Collins A - Search Results

1

Describing the psychosocial profile and unmet support needs of parents caring for a child with a life-limiting condition: A cross-sectional study of caregiver-reported outcomes.

Collins A, Burchell J, Remedios C, Thomas K. Collins A, et al. Palliat Med. 2020 Mar;34(3):358-366. doi: 10.1177/0269216319892825. Epub 2020 Feb 27. Palliat Med. 2020. PMID: 32103697

2

The challenges and suffering of caring for people with primary malignant glioma: qualitative perspectives on improving current supportive and palliative care practices.

Collins A, Lethborg C, Brand C, Gold M, Moore G, Sundararajan V, Murphy M, Philip J. Collins A, et al. BMJ Support Palliat Care. 2014 Mar;4(1):68-76. doi: 10.1136/bmjspcare-2012-000419. Epub 2013 Jun 1. BMJ Support Palliat Care. 2014. PMID: 24644774

3

Predicting distress among people who care for patients living longer with high-grade malignant glioma.

Russell B, Collins A, Dowling A, Dally M, Gold M, Murphy M, Burchell J, Philip J. Russell B, et al. Among authors: collins a. Support Care Cancer. 2016 Jan;24(1):43-51. doi: 10.1007/s00520-015-2739-0. Epub 2015 Apr 25. Support Care Cancer. 2016. PMID: 25910750

4

Lived experiences of parents caring for a child with a life-limiting condition in Australia: A qualitative study.

Collins A, Hennessy-Anderson N, Hosking S, Hynson J, Remedios C, Thomas K. Collins A, et al. Palliat Med. 2016 Dec;30(10):950-959. doi: 10.1177/0269216316634245. Epub 2016 Mar 7. Palliat Med. 2016. PMID: 26951065

5

Initial perceptions of palliative care: An exploratory qualitative study of patients with advanced cancer and their family caregivers.

Collins A, McLachlan SA, Philip J. Collins A, et al. Palliat Med. 2017 Oct;31(9):825-832. doi: 10.1177/0269216317696420. Epub 2017 Apr 3. Palliat Med. 2017. PMID: 28367679

6

Communication about palliative care: A phenomenological study exploring patient views and responses to its discussion.

Collins A, McLachlan SA, Philip J. Collins A, et al. Palliat Med. 2018 Jan;32(1):133-142. doi: 10.1177/0269216317735247. Epub 2017 Nov 13. Palliat Med. 2018. PMID: 29130425

7

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. Collins A, et al. Palliat Med. 2018 Apr;32(4):861-869. doi: 10.1177/0269216317746584. Epub 2017 Dec 13. Palliat Med. 2018. PMID: 29235421

8

Transition Points for the Routine Integration of Palliative Care in Patients With Advanced Cancer.

Collins A, Sundararajan V, Burchell J, Millar J, McLachlan SA, Krishnasamy M, Le BH, Mileshkin L, Hudson P, Philip J. Collins A, et al. J Pain Symptom Manage. 2018 Aug;56(2):185-194. doi: 10.1016/j.jpainsymman.2018.03.022. Epub 2018 Mar 30. J Pain Symptom Manage. 2018. PMID: 29608934 Free article.

9

Responding to urgency of need: Initial qualitative stage in the development of a triage tool for use in palliative care services.

Russell B, Sundararajan V, Hennesy-Anderson N, Collins A, Burchell J, Vogrin S, Le B, Brand C, Hudson P, Philip J. Russell B, et al. Among authors: collins a. Palliat Med. 2018 Jul;32(7):1246-1254. doi: 10.1177/0269216318773221. Palliat Med. 2018. PMID: 29936903

10

The trajectory of patients who die from metastatic prostate cancer: a population-based study.

Collins A, Sundararajan V, Millar J, Burchell J, Le B, Krishnasamy M, McLachlan SA, Hudson P, Mileshkin L, Philip J. Collins A, et al. BJU Int. 2019 May;123 Suppl 5:19-26. doi: 10.1111/bju.14593. Epub 2018 Nov 25. BJU Int. 2019. PMID: 30371986

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