A spoonfull of sugar
medicines management in NHS hospitals
The Audit Commission promotes the best use of
public money by ensuring the proper stewardship of public
finances and by helping those responsible for public services to
achieve economy, efficiency and effectiveness.
The Commission was established in 1983 to appoint and regulate the
external auditors of local authorities in England and Wales. In 1990 its role
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Sir Andrew Foster, Controller, The Audit Commission,
1 Vincent Square, London SW1P 2PN, Tel: 020 7828 1212
Optimising the use of medicines hospitals is central to the quality of
patient care in hospitals.
Expenditure on medicines is rising as new therapies are developed
and as more patients are being treated.
Strategic Challenges
Hospitals face several challenges in optimising the use of medicines.
Obstacles to Progress and How to
In order to meet the strategic challenges presented by the medicines
management agenda, hospitals need to elevate the status of some
pharmacy services
Urgent action and investment are needed in many hospitals to bring
medicines management arrangements up to the level of the best.
The Way Forward
5 The NHS Plan
What should trust boards do?
1 Why has this report been
The DoH medicines
Local audits
Why trust boards should review
medicines management now
Appendix 1
3 Linking medicines management
Appendix 2
to clinical governance
External advisors and study
methodology
Forming effective relationships
with primary care
Obstacles to Progress and
How to Overcome Them
The status of pharmacy services 44
Staffing 46
Audit Commission 2001
First published in December 2001 by the Audit Commission for Local Authorities
and the National Health Service in England and Wales, 1 Vincent Square,
Typeset by Eighteeno4 Design, Woodbridge, Suffolk
Printed in the UK for the Audit Commission by Holbrooks Printers, Portsmouth
ISBN 1 86240 321 X
David Campione/Science Photo Library (cover), Jacky Chapman/Format (pp 3, 7,
8), Steve Horrell/Science Photo Library (p 4), Adam Hart-Davis/Science Photo
Library (p 11), Thierry Dosogne/The Image Bank (p 13), Steve McAllister/The
Image Bank (pp 36, 47), Steve Taylor/Stone (p 38), David Mansell (p 42),
SF/Medipics (p 43), Simon Fraser/Science Photo Library (p 45), Royal
Pharmaceutical Society of Great Britain (p 56), Oscar Burriell/Science Photo
Preface
The Audit Commission has been responsible for the external audit of
local authorities in England and Wales since 1983, and in 1990 it
assumed responsibility for auditing the NHS. As well as reviewing the
financial accounts of local government and health service bodies, the
Commission's auditors have a statutory duty to examine the economy,
efficiency and effectiveness of the use of resources. The Commission aims
to help those who manage and work in local authorities and the NHS to
deliver the best possible services with the money that is available so that
public expenditure makes the maximum contribution to society.
This report seeks to emphasise to NHS trust boards the importance ofmedicines management as a very significant part of their clinicalgovernance responsibilities. It is one of a number of complementaryinitiatives seeking to raise the profile of medicines management:
in 1999, the Department of Health (DoH) introduced the ControlsAssurance Framework, which includes a section devoted to reducingthe risk involved in the use of medicines (Ref. 1);
in 2000/01, hospitals in England have assessed their services againstthe DoH's Medicines Management Framework, which has highlightedpriority action areas (Ref. 2);
in concert with this exercise, the Audit Commission is currentlycollecting baseline data about medicines management arrangements,which will enable local auditors to work with hospitals, and withchief pharmacists in particular, to improve services;
the Audit Commission will work with chief pharmacists' groupsto interpret and analyse these data; and
in 2002, the Audit Commission will produce an internet site toprovide guidance on the self-administration of medicines by hospitalpatients.
This report, and the associated audit guide, data collection and training,was prepared by Michael Yeats, Ian Jones, Amy Kerbel, Emma Cox, andNick Mapstone with direction from Jonathan Boyce.
A number of individuals have provided support and guidance to the studyteam as the work has developed. They are listed in Appendix 1, togetherwith the organisations visited and the underlying study methodology. TheCommission is very grateful for their contribution though, as always,responsibility for the findings and conclusions of the study rests with theCommission alone.
Optimising the use of medicines hospitals is central to the
quality of patient care in hospitals. But many hospitals face
significant service pressures that prevent them improving
the quality of care given to patients.
A hospital patient discusses her medication with the healthcare teamon their ward round. The pharmacist team-member explains proposedchanges to the medication, which the patient will administer herself.
The pharmacist also discusses learning points with other team members.
