The Hospice e-News

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

Week of September 19, 2006

…a service of Florida Hospices and Palliative Care

 


 

CLINICIANS GIVEN ADVICE ON LAST HOURS OF LIVING

 

“The Last Hours of Living:  Practical Advice for Clinicians,” by Doctors Linda Emanuel, Frank D. Ferris, Charles F. von Gunten and Jamie H. Von Roenn, provides continuing education credit for physicians and nurses.  Topics included are introduction to and preparing for the last hours of life, physiologic changes, symptom management, typical last hours, pronouncing a patient dead and notifying the family.  The program is online at www.medscape.com/viewprogram/5808?src=mp. 

 

The authors say that advance preparation and education of all persons who are around the patient are essential if the end of the patient’s life is to be as positive as possible.  They should “be knowledgeable about the potential time course, signs, and symptoms of the dying process, and their potential management.”  Additionally, say the authors, family members should “understand that what they see may be very different from the patient's experience.”

 

The online course details the changes during the dying process and describes the signs of each change.  Examples of the changes are fatigue and weakness, skin breakdown and wounds, decreased appetite and fluid intake and heart and kidney failure.  Neurologic dysfunctions include decreased levels of consciousness and ability to communicate, delirium, respiratory distress, inability to swallow, incontinence, pain, and the inability to close the eyes.  Uncommon events may include asphyxiation, aspiration or a burst of energy just before death.

 

The authors list two “roads to death.”  The “usual” road includes sleepiness, lethargy, obtundedness, a semicomatose state and then coma and death.  The “difficult” road includes restlessness, confusion, quivering or shaking, hallucinations, delirium, jerking, seizures, light coma and then coma and death. 

 

The authors suggest that families need to know the signs that death has occurred.  They are:  cessation of heartbeats and respiration, fixed and dilated pupils, paleness of the body, drop in body temperature, muscle relaxation, sphincter relaxation and possible passage of stool and urine.  The eyes may remain open, the jaw may fall open and bystanders may be able to hear internal fluids trickling. 

 

Once a patient has died, say the authors, both caregivers and family may need permission to spend time with the deceased.  A health professional, if possible, should straighten the body and the bed, remove any machinery and catheters and clean up any mess.  Allow as much time as needed for loved ones to say goodbye.

 

When communicating the news to those who were not present at the death, the authors say, healthcare professionals should try to avoid doing so by telephone.  Provide a comfortable setting, break the news gently and respond with empathy to any expressions of grief.  Conclude the meeting with a plan for the tasks that need to be done.

 

Local laws vary about what has to be done to pronounce death.  When a patient dies at home under hospice care, the nurse may be able to make the pronouncement.  If the patient is not in hospice, but the death was expected and the physician is willing to sign a death certificate, there may not be a need to transport the deceased to a hospital to be pronounced.  Physicians called to pronounce a death should find out if the family is present, if an autopsy has been requested or is needed and whether there is any possibility of organ donation.  If the family is present, the physician should explain why he or she is there, empathize with the family and answer questions.  The article lists the tasks to be done in determining death and recording the event in the medical record. 

 

The authors conclude with a number of key points to remember, some of which are:

          *  You only have one chance to get it right when managing the last hours of someone’s life.

          *  Dying patients often need skilled nursing care around the clock.

          *  Fatigue in a dying patient is expected and, in most cases, should not be treated.

*  Loss of appetite and thirst are normal, and the ketosis which results from decreased food intake can “lead to a greater sense of well-being and diminish pain.”  Dehydration “may stimulate endorphin release that adds to the patient’s sense of well-being.”

*  Terminal delirium (moaning, grimacing, agitation, restlessness, etc.) may be misinterpreted as pain and sedating neuroleptics may be required.

          *  Avoid maintaining parenteral fluids, oropharyngeal suctioning,and removing the body prematurely. 

 

The authors also suggest that only essential medications be used, that the clinician be familiar with the signs of the dying process, and that family and caregivers be drawn in as partners in care.  (Medscape Today, 8/28)

 

 

DEA REVISES PAINKILLER PRESCRIPTION RULE

 

According to an article in The Washington Post, the Drug Enforcement Administration recently rescinded a two-year-old policy that kept physicians from writing multiple, post-dated prescriptions for opioids.  Physicians can now write three 30-day prescriptions, with two of the prescriptions having future dates, to be filled at least one month apart.  Two years ago, the DEA revoked a similar policy and physicians began requiring patients to come for monthly visits which “many doctors considered medically unnecessary but essential to keep them out of trouble with the DEA.

 

DEA administrator Karen Tandy said that the DEA had been wrong to revoke the prior rule, and had gotten more than 600 comments about it from doctors, patients and others.  Howard Heit, a pain and addiction specialist, says that Tandy’s actions were “a very positive step forward in restoring that necessary cooperation between practicing physicians and the DEA.”  But Siobhan Reynolds, founder of the Pain Relief Network, says that little has changed.  “Ms. Tandy states here, as she has on many occasions, that doctors need not fear criminal prosecution as long as they practice medicine in conformity with what these drug cops think is appropriate.  If that isn’t a threat, it will certainly pass for one within the thoroughly intimidated medical community,” Reynolds said.  (The Washington Post, 9/7)

 

 

RESEARCH & RESOURCE NOTES

 

*  A study examining the outcomes of sustained-release opioids in hospice patients looked at pain score, severity of constipation and the patient’s ability to communicate with caregivers.  Scores on pain and severity of constipation were about the same for all three medications – sustained-release morphine, oxycodone and transdermal fentanyl.  Patients receiving transdermal fentanyl had more communication problems than those receiving the other two and also had a shorter length of hospice stay.  (Medical Devices & Surgical Technology Week, 9/17)

