Direct Umbilical Vein Injection of Epinephrine with Cut-Cord Milking in an Ovine Model of Neonatal Resuscitation

Author:

Vali Payam1,Chen Peggy2,Giusto Evan13ORCID,Lesneski Amy4,Hardie Morgan E.5,Knych Heather K.6,Sankaran Deepika1ORCID,Alhassen Ziad7,Joudi Houssam M.1,Lakshminrusimha Satyan1ORCID

Affiliation:

1. Division of Neonatology, Department of Pediatrics, University of California Davis, Sacramento, CA 95817, USA

2. Division of Neonatology, Miller Children’s & Women’s Hospital Long Beach, Long Beach, CA 90806, USA

3. D-5 Neonatal Units, Patient Care Services, University of California Davis, Sacramento, CA 95817, USA

4. Department of Stem Cell Research, University of California Davis, Sacramento, CA 95817, USA

5. School of Veterinary Medicine, University of California Davis, Davis, CA 95616, USA

6. K.L. Maddy Equine Analytical Pharmacology Laboratory, Department of Veterinary Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, CA 95616, USA

7. Division of Neonatology, Children’s Hospital of Orange County, Orange, CA 92868, USA

Abstract

Background: An umbilical venous catheter (UVC) is the preferred route of epinephrine administration during neonatal resuscitation but requires specialized equipment, expertise, and time. Hypothesis: Direct injection of epinephrine into the umbilical vein (UV) followed by milking a ~20 cm segment of cut umbilical cord to flush the epinephrine (DUV + UCM) will lead to a quicker administration and earlier return of spontaneous circulation (ROSC) compared with epinephrine given through a UVC. Design: Eighteen near-term asphyxiated lambs were randomized to receive a low-UVC or DUV + UCM of epinephrine at 0.02 or 0.03 mg/kg doses. Outcome measures: A total of 16/18 lambs achieved ROSC with a similar mean (±SEM) time to ROSC [DUV + UCM vs. low-UVC (4.67 ± 0.67 vs. 3.99 ± 0.58 min); p = 0.46]. Two out of ten lambs in the DUV + UCM group required UVC placement for additional epinephrine. The administration of the first dose of epinephrine was similar (DUV + UCM—2.97 ± 0.48 vs. UVC—4.23 ± 0.58 min; p = 0.12). Both methods yielded similar epinephrine concentrations (peak concentrations of 253 ± 63 and 328 ± 80 ng/mL for DUV + UCM and UVC EPI, respectively). Conclusions: DUV + UCM resulted in a ROSC success of 78% following the first epinephrine dose and showed similar epinephrine concentrations to UVC. Clinical studies evaluating DUV + UCM as an alternate route for epinephrine while intravenous access is being established are warranted.

Funder

NIH

the National Center for Advancing Translational Sciences

CTSC

Publisher

MDPI AG

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