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Adverse events after protamine administration following cardiopulmonary bypass in infants and children

  • Harry A. Seifert
  • , David R. Jobes
  • , Thomas Ten Have
  • , Stephen E. Kimmel
  • , Lisa M. Montenegro
  • , James M. Steven
  • , Susan C. Nicolson
  • , Brian L. Strom
  • University of Pennsylvania
  • GlaxoSmithKline

Producción científicarevisión exhaustiva

44 Citas (Scopus)

Resumen

We performed this study to determine the incidence of and risk factors for adverse events (AEs) in infants and children after the IV administration of protamine after cardiopulmonary bypass. In a retrospective cohort study, all relevant anesthesia records from a 3-yr period were examined to identify AEs after protamine. The AEs were then grouped into three categories by applying increasingly strict criteria. Among 1249 anesthesia records, there were no documented episodes of isolated or hypotension-associated right-sided cardiac failure or acute pulmonary dysfunction. The incidence of systemic hypotension after protamine was between 1.76% (95% confidence interval [CI], 1.11%-2.65%) and 2.88% (95% CI, 2.03%-3.97%), depending on the strictness of case definition. To identify risk factors, we performed a nested case-control study in which unmatched controls were randomly selected from the parent cohort at a 4:1 ratio to cases. Cases of hypotension after protamine were more likely during operations on girls (odds ratio [OR], 6.47; 95% CI, 1.66 -32.8), after larger doses of protamine (OR, 1.88; 95% CI, 1.03-3.63), or after smaller doses of heparin (OR, 0.49; 95% CI, 0.17-0.67).

Idioma originalEnglish
Páginas (desde-hasta)383-389
Número de páginas7
PublicaciónAnesthesia and Analgesia
Volumen97
N.º2
DOI
EstadoPublished - 1 ago 2003
Publicado de forma externa

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