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Behavioural symptoms among people with severe and profound intellectual disabilities: A 26-year follow-up study

Published online by Cambridge University Press:  02 January 2018

Christina L. Thompson*
Affiliation:
Tayside Primary Care NHS Trust, Clinical Psychology Department, Wedderburn House, Dundee
Andrew Reid
Affiliation:
Carseview Centre, Ninewells Medipark, Dundee
*
Dr Andrew Reid, Carseview Centre, 4 Tom McDonald Avenue, Ninewells Medipark, Dundee DD2 INH, UK
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Abstract

Background

Very little is known about the natural history of challenging behaviour and psychiatric disorder in people with severe and profound degrees of intellectual disability.

Aims

To clarify the natural history of challenging behaviour and psychiatric disorder in this population through a long-term prospective cohort study over a 26-year period.

Method

One hundred individuals with severe or profound intellectual disability were randomly selected in 1975. Their behaviour was recorded through carer and psychiatrist ratings using the Modified Manifest Abnormality Scale of the Clinical Interview Schedule. The presence and severity of psychiatric disorder were also recorded. The study was repeated in 1981/82 and 1992/93. We repeated the study again in 2001, supplementing the original observational data with the Checklist of Challenging Behaviour.

Results

Behavioural symptomatology is remarkably persistent, particularly stereotypy, emotional abnormalities, eye avoidance and overactivity although the severity of overall psychiatric disorder does show some abatement through time.

Conclusions

These findings influence the prospects of success in relocating adults with severe and profound degrees of intellectual disability back into the community.

Type
Papers
Copyright
Copyright © 2002 The Royal College of Psychiatrists 

Psychiatric symptoms and challenging behaviour often coexist in adults with severe and profound intellectual disabilities. These phenomena tend to persist over time (Reference Kiernan and AlborzKiernan & Alborz, 1996; Reference Nottestad, Stromgren and LinakerNottestad et al, 2000) and can be difficult to distinguish (Reference Moss, Emerson and KiernanMoss et al, 2000). It is important to establish the natural history of these behavioural symptoms and psychiatric disorders so that we can assess the efficacy of management and treatment procedures. This is particularly relevant because people with severe intellectual disability are now living longer (Reference Day and JancarDay & Jancar, 1994) and the needs of this ageing population are becoming increasingly important (Reference HollandHolland, 2000). However, it is an underresearched area and this cohort study, which charts the challenging behaviour and psychiatric symptoms of a group of adults with severe and profound intellectual disabilities over a 26-year period, offers a unique perspective on these issues.

METHOD

In 1975/76 the second author, with colleagues, randomly selected 100 adults with severe and profound degrees of intellectual disabilities and studied their behavioural patterns and psychiatric syndromes (Reference Reid, Ballinger and HeatherReid et al, 1978).

The data collection was repeated in 1981/82 (Reference Reid, Ballinger and HeatherReid et al, 1984) and again in 1992/93 (Reference Reid and BallingerReid & Ballinger, 1995). We have repeated the assessments once again and present the results of a comparison of the 1975/76 data with the 2001 data to establish possible changes in behavioural and psychiatric patterns.

Design and participants

The study is a longitudinal, within-participant design, following the cohort over a 26-year period. The original 1975/76 sample consisted of 100 individuals living at a long-stay hospital for people with intellectual disabilities: 45 males and 55 females with a mean age of 35 years (range 17-78), 49 of them with severe intellectual disability and 51 with profound intellectual disability. Subsequently, two individuals were excluded because it emerged that they were functioning above the ‘severe’ level of intellectual disability. Of the remaining 98, 54 are still living. One individual was not followed up in 2001 because she was relocated repeatedly throughout the data collection period. The study is, therefore, a behavioural comparison of the 53 survivors in 2001 from the original cohort with those same 53 individuals in 1975.

The present sample consisted of 21 males and 32 females with a mean age of 57.6 years (range 42-92): 26 (49.1%) with severe intellectual disability, 18 (34%) with profound intellectual disability and 9 (17%) whose level of intellectual disability varied on the border between severe and profound. In 28 out of 53 (52.8%) the intellectual disability was of unknown aetiology, with other causes including hydrocephalus (1 out of 53, 1.9%) and Down's syndrome (4 out of 53, 7.5%).

