Approaches to primary care of adults with intellectual and developmental disabilities

Health disparities framework

In 2006, Canadian Family Physician published “Consensus guidelines for primary health care of adults with developmental disabilities” (hereafter referred to as the guidelines).¹⁰ These guidelines drew attention to the reality that adults with IDD have a high risk of poor health and premature death owing in part to health disparities unique to adults with IDD.^11,12 The 2006 guidelines, and their revision in 2011,¹³ sought to increase primary care providers’ capacity to identify these disparities and address them through preventive and other health care interventions.

The health disparities framework adopted by the 2006 and 2011 guidelines is based on the ethical principle that health care is a fundamental human right and that access by all to the highest standard of health care possible in their community is part of the common good. Hence, addressing health disparities unique to adults with IDD is a matter of good medical practice and social justice. These principles have been affirmed by the United Nations’ Convention on the Rights of Persons with Disabilities, which the federal government of Canada ratified on March 10, 2011, with agreement by every province and territory. Article 25 of the Convention stipulates that people with disabilities have the “right to the enjoyment of the highest attainable standard of health without discrimination on the basis of disability.”¹⁴ States are obligated to provide health care that people with disabilities need “specifically because of their disabilities.”¹⁴ Health care professionals have the responsibility to provide care of the same quality to people with disabilities as to others and to fulfil that responsibility through “training and the promulgation of ethical standards.”¹⁴ Hubert H. Humphrey has said that the moral test of government is how that government treats those who are in the dawn of life, the children; those who are in the twilight of life, the elderly; those who are in the shadows of life, the sick, the needy and the handicapped.¹⁵

These words apply not only to governments but also to those involved in the provision of health care.

Health complexity framework

The revised 2018 guidelines published in Canadian Family Physician,¹⁶ together with this special issue of articles on certain recommendations,¹⁷ are also shaped by a health complexity framework. This approach involves accounting for multiple, interacting, and often compounding factors that influence the health and functioning of people with IDD. These factors include their health characteristics, environments, communication challenges, systems of health care, and social supports. In providing primary care to adults with IDD, family physicians often make decisions under conditions in which there are high levels of uncertainty¹⁸ and ambiguity.¹⁹ To make the best possible decisions under such conditions, family physicians need knowledge derived from research on a patient’s local context and from the practical wisdom of experienced clinician experts.²⁰ Family physicians also need to understand the preferences and values of patients and their caregivers to deliberate with them regarding intervention options that are appropriate for the circumstances of these patients and that are acceptable to them. These distinct types of knowledge form a basis for each of the 2018 guideline recommendations just as each type of knowledge addresses a different basis for clinical decisions in complex health care.²¹

Relational and person-centred care framework

The 2006, 2011, and 2018 guidelines, and the articles in this special issue, all adopt a relational and person-centred care framework in forming recommendations.²² In the 2018 guidelines, this framework is made explicit in the new section on approaches to care, which begins with a guideline on person-centred care (guideline 1).¹⁶ This approach is defined as one in which health care relationships put the person with IDD at the centre of communication, planning, and decisions regarding care. This might require more time than that allocated to the typical office visit, getting to know the patient as a person and the patient’s community, and engaging additional supports.¹⁶

The important concepts here are the relational aspect of health care and the central place of the person with IDD. These concepts are evident, for example, in the revised guideline on decision making (guideline 3).¹⁶ This guideline highlights supported and shared decision making as a way for adults with IDD to contribute optimally to decisions affecting their health care with the support of their family physicians and trusted caregivers. This approach to health care decision making might also avoid the need for legal appointment of others to make decisions on behalf of a patient who is assessed to lack some aspect of decision-making capacity (eg, a guardian who might not know such a patient well).

The relational and person-centred care framework also shapes the guideline on behaviours that challenge (guideline 27).¹⁶ Such behaviour often emerges from an interaction between a person with unique needs and his or her environment. They might signal the absence of necessary environmental accommodations or insufficient supports. Behaviours that challenge can be the way a person with IDD communicates distress.²³ Guideline 27 presents a comprehensive and systematic approach by which family physicians and others can assess the causes (which might be multiple) of a person with IDD’s distress.¹⁶

The relational and person-centred care framework of the 2018 guidelines also shapes a new guideline regarding life transitions (guideline 12).¹⁶ These are life phases during which people with IDD require different or greater supports, such as during their transitions to adolescence, adulthood, frailty, and the end of life. People with IDD can develop decision-making, coping, and other life skills for these transitions with the support of others. Continuity in core relationships in health care, and a coordinated care plan for moving toward different and new supports, can minimize the distress of people with IDD and their caregivers and provide beneficial support during these important periods of change in their lives.

Because people with IDD benefit especially from holistic, biopsychosocial approaches to health care and from support from others for their developmental and caregiving needs, integration of their primary health care should cover the various health and allied health care specialties that are engaged, as well as their network of supports.²⁴ Family physicians play a key role in this integration as the central hub for the timely provision and coordination of all physical and mental health care needs of adults with IDD. They also provide a stable and core health care relationship on which these patients, their families, and other caregivers can rely. The objectives of the Patient’s Medical Home model that the College of Family Physicians of Canada has articulated²⁵ can be used in conjunction with the 2018 guidelines as standards for relational and person-centred primary care of adults with IDD.