What are the benefits?
Publications > Recommended minimum data set > What are the benefits?
- It will enable comparative clinical audit
- Unless we are measuring pre-hospital
care against the same variables it is impossible to draw any
comparison or conclusion and the data again becomes meaningless.
If future collaboration and comparisons are to be made, common data
sets and definitions must be used. Also, in this new age of
clinical governance, collaboration, national service/ performance
frameworks, and benchmarking, it is vital that all data collection is
uniform and accurate i.e. the minimum data set is adopted as common
practice, otherwise poor information will become an excuse for poor
performance and the real reasons for disparities in the provision of
pre-hospital health care will not be uncovered.
As stated previously, the minimum data set is not an audit tool in
itself. However, by adopting the minimum data set robust clinical
audit tools can be developed into which truly comparative information
can be fed and firm conclusions drawn without any disclaimers covering
the quality and definition of the data.
- It will facilitate the implementation of
integrated care pathway's.
- It is equally important that the
collection of this minimum data set goes hand in hand with the
collection of data on patient progress through A&E and beyond.
Only when measurable outcomes can be collected will we be able to
truly evaluate the service we provide in the pre-hospital environment.
We must be able to close the audit loop and evaluate the outcome of
care. This should include common ways of following patients through
the health care system and linking the relevant pre-hospital, hospital
and other health care databases.
- It will focus risk management policies
Clinical governance equates to clinical
responsibility. Taking the example of the Bolam principal - peer
opinion states that if the majority of other processional clinicians
would have done exactly the same under the given circumstances, then
protection for the action is guaranteed. This has relevance to clinical
risk, clinical governance and the closure of the paramedic title.
Through governance, education and the obligation to audit practice, each
individual will be responsible for their actions. It is therefore
vitally important that, to achieve the security of the Bolam principal,
the minimum data set must be recorded to allow for clinical audit and
clinical risk management. This includes the recording of pertinent
negatives (i.e. why something was not done) to ensure all clinical
decisions are documented.
We must therefore, in conjunction
with the minimum data set, collect all data from all patient report
forms (PRF'S) to ensure we know we are doing the right things and
doing the right things right. The minimum data set should be recorded
somewhere and somehow whether on the PRF or elsewhere as long as all
databases are able to be cross-referenced and the data is retrievable.
This will not mean prescriptive PRF designs or
content. Hopefully however, greater collaboration and the adoption of a
common data set with common audit tools will lead to sharing of good
ideas and best practice creating a streamlining of PRF designs.
- It will result in clinically effective
practice.
Without a minimum data set we can't produce a robust evidence base
from which decisions on clinical effectiveness can be based. Only when
true comparisons are made through benchmarking of identical data sets
and definitions can a robust evidence base be built.
Examples:
- South East Ambulances Clinical Audit
Group - Although a regional evidence based protocol was developed
for the treatment of pre-hospital hypoglycaemia, there were several
large obstacles which had to be tackled in order to compare data sets
collected by the seven collaborating services. These included
different standards/ protocols and differing data sets. Some services
had to collect extra data whilst others ignored data they already
collected.
- National Service Frameworks - unless
all UK ambulance services are collecting the same data it would be
impossible to benchmark performance and decide which is the most
clinically effective practice based on the evidence.
- Nationally recommended protocols/
standards - a commonly adopted minimum data set will allow for
direct comparison of which standards/ protocols are effective. Again
benchmarking exercises can highlight good practice and lead to the
development of common standards based on the evidence, with the
minimum data set as their foundation.
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