Forty-two of the cohort are currently living in the community, with the remainder either living in the same long-stay hospital as in 1975/76 or in specialist accommodation. As a group, the participants have been resident in hospital for a mean of 36.7 years (range 10-67).

Measures taken

In both the 1975/76 and the 2001 study, the following demographic data were noted: age, gender, cause of intellectual disability (if known), level of intellectual disability, continence level, whether the individual had epilepsy and whether they had significant impairment of vision, hearing or mobility. We adopted the same definition of epilepsy in 2001 as in 1975/76, defining a patient as having epilepsy if he or she had suffered three or more fits over the last 2 years or was receiving any anticonvulsant medication for previous epilepsy (Reference Gunn and FentonGunn & Fenton, 1969).

Participants were also assessed in the following two ways. First, staff informant interviews, originally devised by Reid et al in Reference Reid, Ballinger and Heather1978, asked primary carers if participants had shown significant abnormality during the preceding week in relation to social withdrawal, overactivity, stereotypies, irritability, nosiness, self-injury, stripping, sleep disturbance or feeding disorder: ‘ 0’ indicated that the symptom was absent and ‘1’ indicated that it was present. This information represents dichotomous data and the ratings are referred to as ‘carer ratings’. Second, each participant was interviewed/observed for approximately 20 min using the Modified Manifest Abnormality Scale (MMAS) of the Clinical Interview Schedule (Reference Goldberg, Cooper and EastwoodGoldberg et al, 1970).

The MMAS (see Appendix) defines and records 19 behaviours and psychiatric symptoms on a five-point rating scale: a zero rating indicates that the symptoms are absent, whereas ratings of 1-4 represent increasing degrees of severity. Ballinger et al (Reference Ballinger, Armstrong and Presly1975) had previously shown this modified scale to be a reasonably valid and reliable instrument in this population, although the numbers involved in the original reliability study were small and correlations for some of the items, for example ‘histrionic’, ‘anxious’ and ‘hostile irritability’, did not reach statistical significance. Some other items, for example ‘delusions, misinterpretations and thought disorder’ and ‘pica’, were also recorded so rarely that statistical analysis made little sense. The interpretation of significant changes/lack of changes on these symptoms should therefore be viewed cautiously.

For the 1975/76 data, observations of behaviour and mental state were made by psychiatrists. For the 2001 data, these same observations were made by a research psychologist. The reliability of these ratings was not established, but the psychologist had extensive research and clinical experience with this population, with particular reference to behavioural observation. The authors, therefore, would have no concern about the psychologist's expertise in assessing and rating psychopathology. For the purposes of consistency between published papers, the psychologist's ratings are referred to in this follow-up study as ‘psychiatrist ratings’.

These two sources of information were then reviewed and a decision was made by the psychiatrist/psychologist as to whether each participant showed evidence of a psychiatric disorder.

As with the previous studies, psychiatric disorder was defined as follows: ‘abnormalities of emotions, behaviour, relationships, or thinking which are inconsistent with the patient's intellectual level and of sufficient duration or severity to cause persistent suffering or handicap to the person and/or distress and disturbance to those in daily contact with him/her’. This definition was derived from that of Rutter & Graham (Reference Rutter and Graham1968). We rated psychiatric disorder thus defined on a five-point scale: 0=no disorder, 1=personality quirks or eccentricities of behaviour, not amounting to overt psychiatric disorder or sufficient to cause management problems; 2, 3 and 4 indicate mild, moderate and severe degrees of psychiatric disorder, respectively. The second author has used this five-point scale previously for rating psychiatric disorder in a population with intellectual disability (Reference Ballinger and ReidBallinger & Reid, 1977). It was used in both the 1975/76 and 2001 studies to estimate, at the time of interview, the presence or absence and degree of severity of psychiatric disorder. It represents a subjective opinion by the interviewer and the data are referred to as ‘overall’ ratings.

In addition, for the 2001 study, data were collected using the Checklist of Challenging Behaviour (CCB; Reference Harris, Humphreys and ThomsonHarris et al, 1994). This checklist aims to identify: the type and number of challenging behaviours exhibited by residents and explores how often an individual displays these behaviours; if staff find these behaviours difficult to manage; and if any injuries have been caused as a result within the 3 months prior to administration of the assessment. The CCB has been found to be useful as a screening tool for both challenging behaviour and mental health problems (Reference Jenkins, Rose and JonesJenkins et al, 1998) and it is used here to lend validity to the subjective ‘overall’ interviewer ratings.

