The Hospice e-News

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

Week of August 22, 2006

…a service of Florida Hospices and Palliative Care

 


 

ASSISTED LIVING CENTERS AND HOSPICES FORM PARTNERSHIPS

 

An article in Assisted Living Executive looks at the partnerships formed between assisted living centers and hospices to provide care until the end of life.  “Seniors move to assisted living because they want a home, so partnering with a hospice means they can stay home through the rest of their life,” the article says.  The article notes, however, that not all states permit hospice residents to live in assisted living communities, but both NHPCO and Assisted Living Foundation of America hope to change that.

 

Joan Linsky, senior clinical liaison for Allegiance Hospice and Palliative Care, based in Lowell, Massachusetts, thinks it’s a good idea.  Her mother-in-law lives in an assisted-living community and requires hospice care.  She can eat with other residents if she chooses, but, if not, a hospice staff member will prepare breakfast for her in her own apartment.  She once told Linsky she never thought dying could feel so good.

 

Linsky says that such partnerships assure consistency of care with a community’s culture and can be a “powerful sales tool” if communicated well.  Linsky urges senior housing providers not to fear telling current and potential residents about hospice.  The key is educating people about what hospice is.  “It doesn’t mean that their place is going to be associated with dying because hospice is not about dying,” she says. “It’s about living.”

 

Linsky also sees the partnerships as a way to encourage earlier entry into hospice for those who need it.  “Hospices can provide assisted living providers with the training and tools both to recognize residents who become eligible for hospice care and to educate those residents about the benefits of hospice care,” the author says.  “And senior housing providers can help hospice providers with the referrals they need to assure people are getting the greatest benefit from hospice.”  Holli Hallmark, a senior director for VITAS, says, “You have to recognize someone who has a need for hospice care.  If you miss, that person may end up in a hospital or nursing home and not be able to come back to assisted living.”

 

Sunrise Senior Living has recently formed partnerships with VITAS Healthcare Corp. and VistaCare Inc. for hospice services.  It also has local and regional partnerships and does not mandate that any resident use a hospice that it has partnered with, leaving them free to choose another hospice if they wish.  Vice-president Gregg Colon says, “The ‘why’ is pretty basic.”  “Our mission at Sunrise is to champion quality of life for all seniors. Part of this is trying to provide a dying process that is as compassionate as it can be.”

 

One of the benefits of the partnerships, says the article, is the ease of developing consistent programs to educate residents and staff about hospice and end-of-life issues.  Another is that the senior housing provider can train hospice staff about its best practices.  Colon suggests that the housing provider define clear measures of what a successful partnership should be and evaluate whether the partnership is meeting residents’ needs.

 

In other cases, such as Silverado Senior Living Inc., the senior living company establishes its own hospice division.  Scott Robinson, vice-president of hospice for Silverado, says that getting into the hospice business yourself is the “ultimate way” to make sure that end-of-life care meets the expectations of your company’s standards and can also be a good source of new revenue.  Robinson thinks you need “a very large base of operations” to successfully operate your own hospice.  “If you’re serving five to 10 residents with hospice, you’re better off partnering because Medicare will pay for the hospice costs but will not cover over-head,” he says.

 

The article suggests five questions to be answered before a housing community decides to get into the hospice business.

 

          *  Who will your hospice serve – just your residents, or the larger community?

          *  If just your residents, what will your average hospice census need to be just to break even?

          *  What will you have to do in order to be licensed as a hospice?

          *  How long will it take you to obtain a license?

          *  Are there places that you can share staff to control costs?

 

          VITAS’ Hallmark recommends asking the following questions of any potential hospice partner.

          *  Is the hospice properly licensed and certified?  If so, can they provide all the levels of care needed by residents?

          *  What kinds of grief counseling and support does the hospice offer for family members, residents and staff?

          *  Is everybody, from senior executives down to community leaders, on board with the program?  (Assisted Living Executive, 6/2006)

 

 

MANY FACTORS IMPACT HOW CHILDREN DEAL WITH GRIEF

 

An article in Chicago Hospital News says, “Children are unique in their understanding of death and their response to grief, depending on their developmental level, cognitive skills, personality and religious and cultural beliefs, as well as input from the media and what they learn about death and grief from the adults in their lives.”  The article uses five stages of childhood to suggest concepts of death and grief responses but says that readers should keep in mind “that no child falls neatly into any one category.”

