Role of Psychiatry in Palliative Care - A Case Report
Role of Psychiatry in Palliative Care - A Case Report
11(09), 204-207
Article DOI:10.21474/IJAR01/17521
DOI URL: http://dx.doi.org/10.21474/IJAR01/17521
RESEARCH ARTICLE
ROLE OF PSYCHIATRY IN PALLIATIVE CARE - A CASE REPORT
dying patients and the support of their families. This article briefly defines palliative care and summarizes the
evidence for its benefits, to describe the roles of psychiatry within palliative care in the form of a case report.
Palliative care is specialized medical care for people with serious illnesses. This care is focused on providing
patients with relief from the symptoms, pain, and stress of a serious illness – whatever the diagnosis. The goal is to
improve the quality of life for both the patient and the family. Palliative care is provided by a team of doctors,
nurses, and other specialists who work with a patient's other doctors to provide an extra layer of support. Palliative
care can be appropriate at any age and at any stage in a serious illness and can be provided together with curative
treatment” [1].
The most important – and frequently misunderstood – elements of this definition include the focus on preserving the
quality of life, attention to suffering in both the patient and caregivers, care that is provided by a team with
interdisciplinary expertise, and support that can complement disease-oriented treatments throughout the entire
course of an illness for persons of any age.
Palliative care is different from Hospice, as when a cure is no longer possible, or when disease-modifying treatment
is no longer desired, palliative care may become the sole focus of care. Hospice delivers enhanced palliative care,
wherever patients live, when the prognosis is short and the goals of therapy are to optimize quality of life and
function in the final phase of life. Uniquely, hospice services also include bereavement care for family members up
to and after a patient's death [2]. In the United States, hospice care is available to patients with a prognosis of 6
months or less, and the services provided are largely governed by the guidelines of the federal healthcare benefit.
Case presentation
We present the case of a 6-year-old male, with a history of adenovirus pneumonia at age 4, followed by multiple
recurrent lung infections and pneumonia that were not adequately treated due to the family’s religious beliefs. The
boy was brought to the paediatrician after his 6th birthday for his follow-up vaccination when the paediatrician
noted the boy was having difficulty breathing. On obtaining an X-ray of the chest, the boy was diagnosed with
complicatedpost-infectious bronchiolitis obliterans with hypoxemic and hypercapnic acute on chronic respiratory
failure.
With poor feeding and aspiration due to coughing, the boy had also developed liver dysfunction, portal vein
thrombosis, oesophageal varices, and malnutrition. He was a candidate for a lung transplant, but due to a
complicated case and few chances of survival, he was denied a lung transplant atChildren’s Hospital.
With worsening respiratory failure and BIPAP dependence, the patient has been transitioned to comfort care and is a
candidate for hospice.
Palliative care was started and the parents were informed about the patient's terminal diagnosis. The boy developed
increased anxiety due to difficulty breathing and was not able to tolerate BiPap, due to a fear of desaturating. The
boy also had a panic attack while going for a DEXA Scan. The psychiatry team was consulted along with
psychologists and a treatment plan was set.
Psychiatry prescribed- Hydroxyzine 2.5 mg as needed, to decrease anxiety with Lorazepam 2mg as needed for
second line.
Psychologists along with palliative care specialists, helped with therapy and tried to make him comfortable with the
hospital environment.
Discussion:-
All physicians, regardless of specialty, should be competent in providing basic or “primary” palliative care:
attending to whole-person and family concerns, rooting treatment in an understanding of the illness experience,
clarifying basic goals of therapy, and giving due weight to symptom relief and quality of life. A subset of
physicians, with further experience or formal training in this set of skills and knowledge, will practice specialized or
“secondary” palliative care, often in the role of palliative care consultants and part of a multidisciplinary team.
Finally, “tertiary” palliative care is needed for the most challenging cases; it is provided by experts who are also
involved in the research and education of new trainees in the subspecialty [3].
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Lastly, Hospice and Palliative Medicine is a subspecialty medical field, formally recognized in 2006 by the
American Board of Medical Specialties and the Accreditation Council for Graduate Medical Education. Ten medical
boards, including the American Board of Psychiatry and Neurology, sponsor the Hospice and Palliative Medicine
subspecialty certification. As of 2012, qualification for the Hospice and Palliative Medicine subspecialty board
required completion of an ACGME-accredited 1-year postgraduate fellowship [4]. As mentioned, palliative care is
provided by interdisciplinary specialty teams, and specialist-level training experiences and/or competencies also
exist for palliative care nursing [5], social work [6], and chaplaincy [7].
Quality of Care
A number of studies have looked at clinical outcomes in different palliative care settings. These include
observational and quasi-experimental designs, and, more recently, randomized trials. In general, many of these show
improvements in symptom relief, and most show improvements in quality of life. For example, in a retrospective
study of over 400 cancer patients, an outpatient palliative care intervention was associated with significant
reductions in pain, fatigue, dyspnoea, insomnia, depression, and anxiety, as well as significant improvements in
overall quality of life [9]. In addition, surveys have consistently reported high levels of satisfaction among families
and caregivers. In a nationally representative sample of family members of deceased patients, for example, those
who used home-based hospice services (as compared to home health, nursing home, or hospital) reported improved
relief of pain, higher levels of emotional support for both patient and family, increased treatment with respect, and
higher overall quality of care [10].
Survival
Concerns are sometimes raised that the cost savings associated with palliative care stem from poorer survival among
patients receiving these services; i.e. “palliative care saves money by shortening life.” To the contrary, recent data
from well-designed trials indicates that, in some conditions, palliative care interventions may confer a survival
benefit. In a 2010 study of adults with metastatic lung cancer at the time of diagnosis, participants were randomized
in two treatment arms: standard cancer care alone, or standard cancer care plus palliative care. Patients in the
palliative care arm experienced higher scores on measures of quality of life, reductions in depressive symptoms,
reduced exposure to “aggressive” care, and improved survival – living on average more than two and a half months
longer than their counterparts [14].
Conclusion:-
Palliative care achieves better clinical outcomes than standard care alone. Patients feel better, they report improved
quality of life, and caregivers report higher levels of satisfaction. When delivered by a specialist consultation team in
a hospital, or in the hospice setting at the end of life, palliative care appears to be less costly than standard care
alone, when matched by diagnosis and severity of illness. And finally, emerging data from at least one well-
designed study suggests that under some circumstances there may be improvements in survival as well.
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