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Letters to the Editor
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Patient safety
Auditing medication practice
From Professor D. H. Cousins, MRPharmS
I write in response to Brian Hebron’s article entitled “Audits:
pitfalls and good practice” (PJ, 1 March 2008, p250).
Recognising time and resource constraints that NHS organisations face
the National
Patient
Safety Agency took a pragmatic approach in designing our audit forms.
We did not include the need to calculate sample size or confidence intervals.
Denominator data, such as the total number of patients started on anticoagulants,
or children treated with hypotonic infusions, are not easily found in most
organisations and would have been a barrier to audit. The NPSA identified more
straightforward organisational and observational measures to provide meaningful
information on the implementation of safe medication recommendations.
Over time healthcare organisations and researchers can refine audit methodology,
including the use of statistical methods, to provide increased levels of information
and, hopefully, produce audit reports for journal publications on the management
of medication risks in the NHS.
As regards warfarin regimens and strength of tablets used, the NPSA does not
recommend changing the warfarin tablet strengths for patients who are stable
and coping well with their regimens. Where patients are having difficulties
or where difficulties can be anticipated (eg, taking large numbers of tablets
each day, alternate day dosing, or having to split tablets), then therapeutic
practice should be flexible.
Allowing the use of the most appropriate tablet
strengths and constant daily dosing regimens will better meet individual
patients’ needs. David Cousins
Head of Safe Medication Practice,
National Patient Safety Agency |