 

*  Infants to second birthday:  They don’t understand death, but are aware of separation and loss, reacting more to the emotions of the adults in their lives.  Grief reactions may include a change in sleep habits, protest, weight loss or decreased activity.

*  Two to four year olds:  Death is temporary and, in their thinking, can be reversed.  They are usually “more concerned about altered patterns of care or the emotional reactions of adults in their lives.”  They may experience frightening dreams, be agitated at bedtime or show regressive behavior, such as wetting the bed.

*  Four to seven year olds:  Death is still seen as reversible, but the child may use “magical thinking,” believing that their own thoughts or actions are responsible for the death.  Their reactions may include “repetitive questioning about the death process,” or they may act as if nothing has happened.  Eating and sleeping difficulties can occur, as well as anger, sadness or regressive behavior.

*  Seven to eleven year olds:  Children in this age group can recognize that death is final, though they don’t want to see it that way.  They may think that their own efforts can keep death from occurring.  They are concerned with specific details about the death and about how others feel about it.  School difficulties are common and sadness and anger may be acted out.  Some become worried about their own health.  Other responses may include denial, sadness, shock and regression.

*  Adolescents:  They “recognize death as final and irrevocable.”  They may express grief with physical symptoms such as head or stomach aches, mood swings or anger.  Some may withdraw while others act out with inappropriate behavior.  Depression and/or sleep disturbances can occur.  Some may idealize their deceased loved ones, wearing their clothes and adopting their mannerisms.  (Chicago Hospital News, 7/2006)

 

 

RESEARCH & RESOURCE NOTES

 

*  Raising an Emotionally Healthy Child When a Parent is Sick is reviewed by Dr. John Glazer of The Cleveland Clinic Foundation.  Glazer says that the book establishes a foundation in normal child development and “subsequent chapters address in specific, informed detail every conceivable issue, practical, behavioral, and psychological, apt to be encountered by an ill parent and/or his or her partner.”  “I recommend it to professionals and parents alike – be they ill or well,” he says.  (Journal of the American Academy of Child and Adolescent Psychiatry, 2006;45(7):887)

 

*  Harry Moody, director of academic affairs for AARP , calls services such as those offered by elder-care mediators “silver industries, services developed to respond to the special needs of an aging population.”  Elder-care mediators, many of whom have a legal background, “work with families and seniors to develop solutions for conflicts around such issues as housing, health care, end-of-life directives, emergency situations, finances and even when mom or dad should hang up the car keys.” (The Hartford Courant, 8/16)

 

*  September is again Pain Awareness Month, and the American Society of Pain Educators (ASPE) will have several events to educate healthcare providers on pain management.  Two critical factors drive the current focus – the inadequate pain management education that physicians receive during their training and “the serious need for evidence-based pain management education among healthcare professionals treating the growing population of aging adults and the elderly.”  Clinicians may register for a variety of resources at the ASPE website at http://www.paineducators.org/PainAwarenessMonth.asp.  (Medical Device Law Weekly, 8/27)


PAIN AND END-OF-LIFE NOTES

 

*  Children watching TV have less pain than those who don’t.  An even more disturbing factor, according to the author of a recent study from the British Archives of Diseases in Childhood, is that Mom is less comforting than cartoons.  Other experts agree, saying that parental attempts at comforting often backfire, because the child thinks “something must really be bad” if they need soothing.  Experts have long known that distraction helps divert children’s attention from pain, but Dr. Stephen Hays, of Vanderbilt Children’s Hospital, says it has to be a passive distraction, like TV, because when children are asked to actively play, they report increased pain levels.  (The Hattiesburg American, 8/18)

 

