Literature DB >> 27378079

Unmet information needs and limited health literacy in newly diagnosed breast cancer patients over the course of cancer treatment.

Sarah Maria Halbach1, Nicole Ernstmann2, Christoph Kowalski3, Holger Pfaff4, Timo-Kolja Pförtner4, Simone Wesselmann3, Anna Enders4.   

Abstract

OBJECTIVE: To investigate unmet information needs in newly diagnosed breast cancer patients over the course of cancer treatment and its association with health literacy.
METHODS: We present results from a prospective, multicenter cohort study (PIAT). Newly diagnosed breast cancer patients (N=1060) were surveyed directly after breast cancer surgery, 10 and 40 weeks later. Pooled linear regression modeling was employed analyzing changes in unmet information needs over time and its association with health literacy.
RESULTS: Unmet information needs on side effects and medication and medical examination results and treatment options were high and increased during the first 10 weeks after breast cancer surgery. Considering health promotion and social issues, unmet information needs started high and decreased during post-treatment. Patients with limited health literacy had higher unmet information needs.
CONCLUSION: Our results indicate a mismatch in information provision and breast cancer patients' information needs. Patients with limited health literacy may be at a distinct disadvantage in having their information needs met over the course of breast cancer treatment. PRACTICE IMPLICATIONS: Strategies are needed to reduce unmet information needs in breast cancer patients considering treatment-phase and health literacy and thereby enable them to better cope with their diseases.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Breast cancer; Health literacy; Longitudinal study; Unmet information needs

Mesh:

Year:  2016        PMID: 27378079     DOI: 10.1016/j.pec.2016.06.028

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  36 in total

1.  Improving Communication in Breast Cancer Treatment Consultation: Use of a Computer Test of Health Numeracy.

Authors:  Marilyn M Schapira; Kathlyn E Fletcher; Pamela S Ganschow; Elizabeth A Jacobs; Cindy M Walker; Alicia J Smallwood; Denisse Gil; Arshia Faghri; Amanda L Kong; Tina W Yen; Susan McDunn; Elizabeth Marcus; Joan M Neuner
Journal:  J Womens Health (Larchmt)       Date:  2019-06-25       Impact factor: 2.681

2.  Rural Disparities in Treatment-Related Financial Hardship and Adherence to Surveillance Colonoscopy in Diverse Colorectal Cancer Survivors.

Authors:  Jean A McDougall; Matthew P Banegas; Charles L Wiggins; Vi K Chiu; Ashwani Rajput; Anita Y Kinney
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2018-03-28       Impact factor: 4.254

3.  Development of the Cancer Survivor Profile-Breast Cancer (CSPro-BC) app: patient and nurse perspectives on a new navigation tool.

Authors:  Amanda Gehrke; Sukhyung Steve Lee; Karrie Hilton; Barbara Ganster; Rebecca Trupp; Corinne McCullough; Elizabeth Mott; Michael Feuerstein
Journal:  J Cancer Surviv       Date:  2018-03-09       Impact factor: 4.442

4.  Health literacy: Impact on quality of life in head and neck cancer survivors.

Authors:  Marci Lee Nilsen; Jessica Moskovitz; Lingyun Lyu; Christine Harrison; Evan Randazza; Shyamal Das Peddada; Jonas T Johnson
Journal:  Laryngoscope       Date:  2019-12-04       Impact factor: 3.325

5.  Supportive care priorities of low-income Latina breast cancer survivors.

Authors:  Alix G Sleight; Kathleen Doyle Lyons; Cheryl Vigen; Heather Macdonald; Florence Clark
Journal:  Support Care Cancer       Date:  2018-05-16       Impact factor: 3.603

6.  Health Literacy, Language, and Cancer-Related Needs in the First 6 Months After a Breast Cancer Diagnosis.

Authors:  Christine M Gunn; Michael K Paasche-Orlow; Sharon Bak; Na Wang; Jennifer Pamphile; Kerrie Nelson; Samantha Morton; Tracy A Battaglia
Journal:  JCO Oncol Pract       Date:  2020-03-27

Review 7.  The Dyadic Cancer Outcomes Framework: A general framework of the effects of cancer on patients and informal caregivers.

Authors:  Tess Thompson; Dana Ketcher; Tamryn F Gray; Erin E Kent
Journal:  Soc Sci Med       Date:  2021-08-30       Impact factor: 5.379

8.  Understanding the role of health information in patients' experiences: secondary analysis of qualitative narrative interviews with people diagnosed with cancer in Germany.

Authors:  Susanne Blödt; Maleen Kaiser; Yvonne Adam; Sandra Adami; Martin Schultze; Jacqueline Müller-Nordhorn; Christine Holmberg
Journal:  BMJ Open       Date:  2018-03-12       Impact factor: 2.692

9.  Using a Mobile App-Based Video Recommender System of Patient Narratives to Prepare Women for Breast Cancer Surgery: Development and Usability Study Informed by Qualitative Data.

Authors:  Ilja Ormel; Charles C Onu; Mona Magalhaes; Terence Tang; John B Hughes; Susan Law
Journal:  JMIR Form Res       Date:  2021-06-02

10.  The impact of doctor-patient communication on patients' perceptions of their risk of breast cancer recurrence.

Authors:  Nancy K Janz; Yun Li; Brian J Zikmund-Fisher; Reshma Jagsi; Allison W Kurian; Lawrence C An; M Chandler McLeod; Kamaria L Lee; Steven J Katz; Sarah T Hawley
Journal:  Breast Cancer Res Treat       Date:  2016-12-09       Impact factor: 4.624

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