Literature Review

How to responsibly use AI in palliative care and hematologic malignancies CancerNetwork; podcast by Ram Prakash Thirugnanasambandam, MBBS; 2/2/26 In a conversation with CancerNetwork®, Ram Prakash Thirugnanasambandam, MBBS, discussed the evolving roles that artificial intelligence (AI)–based tools may play in palliative care and the management of different hematologic malignancies. ... According to Thirugnanasambandam, implementing AI into one’s workflow may help accurately predict disease subtypes and burdens among patients with leukemia, lymphoma, or multiple myeloma. ... Thirugnanasambandam also discussed some of the ethical considerations surrounding the growth of AI-based tools, highlighting information privacy concerns and potentially biased datasets as notable issues with these platforms. Although AI may assist with decision-making, Thirugnanasambandam stated that it ultimately cannot replace a human’s nuanced clinical judgment and empathy.

Awards and Recognitions: January 2026

Cultivating leaders in medicine: We can do better Medscape; by Aba Black, MD, MHS; 1/29/26 ... there’s no question that medicine as a field has lagged when it comes to propagating tenets of effective leadership. ... [Too] many doctors make it through the endurance run that is medical education without ever being told what makes a good leader. There’s good reason to want more doctors in leadership roles, as healthcare administrators with clinical expertise bring an important skill set to the challenges facing our healthcare system. While hospitals led by economists may fare better financially, physician-led hospitals are associated with lower mortality rates and higher patient satisfaction. 

Evaluating palliative care needs in patients with advanced non-malignant chronic conditions: An umbrella review of needs assessment tools Healthcare; by Chrysovalantis Karagkounis, Stephen Connor, Danai Papadatou, Thalia Bellali; 12/24/25 Patients with advanced non-malignant chronic conditions experience illness burdens and palliative care needs comparable to those of oncology patients, yet palliative care is often introduced late. Identifying individuals with potential palliative care needs is complex, and although multiple tools exist, the most appropriate approach for assessing needs in this population remains unclear. This umbrella review aimed to identify and evaluate tools used to systematically assess palliative care in adults with advanced non-malignant chronic conditions, with a specific focus on their content, structure, and psychometric properties.

Integrating psychiatric and hospice services: Legal and clinical considerations for involuntary commitment in multimorbid end-of-life care American Journal of Hospice and Palliative Medicine; by Ilana Marmershteyn, BS, Darian Peters, BS, Victor Milev, BS, Mario Jacomino, MD, MPH, and George Luck, MD, FAAHPM; 1/28/26  Multimorbid patients at the end-of-life face complex medical, psychosocial, and psychiatric challenges. Hospice care aims to address physical, emotional, and spiritual needs; however, psychiatric comorbidities, particularly acute crises, remain under-recognized and inconsistently managed. The intersection of psychiatric intervention, hospice care, and legal frameworks such as involuntary commitment presents significant clinical and ethical challenges.

Meant to Be: Denise's journey into hospice nursing The McKenzie, Tennessee Banner; 1/27/26 When Denise lost her husband, Tony, to leukemia at only 39, her world shifted forever. She was 29. ... In her thirties, ... she enrolled in nursing school, determined to rebuild her own story, one chapter at a time. ...Then came a nursing hospice opportunity. ... For Denise, hospice nursing isn't about endings; it's about helping families find peace, honesty, dignity, and hope in the final chapter. She carries the responsibility with deep reverence. "We're the last chapter," she says softly. "And if that chapter ends poorly, a lot of it is on us." ... Denise's journey reminds us that sometimes the hardest heartbreaks lead us to the most meaningful callings. Editor's Note: [Full access to this may require a subscription.] What personal life experiences brought many of your clinicians to end-of-life care? You may be surpised how little you know about them; what brings meaning and purpose for them; how seeing their journeys inspires you in your leadership role.

