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Emotional Pain Following a Cancer Diagnosis

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The agreed definition of pain put forward by the experts' the IASP in 1994 is: ... Changes made to names and only brief vignette's given to protect identity ... – PowerPoint PPT presentation

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Title: Emotional Pain Following a Cancer Diagnosis


1
Emotional Pain Following a Cancer Diagnosis
  • Wendy Johnson.
  • MSc. In Practice Development
  • Pain Management
  • Completed 2006

2
  • Definition of pain
  • The agreed definition of pain put forward by the
    experts the IASP in 1994 is
  • an unpleasant sensory and emotional experience
    associated with actual or potential tissue
    damage
  • Do we agree with this?

3
The Study
  • To look at emotional pain specifically relating
    to
  • psycho-social issues in palliative patients.

4
WHO DEFINITION OF PALLIATIVE CARE (2008)
An approach that improves the quality of life of
patients associated with life-threatening
illness, through the prevention and relief of
suffering by means of early identification and
impeccable assessment and treatment of pain and
other problems, physical, psychosocial and
spiritual
5
Aims of the Study
  • Identify whether patients do experience emotional
    pain.
  • Identify how emotional pain is related to their
    psychosocial well-being and whether this is
    recognised by professionals.
  • Explore how professionals identify these emotions
    and deal with this aspect of pain.
  • Determine if the support received by patients
    meets their needs.
  • Identify if there are any educational needs for
    professionals

6
Methodology
  • Qualitative research descriptive rather than
    quantities using in depth interviews
  • Narrative analysis using the patients story and
    putting together themes which were then analyzed
    in relation to the patients own agenda.
  • Finally to offer recommendations for practice

7
What is narrative analysis?
  • Narratives as they are known are stories given
    by an individual to give an insight into their
    experiences
  • It allows the practitioner/researcher become part
    of the individuals world letting them share
    their story
  • The individuals story is allowed to reported
    using their own words

8
Why use narrative analysis?
  • Allows the person to regain form and meaning to
    their lives (Carlick and Biley 2004)
  • Allows life and pain to be freed from its chaos
    by sequencing events and giving order
  • (Frank 2004)
  • It is the persons own perception allowing their
    viewpoint (Kinsella 2005)
  • As nurse we should develop an understanding of
    individuals experience and their personal truths
    through stories through stories rather than the
    biophysical (Payne 2004)

9
Participants
  • 3 participants one male and two female
  • Age group 48-64
  • Two were seen at home one at centre (patient
    choice)
  • Patients were aware they could exit the study at
    any time
  • Back-up counselling support offered, but not
    taken up
  • Changes made to names and only brief vignettes
    given to protect identity

10
Four Core Themes
  • 1.Changes in social/family status
  • 2. Patients expectations of professionals
  • 3. Attitudes of others towards cancer
  • 4. Reaction to diagnosis

11
Core Theme Changes in social/family status
  • Storyteller 1 Dianne
  • Stories of a changing life in a
  • nice family

Dianne the mother of the family. A true
matriarch she had a responsible job as a
supervisor over 250 staff in healthcare.
12
Core ThemePatients expectations of Professionals
  • Storyteller 2 -Jim
  • Stethoscopes and Tissues
  • Jim Known as the big guy had been an
    electrician travelling all over the country.
    Always ready to help family and friends.
  • A discerning man who often spoke in metaphors.

13
Core ThemeAttitudes of others towards cancer
  • Storyteller 1 Dianne
  • Stories of being distanced
  • Dianne the mother of the family. A true
    matriarch she had a responsible job as a
    supervisor over 250 staff in healthcare.

14
Core ThemeReaction to diagnosis
  • Storyteller 3 Mary
  • Stories of the comforter
  • Mary called herself a carer and a family
    person, she was main carer to her husband who had
    a major stroke, and in the past had cared for her
    mother and father

15
How then does this affect our practice?
  • Patients when given the opportunity are very
    willing to share their story
  • Holistic interviews with patients should be on
    their terms and their agenda
  • Professionals need to set aside time to discuss
    these issues
  • Professionals need to be aware of the impact of
    their actions/comments

16
Discussion
  • Emotional pain of living with cancer issues not
    new ones, difficult to put into a particular
    model as they are intertwined
  • Educational needs. Communication is still a
    key issue surrounding a cancer diagnosis. These
    issues can have resounding impact on the patient
    and family.
  • Patients own story. May be part of the process
    of re-ordering their life.

17
Recommendations
  • Patients needs should be identified using a
    person centred approach in order that their main
    concerns can be identified
  • Professionals should continue to be educated in
    end of life care particularly communication
    skills in order to elicit this information
  • Narratives/storytelling should be identified as a
    tool not only in the research arena, but also in
    patient assessment
  • The time and effort needed to develop a
    therapeutic relationship should be acknowledged
    as part of nursing activities

18
Conclusion
  • The study, though small was rich in textual
    evidence. It highlighted the emotional needs/pain
    of those who have a cancer diagnosis.
  • It identified that though we (professionals)
    acknowledge the total pain model. We may not
    fully appreciate the impact of living with
    cancer
  • It highlighted that it is not just physical pain
    eg. Tissue damage that can cause pain.
  • It identified the need for ongoing education and
    planning in end of life' patient services.

19
.....and finally
  • As a researcher the study allowed me to become
    part of the patients world. I became privy to
    information they had previously not thought I
    would be interested in, but as the interviews
    showed, were truly important.
  • Given the time, and their own agenda patients
    are willing to tell you their own story about
    living with cancer.
  • ... and I felt privileged that they did.

20
Thankyou
  • ..any questions?

21
ReferencesWorld Health Organisation (2006).
http/www.who.int/cancer/palliative/definition/en/
. WHO definition of Palliative Care. Accessed
24.3.06Carlick.A, and Biley.F.C (2004).
Thoughts on the therapeutic use of narrative in
the promotion of coping in cancer care. European
Journal of Cancer Care.13 308-317. Frank.A.
(2004) Asking the Right Question About Pain
Narrative and Phronesis.Literature and
Medicine23.nno2 (Fall 2004) 209-225. The John
Hopkins University PressIASP (2006)httpwww.iasp
-pain.org/ter.s-phtml. Pain terminology. Pain
terms updated 1994. Date accessed
24.3.06.Kinsella.E.A (2005) Constructions of
self-ethical overtones in surprising locations.
J.Med EthicsMedical Humanities
20053161-71Payne.S, Seymour J, Ingleton C.
(2004) Palliative Care Nursing Principles and
Evidence for Practice Open University Press
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