Literature DB >> 23576528

Psychosocial support in patients with multiple myeloma at time of diagnosis: who wants what?

Jette Lamers1, Mechthild Hartmann1, Hartmut Goldschmidt2,3, Anette Brechtel1, Jens Hillengass2, Wolfgang Herzog1.   

Abstract

OBJECTIVE: The aim of this study was to examine interest in psychosocial interventions among patients with multiple myeloma at time of diagnosis as well as associated factors.
METHODS: Patients with newly diagnosed multiple myeloma were recruited from our outpatient myeloma unit at the Heidelberg University Hospital. Patients completed questionnaires that included a checklist on desired psychosocial interventions and the Patient Health Questionnaire 9-item (PHQ-9) depression and Generalized Anxiety Disorder 7-item scale (GAD-7) anxiety scales. Medical data were extracted from the patients' electronic records.
RESULTS: The survey was completed by 114 out of the 130 myeloma patients. Half of the patients (51%) desired psychosocial interventions. The most common preferences were relaxation techniques (21%), psychological counseling (20%), and peer support groups (18%). Approximately 24% of the patients reported symptoms of depression, and 8% reported symptoms of anxiety. Patients with symptoms of depression had twice as many preferences for psychosocial interventions as nondepressed patients. They more frequently desired individual psychotherapy (p = 0.035) and peer support groups (p = 0.015). In general, lower age was associated with greater interest in psychosocial interventions. Medical status was not strongly associated with interest in psychosocial interventions.
CONCLUSIONS: A high percentage (51%) of patients with multiple myeloma has psychosocial intervention desires at the time of diagnosis. The greatest interest was found in depressed and younger patients. However, depressed patients do not prefer a single intervention form but rather show a broad variability of wishes, so 'one size does not fit all'. Therefore, to reach all patients in need, a choice of psychosocial interventions should be offered.
Copyright © 2013 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer; multiple myeloma; oncology; psychosocial care; treatment preferences

Mesh:

Year:  2013        PMID: 23576528     DOI: 10.1002/pon.3284

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  10 in total

1.  Health-related quality of life in patients with multiple myeloma participating in a multidisciplinary rehabilitation program.

Authors:  Lene Kongsgaard Nielsen; Rikke Faebo Larsen; Lene Jarlbaek; Sören Möller; Eva Jespersen
Journal:  Ann Hematol       Date:  2021-01-06       Impact factor: 3.673

2.  Factors influencing supportive care needs of multiple myeloma patients treated with chemotherapy.

Authors:  Yoo-Rin Cho; Yang-Sook Yoo
Journal:  Support Care Cancer       Date:  2019-07-18       Impact factor: 3.603

3.  Resting-state brain metabolic fingerprinting clusters (biomarkers) and predictive models for major depression in multiple myeloma patients.

Authors:  Xiaofei Wang; Joshua Eichhorn; Iqbal Haq; Ahmad Baghal
Journal:  PLoS One       Date:  2021-05-06       Impact factor: 3.240

4.  Psychological Treatment for Patients Receiving Radiation: Results of NRG Oncology/RTOG 0841.

Authors:  William Small; Stephanie L Pugh; Lynne I Wagner; Jeffrey Kirshner; Kulbir Sidhu; Martin J Bury; Albert S DeNittis; Tracy E Alpert; Binh Tran; Beatrice F Bloom; Julie Mai; Deborah Watkins Bruner
Journal:  Int J Radiat Oncol Biol Phys       Date:  2021-02-07       Impact factor: 8.013

5.  Quality of Patient-Centered Care Provided to Patients Attending Hematological Cancer Treatment Centers.

Authors:  Flora Tzelepis; Tara Clinton-McHarg; Christine L Paul; Robert W Sanson-Fisher; Douglas Joshua; Mariko L Carey
Journal:  Int J Environ Res Public Health       Date:  2018-03-19       Impact factor: 3.390

6.  Association of resilience with health-related quality of life and depression in multiple myeloma and its precursors: results of a German cross-sectional study.

Authors:  Imad Maatouk; Susanne He; Natalia Becker; Manuela Hummel; Stefan Hemmer; Michaela Hillengass; Hartmut Goldschmidt; Mechthild Hartmann; Dieter Schellberg; Wolfgang Herzog; Jens Hillengass
Journal:  BMJ Open       Date:  2018-07-30       Impact factor: 2.692

7.  The work of managing multiple myeloma and its implications for treatment-related decision making: a qualitative study of patient and caregiver experiences.

Authors:  Cheryl Pritlove; Mobin Jassi; Bridget Burns; Arleigh McCurdy
Journal:  BMC Cancer       Date:  2021-07-08       Impact factor: 4.430

8.  Treat patient, not just the disease: holistic needs assessment for haematological cancer patients.

Authors:  Md Serajul Islam
Journal:  Oncol Rev       Date:  2018-07-04

9.  Patients with precursor disease exhibit similar psychological distress and mental HRQOL as patients with active myeloma.

Authors:  Imad Maatouk; Susanne He; Manuela Hummel; Stefan Hemmer; Michaela Hillengass; Hartmut Goldschmidt; Mechthild Hartmann; Wolfgang Herzog; Jens Hillengass
Journal:  Blood Cancer J       Date:  2019-01-21       Impact factor: 11.037

10.  Quality of life and distress assessed with self and external assessment screening tools in patients with hematologic malignancies attending treatment in an acute hospital.

Authors:  Bianca Senf; Kirsten Grabowski; Natascha Spielmann; Jens Fettel
Journal:  Qual Life Res       Date:  2020-08-19       Impact factor: 4.147

  10 in total

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