|
Sign In to gain access to subscriptions and/or personal tools.
|
Hope and Probability: Patient Perspectives of the Meaning of Numerical Information in Cancer Communication
Sally Thorne
University of British Columbia School of Nursing in Vancouver, British Columbia, Canada.
T. Gregory Hislop
British Columbia Cancer Research Centre in Vancouver, British Columbia, Canada.
Margot Kuo
Elizabeth-Anne Armstrong
University of British Columbia School of Nursing in Vancouver, British Columbia.
Although the complexities inherent in human communication make it a difficult target for empirical investigation and systematic interpretation, it is well recognized that patientprovider 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.
Key Words: cancer communication physician-patient relations informed consent
Qualitative Health Research, Vol. 16, No. 3,
318-336 (2006)
DOI: 10.1177/1049732305285341

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. Olumide Olufowote
A Structurational Analysis of Informed Consent to Treatment: (Re)productions of Contradictory Sociohistorical Structures in Practitioners' Interpretive Schemes
Qual Health Res,
June 1, 2009;
19(6):
802 - 814.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
S. S. Y. Ching, I. M. Martinson, and T. K. S. Wong
Reframing: Psychological Adjustment of Chinese Women at the Beginning of the Breast Cancer Experience
Qual Health Res,
March 1, 2009;
19(3):
339 - 351.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
L. R. Evans, E. A. Boyd, G. Malvar, L. Apatira, J. M. Luce, B. Lo, and D. B. White
Surrogate Decision-Makers' Perspectives on Discussing Prognosis in the Face of Uncertainty
Am. J. Respir. Crit. Care Med.,
January 1, 2009;
179(1):
48 - 53.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Audrey, J. Abel, J. M Blazeby, S. Falk, and R. Campbell
What oncologists tell patients about survival benefits of palliative chemotherapy and implications for informed consent: qualitative study
BMJ,
July 31, 2008;
337(jul31_3):
a752 - a752.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Donovan-Kicken and J. J. Bute
Uncertainty of Social Network Members in the Case of Communication-Debilitating Illness or Injury
Qual Health Res,
January 1, 2008;
18(1):
5 - 18.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
K. Moore Schaefer
Patients with cancer used numerical information to calculate the odds and mobilise their coping responses
Evid. Based Nurs.,
January 1, 2007;
10(1):
31 - 31.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
O. Dammann and A. Leviton
Neuroimaging and the Prediction of Outcomes in Preterm Infants.
N. Engl. J. Med.,
August 17, 2006;
355(7):
727 - 729.
[Full Text]
[PDF]
|
 |
|
|
|