Literature DB >> 20439217

Time since diagnosis as a predictor of symptoms, depression, cognition, social concerns, perceived benefits, and overall health in cancer survivors.

Jill A Bennett1, Linda D Cameron, Paul M Brown, Lisa C Whitehead, David Porter, Tanja Ottaway-Parkes, Elizabeth Robinson.   

Abstract

PURPOSE/
OBJECTIVES: To assess whether health and other factors are different in short-term cancer survivors (less than five years since diagnosis), long-term survivors (5-10 years), and very long-term survivors (more than 10 years).
DESIGN: A cross-sectional survey.
SETTING: New Zealand. SAMPLE: 836 survivors of adult-onset cancers (6 months to 43 years since diagnosis).
METHODS: Survivors were recruited using community-based methods and answered a mailed questionnaire. MAIN RESEARCH VARIABLES: Physical and emotional health, depression, symptoms, cognitive difficulty, social concerns, and perceived benefits of cancer.
FINDINGS: Physical and emotional health, depression, physical symptoms, and perceived benefits of cancer were not associated with time since diagnosis, but longer time since diagnosis was associated with decreases in cognitive difficulties and social concerns. The survivors in this study reported a mean of 8.4 physical symptoms, regardless of time since diagnosis, with the most frequent being fatigue (76%), aches and pain (75%), and trouble sleeping (68%).
CONCLUSIONS: Most survivors enjoyed a moderately good level of health. However, some adverse effects, such as symptoms, were similar in short-, long-, and very long-term survivors, suggesting that interventions may be needed to prevent persistent issues as time progresses. IMPLICATIONS FOR NURSING: The findings suggest a need to reconsider the common attitude that survivors who finish treatment should be able to return to normal life. Assessment of symptoms, particularly fatigue, pain, and sleep issues, is important even in very long-term survivors.

Entities:  

Mesh:

Year:  2010        PMID: 20439217     DOI: 10.1188/10.ONF.331-338

Source DB:  PubMed          Journal:  Oncol Nurs Forum        ISSN: 0190-535X            Impact factor:   2.172


  6 in total

1.  Quality of life, fatigue and depression in Italian long-term breast cancer survivors.

Authors:  Francesca Romito; Claudia Cormio; Francesco Giotta; Giuseppe Colucci; Vittorio Mattioli
Journal:  Support Care Cancer       Date:  2012-03-08       Impact factor: 3.603

2.  Comparison of quality of life between Native and non-Native cancer survivors: Native and non-Native cancer survivors' QOL.

Authors:  Linda Burhansstipanov; Mark Dignan; Katherine L Jones; Linda U Krebs; Paula Marchionda; Judith Salmon Kaur
Journal:  J Cancer Educ       Date:  2012-04       Impact factor: 2.037

3.  Racial and ethnic differences in health status and health behavior among breast cancer survivors--Behavioral Risk Factor Surveillance System, 2009.

Authors:  Arica White; Lori A Pollack; Judith Lee Smith; Trevor Thompson; J Michael Underwood; Temeika Fairley
Journal:  J Cancer Surviv       Date:  2012-12-05       Impact factor: 4.442

4.  Pain in long-term breast cancer survivors: the role of body mass index, physical activity, and sedentary behavior.

Authors:  Laura P Forsythe; Catherine M Alfano; Stephanie M George; Anne McTiernan; Kathy B Baumgartner; Leslie Bernstein; Rachel Ballard-Barbash
Journal:  Breast Cancer Res Treat       Date:  2012-12-15       Impact factor: 4.872

5.  Sharing Wisdom, Sharing Hope: Strategies Used by Native American Cancer Survivors to Restore Quality of Life.

Authors:  Tiana D Bastian; Linda Burhansstipanov
Journal:  JCO Glob Oncol       Date:  2020-02

6.  Coexistence of urinary incontinence and major depressive disorder with health-related quality of life in older Americans with and without cancer.

Authors:  Alexandra J White; Bryce B Reeve; Ronald C Chen; Angela M Stover; Debra E Irwin
Journal:  J Cancer Surviv       Date:  2014-04-26       Impact factor: 4.442

  6 in total

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