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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.
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.
Abstract:
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.
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