# 192 Palliative Care for Adults with Developmental Disabilities


Author(s): Neil M Ellison MD and Drew A Rosielle MD

Introduction   The life expectancy for adults with developmental disabilities (DD) is now within 5 years of the general population. This has resulted in an increased frequency of death from age related illnesses such as cancer, heart disease, and chronic lung disease. This Fast Fact will review special issues in the care of developmentally disabled people with life-limiting diseases. Fast Fact #193 will discuss decision making around life-threatening diseases for adults with DD.

Background Adults   with DD may be defined as persons with impaired social functioning and decreased ability (mild to profound) to comprehend new or complex information or to learn new skills. These disabilities begin prior to age 18. Examples include people with autism, Down syndrome, and cerebral palsy associated mental retardation. During the past decades there has been a move towards decreased institutionalization with mainstreaming of persons with DD to the community. Home care is often provided by elderly parents. Community housing may be supervised by individuals with little familiarity with the patient.

Barriers to medical and palliative care for adults with DD

  • Suboptimal nutrition, limited exercise, decreased utilization of health screening often negatively impact developmentally disabled people’s health.
  • Communication barriers can lead to more advanced illness presentation.
  • Lack of clarity of goals of care and poorly defined decision-makers (see Fast Fact #193).
  • Developmentally disabled people may not be allowed appropriate bereavement:
    • Deprived of the knowledge of death of their caregivers and loved ones.
    • Excluded from funerals, memorial services, or other bereavement activities.
  • Patient lack of comprehension of their illness, its symptoms, or its treatments:
    • May interpret illness or treatments as punishment for wrong-doing.
    • May not be able to understand death and why their family/caregivers are sad around them.
  • Symptom assessment may be compromised by an inability to communicate:
    • Individuals demonstrate a wide range of behaviors indicating discomfort, some of which may be subtle and only apparent to people who know them well, if at all.
    • Signs of distress may be apparent even though it is unclear what is causing the distress: pain, other somatic symptoms, anxiety/fear, sadness?

Providing effective palliative and supportive care to adults with DD

  • Work closely with caregivers to maximize time in familiar surroundings, with familiar people and objects, in identifying routines and activities enjoyable to the patient, and in ways to offer emotional reassurance.
  • Communicate about symptoms understandable to the patient, as opposed to abstract diseases.
    • Symptom assessment and management (see also Fast Fact #126):
    • Research has supported the finding that symptom assessment needs to be individualized to the patient, based on the experience of a patient’s closest caregivers.
    • DisDAT – a distress assessment tool – has been developed to help clinicians and caregivers identify, communicate about, and document an individual’s signs of distress and contentment (3,4).
    • Symptom management should focus on careful examination of patterns of distress, a thorough physical examination, judicious use of diagnostic testing, and empiric use of comfort medications based on what is felt to be the most likely cause. Trial and error, with constant monitoring of adverse medication effects, is often necessary.


  1. Read S. Learning Disabilities and Palliative Care: Recognizing Pitfalls and Exploring Potential. Intl J Palliat Nurs. 2003; 11:15-20.
  2. Tuffrey-Wijne I. The palliative care needs of people with intellectual disabilities: a literature review. Palliat Med. 2003; 17:55-62.
  3. Regnard C, Reynolds J, Watson B, et al. Understanding distress in people with severe communication difficulties: developing and assessing the Disability Distress Assessment Tool (DisDAT). J Intellect Disability Res. 2007;51:277-292. (Further discussion of and examples of DisDAT are available at: http://www.disdat.co.uk.)

Fast Facts and Concepts are edited by Drew A Rosielle MD, Palliative Care Center, Medical College of Wisconsin. For more information write to: drosiell@mcw.edu. More information, as well as the complete set of Fast Facts, are available at EPERC: www.eperc.mcw.edu.

Version History: Originally published November 2007. Current version re-copy-edited in May 2009.

Copyright/Referencing Information: Users are free to download and distribute Fast Facts for educational purposes only. Ellison N, Rosielle D. Palliative Care for Adults with Developmental Disabilities. Fast Facts and Concepts. November 2007; 192. Available at: http://www.eperc.mcw.edu/EPERC/FastFactsIndex/ff_192.htm.

Disclaimer: Fast Facts and Concepts provide educational information. This information is not medical advice. Health care providers should exercise their own independent clinical judgment. Some Fast Facts cite the use of a product in a dosage, for an indication, or in a manner other than that recommended in the product labeling. Accordingly, the official prescribing information should be consulted before any such product is used.

ACGME Competencies: Medical Knowledge

Keyword(s): Non-pain Symptoms and Syndromes, Other Neurological Disorders