Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening
Newborn 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...
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| Format: | Article |
| Language: | Spanish |
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Elsevier
2019-04-01
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| Series: | Anales de Pediatría (English Edition) |
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2341287919300390 |
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| language |
Spanish |
| format |
Article |
| sources |
DOAJ |
| author |
Silvia Gartner Pedro Mondéjar-López Óscar Asensio de la Cruz María José Alonso Marina Álvarez Anselmo Andrés Martín María Isabel Barrio Gómez de Agüero María Jesús Cabero Pérez Pilar Caro Aguilera María Cols Roig Isidoro Cortell Aznar-Pérez Jordi Costa Colomer Isabel Delgado Pecellín Amparo Escribano Montaner Joan Figuerola Mulet Gloria García Hernández Pilar Guayarte David Gil Ortega David Gómez Pastrana Adelaida Lamas Ferreiro José Luis Marín Soria Carlos Martín de Vicente Martín Navarro Merino Concepción Oliva Hernández Javier Pérez Frías Estela Pérez Ruiz Sandra Rovira Amigo Antonio Salcedo Posadas Manuel Sánchez-Solís Josep Sirvent Gómez Carlos Vázquez Cordero José Ramón Villa Asensi |
| spellingShingle |
Silvia Gartner Pedro Mondéjar-López Óscar Asensio de la Cruz María José Alonso Marina Álvarez Anselmo Andrés Martín María Isabel Barrio Gómez de Agüero María Jesús Cabero Pérez Pilar Caro Aguilera María Cols Roig Isidoro Cortell Aznar-Pérez Jordi Costa Colomer Isabel Delgado Pecellín Amparo Escribano Montaner Joan Figuerola Mulet Gloria García Hernández Pilar Guayarte David Gil Ortega David Gómez Pastrana Adelaida Lamas Ferreiro José Luis Marín Soria Carlos Martín de Vicente Martín Navarro Merino Concepción Oliva Hernández Javier Pérez Frías Estela Pérez Ruiz Sandra Rovira Amigo Antonio Salcedo Posadas Manuel Sánchez-Solís Josep Sirvent Gómez Carlos Vázquez Cordero José Ramón Villa Asensi Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening Anales de Pediatría (English Edition) Fibrosis quística Cribado neonatal Protocolo de diagnóstico y seguimiento |
| author_facet |
Silvia Gartner Pedro Mondéjar-López Óscar Asensio de la Cruz María José Alonso Marina Álvarez Anselmo Andrés Martín María Isabel Barrio Gómez de Agüero María Jesús Cabero Pérez Pilar Caro Aguilera María Cols Roig Isidoro Cortell Aznar-Pérez Jordi Costa Colomer Isabel Delgado Pecellín Amparo Escribano Montaner Joan Figuerola Mulet Gloria García Hernández Pilar Guayarte David Gil Ortega David Gómez Pastrana Adelaida Lamas Ferreiro José Luis Marín Soria Carlos Martín de Vicente Martín Navarro Merino Concepción Oliva Hernández Javier Pérez Frías Estela Pérez Ruiz Sandra Rovira Amigo Antonio Salcedo Posadas Manuel Sánchez-Solís Josep Sirvent Gómez Carlos Vázquez Cordero José Ramón Villa Asensi |
| author_sort |
Silvia Gartner |
| title |
Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| title_short |
Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| title_full |
Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| title_fullStr |
Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| title_full_unstemmed |
Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| title_sort |
follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening |
| publisher |
Elsevier |
| series |
Anales de Pediatría (English Edition) |
| issn |
2341-2879 |
| publishDate |
2019-04-01 |
| description |
Newborn 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. Resumen: El diagnóstico de fibrosis quística (FQ) a través del cribado neonatal (CN) está bien establecido en muchos países y brinda la oportunidad de un diagnóstico y tratamiento temprano antes del desarrollo de daño estructural pulmonar irreversible.En 1999, Cataluña, Castilla-León y las Islas Baleares iniciaron el programa CN para FQ. En los últimos 10 años su implementación se extendió rápidamente y todas las autonomías ofrecen el programa CN para FQ desde 2015. Hay varias estrategias diferentes en toda España. Creemos que es muy oportuno contar con una guía actualizada y consensuada para el diagnóstico, el seguimiento y el tratamiento de los pacientes diagnosticados de FQ mediante CN. |
| topic |
Fibrosis quística Cribado neonatal Protocolo de diagnóstico y seguimiento |
| url |
http://www.sciencedirect.com/science/article/pii/S2341287919300390 |
