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Factors Associated with Quality of Life at the Last Month of Life in the United States

Yıl 2025, Cilt: 14 Sayı: 1, 119 - 137
https://doi.org/10.15869/itobiad.1517005

Öz

Recently, increasing aging rates and prolonged dying processes have significantly influenced the quality of life during the end-of-life period. The concept of quality of life at this stage has become a topic of growing debate, with a particular focus on alleviating symptoms and preserving functionality. This study aims to evaluate the quality of life among adults aged 65 and older in their last month of life in the United States and to identify associated risk factors. Utilizing data from the National Health and Aging Trends Study (NHATS), covering the period from 2011 to 2021 across ten waves, the analysis included 1,722 participants. Weighted prevalence estimates and multivariable regression models were employed. The results indicated that participants had an average quality of life score of 2.10 out of 5. Among the participants, 57.35% were conscious, and 42.36% were able to get out of bed without assistance. Additionally, 26.62% reported no pain, 40.61% did not experience respiratory issues, and 43.84% did not report feelings of sadness or anxiety. The study identified several risk factors associated with lower quality of life at the end of life, including race/ethnicity, living alone, multiple chronic conditions, and limitations in daily activities. These findings highlight critical implications for social policy and social work. Specifically, they underscore the importance of end-of-life care that not only extends life but also enhances the experience for patients and their families. Achieving this requires comprehensive support in personal care, socio-psychological assistance, and effective symptom management. The study further emphasizes the necessity of broader adoption of advance directives to align care with the priorities and preferences of patients and their families. Moreover, the use of evidence-based symptom assessment tools is essential for early detection and effective management of symptoms. Finally, the development of social work practices and policies tailored to socially disadvantaged and high-risk groups can play a pivotal role in mitigating challenges associated with end-of-life care, ultimately improving overall quality of life.

