Hospice eNews       

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

Week of October 17, 2005

…a service of Florida Hospices and Palliative Care

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JAMA EXAMINES PALLIATIVE SEDATION IN DYING PATIENTS

 

            The story of Mrs. B, a 49-year-old woman dying of metastatic breast cancer, is used in the current JAMA to illustrate the issues involved in the use of palliative sedation.  The term palliative sedation is used rather than terminal sedation for the administration of sedatives to induce unconsciousness “to avoid any implication that the intention of such treatment is to cause the patient’s death.”

 

            Traditionally, the article says, the justification for palliative sedation is the “doctrine of double effect, which draws a moral distinction between what a person intends and what is accepted as a foreseen but unintended side effect.”  The double effect doctrine holds that intentionally causing death is not acceptable but prescribing high doses of sedatives and opioids to relieve pain is, even if the resulting death is foreseen. 

 

            There are three characteristics of cases in which palliative sedation may be justified, say the authors. 

            *  Alternative means of relieving symptoms either are ineffective or have intolerable adverse effects.”

            *  The goal or intention of sedation is to relieve symptoms, not to shorten life.”

            *  The patient is ‘at the point of death, in a dying state, or close to death.’”

 

            Additionally, other double effect doctrine conditions must be met. 

            *  The action itself [such as the administration of opioids and/or sedatives] must not be morally wrong, independent of its consequences.”

            *  The resulting secondary effect, such as respiratory depression or death, “must not be the means to accomplish the primary beneficial effect (relief of suffering).”

            *  There must be proportionality between the intended primary effects and the unintended but foreseen secondary effect.  With palliative sedation, proportionality is established by the terminal condition of the patient, the urgent need to relieve suffering, and the consent of the patient or proxy.”

            *  There must be no less harmful option for achieving the goal of relieving suffering.”

 

            The authors make it clear that palliative sedation should be used only as a last resort for intractable pain that can’t be controlled by any other means.  Patients whose pain is not controlled by opioids should be switched to another opioid, offered other modalities such as palliative chemotherapy or radiation and offered interventions that address other issues that might exacerbate pain.  A palliative care specialist or pain specialist, or both, should be consulted.

            “Broader uses of palliative sedation … are ethically controversial,” the authors write.  They give examples of such broader uses as when a patient is terminally ill but not “moribund,” when palliative sedation is combined with the withdrawal of other life-sustaining measures (especially artificial nutrition or hydration), or when “the refractory symptom is existential or spiritual suffering rather than physical symptoms.” 

 

            The article suggests several key points, which should be made when physicians discuss palliative sedation with other members of the healthcare team and family.

            *  The patient’s unbearable suffering cannot be controlled in any other way.

            *  Be explicit about goals and outcomes.”  The patient probably will not regain consciousness, and will die.

            *  Many people “are ambivalent or uncertain about palliative sedation.”  Discuss concerns and possible misunderstandings.

            *  Anticipate questions about the process of dying.

            *  Explain that palliative sedation is not the same as euthanasia, and is “ethically and legally acceptable.”

            *  Ask about things, which can be done for the patient to provide closure and comfort, such as allowing people to say goodbye, or conducting specific religious rituals.

 

            The authors list several points for consideration when a decision for palliative sedation is being made:

            *  If a palliative or pain specialist is readily available, arrange for a consultation.

            *  Discuss the decision with all caregivers.

            *  Clearly distinguish between euthanasia and palliative sedation.

            *  Get informed consent from the patient or surrogate.

            *  Document an explicit plan that includes drugs, dosages and criteria for increasing the dosages.

            *  The site of care should provide an appropriate level of monitoring and nursing care.

            *  Document the procedure carefully in the patient’s chart.

            *  Elicit, and respond to, questions, suggestions and concerns.

            *  After death, hold follow-up discussions with both the family and the healthcare team.

            *  Review, and if necessary, revise hospital policies concerned with palliative sedation.

