Hospice eNews

What the Media Said about End-of-Life Care This Week

Week of February 14, 2005

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VA & NHPCO RELEASE REPORT ON EOL CARE FOR VETERANS

 

                        “VA Transforms End-of-Life Care for Veterans” is a newly released monograph that notes the “advancements made in end-of-life care for veterans and examines successful hospice-veterans partnerships.”  A joint project of the Department of Veterans Affairs (VA) and NHPCO, the report examines the unique needs of veterans and emphasizes “the importance of quality, compassionate care for dying veterans and their families.”

 

                        US veteran deaths average 54,000 per month, nearly a quarter of all US deaths.  The report shares individual stories of some of these veterans.  Vietnam veteran Paxson Parsons encourages other veterans to “be open to hospice care.”  “It’s not about dying – that part’s up to you.  Hospice is just a helping hand, helping you to live with the disease.  It’s helped me a lot.”  The Hospice of the Florida Suncoast in Largo cared for Parsons.  In an interview with the author, Parsons also complimented Bay Pines VA Medical Center, saying, “I’ve gotten better thanks to the Bay Pines VAMC.  They helped because they treated me like a person.”

 

                        In a preface to the monograph, VA Secretary Anthony J. Principi, says, “VA’s palliative and end-of-life care offers an opportunity to provide veterans a peaceful journey across life’s last years, as well as an opportunity to provide them the respect and recognition they so well deserve through dignified, quality care.  Ours, then, is a final chance to fulfill a last promise.”  Dr. Thomas Edes, Chief of Home and Community-Based Care for the VA, says, “We are raising expectations at the national and local levels, so that a terminally ill veteran can go to any VA facility and obtain hospice care.  If needed hospice care is not forthcoming, we want them to contact us.”

 

                        Saying that the VA has a mandate “to honor veterans’ preferences for end-of-life care,” Principi noted the following commitments to achieving that mandate:

                        *  All enrolled veterans have hospice and palliative care as a covered benefit.

                        *  Every VA healthcare facility has either hospice and palliative care consult teams or inpatient units.

                        *  VA purchases, as a standard practice, comprehensive hospice services in local communities.

                        *  Management is actively institutionalizing hospice and palliative care in all VA healthcare operations, including ongoing training of healthcare personnel.

                        *  Home hospice care is included in this year’s annual budget submission to Congress.

                        *  VA uses its Hospice-Veteran Partnership to “build solid working relationships with the hospice community” to provide comprehensive home hospice services.  The VA anticipates having working partnerships in every state by the end of fiscal year 2005. 

 

                        The report says that VAMC’s are largely autonomous and may address end-of-life care according to patients’ needs.  National policy and standards stipulate, however, that every VA facility must have the following services:

                        *  A person designated as the hospice contact who serves as “part of an integrated network for local and national communications and information dissemination”;

                        *  Hospice services provided in all settings;

                        *  Inpatient hospice beds or community access to them;

                        *  An interdisciplinary palliative care consult team;

                        *  Referral assistance to area community hospices; and

                        *  Tracking of provided palliative care and hospice services in all settings.

 

                        The VA’s current philosophy about hospice and palliative care owes much to Dr. Kenneth Kizer, Under Secretary for Health from 1994 to 1999.  In 1997, Kizer called a VA End-of-Life Summit, which led to “the development of national outcomes measures reflecting greater accountability for appropriate end-of-life care.”  In the years following the summit, the VA and other national organizations have funded several projects that focused on improving quality of care and training of healthcare personnel.  Among them are:

                        *  The VA Faculty Leader Project for Improved Care at the End of Life, partially funded by the Robert Wood Johnson Foundation;

                        *  Training and Program Assessment for Palliative Care, in conjunction with the VA’s Office of Academic Affiliations;

                        *  Interprofessional Fellowship Program in Palliative Care, administered by the VA’s Office of Academic Affiliations;

                        *  VA Hospice and Palliative Care Initiative, supported by Rallying Points and NHPCO;

                        *  National Hospice-Veteran Partnership Program, with Rallying Points, and

                        *  Accelerated Administrative and Clinical Training, together with Geriatrics and Extended Care in collaboration with the VA’s Employee Education System and the Office of Academic Affiliations.