Kaynakça

  • Birkholz, L., & Haney, T. (2018). Using a dyspnea assessment tool to improve care at the end of life. Journal of Hospice & Palliative Nursing, 20(3), 219-227. Doi: https://doi.org/10.1097/NJH.0000000000000432
  • Büken, N. Ö. (2016). Yaşamın Sonunda Klinik Etik Karar Verme Süreci ve Belirleyici Faktörler. Türkiye Klinikleri Tıp Etiği-Hukuku-Tarihi Özel, 2(3), 24-33.
  • Campbell, M. L., Kiernan, J. M., Strandmark, J., & Yarandi, H. N. (2018). Trajectory of dyspnea and respiratory distress among patients in the last month of life. Journal of Palliative Medicine, 21(2), 194-199. Doi: https://doi.org/10.1089/jpm.2017.0265
  • Chi, N. C., & Demiris, G. (2017). Family caregivers’ pain management in end-of-life care: A systematic review. American Journal of Hospice and Palliative Medicine®, 34(5), 470-485. Doi: https://doi.org/10.1177/1049909116637359
  • Cohen-Mansfield, J., Cohen, R., Skornick-Bouchbinder, M., & Brill, S. (2018). What is the end of life period? Trajectories and characterization based on primary caregiver reports. The Journals of Gerontology: Series A, 73(5), 695-701. Doi: https://doi.org/10.1093/gerona/glx195
  • Conill, C., Verger, E., Henríquez, I., Saiz, N., Espier, M., Lugo, F., & Garrigos, A. (1997). Symptom prevalence in the last week of life. Journal of Pain and Symptom Management, 14(6), 328-331. Doi: https://doi.org/10.1016/s0885-3924(97)00263-7
  • Davidoff, A. J., Canavan, M. E., Prsic, E., Saphire, M., Wang, S. Y., & Presley, C. J. (2021). End-of-life patterns of symptom management and cancer-directed care among Medicare beneficiaries with lung cancer: a claims-based analysis. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 29(7), 3921–3932. Doi: https://doi.org/10.1007/s00520-020-05964-2
  • Drageset, J., Corbett, A., Selbaek, G., & Husebo, B. S. (2014). Cancer-related pain and symptoms among nursing home residents: A systematic review. Journal of Pain and Symptom Management, 48(4), 699-710. Doi: https://doi.org/10.1016/j.jpainsymman.2013.12.238
  • Duncan-Daston, R., Foster, S., & Bowden, H. (2016). A look into spirituality in social work practice within the hospice setting. Journal of Religion & Spirituality in Social Work: Social Thought, 35(3), 157-178. Doi: https://doi.org/10.1080/15426432.2015.1102672
  • Düzgün, G., Yönt, G. H., & Polat, G. (2023). Yaşam Sonu Bakımda Onurun Korunması. Sağlık Akademisi Kastamonu, 8(3), 590-598.
  • Enguidanos, S., & Ailshire, J. (2017). Timing of advance directive completion and relationship to care preferences. Journal of pain and symptom management, 53(1), 49-56. Doi: https://doi.org/10.1016/j.jpainsymman.2016.08.008
  • Freedman, V. A., & Kasper, J. D. (2019). Cohort profile: the national health and aging trends study (NHATS). International journal of epidemiology, 48(4), 1044-1045g.
  • Freedman, V. A., Hu, M., DeMatteis, J., & Kasper, J. D. (2020). Accounting for sample design in NHATS and NSOC analyses: Frequently asked questions. NHATS Technical Paper, 23, 2021.
  • Gawande, A. (2010). Letting go. The New Yorker, 2, 36-49.
  • Gawande, A. (2014). Being mortal: illness, medicine and what matters in the end. London: Profile Books.
  • Hendriks, S. A., Smalbrugge, M., Hertogh, C. M., & van der Steen, J. T. (2014). Dying with dementia: Symptoms, treatment, and quality of life in the last week of life. Journal of Pain and Symptom Management, 47(4), 710- 720. Doi: https://doi.org/10.1016/j.jpainsymman.2013.05.015
  • Kasper, J. D., & Freedman, V. A. (2014). Findings from the 1st round of the National Health and Aging Trends Study (NHATS): Introduction to a special issue. Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 69(1), 1-7.
  • Kehl, K. A., & Kowalkowski, J. A. (2013). A systematic review of the prevalence of signs of impending death and symptoms in the last 2 weeks of life. American Journal of Hospice and Palliative Medicine®, 30(6), 601-616. Doi: https://doi.org/10.1177/1049909112468222
  • Kozlov, E., Phongtankuel, V., Prigerson, H., Adelman, R., Shalev, A., Czaja, S., ... & Reid, M. C. (2019). Prevalence, severity, and correlates of symptoms of anxiety and depression at the very end of life. Journal of Pain and Symptom Management, 58(1), 80-85. Doi: https://doi.org/10.1016/j.jpainsymman.2019.04.012
  • Lee, H. J., Small, B. J., & Haley, W. E. (2020). Health and well-being in the year before death: The association with quality of life and care at the end-of-life. Journal of Aging and Health, 32(10), 1475-1485. Doi: https://doi.org/10.1177/0898264320935297
