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Validation of an IGF1 Screening Method for Retinopathy of Pre-maturity.
Pérez-Muñuzuri, Alejandro; López-Suárez, Olalla; Mandiá-Rodríguez, Natalia; López-Sanguos, Carolina; Blanco-Teijeiro, María José; Couce, María Luz.
Afiliação
  • Pérez-Muñuzuri A; Neonatology Unit, University Clinical Hospital of Santiago, Santiago, Spain.
  • López-Suárez O; Department of Forensic Sciences, Pathology, Gynecology and Obstetrics, and Paediatrics, Health Research Institute of Santiago (IDIS), University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Mandiá-Rodríguez N; Neonatology Unit, University Clinical Hospital of Santiago, Santiago, Spain.
  • López-Sanguos C; Department of Forensic Sciences, Pathology, Gynecology and Obstetrics, and Paediatrics, Health Research Institute of Santiago (IDIS), University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Blanco-Teijeiro MJ; Neonatology Unit, University Clinical Hospital of Santiago, Santiago, Spain.
  • Couce ML; Department of Forensic Sciences, Pathology, Gynecology and Obstetrics, and Paediatrics, Health Research Institute of Santiago (IDIS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Front Pediatr ; 8: 615716, 2020.
Article em En | MEDLINE | ID: mdl-33381481
Retinopathy of pre-maturity (ROP) is a retinal disease that causes arrest of vascularization of the retina and can result in retinal detachment and blindness. Current screening protocols may not be sufficiently accurate to identify all at-risk patients. The aim of this study is to validate a method for improved identification of newborns at risk of ROP. We conducted a prospective clinical trial of pre-term newborns <32 weeks of gestation and/or <1,500 g birth weight during a 6-year period in a tertiary care hospital. We applied our new method based on measurement of insulin-like growth factor 1 (IGF1) levels at 3 weeks of age and the presence of sepsis during the first 3 weeks of life. Our screening protocol allowed exclusion of 121 (79.1%) patients for whom American Academy of Pediatrics (AAP) guidelines recommended screening, had a negative predictive value of 100%, and correctly identified all patients with ROP. Following retrospective assessment of our data based on these findings, we propose further restriction of the current AAP indications for screening to <1,100 g and <28 weeks of gestation in order to improve diagnostic efficacy while ensuring optimal use of restriction of human and material resources.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article