 

*  When a person is seriously ill, family and friends need to know how they are doing and express concern, but the patient can’t keep everyone up to date.  A website, www.thestatus.com, is designed to do exactly that – provide “free, easy, secure, private web communications for patients, family, friends.”  Patients can create their own personal pages in English, French or Spanish, which may be password protected or left open for public view.  Other languages will be added later.  (The New York Times, 9/12; The Status Website)

 

*  A survey of parents whose children died in a pediatric intensive care unit identified issues that they considered important:  complete and honest information, easy access to staff, coordination of communication and care, “real feelings” and support by the staff, “preservation of the integrity of the parent-child relationship” and faith.  An abstract of the article, which originally appeared in the journal Pediatrics, is online at patient.cancerconsultants.com/news.aspx?id=38053.  (CancerConsultants.com) 

 

*  The reviewers of the new edition of Weiner’s Pain Management are especially complimentary of the editors’ and authors’ coverage of complementary and alternative treatments of pain.  The editors of the book intend it to be a “first and last” source for information about pain management for most clinicians, a goal that the reviewers say they don’t quite achieve.  Better texts are available dealing with the science of pain, the reviewers note, even as they commend the editors and authors “for their enormous effort in providing a unique work of such breadth.”  (JAMA, 2006;296:1297-1298)

 

*  According to Yahoo! News, a report from the Harvard School of Public Health says that place of residence, race and income play “a huge role in the nation’s health disparities, differences so stark … it’s as if there are eight separate Americas instead of one.”  Asian-American women in Bergen County, New Jersey, typically live until they are 92, while American Indian men in areas of South Dakota only make it to 58.  Dr. Christopher Murray, lead researcher on the study, says “Millions of the worst-off Americans have life expectancies typical of developing countries.”  (Yahoo! News, 9/11)

 

*  In a review of Arnold Kling’s Crisis of Abundance:  Rethinking How We Pay for Health Care, reviewer Dr. Arnold S. Relman highly recommends the book, in spite of disagreeing with the author on many assumptions and conclusions.  He takes issue with Kling’s assertions that “Prices in health care are related to costs of production, that we cannot have health care that is both accessible and affordable while still insulating consumers from its cost, that professional regulation mainly serves the interests of physicians who wish to restrict competition, and that the best way to control costs is to shift more responsibility to patients of all ages through health savings accounts and insurance with high deductibles.”  Most of all, Relman says, Kling is “terribly mistaken in believing … that free markets can largely replace government in protecting the public’s interest in health care.”  But Relman agrees with Kling on a number of other issues and was “attracted by a certain freshness and directness in much of Kling’s argument.”  He “warmly recommends” the book “to general readers who want to understand what economics has to say about health care.”  (NEJM, 2006;355:1073-1074)

 

*  In the current issue of JAMA, Dr. Sharon K. Hull reviews The Soul of a Doctor, a collection of essays of Harvard medical students, in the current JAMA.  Calling the book “both captivating reading and an instructive cautionary tale,” Hull says, “The student contributors write from their souls, providing a frontline report on the process of acculturation into the profession.”  She closes by saying, “The  reader who expects to ever be a patient in today's health care system or who is a physician at any point in the developmental journey will find the stories in this volume at times heartening, at times frightening, and always enlightening.” (JAMA, 2006;296:1141)

 

 

OTHER NOTES

 

*  In west Texas, the battle to save eight-year-old Luis Carranza from dying of cancer has meant that he was separated from his mother.  She brought him to Texas, illegally, from their home in Mexico, hoping for treatment that might save him.  She found the treatment but was deported and, in spite of the efforts of legal and medical volunteers in the US, was unable to see him for months.  Finally she was granted a humanitarian parole visa and allowed to come back to Texas, where she cares for her son with the help of hospice.  (AP, 9/9)

 

*  At a recent forum in San Bernadino, attorneys and physicians met to attempt to understand each others’ point of view in end-of-life matters and assisted suicide.  Susan L. Penney, legal counsel for the California Medical Association, says it’s important that attorneys and physicians understand each other, particularly as medical situations become more complex.  In San Bernadino County, the county medical society and bar association have been meeting every other year for twenty years to discuss topics of mutual interest.  (San Bernadino Sun, 9/14)

 

*  In the Catholic Health Association, 90% of the hospitals and 95% of its member health systems have revised guidelines for “planning, measuring and documenting community benefits.”  The new guidelines are intended to ensure that institutions meet the requirements for non-profit organizations under the federal tax code.  US Senator Chuck Grassley (R-Iowa) asked the IRS to adopt the new CHA guidelines “for calculating and publicly reporting community benefits and charity care.”  (Modern Healthcare, 9/11; Modern Healthcare’s Daily Dose, 9/12)

 

*  The lack of available spots in nursing schools for new applicants is the driving force in the nursing shortage in Orange County, California.  Becky Miller, director of Santa Ana College’s nursing program, says she has a waiting list of 400 for 96 openings.  “With the entry list being so long, the students look at that and say, ‘I'm going to go into something else,’” Miller said.  (The Orange County Register, 9/4)

 

*  An article about Georgia’s nursing shortage in the Atlanta Business Chronicle calls the state’s moratorium on establishing new nursing schools “puzzling and counterproductive in a state where 3,100 new and replacement registered nurses will be needed annually over the next six years.”  The freeze was established by the Georgia Board of Nursing, because it says there aren’t enough nursing faculty members to staff new programs.  The article says, “Increasing objections to the nursing school freeze -- many from nurse-depleted hospitals and technical schools -- are building the momentum to have the ban lifted.” (Atlanta Business Chronicle, 9/11)

 

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.