Literature DB >> 21116176

Breast cancer patients' use of health information in decision making and coping.

M Elise Radina1, Amanda C Ginter, Julie Brandt, Jan Swaney, Daniel R Longo.   

Abstract

BACKGROUND: Breast cancer patients are some of today's most proactive healthcare consumers. Given how the media has highlighted the many issues involved in breast cancer, the unprecedented rise of consumerism in general, and the rise of healthcare consumerism specifically, a plethora of information on breast cancer has emerged in both scientific and popular media. It is timely and appropriate to consider breast cancer patients' perspectives regarding their search for health-related information and its use for treatment decision making and coping.
OBJECTIVE: The present study explores health information-seeking behaviors (passive and active), use of health information, sources of health information, and how such information is or is not used in patients' decision making about their treatment.
METHODS: This study used a secondary analysis of data regarding health information-seeking behaviors and treatment decisions from 2 separate but compatible qualitative data sets based on in-depth interviews with a total of 35 breast cancer survivors. Data were analyzed using thematic analysis.
RESULTS: The majority of participating women were active information seekers (n = 26). Of the subsets of women who described their level of involvement in treatment decision making, the largest number (n = 13) reported a shared responsibility for decision making with their physician, and the next largest subset (n = 9) reported making the final decision themselves.
CONCLUSION: These findings provide an enhanced understanding of the preferred source and method of delivery of information given health information-seeking behaviors and decision-making strategies. IMPLICATIONS FOR PRACTICE: How health information is delivered in the future given these findings is discussed with specific attention to matching patient preferences with delivery methods to potentially enhance patients' sense of agency with regard to treatment, which has been shown to improve patients' psychosocial outcomes.

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Year:  2011        PMID: 21116176     DOI: 10.1097/NCC.0b013e3181faab7c

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  9 in total

1.  Communication competence, psychological well-being, and the mediating role of coping efforts among women with breast cancer: cross-sectional and longitudinal evidence.

Authors:  Minsun Shim; Laura M Mercer Kollar; Linda J Roberts; David H Gustafson
Journal:  Women Health       Date:  2015-03-20

2.  "It's a mess sometimes": patient perspectives on provider responses to healthcare costs, and how informatics interventions can help support cost-sensitive care decisions.

Authors:  Olivia K Richards; Bradley E Iott; Tammy R Toscos; Jessica A Pater; Shauna R Wagner; Tiffany C Veinot
Journal:  J Am Med Inform Assoc       Date:  2022-05-11       Impact factor: 7.942

Review 3.  Self-advocacy and cancer: a concept analysis.

Authors:  Teresa L Hagan; Heidi S Donovan
Journal:  J Adv Nurs       Date:  2013-01-24       Impact factor: 3.187

4.  Health information seeking behaviors of ethnically diverse adolescents.

Authors:  Anastasia E Okoniewski; Young Ji Lee; Martha Rodriguez; Rebecca Schnall; Alexander F H Low
Journal:  J Immigr Minor Health       Date:  2014-08

5.  Knowledge gaps among public librarians seeking vaccination information: A qualitative study.

Authors:  Catherine Arnott Smith; Savreen Hundal; Alla Keselman
Journal:  J Consum Health Internet       Date:  2014-02-24

6.  Lived experiences of breast cancer survivors after diagnosis, treatment and beyond: qualitative study.

Authors:  Faustine Williams; Stephen C Jeanetta
Journal:  Health Expect       Date:  2015-05-07       Impact factor: 3.377

Review 7.  Information Needs of Breast Cancer Patients: Theory-Generating Meta-Synthesis.

Authors:  Hongru Lu; Juan Xie; Lynette Hammond Gerido; Ying Cheng; Ya Chen; Lizhu Sun
Journal:  J Med Internet Res       Date:  2020-07-28       Impact factor: 5.428

Review 8.  Incorporating the patient perspective: a critical review of clinical practice guidelines for implantable cardioverter defibrillator therapy.

Authors:  Kerry E Joyce; Stephen Lord; Daniel D Matlock; Janet M McComb; Richard Thomson
Journal:  J Interv Card Electrophysiol       Date:  2012-12-19       Impact factor: 1.900

9.  Challenges and Opportunities with Empowering Baby Boomers for Personal Health Information Management Using Consumer Health Information Technologies: an Ecological Perspective.

Authors:  Cynthia M LeRouge; Donghua Tao; Jennifer Ohs; Helen W Lach; Keri Jupka; Ricardo Wray
Journal:  AIMS Public Health       Date:  2014-09-02
  9 in total

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