  • Lobchuk, M. M., & Degner, L. F. (2002). Symptom experiences: Perceptual accuracy between advanced-stage cancer patients and family caregivers in the home care setting. Journal of Clinical Oncology, 20(16), 3495- 3507.
  • Meier, E. A., Gallegos, J. V., Thomas, L. P. M., Depp, C. A., Irwin, S. A., & Jeste, D. V. (2016). Defining a good death (successful dying): Literature review and a call for research and public dialogue. The American Journal of Geriatric Psychiatry, 24(4), 261-271. Doi: https://doi.org/10.1016/j.jagp.2016.01.135
  • National Center for Health Statistics. (2022). National Vital Statistics System, Mortality Data File. 10.07.2024 tarihinde https://www.cdc.gov/nchs/data/databriefs/db492-tables.pdf#4 adresinden alındı.
  • National Institute on Aging [NIH]. (2024). Providing Care and Comfort at the End of Life. 10.07.2024 tarihinde https://www.nia.nih.gov/health/end-life/providing-care-and-comfort-end-life#what adresinden alındı.
  • Özçelik, H. (2017). Palyatif bakım ve ölmekte olan hastaya yaklaşım. Turkiye Klinikleri Anesthesiology Reanimation-Special Topics, 10(1), 87-93.
  • Özdemir, Z., & Çelik, S. Ş. (2011). Terminal dönemde olan hastanın bakımı. Turkiye Klinikleri Journal of Nursing Sciences, 3(2), 81-88.
  • Perry, L. M., Walsh, L. E., Horswell, R., Miele, L., Chu, S., Melancon, B., ... & Hoerger, M. (2021). Racial disparities in end-of-life care between Black and White adults with metastatic cancer. Journal of Pain and Symptom Management, 61(2), 342-349. Doi: https://doi.org/10.1016/j.jpainsymman.2020.09.017
  • Peterson, L. J., Hyer, K., Meng, H., Dobbs, D., Gamaldo, A., & O’Neil, K. (2019). Discussing end-of-life care preferences with family: Role of race and ethnicity. Research on Aging, 41(9), 823-844. Doi: https://doi.org/10.1177/0164027519858716
  • Prieto-Lobato, J. M., De la Rosa-Gimeno, P., Rodríguez-Sumaza, C., Marquina-Márquez, A., & Lucas-García, J. A. (2024). Social work at the end of life: Humanization of the process. Journal of Social Work, 24(2), 240-258. Do: https://doi.org/10.1177/14680173231206713
  • Rome, R. B., Luminais, H. H., Bourgeois, D. A., & Blais, C. M. (2011). The role of palliative care at the end of life. The Ochsner Journal, 11(4), 348-352.
  • Saphire, M. L., Prsic, E. H., Canavan, M. E., Wang, S. Y. J., Presley, C. J., & Davidoff, A. J. (2020). Patterns of symptom management medication receipt at end-of-life among Medicare beneficiaries with lung cancer. Journal of Pain and Symptom Management, 59(4), 767-777. Doi: https://doi.org/10.1016/j.jpainsymman.2019.11.015
  • Schmidt, W. C. (2015). Proxy decision-making: A legal perspective. C. Foster, J. Herring, & I. Doron içinde, The Law and Ethics of Dementia (s. 311-326). Oxford, UK: Hart Publishing.
  • Sharma, R. K., Freedman, V. A., Mor, V., Kasper, J. D., Gozalo, P., & Teno, J. M. (2017). Association of racial differences with end-of-life care quality in the United States. JAMA internal medicine, 177(12), 1858-1860. Doi: https://doi.org/10.1001/jamainternmed.2017.4793
  • Smith, A. (2000). Researching Quality of Life of Older People: Concepts, Measures and Findings. Staffordshire: Keele University.
  • Solon, G., Haider, S. J., & Wooldridge, J. M. (2015). What are we weighting for?. Journal of Human resources, 50(2), 301-316.
  • Sudore, R. L., Lum, H. D., You, J. J., et al. (2017). Defining advance care planning for adults: A consensus definition from a multidisciplinary Delphi Panel. Journal of Pain and Symptom Management, 53(5), 821–832. Doi: https://doi.org/10.1016/j.jpainsymman.2016.12.331
  • Teoli, D., & Bhardwaj, N. (2023). Definition/Introduction. 10.07.2024 tarihinde https://www.ncbi.nlm.nih.gov/books/NBK536962/#:~:text=Definition%2FIntroduction,a%20specific%20point%2 0in%20time adresinden alındı.
  • Tilden, V. P., Tolle, S., Drach, L., & Hickman, S. (2002). Measurement of quality of care and quality of life at the end of life. The Gerontologist, 42(3), 71-80. Doi: https://doi.org/10.1093/geront/42.suppl_3.71
  • Tuncay, T. (2013). Yaşam sonu bakımda sosyal hizmet uzmanının rolleri. Toplum ve Sosyal Hizmet, 24(2), 145- 154.
  • Ware, J. E. (2003). Conceptualization and measurement of health-related quality of life: Comments on an evolving field. Archives of Physical Medicine and Rehabilitation, 84(2), 43-51.
  • Wildiers, H., & Menten, J. (2002). Death rattle: Prevalence, prevention and treatment. Journal of Pain and Symptom Management, 23(4), 310-317. Doi: https://doi.org/10.1016/s0885-3924(01)00421-3
  • Zhu, Y., & Enguidanos, S. (2022). Advance directives completion and hospital out‐of‐pocket expenditures. Journal of Hospital Medicine, 17(6), 437-444. Doi: https://doi.org/10.1002/jhm.12839

