Semin Respir Crit Care Med 2009; 30(5): 569-578
DOI: 10.1055/s-0029-1238915
© Thieme Medical Publishers

Anxiety and Depression in Cystic Fibrosis

Ivette Cruz1 , Kristen K. Marciel1 , Alexandra L. Quittner1 , Michael S. Schechter2 , 3
  • 1Departments of Psychology and Pediatrics, University of Miami, Coral Gables and Miami, Florida
  • 2Department of Pediatrics, Division of Pulmonary, Allergy/Immunology, Cystic Fibrosis and Sleep, Emory University School of Medicine, Atlanta, Georgia
  • 3Children's Healthcare of Atlanta, Atlanta, Georgia
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Publikationsdatum:
16. September 2009 (online)

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ABSTRACT

Symptoms of anxiety and depression have important consequences for patients with chronic disease, including lower rates of adherence and increased morbidity. This review discusses the prevalence of anxiety and depression in patients with cystic fibrosis (CF) across the life span and highlights current understanding of how these symptoms affect adherence, health outcomes, and health-related quality of life (HRQOL). Anxiety and depression appear to be more common in patients with CF than in the general population. Recent studies also indicate that symptoms of anxiety occur more frequently than depression in this population. Both anxiety and depression have been shown to be associated with poorer disease outcomes, including HRQOL. Depression, specifically, leads to lower adherence to recommended therapies. Given the prevalence and impact of anxiety and depression in CF, it seems appropriate to recommend annual screening using a validated approach, with referral for either pharmacotherapy or cognitive behavioral therapy of those with apparent symptoms. A large-scale epidemiological study of anxiety and depression in CF is under way and should provide better prevalence estimates and more information on the effects of these psychological symptoms.

REFERENCES

Ivette CruzM.S. 

Department of Psychology, University of Miami

5665 Ponce de Leon Blvd., Coral Gables, FL 33146

eMail: i.cruz1@umiami.edu