Telehealth cancer care consultations during the COVID-19 pandemic: a qualitative study of the experiences of Australians affected by cancer.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 21 12 2021
accepted: 29 03 2022
pubmed: 4 5 2022
medline: 24 6 2022
entrez: 3 5 2022
Statut: ppublish

Résumé

In response to the onset of the COVID-19 pandemic, telehealth was rapidly rolled out in health services across Australia including those delivering cancer care. This study aimed to understand people with cancer and carers' experiences with telehealth for cancer care during the COVID-19 pandemic and associated restrictions. Semi-structured interviews conducted with people with cancer and carers via telephone or online video link between December 2020 and May 2021. Participants were recruited through cancer networks and social media. Interviews were transcribed and thematic analysis undertaken. Twenty-three patients and 5 carers were interviewed. Telephone-based appointments were most common. Responses to telehealth were influenced by existing relationships with doctors, treatment/cancer stage and type of appointment. Four themes were derived: (i) benefits, (ii) quality of care concerns, (iii) involving carers, and (iv) optimising use of telehealth. Benefits included efficiency and reduced travel. Quality of care concerns identified subthemes: transactional feel to appointments; difficulties for rapport; suitability for appointment type and adequacy for monitoring. Both patients and carers noted a lack of opportunity for carers to participate in telephone-based appointments. Aligning appointment mode (i.e. telehealth or in person) with appointment purpose and ensuring telehealth was the patient's choice were seen as essential for its ongoing use. While telehealth has benefits, its potential to reduce the quality of interactions with clinicians made it less attractive for cancer patients. Patient-centred guidelines that ensure patient choice, quality communication, and alignment with appointment purpose may help to increase telehealth's utility for people affected by cancer.

Sections du résumé

BACKGROUND BACKGROUND
In response to the onset of the COVID-19 pandemic, telehealth was rapidly rolled out in health services across Australia including those delivering cancer care. This study aimed to understand people with cancer and carers' experiences with telehealth for cancer care during the COVID-19 pandemic and associated restrictions.
METHOD METHODS
Semi-structured interviews conducted with people with cancer and carers via telephone or online video link between December 2020 and May 2021. Participants were recruited through cancer networks and social media. Interviews were transcribed and thematic analysis undertaken.
RESULTS RESULTS
Twenty-three patients and 5 carers were interviewed. Telephone-based appointments were most common. Responses to telehealth were influenced by existing relationships with doctors, treatment/cancer stage and type of appointment. Four themes were derived: (i) benefits, (ii) quality of care concerns, (iii) involving carers, and (iv) optimising use of telehealth. Benefits included efficiency and reduced travel. Quality of care concerns identified subthemes: transactional feel to appointments; difficulties for rapport; suitability for appointment type and adequacy for monitoring. Both patients and carers noted a lack of opportunity for carers to participate in telephone-based appointments. Aligning appointment mode (i.e. telehealth or in person) with appointment purpose and ensuring telehealth was the patient's choice were seen as essential for its ongoing use.
DISCUSSION AND CONCLUSIONS CONCLUSIONS
While telehealth has benefits, its potential to reduce the quality of interactions with clinicians made it less attractive for cancer patients. Patient-centred guidelines that ensure patient choice, quality communication, and alignment with appointment purpose may help to increase telehealth's utility for people affected by cancer.

Identifiants

pubmed: 35503140
doi: 10.1007/s00520-022-07021-6
pii: 10.1007/s00520-022-07021-6
pmc: PMC9062284
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6659-6668

Informations de copyright

© 2022. The Author(s).

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Auteurs

Victoria White (V)

School of Psychology, Faculty of Health, Deakin University, Geelong, VIC, Australia. Vicki.white@deakin.edu.au.

Alice Bastable (A)

Cancer Council Victoria, Melbourne, VIC, Australia.

Ilana Solo (I)

Loddon Mallee Integrated Cancer Service, Bendigo, VIC, Australia.

Seleena Sherwell (S)

Southern Melbourne Integrated Cancer Service, Melbourne, VIC, Australia.

Sangeetha Thomas (S)

School of Psychology, Faculty of Health, Deakin University, Geelong, VIC, Australia.

Rob Blum (R)

Loddon Mallee Integrated Cancer Service, Bendigo, VIC, Australia.
Bendigo Health, Bendigo, VIC, Australia.

Javier Torres (J)

Goulburn Valley Health, Shepparton, VIC, Australia.

Natalie Maxwell-Davis (N)

Consumer Representative, Melbourne, VIC, Australia.

Kathy Alexander (K)

Consumer Representative, Melbourne, VIC, Australia.

Amanda Piper (A)

Cancer Council Victoria, Melbourne, VIC, Australia.

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