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DOI 10.3390/ijns10040069

Медицинская библиотека · International journal of neonatal screening · 2024

Newborn Screening for Sickle Cell Disease in Catalonia between 2015 and 2022-Epidemiology and Impact on Clinical Events.

González de Aledo-Castillo José Manuel, Argudo-Ramírez Ana, Beneitez-Pastor David, Collado-Gimbert Anna, Almazán Castro Francisco, Roig-Bosch Sílvia, Andrés-Masó Anna, Ruiz-Llobet Anna, Pedrals-Portabella Georgina, Medina-Santamaria David, Nadal-Rey Gemma, Espigares-Salvia Marina, Coll-Sibina Maria Teresa, Algar-Serrano Marcelina, Torrent-Español Montserrat, Leoz-Allegretti Pilar, Rodríguez-Pebé Anabel, García-Bernal Marta, Solà-Segura Elisabet, García-Gallego Amparo, Prats-Viedma Blanca, López-Galera Rosa María, Paredes-Fuentes Abraham J, Pajares García Sonia, Delgado-López Giovanna, Blanco-Álvarez Adoración, Tazón-Vega Bárbara, Díaz de Heredia Cristina, Mañú-Pereira María Del Mar, Marín-Soria José Luis, García-Villoria Judit, Velasco-Puyó Pablo, On Behalf Of The Sickle Cell Disease Newborn Screening Group Of Catalonia

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Аннотация

In 2015, Catalonia introduced sickle cell disease (SCD) screening in its newborn screening (NBS) program along with standard-of-care treatments like penicillin, hydroxyurea, and anti-pneumococcal vaccination. Few studies have assessed the clinical impact of introducing NBS programs on SCD patients. We analyzed the incidence of SCD and related hemoglobinopathies in Catalonia and the change in clinical events occurring after introducing NBS. Screening 506,996 newborns from 2015 to 2022, we conducted a retrospective multicenter study including 100 screened (SG) and 95 unscreened (UG) SCD patients and analyzed SCD-related clinical events over the first six years of life. We diagnosed 160 cases of SCD, with an incidence of 1 in 3169 newborns. The SG had a significantly lower median age at diagnosis (0.1 y vs. 1.68 y, p < 0.0001), and initiated penicillin prophylaxis (0.12 y vs. 1.86 y, p < 0.0001) and hydroxyurea treatment earlier (1.42 y vs. 4.5 y, p < 0.0001). The SG experienced fewer median SCD-related clinical events (vaso-occlusive crisis, acute chest syndrome, infections of probable bacterial origin, acute anemia requiring transfusion, acute splenic sequestration, and pathological transcranial Doppler echography) per year of follow-up (0.19 vs. 0.77, p < 0.0001), a reduced number of annual emergency department visits (0.37 vs. 0.76, p < 0.0001), and fewer hospitalizations (0.33 vs. 0.72, p < 0.0001). SCD screening in Catalonia's NBS program has effectively reduced morbidity and improved affected children's quality of life.

Для цитирования: González de Aledo-Castillo José Manuel, Argudo-Ramírez Ana, Beneitez-Pastor David, Collado-Gimbert Anna, Almazán Castro Francisco, Roig-Bosch Sílvia, Andrés-Masó Anna, Ruiz-Llobet Anna, Pedrals-Portabella Georgina, Medina-Santamaria David, Nadal-Rey Gemma, Espigares-Salvia Marina, Coll-Sibina Maria Teresa, Algar-Serrano Marcelina, Torrent-Español Montserrat, Leoz-Allegretti Pilar, Rodríguez-Pebé Anabel, García-Bernal Marta, Solà-Segura Elisabet, García-Gallego Amparo, Prats-Viedma Blanca, López-Galera Rosa María, Paredes-Fuentes Abraham J, Pajares García Sonia, Delgado-López Giovanna, Blanco-Álvarez Adoración, Tazón-Vega Bárbara, Díaz de Heredia Cristina, Mañú-Pereira María Del Mar, Marín-Soria José Luis, García-Villoria Judit, Velasco-Puyó Pablo, On Behalf Of The Sickle Cell Disease Newborn Screening Group Of Catalonia. Newborn Screening for Sickle Cell Disease in Catalonia between 2015 and 2022-Epidemiology and Impact on Clinical Events.. International journal of neonatal screening. 2024. DOI: 10.3390/ijns10040069.
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