 

            The authors conclude by saying, “Because palliative sedation should be considered a last resort, it usually occurs in complicated cases, under stressful conditions, and with time constraints.  Although palliative sedation should never be easy for caregivers, it is immensely rewarding to relieve a dying patient’s suffering, without crossing the line into ethically controversial ground.” 

 

            The full text of the patient page on this topic is online at

jama.ama-assn.org/cgi/collection/patient_page.  Other recent pages on related topics, available at the same URL, include a page on palliative care (3/15/2005), one on hospice care (2/21/2001) and a page on end-of-life care (11/1/2000).  (JAMA, 2005;294:1810-1816)

 

 

PAIN STUDIES REVEAL MORE ABOUT PLACEBO EFFECT IN BRAIN

 

            JAMA includes an article titled, “Pain Studies Illuminate the Placebo Effect.”  Magnetic resonance imaging (MRI) and positron emission tomography (PET) scans show that activity at the brain’s opioid receptors “mediates the placebo effect.”  These findings, and others that identify brain areas that are active when a placebo is given, “demonstrate a mechanism through which the patient’s expectation of pain relief can alter their experience of pain and their emotional state.” 

 

            The University of Michigan Medical School study injected a saltwater solution into the jaws of health volunteers.  While undergoing PET scans, the men received a placebo described to them as something “that might relieve their pain.”  At 15-second intervals, the men described their pain and the descriptions were correlated with the brain images.  The results show that endogenous opioids, which were released in several areas of the brain and in the dorsal lateral prefrontal cortex, correlated with how effective the patient expected the placebo to be.

 

            Tor Wager, PhD, assistant professor of psychology at Columbia University, says, “This study shows changes in opiate release occur directly in the brain, in the regions of the brain most closely associated with subjective feelings, reward and pain experience. … This circuitry is directly affected by how you think about a situation.”  The study suggests that “a patient’s assessment of a situation could have important clinical implications.” 

 

            Dr. Jon-Kar Zubieta, the professor who led the study, thinks that a strong placebo response in individuals may provide an adaptive advantage to individuals who have it.  “You can interpret this as a resiliency mechanism that you want to preserve and enhance,” he said.

 

            In the future, medications may target these areas of the brain to enhance the placebo effect.  Psychosocial interventions, in conjunction with medication, may reduce pain.  Researchers say that much more study is needed, because the placebo effect can “confound the results of clinical trials.”  Wager says that too many researchers “fail to take into account the consequences of a patient’s psychological state” on the patient’s health.  “Clinical trials as they are conducted now don’t do a good job of separating drug effects from the effects of expectations and belief.”  Researchers are beginning to study the effects of drugs “when patients know they are receiving it vs when the pain is administered covertly.”  (JAMA, 2005;294:1750-1751)


RESEARCH AND RESOURCE NOTES

 

            *  Narrative, Pain, and Suffering, volume 34 of Progress in Pain Research and Management, is reviewed in the current NEJM.  The physician’s understanding of the patients’ narrative of pain experience is seen as essential to good diagnosis and therapy, communication and empathy with the patient.  Reviewer Philip R. Appel says, “The editors have created a work that addresses several topics stemming from the challenge of understanding what is happening in the patient’s brain as he or she relates the experience of pain.”  (NEJM, 2005;353:1637)

 

            *  A recently released report summarizes the results of last fall’s Maryland Pediatric Care Summit.  The report, Challenges and Opportunities to Improve Pediatric Palliative Care in Maryland, recommends making palliative care family-centered, integrating palliative and curative care, developing innovative care deliver models, improving facilities and spaces which provide end-of-life and palliative care, developing policies and practices that focus on pediatrics, developing a state-wide interdisciplinary model of palliative care for children and adolescents, establishing resource networks for healthcare professionals and families and educating healthcare professionals, families and the public.  (Elder Law Weekly, 10/19)

 

