Literature DB >> 17133896

A qualitative study of the trauma and posttraumatic growth of multiple myeloma patients treated with peripheral blood stem cell transplant.

Jacqueline Fine Dahan1, Carl F Auerbach.   

Abstract

OBJECTIVE: The study was conducted to understand the emotional impact of multiple myeloma, as well as the impact of its principle treatment, peripheral blood stem cell transplant (PBSCT). The absence of psycho-oncology research literature on this population prompted the need for a hypothesis-generating investigation. Thus, a qualitative design was used to construct a theoretical model of the trauma relating to diagnosis and treatment of myeloma. The study also incorporates the important period of reflection and growth following treatment.
METHODS: The sample consisted of 3 women and 3 men treated for myeloma at a New York City-based cancer treatment center. Data from individual interviews were audiotaped and transcribed. After extensive review, the data were categorized into groups of repeating ideas, themes and broad theoretical constructs.
RESULTS: A five-construct model emerged from the data analysis that integrated a model of trauma and growth presented in earlier work (Auerbach et al., 2006). These constructs roughly correspond with stages of illness, but do not necessarily imply a linear process, as suggested by stage models. The first construct is diagnosis. Patients receive the news that they have multiple myeloma. Initial reactions are discussed and a treatment plan takes form. In the second construct, treatment, patients highlight the physical and emotional hurdles confronted throughout treatment. The third construct, network of safety, presents social factors that play a role in comforting patients throughout illness. Patients recognize the importance of a strong support system during their experiences. In the fourth construct, recuperation, physical energy is regained after an arduous recovery period. This contributes to higher spirits and a motivation to reengage with life. The fifth construct is reflection and new existence. Patients strive to balance a new reality that relapse and death are inevitable, along with their need to live a meaningful life. Many do not yet appreciate how their disease has impacted them, but describe how their interpersonal lives and perceptions have changed, both positively and negatively. SIGNIFICANCE OF
RESULTS: Limitations of the study, future directions for research and clinical implications are discussed.

Entities:  

Mesh:

Year:  2006        PMID: 17133896     DOI: 10.1017/s1478951506060470

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  8 in total

1.  Living with multiple myeloma: experiences of patients and their informal caregivers.

Authors:  Alex Molassiotis; Barbara Wilson; Susan Blair; Tracy Howe; James Cavet
Journal:  Support Care Cancer       Date:  2009-12-09       Impact factor: 3.603

2.  Improving the assessment of quality of life in the clinical care of myeloma patients: the development and validation of the Myeloma Patient Outcome Scale (MyPOS).

Authors:  Thomas R Osborne; Christina Ramsenthaler; Stephen A Schey; Richard J Siegert; Polly M Edmonds; Irene J Higginson
Journal:  BMC Cancer       Date:  2015-04-14       Impact factor: 4.430

3.  Patient-Centered Insights on Treatment Decision Making and Living with Acute Myeloid Leukemia and Other Hematologic Cancers.

Authors:  Rebecca Crawford; Kate Sully; Rebecca Conroy; Chloe Johnson; Lynda Doward; Timothy Bell; Verna Welch; Francois Peloquin; Adam Gater
Journal:  Patient       Date:  2020-02       Impact factor: 3.883

4.  Interrupted Identities: Autologous Stem Cell Transplant in Patients With Multiple Myeloma.

Authors:  Sean N Halpin; Michael Konomos; Ivey Jowers
Journal:  J Patient Exp       Date:  2021-03-03

5.  Understanding what matters most to people with multiple myeloma: a qualitative study of views on quality of life.

Authors:  Thomas R Osborne; Christina Ramsenthaler; Susanne de Wolf-Linder; Stephen A Schey; Richard J Siegert; Polly M Edmonds; Irene J Higginson
Journal:  BMC Cancer       Date:  2014-07-09       Impact factor: 4.430

6.  Challenges in the cultural adaptation of the German Myeloma Patient Outcome Scale (MyPOS): an outcome measure to support routine symptom assessment in myeloma care.

Authors:  Christina Gerlach; Katherine Taylor; Marion Ferner; Markus Munder; Martin Weber; Christina Ramsenthaler
Journal:  BMC Cancer       Date:  2020-03-23       Impact factor: 4.430

Review 7.  Post-traumatic growth after cancer: a scoping review of qualitative research.

Authors:  Fiona Menger; Nurul Asyiqin Mohammed Halim; Ben Rimmer; Linda Sharp
Journal:  Support Care Cancer       Date:  2021-05-20       Impact factor: 3.603

8.  Living With Multiple Myeloma: A Focus Group Study of Unmet Needs and Preferences for Survivorship Care.

Authors:  Leanne Monterosso; Karen Taylor; Violet Platt; Elizabeth Lobb; Toni Musiello; Caroline Bulsara; Kendall Stratton; David Joske; Meinir Krishnasamy
Journal:  J Patient Exp       Date:  2017-07-26
  8 in total

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