New medication is agreed between members of the clinical team andordered at the bedside though a radio computer link to an automateddispensary, where robotic systems pick the new medicines and dispatchthem to the patient's ward via a pneumatic tube.
Computer technology updates the electronic patient record, to which thepatient's GP has access. The medication that has been issued issimultaneously recorded to update stock records and order fresh supplies.
The scenario described above is not necessarily a fanciful vision. The
best hospitals in the UK are only a few steps away from working like this.
But for many, the vision is a pipe-dream. In these hospitals, many aspectsof medicines management arrangements and practice remain rooted in the1970s. But 30 years ago, the pace of life was slower – the average lengthof stay in hospital was 15 days and bed occupancy ran at 70 per cent.
Today, average lengths of stay are less than seven days; bed occupancy
runs at over 95 per cent in some hospitals; patients are more chronicallyill; and are more likely to be transferred between wards. The increasedpace and complexity of work means that the use of medicines is notalways managed to best effect.
Workload pressures are mounting at a time when medicines are
becoming ever-more powerful and complex. This means that the risk ofmedication errors is increasing, and there are longer delays in supplyingmedicines. This scenario increases staff stress and turnover, creating adownward spiral that makes significant service improvement a challengetoo far.
Great strides are needed to make medicines management practice in
all UK hospitals match the level of the best. A definition of medicinesmanagement illustrates the extensive and inclusive nature of the agenda
Medicines management defined
Medicines management in hospitals encompasses the entire way that
medicines are selected, procured, delivered, prescribed, administered and
reviewed to optimise the contribution that medicines make to producing
informed and desired outcomes of patient care.
Source: Audit Commission
There are some important obstacles to improving medicines
management arrangements:
many boards are concerned with short-term financial targets and are
many of the specific
unwilling or unable to invest money to achieve sustainable qualityand cost improvements;
objectives that are set
there are serious recruitment and retention problems in some hospital
out in the NHS Plan
pharmacy services;
and Improving Health
some pharmacists are content with their traditional dispensing andmonitoring functions – the word ‘pharmacy' conjures up in their
minds a room in a hospital, not a patient-centred service where thepharmacist is a key member of the clinical team; and
some doctors and nurses have neither the will nor the incentives tochange traditional ways of working.
But the status quo is unsustainable:
hospital medication errors are unacceptably common;
the efficacy of medicines is increasing, but costs are rising;
the complexity of ensuring the safe use of new medicines is growing;and
there is an urgent need to review medicines management across wholehealth economies, as the distinction between primary and secondarycare becomes increasingly blurred.
Moreover, improved medicines management underpins many of the
specific objectives that are set out in the NHS Plan and Improving Healthin Wales (Refs. 3 and 4). For example, these include:
providing new mechanisms to satisfy patients that the care they get isquality assured;
reducing the ‘postcode lottery' in the prescribing of anti-cancermedicines;
establishing rapid access to chest-pain clinics;
ensuring that mental health teams provide an immediate response tocrises; and
reducing the number of patients who are dying or being paralysedfrom accidents involving spinal injections.
Why has this report
This report has important strategic recommendations for the DoH
and the National Assembly for Wales (the National Assembly). But it is
primarily aimed at board members of NHS trusts, and concentrates onthe issues that they have to address. It has two aims:
to raise the profile of medicines management in hospitals; and
to make the case for providing adequate investment to enablestandards to be raised.
All members of the clinical team need to work together to manage
medicines effectively. Non-clinical staff too have to ensure effectivefinancial management, procurement and logistics. But before they cansucceed, there are systemic and resource issues that boards must address.
The strategic challenges facing boards are described, together with
the main obstacles and possible solutions. They should use this reportto identify how well their hospital manages medicines, what the mostimportant local priorities are, and how to deliver them.
Expenditure on medicines is rising as new therapies are
developed and as more patients are being treated. These cost
pressures need to be viewed as part of the overall package of
patient care – for some conditions, medicines expenditure
should be rising because an increase in spending
provides a cost-effective way of increasing
health gain for the population.
Medicines management is central to the quality of healthcare.
Nearly all patients are given medication as a result of a visit to hospital –7,000 individual doses are administered daily in a ‘typical' hospital; andup to 40 per cent of nurses' time is spent administering medicines.
In 1999/2000, NHS hospitals spent over £1.5 billion on medicines,
which accounted for 4.6 per cent of their costs. In addition, pharmacystaff cost £300 million a year.
Relative spending on hospital medicines has risen over the last ten
years, and in the last five it has outstripped growth in primary care
medicines expenditure [EXHIBIT 1].