Amerika Birleşik Devletleri'nde Hayatın Son Ayında Yaşam Kalitesini Belirleyici Faktörlerin Analizi

Yıl 2025, Cilt: 14 Sayı: 1, 119 - 137
https://doi.org/10.15869/itobiad.1517005

Öz

Günümüzde artan yaşlanma oranları ve uzayan ölüm süreçleri, hayat sonu dönemdeki bireylerin yaşam kalitesi üzerinde önemli etkiler doğurmaktadır ve bu konu son yıllarda artan bir şekilde tartışılmaktadır. Hayat sonunda yaşam kalitesi, semptomların hafifliği ve işlevselliğin korunmasıyla ölçülmektedir. Bu çalışma, Amerika Birleşik Devletleri'nde 65 yaş üstü bireylerin hayatlarının son bir ayındaki yaşam kalitelerini değerlendirmeyi ve bu süreci etkileyen risk faktörlerini belirlemeyi amaçlamaktadır. Çalışmada, 2011-2021 yılları arasını kapsayan National Health and Aging Trends Study (NHATS) verilerinden elde edilen on etaplı örnekleme üzerinde yapılan analizde, 1,722 katılımcı incelenmiştir. Ağırlıklandırılmış prevalans ve ağırlıklandırılmış çok değişkenli regresyon modeli kullanılarak araştırma yürütülmüştür. Bulgularımıza göre, katılımcıların yaşam kalitesi skoru 5 üzerinden 2,10 olarak belirlenmiştir. Katılımcıların %57,35'inin bilinci açıkken, %42,36'sı yataktan desteksiz kalkabilmektedir. Ayrıca, %26,62'si ağrı/acı deneyimlememiş, %40,61'i solunum sorunu yaşamamış ve %43,84'ü üzüntü/kaygı hissetmemiştir. Hayat sonunda düşük yaşam kalitesi ile ilişkilendirilen risk faktörleri arasında ırk/etnisite, yalnız yaşamak, birden fazla kronik hastalığa sahip olmak ve günlük aktivitelerde kısıtlılık bulunmaktadır. Bu bulgular, önemli sosyal politika ve sosyal hizmet önerileri sunmaktadır. Özellikle hayat sonu bakımın sadece süreyi uzatmaktan öte, hastaların ve ailelerinin bu süreci nasıl deneyimlediğine odaklanması gerektiğini vurgulamaktadır. Bu süreçte bütüncül bakış açısı ile kişisel bakım, sosyo-psikolojik destek ve etkili semptom yönetimi konularında destek sağlanmalıdır. Hastaların ve ailelerinin önceliklerinin ve isteklerinin uygulanabilmesi için ileri direktiflerin daha yaygın bir şekilde kullanılması önem arz etmektedir. Ayrıca, semptomların tespiti konusunda kanıta dayalı semptom değerlendirme ölçeklerinin kullanımı yaygınlaştırılmalıdır. Son olarak, düşük yaşam kalitesine yönelik risk faktörleri göz önünde bulundurularak, sosyal olarak dezavantajlı yüksek risk gruplarına yönelik sosyal hizmet uygulamaları ve sosyal politikalar geliştirilerek, hayat sonu bakımında karşılaşılan zorlukların azaltılması ve yaşam kalitesinin artırılmasına önemli katkı sağlanabilir.

