Aging with Disability
Increased life
expectancy
Until recently, individuals with a disability
seldom enjoyed the same life expectancy as their
peers without disabilities. Secondary medical
conditions such as respiratory illness, renal
failure, accidents, infections, and depression,
coupled with a general lack of adequate primary
medical care, prevented most persons from
experiencing their true life expectancy. Today,
advances in medicine and rehabilitation have
made the expectation of living to late life
fairly reasonable for most persons, even those
with a significant disability. In fact, aging
with a disability has been described as one of
the most important new developments in
rehabilitation.
Disability changes
over the lifetime
Research on aging with a disability has been
ongoing for only about 15 years, but many new
discoveries have already challenged previously
accepted beliefs. The single most important
finding is that "chronic disability" is not at
all static over the life span. Many, if not
most, persons who live 20+ years with a
disability or who are 40 years of age or older
encounter substantial new medical, functional,
and psycho-social problems that were neither
expected nor planned for at an in earlier age.
Many of these changes are well underway by
middle age; some are even underway by age 30 or
as soon as 10 years after one acquires a
disability. While the exact causes of this
"premature aging" are unknown, the following
discussion shows that persons with disability do
not age in a typical matter.
The phenomenon of
aging.
To the gerontologist, the term aging refers to
the natural progression of biological,
psychological and social functioning after the
point of maximum development (Birren and Schaie,
1985). The goal of aging research is to gain
understanding and control of the genetic,
environmental, health, and lifestyle variables
that affect the processes of aging so that each
person can live a quality life for the maximum
number of years. Aging is not the same as being
aged. Biological aging actually begins when a
person is about 25 years of age. By then, organ
systems begin to lose 1% of their function per
year. The significance of this is that research
on aging must begin with people who are still in
their 20's. Traditionally, gerontologists
distinguish three kinds of aging: biological,
psychological and social. Biological capacity
peaks earliest, and then slowly begins to
decline. Despite this decline, physical
illnesses do not show a rapid increase in
prevalence until after age 70 because all organ
systems have large reserve capacities.
Psychological maturity reaches a peak at about
age 35 as measured by learning ability,
intelligence, creativity and skilled
performance. Psychological aging declines at a
slower rate than physical aging because people
learn compensatory abilities. Social maturity
peaks last, about 55 years of age as measured by
income, number of important social roles and
career advancement. Normally, individuals can
maintain social roles well into their 70's and
80's. Decades of studies on normal aging (such
as the Baltimore Longitudinal Studies) have
provided baseline data on physical,
psychological and social aging that are helpful
for gauging both normal and atypical aging
patterns, such as among people with disability.
Medical problems
Whereas typical aging is not accompanied by a
high rate of medical and functional problems
until after 70-75 years of age, people with
disability show these higher rates 20-25 years
sooner. People with disabilities also have 3 to
4 times the number of secondary health problems
compared to their age-matched peers without
disabilities. In fact,
-
Rates of respiratory illnesses are four times
higher in persons with post-polio syndrome;
-
Diabetes is five to six times higher in many
disability groups;
- Cardiovascular disease is the second leading
cause of death in persons with spinal cord
injury;
-
Fractures are five times more common in persons
aging with cerebral palsy, and
-
Osteoporosis affects nearly 70% of people with
disability whose mobility is affected by
disability.
Other problems with especially high rates
include hypertension, pressure sores, high
cholesterol, obesity, heart disease, diabetes,
respiratory illness and osteoporosis Reasons for
these conditions are not yet well understood;
they are probably multi-factorial and act
together. A person acquiring a disability early
in life may have reduced reserve capacity in one
or more organ systems. Combined with normal
aging, more illnesses may then occur.
Some
problems may be linked to widespread changes in
physiology. For example, cholesterol levels of
persons with spinal cord injury are abnormal at
an early age (Bauman and Spungen, 1996) and
persons with polio who develop post-polio
syndrome have higher numbers with elevated
cholesterol compared to persons with polio who
stay ambulatory or compared to a nondisabled
controls (Kemp and Campbell, 1993).
Orthopedic
problems that produce severe consequences for
daily functioning and quality of life include
bone loss, fractures, dislocations, rotator cuff
injuries, scoliosis and over-use syndrome
(Murphy et al., 1995; Sie et al., 1992; Waters
et al., 1995; Garland et al., 1993). Orthopedic
problems arise because of excess wear and tear
(due to compensations for postural or ambulatory
effects of disability, accidents, deconditioning
and metabolic conditions (e.g., osteoporosis).
Functional problems.
The early onset of new functional problems
impacts Activities of Daily Living (mobility,
dressing, toileting, etc.), Instrumental
Activities of Daily Living (IADLs) (shopping,
transportation, money management, etc.), work
and recreation. Such changes are common to
many, if not most, persons aging with
disability, regardless of the original
disability. These problems often begin with
loss of strength, endurance and range of motion,
along with increased pain. This complex of
symptoms may be the most characteristic
age-associated functional change with age.
This complex, together with decreased function
constitute "post-polio syndrome," affecting up
to 80% of people with a history of polio
(Halstead, 1991) However, this complex also
affects others and it is becoming increasingly
likely that this may constitute a
"post-disability syndrome" common among many
impairment groups. For example, Gerhart et al.,
(1993) found that approximately one-third of
persons aging with spinal cord injury in England
underwent such changes. Kemp and Thompson
(1997) studied 150 persons from a United States
Spinal Cord Injury Center and found that 26% of
those who had durations of five years or more
reported changes in function, most often
beginning with excess fatigue.
Similar results
have been found in persons with cerebral palsy
(Murphy et al., 1995) and rheumatoid arthritis
(Campbell et al., 1998). A recent study by
Olsen and Hutchings (1998) demonstrated that the
physical nature of a disability is the key
factor in these changes. In their study,
persons aging with mental retardation had far
fewer of these functional changes compared to
persons aging with physical disabilities.