Expenditure is rising because:
new, more expensive therapies are always being developed;
more patients are being treated;
the population is ageing and has more chronic illness; and
medicines are being used in preference to invasive treatments.
Cash outturn £m
Percentage of total NHS medicines spend by hospitals
NHS expenditure on medicines by
hospitals and its contribution to
total NHS medicines expenditure
Spending on medicines rose sharply
over the last ten years, and in the last
five years it accounted for a steadily
increasing percentage of totalexpenditure on medicines.
1990–91 1991–92 1992–93 1993–94 1994–95 1995–96 1996–97 1997–98 1998–991999–2000
Hospital and community health
Hospital spend as a percentage
services cash outturn
Source: Audit Commission analysis of dataobtained from the DoH
There are, of course, differences in the relative amount of money that
For some conditions,
hospitals spend on medicines. But even after accounting for differences in
activity, there remains a significant variation between similar hospitals
should be rising
in the proportion of their non-pay expenditure on medicines [EXHIBIT 2].
because it would be a
It is not known how much of the variation is explained by differences
in the age and medical condition of the patients treated because:
cost-effective way of
hospitals use different descriptions of medicines;
increasing health
hospitals do not use a common coding system;
gain for the
medicines are commonly used to treat multiple conditions; and
there are no nationally accepted ways of aggregating data to accountfor differences in the age or illness of the patients treated.
What is clear, however, is that some hospitals are experiencing
significant increases in their medicines expenditure [EXHIBIT 3]. In recent
years, these cost pressures have been driven by the introduction of new
medicines to treat cancer, heart disease, arthritis, and a range of
psychiatric conditions. In London alone, expenditure on anti-retroviral
medicines for the treatment of AIDS/HIV has risen to £51 million – over
one-sixth of the total expenditure on medicines by London hospitals.
These cost pressures are cause for concern for many trust boards, but
they need to be viewed as part of the overall package of patient care. Forsome conditions, medicines expenditure should be rising because it wouldbe a cost-effective way of increasing health gain for the population. Forexample, expenditure on proton pump inhibitors and H2 antagonistsshould be rising because their use improves the quality of patients'lives and saves money by preventing invasive surgery.
Percentage of non-pay spend on medicines
Proportionate expenditure on
medicines
There is a two-fold variation between
similar trusts' standardisedexpenditure on medicines.
Source: Audit Commission analysis of
1999/2000 TFR3 data
Percentage increase in medicines expenditure 1998/99 to 2000/01
Average increases in medicines
expenditure over the last three
Some trusts have experiencedsignificant increases in medicines
Source: Audit Commission acute hospitals
portfolio data
Why trust boards
It is timely for trust boards to review medicines management
arrangements because:
The DoH's report, An Organisation with a Memory, found that10,000 hospital patients each year have serious adverse reactions to
medicines, and one-fifth of clinical negligence litigation stems fromhospital medication errors (Ref. 5). The Chief Medical Officer has settrusts a target to reduce serious medication errors by 40 per centby 2005 (Ref. 6).
Spending on medicines has been identified as a key area forexamination by the government's efficiency task force. In response,the DoH has produced a Medicines Management Framework thatwill be applied to all acute trusts, with reports being made toregional directors of performance review (Ref. 2).
The report of the Task and Finish Group for Prescribing in Walesto the the National Assembly seeks to ‘assure high standards in theclinical care of patients and to enhance professional fulfilment inthose concerned with patients through the prescribing ofmedicines' (Ref. 7).
Medicines management is an important part of the DoH's ControlsAssurance Framework, which seeks to manage risk (Ref. 1).
The recent review of NHS procurement requires all boards to agreea written procurement strategy that includes medicines, as a majorexpenditure item (Ref. 8).
New money was announced in the NHS Plan explicitly to improveIT expertise and capacity (Ref. 3). High priority needs to be given toelectronic patient records and to electronic prescribing, which shouldprovide significant understanding of the effectiveness of medicinesand help to track patients between hospital and primary care.
The NHS Plan also states that by 2004 over one-half of the nursingworkforce, together with pharmacists and allied health professionals,will be able to supply medicines (Ref. 3). This is a major change forwhich trust boards need to prepare.
In September 2000, the DoH published Pharmacy in the Future –Implementing the NHS Plan, which set out a programme forpharmacy services (Ref. 9). It says that hospital pharmacists will‘ensure that inpatients' medication is got right early in their stay andthat they have the medicines they need as soon as they are ready tobe discharged.'
The National Service Framework for Older People emphasises the
importance of medicines management arrangements (Ref. 10) [BOX B].
