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Home » End-of-Life Care
 
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To Reduce Futile Care, Build Trust
September 6, 2012
“I’m Not Going to Treat Your Cancer”
ONCOLOGY,  March 30, 2012


 

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End-of-Life Care

 
FEATURED CONTENT

Early End-of-Life Discussions Affect Aggressiveness in Treating Incurable Cancers
Leah Lawrence , December 11, 2012

Initiating discussions about end-of-life care with patients with incurable cancers early in their disease was associated with a decrease in late-stage aggressive cancer treatments such as chemotherapy or acute care, and with an increase in the use of hospice care at the end of life.

End-of-Life Parenteral Hydration Did Not Improve Symptoms, Quality of Life
Leah Lawrence , December 4, 2012

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 of life, or survival, according to a randomized, placebo controlled study.

Use of Advanced Radiation Techniques Increased During Last Year of Life
Leah Lawrence , November 19, 2012

Although the number of metastatic cancer patients receiving radiation in the last year of life did not significantly change from 2000 to 2007, a new study has found a shift in radiation use from the simplest radiation treatments to more advanced treatment.

Study: In Final Months, Older Cancer Patients Pain Under-Addressed
Leah Lawrence , November 7, 2012

A new study in the United Kingdom has found an increasing trend in opioid prescribing by general practitioners for cancer pain during a patient’s last 3 months of life. However, data also revealed that older patients had a significantly lower chance of receiving opioids to address cancer pain compared with patients aged 50 years or younger.

Palliative Care for Oncology Patients
Thomas J. Smith, MD1 , November 2, 2012

In this podcast we discuss integrating palliative care into standard oncology care with Thomas J. Smith, director of palliative medicine at Sidney Kimmel Comprehensive Cancer Center.

ASTRO: Many Terminal Lung Cancer Patients Believe Palliative Radiation Therapy Is a Cure
Dave Levitan , October 31, 2012

A significant portion of patients with incurable lung cancer believe that palliative radiation therapy will cure the disease or at least help them live longer, according to a new study. Only about one-third of patients acknowledged that the treatment was not at all likely to cure their cancer.

Adolescents, Young Adults Seek Involvement in End-of-Life Planning
Leah Lawrence , October 22, 2012

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 decisions helpful, according to the results of a recently published study.

Communication Key to Parental Decision Making for Children at End of Life
Leah Lawrence , October 9, 2012

When facing decisions involving children with cancer at the end of life, three themes drove parental decision making--communication, extending time, and understanding prognosis, according to a recent meta-analysis.

Am I Obligated to Give Therapy Against My Better Judgment?
Paul R. Helft, MD , September 27, 2012

The family of a young woman with a brainstem glioma has been haranguing her physician to continue bevacizumab treatment despite a significant decline in her functional status. How to respond?

To Reduce Futile Care, Build Trust
Paul R. Helft, MD , September 6, 2012

I have come to the conclusion that a successful systematic approach to earlier transitions from disease-directed cancer therapy to end-of-life and palliative care can only come from better communication in the context of more trusting relationships.

Showing 1 - 10 of 42 results.
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More on End of Life

Oncology NEWS International. Vol. 15 No. 8
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Palliative Care Service at NIH Is Integral Part of Treatment

August 1, 2006

WASHINGTON—In an ideal world, palliative care would be integrated into therapeutic care from the time of cancer diagnosis—not limited to hospice or end-of-life care. An interdisciplinary palliative care team would regularly assess each patient's needs, not only for pain and symptom relief but also for psychosocial and spiritual needs. Their activities and recommendations would be closely coordinated with clinicians on the curative team.

This is no pipe dream, according to Ann Berger, MD, chief of the Pain and Palliative Care Service (PPCS) at NIH's Clinical Center, where she is working to turn this vision into reality. The NIH Clinical Center is a clinical research hospital, and all patients participate in clinical research studies.

Speaking at the World Cancer Congress, convened by the International Union Against Cancer (UICC), Dr. Berger described the philosophy and methods that are enabling NIH to integrate palliative care into the treatment of cancer patients and those with other diseases on therapeutic research protocols (abstract 6-2).

"Palliative care is optimized when initiated at the time of diagnosis and comprehensively utilized throughout the disease," Dr. Berger said. "We're there the whole way through."

At NIH, the PPCS is addressing those needs through a core team consisting of a chief physician, a palliative care advanced practice nurse, a nurse practitioner, a nurse thanatologist, and an administrative coordinator. Designated liaisons in Clinical Center departments also work with the PPCS.

The Quality-of-Life Team

A key tool for the PPCS team is going on rounds with the curative team. "Clinical presence at the bedside is paramount," Dr. Berger said. One challenge at the outset was the perception that the start of palliative care equals the end of hope for cure or long-term remission. Changing terminology helped. "We call ourselves the quality-of-life team," Dr. Berger said. "That's acceptable to patients."

A second critical step is daily follow-up visits to anchor symptom management in the research protocol. And a third is documentation in a consult format, providing a rationale for interventions.

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JOURNAL SCAN
Asking next-of-kin of recently deceased cancer patients to take part in research: 11 of 20 surveyed found it a positive experience
ebn.bmj.com - 3/7/13

Commentary on: Koffman J, Higginson IJ, Hall S, et al. Bereaved relatives’ views about participating in cancer research. Palliat Med 2012;26:379–83.

Implications for practice and research

  • These results will aid the development of protocols for screening bereaved individuals who are eligible for study participation.

  • These results provide insight into bereaved participants’ preferences for

  • The majority of nurses first experience death in or before their first year of practice, and the experience can provoke feelings of helplessness, guilt and ongoing distress
    ebn.bmj.com - 2/27/13

    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.

  • EBN resources page
    ebn.bmj.com - 7/3/12
    RNAO clinical best practice guideline end-of-life care in the last days and hours (September 2011)

    http://www.rnao.org/Page.asp?PageID=924&ContentID=3592

    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

    Knowledge, attitudes, experiences, and confidence of nurses in completing advance directives: a systematic synthesis of three studies.
    pubmed.gov - 6/1/12
    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: does its use differ in vulnerable patient groups? A systematic review and meta-analysis.
    pubmed.gov - 4/2/12
    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

    Result Pages: 1 2 Next



    VIDEO: Discussing End-of-Life Care With a Patient

     

    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.
     

     
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