COVID-19 and cystic fibrosis. Background and recommendations

Authors

  • Francisco Cammarata-Scalisi Servicio de Pediatría, Hospital Regional de Antofagasta, Chile https://orcid.org/0000-0002-0193-2171
  • Antonio Cárdenas-Tadich Servicio de Pediatría, Hospital Regional de Antofagasta, Chile
  • Marco Medina Servicio de Pediatría, Hospital Regional de Antofagasta, Chile
  • Marcia Vega Servicio de Pediatría, Hospital Regional de Antofagasta, Chile
  • Michele Callea Unit of Dentistry, Bambino Gesú Children’s Hospital, IRCCS, Rome, Italy

DOI:

https://doi.org/10.35839/repis.4.3.736

Abstract

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References

Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, et al. Diagnosis of cystic fibrosis: Consensus guidelines from the Cystic Fibrosis Foundation. J Pediatr 2017; 181S: S4-15.e1.

Bareil C, Bergougnoux A. CFTR gene variants, epidemiology and molecular pathology. Arch Pediatr 2020; 27 Suppl 1: eS8‐12.

Orientaciones técnicas para la atención integral de fibrosis quística. 2019. Segunda Edición. Grupo Técnico, Programa de Fibrosis Quística Departamento Procesos Clínicos Integrados Subsecretaría de Redes Asistenciales Ministerio de Salud.

Informe de evaluación científica basada en la evidencia disponible. Condición de Salud: Fibrosis Quística. 2017. https://www.minsal.cl/wp-content/uploads/2017/10/fibrosis_quistica-OK.pdf.

Colombo C, Burgel PR, Gartner S, van Koningsbruggen-Rietschel S, Naehrlich L, Sermet-Guadeus I, et al. Impact of COVID-19 on people with cystic fibrosis. Lancet Respir Med 2020; S2213-2600(20)30177-6.

Poli P, Timpano S, Goffredo M, Padoan R, Badolato R. Asymptomatic case of COVID-19 in an infant with cystic fibrosis. J Cyst Fibros 2020; S1569-1993(20)30096-5.

Published

2020-06-19

Issue

Section

Cartas al Editor

How to Cite

1.
COVID-19 and cystic fibrosis. Background and recommendations. Rev Peru Investig Salud [Internet]. 2020 Jun. 19 [cited 2025 Sep. 8];4(3):132-3. Available from: http://revistas.unheval.edu.pe/index.php/repis/article/view/736

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