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Vol. 54, No. 4, April 2008, pp.568 - 571.e6 Copyright © 2008 by The College of Family Physicians of Canada
Medical students views on training in intellectual disabilitiesPhilip Burge, MSWAssistant Professor in the Department of Psychiatry at Queens University in Kingston, Ont
Hélène Ouellette-Kuntz, MSc
Barry Isaacs, MA PhD
Yona Lunsky, MA PhD
Undergraduate Medical Education in Intellectual Disabilities Group at Queens University
Correspondence to: Mr Philip Burge, Queens University, c/o Ongwanada, 191 Portsmouth Ave, Kingston, ON K7M 8A6; telephone 613 549-7944; e-mail burgep{at}queensu.ca There is an urgent need for well trained physicians to care for people with intellectual disabilities (ID). Intellectual disabilities are also referred to as developmental disabilities (in Canada), learning disabilities (in the United Kingdom), and mental retardation (in the Diagnostic and Statistical Manual of Mental Disorders, 4th edition). People with ID have substantial limitations in both intellectual functioning and adaptive skills. Such limitations become apparent before the age of 18 years.1 While those with ID make up only 1% to 3% of the population in Canada,2–4 they have a greater number and variety of health care needs, as well as substantially higher mortality rates, than do people in the general population.5–7 A key barrier to adequate health care for people with ID is physicians lack of experience in caring for this population.8,9 The need for advanced knowledge and skills to serve people with ID adequately has been widely recognized.10–14 A report prepared by the International Association for the Scientific Study of Intellectual Disabilities for the World Health Organization noted the lack of general training in ID among primary health care providers. The report recommended that nations ensure that medical and health care personnel receive sufficient training in care of people with ID to provide appropriate preventive and treatment-oriented health and social services to them.15 Authors of some Canadian studies have argued that more attention to training medical students in this area is a key component of improving the health care of those with ID.7,16–20 The need for adequate training is more pressing because of changes in Canadian social policy. Over the past 30 years, there has been a steady trend in most Canadian provinces toward community living rather than institutionalization for people with ID. As a result, people with ID and, indeed, the governments and agencies that support them expect health care to be provided by the generic health care services in the community, including by public hospitals. While few practitioners in these settings have expertise in working with people with ID, there is an increasing recognition and acceptance of the fact that all physicians will be required to assess and treat those with ID, regardless of specialty. The need for better patient care for people with ID was the main reason that a group of concerned physicians and allied health care providers recently authored and promoted primary care guidelines for Canadian physicians treating adults with ID.21 This group also recommended a minimum of 22 curriculum hours of training be devoted to care of people with ID in all Canadian medical schools (personal communication from Dr William Sullivan, Assistant Professor, Department of Family and Community Medicine, University of Toronto, April 24, 2007). While few Canadian medical schools currently include specific training in ID as part of their undergraduate medical education programs,17 Queens University (Queens) in Kingston, Ont, and more recently the University of Toronto (U of T) in Ontario have developed a full day of teaching on ID within the 6-week clerkship psychiatry rotation in addition to other lectures and problem-based learning modules specific to care of people with ID offered throughout the 4 years of training. This study involved collaboration between these 2 universities in order to understand better the perspectives of upper-year undergraduate medical students on preparation for working with people with ID. Results of this study will guide efforts to improve the medical training of students in this field and, by extension, might improve the future health care of people with ID.
This cross-sectional survey was administered to upper-year undergraduate medical students who were completing the clinical portion of their education (ie, students often referred to as clinical clerks or clerks) at Queens and U of T during 2006. Ethical approval for the study was received from the research ethics boards of both universities. In all, 346 students enrolled in psychiatry clerkship rotations between November 7, 2005, and December 31, 2006, were eligible to complete the survey on a voluntary basis at the beginning and end of this rotation. All findings presented in this paper are taken from surveys completed at the end of the rotation.
Research instrument
Programs All clerks at Queens were likely to have attended 1 specific lecture in ID during their first or second year, and some would also have been assigned an ID-related problem-based learning case before their clerkship. During their rotation in psychiatry, clerks who were placed locally typically attended a mandatory, clinically focused, day-long trip to a residential institution for adults with ID, and about a quarter were also assigned to take part in a community-based day on caring for people with ID. Chance clinical encounters with patients with ID might also have occurred during day-to-day work while these clerks were on psychiatry placements. In many instances at Queens, clerks who were placed considerable distances away did not receive the formal day-long training nor have an opportunity to complete post-rotation surveys. All except 36 clerks from U of T attended a full community-based day in care of people with ID. These 36 clerks might have received some training in ID during rotations (eg, approximately 20% of participants would have received a 2-hour seminar on dual diagnosis given by a psychiatrist at the psychiatric hospital) or earlier in their training; they were given the opportunity to complete post-rotation surveys.
Data analysis
Response rate and respondents characteristics Of the 346 clerks enrolled during the study period (248 at U of T and 98 at Queens), 196 completed post-rotation surveys for an overall response rate of 56.6% (52.8% for U of T and 66.3% for Queens). Many nonrespondents missed the opportunity to complete post-rotation surveys because they were ill or absent for various reasons or were on placements elsewhere. Nonrespondents did not differ from respondents as to proportion of men and women, but no additional information was available on them. Of the 196 medical students who completed the survey, 131 (66.8%) were enrolled at U of T. Table 123 shows respondents demographic characteristics and the amount and type of contact they had had with people with ID.
Perceptions of training A high proportion of clerks at both universities (85.6%) indicated that they had received specific didactic education on ID during medical school. Two-thirds or more of the clerks noted that 6 of 12 topics had been covered (Table 2). The quality of instruction on the 12 topics was rated as good or better by 68.4% of clerks. The quantity of undergraduate didactic instruction was rated inadequate by 50.8% of clerks and adequate or extensive by the remainder.