Employment seems to be a
functional activity especially vulnerable to the
effects of aging. Because employment is such a
valued and important activity, many persons
aging with disability who experience problems
with fatigue, pain and weakness try to maintain
work roles above all else. Our studies indicate
that individuals decrease recreation, get more
help with IADLs, and try to get more rest in
order to preserve their work capacity.
However,
these efforts may not suffice. In a recent
study conducted at the Rehabilitation Research
and Training Center on Aging with Disability at
Rancho Los Amigos Medical Center, McNeal,
Somerville, and Wilson (1996) found that over
50% of persons with polio had to adjust work
roles, reduce effort and hours, or else retire
altogether by the age of 50 because of these
problems. Over one-third of persons with spinal
cord injury showed similar results;
however, the
persons with spinal cord injury were 10 years
younger on average than the persons with polio
and they may eventually reach the same degree of
change.
To summarize, as persons
with disability begin to reach age 50, many show
the kind of functional changes that would not be
expected until age 70-75 in people without
disabilities. It is not yet clear whether this
"aging gap" is independent of the medical
problems discussed earlier or is somehow related
to them. However, what is clear is that
service providers need to learn more about these
recent discoveries in order to better plan and
provide services.
Psychosocial changes
Psychosocial changes are important not only
because they affect individuals who are aging,
but also involve their families. Quality of
life (QOL) is negatively affected by age-related
changes in function and health. Gerhart, et.
al. (1993) found that persons with spinal cord
injury who had decreased function rated their
lives as less satisfying than persons who had
not changed function.
Krause (1990) had earlier
shown that life satisfaction normally increases
as one ages with a disability as long as major
functional changes do not occur. Similarly,
Fuhrer et al., (1992) and Dijkers (1996) showed
that life satisfaction was only slightly lower
among persons with a disability compared to
people without disabilities, and what
differences did exist were due to health,
mobility, work and social problems. In addition
to lower QOL, decline in health and functioning
often result in psychological distress or
depression.
Overall rates of depressive
disorder are 2-3 times higher among persons
aging with disability compared to age-matched
non-disabled persons (Fuhrer et al., 1993; McColl and Rosenthal, 1994; Kemp et al., 1997).
This finding is of major importance because
depression itself is a disabling condition and
in conjunction with a physical disability can
cause excessive health, functional and family
problems. Contrary to popular belief though,
depression is not a "natural" consequence of
disability or age and does not correlate with
the severity of impairment, or even with the
level of disability (Fuhrer et al., 1993;
Reinhardt, 1996; Tate, et. al., 1994; McColl
and Rosenthal, 1994). However, it does
correlate with difficulty coping with changes in
health, function and social roles that accompany
age.
Kemp, Adams and Campbell et. al. (1997)
found that among persons aging with polio,
depression scores were higher only if
individuals had more post-polio changes and/or
had poor family cohesion. Hansen et al., (1998)
recently showed that poor coping in the form of
using escape-avoidance techniques was related to
poorer psychological outcomes.
The impact of health and
functional changes on the family is equally
important. As changes in ability occur in the
person with disability, families are usually the
first one called upon to provide increased
assistance. However, this may not be something
families are ready for or capable of doing.
Recent reports indicate that families experience
worry and stress, including individuals with
mental retardation (Heller and Factor, 1991) or
physical disabilities (Holicky, 1996). Richards
and Shewchuck (1996) reported that spouses
actually had higher average depression scores
than the individuals who had a disability.
McColl and Rosenthal (1994) found that family
support was highly correlated with both
depression (a negative correlation) and with
life-satisfaction (a positive correlation) among
persons aging with disability. Therefore,
quality of life, depression and personal
assistance/caregiving issues are all related to
and impacted by physical and functional changes
affecting persons aging with disability.
Possible Causes.
The age-related problems described above are not
yet well understood. We do not yet have
sufficient data to know the eventual course of
aging with a disability, how these changes may
vary by such factors as gender or ethnicity, nor
do we yet fully understand the causes of these
problems. At least five hypotheses have been
proposed in the literature to explain these
changes, and more than one may be correct.
1. Accelerated biological aging processes. Is
there something inherent in disability that
alters the course or rate of aging at the
cellular or organ system level?
2.
Wear and Tear. Does living with a disability
for a long period of time place increased stress
on the body?
3.
The era of onset. Is the critical variable
really when the person became disabled? People
with disabilities of 20, 25, and 30 years
duration received rehabilitation in a different
era. Medical and rehabilitation care,
technology, and social factors have changed
markedly over the years. Are the problems
observed today caused by the care that was given
then?
4.
Latent illness. Does a major impairment like
polio or cerebral palsy start a cascade of
metabolic changes at culminate in a variety of
illnesses that were not diagnosed in earlier
decades because people didn't live long enough
to develop them?
5. Environmental causes. Are excess disability and
health problems due to living for years in an
unaccommodating, disability-causing environment?
The RRTC on Aging with a Disability approach to
the research program. These are complex issues
and testing hypotheses like these require
sophisticated research designs and large
samples, both of which we will provide.
Moreover, understanding the causes of these
problems is not enough. It is time to test
interventions and to disseminate current
information.
Our research has two goals:
1) to
conduct studies that further basic knowledge
about the natural course of aging.
2) to
test interventions designed to help alleviate
the problems found in persons aging with
disability.
Our strategy for the first goal is
to conduct the largest cross-disability
longitudinal study of people aging with
disability to date. To do this, we will use the
1,000+ person database we compiled from earlier
research. This database includes persons with
cerebral palsy, polio, spinal cord injury,
rheumatoid arthritis, stroke and also a control
group without disability.