Volume 57, Issue 2 pp. 347-360
REVIEW

Cystic fibrosis year in review 2020: Section 2 pulmonary disease, infections, and inflammation

Nicholas J. Antos MD

Corresponding Author

Nicholas J. Antos MD

Department of Pediatrics, Division of Pulmonary and Sleep Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, USA

Department of Pediatric Pulmonology, Children's Wisconsin, Milwaukee, Wisconsin, USA

Correspondence Nicholas J. Antos, MD, Department of Pediatrics, Division of Pulmonary and Sleep Medicine, Medical College of Wisconsin, 9000 W Wisconsin Ave, PO Box 1997, Suite B620, Milwaukee, WI 53201, USA.

Email: [email protected]

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Adrienne P. Savant MD, MS

Adrienne P. Savant MD, MS

Department of Pediatrics, Children's Hospital of New Orleans, New Orleans, Louisiana, USA

Department of Pediatrics, Tulane University, New Orleans, Louisiana, USA

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First published: 25 May 2021
Citations: 4

Abstract

The outlook for those with cystic fibrosis (CF) has never been brighter with ever increasing life expectancy and the approval of the highly effective CFTR modulators, such as elexacaftor/tezacaftor/ivacaftor. With that being said, the progressive pulmonary decline and importance of lung health, infection, and inflammation in CF remains. This review is the second part in a three-part CF Year in Review 2020. Part one focused on the literature related to CFTR modulators while part three will feature the multisystem effects related to CF. This review focuses on articles from Pediatric Pulmonology, including articles from other journals that are of particular interest to clinicians. Herein, we highlight studies published during 2020 related to CF pulmonary disease, infection, treatment, and diagnostics.

CONFLICT OF INTERESTS

The authors declare that there are no conflict of interests.

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