Delirium in Palliative Care Miriam M. Friedlander, MD1, Yanina Brayman, BA2, William S. Breitbart, MD3, October 1, 2004
Delirium is highly prevalent in cancer patients with advanced disease.
Frequently a preterminal event, the condition is a sign of significant
physiologic disturbance, typically involving multiple medical etiologies
including infection, organ failure, adverse medication effects,
and in rare situations, paraneoplastic syndromes. Unfortunately, delirium
is frequently underrecognized or misdiagnosed and, therefore,
inappropriately treated or untreated in terminally ill patients. The clinical
features of delirium are numerous and encompass a variety of neuropsychiatric
symptoms common to other psychiatric disorders. Three
clinical subtypes of delirium, based on arousal disturbance and psychomotor
behavior, have been described: hyperactive, hypoactive, and
mixed. The differential diagnosis for delirium includes depression,
mania, psychosis, and dementia. Numerous instruments have been developed
to aid the clinician in rapidly screening for the disorder. Standard
management requires an investigation of the etiologies, correction
of the contributing factors, and management of symptoms. Symptomatic
and supportive therapies, including numerous pharmacologic
approaches, are important, but several aspects of the use of neuroleptics
and other agents in the management of delirium in the dying patient
remain controversial.
The term “supportive oncology” refers to those aspects of medical care
concerned with the physical, psychosocial, and spiritual issues faced
by persons with cancer, their families, their communities, and their healthcare
providers. In this context, supportive oncology describes both those interventions
used to support patients who experience adverse effects caused by antineoplastic
therapies and those interventions now considered under the broad rubric of palliative
care. At its core, palliative care is concerned with providing the maximum
quality of life to the patient/family unit.
A federal judge in Oregon has temporarily blocked Attorney General John Ashcroft’s ability to prosecute Oregon physicians who use controlled substances to help a patient in pain end his or her life. Mr. Ashcroft’s announcement in early
SAN FRANCISCO—More than four out of 10 cancer patients received chemotherapy during their last year of life, according to a study of Medicare patients in Massachusetts. Even a proportion of patients with tumors considered unresponsive to chemotherapy received treatments within 1 month of their death.
Sedation is a clinically important therapeutic intervention in the imminently dying patient. As the patient with an advanced, irreversible illness nears the end of life, symptoms accumulate that are progressively more difficult to
CLEVELAND—While the majority of Americans wish to die in the comfort of their homes, most are actually dying in institutions, often with pain and other symptoms poorly controlled.
Author: Daniel R. Tobin, MD Publisher: Perseus Books, Reading, Massachusetts Pages: 210, No illustrations Price: $14.00
Reviewed by J. Cameron Muir, MD, Fellow, Department
of Medicine, Division of Hematology/Oncology, Northwestern
University, Chicago, Illinois
, August 1, 1999
Peaceful Dying is a work of considerable effort and organization. Dr. Tobin has painstakingly analyzed his experience as a physician caring for patients with terminal illness and compiled a step-by-step guide to help both patients and their families
Elizabeth B. Lamont, MD
Robert Wood Johnson Clinical Scholars Program, Department of Medicine Nicholas A. Christakis, MD, PhD, MPH Departments of Sociology and Medicine, University of Chicago,
Chicago, IL
, August 1, 1999
Predicting the survival of terminal cancer patients is a difficult task. To better understand this difficulty, we divide prognostication into two distinct elements: foreseeing and foretelling. Foreseeing is a physician’s silent cognitive
Walter F. Baile, MD Chief, Section of Psychiatry, Department of Neuro-Oncology Gary A. Glober, MD, and Renato Lenzi, MD Department of Gastrointestinal Medical Oncology and Digestive Diseases Estela A. Beale, MD Department of Neuro-Oncology Andrzej P. Kudelka, MD Department of Clinical Investigation, The University of Texas M.
D. Anderson Cancer Center, Houston, Texas
, July 1, 1999
Because most patients now want to know the truth about their diagnosis and prognosis, the ability to discuss the cancer diagnosis, disease recurrence, or treatment failure, and to solicit patients’ views about resuscitation
Initiating discussions about end-of-life care with patients with incurable cancers early in their disease was associated with a decrease in late-stage... More »
Giving patients at the end of life regular parenteral hydration of 1 L of saline per day did not improve symptoms associated with hydration, quality... More »
A significant portion of patients with incurable lung cancer believe that palliative radiation therapy will cure the disease or at least help them... More »
Adolescents and young adults want to be more involved in specific aspects of their end-of-life care and found a planning document to aid in those... More »
When facing decisions involving children with cancer at the end of life, three themes drove parental decision making--communication, extending time,... More »
Commentary on: Kent B, Anderson NE, Owens RG. Nurses’ early experiences with patient death: the results of an on-line survey of Registered Nurses in New Zealand. Int J Nurs Stud 2012;49:1255–65.
Implications for practice and research
The study draws attention to the issue of patient death and its impact on staff well-being, moral and mental health, calling for these areas to be taken more seriously.
This Registered Nurses' Association of Ontario (RNAO) clinical best practice guideline provide evidence-based recommendations for registered nurses and registered practical nurses on best nursing practices for end-of-life care during the last day
Advance directives (ADs) are one of the few means for patients to indicate their end-of-life (EOL) treatment option preference. An effective and consistent solution for increasing the AD completion rate remains elusive. A literature search revealed three studies completed in the United States that employed an identical methodology and focused on registered nurses (RNs). These studies examined a variety of concepts, including nurses' knowledge, attitudes, experience, and confidence with regard to ADs.|This review completed a systematic synthesis of reported results from three survey studies that focused, respectively, on oncology, critical care, and emergency RNs who were members of various professional nursing organizations.|Our investigation addressed the following research questions: What are the knowledge, attitudes, experience, and confidence of RNs with regard to ADs, and what is the relationship among these study variables? Each study used the Knowledge, Attitudes, and
Medical end-of-life decisions, defined as end-of-life practices with a potential or certain life-shortening effect, precede almost 50% of deaths in Western countries, and receive ample medical-ethical attention. This systematic review aims to detect whether there are differences in the prevalence of medical end-of-life decisions in 'vulnerable' patient groups. In 2009, five major databases were scrutinized for publications containing original data on the prevalence of euthanasia/physician-assisted suicide, life-ending without explicit patient request, intensified symptom alleviation, non-treatment decisions and palliative sedation by social factors (eg age, gender and SES). Heterogeneous findings were pooled using a random effects model. We identified 6377 papers of which 51 papers were selected, involving over 1.09 million patients. Most publications reported the prevalence of non-treatment decisions. The most studied social factors were age and gender. Among patients older than
William S. Breitbard, MD, acting chair at the department of psychiatry and behavioral sciences and chief of psychiatry service at Memorial Sloan-Kettering Cancer Center, discusses how to have an effective end-of-life conversation with a patient.
Key Differences between FQHCs and RHCs Chastity Werner, RHIT, June 13, 2013 FQHCs and RHCs take up a unique niche among physician practices. And that affects compensation and billing.
Improving Care Coordination in Your Practice Susanne Madden, June 12, 2013 Practices are feverishly working to control the rising costs of healthcare - effective care coordination can help.
Refunding Overpayments: Two Options for Medical Practices Ericka L. Adler, June 12, 2013 Medicare and Medicaid providers must return overpayments once identified. Here are two different refund approaches for practices to consider when necessary.
iPad Alternatives for Mobile Physicians Marisa Torrieri, June 11, 2013 As more physicians are seeing the merits of media tablets, the market is expanding, too.