Etik Beyan

Bu çalışma Etik Kurul Onayı Gerektirmemektedir.

Kaynakça

  • Birkholz, L., & Haney, T. (2018). Using a dyspnea assessment tool to improve care at the end of life. Journal of Hospice & Palliative Nursing, 20(3), 219-227. Doi: https://doi.org/10.1097/NJH.0000000000000432
  • Büken, N. Ö. (2016). Yaşamın Sonunda Klinik Etik Karar Verme Süreci ve Belirleyici Faktörler. Türkiye Klinikleri Tıp Etiği-Hukuku-Tarihi Özel, 2(3), 24-33.
  • Campbell, M. L., Kiernan, J. M., Strandmark, J., & Yarandi, H. N. (2018). Trajectory of dyspnea and respiratory distress among patients in the last month of life. Journal of Palliative Medicine, 21(2), 194-199. Doi: https://doi.org/10.1089/jpm.2017.0265
  • Chi, N. C., & Demiris, G. (2017). Family caregivers’ pain management in end-of-life care: A systematic review. American Journal of Hospice and Palliative Medicine®, 34(5), 470-485. Doi: https://doi.org/10.1177/1049909116637359
  • Cohen-Mansfield, J., Cohen, R., Skornick-Bouchbinder, M., & Brill, S. (2018). What is the end of life period? Trajectories and characterization based on primary caregiver reports. The Journals of Gerontology: Series A, 73(5), 695-701. Doi: https://doi.org/10.1093/gerona/glx195
  • Conill, C., Verger, E., Henríquez, I., Saiz, N., Espier, M., Lugo, F., & Garrigos, A. (1997). Symptom prevalence in the last week of life. Journal of Pain and Symptom Management, 14(6), 328-331. Doi: https://doi.org/10.1016/s0885-3924(97)00263-7
  • Davidoff, A. J., Canavan, M. E., Prsic, E., Saphire, M., Wang, S. Y., & Presley, C. J. (2021). End-of-life patterns of symptom management and cancer-directed care among Medicare beneficiaries with lung cancer: a claims-based analysis. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 29(7), 3921–3932. Doi: https://doi.org/10.1007/s00520-020-05964-2
  • Drageset, J., Corbett, A., Selbaek, G., & Husebo, B. S. (2014). Cancer-related pain and symptoms among nursing home residents: A systematic review. Journal of Pain and Symptom Management, 48(4), 699-710. Doi: https://doi.org/10.1016/j.jpainsymman.2013.12.238
  • Duncan-Daston, R., Foster, S., & Bowden, H. (2016). A look into spirituality in social work practice within the hospice setting. Journal of Religion & Spirituality in Social Work: Social Thought, 35(3), 157-178. Doi: https://doi.org/10.1080/15426432.2015.1102672
  • Düzgün, G., Yönt, G. H., & Polat, G. (2023). Yaşam Sonu Bakımda Onurun Korunması. Sağlık Akademisi Kastamonu, 8(3), 590-598.
  • Enguidanos, S., & Ailshire, J. (2017). Timing of advance directive completion and relationship to care preferences. Journal of pain and symptom management, 53(1), 49-56. Doi: https://doi.org/10.1016/j.jpainsymman.2016.08.008
  • Freedman, V. A., & Kasper, J. D. (2019). Cohort profile: the national health and aging trends study (NHATS). International journal of epidemiology, 48(4), 1044-1045g.
  • Freedman, V. A., Hu, M., DeMatteis, J., & Kasper, J. D. (2020). Accounting for sample design in NHATS and NSOC analyses: Frequently asked questions. NHATS Technical Paper, 23, 2021.
  • Gawande, A. (2010). Letting go. The New Yorker, 2, 36-49.
  • Gawande, A. (2014). Being mortal: illness, medicine and what matters in the end. London: Profile Books.