How do I tell my patient they’re dying? Medscape; by Lisa Mulcahy; 1/27/26 Ruth Parry, PhD, still remembers a conversation she mishandled as a junior National Health Service stroke rehabilitation physiotherapist many years ago. ... Since then, Parry has analyzed nearly 100 video consultations between practitioners and patients with poor prognoses in stroke and head injury and with terminal diagnoses. Her research explores a critical clinical dilemma: How do doctors navigate the delicate balance of providing fair, accurate information about dire prognoses while respecting a patient’s feelings and personal choices?

Stroke survivors in DFW find new hope with Sovereign Hospice Home Care Holliston Town News, Aubrey, TX; by Sovereign Hospice; 1/26/26 Stroke survivors and their families often encounter unexpected challenges ... Sovereign Hospice in Aubrey, Texas, addresses these complex needs through targeted palliative care programs designed specifically for post-stroke complications. ... Post-stroke pain affects approximately 30% of survivors, manifesting as headaches, muscle spasticity, or neuropathic sensations. Fatigue represents another common issue, with many patients reporting exhaustion after minimal activity. Depression occurs in roughly one-third of stroke survivors, creating additional barriers to recovery. 

Improving timeliness of palliative care referrals within the ICU: A quality improvement project Dimensions of Critical Care Nursing (DCCN); by Stephanie Fiore, Simone O'Donovan, Kerry A Milner; 1/23/26 ... Using the Model for Improvement, this quality improvement project was conducted over 7 months, including a 4-month baseline phase and a 3-month implementation phase. ICU nurses used a PC screening tool to evaluate patients within 48 hours of admission. The project aimed to increase PC screenings to 75% and ensure PC referrals within 48 hours. ...  The implementation phase saw a significant increase in PC screenings, with compliance reaching 90.9% after process adjustments. 

Patients' perceptions of autonomy in palliative care: Two patient interview exemplars Palliative Care and Social Practice; by Kristen Tulloch, Julia Acordi Steffen, John P Rosenberg; 1/19/26 Results: Four themes were identified: (a) my involvement in healthcare decisions, (b) change to my autonomy during illness progression, (c) self-assessing my abilities to exercise autonomy and (d) my coping mechanisms for loss of autonomy. Palliative care patients perceived and managed their autonomy amidst their illnesses, revealing a sense of loss of autonomy extending beyond healthcare into many daily activities. Participants wished to exercise autonomy in nuanced ways, varying in intensity across many aspects of their lives, underscoring the importance of recognising and respecting individuals' wishes for autonomy.Editor's Note: The authors’ focus on coping with loss of autonomy is essential. As illness progresses, autonomy can erode not only in medical decisions but across daily life, identity, and meaning—losses that are too often overlooked in clinical care. The frequently misapplied “Five Stages of Grief” can further blur this reality, reducing complex, personal experiences to linear expectations not supported by contemporary grief research. Understanding how patients adapt to loss of autonomy is foundational to truly person-centered palliative care.

Why asking about “critical abilities” is misguided: Lessons learned from the updated Serious Illness Conversation Guide Journal of General Internal Medicine; by Joel Michael Reynolds, PhD and Michael Pottash, MD, MPH; 1/20/26 The Ariadne Labs’ Serious Illness Care Program is a care delivery model that aims to improve conversations between patients and their clinicians about serious illness. This is accomplished through its foundational tool: the serious illness conversation guide. ... As of 2022, the Serious Illness Care Program has a footprint in over 44 countries and in all 50 states. The conversation guide had been translated into over 13 languages and nearly 18,000 clinicians had been trained on its use. In 2023, the Serious Illness Care Program released an updated conversation guide. ... Gone was the future-oriented question about critical abilities: “What abilities are so critical to your life that you can’t imagine living without them?” A more present-focused question about activities replaced it: “What activities bring joy and meaning to your life?” ... The revision of the Serious Illness Conversation Guide signals more than a semantic change. Its revision of the critical abilities question instead reflects a deeper reckoning with the ethical limitations of traditional advance care planning and with the import of disability bioethics.