 hours)Perioperative bleeding

Secondary

MeasureTime frameDescription
Anesthetic complicationsFrom beginning to end of cesarean section (2 hours)Failed epidural
Neonatal complications1 and 5 minutes after deliveryApgar scores
Other anesthetic complicationsFrom beginning to end of cesarean section (2 hours)Intraoperative hypotension

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026