American Journal of Hospice & Palliative Medicine
Scope & Guideline
Exploring insights that enhance quality of life for patients with serious illnesses.
Introduction
Aims and Scopes
- Palliative Care Model Development:
Focuses on creating and evaluating innovative models of care delivery, particularly in the context of serious illness, to improve patient outcomes and experiences. - Interdisciplinary Care Approaches:
Emphasizes the importance of interdisciplinary collaboration among healthcare providers to enhance the quality of palliative care and address complex patient needs. - Patient and Family Perspectives:
Incorporates research that prioritizes the voices and experiences of patients and their families, ensuring that care aligns with their values, preferences, and goals. - Cultural Competence in Palliative Care:
Explores the impact of cultural, ethnic, and socioeconomic factors on palliative care delivery and seeks to improve accessibility and quality of care for diverse populations. - Education and Training in Palliative Care:
Focuses on the development and evaluation of educational programs for healthcare professionals to enhance their competencies in providing palliative and end-of-life care. - Policy and Ethical Considerations:
Investigates the implications of healthcare policies and ethical dilemmas in palliative care, aiming to inform best practices and advocate for patient rights.
Trending and Emerging
- Telehealth and Virtual Care Integration:
The rise of telehealth during the COVID-19 pandemic has led to an increased focus on how virtual care can enhance access to palliative services, particularly for underserved populations. - Advance Care Planning and Decision-Making:
There is a growing emphasis on advance care planning, with research highlighting its importance in improving communication and aligning treatment decisions with patient preferences. - Mental Health and Palliative Care:
An increasing number of studies are addressing the intersection of mental health and palliative care, recognizing the psychological dimensions of serious illness and the need for integrated support. - Social Determinants of Health:
Research is increasingly examining how social determinants, such as socioeconomic status and access to care, impact outcomes in hospice and palliative care settings. - Innovative Care Models for Diverse Populations:
Emerging studies focus on tailored palliative care models for specific demographics, including racial and ethnic minorities, to reduce disparities and enhance culturally competent care.
Declining or Waning
- Traditional Pain Management Techniques:
There has been a noticeable decrease in research centered on conventional pain management strategies, such as opioids, as the field shifts towards exploring integrative approaches and non-pharmacological interventions. - General Palliative Care Awareness:
The emphasis on broad awareness campaigns for palliative care has waned, with more research focusing on specific populations or conditions rather than generalized awareness efforts. - End-of-Life Care in Non-Cancer Populations:
Research specifically targeting end-of-life care in non-cancer populations, such as those with chronic diseases, has become less prevalent, as the focus has shifted toward cancer-related palliative care.
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