National Service Framework for Older People – the relevance of medicines
As people get older, their use of medication tends to increase. Four in
5 people over 75 take at least 1 prescribed medicine, with 36 per cent
taking 4 or more medicines (Ref. 11).
The ageing process affects the body's capacity to handle medicines.
Multiple diseases and complicated medication regimes may affect the
patients' capacity and ability to manage their own medication regime.
Adverse reactions are implicated in 5 per cent to 17 per cent of hospital
admissions of older people (Refs. 12 and 13).
While in hospital, 6 per cent to 17 per cent of older inpatients
experience adverse drug reactions (Ref. 14).
As many as 50 per cent of older people do not take their medication
as intended (Ref. 15).
Unintentional changes in medication after discharge from hospital
happen too frequently (Ref. 16).
There is often poor communication between hospital and primary care
and vice-versa. Communication needs to be improved to reduce delay in
the transfer of medication recommendations to primary care; to ensure
treatment that was only intended as short-term, while in hospital, is
discontinued on discharge; and to improve explanations of medication
changes. In primary care, the interpretation and actioning of discharge
medication histories is not always optimal (Ref. 17).
Older people who are taking four or more medicines have an increased
risk of suffering an adverse reaction to a medicine and being
readmitted to hospital as a result (Refs. 18 and 19).
The National Service Framework for Older People states that by 2002,
all hospitals should have one-stop dispensing or dispensing for
discharge schemes and, where appropriate, self-administration
schemes for medicines for older people (Ref. 10).
Hospitals face several challenges in optimising the use of
medicines. They need to link medicines management to
clinical governance and, in particular, introduce processes
to reduce risk and the number of medication errors.
Hospitals must also manage medicines across their local
health economies and work with commissioners and
primary care to improve financial planning.
There are four strategic challenges facing hospitals in relation to
linking medicines management to clinical governance;
forming effective relationships with primary care; and
improving financial planning.
The role of the trust board in medicines
Under the 1999 Health Act, boards must assure the quality of patient
care (Ref. 20). Their clinical governance development plans need to containspecific arrangements to implement quality assurance and monitoringmeasures for key activities, such as medicines management. Thesearrangements should supplement and deepen existing professionaland statutory controls.
Shortcomings in medicines management arrangements are evident
in many hospitals:
Pharmacy services have traditionally established quality controlmechanisms, such as prescription monitoring, but these can fall shortof the ideal – medicines management now needs to be developed tofit into an overall structure for clinical governance.
Only 11 out of 105 hospital consultants surveyed in 4 hospitalsvisited reported that reviews of the use of medicines fed into widerclinical audit work and their clinical governance agendas.
Reviews of board meetings' minutes show that many have notconsidered important aspects of medicines management. A commonresponse is that medicines management is the responsibility of Drugsand Therapeutics Committees (DTCs). However, analysis of theiractivities shows that there are not always systematic reviews of thecost and efficacy of the most significant medicine categories.
Individual consultants' clinical freedom still takes precedence overcorporate clinical responsibility, and prescribing practice is seldomreviewed systematically. Only 9 of 105 consultants surveyed reportedthat prescribing practice formed part of their regular performancereview meetings with clinical directors.
Information systems have shortcomings: only 17 of 105 consultantssurveyed felt that they receive adequate information about how theirprescribing practice compares with colleagues in their specialty. Mostdata that are available relate to the cost of medicines, without properconsideration of their efficacy or health outcomes.
These findings suggest that some trust boards are neglecting an
important aspect of their clinical governance duties. As a starting point,they should use the DoH's Medicines Management Framework inconjunction with the Audit Commission's diagnostic to monitormedicines management arrangements and develop local action plans
[BOX C] (Ref. 2).I
Board-level involvement in medicines management can reduce costs
as well as improve quality [CASE STUDY 1, overleaf].
Quality standards and targets for medicines management
Is there effective
Relative expenditure changes
by BNF formulary chapter
Pharmacy service staff
numbers, cost and skill mix
Is staffing adequate for
the services that
should be provided?
Hospital activity per member
of pharmacy staff
Does the trust
Costed staff activity in
provide an
Amount of time spent
on clinical pharmacy
Do pharmacy staff
devote enough time
to direct patient care?
Use of original packs
introduced processes
in line with accepted
Use of joint formularies
Source: Audit Commission
Medicines management is included in the Audit Commission's Acute Hospitals Portfolio –data from all acute trusts on each area referred to in Box C will be collected during2001. The data will be analysed and the results reported to trusts as part of the 2001/02audit programme.
