Gartner, SilviaMondéjar-López, PedroAsensio de la Cruz, ÓscarGrupo de Trabajo de Fibrosis Quística de la Sociedad Española de Neumología Pediátrica2025-01-072025-01-072018-12-28https://hdl.handle.net/10668/25081Newborn screening (NBS) for cystic fibrosis (CF) is well-established in many countries and provides the opportunity for an early diagnosis and treatment before the development of irreversible structural lung damage. In 1999, Catalonia, Castilla-León, and the Balearic Islands started the NBS programme for CF. In the last 10 years its implementation rapidly spread and all the autonomies offer the NBS programme for CF since 2015. There are many different strategies across Spain. It is believed that it is very opportune to have an updated and consensual guide for the diagnosis, follow-up, and treatment of patients diagnosed by neonatal screening.esAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/Cribado neonatalCystic fibrosisFibrosis quísticaGuidelines for diagnosis and treatmentNewborn screeningProtocolo de diagnóstico y seguimientoAftercareCystic FibrosisHumansInfant, NewbornNeonatal ScreeningPractice Guidelines as TopicSpain[Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening].Protocolo de seguimiento de pacientes con fibrosis quística diagnosticados por cribado neonatal.research article30598406open access10.1016/j.anpedi.2018.11.0092341-2879https://doi.org/10.1016/j.anpedi.2018.11.009