Cesarean Delivery Clinical Trial
Official title:
A Retrospective Comparison of Neonatal Acid-base Status After Cesarean Delivery (CD) at NYPresbyterian/Columbia University Medical Center (CUMC) Before January, 2015 and After January, 2016
The objective is to retrospectively gather peri-operative data on neonatal outcomes, primarily neonatal acid-base status, based on umbilical cord gas analysis, for the 23 months preceding and 23 months following the conduct of the "tilt versus supine study". The investigators hypothesize that there will be no difference in mean neonatal umbilical artery base excess in neonates delivered by cesarean section during the period before and after conduct of the study, for elective, urgent and emergent deliveries.
For decades, obstetric anesthesia dogma for term women undergoing cesarean delivery (CD)
includes maintenance of left lateral tilt for uterine displacement until delivery, based on
the premise that the supine position will result in aortocaval compression (ACC), maternal
hypotension and fetal compromise. More recent evidence suggests that even in 15 degrees of
left tilt, there is minimal relief of aortocaval compression. Furthermore, there is evidence
that most practitioners never achieve 15 degrees of tilt anyway.
Between January 2015 and January 2016, the investigators conducted a randomized clinical
trial at NewYork Presbyterian/The Allen Hospital in which healthy women undergoing elective
CD were randomized (non-blinded) to supine horizontal (SUPINE, N=50) or 15° left tilt of the
surgical table (TILT, N= 50) following spinal anesthesia (hyperbaric bupivacaine 12 mg,
fentanyl 15 μg, preservative-free morphine 150 μg). Lactated Ringer's 10ml/kg and a
phenylephrine (PE) infusion titrated to 100% baseline systolic blood pressure (SBP) were
initiated with intrathecal injection. The primary outcome was umbilical artery base excess
(UA-BE). There were no differences in UA-BE or pH between groups. The mean UA-BE (± SD) was
-0.5 mmol/L (± 1.6) in the SUPINE group (n=50) versus -0.6 mmol/L (± 1.5) in the TILT group
(n=47) (p= 0.64). The conclusion was that maternal supine position during elective CD with
spinal anesthesia in healthy term women does not impair neonatal acid-base status compared to
15° left tilt, when maternal SBP is maintained with a coload and PE infusion. The
investigators understood that the findings may not be generalized to emergency situations or
non-reassuring fetal status.
Since the end of the study, discussion of the findings with colleagues at Departmental grand
rounds and national conferences, and a publication in the journal Anesthesiology,
practitioners have reported feeling more comfortable with maternal supine position during
cesarean delivery, as long as maternal SBP is kept at or near to baseline with crystalloid
infusion and a PE infusion. It is routine practice at CUMC to use a prophylactic PE infusion
for maintenance of maternal SBP close to or at baseline. It is also routine at CUMC to send
samples of umbilical arterial and venous blood for analysis. Much of the dosing for neuraxial
anesthesia (spinal, combined spinal epidural anesthesia and epidural doses) are standardized
at CUMC. The investigators believe that since there has been a noticeable practice shift with
practitioners anecdotally reporting that they have discontinued the routine use of left
maternal tilt intraoperatively, the investigators will be able to collect useful data on
cases which had not been studied - these include cases with preeclampsia, morbid obesity and
emergencies.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03236324 -
Transversalis Fascia Plane Blocks for Analgesia Post-cesarean Delivery
|
Phase 2 | |
Recruiting |
NCT04058444 -
The First ERAS Protocol for Cesarean Delivery in Serbia at the University Hospital
|
N/A | |
Completed |
NCT03150641 -
Delayed Cord Clamping at Term Cesarean
|
N/A | |
Recruiting |
NCT06247852 -
Persistent Pain After Cesarean Delivery - A Danish Multicenter Cohort Study
|
||
Completed |
NCT02846129 -
Incidence of Complications Associated With Anesthesia in Multiple Gestation Undergoing Cesarean Delivery
|
N/A | |
Completed |
NCT00799955 -
Comparing 2 Types of Pain Relief After Cesarean Delivery: Spinal Morphine and TAP Block
|
N/A | |
Completed |
NCT03336541 -
Low-dose Ketamine and Postpartum Depression in Parturients With Prenatal Depression
|
Phase 4 | |
Completed |
NCT04358757 -
Immune and Physical Recovery Following Cesarean Delivery
|
||
Completed |
NCT01755026 -
Serum and Tissue Cefazolin Concentrations in Patients Undergoing Cesarean Delivery
|
Phase 4 | |
Recruiting |
NCT03746678 -
Patient-Centred Perioperative Mobile Application
|
||
Completed |
NCT03349151 -
Postoperative Results of Early Versus On-demand Maternal Feeding After Cesarean Delivery
|
N/A | |
Completed |
NCT03729076 -
Crystalloid Versus Colloid Rapid Co-load for Cesarean Delivery Under Spinal Anesthesia
|
N/A | |
Completed |
NCT04799587 -
Accupressure of P6 to Reduce Nausea During Cesarean Section
|
N/A | |
Not yet recruiting |
NCT05758012 -
Carbetocin Compared To Oxytocin During Cesarean Delivery
|
||
Completed |
NCT03781388 -
ED90 for Hyperbaric Bupivacaine in Super Obese Parturients
|
Phase 4 | |
Completed |
NCT04349215 -
Validation of the Chinese ObsQoR-11
|
||
Completed |
NCT04812223 -
Timing of Umbilical Cord Clamping in Term Cesarean Deliveries
|
N/A | |
Recruiting |
NCT05279703 -
Epinephrine Infusion for Prophylaxis Against Maternal Hypotension During Cesarean Delivery
|
Phase 4 | |
Completed |
NCT01550640 -
Pharmacogenetics of Remifentanil in Patients With Hypertension Undergoing Cesarean Delivery Under General Anesthesia
|
N/A | |
Completed |
NCT00884026 -
Can Augmentation Index (AIx) be Used to Predict Hypotension After Spinal Anesthesia?
|
N/A |