CASE STUDY 1
North Staffordshire Hospitals NHS Trust – medicines management
To encourage all clinical directorates to focus on prescribing issues, a series
of reports are presented quarterly to the board. They include a summary
table showing the medicine budgets and actual expenditure for the trust as
a whole and for each directorate.
A narrative reporting the recent decisions of the DTC and the Medicines
Management Group, as well as identifying key prescribing issues in each
directorate, supplements this financial information.
Prescribing is also made a regular feature of performance review meetings
between the chief executive and clinical directors.
Better use of medicines has been demonstrated by these actions, and
savings have resulted (see Exhibit 11.)
Source: Audit Commission study site
The role of the Drugs and Therapeutics
Committee
.establishing an agreed
A process of establishing an agreed formulary is the cornerstone of
effective medicines management. There are a number of quality and cost
formulary is the
consequences if formularies are not developed:
cornerstone of
greater diversity of prescribing practice resulting in an increased risk
of medication errors;
higher medicine costs;
an increased chance of medicines being out of stock;
a greater risk of passing medicine expiry dates; and
higher administrative costs because more lines have to be ordered.
An effective DTC will help to ensure that:
national and locally agreed treatment guidelines are adhered to;
therapeutic categories with high-risk, high-volume or expensivemedicines are regularly reviewed;
non-formulary medicines are not routinely stocked;
prescribers are monitored for excessive use of non-formularymedicines;
the formulary is evaluated periodically for ineffective and obsoletemedicines; and
the quality and cost impact of new medicines is always assessed.
In the more progressive hospitals the role of the DTC is developing.
A criticism of the traditional formulary is that it is simply a list ofmedicines: the formulary only becomes a live operational documentonce the medicines are tied to a diagnosis.
Chief executives and medical directors should make the DTC at their
trust accountable to the trust board for the introduction of evidence-based formularies which are linked to clinical and National Institute forClinical Excellence (NICE) guidelines. These should describe howcommon conditions are to be treated, including the medicines to be used.
To ensure the best treatment for patients, the information is best stored inelectronic format so that it is available at the time that prescribingdecisions are made.
These systems will become more important with the growth of
prescribing by nurses and other healthcare professionals. The Governmenthas announced that £10 million has been allocated from 2001 to 2004to train 10,000 nurses (in primary care and in hospitals) to prescribemedicines independently for common conditions in the areas of minorailments, minor injuries, health promotion and palliative care.
DTCs also have a strategic role in monitoring prescribing practice.
While detailed analysis is in the domain of clinical audit, the DTC shouldanalyse data on medicines use at an aggregate level, both over time andin comparison to similar hospitals. For example, DTCs might monitoraspects of the hospital's practice with regard to the prescription ofantibiotics, an area where there is wide variation between similar trusts
[EXHIBIT 4]. Analysis of this sort could generate reviews of local practice.I
High levels of use of antibiotics may not necessarily be ‘bad' – it could indicate asuccessful policy of discharging those patients who can take antibiotics orally.
Percentage expenditure on oral vs IV antibiotics
Comparison of hospitals'
expenditure on antibiotics
administered orally vs.
There is wide variation betweensimilar trusts in the use of oral vs.
Source: Audit Commission study sites
DTCs will increasingly become involved in whole health economy
prescribing practice. This development is foreshadowed by the proposalin the Task and Finish Group in Wales that more of DTCs' responsibilitiesshould be devolved to local health groups (LHGs) (Ref. 7).
A serious problem?
Linking medicines management to clinical governance will help to
assure effective clinical practice, and minimise the risk of medication
errors,I which are an important cause of morbidity in hospitals [BOX D]
(Refs. 21, 22, 23, 24). They account for about one-fifth of deaths due to all
types of adverse event in hospital and are also an increasingly common
stimulus to litigation (Ref. 25).II
In the USA, the number of deaths because of medication errors and
the adverse effects of medicines used in hospitals increased from 2,876 in
1983 to 7,391 in 1993 (Ref. 24). There is also evidence of an upward trend
in the UK [EXHIBIT 5]). Such trends may be due to the increasing pace of
work in hospitals and to the greater toxicity of modern medicines. During
2001, the DoH has had to publish guidance on preventing medication
errors involving spinal injections, in response to a high profile incident
(Refs. 28 and 29).
Although much of the academic literature on this subject comes from
overseas, it is now accepted that these findings can be transferred to theNHS (Ref. 30). It is recognised that medication errors alone cost the NHSabout £500 million a year in additional days spent in hospital (Ref. 6).
