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Low palliative care utilization is associated with higher risk of mental health challenges among patients with pancreatic cancer, recent research found. Researchers dug into patients’ data to examine palliative care utilization and delivery of mental health services and pharmacotherapies between January 1, 2010, and December 31, 2018. Roughly 22.8%
How can we make sure that people living with serious illnesses are given the information they need about their disease that prevents surprises in their disease trajectories that increase psychological and physical suffering? Julia Frydman, senior medical director at Nashville-based Thyme Care, runs its palliative care wing.
The Pennant Group has been quietly building palliative care programs driven by its local leaders with support from the corporate offices Service Center. Pennant is the holding company for a group of independent hospice, home health and senior living providers located across 13 states.
Care coordination between providers: Thyme Care coordinates with a members oncologist, primary care physician and other specialists to ensure everyone has the right information at the right time to make informed care decisions. A new partnership between Humana Inc. The company offers palliative care in addition to other services.
Patients have greater access to information about their condition, for example. A key component of palliative care is understanding that chronic conditions may not be cured, but rather need to be managed, sometimes for many years. Pharmacological drugs have their limitations and they have side effects.
We hope to inform policy through recommendations and demonstrations on how innovation can make a real difference to reduce cost and improve patient outcomes. Global Partners in Care (GPIC) and Elea Institute have formed a partnership designed to extend access to palliative care services worldwide.
Michigan-based Corewell Health Childrens program has expanded and diversified the scope of its pediatric services during the last decade of operations. Delivering goal concordant care has been the largest strategic lever to its growth. Corewell Health Childrens program began in January 2015 and now features more than 70 health care specialty areas.
Some patients wish to seek out alternative medicine therapies while receiving palliative care, and providers can benefit from understanding the nature and possible outcomes of these interventions, recent research has found. Alternative medicine includes any of a range of medical therapies that are not regarded as orthodox by the medical profession.
Demographic trends were among the key factors that drove the program forward, said Monica Escalante, chief strategy and information officer at Hospice of the Chesapeake. The new program provides patients and their caregivers with direct support from Hospice of the Chesapeake’s interdisciplinary care team. “One
Improved patient and staff satisfaction are among the most significant returns on investment for hospices that are pouring greater resources into trauma-informed training. Trauma-informed education should be a normalized part of hospice’s interdisciplinary training to help staff recognize and respond to a range of experiences, Ash indicated.
The most important thing that can be done at the bedside is to make sure the patient and family are not extremely distressed when providing information,” Hotchkiss said. The nonprofit has narrowed the focus of its retention initiatives toward reducing staff turnover.
We dont always have information about someone before they enter hospice. Some payment value-based demonstration projects have already given us that information. What are the other services or programs that Hospice of the Valley offers? At least half of our census receives services that are not hospice.
The collaborative provides a shared pool of services such as accounting, payroll, revenue cycle and treasury management, information technology (IT), human resources, compliance, education, and marketing and communications. The partners will provide durable medical equipment and supplies to patients in Colorados Front Range region.
How will your past experiences help inform your future policy and advocacy efforts in the home-based landscape? It was also activating the team from a grassroots perspective when it was time to take action, making sure that leaders were paying attention and providing the right information.
As Contessa Health pioneers a growing value-based palliative care-at-home program, they’ve encountered some learning curves when it comes to operating within a new payment system. Contessa is a subsidiary of Amedisys (NASDAQ: AMED), which the home health and hospice provider acquired in 2021 for $250 million.
Palliative care delivery approaches that are not gender-inclusive can contribute to significant quality issues in caring for transgender populations. It’s important to understand that just because you have a transgender patient does not mean that being transgender is the main thing you focus on,” Fried said. Furthermore, 85.3% Furthermore, 85.3%
The agency’s findings will likely inform the development of future payment models as the U.S. When deployed at scale, palliative care can help achieve many of the health care systems current goals, including reduced costs, improved patient satisfaction and quality of life.
While pediatric palliative care nurses were viewed as helpful in addressing the needs of children with serious illnesses, “service gaps” were found in terms of a need for better medical care collaboration and coordination of supportive resources and information, researchers indicated. Helping them understand is a very important role for us.”
Hierarchical Condition Category (HCC) scores within Medicare payment assign numeric values to each beneficiary and are designed to help predict future health care costs based on a patient’s diagnostic information. The ACO reimbursement landscape includes incentives and quality measures designed to improve outcomes based on population needs.
We combined our administrative claims data, our predictive modeling output and basically a template that we could use to prompt AI to pretend as if it was a nurse practitioner and synthesize all the information at the member-specific level,” Carlin Brickner, vice president of data Science at VNS Health, told Palliative Care News.
We need to be really thoughtful about how we work with primary care providers and utilize palliative care experts to better train and inform our primary care providers,” he said. “We She added that these services are now being offered in diverse settings, including outpatient and home-based care models.
About 71% indicated that they were not “sufficiently informed” to counsel patients on its use, according to a recent study in the Journal of Pain and Symptom Management. A majority of palliative care and hospice clinicians feel unprepared to discuss medical cannabis with their patients. Currently, close to 3.9
Seriously ill children may be at increased risk of experiencing abuse and neglect, an issue challenging palliative care providers’ ability to deliver trauma-informed care among pediatric populations. Training interdisciplinary staff to recognize the signs of abuse and neglect is a key part of trauma informed care delivery, Tyson said.
