Pulmonary Complications in Adult Patients with Cystic Fibrosis
Overview
Authors
Affiliations
Early diagnosis, treatments of acute exacerbations, and chronic therapies have all improved the lifespan of cystic fibrosis patients; however, the natural history remains one of worsening bronchiectasis and obstructive airways impairment. The progression of disease leads to eventual respiratory failure, but some will have other acute respiratory complications that require intervention. In this report, we review the most common life-threatening respiratory complications of cystic fibrosis, including pneumothorax, massive hemoptysis, and respiratory failure.
Pediatric Endoscopy and High-risk Patients: A Clinical Report From the NASPGHAN Endoscopy Committee.
Lightdale J, Liu Q, Sahn B, Troendle D, Thomson M, Fishman D J Pediatr Gastroenterol Nutr. 2019; 68(4):595-606.
PMID: 30664560 PMC: 8597353. DOI: 10.1097/MPG.0000000000002277.
Grossmann R, Zughaier S, Kumari M, Seydafkan S, Lyles R, Liu S Dermatoendocrinol. 2012; 4(2):191-7.
PMID: 22928076 PMC: 3427199. DOI: 10.4161/derm.20332.
[Emergencies in adult mucoviscidosis patients].
Smaczny C, Born T, Wagner T Internist (Berl). 2012; 53(5):575-84.
PMID: 22527665 DOI: 10.1007/s00108-012-3019-4.
"Bong lung" in cystic fibrosis: a case report.
Gao Z, Wood-Baker R, Harle R, Muller K, Hauser J, Reid D J Med Case Rep. 2010; 4:371.
PMID: 21092085 PMC: 2998526. DOI: 10.1186/1752-1947-4-371.
Khazai N, Judd S, Jeng L, Wolfenden L, Stecenko A, Ziegler T J Clin Endocrinol Metab. 2009; 94(6):2037-43.
PMID: 19336509 PMC: 2690417. DOI: 10.1210/jc.2008-2012.