However, the true extent of medication errors is unknown because of
inadequate definitions and different reporting arrangements. Only onehospital visited had a comprehensive error and near-miss reportingsystem in place.
A medication error may be defined as ‘.any preventable event that may cause or leadto inappropriate medication use or patient harm, while the medication is in the controlof the health care professional, patient, or consumer. Such events may be related toprofessional practice, health care products, procedures, and systems including:prescribing; order communication; product labelling, packaging and nomenclature;compounding; dispensing; distribution; administration; education; monitoring; and use'.
Medical Defence Union data show that one-quarter of all indemnity paid out followinglitigation claims after adverse events in general practice results from medication errors.
Their contribution to adverse events in hospital is not known but is unlikely to be smaller,in view of the scale and complexity of hospital medicines prescribing. Litigation claimscost the NHS £400 million in 1998/99.
Evidence of adverse events in hospitals
From the USA
From the UK
Examples of errors at one hospital
Incidence of iatrogenic disease
10.8 per cent of patients on
A patient on the anti-cancer
is 4 per cent or 1 million cases
medical wards experience an
medicine tamoxifen was
per year in the USAI
adverse event, 46 per cent of
prescribed the sleeping tablet
There are four times as many
which were judged to be
temazepam instead
deaths from iatrogenic disease
A contraceptive steroid was
(180,000 a year) as from road
One-third lead to greater
prescribed instead of an anti-
traffic accidents (45,000)
morbidity or death
psychotic injection
Over 69 per cent of iatrogenic
Each event leads to an average
A toxic medicine to be given
accidents were considered
of 8.5 additional days in
weekly was prescribed daily
An anti-cancer medicine was
20 per cent of adverse events
If the data from the sample
prescribed at 1,000 times the
were related to medicines use
trusts are representative and
extrapolated across the NHS,
this costs the NHS £1.1 billion
12 per cent of adverse events
were related to medicines use
Source: Ref. 26
Source: Ref. 27
Source: Clinical audit review at one studysite
Iatrogenic disease is that caused by a clinician's intervention.
Number of deaths
The number of deaths in England
and Wales from medication errors
and the adverse effects of
medicines, 1990 to 2000
The number of reported deaths shows
an upward trend.
Medication errors
Adverse effects of medicines in therapeutic use
Source: ICD9 and ICD10 data
The DoH's proposals to address these issues centre upon the
establishment of the National Patient Safety Agency. The establishmentof standard nation-wide definitions and categories of medication errorsand ‘near-misses' should be an early priority for the Agency. Trustsshould be required to adopt such systems as part of their clinicalgovernance arrangements and report progress in their annual reports, aswell as reporting along the lines proposed in Building a Safer NHS (Ref. 6).
Following agreement of standard definitions and categories of
medication errors, baseline audits should be undertaken with centralfunding at a representative sample of hospitals. This will calibrate thecurrent situation in order that improvement targets can be set and theirachievement monitored. Work should prioritise specialties or areas withthe highest likely risk (for example, ITUs, paediatrics, antibiotics, andnutrition).
The pharmacist's role in reducing medication
errors
Pharmacists have traditionally had an important quality control
role in checking patients' medication. Typically, between one-fifth and
one-quarter of inpatient prescription charts are amended by pharmacists
for a variety of reasons that reflect shortcomings in the basic rules for
safe prescribing [EXHIBIT 6].
Nature of errors on medicine charts
identified by pharmacists
Prescription charts are amended by
pharmacists for a variety of reasons.
Percentage errors identifed by pharmacists
Type of error
Patient's name incorrect
Form of drug incorrect
Adverse drug reaction warning
Frequency of dose incorrect
Administration route incorrect
Source: Analysis of data collected from sixhospitals in the Oxford region
Concerns have recently been expressed that the core curricula at
medical schools do not provide a thorough knowledge of safe medicines
prescribing and administration (Ref. 31). Shortcomings in doctors'
knowledge means that there is a particular risk of medication errors
when they first arrive in hospital. Only a small proportion of new
doctors believe that their induction dealt adequately with medicines
management issues [EXHIBIT 7].
Medication errors are common because of major systemic weaknesses
in prescribing arrangements. About 70 per cent of prescribing decisionsare made by house officers and senior house officers even though theyhave little experience of medicines. Studies have also shown that they areprone to increasing error rates when they are stressed, tired, distracted,or are working in unfamiliar surroundings – almost a stereotype ofhospital life (Refs. 32 and 33).
Can medication errors be avoided?
