Childhood cancer survivorship: barriers and preferences. Issue Volume 12:Issue e5(2022) (11th November 2019)
- Record Type:
- Journal Article
- Title:
- Childhood cancer survivorship: barriers and preferences. Issue Volume 12:Issue e5(2022) (11th November 2019)
- Main Title:
- Childhood cancer survivorship: barriers and preferences
- Authors:
- Signorelli, Christina
Wakefield, Claire
McLoone, Jordana K
Fardell, Joanna
Jones, Janelle M
Turpin, Kate H
Emery, Jon
Michel, Gisela
Downie, Peter
Skeen, Jane E
Cohn, Richard - Other Names:
- author non-byline.
Alvaro Frank author non-byline.
Cohn Richard author non-byline.
Corbett Rob author non-byline.
Downie Peter author non-byline.
Egan Karen author non-byline.
Ellis Sarah author non-byline.
Emery Jon author non-byline.
Fardell Joanna author non-byline.
Foreman Tali author non-byline.
Gabriel Melissa author non-byline.
Girgis Afaf author non-byline.
Graham Kerrie author non-byline.
Johnston Karen author non-byline.
Jones Janelle author non-byline.
Lockwood Liane author non-byline.
Maguire Ann author non-byline.
McCarthy Maria author non-byline.
McLoone Jordana author non-byline.
Mechinaud Francoise author non-byline.
Molloy Sinead author non-byline.
Moore Lyndal author non-byline.
Osborn Michael author non-byline.
Signorelli Christina author non-byline.
Skeen Jane author non-byline.
Tapp Heather author non-byline.
Till Tracy author non-byline.
Truscott Jo author non-byline.
Turpin Kate author non-byline.
Wakefield Claire author non-byline.
Williamson Jane author non-byline.
Walwyn Thomas author non-byline.
Yallop Kathy author non-byline.
… (more) - Abstract:
- Abstract : Objective: Many survivors are disengaged from follow-up, mandating alternative models of survivorship-focused care for late effects surveillance. We explored survivors' barriers to accessing, and preferences for survivorship care. Methods: We invited Australian and New Zealand survivors of childhood cancer from three age groups: <16 years (represented by parents), 16–25 years (adolescent and young adults (AYAs)) and >25 years ('older survivors'). Participants completed questionnaires and optional interviews. Results: 633 survivors/parents completed questionnaires: 187 parents of young survivors (mean age: 12.4 years), 251 AYAs (mean age: 20.6 years) and 195 older survivors (mean age: 32.5 years). Quantitative data were complemented by 151 in-depth interviews. Most participants, across all age groups, preferred specialised follow-up (ie, involving oncologists, nurses or a multidisciplinary team; 86%–97%). Many (36%–58%) were unwilling to receive community-based follow-up. More parents (75%) than AYAs (58%) and older survivors (30%) were engaged in specialised follow-up. While follow-up engagement was significantly lower in older survivors, survivors' prevalence of late effects increased. Of those attending a follow-up clinic, 34%–56% were satisfied with their care, compared with 14%–15% of those not receiving cancer-focused care (p<0.001). Commonly reported barriers included lack of awareness about follow-up availability (67%), followed by logistical (65%),Abstract : Objective: Many survivors are disengaged from follow-up, mandating alternative models of survivorship-focused care for late effects surveillance. We explored survivors' barriers to accessing, and preferences for survivorship care. Methods: We invited Australian and New Zealand survivors of childhood cancer from three age groups: <16 years (represented by parents), 16–25 years (adolescent and young adults (AYAs)) and >25 years ('older survivors'). Participants completed questionnaires and optional interviews. Results: 633 survivors/parents completed questionnaires: 187 parents of young survivors (mean age: 12.4 years), 251 AYAs (mean age: 20.6 years) and 195 older survivors (mean age: 32.5 years). Quantitative data were complemented by 151 in-depth interviews. Most participants, across all age groups, preferred specialised follow-up (ie, involving oncologists, nurses or a multidisciplinary team; 86%–97%). Many (36%–58%) were unwilling to receive community-based follow-up. More parents (75%) than AYAs (58%) and older survivors (30%) were engaged in specialised follow-up. While follow-up engagement was significantly lower in older survivors, survivors' prevalence of late effects increased. Of those attending a follow-up clinic, 34%–56% were satisfied with their care, compared with 14%–15% of those not receiving cancer-focused care (p<0.001). Commonly reported barriers included lack of awareness about follow-up availability (67%), followed by logistical (65%), care-related beliefs (59%) and financial reasons (57%). Older survivors (p<0.001), living outside major cities (p=0.008), and who were further from diagnosis (p=0.014) reported a higher number of barriers. Conclusions: Understanding patient-reported barriers, and tailoring care to survivors' follow-up preferences, may improve engagement with care and ensure that the survivorship needs of this population are met. … (more)
- Is Part Of:
- BMJ supportive & palliative care. Volume 12:Issue e5(2022)
- Journal:
- BMJ supportive & palliative care
- Issue:
- Volume 12:Issue e5(2022)
- Issue Display:
- Volume 12, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 12
- Issue:
- 5
- Issue Sort Value:
- 2022-0012-0005-0000
- Page Start:
- e687
- Page End:
- e695
- Publication Date:
- 2019-11-11
- Subjects:
- barriers -- paediatric oncology -- survivorship -- models of care -- long-term follow-up -- patient preferences
Palliative treatment -- Periodicals
Terminal care -- Periodicals
616.029 - Journal URLs:
- http://www.bmj.com/archive ↗
http://spcare.bmj.com/ ↗ - DOI:
- 10.1136/bmjspcare-2019-002001 ↗
- Languages:
- English
- ISSNs:
- 2045-435X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24498.xml