*  Art Buchwald isn’t the only hospice patient to outlive his doctor’s prognosis.  “Doctors are notoriously poor at prognosis,” says Dr. Andrea Miller, medical director for Wuesthoff Brevard Hospice and Palliative Care.  But, Miller adds, they usually overestimate how long a patient will live, rather than underestimate.  Some estimates suggest that 8% of hospice patients that are given a six-month prognosis live longer than a year.  One reason is that the type of patients seen by hospices is shifting, with more chronic and not immediately life-threatening illnesses.  (Florida Today, 8/15)

 

*  An editorial in The Columbus Dispatch suggested that Kansas Senator Sam Brownback’s (R) Assisted Suicide Prevention Act is a violation of the states’ right to regulate the practice of medicine.  The writer says that states “should be free to try new approaches to solving problems without fear of the federal government pouncing on them…  Perhaps the people of Oregon and elsewhere will decide that assisted suicide is the wrong path.  But the resolution should come from those involved in the experiment and should not be imposed by Congress.”  (The Columbus Dispatch, 8/14)

 

*  Debbie Gunter, director of clinical services at the hospice inpatient unit at Atlanta’s Budd Terrace, believes there’s a difference in telling the truth and being honest with terminally ill patients.  Telling the truth means using medical terminology, she says, but “being honest means telling them what that means and what choices they have for managing their disease.”  Gunter has been interested in palliative care since she was in nursing school more than 25 years ago and has worked as a palliative care practitioner with elderly patients.  Gunter took her definition of hope from a physician, who said, “When there isn’t hope for a cure, there is always hope for other things.”  (Atlanta Hospital News, 8/7)

 

 

NURSING SHORTAGE NOTES

 

*  Detroit’s St. John Health System is trying to recruit foreign nurses to fill a 300-vacancy shortage.  The healthcare system is offering to help the nurses get Michigan licenses, will offer a 12-week orientation “that includes a ‘culturally minded introduction’ to southeast Michigan and will conduct an ‘accident reduction’ course to help the new nurses speak better English.”  The Michigan Department of Labor and Economic Growth projects a statewide nursing shortage of 7,000 nurses by 2010, and almost 18,000 by 2015.  (The Detroit News, 8/17)

 

*  The National League for Nursing says that baccalaureate nursing programs saw an 16% increase in applicants last year, and associate degree programs had a 28% increase.  But nearly 150,000 qualified applicants, 18% more than in 2004, were turned away because there aren’t enough nursing professors.  Nursing professors make only about half as much as clinical nurses.  Another problem is a lack of clinical placements to train students.  (The New York Times, 8/13)

 

 

OTHER NOTES

 

*  Michael Schiavo has emerged as “a political weapon in this year’s midterm elections.”  Schiavo “did not vote or follow the news until recently,” but spoke on behalf of Democrat Ned Lamont, who defeated Senator Joe Lieberman in the recent Connecticut primary.  Schiavo told voters that Lieberman had “supported an emergency bill asking a federal court to consider reinserting Ms. Schiavo’s feeding tube…”  (The New York Times, 8/16)

 

*  In an article on Fairfax County chaplains, Capital Hospice chaplain Diana Gomez de Molina says her faith “never wavers” but that she regularly gets angry over deaths that seem senseless.  “I’ll be giving God a good piece of my mind,” Molina says, adding that she has the kind of relationship with God where she’s free to be angry and unhappy with things that are happening.  “You can be facing something that’s inevitable, but you don’t have to put a plastic smile on your face.”  (The Fairfax County Times, 8/9)

 

*  The cost of a dose of Erbitux to a patient whose insurance won’t cover it is more than $18,000 and increasing number of patients are facing the choice of paying for treatments as they live longer with terminal disease.  The high costs of extraordinary care for the dying creates a dilemma that is “challenging governments, employers and insurers, who all help finance America's longer life spans and innovative technologies.”  Some doctors, ethicists and economists say money expended to extend life by a few weeks or months would be better spent to screen and treat diseases in earlier stages.  (AP, 8/13)

 

 

Glatfelter Insurance Group is the national sponsor of Hospice News Network for 2006.  Glatfelter Insurance Group provides property and liability insurance for hospices and home healthcare agencies through their Hospice and Community Care Insurance Services division.  Ask your insurance agent to visit their website at www.hccis.com. 

 

 

* There will be no publication of The Hospice e-News on the week of September 12, 2006. *