It is important not to under-estimate the task of minimising
medication errors. The prescriber has to be knowledgeable enough tochoose an effective treatment that is suitable for the individual patient,taking into account age, infirmity, and possible interactions with othermedicines. Having selected the right medicine and the correct dose, theprescriber has to transmit the message to the dispenser. They then have tohand the medicine to the patient, or to a carer or nurse, who has to seethat the medicine is given in the correct way and at the specified times.
Timeliness of advice
The perceptions of doctors in
medicines is adequate
training of support in medicines
management issues
Only a small proportion of doctors in
Quality of advice
training report that their induction
dealt adequately with medicines
medicines is adequate
management issues.
information about
pharmacy services
10% 20% 30% 40% 50% 60% 70% 80% 90% 100%
Percentage of doctors agreeing with the statement
Source: Audit Commission study sites
Medication errors occur because of the complexity of this process,
but there are several ways in which risk can be minimised:
changing the risk management culture;
induction and training;
redesigning processes and using computer technology to reduceerrors; and
developing clinical pharmacy services.
Changing the risk management culture
.senior managers
A typical response to errors in hospitals is to identify those involved
and castigate them (Ref. 26). The UKCC has recorded its concern that
should also seek
nurses who made mistakes under pressure of work, and were honest and
assurance that actual
open about those mistakes to senior staff, have often been subject todisciplinary action. This discourages incident reporting and is potentially
clinical practice
detrimental to patient care.
reflects agreed
Hospitals need to learn from the practices of other high-risk industries
where risk management concentrates on ‘near misses' as a way ofreducing systemic errors (Ref. 34). The government's view of clinicalgovernance emphasises the need to adopt ‘a systematic approach toquality assurance and improvement . above all, clinical governance isabout changing organisational culture . away from a culture of blameto one of learning so that quality infuses all aspects of the organisation'swork'(Ref. 3).
Trust boards should distinguish between cases where the error is the
result of reckless practice and those that have been the result of seriouspressure of work and where an immediate, honest disclosure is made. Allerrors and incidents require thorough and careful investigation that takesfull account of the circumstances and context of the event and theunderlying systemic causes.
Trust boards and senior managers should also seek assurance that
actual clinical practice reflects agreed protocols. The recent events atQueen's Medical Centre illustrate how day-to-day pressures can lead toacknowledged best practice being ignored (Ref. 35). There were particularconcerns expressed at some hospitals visited of aseptic preparations beingmade-up on wards, despite protocols stating that they would be preparedin the safer, better quality-assured, facilities in pharmacies. Such practicehas been shown to represent a significant risk to patients because of therisks of microbial and medication errors associated with the preparationof intravenous medicines at ward level (Ref. 36).
Induction and training
Lead clinicians must ensure that all new clinical staff are provided
with a formal induction, which should include the provision of guidelinesand protocols covering prescribing practice, medicines administration anderror reporting arrangements. New members of staff should sign toacknowledge receipt and understanding of the guidelines. Inductioncourses should also introduce new clinicians to contact points inthe hospital's pharmacy service.
After initial induction, there is a need for continuing training and
competency assessments for all clinicians who are involved in theprescription and administration of medicines. No one can prespecifytheir own ignorance, so constant vigilance and a robust safety culturewill always be required to prevent accidents.
Redesigning processes and using computer technology to
reduce errors
Complications arising from medicines treatment are the most
common cause of adverse events in hospital patients (Refs. 37 and 38) and
generate adverse publicity for the NHS [BOX E]. Errors may occur from
the initial decision to prescribe to the final administration of the medicine,
and these include choice of the wrong medicine, dose, route, form, and
frequency or time of administration (Refs. 39 and 40).
Most errors are caused by the prescriber not having immediate
access to accurate information about either the medicine (its indications,
contraindications,I interactions, therapeutic dose, or side effects); or
the patient (allergies, other medical conditions, or the latest laboratory
results) (Refs. 40, 41 and 42).
Contraindication – any condition that renders a particular line of treatment improper orundesirable.
Examples of adverse publicity involving medication errors
Source: Audit Commission
Hand-written prescriptions or patients' notes also contribute to errors
as they may be illegible, incomplete, subject to transcription errors or
make use of inappropriate ‘shorthand' [BOX F]. Prescription sheets
themselves may also be temporarily unavailable or lost. To add to the
risk of confusion, different medicines are sometimes contained in
similar packages [BOX G].
Example of patient's notes
Hand-written prescriptions or patients' notes also contribute to errors as
they may be illegible, incomplete, subject to transcription errors or may
make use of inappropriate ‘shorthand'.
