Olivia A Nelson

Dr. Olivia A Nelson

orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 August 2022 in Pediatric Anesthesia
Verified
Journal Article
Closed access
MKMichael R. King
Michael R. King
SSSteven J Staffa
Steven J Staffa
PSPaul Stricker
Paul Stricker
CPCarolina Pérez‐Pradilla
Carolina Pérez‐Pradilla
ONOlivia A Nelson
Olivia A Nelson
TGthe Pediatric Craniofacial Collaborative Group
the Pediatric Craniofacial Collaborative Group

7 November 2021 in Pediatric Anesthesia
Verified
Journal Article
Closed access
PDF file
KYKai Yuan
Kai Yuan
ONOlivia A Nelson
Olivia A Nelson
GBGordon A Barr
Gordon A Barr
BZBingqing Zhang
Bingqing Zhang
ATAlexis A Topjian
Alexis A Topjian
AGArjunan Ganesh
Arjunan Ganesh


14 January 2025 in Transfusion
Verified
Journal Article
Open access
ONOlivia A Nelson
Olivia A Nelson
RJRebecca Jones
Rebecca Jones
JMJulie S. Moldenhauer
Julie S. Moldenhauer
NRNatalie E. Rintoul
Natalie E. Rintoul
HHHolly L. Hedrick
Holly L. Hedrick
SCStella T. Chou
Stella T. Chou
Background: Neonates with congenital anomalies frequently require perioperative allogeneic red blood cell (RBC) transfusion. Whole cord blood for autologous transfusion to neonates may provide an alternative RBC source, but whether sufficient volumes can be collected after delayed cord clamping to reduce allogeneic RBC requirements is unknown.Study Design and Methods: Inclusion criteria were mothers delivering a viable infant >34 weeks' gestation. Sterile cord blood collection from the umbilical cord was performed at delivery as per routine obstetric indications. During storage at 4°C, we performed weekly blood gases. Blood culture, complete blood count, and hemolysis tests were performed at baseline and day 21. We compared the whole cord blood volume collected with each infant's allogeneic transfusion requirements.Results: 54 collection attempts yielded 49 collections with a mean volume of 54.1 mL (±20.3) after median delayed cord clamping of 46 seconds (IQR 12.0, 60.0). Among 39 blood cultures obtained, 3 grew organisms after vaginal delivery (3/27, 11.0% vs. 0/12, 0% cesarean delivery, p = .54). Hemolysis was stable during storage (baseline vs. day 21, median [IQR], 0.7% [0.4%–0.9%] vs. 0.7% [0.6%–1.1%], p = .08).Conclusions: Whole cord blood collection following delayed cord clamping was feasible, with volumes equal to 16.7 mL/kg, or one transfusion. Hemolysis was low, and although potassium increased during storage, it was consistent with patterns observed with adult donor stored whole blood. There were no positive blood cultures from collections during cesarean deliveries. Studies are needed to determine whether whole cord blood transfusions improve patient outcomes.

12 September 2020 in Journal of Clinical Monitoring and Computing
Verified
Journal Article
Closed access
PDF file
ASAllan F. Simpao
Allan F. Simpao
ONOlivia A Nelson
Olivia A Nelson
LALuis M. Ahumada
Luis M. Ahumada

1 March 2025 in Journal of Anesthesia and Translational Medicine
Verified
Journal Article
Open access
ONOlivia A Nelson
Olivia A Nelson
ELElaina E. Lin
Elaina E. Lin
Fetal surgery is an expanding domain in which the developing fetus receives therapeutic interventions aimed at reducing mortality and/or morbidity. It presents unique challenges to the anesthesiologist, as it involves managing two simultaneous patients and necessitates the integration of both obstetric and pediatric anesthesia. Fetal therapies range from minimally invasive techniques to open mid-gestation procedures to near-term procedures performed with the fetus partially delivered while on placental circulation. In this overview, we delineate the indications for fetal surgery, review the principles for administering anesthesia in these cases, and outline the anesthetic strategies for minimally invasive, open mid-gestation, and ex utero intrapartum treatment (EXIT) procedures.