The CCB is divided into two parts: Part 1 consists of 14 aggressive behaviours that involve physical contact with other people and self-injury; and Part 2 consists of 18 other types of challenging behaviours, such as absconding and stereotypical behaviours. Both parts are rated on a five-point scale: Part 1 for frequency, management difficulty and severity; and Part 2 for frequency and management difficulty. Within each scale, a higher number denotes a more frequent behaviour, difficult behaviour or severe injury. For example, the frequency scale ranges from ‘1: never occurred’ to ‘ 5: occurs daily or more often’.

For the purposes of this study, the rating scale was modified to ‘ 0-4’ rather than ‘1-5’ because it was felt that the original scale was subject to false inflation of scores. On the original scale, an individual who displayed no challenging behaviours would have received a score of 32. By modifying the scale, the same individual would now receive a more authentic score of zero; if a behaviour has not occurred, it is rated as zero across all scales.

RESULTS

Other disabilities

Of the sample, 17 (32.1%) were epileptic, 7 (13.2%) were visually impaired or registered blind, 2 (3.8%) were hearing impaired or deaf, 36 (68%) were partially or fully incontinent and 16 (30.2%) had mobility difficulties or were immobile. The corresponding figures for 1975/76 were 15 (28.3%), 6 (11.3%), 4 (7.5%), 31 (58.5%) and 6 (11.3%). The Wilcoxon signed rank test indicated a significant increase at follow-up in the number of individuals who were immobile or who required assistance to get around. No other significant differences were found between the 1975/76 and 2001 studies for the other disabilities.

Carer ratings

Table 1 compares the carer ratings for the 53 survivors between 1975/76 (base-line) and 2001 (follow-up). Because the data for these ratings are dichotomous, correlation coefficient ϕ was used to explore the relationships between ratings. This indicated three categories that showed a significant correlation between assessment points: noisy, social withdrawal and overactive. It should be noted, however, that all three correlation coefficients were fairly weak. The remaining behaviours were not found to be significantly correlated despite showing similar percentages between assessment periods.

Table 1 Carer ratings: baseline and follow-up comparison

Category Baseline (1975) n(%) Follow-up (2001) n(%) Correlation coefficient ϕ and significance
Noisy 19 (35.8) 28 (52.8) 0.39 (P<0.005)
Social withdrawal 10 (18.9) 9 (17.0) 0.29 (P<0.05)
Overactive 26 (49.1) 12 (22.6) 0.28 (P<0.05)
Irritability 36 (67.9) 25 (47.2) NS
Self-injurious behaviour 23 (43.4) 10 (18.9) NS
Stereotypy 20 (37.7) 22 (41.5) NS
Feeding disorder 13 (24.5) 12 (22.6) NS
Sleeping disturbance 8 (15.1) 8 (15.1) NS
Stripping 6 (11.3) 11 (20.8) NS

Psychiatrist ratings

Table 2 compares the interviewer ratings of manifest abnormalities between 1975/76 and 2001 using the Wilcoxon signed rank test. Ratings of slow, lability of mood, and depressed show a significant increase over assessment periods.

Table 2 Psychiatrist ratings: baseline and follow-up comparison

Category Baseline (1975) n(%) Follow-up (2001) n(%) Wilcoxon signed rank test (two-tailed)
Slow 9 (17.0) 18 (34.0) Z=-2.340 (P<0.05)
Lability of mood 1 (1.9) 4 (7.5) Z=-2.226 (P<0.05)
Depressed 1 (1.9) 5 (9.4) Z=-2.203 (P<0.05)
Stereotypy 32 (60.4) 34 (64.2) NS
Flattened 15 (28.3) 8 (15.1) NS
Eye avoidance 14 (26.4) 14 (26.4) NS
Overactivity 13 (24.5) 7 (13.2) NS
Elated 9 (17.0) 6 (11.3) NS
Suspicious 8 (15.1) 3 (5.7) NS
Distractibility 7 (13.2) 3 (5.7) NS
Anxious 6 (11.3) 12 (22.6) NS
Hostile irritability 4 (7.5) 4 (7.5) NS
Histrionic 3 (5.7) 1 (1.9) NS
Self-injurious behaviour 3 (5.7) 6 (11.3) NS
Pica 2 (3.8) 0 NS
Delusions 0 0 NS
Hallucinations 0 0 NS
Excessive concern with body 0 0 NS
Depressive thoughts 0 0 NS

Among the other symptoms, four were not present at either period and the remainder showed no significant differences over time, indicating their persistence. Stereotype, in particular, is present in over 60% of the cohort at both periods.

