Palliative Care in the 21st Century: Multidisciplinary Collaboration, Digital Health, and Equitable Access
Downloads
Background: Palliative care is a fundamental component of modern healthcare, aiming to improve the quality of life for patients with serious, life-limiting illnesses and their families. Despite global recognition of its importance, access remains limited, particularly in low- and middle-income countries, highlighting systemic, structural, and workforce-related disparities.
Objective: This review provides a comprehensive analysis of contemporary palliative care, emphasizing multidisciplinary collaboration, workforce development, digital innovation, ethical considerations, and strategies for equitable global access.
Methods: A narrative synthesis of recent literature was conducted, focusing on international guidelines, empirical studies, and evidence-based interventions. Key themes included holistic patient-centered approaches, interdisciplinary teamwork, public education, digital health applications, caregiver involvement, and economic and ethical frameworks supporting palliative care delivery.
Results: Effective palliative care requires early integration alongside disease-directed treatments, robust multidisciplinary teams—including physicians, nurses, social workers, psychologists, and spiritual care providers—and structured workforce education. Digital innovations, such as telepalliative care, electronic patient-reported outcomes, and mHealth applications, expand access, enhance continuity of care, and empower patients and caregivers. Engagement of family caregivers improves symptom management and overall patient outcomes. Ethical frameworks and culturally sensitive practices are essential for aligning care with patient values, reducing professional moral distress, and addressing global disparities. Economic analyses demonstrate that timely, home- and community-based interventions reduce unnecessary hospitalizations and optimize healthcare resources.
Conclusion: Modern palliative care is defined by the integration of clinical excellence, interdisciplinary collaboration, digital innovation, and ethical, culturally sensitive frameworks. Achieving equitable access worldwide requires coordinated policy efforts, workforce capacity-building, and the adaptation of services to diverse contexts. Early, patient- and family-centered palliative interventions improve clinical outcomes, enhance quality of life, and ensure that individuals facing life-limiting illnesses receive compassionate, comprehensive, and culturally competent care globally.
Downloads
Barnestein-Fonseca P, González-Martínez P, Navarro-Illana P, et al. Societal engagement and culturally sensitive palliative care interventions. Palliat Med. 2024;38(3):456–470.
Bush, S., Perez, N., Baum, C., & Nair, V. (2023). Telehealth and remote monitoring in palliative care: Opportunities for quality assessment. Current Opinion in Supportive and Palliative Care, 17(2), 103–112. https://doi.org/10.1097/SPC.0000000000000681
Cherny, N., Radbruch, L., & Board, I. (2023). Palliative care: Current challenges and future directions. Lancet Oncology, 24(6), 600–614.
Choo SL, Low JH, Chan SWC. Interdisciplinary collaboration in palliative care: a scoping review. BMJ Support Palliat Care. 2023;13:345–356.
Connor, S., & Bermedo, M. C. S. (Eds.). (2020). Global atlas of palliative care (2nd ed.). World Health Organization. https://www.who.int/publications/i/item/9789240034461
Dalgaard KM, Jensen AB, Guldin MB. Knowledge gaps in palliative care among health professionals: a systematic review. Palliat Med. 2014;28(4):287–303.
Dionne-Odom JN, Ornstein KA, Kent EE. Patient and family engagement in palliative care: a critical review. J Pain Symptom Manage. 2019;58(5):895–907
Downar, J., MacDonald, S., & Buchman, S. (2023). Medical assistance in dying, palliative care, safety, and structural vulnerability. Journal of Palliative Medicine, 26(9), 1175–1179. https://doi.org/10.1089/jpm.2023.0210
Hayek S, Hui D, Bruera E. Education and referral criteria in palliative care: improving integration across specialties. Support Care Cancer. 2025;33:1125–1137.
Hui D, Bruera E. Models of outpatient and home-based palliative care. Curr Opin Support Palliat Care. 2016;10(4):349–356.
Kaasa S, Loge JH, Aapro M, et al. Integration of palliative care into oncology: ESMO Clinical Practice Guidelines. Ann Oncol. 2018;29(Suppl 4):iv120–iv142.
Knaul, F., Farmer, P., Krakauer, E., De Lima, L., Bhadelia, A., Jiang, Kwete, X., … Foley, K. (2018). Lancet Commission on Palliative Care and Pain Relief. The Lancet.
Li Q, Chhabra K, Singh A. Digital innovations in palliative care: enhancing access and quality of care. J Palliat Med. 2021;24(5):700–712.
May, P., Normand, C., Cassel, J., & Morrison, R. S. (2020). Economic impact of timely palliative care interventions in oncology. Journal of Clinical Oncology, 38(10), 1045–1054.
McIlfatrick S, Hasson F, McKenna H, O’Connor M. Public knowledge and attitudes toward palliative care in Europe: a systematic review. BMC Palliat Care. 2021;20:59.
Nair, D., Paul, A. S., & Raveendran, K. U. (2023). Palliative care development in India: New WHO conceptual model. BMJ Supportive & Palliative Care, 13(3), 298–304. https://doi.org/10.1136/spcare 2022 004062
Rajagopal, M., & Kumar, S. (2022). Palliative care in low- and middle-income countries: Challenges and strategies. Journal of Pain and Symptom Management, 63(5), 1001–1012.
Rid, A., Wendler, D., & Mattson, J. (2023). Ethical frameworks in palliative care. The Lancet Oncology, 24(5), e200–e210. https://doi.org/10.1016/S1470-2045(23)00123-4
Sanders T, Verhoef M, Flaherty M, et al. Continuity of care in palliative services: coordination between outpatient and inpatient care. J Palliat Med. 2024;27(1):12–23.
Sleeman, K., de Brito, M., Etkind, S., Nkhoma, K., Guo, P., Murtagh, F., … Higginson, I. (2019). The burden of serious health-related suffering among adults in low- and middle-income countries: Global estimates. Lancet Global Health, 7(3), e321–e331.
Sleeman, K. E., Timms, A., Gillam, J., Anderson, J. E., Harding, R., Sampson, E. L., & Evans, C. J. (2021). Priorities and opportunities for palliative and end of life care in United Kingdom health policies: A national documentary analysis. BMC Palliative Care, 20, Article 108. https://doi.org/10.1186/s12904 021 00802 6.
Smith, S., Johnson, L., Brown, K., & Thompson, R. (2022). Evaluating the effectiveness of home- and community-based palliative care: Outcomes and cost-efficiency. Palliative Medicine, 36(4), 567–579.
Sudore, R. L., Landefeld, C. S., & Knight, S. J. (2017). Engaging patients in advance care planning: Challenges and opportunities. JAMA Internal Medicine, 177(5), 676–682. https://doi.org/10.1001/jamainternmed.2017.0106
Weiss, M., Sabo Wagner, S., Frydman, J., & Pramesh, C. S. (2025). Addressing barriers in palliative care for rural and underserved communities. American Society of Clinical Oncology Educational Book, 45(3), e472842. https://doi.org/10.1200/EDBK-25-472842
World Health Assembly. (2014). Strengthening of palliative care as a component of comprehensive care throughout the life course (WHA Resolution 67.19). https://apps.who.int/gb/ebwha/pdf_files/WHA67/A67_R19-en.pdf
Worldwide Hospice Palliative Care Alliance & World Health Organization. (2020). Global atlas of palliative care (2nd ed.). https://www.thewhpca.org/resources/global-atlas-on-end-of-life-care
Zhi Y, Smith AK. Misconceptions about palliative care among healthcare professionals: impact on early integration. J Pain Symptom Manage. 2015;50(6):785–790.
Copyright (c) 2025 Georgian Scientists

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

