The first five-year evaluation of cystic fibrosis neonatal screening program in São Paulo State, Brazil

Léa Maria Zanini Maciel1, Patrícia Künzle Ribeiro Magalhães1, Ieda Regina Lopes Del Ciampo1

  • 1Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brasil.

Cadernos De Saude Publica
|October 28, 2020
PubMed

Insights

Brazil

Area of Science:

  • Medical Genetics
  • Pediatrics
  • Public Health

Background:

  • Cystic Fibrosis (CF) screening implemented in São Paulo State, Brazil, via court order since 2010.
  • The study evaluates the initial five years of the CF newborn screening program at the Hospital of the Ribeirão Preto Medical School.
  • The program utilized the original immunoreactive trypsinogen (IRT)/IRT screening protocol adopted in Brazil.

Purpose of the Study:

  • To evaluate the effectiveness and outcomes of the first five years of the cystic fibrosis newborn screening program in São Paulo State, Brazil.
  • To determine the incidence of CF and analyze screening protocol performance.
  • To highlight the importance of clinical awareness for CF diagnosis despite screening results.

Main Methods:

  • Screened 173,571 newborns using the IRT/IRT protocol.
  • Followed up on elevated IRT1 results with repeat IRT2 testing.
  • Identified CF cases and analyzed mutation frequencies (F508del).

Main Results:

  • Identified 26 CF cases with an incidence of 1:6,675 newborns.
  • 1.1% showed elevated IRT1, and 5.2% of those had elevated IRT2.
  • Three CF cases were missed by the screening program, presenting early clinical manifestations.

Conclusions:

  • The CF newborn screening program identified a significant number of cases, but false negatives occurred.
  • Early detection and treatment were facilitated by active search efforts.
  • Pediatricians must maintain clinical suspicion for CF, even with negative newborn screening results, due to early disease onset.

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