Overall ratings

Table 3 compares overall ratings for psychiatric disorder between 1975/76 and 2001. Results indicate that the number of individuals receiving an overall score of 3 or 4 in 2001 had decreased from 1975/76, whereas the numbers who received a less severe score of 1 had increased. The Wilcoxon signed rank test found these differences to be significant.

Table 3 Overall psychiatric ratings: baseline and follow-up comparison

Overall rating Baseline (1975) n(%) Follow-up (2001) n(%)
0 8 (15.1) 7 (13.2)
1 16 (30.2) 26 (49.1)
2 16 (30.2) 15 (28.3)
3 5 (9.4) 3 (5.7)
4 8 (15.1) 2 (3.8)
Mean score 1.79 1.38

Overall ratings from the 2001 data were also compared for frequency, management difficulty and severity scores on the CCB. Two-tailed Spearman's correlation coefficient ρ indicated a significant correlation between overall ratings and frequency ratings (ρ=0.331, P<0.05). No significant correlation was found for overall ratings and either management difficulty or severity ratings.

Additional comparisons

We also looked at the 2001 overall ratings in relation to the participants' age, gender, place of residence and level of intellectual disability. These figures are shown in Table 4. Comparison of scores by place of residence and age group both show a significant difference, with those living in the hospital and those aged 59 years and under, recording a higher mean overall rating for psychiatric disorder (for place of residence, those living in specialist provision were placed within the hospital group). No significant differences were found between males and females or levels of intellectual disability.

Table 4 Comparison of cohort characteristics and overall psychiatric rating

Variable Overall rating for psychiatric disorder at 2001 n(mean) Mann—Whitney Utest (two-tailed)
Place of residence Z=-2.77 (P < 0.01)
Community 42 (1.17)
Hospital 11 (2.18)
Age (years) Z=-2.20 (P < 0.05)
≤ 59 35 (1.57)
≥ 60 18 (1.11)
Gender NS
Male 21 (1.48)
Female 32 (1.38)
Level of intellectual disability NS
Severe 26 (1.08)
Profound 18 (1.44)
Not conclusive 9 (2.11)

Finally, we compared the 1975/76 data of those still living with those of the original cohort who are now deceased, in order to examine differences, if any, between these two groups and identify possible mortality trends. As an original cohort of 98, the living and deceased groups were fairly evenly matched. We found no significant differences between groups for overall ratings for psychiatric disorder. Among the deceased group, we did find a significantly lower level of psychiatrist ratings of stereotypy, eye avoidance, elation and overactivity, and a higher level of hostile irritability, but carer ratings showed no differences between the two groups. Our confidence in these differences is therefore limited.

An easier explanation would be that more individuals within the deceased group were of profound intellectual disability, and more were older at the baseline assessment period, which would account quite readily for any differential mortality.

DISCUSSION

The persistence of symptoms and psychiatric disorder

In this study, we were able to show that a high number of behavioural symptoms persisted over a 26-year period, particularly overactivity, which was noted by both psychiatrists and carers to be significantly persistent. This is very much in accordance with clinical experience.

The cohort is clearly showing a similar behaviour pattern at both assessment points on psychiatrist ratings. From 1975/76 to 2001 three symptoms — slow, lability of mood and depressed — show notable increases. The other symptoms are remarkably persistent.

The carer ratings are less robust and can be somewhat misleading at first glance. Only three behaviour ratings were found to be persistent over time and the correlations were fairly weak. Figures from Table 1 (percentages of population showing each behaviour) show some behaviours where, at first glance, a perfect correlation would be expected, for example sleep disturbance. However, although the same number of individuals are showing that behaviour, they are not the same individuals. Careful consideration should therefore be given to dichotomous data such as this, because an exploration of numbers and/or percentages alone may lead to false demonstration of persistence.

