Abstract 4358117: Hyperoxia During Cardiopulmonary Bypass in Neonatal Congenital Heart Surgery is Associated with Worse Clinical Outcomes: A Multi-Institutional Study
Abstract
Background: Neonates undergoing cardiac surgery with cardiopulmonary bypass (CPB) may be exposed to supraphysiologic oxygen (O 2 ) concentrations, termed hyperoxia, which has been associated with worse outcomes in single center studies. We aimed to describe variation in oxygen exposure during CPB within and across centers and determine if hyperoxia was associated with worse outcomes in a multicenter cohort of neonates undergoing cardiac surgery. Methods: We performed a retrospective study across 29 centers enrolled in CoRe-PCICS: Collaborative Research from the Pediatric Cardiac Intensive Care Society. Neonates (< 30d) who underwent Society of Thoracic Surgery STAT category 2–5 surgery with CPB between 01/2021 and 12/2022 were included. Clinical outcomes of interest were operative mortality and the composite outcome of major adverse cardiovascular events (MACE), including: cardiac arrest, extracorporeal support, stroke, and operative mortality. Logistic regression was performed to determine association between median PaO 2 during CPB and outcomes. Post-hoc subset analyses were performed on neonates with single ventricle (SV) anatomy. Results: We reviewed 1,175 neonates (median 48 per center), including 357 with SV anatomy. Variation in O 2 exposure during CPB is shown in Figure 1. There were 54 mortalities (5%) (Figure 2) and 203 MACE (17%) in total and 35 mortalities (10%) and 111 MACE (31%) in patients with SV anatomy. We observed no mortalities in neonates with median PaO 2 < 200mmHg (n=161). Analysis identified a median PaO 2 cut point of 221 mmHg as having modest predictive value for mortality (96% sensitivity, 19% specificity, Youden’s index score 0.16). In multivariate regression, hyperoxia (median PaO 2 > 221mmHg) was associated with mortality and MACE, controlling for birth weight, ventricular anatomy, non-cardiac anomalies, and CPB duration, however, not associated when also controlling for center. In a similar model among neonates with SV anatomy, hyperoxia was associated with mortality ( p =0.022) and MACE (p=0.008) (Table 1). Conclusions: In a multicenter study of neonates who underwent cardiac surgery, variation of O 2 exposure during CPB was apparent within and across centers and supraphysiologic PaO 2 values were common. Hyperoxia was associated with worse morbidity and mortality, particularly in neonates with SV anatomy. These findings underscore the need for a trial to determine if conservative oxygen titration during CPB leads to improved outcomes.
Article Details
Authors (33)
Asaad Beshish
EMORY UNIVERSITY, Atlanta, Georgia, United States
David Kwiatkowski
LUCILE PACKARD STANFORD, Palo Alto, California, United States
Nathaniel Sznycer-Taub
UNIVERSITY MICHIGAN, Ann Arbor, Michigan, United States
John Costello
School of Physical Sciences Dublin City University Dublin 9 Ireland
Andrew Jergel
Emory University, Atlanta, Georgia, United States
Scott Gillespie
Katherine Cashen
Duke University School of Medicine, Durham, North Carolina, United States
Ahmed Asfari
University of Alabama at Birmingham, Birmingham, Alabama, United States
Maria Batsis
LUCILE PACKARD STANFORD, Palo Alto, California, United States
Jason Buckley
Medical Univ. of South Carolina, Charleston, South Carolina, United States
Meghan Chlebowski
Cincinnati Children's Hospital, Cincinnati, Ohio, United States
Saul Flores
Texas Children's Hospital, Houston, Texas, United States
Nimrod Goldshtrom
Columbia University Irving Medical, New York, New York, United States
Karl Migally
Northwestern, Lurie Childrens, Chicago, Illinois, United States
Kimberly Mills
Boston Children's Hospital, Boston, Massachusetts, United States
Monique Radman
Seattle Children's Hospital, Seattle, Washington, United States
Chetana Reddy
St. Louis University School of Medicine, St. Louis, Missouri, United States
Brittany Shutes
Nationwide Children’s Hospital and the Ohio State University College of Medicine, Columbus, Ohio, United States
Christine Riley
Children's National Hospital, Silver Spring, Maryland, United States
Sukumar Suguna Narasimhulu
Shands Hospital for Children, Gainesville, Florida, United States
Dana Mueller
Rady Children's, San Diego, California, United States
Venugopal Amula
University of Utah, SLC, Utah, United States
Raji Venkitachalam
Medical College of Wisconsin, Milwaukee, Wisconsin, United States
Brian Joy
University of Minnesota Medical School, Minneapolis, Minnesota, United States
Karan Karki
UTHSC, Memphis, Tennessee, United States
Scott Leopold
University of Wisconsin Schol of Medicine and Public Health, Madison, Wisconsin, United States
Jennifer Schramm
Johns Hopkins University, Baltimore, Maryland, United States
Christine Capone
Zucker School of Medicine at Hofstra/Northwell, New Hyde Park, New York, United States
Scott Aydin
Icahn School of Medicine at Mount Sinai, New York, New York, United States
Adnan Bakar
Albany Medical College, Albany, New York, United States
Kieran Leong
University of North Carolina School of Medicine, Chapel Hill, North Carolina, United States
Agnieszka Kulikowska
University of Illinois College of Medicine at Peoria/Children’s Hospital of Illinois, Peoria, Illinois, United States
Christopher Mastropietro
Indiana University School of Medicine, Indianapolis, Illinois, United States