  • Hendriks, S. A., Smalbrugge, M., Hertogh, C. M., & van der Steen, J. T. (2014). Dying with dementia: Symptoms, treatment, and quality of life in the last week of life. Journal of Pain and Symptom Management, 47(4), 710- 720. Doi: https://doi.org/10.1016/j.jpainsymman.2013.05.015
  • Kasper, J. D., & Freedman, V. A. (2014). Findings from the 1st round of the National Health and Aging Trends Study (NHATS): Introduction to a special issue. Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 69(1), 1-7.
  • Kehl, K. A., & Kowalkowski, J. A. (2013). A systematic review of the prevalence of signs of impending death and symptoms in the last 2 weeks of life. American Journal of Hospice and Palliative Medicine®, 30(6), 601-616. Doi: https://doi.org/10.1177/1049909112468222
  • Kozlov, E., Phongtankuel, V., Prigerson, H., Adelman, R., Shalev, A., Czaja, S., ... & Reid, M. C. (2019). Prevalence, severity, and correlates of symptoms of anxiety and depression at the very end of life. Journal of Pain and Symptom Management, 58(1), 80-85. Doi: https://doi.org/10.1016/j.jpainsymman.2019.04.012
  • Lee, H. J., Small, B. J., & Haley, W. E. (2020). Health and well-being in the year before death: The association with quality of life and care at the end-of-life. Journal of Aging and Health, 32(10), 1475-1485. Doi: https://doi.org/10.1177/0898264320935297
  • Lobchuk, M. M., & Degner, L. F. (2002). Symptom experiences: Perceptual accuracy between advanced-stage cancer patients and family caregivers in the home care setting. Journal of Clinical Oncology, 20(16), 3495- 3507.
  • Meier, E. A., Gallegos, J. V., Thomas, L. P. M., Depp, C. A., Irwin, S. A., & Jeste, D. V. (2016). Defining a good death (successful dying): Literature review and a call for research and public dialogue. The American Journal of Geriatric Psychiatry, 24(4), 261-271. Doi: https://doi.org/10.1016/j.jagp.2016.01.135
  • National Center for Health Statistics. (2022). National Vital Statistics System, Mortality Data File. 10.07.2024 tarihinde https://www.cdc.gov/nchs/data/databriefs/db492-tables.pdf#4 adresinden alındı.
  • National Institute on Aging [NIH]. (2024). Providing Care and Comfort at the End of Life. 10.07.2024 tarihinde https://www.nia.nih.gov/health/end-life/providing-care-and-comfort-end-life#what adresinden alındı.
  • Özçelik, H. (2017). Palyatif bakım ve ölmekte olan hastaya yaklaşım. Turkiye Klinikleri Anesthesiology Reanimation-Special Topics, 10(1), 87-93.
  • Özdemir, Z., & Çelik, S. Ş. (2011). Terminal dönemde olan hastanın bakımı. Turkiye Klinikleri Journal of Nursing Sciences, 3(2), 81-88.
  • Perry, L. M., Walsh, L. E., Horswell, R., Miele, L., Chu, S., Melancon, B., ... & Hoerger, M. (2021). Racial disparities in end-of-life care between Black and White adults with metastatic cancer. Journal of Pain and Symptom Management, 61(2), 342-349. Doi: https://doi.org/10.1016/j.jpainsymman.2020.09.017
  • Peterson, L. J., Hyer, K., Meng, H., Dobbs, D., Gamaldo, A., & O’Neil, K. (2019). Discussing end-of-life care preferences with family: Role of race and ethnicity. Research on Aging, 41(9), 823-844. Doi: https://doi.org/10.1177/0164027519858716
  • Prieto-Lobato, J. M., De la Rosa-Gimeno, P., Rodríguez-Sumaza, C., Marquina-Márquez, A., & Lucas-García, J. A. (2024). Social work at the end of life: Humanization of the process. Journal of Social Work, 24(2), 240-258. Do: https://doi.org/10.1177/14680173231206713