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doaj-8dd249170a644c38af89ff7e0f7331842021-05-20T07:51:08ZspaElsevierAnales de Pediatría (English Edition)2341-28792019-04-01904251.e1251.e10Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screeningSilvia Gartner0Pedro Mondéjar-López1Óscar Asensio de la Cruz2María José Alonso3Marina Álvarez4Anselmo Andrés Martín5María Isabel Barrio Gómez de Agüero6María Jesús Cabero Pérez7Pilar Caro Aguilera8María Cols Roig9Isidoro Cortell Aznar-Pérez10Jordi Costa Colomer11Isabel Delgado Pecellín12Amparo Escribano Montaner13Joan Figuerola Mulet14Gloria García Hernández15Pilar Guayarte16David Gil Ortega17David Gómez Pastrana18Adelaida Lamas Ferreiro19José Luis Marín Soria20Carlos Martín de Vicente21Martín Navarro Merino22Concepción Oliva Hernández23Javier Pérez Frías24Estela Pérez Ruiz25Sandra Rovira Amigo26Antonio Salcedo Posadas27Manuel Sánchez-Solís28Josep Sirvent Gómez29Carlos Vázquez Cordero30José Ramón Villa Asensi31Unidad de Fibrosis Quística y Neumología Pediátrica, Hospital Universitari Vall d’Hebron, Barcelona, Spain; Corresponding author.Unidad de Neumología Pediátrica y Fibrosis Quística, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, SpainUnidad de Fibrosis Quística y Neumología y Alergia Pediátrica, Hospital de Sabadell, Parc Taulí Hospital Universitario, Barcelona, SpainInstituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, ValladolidPaediatric Gastroenterology, Hepatology and Nutritional Support Unit, Hospital Universitari Vall d’Hebron, BarcelonaDepartment of Paediatric Pulmonology, Department and Clinical Management Unit of Paediatrics, Hospital Universitario Virgen Macarena, SevillePaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario La Paz, MadridPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Marqués de Valdecilla, SantanderPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Materno-Infantil Universitario de Málaga, MalagaPaediatric Pulmonology and Cystic Fibrosis Unit, Department of Paediatrics, Hospital Sant Joan de Déu, BarcelonaDepartment of Paediatric Allergy and Pulmonology, Hospital Universitario La Fe, ValenciaPaediatric Pulmonology and Cystic Fibrosis Unit, Department of Paediatrics, Hospital Sant Joan de Déu, BarcelonaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario Virgen del Rocío, SevillePaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Clínico Universitario de Valencia, Universitat de València, ValenciaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario Son Espases, Palma de MallorcaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario 12 de Octubre, MadridPaediatric Gastroenterology Unit, Hospital Universitario Parc Taulí, SabadellPaediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario Virgen de la Arrixaca, MurciaPaediatric Pulmonology Unit, Hospital de Jerez, Jerez de la FronteraCystic Fibrosis Unit, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), MadridNeonatal Screening Laboratory of Catalonia, Hospital Clinic, BarcelonaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario Miguel Servet, ZaragozaDepartment of Paediatric Pulmonology, Department and Clinical Management Unit of Paediatrics, Hospital Universitario Virgen Macarena, SevilleHospital Universitario Nuestra Señora de la Candelaria, Santa Cruz de TenerifePaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Materno-Infantil Universitario de Málaga, MalagaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Materno-Infantil Universitario de Málaga, MalagaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Vall d’Hebron, BarcelonaCystic Fibrosis Unit, Hospital Universitario del Niño Jesús-Hospital Universitario Gregorio Marañón, MadridPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario Virgen de la Arrixaca, MurciaPaediatric Pulmonology Unit, Hospital Materno Infantil, Complexo Hospitalario Universitario A Coruña, A CoruñaPaediatric Pulmonology and Cystic Fibrosis Unit, Hospital Universitario Cruces, BilbaoPulmonology and Cystic Fibrosis Unit, Hospital Universitario del Niño Jesús, MadridNewborn 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. Resumen: El diagnóstico de fibrosis quística (FQ) a través del cribado neonatal (CN) está bien establecido en muchos países y brinda la oportunidad de un diagnóstico y tratamiento temprano antes del desarrollo de daño estructural pulmonar irreversible.En 1999, Cataluña, Castilla-León y las Islas Baleares iniciaron el programa CN para FQ. En los últimos 10 años su implementación se extendió rápidamente y todas las autonomías ofrecen el programa CN para FQ desde 2015. Hay varias estrategias diferentes en toda España. Creemos que es muy oportuno contar con una guía actualizada y consensuada para el diagnóstico, el seguimiento y el tratamiento de los pacientes diagnosticados de FQ mediante CN.http://www.sciencedirect.com/science/article/pii/S2341287919300390Fibrosis quísticaCribado neonatalProtocolo de diagnóstico y seguimiento |