Download PDF
Schlaf 2016; 5(01): 16-19
DOI: 10.1055/s-0037-1618333
Review
Schattauer GmbH

Mukoviszidose & Schlaf

Richard Schulz
Further Information

Publication History

Publication Date:
12 February 2018 (online)

    Permissions and Reprints

Die Mukoviszidose oder zystische Pankreasfibrose (Englisch: cystic fibrosis, [CF]) kann mit Schlafstörungen verbunden sein, wobei es sich nicht nur um solche handelt, die die Atmung betreffen. Die Schlafstörungen bei CF sind noch nicht in allen Aspekten erforscht, haben aber wahrscheinlich weitreichende Konsequenzen für die betroffenen Patienten. Hinzu kommt, dass aufgrund verbesserter Therapiemöglichkeiten die Lebenserwartung der CF-Patienten immer weiter ansteigt und deshalb auch der „Erwachsenen”-Mediziner bzw. Schlafmediziner Kenntnisse über diese Zusammenhänge haben sollte.

 

  • Literatur

  • 1 Pletz MW, Sauer-Heilborn A, Köhnlein T, Seidler U, Lamprecht G. Mukoviszidose im Erwachsenenalter. Internist 2010; 51 (Suppl. 01) 277-288.
    CrossrefPubMedGoogle Scholar
  • 2 Milross MA, Piper AJ, Dobbin CJ, Bye PT, Grunstein RR. Sleep disordered breathing in cystic fibrosis. Sleep Med Rev 2004; 8: 295-308.
    CrossrefPubMedGoogle Scholar
  • 3 van der Giessen L, Loeve M, de Jongste J, Hop W, Tiddens H. Nocturnal cough in children with stable cystic fibrosis. Pediatr Pulmonol 2009; 44: 859-865.
    CrossrefPubMedGoogle Scholar
  • 4 Flume PA, Ciolino J, Gray S, Lester MK. Patient-reported pain and impaired sleep quality in adult patients with cystic fibrosis. J Cyst Fibros 2009; 8: 321-325.
    CrossrefPubMedGoogle Scholar
  • 5 Spicuzza L, Sciuto C, Leonardi S, La Rosa M. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Arch Pediatr Adolesc Med 2012; 166: 1165-1169.
    CrossrefPubMedGoogle Scholar
  • 6 Hayes D. Restless legs syndrome manifested by iron deficiency from chronic hemoptysis in cystic fibrosis. J Cyst Fibros 2007; 6: 234-236.
    CrossrefPubMedGoogle Scholar
  • 7 Milross MA, Piper AJ, Norman M, Dobbin CJ, Grunstein RR, Sullivan CE, Bye PT. Subjective sleep quality in cystic fibrosis. Sleep Med 2002; 3: 205-212.
    CrossrefPubMedGoogle Scholar
  • 8 Dancey DR, Tullis ED, Heslegrave R, Thornley K, Hanly PJ. Sleep quality and daytime function in adults with cystic fibrosis and severe lung disease. Eur Respir J 2002; 19: 504-510.
    CrossrefPubMedGoogle Scholar
  • 9 Naqvi SK, Sotelo C, Murry L, Simakajornboon N. Sleep architecture in children and adolescents with cystic fibrosis and the association with severity of lung disease. Sleep Breath 2008; 12: 77-83.
    CrossrefPubMedGoogle Scholar
  • 10 Perin C, Fagondes SC, Casarotto FC, Pinotti AFF, Menna Barreto SS, Dalcin PR. Sleep findings and predictors of sleep desaturation in adult cystic fibrosis patients. Sleep Breath 2012; 16: 1041-1048.
    CrossrefPubMedGoogle Scholar
  • 11 Dobbin CJ, Bartlett D, Melehan K, Grunstein RR, Bye PT. The effect of infective exacerbations on sleep and neurobehavioral function in cystic fibrosis. Am J Respir Crit Care Med 2005; 172: 99-104.
    CrossrefPubMedGoogle Scholar
  • 12 Bouka A, Tiede H, Liebich L, Dumitrascu R, Hecker C, Reichenberger F, Mayer K, Seeger W, Schulz R. Quality of life in clinically stable adult cystic fibrosis out-patients : associations with daytime sleepiness and sleep quality. Respir Med 2012; 106: 1244-1249.
    CrossrefPubMedGoogle Scholar
  • 13 Young AC, Wilson JW, Kotsimbos TC, Naughton MT. The impact of nocturnal oxygen desaturation on quality of life in cystic fibrosis. J Cyst Fibros 2011; 10: 100-106.
    CrossrefPubMedGoogle Scholar
  • 14 Dwyer TJ, Robbins L, Kelly P, Piper AJ, Bell SC, Bye PT. Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: a randomized trial. J Physiother 2015; 61: 142-147.
    CrossrefPubMedGoogle Scholar