Publications by authors named "G Stephen Nace"

Background: Blunt hollow viscus injuries (HVIs) are relatively rare and difficult to diagnose. Whether a delay in operative intervention impacts outcomes for pediatric patients with blunt HVI has not been investigated via analysis of multicenter databases.

Methods: We queried the Trauma Quality Improvement Program database from 2016 to 2020 for patients younger than 18 years who underwent an operation of the stomach, small intestine, large intestine, or rectum within 72 hours of emergency department arrival after blunt injury.

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Introduction: Among premature infants, the incidence of inguinal hernias (IH) has been reported to be as high as 10-30%. We performed this study to characterize the association between individual and systemic variables that may affect diagnosis to definitive operative repair of the premature neonatal IH in the outpatient setting.

Methods: A single center cohort retrospective review analyzing IH repair in the premature neonatal (<37 GA) population was performed.

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Introduction: Recent quality improvement (QI) initiatives indicate that pediatric patients with uncomplicated ileocolic intussusception can be safely discharged from the emergency department (ED) after fluoroscopic reduction. These programs improve patient experience and reduce cost. We sought to build on these efforts by developing a QI initiative at our own institution that included patients transferred from a satellite campus and focused on iterative improvement of our treatment pathway based on continual reassessment of our processes and data.

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Article Synopsis
  • The study evaluates the use and effectiveness of genetic testing in diagnosing infants with esophageal atresia (EA) and tracheoesophageal fistula (TEF) over a 12-year period to improve future care and management.
  • It involves a retrospective analysis of 212 infants, identifying different classifications (complex/syndromic, isolated/nonsyndromic) and noting varying success rates for different genetic tests performed.
  • The findings suggest that EA/TEF has a complex genetic landscape, highlighting the need for advanced testing methods like exome sequencing to better understand its causes and improve diagnosis.
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