It is interesting to note that overall ratings continue to show a high number of behavioural symptoms for the cohort, but the severity of these symptoms has decreased, suggesting that the group has become easier to manage. The high percentage of the cohort that has been relocated to the community supports this suggestion.

Implications for care

Any conclusions drawn from this study about the persistence of symptoms are obviously coloured by the use of older methodologies and definitions in 1975/76. Ways of investigating and measuring behavioural and psychiatric symptoms have improved in the intervening period. The comparison of overall ratings with the CCB, however, does provide a measure of validity between overall ratings and frequency, and this allows us to be more confident in our findings.

It is predictable that individuals with higher levels of challenging behaviour are to be found within the hospital rather than community settings. In this study, individuals resident in hospital show, on average, almost twice as much challenging behaviour as individuals resident in the community. It is also predictable that behavioural symptoms are likely to decrease in severity with age. We found this to be the case, with individuals over 60 years of age being given lower overall ratings for psychiatric disorder. This is not surprising, given the noted increase in mobility problems from 1975/76 to 2001 for the cohort as a whole.

The passage of time

In 1995, the second author concluded by stating that the passage of time was unlikely per se to bring about more than a modest abatement in the disordered behaviour of such a challenging group. This view is supported in this study by the continued persistence of the majority of the symptoms investigated. However, although the passage of time may not have fundamentally changed the behaviour patterns of this population with severe and profound intellectual disability, there has been a reduction in the severity of the symptomatology.

CLINICAL IMPLICATIONS

  1. Challenging behaviour is persistent over time, although its severity diminishes.

  2. The study serves as a baseline against which to assess the impact of treatment procedures.

  3. Severe challenging behaviour is an impediment to successful relocation to the community.

LIMITATIONS

  1. The methodology inevitably draws on an out-of-date protocol.

  2. The study utilised a trained, but different observer on this occasion, although this lent a degree of objectivity and reduced any practice effect.

  3. Carer ratings were less convincing than observer ratings.

APPENDIX

Modified Manifest Abnormality Scale (MMAS; Reference Ballinger, Armstrong and PreslyBallinger et al, 1975)

The following list gives the 19 rating items (in bold) along with their definitions:

Slow, lacking spontaneity and definition

delayed verbal responses, reduced motor activity

Suspicious, defensive

reluctant to respond/refusal/requests to leave interview situation

Histrionic

exaggeration of symptoms for effect/extravagant gestures/grossly manipulative behaviour

Depressed

gloominess/clinically depressed/suicidal

Anxious/agitated

apprehensive/in need of reassurance/inability to relax/motor agitation

Elated/euphoric

cheerful, high spirits/marked elation of mood/infectious laughter and jollity

Flattened, incongruous

lack of emotional tone/impaired or incongruous emotional responses

Delusions/misinterpretations/thought disorder

eccentric beliefs/over-valued ideas/undoubted delusions/complex delusional symptoms

Hallucinations

hypnogogic or eidetic images/false perceptions with or without insight

Excessive concern with bodily functions

over-concerned with health or bodily functions/reluctance to move to other topics

Depressive thoughts

morbid pessimism/feelings of inferiority, shame and guilt/nihilistic delusions

Overactivity

fidgety, restless, pacing, frequent unnecessary movements

Distractibility

stops talking, changes subject/distracted by trivial noises or events outside of room/turns attention to furniture

Stereotypies

constant repetition of movements or postures such as rocking, rubbing, nodding or grimacing

Hostile irritability

uncooperative, irritable, angry, overtly hostile, discontented, haughty, antagonistic

Lability of mood

whether lability of one mood or changing from one mood to another

Pica

eating or attempting to eat substances that are not food

Self-injury

activities that cause or are likely to cause actual bodily harm (e.g. hitting self, biting self, excessive scratching, pulling hair out, striking body on furniture, etc.)/excluding accidents and nailbiting

Eye avoidance

failure to maintain eye contact during interview or failure to establish eye contact at all

Footnotes

Declaration of interest

None.

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Figure 0

Table 1 Carer ratings: baseline and follow-up comparison

Figure 1

Table 2 Psychiatrist ratings: baseline and follow-up comparison

Figure 2

Table 3 Overall psychiatric ratings: baseline and follow-up comparison

Figure 3

Table 4 Comparison of cohort characteristics and overall psychiatric rating

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