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Journal Abstract Search

474 related items for PubMed ID: 28367679

  • 1. Initial perceptions of palliative care: An exploratory qualitative study of patients with advanced cancer and their family caregivers.
    Collins A, McLachlan SA, Philip J.
    Palliat Med; 2017 Oct; 31(9):825-832. PubMed ID: 28367679
    [Abstract] [Full Text] [Related]

  • 2. How should we talk about palliative care, death and dying? A qualitative study exploring perspectives from caregivers of people with advanced cancer.
    Collins A, McLachlan SA, Philip J.
    Palliat Med; 2018 Apr; 32(4):861-869. PubMed ID: 29235421
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  • 3. Communication about palliative care: A phenomenological study exploring patient views and responses to its discussion.
    Collins A, McLachlan SA, Philip J.
    Palliat Med; 2018 Jan; 32(1):133-142. PubMed ID: 29130425
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  • 4. Perceptions of the care received from Australian palliative care services: A caregiver perspective.
    Pidgeon TM, Johnson CE, Lester L, Currow D, Yates P, Allingham SF, Bird S, Eagar K.
    Palliat Support Care; 2018 Apr; 16(2):198-208. PubMed ID: 28357973
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  • 5. The experiences of patients with advanced cancer and caregivers presenting to Emergency Departments: A qualitative study.
    Philip J, Remedios C, Breen S, Weiland T, Willenberg L, Boughey M, Jelinek G, Lane H, Marck C, Weil J.
    Palliat Med; 2018 Feb; 32(2):439-446. PubMed ID: 29130378
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  • 6. The experience of palliative care service provision for people with non-malignant respiratory disease and their family carers: An all-Ireland qualitative study.
    Mc Veigh C, Reid J, Larkin P, Porter S, Hudson P.
    J Adv Nurs; 2018 Feb; 74(2):383-394. PubMed ID: 28910509
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  • 7. Patients', family caregivers', and professionals' perspectives on quality of palliative care: a qualitative study.
    Vedel I, Ghadi V, Lapointe L, Routelous C, Aegerter P, Guirimand F.
    Palliat Med; 2014 Oct; 28(9):1128-38. PubMed ID: 24821709
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  • 8. Service user perspectives on palliative care education for health and social care professionals supporting people with learning disabilities.
    McLaughlin D, Barr O, McIlfatrick S, McConkey R.
    BMJ Support Palliat Care; 2015 Dec; 5(5):531-7. PubMed ID: 24644213
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  • 12. Resilience for family carers of advanced cancer patients-how can health care providers contribute? A qualitative interview study with carers.
    Røen I, Stifoss-Hanssen H, Grande G, Brenne AT, Kaasa S, Sand K, Knudsen AK.
    Palliat Med; 2018 Sep; 32(8):1410-1418. PubMed ID: 29852808
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  • 14. Preparedness for caregiving: A phenomenological study of the experiences of rural Australian family palliative carers.
    Mason N, Hodgkin S.
    Health Soc Care Community; 2019 Jul; 27(4):926-935. PubMed ID: 30810249
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  • 15. 'I am part of the community but...' The changing context of rural living for persons with advanced cancer and their families.
    Duggleby WD, Penz K, Leipert BD, Wilson DM, Goodridge D, Williams A.
    Rural Remote Health; 2011 Jul; 11(3):1733. PubMed ID: 21787109
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  • 16. The 'safe death': An ethnographic study exploring the perspectives of rural palliative care patients and family caregivers.
    Rainsford S, Phillips CB, Glasgow NJ, MacLeod RD, Wiles RB.
    Palliat Med; 2018 Dec; 32(10):1575-1583. PubMed ID: 30229700
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  • 17. An ethnography of managing emotions when talking about life-threatening illness.
    Ayers NE, Vydelingum V, Arber A.
    Int Nurs Rev; 2017 Dec; 64(4):486-493. PubMed ID: 28151559
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