 

                        Last year, ten state hospice and palliative care organizations received grants from NHPCO to support their efforts to develop stronger relationships with VA medical centers.  Other end-of-life advocates also promote these partnerships and the report suggests a number of ways that community hospices and VA medical centers can work together.

 

                        The press release and monograph are available from NHPCO at www.nhpco.org.  Click on “About NHPCO,” then on “Press Releases.”  (“VA Transforms End-of-Life Care for Veterans,” NHPCO Press Release, 2/10)

 

 

PAIN AND PALLIATIVE CARE NOTES

 

                        *  This week, the FDA will discuss the fate of COX-2 inhibitors, painkillers that include Vioxx and Celebrex.  Though not proven to be more effective than NSAIDs, they were believed to have fewer digestive system complications.  Recent concerns about adverse cardiovascular effects have prompted a re-examination.  (USA Today, 2/10)

 

                        *  Researchers at the University of Michigan and the University of South Florida say that adults over 50 are better able to cope with chronic pain and experience less depression associated with chronic pain than younger adults.  Senior author Dr. Carmen R. Green says, “Our study suggests that age is a significant factor across races and ethnicities, and that the impact of pain may differ even with racial and ethnic groups.”  (Forbes.com, 1/28)

 

                        *  Scientists evaluate whether tropical frogs are poisonous by licking their backs.  It’s all for a good cause, because some of the toxins are leading to new painkilling drugs.  The raw chemical epibatadine, found in the phantasmal poison frog, is 200 times more potent than morphine.  While it can’t be used directly, it does serve as a model for developing other drugs.  (Science World, 1/3)

 

                        *  DEA war on drugs no help to chronic pain sufferers” is a headline in the Arkansas Democrat-Gazette.  Arkansas has 47 pain specialists registered at the Doctors for Pain website, www.doctorsforpain.com.  That is fewer than one per county, the article says, and “the loss of a single physician can cut off hundreds of Arkansans from access to pain care.  To the Drug Enforcement Agency (DEA), this fragile network of care is a tempting law enforcement target.”  (Arkansas Democrat-Gazette, 2/6)

 

                        *  Writing in the Rochester Democrat and Chronicle, guest essayist Dr. Patricia Bomba encourages support for New York’s Assembly bill, the Pain Management Legislation, A.10407.  Bomba says “It’s time to create system-based solutions to improve the quality of life for those who suffer needlessly with undertreated pain.”  (Rochester Democrat and Chronicle, 2/4)

 

                        *  If a budget amendment asking for $500,000 to support palliative care training in Virginia is funded, palliative care programs at Virginia Commonwealth University and the Capital Hospice Institute for Education and Leadership in Northern Virginia would provide training in palliative care principles and services across the state.  The wife of major league baseball manager Johnny Oates, who recently died of a brain tumor, is asking the legislature to pass the resolutions that would provide the funding.  (Richmond Times Dispatch, 2/3)

 

                        *  Purdue Pharma has begun shipping Palladone, a long-acting hydromorphone formulation, to wholesale drug distributors.  The company’s press release says that Palladone should be used only for those patients who are opioid tolerant and are already receiving opioids.  Palladone should not be prescribed for the first use of opioids by a patient or for short-term use.  (Biotech Week, 2/9) 

 

 

PAS & END-OF-LIFE NOTES

 

                        *  A male infant named Sun, whose skeletal abnormality is slowly suffocating him, is the center of a court battle over whether to terminate life support.  Doctors at Texas Children’s Hospital in Houston say continuing life support is unethical, but when Sun’s mother, Wanda Hudson, objected, the hospital agreed to let the court decide and is paying for his mother’s lawyer.  The hospital’s decision was made, in part, out of concern for Hudson’s competence.  Hudson maintains that the infant was fathered “by the sun that shines in the sky.”  (The Dallas Morning News, 2/9)

 

                        *  At a recent joint hearing of the California Assembly Committee on Aging and Long-Term Care and the Assembly Judiciary Committee, committee members heard testimony about whether or not California should enact a law similar to Oregon’s Death With Dignity Act.  Two state legislators plan to introduce a bill allowing physicians to prescribe lethal doses of medication to terminally ill patients who wish to choose the time of their deaths.  (Sacramento Bee, 2/5)

 

