Your browser doesn't support javascript.
loading
Refining The Society of Thoracic Surgeons Congenital Heart Surgery Database Mortality Risk Model With Enhanced Risk Adjustment for Chromosomal Abnormalities, Syndromes, and Noncardiac Congenital Anatomic Abnormalities.
Jacobs, Jeffrey P; O'Brien, Sean M; Hill, Kevin D; Kumar, S Ram; Austin, Erle H; Gaynor, J William; Gruber, Peter J; Jonas, Richard A; Pasquali, Sara K; Pizarro, Christian; St Louis, James D; Meza, James; Thibault, Dylan; Shahian, David M; Mayer, John E; Jacobs, Marshall L.
Afiliação
  • Jacobs JP; Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland; Division of Cardiovascular Surgery, Department of Surgery, Johns Hopkins All Children's Heart Institute, Johns Hopkins All Children's Hospital and Florida Hospital for Children, Sain
  • O'Brien SM; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Hill KD; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Kumar SR; Heart Institute, Children's Hospital of Los Angeles, Keck School of Medicine of the University of Southern California, Los Angeles, California.
  • Austin EH; Department of Cardiovascular and Thoracic Surgery, University of Louisville, Louisville, Kentucky; Norton Children's Hospital, Louisville, Kentucky.
  • Gaynor JW; The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Gruber PJ; Yale University School of Medicine, New Haven, Connecticut.
  • Jonas RA; Children's National Health System, Washington, DC.
  • Pasquali SK; C. S. Mott Children's Hospital, University of Michigan, Ann Arbor, Michigan.
  • Pizarro C; Alfred I. duPont Hospital for Children, Wilmington, Delaware.
  • St Louis JD; Department of Surgery, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Meza J; Duke Clinical Research Institute, Duke University, Durham, North Carolina; The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Thibault D; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Shahian DM; Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Mayer JE; Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts.
  • Jacobs ML; Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ann Thorac Surg ; 108(2): 558-566, 2019 08.
Article em En | MEDLINE | ID: mdl-30853592
ABSTRACT

BACKGROUND:

The Society of Thoracic Surgeons Congenital Heart Surgery Database Mortality Risk Model adjusts not only for procedure and age group pairings but also for additional patient factors, including the binary presence or absence of a chromosomal abnormality (CA), syndrome (S), and/or a noncardiac congenital anatomic abnormality (NCAA). This analysis refines case-mix adjustment by adding more granular adjustment for individual conditions (CA, S, and NCAA), consistent with a hypothesis that associated risk of mortality differs between individual conditions.

METHODS:

CA/S corresponding to the same condition were merged to a single condition code. Odds ratios were estimated for all CA/S. For CA/S associated with at least 10 deaths in neonates and infants and at least 10 deaths in children and adults, odds ratios were estimated for the effect of the CA/S separately in neonates/infants and in children/adults. In addition to these condition/age interactions, condition/age/procedure interactions were explored (eg, effect of Down syndrome was estimated based on age and procedure subgroups, including atrioventricular canal repair and single-ventricle palliation). Bayesian modeling was used to create 5 maximally homogeneous groups of CA/S from 81 candidate CA/S variables. A standard logistic regression model then incorporated indicator variables for the 5 categories of CAs/Ss, 7 unique NCAAs, and all other covariates in the previously published Society of Thoracic Surgeons Congenital Heart Surgery Database Mortality Model.

RESULTS:

Analysis included 107,062 operations in 100 centers (2010 to 2015). Operative Mortality was 3,629 (3.4%). In the development sample, the C statistics of the original nonaugmented model and the augmented model were 0.872 and 0.875, respectively.

CONCLUSIONS:

The Society of Thoracic Surgeons Congenital Heart Surgery Database Mortality Risk Model has been augmented by addition of covariates representing individual CAs, Ss, and NCAAs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sociedades Médicas / Cirurgia Torácica / Modelos Estatísticos / Medição de Risco / Transtornos Cromossômicos / Cardiopatias Congênitas / Procedimentos Cirúrgicos Cardíacos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sociedades Médicas / Cirurgia Torácica / Modelos Estatísticos / Medição de Risco / Transtornos Cromossômicos / Cardiopatias Congênitas / Procedimentos Cirúrgicos Cardíacos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article