About You
From concept to implementation,
Dr Iain Carpenter has been closely with the development of MDS
forms for the UK health and care community.
Tell us about your background as a
practitioner and how you came to be interested in
assessment.
From the time I first started as a
consultant geriatrician in Winchester I have always been
interested in what happened to older people before they came
into hospital. I did a project screening people aged 75 and
over, using a very simple questionnaire to detect early
changes in their ability. The idea was that any early change
may indicate problems around the corner. The project was very
successful.
Then I went on to do some work for the NHS
National Casemix Office, looking at a way of identifying the
clinical problems associated with costs of care in older
people. This lead me to read about a system developed in the
United States that dealt with the problems that older people
face. I thought it made very good sense. We ran a validation
project in the early 1990s which again was remarkably
successful, as it showed that you could clearly identify
people with similar conditions who had similar costs of care.
In the course of that work I met a group of people in Italy
who had an interest in this thing called the ‘Minimum Data Set
Resident Assessment Instrument’. They were so enthusiastic
about it that we decided to see if there would be any value in
having an international collaborative project based upon it.
What’s the philosophy behind
MDS?
It’s unique. Professionals base an older
person’s care plans on their assessment of the care need. The
principle behind MDS is that
you do it in a structured way. Expanding on that, the information in an MDS assessment is
put into a structured format. This enables all the benefits of aggregated information
- on outcome, quality of care, cost of care and so on – to
be based solely on a comprehensive assessment carried out for the purposes of caring for the
person who is in front of you.
So how was the MDS originally
developed?
The Minimum Data Set Resident Assessment
Instrument – that’s the MDS for Nursing Home Care - was
originally developed in the United States to improve the
quality of care in their nursing homes. * As evidence showed
that good assessment could drive up the quality of care, a
research group within the United States set about developing a
rigorous system that would not only thoroughly assess need,
but would also assist care planning and improve all round
skills. That took place at the end of the 1980s and it was
introduced in 1992.
The international initiative you
mentioned earlier: was that interRAI?
That’s right. interRAI was formed in
1992, and we immediately recognised that community care was
crucially important in care of older people. We therefore set
about developing the MDS for Home Care. By now interRAI
spanned 20 countries and represented extremely able scientists
and professionals in leading organisations.
We set about the process of identifying
those areas that were important for maintaining older people
as independently as possible in their own homes. This came to
a list of about 36, which we reduced to 30, and shared out
into groups with expertise in specific domains.
We researched the literature and
constructed separate protocols for each domain. These
protocols all have a similar structure: they define the
problem, they give information about the nature of the problem
- why it is important and how common it is, and then offer
more detailed guidance on how to deal with it, either by more
detailed assessment or referral to a specific expert or
specialist advice. We then sent the protocols out for
consultation and review by panels with expertise in those
areas and revised them.
From that process we succeeded in
specifying the minimum set of questions that could identify
whether or not a person had a particular problem, or was at
risk of developing a problem. * Those questions became the
items in the assessment instrument, hence the name ‘Minimum
Data Set’.
The assessment instrument was compiled
in this way, and then rigorously tested for reliability and
validity. To test for reliability, we had different people
assessing the same person to ensure they come up with the same
answer.
To test for validity, we made sure that
what people thought they were assessing was what they actually
were assessing. So now we are confident that there is a highly
systematic scientific basis for these assessment instruments.
What can you tell us about the use
of MDS internationally?
InterRAI now encompasses 29 countries
around the world and the MDS instruments are used widely. Not
only are there instruments for Nursing Home and Community
Care, they also exist for Mental Health, Community Mental
Health, Palliative Care, Post Acute Care and what the North
Americans call Assisted Living.
The Nursing Home assessment is used in
every nursing home in the United States, the majority of the
chronic care hospitals and nursing homes in many of the
territories and provinces in Canada, and every nursing home in
Iceland. Its use is rapidly expanding in Germany, Finland,
Italy, Switzerland and it is being actively evaluated in
several other countries.
The Minimum Data Set for Homecare is
used in most of the territories and provinces in Canada. It
has been adopted voluntarily (as opposed to mandated) in 16
States in the USA, and it is the commonest of 4 recommended
instruments in use in Japan. It is also in use in Hong Kong,
South Korea, Italy, Switzerland and many Scandinavian and
European countries. It is currently being investigated in
Australia and New Zealand for widespread implementation. The
Nursing Home instrument first came into place in 1992 and in
the past 2-3 years has really taken off.
Why is it that the quality of data
gathered using MDS is so good?
Principally because it’s completely
relevant to the task in hand. The information you collect in
the MDS is the only information that you need for the care of
that person. You don’t ask questions just to complete scales
or for administrative purposes.
Also, it is very precise. When people
first see the instrument they are often frightened by the
structure, but very soon they come to recognise how beneficial
it is. It works very well as a basis for discussion between
professionals.
Our research in the United Kingdom shows
if Care Managers use the MDS for Homecare, 95% of all the
items in all the people assessed are completed compared with
40-60% in the current use of assessment instruments. Another
reason is that it is enormously effective for determining the
resident nurse contribution to care for people admitted to
nursing homes, and identifying people who are eligible for NHS
continuing care. We’ve identified these areas as a common
source of conflict between health and social services and a
common source of concern for older people themselves.
MDS is a very objective measure, so it
is a very reliable and fair indicator of these eligibility
levels. On the basis of this information, the professionals
and people for whom they are caring find they can resolve
disagreement and come to a conclusion on appropriate funding
levels with which they are both very happy.
Given the overall context of the
single assessment process, where do you see these assessment
forms being used?
The nice thing about the MDS assessment
instruments is that they really do cover all the important
domains. Because we have a lot of research evidence, we have
also been able to produce evidence-based components of the MDS
for use at different levels of assessment.
This means that the contact assessment
contains the basic information that one would ask about the
person in any case, but only a very small number of questions
that indicate what we call self-reliance. People who are
self-reliant really do not need any further assessment, while
people who are not self-reliant can be referred on for an
overview assessment.
The overview assessment is a very
effective way of gathering the appropriate information that
one would gather in an overview screening process. It also
works very well as an admission assessment, for example: into
intermediate care services. In intermediate care, we found
that the use of the MDS has helped identify the sorts of
people for whom the different forms of intermediate care
service are most appropriate.
We have been able to use them for
evaluating intermediate care and even for determining what
affects hospital bed requirements. In this way the MDS is
useful for the person doing the assessment because it gathers
the information they need, in their discussion with their
patient or client, in order to develop a best care plan for
them. The information from the assessment can then be
aggregated and used to look at outcomes, quality of care
indicators, costs of care and, of course, eligibility for
different levels of care.
The MDS also has a use in working out
the underlying causes for delayed discharges. If people whose
discharges are delayed are assessed using an MDS assessment,
it is possible to identify what sorts or services are the ones
that are consistently causing the delay.
To sum up, the MDS provides an extremely sound evidence base for identifying
who needs specialist or comprehensive assessment, for the provision and valuation of services, and
for determining the cost effectiveness of services. All this can be generated from the routine practice of
health and social care practitioners focussing solely on planning the care of their
client. .
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