Literature DB >> 11825221

The natural history of the use of healthcare information by women with breast cancer: a conceptual model.

D R Longo1, T B Patrick, R L Kruse.   

Abstract

The overall goal of our research agenda is to contribute to improved quality of healthcare by identifying factors that foster or inhibit the use of healthcare information by patients to make informed healthcare decisions. We propose to study the natural history of the use of healthcare information by women with breast cancer to support decisions about health care. To do so in this paper we propose a conceptual model developed based on an extensive literature review and critique that describes patients' health information use over the disease course. It will guide our further investigation of the complex relationships among patients' personal circumstances, the progress of their medical treatment, and their satisfaction and empowerment as informed decision-makers. The model will help policy makers and health professionals identify the best means to provide patients with useful information, and help all stakeholders in health care acquire information needed to improve healthcare quality.

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Mesh:

Year:  2001        PMID: 11825221      PMCID: PMC2243472     

Source DB:  PubMed          Journal:  Proc AMIA Symp        ISSN: 1531-605X


  21 in total

Review 1.  What do consumers want and need to know in making health care choices?

Authors:  J S Lubalin; L D Harris-Kojetin
Journal:  Med Care Res Rev       Date:  1999       Impact factor: 3.929

2.  Consumer perceptions of health care services: implications for academic medicine.

Authors:  J E Ware; W R Wright; M K Snyder; G C Chu
Journal:  J Med Educ       Date:  1975-09

3.  A meta-analysis of studies of the Health Belief Model with adults.

Authors:  J A Harrison; P D Mullen; L W Green
Journal:  Health Educ Res       Date:  1992-03

Review 4.  The importance of information giving for patients newly diagnosed with cancer: a review of the literature.

Authors:  M E Mills; K Sullivan
Journal:  J Clin Nurs       Date:  1999-11       Impact factor: 3.036

5.  The information needs of patients with breast cancer.

Authors:  D J Perez; S G Allan; G P Humm; C J Wynne
Journal:  Aust N Z J Med       Date:  1995-10

6.  On the foundation and structure of medical informatics.

Authors:  Z Li; J Mitchell; A Tian; A Rikli
Journal:  Medinfo       Date:  1995

7.  Patient practice variation. A call for research.

Authors:  D R Longo
Journal:  Med Care       Date:  1993-05       Impact factor: 2.983

8.  The clinical application of the biopsychosocial model.

Authors:  G L Engel
Journal:  Am J Psychiatry       Date:  1980-05       Impact factor: 18.112

9.  Cognitive predictors of compliance in chronic disease patients.

Authors:  V T Nagy; G R Wolfe
Journal:  Med Care       Date:  1984-10       Impact factor: 2.983

Review 10.  Assessing, accommodating, and interpreting the influences of heterogeneity.

Authors:  T A Louis
Journal:  Environ Health Perspect       Date:  1991-01       Impact factor: 9.031

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  3 in total

1.  Understanding health information, communication, and information seeking of patients and consumers: a comprehensive and integrated model.

Authors:  Daniel R Longo
Journal:  Health Expect       Date:  2005-09       Impact factor: 3.377

2.  Internet access and empowerment: a community-based health initiative.

Authors:  Christopher M Masi; Yolanda Suarez-Balcazar; Margaret Z Cassey; Leah Kinney; Z Harry Piotrowski
Journal:  J Gen Intern Med       Date:  2003-07       Impact factor: 5.128

3.  Information Access and Use by Patients With Cancer and Their Friends and Family: Development of a Grounded Theory.

Authors:  Maclean Thiessen; Shane Sinclair; Patricia A Tang; Shelley Raffin Bouchal
Journal:  J Med Internet Res       Date:  2020-10-29       Impact factor: 5.428

  3 in total

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