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Outcomes Following Post-Hemorrhagic Ventricular Dilatation among Infants of Extremely Low Gestational Age.
Shankaran, Seetha; Bajaj, Monika; Natarajan, Girija; Saha, Shampa; Pappas, Athina; Davis, Alexis S; Hintz, Susan R; Adams-Chapman, Ira; Das, Abhik; Bell, Edward F; Stoll, Barbara J; Walsh, Michele C; Laptook, Abbot R; Carlo, Waldemar A; Van Meurs, Krisa P; Sánchez, Pablo J; Ball, M Bethany; Hale, Ellen C; Seabrook, Ruth; Higgins, Rosemary D.
Afiliação
  • Shankaran S; Department of Pediatrics, Wayne State University, Detroit, MI. Electronic address: sshankar@med.wayne.edu.
  • Bajaj M; Department of Pediatrics, Wayne State University, Detroit, MI.
  • Natarajan G; Department of Pediatrics, Wayne State University, Detroit, MI.
  • Saha S; Social, Statistical and Environmental Sciences Unit, RTI International, Research Triangle Park, NC.
  • Pappas A; Department of Pediatrics, Wayne State University, Detroit, MI.
  • Davis AS; Department of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine and Lucile Packard Children's Hospital, Palo Alto, CA.
  • Hintz SR; Department of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine and Lucile Packard Children's Hospital, Palo Alto, CA.
  • Adams-Chapman I; Emory University School of Medicine, Department of Pediatrics, Children's Healthcare of Atlanta, Atlanta, GA.
  • Das A; Social, Statistical and Environmental Sciences Unit, RTI International, Rockville, MD.
  • Bell EF; Department of Pediatrics, University of Iowa, Iowa City, IA.
  • Stoll BJ; Department of Pediatrics, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, TX.
  • Walsh MC; Department of Pediatrics, Rainbow Babies & Children's Hospital, Case Western Reserve University, Cleveland, OH.
  • Laptook AR; Department of Pediatrics, Women & Infants Hospital, Brown University, Providence, RI.
  • Carlo WA; Division of Neonatology, University of Alabama at Birmingham, Birmingham, AL.
  • Van Meurs KP; Department of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine and Lucile Packard Children's Hospital, Palo Alto, CA.
  • Sánchez PJ; Department of Pediatrics, Nationwide Children's Hospital, Ohio State University College of Medicine, Columbus, OH.
  • Ball MB; Department of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine and Lucile Packard Children's Hospital, Palo Alto, CA.
  • Hale EC; Emory University School of Medicine, Department of Pediatrics, Children's Healthcare of Atlanta, Atlanta, GA.
  • Seabrook R; Department of Pediatrics, Nationwide Children's Hospital, Ohio State University College of Medicine, Columbus, OH.
  • Higgins RD; College of Health and Human Services, George Mason University, Fairfax, VA.
J Pediatr ; 226: 36-44.e3, 2020 11.
Article em En | MEDLINE | ID: mdl-32739261
OBJECTIVE: To assess outcomes following post-hemorrhagic ventricular dilatation (PHVD) among infants born at ≤26 weeks of gestation. STUDY DESIGN: Observational study of infants born April 1, 2011, to December 31, 2015, in the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network and categorized into 3 groups: PHVD, intracranial hemorrhage without ventricular dilatation, or normal head ultrasound. PHVD was treated per center practice. Neurodevelopmental impairment at 18-26 months was defined by cerebral palsy, Bayley Scales of Infant and Toddler Development, 3rd edition, cognitive or motor score <70, blindness, or deafness. Multivariable logistic regression examined the association of death or impairment, adjusting for neonatal course, center, maternal education, and parenchymal hemorrhage. RESULTS: Of 4216 infants, 815 had PHVD, 769 had hemorrhage without ventricular dilatation, and 2632 had normal head ultrasounds. Progressive dilatation occurred among 119 of 815 infants; the initial intervention in 66 infants was reservoir placement and 53 had ventriculoperitoneal shunt placement. Death or impairment occurred among 68%, 39%, and 28% of infants with PHVD, hemorrhage without dilatation, and normal head ultrasound, respectively; aOR (95% CI) were 4.6 (3.8-5.7) PHVD vs normal head ultrasound scan and 2.98 (2.3-3.8) for PHVD vs hemorrhage without dilatation. Death or impairment was more frequent with intervention for progressive dilatation vs no intervention (80% vs 65%; aOR 2.2 [1.38-3.8]). Death or impairment increased with parenchymal hemorrhage, intervention for PHVD, male sex, and surgery for retinopathy; odds decreased with each additional gestational week. CONCLUSIONS: PHVD was associated with high rates of death or impairment among infants with gestational ages ≤26 weeks; risk was further increased among those with progressive ventricular dilation requiring intervention.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemorragia Cerebral / Ventrículos Cerebrais / Transtornos do Neurodesenvolvimento / Doenças do Prematuro Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Pediatr Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemorragia Cerebral / Ventrículos Cerebrais / Transtornos do Neurodesenvolvimento / Doenças do Prematuro Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Pediatr Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos