Fatigue and functional impairment in early-stage non-small cell lung cancer survivors. Academic Article uri icon

Overview

abstract

  • CONTEXT: Fatigue is the most common sequela among non-small cell lung cancer (NSCLC) survivors one to six years post-treatment and is associated with functional limitations. OBJECTIVES: This study examined the prevalence, severity, and correlates of fatigue among early stage NSCLC survivors. METHODS: Three-hundred fifty individuals diagnosed and surgically treated for Stage IA or IB NSCLC completed a survey that included the Brief Fatigue Inventory (BFI) to assess the prevalence and severity of fatigue. The Karnofsky Self-Reported Performance Rating scale (SR-KPS) was used as a measure of functional status and was compared with the severity of fatigue through Chi-squared analyses. Demographic, psychological, and medical correlates of fatigue were examined using logistic regression. RESULTS: The prevalence of fatigue was 57%. Forty-one percent (n=142) of participants had mild fatigue and 16.8% (n=59) had moderate or severe fatigue (BFI≥4). Among the individuals reporting moderate or severe fatigue, 23.7% (n=14) had significant functional impairment (SR-KPS≤70%) compared with 2.8% (n=8) with mild or no fatigue (χ(2)=58.1, P<0.001). In the multivariate analysis, NSCLC survivors with pulmonary disease (odds ratio [OR]=2.28), depressive symptoms (OR=6.99), and anxiety symptoms (OR=2.31) were more likely to report experiencing clinically significant fatigue, whereas those who met physical activity guidelines (OR=0.29) reported less fatigue. CONCLUSION: Fatigue is highly prevalent among NSCLC survivors and associated with more functional impairment. A comprehensive approach to the treatment of fatigue includes the screening and management of anxious and depressive symptoms, and pulmonary disorders such as chronic obstructive pulmonary disease.

publication date

  • January 8, 2011

Research

keywords

  • Carcinoma, Non-Small-Cell Lung
  • Fatigue
  • Lung Neoplasms
  • Survivors

Identity

PubMed Central ID

  • PMC3063865

Scopus Document Identifier

  • 79951934118

Digital Object Identifier (DOI)

  • 10.1016/j.jpainsymman.2010.05.017

PubMed ID

  • 21216563

Additional Document Info

volume

  • 41

issue

  • 2