Literature DB >> 25244662

Patient-reported quality of life, unmet needs and care coordination outcomes: Moving toward targeted breast cancer survivorship care planning.

Meagan Elizabeth Brennan1,2, Phyllis Butow3, Andrew John Spillane1,4, Frances Boyle1,2.   

Abstract

AIM: Survivorship care plans (SCPs) have been proposed for universal use with the aim of addressing the many unmet needs of cancer survivors. Trials have failed to find a significant impact of SCPs on quality of life outcomes. This study evaluated quality of life, unmet needs, satisfaction with health care and perception of cancer care coordination at the end of treatment in a cohort of women at the end of treatment for early breast cancer. The aim was to identify specific needs to assist in the design of a tailored SCP.
METHODS: Women completed patient-reported measures of health-related quality of life (FACT-B [ES]), unmet needs (CaSUN), satisfaction with medical care and cancer care coordination. Total scores and subscale scores for the whole cohort and results of analysis comparing three age groups were reported.
RESULTS: Sixty-eight women (mean age 56) participated. Mean score for FACT-B = 108 and FACT-B (ES) = 167.4. Younger women (<51 years) reported a significantly lower quality of life (P = 0.001 for FACT-B, TOI and FACT-B [ES]). Using CaSUN, 76.1% of participants reported at least one unmet need; mean number of unmet needs = 6.2. Younger women reported more unmet needs than older women. The most frequently reported unmet need was fear of cancer recurrence. Overall, participants were very satisfied with medical care and cancer care coordination.
CONCLUSION: Younger women reported poorer quality of life and more unmet needs. SCPs should specifically target younger women and must include strategies to address fear of cancer recurrence if they are to lead to a measureable difference in outcomes.
© 2014 Wiley Publishing Asia Pty Ltd.

Entities:  

Keywords:  breast cancer; follow-up care; quality of life; survivorship care plan; unmet need

Mesh:

Year:  2014        PMID: 25244662     DOI: 10.1111/ajco.12254

Source DB:  PubMed          Journal:  Asia Pac J Clin Oncol        ISSN: 1743-7555            Impact factor:   2.601


  15 in total

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3.  Exploratory Factor Analysis of a Patient-Centered Cancer Care Measure to Support Improved Assessment of Patients' Experiences.

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Authors:  M C Keeman; C A W Bolman; I Mesters; R A Willems; I M Kanera; L Lechner
Journal:  Eur J Cancer Care (Engl)       Date:  2018-01-22       Impact factor: 2.520

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9.  Development and psychometric evaluation of a questionnaire to measure cancer patients' perception of care coordination.

Authors:  Izumi Okado; Kevin Cassel; Ian Pagano; Randall F Holcombe
Journal:  BMC Health Serv Res       Date:  2020-01-21       Impact factor: 2.655

10.  Study protocol of the BLANKET trial: a cluster randomised controlled trial on the (cost-) effectiveness of a primary care intervention for fear of cancer recurrence in cancer survivors.

Authors:  Yvonne L Luigjes-Huizer; Marije L van der Lee; Niek J de Wit; Charles W Helsper
Journal:  BMJ Open       Date:  2019-12-02       Impact factor: 2.692

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