                        *  Michael Schiavo’s attorney, George Felos, says that the Florida appellate court should issue a mandate by February 22, paving the way for Terri Schiavo’s feeding tube to be removed.  The appellate court recently denied, without issuing an opinion, several motions by Terri Schiavo’s parents.  Since no opinion was issued, the decisions cannot be appealed.  The Palm Beach Post says that “Politics and money too often throw Florida’s moral compass off course,” citing Governor Jeb Bush’s (R) efforts to keep Schiavo alive while cutting budget recommendations for Medicaid.  (UPI, 2/8; Palm Beach Post, 2/4)

 

 

PUBLIC POLICY NOTES

 

                        *  The Wyoming Senate Labor, Health and Social Services Committee wants to put durable powers of attorney and living wills into one document, using a form created by the Department of Health.  Some support the move because it would allow persons to designate their healthcare agent without having to pay attorney fees, but others say that individuals will lose the ability to tailor the document to their own situations.  The bill will go to the full Senate.  (Billings Gazette, 2/10)

 

                        *  In the January 28 Federal Register, CMS says that it is open to a demonstration project that allows Medicare beneficiaries to receive hospice care concurrently with life-saving treatment.  Private insurance companies and the Medicare Payment Advisory Commission already support concurrent treatment.  (Home Health Line, 2/4)

 

                        *  President George W. Bush’s (R) proposed budget would end copayments for hospice care for US Veterans.  (PR Newswire, 2/7)

 

 

OTHER NOTES

 

                        *  Lynette Johnson is a portrait photographer who takes photographs of terminally ill children and donates them to the families of the children.  She got started when her sister-in-law asked if she could make photographs of her stillborn child.  Johnson realized that if she could make photographs of her niece, she could do it for others.  She volunteered to make photos at Children’s Hospital in Seattle for parents who were interested.  Hospital grief counselors call Johnson’s photos “anything but ordinary.”  “Lynette helps people heal,” says one nurse manager.  (People, 2/14)

 

                        *  The National Quality Forum recently endorsed a set of voluntary consensus standards for home health performance.  Family evaluation of hospice care, though not included, remains under consideration and “will be adjudicated in an additional round of voting according to procedures spelled out in the NQF’s Consensus Development Process.”  (PR Newswire, 2/7)

 

                        *  A new brain-imaging study suggests that “thousands of brain-damaged people who are treated as if they are almost completely unaware may in fact hear and register what is going on around them but be unable to respond.”  The study, originally reported in the journal Neurology, “could have sweeping implications for how to care best for these patients… [and] could also have consequences for legal cases in which parties dispute the mental state of an unresponsive patient.”  (The New York Times, 2/8)

 

                        *  The National Minority Health Month Foundation, in conjunction with former speaker of the US House of Representatives Newt Gingrich (R) and former Florida representative Peter Deutsch (D), announced the formation of the Congressional Leadership Alliance to Eliminate Health Disparities.  The Alliance, a bipartisan group, wants to “quantify and identify the prevalence of chronic illnesses that disproportionately affect” minority groups.  The press release is online at www.nmhm.org/newsroom02082005.html.  (National Minority Health Month Foundation Website)

 

                        *  University of Iowa medical students learn ethical decision-making that includes learning the fact that what looks like an ethical decision may be “a problem of communication or trust or insufficient medical information.”  Dr. Lauris Kaldjian, who teaches medical ethics to second year students, says, “A physician’s ability to reason ethically can contribute substantially to both the patient-physician interaction and health care delivery.”  The article is online at www.eurekalert.org/pub_releases/2005-02/uoi-tal021005.php.  (EurekAlert, 2/10)

 

                        *  In VistaCare’s report on first quarter results, the company cited record-high hospice admissions of 4,314 for the quarter ending December 31, 2004.  Chairman and Chief Executive Officer Richard Slager says, “"Admissions and revenue are up, while patient care expenses and lengths of stay are trending down. Theaverage length of stay for the quarter was 114 days and the median length of stay was 31 days, down sequentially from 130 days and 37 days respectively reported in the quarter ended September 30, 2004.”  (PR Newswire, 2/8)

 

                        *  Aetna’s fourth quarter report noted capital deployment, which the company says “complement recent policy-related initiatives in racial and ethnic disparities and care at the end of life, further differentiating Aetna in our industry.”  (Business Wire, 2/10)