California hospices have banded together to help address the issue and ensure health plans are better informed. One form of inducement is the payment of kickbacks to other health care organizations or physicians in exchange for referrals.
Adding any new form of coverage to Medicaid takes a substantial commitment of time and resources, including investing and designing the benefit, building out the information technology infrastructure and, critically, securing the federal approvals and financial participation necessary to reduce state costs.
Health literacy is the degree to which individuals can obtain, process and understand basic health information and services needed to make appropriate health decisions, according to the Institute of Medicine. Low health literacy among seriously ill patients can impede access to palliative care and complicate efforts to improve health equity.
Having access to it is one thing, but getting the information is another,” Keith said at the Palliative Care Conference. At least 21 states had some form of palliative care-related public information program in place as of June 30, 2023, according to data from the National Academy for State Health Policy (NASHP).
Others, such as New Jersey, Wisconsin, Oregon, and Florida, require certain providers to inform patients of those health care options in particular circumstances. The Oregon advisory group began producing a website to inform health care providers about palliative care, with a particular focus on long term care organizations.
The Identification of Patients in Need of Palliative Care, or ID-PALL, is a patient screening tool that does not require detailed medical information. The Identification of Patients in Need of Palliative Care, or ID-PALL, is a patient screening tool that does not require detailed medical information.
An assessment of current palliative care awareness in the United States is needed to inform the health care sector’s improving palliative care communication and delivery.” An Irish study found that 4 in 10 adults prefer not to think or discuss palliative care. Prior research has shown that as many as 71% of the U.S. study indicated.
Medicare beneficiaries and their families deserve clear, accurate information to make informed choices,” said Dr. Steve Landers, CEO for the National Alliance for Care at Home, in a statement. NAHC and NHPCO have since combined into the National Alliance for Care at Home.
Furthermore, the guideline development process invites Expert Panel members, in collaboration with ASCO staff, to participate in self-, group- and system-level reflection and critical discourse about the role of health equity in relation to the given topics that will inform oncology practice and provision on national and global scales.”
In my local community, I have definitely had more requests for information about our services since I started sharing Yoda videos on social media,” said Mize. While a critical service for patients with serious illnesses, palliative care is vastly underutilized nationwide. I am magical.”.
Palliative care helps patients and families make informed decisions about their care and manage symptoms effectively.” As value-based models expand and hold health systems accountable for the entire care continuum, palliative care partnerships and joint ventures are growing in attractiveness.
Individuals with rare diseases often do not have sufficient information about their condition, and lack some of the supportive structures that can help navigate their illness compared to other patients, Kaplan stated. “By A big challenge is finding providers that are specialists in an area, or even comfortable taking care of them. “A
Centers for Medicare & Medicaid Services (CMS) in its proposed 2025 hospice rule featured a series of request for information (RFIs) that included questions about the utilization of higher-cost palliative treatments within the Medicare Hospice Benefit. This compared to 22% of patients who received supportive care without radiation.
Telehealth can be just as effective as in-person visits when it comes to palliative care. The American Journal of Managed Care (ALMC) first reported the results. Participating patients had been diagnosed within the 12 weeks prior to their enrollment. Quality-of-life scores were comparable among both groups.
This kind of information can provide a blueprint for how clinical education can be more oriented around patient needs, as well as around pain and symptom management, Bowman said at a recent conference held in collaboration with the Coalition to Transform Advanced Care (C-TAC). “The
A systematic overhaul of the nation’s health care education programs is needed to ensure that future clinicians are prepared to provide palliative and hospice care amid rising demand, according to Dr. Leah McDonald of HopeHealth. McDonald is a hospice and palliative care physician at HopeHealth. Photo courtesy of HopeHealth.
Whether operating under an FFS or a per-member-per-month model, the sustainability and scalability of these programs hinge on prudent financial management and well-informed business decisions. According to the World Health Organization, each year, an estimated 56.8 million people need palliative care.
Centers for Medicare & Medicaid Services’ (CMS) 2025 proposed hospice payment rule contained a request for information (RFI) on the potential implementation of reimbursement pathways for “high intensity palliative care services,” such as chemotherapy, blood transfusion and dialysis.
The United States lacks a robust reimbursement system for palliative care. While stakeholders work towards change, providers are developing innovative ways to work with what they have to bring this care to patients in need. Historically, the U.S. We’ve brainstormed, tried things out that didn’t work and then tried something else.
A group of health plans, policymakers, and insurance companies recently told the Center for Medicare & Medicare Innovation (CMMI) that they needed a standardized definition for palliative care in order to improve access. The talk with CMMI was just the “tip of the iceberg” on sustainable support for palliative care, Fields told Hospice News.
Every visit with a patient reveals new information about how a patient’s disease is progressing, said Anderson. Fragmented health care has significant ties to adverse outcomes in patients with chronic or serious illnesses. This type of coordination can improve outcomes , decrease costs, and offer patients a better quality of life. “We
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