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

Bibliographic Data

ID5230673
AuthorsLéa Maria Zanini Maciel (0000-0003-1447-0794, Universidade de São Paulo), Patrícia Künzle Ribeiro Magalhães (0000-0003-2564-7903, Universidade de São Paulo), Ieda Regina Lopes Del Ciampo (0000-0002-7862-0221, Universidade de São Paulo), Maria Luísa Barato De Sousa (0000-0002-0787-9412, Universidade de São Paulo), Maria Inez Machado Fernandes (0000-0002-0737-5062, Universidade de São Paulo), Regina Sawamura (0000-0001-9688-9382, Universidade de São Paulo), Roberta Rodrigues Bittar (0000-0002-9660-6677, Universidade de São Paulo), Greice Andreotti De Molfetta (0000-0003-0946-5704, Universidade de São Paulo), Wilson Araújo Da Silva Júnior (0000-0001-9364-2886, Universidade de São Paulo)
Year2020
Volume36
Issue10
Pagese00049719-e00049719
Publication date2020-01-01
Open AccessYes
TypeARTICLE
VenueCadernos de Saude Publica (JOURNAL)
Journal identifiersISSN: 0102-311X • E-ISSN: 1678-4464
PublisherFapUNIFESP (SciELO) (PUBLISHER)
DOI10.1590/0102-311x00049719
PMID33111836
OpenAlexW3095122632
SciELOS0102-311X2020001005012
LanguageEN
Citations received1
References cited26

The Hospital of the Ribeirão Preto Medical School, University of São Paulo is one of the three screening centers in São Paulo State, Brazil, and has included a test for cystic fibrosis (CF) since February 6, 2010, by a court order. We evaluated the first five years of this CF-newborn screening program. The original immunoreactive trypsinogen (IRT)/IRT screening protocol was adopted in Brazil. A total of 173,571 newborns were screened, 1,922 (1.1%) of whom showed IRT1 ≥ 70ng/mL. Of these, 1,795 (93.4%) collected IRT2, with elevated results (IRT2 ≥ 70ng/mL) in 102 of them (5.2%). We identified a total of 26 CF cases during this period, including three CF cases that were not detected by the CF-newborn screening. The incidence of the disease among the screened babies was 1:6,675 newborns screened. Median age at the initial evaluation was 42 days, comparable to that of neonates screened with the IRT/DNA protocol. Almost all infants with CF already exhibited some manifestations of the disease during the neonatal period. The mutation most frequently detected in the CF cases was F508del. These findings suggest the early age at the beginning of treatment at our center was due to the effort of the persons involved in the program regarding an effective active search. Considering the false negative results of CF-newborn screening and the early onset of clinical manifestations of the disease in this study, pediatricians should be aware of the diagnosis of CF even in children with negative test

Cystic fibrosis · Disease · Incidence (geometry) · Newborn screening · Cystic Fibrosis Research Advances · Infant Nutrition and Health · Internal Medicine · Medicine · Neonatal Respiratory Health Research · Pediatrics

  • IRT/IRT as a newborn cystic fibrosis screening method

    Open Access•Carolina Godoy, Pedro Paulo Brito et al.•Cadernos de Saude Publica•2024

Citations per year0.5
Citation span2024 - 2024 (1)
Highly citedNo

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