References
- Braun, V., & Clarke, V. (2006). Using thematic analysis in psychology. Qualitative Research in Psychology, 3(2), 77–101. doi:https://doi.org/10.1191/1478088706qp063oa
- Bruera, E., Sweeney, C., Russell, N., Willey, J. S., & Palmer, J. L. (2003). Place of death of Houston area residents with cancer over a two-year period. Journal of Pain & Symptom Management, 26(1), 637–643.
- Campbell, J. L., Quincy, C., Osserman, J., & Pedersen, O. K. (2013). Coding in-depth semistructured interviews: Problems of unitization and intercoder reliability and agreement. Sociological Methods & Research, 42(3), 294–320. doi:https://doi.org/10.1177/0049124113500475
- Carey, E., Dose, A., Humeniuk, K., Kuan, Y., Hicks, A., Ottenberg, A., … Koenig, B. (2018). The experience of hospital death: Assessing the quality of care at an academic medical center. American Journal of Hospice & Palliative Medicine, 35(2), 189–197. doi:https://doi.org/10.1177/1049909116689547
- Gerritsen, R., Koopmans, M., Hofhuis, J., Curtis, R., Jensen, H., Zijlstra, J., … Spronk, P. (2017). Comparing quality of dying and death perceived by family members and nurses for patients dying in US and Dutch ICUs. Chest, 151(2), 298–307. doi:https://doi.org/10.1016/j.chest.2016.09.003
- Gomes, B., & Higginson, I. J. (2008). Where people die (1974–2030): Past trends, future projections and implications for care. Palliative Medicine, 22(1), 33–41. doi:https://doi.org/10.1177/0269216307084606
- Granda-Cameron, C., & Houldin, A. (2012). Concept analysis of good death in terminally ill patients. American Journal of Hospice & Palliative Medicine, 29(8), 632–639.
- Guest, G., MacQueen, K. M., & Namey, E. E. (2011). Applied thematic analysis. Washington, DC: Sage Publishing.
- Hajradinovic, Y., Tishelman, C., Lindqvist, O., & Goliath, I. (2018). Family members´ experiences of the end-of-life care environments in acute care settings: A photo-elicitation study. International Journal of Qualitative Studies on Health & Well-Being, 13(1), 1511767–1511767. doi:https://doi.org/10.1080/17482631.2018.1511767
- Hales, S., Zimmermann, C., & Rodin, G. (2008). The quality of dying and death. Archives of Internal Medicine, 168(9), 912–918. doi:https://doi.org/10.1001/archinte.168.9.912
- Jennings, B., Ryndes, T., D’Onofrio, C., & Baily, M. (2003). Access to hospice care: Expanding boundaries, overcoming barriers. Retrieved from: http://www.thehastingscenter.org/uploadedFiles/Publications/Special_Reports/access_hospice_care.pdf
- Nelson, J. E., Puntillo, K. A., Pronovost, P. J., Walker, A. S., McAdam, J. L., Ilaoa, D., & Penrod, J. (2010). In their own words: Patients and families define high-quality palliative care in the intensive care unit. Critical Care Medicine, 38(3), 808–818. doi:https://doi.org/10.1097/CCM.0b013e3181c5887c
- Rodgers, B. L., & Cowles, K. V. (1993). The qualitative research audit trail: A complex collection of documentation. Research in Nursing & Health, 16(3), 219–226. doi:https://doi.org/10.1002/nur.4770160309
- Roza, K., Lee, E., Meier, D., & Goldstein, N. (2015). A survey of bereaved family members to assess quality of care on a palliative care unit. Journal of Palliative Medicine, 18(4), 358–365. doi:https://doi.org/10.1089/jpm.2014.0172
- Steinhauser, K., Christakis, N., Clipp, E., McNeilly, M., McIntyre, L., & Tulsky, J. (2000). Factors considered important at the end of life by patients, family, physicians and other care providers. JAMA, 284(19), 2476–2482. doi:https://doi.org/10.1001/jama.284.19.2476
- Steinhauser, K. E., Voils, C. I., Bosworth, H., & Tulsky, J. A. (2015). What constitutes quality of family experience at the end of life? Perspectives from family members of patients who died in the hospital. Palliative & Supportive Care, 13(4), 945–952. doi:https://doi.org/10.1001/jama.284.19.2476
- Tenzek, K., & Depner, R. (2017). Still searching: A meta-synthesis of a good death from the bereaved family member perspective. Behavioral Sciences, 7(4), 25. doi:https://doi.org/10.3390/bs7020025
- Vaismoradi, M., Turunen, H., & Bondas, T. (2013). Content analysis and thematic analysis: Implications for conducting a qualitative descriptive study. Nursing & Health Sciences, 15(3), 398–405. doi:https://doi.org/10.1111/nhs.12048
- Virdun, C., Luckett, T., Davidson, P. M., & Phillips, J. (2015). Dying in the hospital setting: A systematic review of quantitative studies identifying the elements of end-of-life care that patients and their families rank as being most important. Palliative Medicine, 29(9), 774–796. doi:https://doi.org/10.1177/0269216315583032
- Witkamp, E., Droger, M., Janssens, R., van Zuylen, L., & van der Heide, A. (2016). How to deal with relatives of patients dying in the hospital? Qualitative content analysis of relatives’ experiences. Journal of Pain & Symptom Management, 52(2), 235–241. doi:https://doi.org/10.1016/j.jpainsymman.2016.02.009
- Witkamp, F., van Zuylen, L., Borsboom, G., van der Rijt, C., & van der Heide, A. (2015). Dying in the hospital: What happens and what matters according to bereaved relatives. Journal of Pain & Symptom Management, 49(2), 203–213. doi:https://doi.org/10.1016/j.jpainsymman.2014.06.013
- Wright, A. A., Keating, N. L., Balboni, T. A., Matulonis, U. A., Block, S. D., & Prigerson, H. G. (2010). Place of death: Correlations with quality of life of patients with cancer and predictors of bereaved caregivers’ mental health. Journal of Clinical Oncology, 28(29), 4457–4464. doi:https://doi.org/10.1200/JCO.2009.26.3863