Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27470
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dc.contributor.authorZomerdijk, Nienke-
dc.contributor.authorJongenelis, Michelle-
dc.contributor.authorYuen, Eva Y N-
dc.contributor.authorTurner, Jane-
dc.contributor.authorHuntley, Kathryn-
dc.contributor.authorSmith, Andrew-
dc.contributor.authorMcIntosh, Megan-
dc.contributor.authorShort, Camille E-
dc.date2021-09-09-
dc.date.accessioned2021-09-13T05:57:56Z-
dc.date.available2021-09-13T05:57:56Z-
dc.date.issued2022-
dc.identifier.citationPsycho-Oncology 2022; 31(3): 416-424en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27470-
dc.description.abstractHaematological cancer patients are particularly vulnerable to the effects of COVID-19. In addition to being immunocompromised, pandemic-related travel restrictions have impacted access to treatments and overseas stem cell donations for patients requiring transplantation. Given this vulnerability, people with haematological cancers are at risk of experiencing heightened distress during the pandemic. This study aimed to explore haematological cancer patients' experiences and needs. Twenty-four Australian haematological cancer patients completed semi-structured interviews exploring their concerns and worries during the pandemic, impact of pandemic on management of disease, access to information and support, lifestyle changes, and attitudes towards emerging models of healthcare during the pandemic. Interview transcripts were thematically analysed. Four themes reflecting the experiences of haematological cancer patients during the pandemic were identified: 'Fears about contracting COVID-19' (behaviour changes to protect health, impact on daily routine and habits, annoyance at dismissive attitude of others toward COVID-19); 'Reduced sense of connection and support' (reduced social support and access to external support services); 'New challenges' (increased financial hardship, worsened health), and; 'Underlying system and communication issues' (access to trusted information, satisfaction/dissatisfaction with care, navigating telehealth). Participants expressed a need for improved access to support services and trusted information. The findings emphasise the additional challenges experienced by haematological cancer patients during the COVID-19 pandemic and their impact on daily life. Results point to the importance of validation of increased distress during periods of uncertainty; reinforcing recommendations about high-quality sources of information; and facilitating access to support services when face-to-face care is limited.en
dc.language.isoeng-
dc.subjectCOVID-19 pandemicen
dc.subjectcanceren
dc.subjecthaematologyen
dc.subjectoncologyen
dc.subjectpsycho-oncologyen
dc.subjectqualitative researchen
dc.subjectsupportive careen
dc.titleExperiences and needs of people with haematological cancers during the COVID-19 pandemic: A qualitative study.en
dc.typeJournal Articleen
dc.identifier.journaltitlePsycho-Oncologyen
dc.identifier.affiliationCancer Care Services, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationFaculty of Health and Medical Sciences, University of Adelaide, South Australia, Australiaen
dc.identifier.affiliationMelbourne School of Psychological Sciences, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationMelbourne School of Psychological Sciences, Melbourne Centre for Behaviour Change, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Health Sciences, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationVictorian Comprehensive Cancer Centre Alliance, Melbourne, Victoria, Australiaen
dc.identifier.affiliationCentre for Quality and Patient Safety Research-Monash Health Partnership, Institute for Health Transformation Deakin University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Nursing and Midwifery, Faculty of Health, Deakin University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Psychology and Public Health, Department of Psychology and Counselling, La Trobe University, Bundoora, Victoria, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen
dc.identifier.affiliationFaculty of Medicine, University of Queensland, Brisbane, Queensland, Australiaen
dc.identifier.affiliationLeukaemia Foundation, Brisbane, Queensland, Australiaen
dc.identifier.affiliationPsycho-oncology Research Uniten
dc.identifier.doi10.1002/pon.5819en
dc.type.contentTexten
dc.identifier.orcid0000-0001-5008-6429en
dc.identifier.orcid0000-0002-0717-1692en
dc.identifier.orcid0000-0002-7956-5797en
dc.identifier.orcid0000-0003-1438-217Xen
dc.identifier.orcid0000-0003-1722-9920en
dc.identifier.orcid0000-0002-9576-4817en
dc.identifier.orcid0000-0003-0933-6718en
dc.identifier.orcid0000-0002-4177-4251en
dc.identifier.pubmedid34500498-
local.name.researcherYuen, Eva Y N
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptPsycho-Oncology Research Unit-
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