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Journal Abstract Search
996 related items for PubMed ID: 28357973
1. 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 [Abstract] [Full Text] [Related]
2. Reliability testing of the FAMCARE-2 scale: measuring family carer satisfaction with palliative care. Aoun S, Bird S, Kristjanson LJ, Currow D. Palliat Med; 2010 Oct; 24(7):674-81. PubMed ID: 20621947 [Abstract] [Full Text] [Related]
3. Association between family satisfaction and caregiver burden in cancer patients receiving outreach palliative care at home. Naoki Y, Matsuda Y, Maeda I, Kamino H, Kozaki Y, Tokoro A, Maki N, Takada M. Palliat Support Care; 2018 Jun; 16(3):260-268. PubMed ID: 28462749 [Abstract] [Full Text] [Related]
5. Caregiver exposure to critical events and distress in home-based palliative care in Germany a cross-sectional study using the Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) scale. Galatsch M, Prigerson HG, Schnepp W, Zu Sayn-Wittgenstein F, Li J. BMC Palliat Care; 2019 Jan 24; 18(1):9. PubMed ID: 30678682 [Abstract] [Full Text] [Related]
8. Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial. Aoun S, Deas K, Toye C, Ewing G, Grande G, Stajduhar K. Palliat Med; 2015 Jun 24; 29(6):508-17. PubMed ID: 25645667 [Abstract] [Full Text] [Related]
10. Prevalence and correlates of unmet palliative care needs in dyads of Chinese patients with advanced cancer and their informal caregivers: a cross-sectional survey. Wang T, Molassiotis A, Tan JY, Chung BPM, Huang HQ. Support Care Cancer; 2021 Mar 24; 29(3):1683-1698. PubMed ID: 32776164 [Abstract] [Full Text] [Related]
11. [Satisfaction of principal caregivers of patients followed-up by palliative care teams]. Fernández-Isla LE, Conde-Valvis-Fraga S, Fernández-Ruíz JS. Semergen; 2016 Oct 24; 42(7):476-481. PubMed ID: 27117786 [Abstract] [Full Text] [Related]
13. Correlation between patient quality of life in palliative care and burden of their family caregivers: a prospective observational cohort study. Krug K, Miksch A, Peters-Klimm F, Engeser P, Szecsenyi J. BMC Palliat Care; 2016 Jan 15; 15():4. PubMed ID: 26767785 [Abstract] [Full Text] [Related]
14. Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool. Aoun SM, Deas K, Kristjanson LJ, Kissane DW. Palliat Support Care; 2017 Feb 15; 15(1):32-43. PubMed ID: 27173737 [Abstract] [Full Text] [Related]
17. The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial. Aoun SM, Grande G, Howting D, Deas K, Toye C, Troeung L, Stajduhar K, Ewing G. PLoS One; 2015 Feb 15; 10(4):e0123012. PubMed ID: 25849348 [Abstract] [Full Text] [Related]
18. 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 15; 31(9):825-832. PubMed ID: 28367679 [Abstract] [Full Text] [Related]
20. A survey of patients' experience of pain and other symptoms while receiving care from palliative care services. Pidgeon T, Johnson CE, Currow D, Yates P, Banfield M, Lester L, Allingham SF, Bird S, Eagar K. BMJ Support Palliat Care; 2016 Sep 15; 6(3):315-22. PubMed ID: 25743438 [Abstract] [Full Text] [Related] Page: [Next] [New Search]