About 70.4% of respondents reported having observed patients with ID in clinics or having treated them professionally during medical training. Around 21% of these clerks saw 5 or more patients; the remainder saw fewer. Almost 55% reported they had seen patients with both ID and another mental disorder; 16.0% of these clerks had seen 5 or more such patients. Among clerks who had seen patients with ID, 76.2% rated the clinical supervision they received as good, very good, or excellent. Clerks indicated that clinical contact with patients with ID tended to occur while they were visiting patients in community agency programs, institutions, or hospitals. By far most clerks (93.3%) agreed that there was a need to improve coverage of care for people with ID during medical training; the remainder reported that there was no need to change the curriculum. Most often endorsed was the view that their training would have been better with more clinical contact with people with ID and more time in the curriculum for training in their care (Table 3).
Most clerks believed that their future practice would likely include patients with ID (88.8%), that all physicians should be trained in care of those with ID (96.4%), and that training in ID is good preparation for other areas of medicine (90.7%). Clerks were asked to provide written comments on how or why training in ID was or was not beneficial to other areas of medicine. Of the approximately one-third who provided details, most indicated that they believed every physician would see patients with ID, regardless of specialty, and, therefore, should be prepared during undergraduate training to care for these patients. Several other positive comments provided more specific details on a range of perceived benefits. One participant wrote that the training prepares "us to be patient, increase communication abilities and techniques, to be empathetic and see everyone as a person." Another commented that skills in caring for those with ID could well be applied to the "care of children, elderly or demented, and those with psychiatric disorders, especially in terms of communication skills." A few clerks indicated that they believed the number of patients with ID was too small to warrant attention during training, and a few said they intended to pursue a certain specialty (eg, pathology) where such training would not be beneficial. Despite the overwhelming endorsement for training in ID for all physicians, 69.4% of clerks believed that specialists in ID should be providing primary care to people with ID.
Our studys key finding is that there was widespread support from the undergraduates surveyed for more training in ID. This might relate to the belief held by many participants that education in ID is good preparation for other areas of medicine. Having the ability to work with patients with ID requires many skills that are considered useful for caring for a spectrum of patients. For instance, an Ontario study of 559 adults with ID living in the community found that 27% were identified as having difficulties with communication.24 Proper medical assessment of such patients usually requires clinicians to be proficient in making these patients feel comfortable in a clinical setting; to use advanced receptive and expressive communication skills, such as communicating in very simple and concrete terms; and to take a history often with considerable participation of informants, such as care providers or family members. Possessing these skills upon graduation would put physicians at an advantage when they are faced with common work scenarios with a range of patients, including those who do not speak the same language as the physician or those who have learning disabilities or communication difficulties due to relatively common medical problems, including hearing impairment, brain injury, and stroke. The advantages associated with these skills were in fact recognized by general psychiatry residents in a recent American study assessing their perceptions of a rotation serving inpatients with ID; 93% of these respondents said their training in ID had assisted them in learning to communicate better with nonverbal patients.25 Written comments provided by many of our respondents concerning the generalizable benefits of training in ID seem to support this view. The high rate of exposure to many of the topics surveyed was expected, given that most clerks attended our formal teaching day on ID. The strong support for increased curriculum time in ID is even more compelling because it is being expressed by students who are already receiving a substantial amount of training in ID relative to students in many other Canadian medical schools. Nevertheless, it should be noted that neither U of T nor Queens consistently meets the suggested benchmark of 22 hours of curriculum time on care of patients with ID. Our key finding is similar to findings reported elsewhere in residency programs17; participants clearly support enhancements in the area of clinical contact with patients with ID. Rather surprising was the finding that, while by far most clerks reported that such training was good preparation for other areas of medicine and expected to care for patients with ID, more than two-thirds of respondents supported the notion that specialists in ID should be providing primary care to patients with ID. This seems to suggest that students expect to care for patients with ID, but would rather not provide this care directly. It is unusual for primary care to be provided by specialists; while such arrangements sometimes occur with certain populations or medical services, they are often viewed as inefficient and economically wasteful. As educators, we are concerned that we might be leaving students with the erroneous impression that working with patients with ID is so complicated that only ID specialists or interprofessional teams can succeed at it. Future research should investigate underlying beliefs about this finding and determine whether it relates to our concerns, as noted above, or to a general lack of understanding regarding the role of family physicians.
Limitations
Conclusion
We thank the clerks who voluntarily completed the survey. The training day in Toronto, Ont, and therefore this research, would not have been possible without the work and support of Elspeth Bradley. We also thank Surrey Place Centre for financial support; we thank William Sullivan and Jodi Lofchy; and we thank Kelly Killip and Ksenija Hotic for administrative support and data collection. Kingston faculty thanks the staff of Ongwanada and the following assistants and consumer educators who were key contributors to our training days: Julyan Adams, Tom Allman, Kevin Beauregard, Margrit and Laura Choy, Annie Milne, Maureen Perrin, Daniel Pinsonneault, and Sharon Thompson. This research was funded through a research grant from the Developmental Disability Program Management Committee at Queens University in Kingston, Ont.
Contributors Mr Burge, Ms Ouellette-Kuntz, Dr Isaacs, and Dr Lunsky assisted with every phase of the study and contributed greatly to research design, modifications to the survey, planning the steps in data analysis, and drafting and editing the manuscript. The Undergraduate Medical Education in Intellectual Disabilities Group members contributed variously to all or many phases of the study. None declared *Full text is available in English at www.cfp.ca. This article has been peer reviewed.
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