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Palliative care is an active, holistic approach aimed at relieving severe or chronic suffering and enhancing the quality of life for individuals with life-threatening illnesses at any stage of the illness trajectory, from diagnosis onward, whether curative treatments continue or not [1-3].
JMIR Cancer 2025;11:e71596
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Multidisciplinary Oncology Education Among Postgraduate Trainees: Systematic Review
These studies included surgical or surgical oncology fields [16-23], hematology or medical or hematology oncology [16,20-22,24,25], geriatrics or geriatric oncology [20,22,26], radiation oncology [16,20,21,23,27], palliative medicine [16,20], radiology [21], pathology [21], genetics [23], dermatology [23], pediatric specialties [28], and other medical fields (eg, internal medicine, nephrology, neurology) [22,23].
JMIR Med Educ 2025;11:e63655
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Palliative care includes the holistic, person-, and family-centered care provided for patients with a life-limiting diagnosis where the primary goal is to optimize quality of life. At the end of life, patients may experience hardship from an array of distressing symptoms including pain, nausea, agitation, and distress, with up to 88% of patients admitted to a palliative care unit enduring terminal delirium [1].
JMIR Res Protoc 2024;13:e55129
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Palliative care interventions in the ED capture high-risk patients at a time of crisis and can change the course of the disease, improving patient-centered outcomes [1]. These patients require skillful communication so that clinicians can tailor care to the patient’s values, goals, and preferences [2,3].
JMIR Med Educ 2023;9:e43710
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One major cause of lower uptake involves unreliability in provider identification of patients who are appropriate for palliative care. Research shows a clinician’s intuition alone is not the most effective method for recognizing individuals in general practice who could benefit from palliative services [10-12].
JMIR AI 2023;2:e42253
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Patient Perspectives on Value Dimensions of Lung Cancer Care: Cross-sectional Web-Based Survey
With regards to treatment, 27% (40/150) stated that they were in remission, 32% (49/150) were under curative care, 11% (16/150) were under palliative care, and 30% (45/150) did not respond to this question.
Caregivers were mostly women (33/35, 94%) and either a relative of a patient (32/35, 91%), such as their child (16/35, 45%), or their partner (14/35, 40%). They were mostly younger than 56 years (29/35, 83%). Overall, they represented between 9% (2/22; Germany) and 41% (15/37; France) of respondents.
JMIR Form Res 2023;7:e37190
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Although actions concerning legacy may be taken at any timepoint along an illness experience, legacy work, when undertaken, is often incorporated into end-of-life care or palliative care, and such interventions have been shown to promote emotional and spiritual care of advanced cancer patients [1,5-8].
Based on a preliminary literature review and previous research [9], we are exploring the conceptual foundations of legacy. We conceptualize 3 types of legacy: primary, secondary, and tertiary.
JMIR Res Protoc 2022;11(12):e40791
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In this paper, we describe the protocol of the Receipt of Curative Resection or Palliative Care for Hepatopancreaticobiliary Tumours (RICOCHET) study. This prospective study aims to define variations in diagnostic and management pathways for patients with suspected HPB malignancies, determine factors associated with these variations, and test the hypothesis that these variations have an impact on patient outcomes.
JMIR Res Protoc 2019;8(7):e13566
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