  • Rome, R. B., Luminais, H. H., Bourgeois, D. A., & Blais, C. M. (2011). The role of palliative care at the end of life. The Ochsner Journal, 11(4), 348-352.
  • Saphire, M. L., Prsic, E. H., Canavan, M. E., Wang, S. Y. J., Presley, C. J., & Davidoff, A. J. (2020). Patterns of symptom management medication receipt at end-of-life among Medicare beneficiaries with lung cancer. Journal of Pain and Symptom Management, 59(4), 767-777. Doi: https://doi.org/10.1016/j.jpainsymman.2019.11.015
  • Schmidt, W. C. (2015). Proxy decision-making: A legal perspective. C. Foster, J. Herring, & I. Doron içinde, The Law and Ethics of Dementia (s. 311-326). Oxford, UK: Hart Publishing.
  • Sharma, R. K., Freedman, V. A., Mor, V., Kasper, J. D., Gozalo, P., & Teno, J. M. (2017). Association of racial differences with end-of-life care quality in the United States. JAMA internal medicine, 177(12), 1858-1860. Doi: https://doi.org/10.1001/jamainternmed.2017.4793
  • Smith, A. (2000). Researching Quality of Life of Older People: Concepts, Measures and Findings. Staffordshire: Keele University.
  • Solon, G., Haider, S. J., & Wooldridge, J. M. (2015). What are we weighting for?. Journal of Human resources, 50(2), 301-316.
  • Sudore, R. L., Lum, H. D., You, J. J., et al. (2017). Defining advance care planning for adults: A consensus definition from a multidisciplinary Delphi Panel. Journal of Pain and Symptom Management, 53(5), 821–832. Doi: https://doi.org/10.1016/j.jpainsymman.2016.12.331
  • Teoli, D., & Bhardwaj, N. (2023). Definition/Introduction. 10.07.2024 tarihinde https://www.ncbi.nlm.nih.gov/books/NBK536962/#:~:text=Definition%2FIntroduction,a%20specific%20point%2 0in%20time adresinden alındı.
  • Tilden, V. P., Tolle, S., Drach, L., & Hickman, S. (2002). Measurement of quality of care and quality of life at the end of life. The Gerontologist, 42(3), 71-80. Doi: https://doi.org/10.1093/geront/42.suppl_3.71
  • Tuncay, T. (2013). Yaşam sonu bakımda sosyal hizmet uzmanının rolleri. Toplum ve Sosyal Hizmet, 24(2), 145- 154.
  • Ware, J. E. (2003). Conceptualization and measurement of health-related quality of life: Comments on an evolving field. Archives of Physical Medicine and Rehabilitation, 84(2), 43-51.
  • Wildiers, H., & Menten, J. (2002). Death rattle: Prevalence, prevention and treatment. Journal of Pain and Symptom Management, 23(4), 310-317. Doi: https://doi.org/10.1016/s0885-3924(01)00421-3
  • Zhu, Y., & Enguidanos, S. (2022). Advance directives completion and hospital out‐of‐pocket expenditures. Journal of Hospital Medicine, 17(6), 437-444. Doi: https://doi.org/10.1002/jhm.12839
Toplam 42 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Yaşam Seyrinin Sosyolojisi
Bölüm Makaleler
Yazarlar

Hazal Swearinger 0000-0001-8573-641X

Erken Görünüm Tarihi 23 Mart 2025
Yayımlanma Tarihi
Gönderilme Tarihi 16 Temmuz 2024
Kabul Tarihi 21 Ocak 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 14 Sayı: 1

Kaynak Göster

APA Swearinger, H. (2025). Amerika Birleşik Devletleri’nde Hayatın Son Ayında Yaşam Kalitesini Belirleyici Faktörlerin Analizi. İnsan Ve Toplum Bilimleri Araştırmaları Dergisi, 14(1), 119-137. https://doi.org/10.15869/itobiad.1517005
İnsan ve Toplum Bilimleri Araştırmaları Dergisi  Creative Commons Atıf-GayriTicari 4.0 Uluslararası Lisansı (CC BY NC) ile lisanslanmıştır.