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Survival and healthcare utilization of infants diagnosed with lethal congenital malformations.
Nguyen, Jacqueline E; Salemi, Jason L; Tanner, Jean P; Kirby, Russell S; Sutsko, Ronald P; Ashmeade, Terri L; Salihu, Hamisu M; Drach, Laura L.
Afiliação
  • Nguyen JE; Division of Neonatology, Morsani College of Medicine University of South Florida, Tampa, FL, USA. jnguye31@jhmi.edu.
  • Salemi JL; Division of Neonatology, Johns Hopkins All Children's Hospital, St. Petersburg, FL, USA. jnguye31@jhmi.edu.
  • Tanner JP; Department of Family and Community Medicine, Baylor College of Medicine, Houston, TX, USA.
  • Kirby RS; Department of Community and Family Health, College of Public Health, University of South Florida, Tampa, FL, USA.
  • Sutsko RP; Department of Community and Family Health, College of Public Health, University of South Florida, Tampa, FL, USA.
  • Ashmeade TL; Department of Community and Family Health, College of Public Health, University of South Florida, Tampa, FL, USA.
  • Salihu HM; Division of Neonatology, Morsani College of Medicine University of South Florida, Tampa, FL, USA.
  • Drach LL; Division of Neonatology, Levine Children's Hospital/Atrium Health, Charlotte, NC, USA.
J Perinatol ; 38(12): 1674-1684, 2018 12.
Article em En | MEDLINE | ID: mdl-30237475
ABSTRACT

OBJECTIVE:

We assessed survival, hospital length of stay (LOS), and costs of medical care for infants with lethal congenital malformations, and also examined the relationship between medical and surgical therapies and survival. STUDY

DESIGN:

Retrospective cohort study including infants born 1998-2009 with lethal congenital malformations, identified using a longitudinally linked maternal/infant database.

RESULTS:

The cohort included 786 infants trisomy 18 (T18, n = 350), trisomy 13 (T13, n = 206), anencephaly (n = 125), bilateral renal agenesis (n = 53), thanatophoric dysplasia/achondrogenesis/lethal osteogenesis imperfecta (n = 38), and infants > 1 of the birth defects (n = 14). Compared to infants without birth defects, infants with T18, T13, bilateral renal agenesis, and skeletal dysplasias had longer survival rates, higher inpatient medical costs, and longer LOS.

CONCLUSION:

Care practices and survival have changed over time for infants with T18, T13, bilateral renal agenesis, and skeletal dysplasias. This information will be useful for clinicians in counseling families and in shaping goals of care prenatally and postnatally.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Aceitação pelo Paciente de Cuidados de Saúde / Custos de Cuidados de Saúde Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Aceitação pelo Paciente de Cuidados de Saúde / Custos de Cuidados de Saúde Idioma: En Ano de publicação: 2018 Tipo de documento: Article