Literature Review

WiHPCA: Applauds State Assembly for approving bill establishing a state Palliative Care Council WisPolitics; 2/22/24[Wednesday,] the [Wisconsin] State Assembly approved Assembly Bill 736, a bill that would establish a state Palliative Care Council. The Wisconsin Hospice and Palliative Care Association (WiHPCA) strongly supports this legislation, which would ultimately help increase awareness and utilization of palliative care throughout the state. The Assembly Committee on Health, Aging, and Long-Term Care voted 16-0 on January 17 to recommend approval of this legislation. This bill would establish a council of individuals with palliative care and other medical expertise to consult and advise the Wisconsin Department of Health Services (DHS) on this type of specialized medical care. 

Understanding the discordance about prognosis between clinicians and terminally ill patients and their surrogates: A conversation with Douglas B. White, MD, MASThe ASCO Post, by Jo Cavallo; 2/25/24Research shows that about half of adults near the end of life in the United States are too ill to participate in decisions about whether to accept life-prolonging treatment, requiring family members and other proxies to serve as surrogate decision-makers for their critically ill loved ones. However, research also shows that surrogates of patients with advanced illness often have optimistic expectations about prognosis, which often lead to the increased use of invasive treatment (including life support) in dying patients and delays in the integration of palliative care.

Rural-urban disparities and trends in utilization of palliative care services among US patients with metastatic breast cancerJ Rural Health; by Jincong Q Freeman, Adam W Scott, and Ted O Akhiwu; 2/20/24Purpose: To assess trends and rural-urban disparities in palliative care utilization among patients with metastatic breast cancer.Conclusions: In this national, racially diverse sample of patients with metastatic breast cancer, the utilization of palliative care services increased over time, though remained suboptimal. Further, our findings highlight rural-urban disparities in palliative care use and suggest the potential need to promote these services while addressing geographic access inequities for this patient population.

Chapters CEO Andrew Molosky: Building an ecosystem of care around the seriously illHospice News, by Jim Parker; 2/13/24Going forward, hospice and other post-acute providers are preparing to operate within a value-based ecosystem, and Florida-based nonprofit Chapters Health System is no exception. ... The organization has been hard at work in recent years to position itself for risk-based relationships and build out a continuum of care for chronically and terminally ill patients, while maintaining positive employee engagement.

Tier - Palliative Care: A population-based care delivery model to match evolving patient needs to palliative care services for community-based patients with heart failure or cancer [This link goes to the more detailed National Institutes of Health (NIH) description of this clinical trial.]Genomics & Genetics Daily, by a news reporter-staff news editor; 2/14/24Staff editors report on the newly launched clinical trial, NCT06228209, which has the following summary description: "TIER-PC is an adaptive model of delivering palliative care that provides the right level of care to the right patients at the right time. It represents an adaption of the Mount Sinai PALLIATIVE CARE AT HOME (PC@H) program, which delivers home-based palliative care. TIER-PC increases the number and intensity of disciplines added to the patient's care team as their symptoms worsen and function declines."

How to support adolescents and young adults with cancer at the end of lifeThe Oncology Nursing Society Voice, by Kimberly Rivera DNP, RN-BC, OCN®, NPD-BC; 2/12/24... [Cancer] is the fourth leading cause of death in adolescents and young adults (AYAs), following accidents, suicide, and homicide. ... Appropriately defining the difference between palliative and end-of-life care can improve AYAs’ engagement with services such as advance care planning—a specific step that increases AYAs’ likelihood of receiving early palliative care. However, many palliative and hospice care services are geared toward pediatric or adult populations and may not meet AYAs’ unique needs, impeding effective care planning.

Palliative care reimbursement, innovation and reformJD Supra - American Health Law Association, by Edo Banach; 2/7/24Sections include:

Joint inpatient palliative care approaches may reduce length of stay in intensive care unitsPhysician's Weekly; 2/7/24Patients in the intensive care unit (ICU) would benefit from having an Inpatient Palliative Care (IPC) team to help them through this difficult chapter in their lives. An IPC team usually help patients manage their symptoms and pain along with providing support to them and their families and assisting with communication to ensure realistic expectations.

Key palliative care trends to watch in 2024Hospice News, by Jim Parker; 1/29/24

The case for palliative care in the ICU Hospice News, by Rachel Edwards; 1/31/24An intensive care unit (ICU) stay often challenges everyone involved. Integrating palliative care could alleviate some of the suffering through symptom management, improved communication about goals and treatment, and better training and resources for staff. As ICU admissions in the final year of life become increasingly common, the need for better holistic critical care is growing.

Series of 19 online videos address paliative care issuesPress-Republican, by Robin Caudell; 1/26/24Project Compassion began with conversations over coffee after Mass between a doctor and a retired priest. Seventy-one percent of U.S. adults have never heard of palliative care. More than 12 million adults are living with a serious illness now and that number is growing exponentially, according to a press release. To help address this need, Project Compassion was developed by Father Charles Vavonese and Dr. Paul Fiacco thanks to a $500,000 grant from the Mother Cabrini Health Foundation.

Substance use disorder in aging and serious illnessGeriPal podcast with Eric Widera, Alex Smith, Katie Fitzgerald Jones, Jessica Merlin, Devon Check; 1/18/24The CDC’s Guideline for Prescribing Opioids for Chronic Pain excludes those undergoing cancer treatment, palliative care, and end-of-life care. In doing so, it seems to give the impression that pain seen in cancer is inherently different than pain seen in other conditions and that those with cancer may not have the same risk for opioid use disorder as compared to other conditions.

Role matters in understanding 'quality' in palliative care: a qualitative analysis of patient, caregiver and practitioner perspectivesBMJ Open, by Laura M Holdsworth, Karleen Giannitrapani, Raziel C Gamboa, Claire O'Hanlon, Nainwant Singh, Anne Walling, Charlotta Lindvall, Karl Lorenz; 1/17/24Objectives: To compare the discussions from two panels on the concept of palliative care quality for patients with advanced cancer, exploring the priorities reflected in each group's perspectives.