Literature DB >> 16449684

Hope and probability: patient perspectives of the meaning of numerical information in cancer communication.

Sally Thorne1, T Gregory Hislop, Margot Kuo, Elizabeth-Anne Armstrong.   

Abstract

Although the complexities inherent in human communication make it a difficult target for empirical investigation and systematic interpretation, it is well recognized that patient-provider communication can have either a powerfully negative or positive influence on the experience of cancer. Drawing on an extensive data set derived from interviews with 200 cancer patients, the authors examine the impact of information provided in numerical form within cancer care communications from the patient perspective. In this context, they present findings related to various uses and abuses of numbers within cancer care communication, and illustrate how numerical information constitutes a specialized communication form with considerable potency for shaping the cancer experience. In particular, accounts of the thematic relationship between numbers and hope, from the perspective of those on the receiving end of cancer care, provide a unique perspective from which to interpret issues of compassion, caring, and informed consent.

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Year:  2006        PMID: 16449684     DOI: 10.1177/1049732305285341

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  19 in total

Review 1.  Why health expectations and hopes are different: the development of a conceptual model.

Authors:  Karen K Leung; James L Silvius; Nicholas Pimlott; William Dalziel; Neil Drummond
Journal:  Health Expect       Date:  2009-08-18       Impact factor: 3.377

2.  Incompatible with Care: Examining Trisomy 18 Medical Discourse and Families' Counter-discourse for Recuperative Ethos.

Authors:  Megan J Thorvilson; Adam J Copeland
Journal:  J Med Humanit       Date:  2018-09

Review 3.  Recommendations for enhancing clinical trials education: a review of the literature.

Authors:  Karen A Stepan; Amy P Gonzalez; Vivian S Dorsey; Debra K Frye; Nita D Pyle; Regina F Smith; Terry A Throckmorton; Louise A Villejo; Scott B Cantor
Journal:  J Cancer Educ       Date:  2011-03       Impact factor: 2.037

4.  Validating measures of scanned information exposure in the context of cancer prevention and screening behaviors.

Authors:  Bridget J Kelly; Jeff Niederdeppe; Robert C Hornik
Journal:  J Health Commun       Date:  2009-12

5.  A framework for health numeracy: how patients use quantitative skills in health care.

Authors:  Marilyn M Schapira; Kathlyn E Fletcher; Mary Ann Gilligan; Toni K King; Purushottam W Laud; B Alexendra Matthews; Joan M Neuner; Elisabeth Hayes
Journal:  J Health Commun       Date:  2008 Jul-Aug

Review 6.  Clinical Use of Placebo Effects in Patients With Pain Disorders.

Authors:  Regine Klinger; Julia Stuhlreyer; Marie Schwartz; Julia Schmitz; Luana Colloca
Journal:  Int Rev Neurobiol       Date:  2018-08-06       Impact factor: 3.230

7.  Odyssey of hope: a physician's guide to communicating with brain tumor patients across the continuum of care.

Authors:  Mark L Rosenblum; Steven Kalkanis; Wendy Goldberg; Jack Rock; Tom Mikkelsen; Sandra Remer; Sarah Whitehouse; David Nerenz
Journal:  J Neurooncol       Date:  2009-04-09       Impact factor: 4.130

8.  Willingness to favor aggressive care and live with disability following severe traumatic brain injury: a survey of healthy young adults in Hawai'i.

Authors:  Kazuma Nakagawa; Kyle K Obana
Journal:  Hawaii J Med Public Health       Date:  2014-07

9.  Surrogate decision-makers' perspectives on discussing prognosis in the face of uncertainty.

Authors:  Leah R Evans; Elizabeth A Boyd; Grace Malvar; Latifat Apatira; John M Luce; Bernard Lo; Douglas B White
Journal:  Am J Respir Crit Care Med       Date:  2008-10-17       Impact factor: 21.405

10.  The Stage IV Shuffle: Elusiveness of Straight Talk About Advanced Cancer.

Authors:  Donald A Brand
Journal:  J Gen Intern Med       Date:  2019-08-05       Impact factor: 5.128

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