            *  Currents:  Pain Management News and Research is the new monthly online magazine of the American Academy of Pain Management.  The newsletter, which is partially supported by Endo Pharmaceuticals, will examine breaking news about pain from an interdisciplinary standpoint and will also have advocacy news and information, Academy news and other stories of interest.  Members of the Academy will receive the publication each month by email and are encouraged to send it on to others who have an interest in pain management.  (Currents, 10/2005)

 

 

PAIN NOTES

 

            *  The results of a new study by researchers from the University of Michigan Health System Department of Anesthesiology show that minorities and lower-income people have less access to pain medications than higher-income whites.  The study, which appears in the Journal of Pain, found that “pharmacies in predominantly minority areas were significantly less likely to have sufficient supplies of prescription opioid analgesic medications … when compared with predominantly white areas.  In addition, the odds of not having sufficient supplies of opioid analgesics … are significantly higher among pharmacies in low-income areas compared with high income areas, regardless of the racial makeup in the vicinity.”  (myDNA News, 10/10)

 

            *  Use of Acupuncture for Chronic Pain:  Optimizing Clinical Practice” examines acupuncture principles, discusses clinical evidence, and “identifies acupuncture resources to optimize practice for chronic pain management.”  A NIH consensus conference held in 1997 “concluded that acupuncture needling releases endorphins and other neurotransmitters in the brain and should be considered as an appropriate pain treatment option.”  (Holistic Nursing Practice, 2005;19(5):217-221)

 

            *  Children are less likely than adults to receive appropriate pain medication” in an emergency room, according to an article in the current Newsweek.  Parents should ask at check-in if the child should receive an analgesic so it can begin to work, stay with children to comfort and distract them and tell them the truth.  (Newsweek, 10/17)

 

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OTHER NOTES

 

            *  On October 12, former HHS Secretary Tommy G. Thompson received the Mattie Stepanek Award from Children’s Hospice International for his “outstanding work on behalf of U.S. children.”  (US Newswire, 10/11)

 

            *  Bill Burke, volunteer at a hospice unit in Oregon and Washington VA Medical Centers, has written a reflection on life in the unit.  Saying that he is reminded often of “a concept that once prevailed in America:  the great melting pot,” Burke says, “Neither rank nor race nor gender nor wealth nor celebrity status” determines care.  “Honor to one is solace for all. … Honor earned.  Honor due.  Honor given 24/7, by a grateful nation.”  (The Washington Times, 10/10)

 

            *  Louisiana Attorney General Charles Foti (D) is investigating allegations of euthanasia of patients at New Orleans Memorial Hospital in the days following the flooding of the city after Hurricane Katrina.  Foti has requested autopsies, including toxicology tests, on 45 patients who died at the hospital.  Hospital staff who cared for patients under “nightmarish conditions” denied the charges.  The investigation is part of a larger inquiry into 13 nursing homes and six hospitals in the state where patients died in the aftermath of Katrina.  (The Houston Chronicle, 10/14; The Washington Post, 10/16)

 

            *  Following the Supreme Court’s hearing of Gonzales vs. Oregon, a nationwide poll found “widespread support” for physician-assisted suicide.  In the HCD Research Inc. poll, 64% percent of the general public and 62% of physicians agreed that “physicians should be given the right to dispense prescriptions to patients to end their life.”  A USA Today-CNN-Gallup Poll taken just before the court hearing reported that 54% supported PAS.  (Gannett News Service, 10/12)

 

            *  Mitch Albom, author of Tuesdays with Morrie, says that even when plans for death are carefully made, the plans may be cast aside in the light of terminal illness, when decisions may be made that were “previously unimaginable.”  Albom, a supporter of Oregon’s Death With Dignity Act, says though he would not choose suicide for himself, the difference between himself and Ashcroft is that “I don’t feel the right to tell other people what to do.”  Albom says. “Laws are written in plush offices under bright lights.  Lying in a deathbed, the light changes.  And sometimes … so does the plan.”  (Detroit Free Press, 10/9)