Source: Audit Commission study site
Example of different medicines in similar packaging
Different medicines are sometimes contained in similar packages.
The packaging of these medicines is almost the same, but prochlorperazine
is an anti-emetic medicine to treat nausea or vertigo; and procyclidine is a
medicine for treating Parkinson's disease.
Source: Audit Commission study site
Electronic prescribing reduces medicine errors significantly by
providing timely, legible information (Refs. 43 and 44). One study concludedthat improved information systems could contribute to the prevention of78 per cent of transcription errors leading to adverse medicine events
(Ref. 40). Computerised systems containing rules to prevent incorrect or
inappropriate prescribing have also reduced the incidence of errors andincreased the appropriateness of medicine treatment (Refs. 45, 46, 47, 48, 49, 50
The role of clinical pharmacy in reducing risk
Clinical pharmacy applies pharmaceutical expertise to help to
maximise medicine efficacy and minimise medicines toxicity in individualpatients. It allows pharmacists to become part of the clinical team and toanticipate medication errors. One of the pharmacist's traditional roles isone of quality control, monitoring and reporting on errors onlyretrospectively. Clinical pharmacy is a move away from re-active qualitycontrol towards pro-active involvement in direct patient care and theanticipation of errors.
DoH policy has long recognised the importance of clinical pharmacy
in minimising both clinical and financial risk (Ref. 52). Enabling
pharmacists to contribute more fully to patient care reduces patient
morbidity and saves money [BOX H] (Ref. 53). In particular, the presence of
a pharmacist on ward rounds as a full member of the patient care team
reduces prescribing errors significantly (Ref. 54). However, there is wide
variation in the amount of time that hospital pharmacists devote to
clinical pharmacy [EXHIBIT 8].
Analysis of clinical pharmacy services that reduce mortality
Clinical pharmacy service
Number of hospitals
Clinical research
Medicines information services
Medicines history taken on admission
Source: Ref. 53
The ‘p' values refer to associations between a particular pharmacy service being presentand adjusted mortality rates – there is not necessarily a causal link.
Calculated from the difference in death rate/admission (presence or absence of theclinical service) * mean number of admissions/hospital/year offering the clinical service.
Percentage of time spent by registered pharmacists on clinical pharmacy activities
Proportion of time spent on clinical
There is wide variation in the
proportion of time that pharmacists
devote to clinical pharmacy.
Source: Audit Commission acute hospitalsportfolio data
Clinical pharmacy activities should also be extended to pharmacist
prescribing and to taking patients' medication histories. There is evidence
that pharmacists are five times more accurate than doctors in writing
discharge prescriptions (Ref. 55). Where it is properly planned and
supported, investment in clinical pharmacy improves the quality of
patient care and reduces costs [CASE STUDY 2] [EXHIBIT 9, overleaf) (Ref. 56).
CASE STUDY 2
North Staffordshire Hospitals NHS Trust – The impact of clinical pharmacy
The medical directorate of the trust, which spends over £1 million annually
on medicines, decided to purchase additional pharmaceutical support to
provide an experienced clinical pharmacy service to all its wards.
Two senior pharmacists were recruited, with the expectation that they
would save more than the cost of their salary each year.
The initiative has reduced prescribing costs by around 25 per cent through
more appropriate prescribing.
The greatest savings came from appropriate reductions in poly-pharmacy
where patients had been given cocktails of medicines that were designed to
overcome the problems caused by other medicines.
Source: Audit Commission study site
Average cost per script
The impact of the introduction of
The initiative has reduced prescribing
costs by around 25 per cent.
Prescribing costs before
Prescribing costs after
Source: North Staffordshire Hospitals NHS
clinical pharmacy
clinical pharmacy
Trust (Ref. 57).
Trusts should undertake reviews of pharmacy staffing levels and
consider whether there are adequate resources to:
provide all aspects of clinical pharmacy services;
meet the demands on pharmacy services of the NHS Plan in respect ofnew consultants and nurse prescribers (Ref. 3);
take patients' medication histories; and
support dispensing for discharge schemes.
The third strategic challenge facing trusts is to build effective
relationships with primary care in order to improve quality and
reduce costs across the local health economy. This requires appropriate
primary care
joint-working arrangements between primary and secondary care and
progress in four key inter-related areas:
Patients' own medicines
Medication review on admission
Original pack dispensing
Since 1st April 1999, healthcare allocations have been unified across
hospital, community health services and general medical services. Thismeans that prescribing costs across health economies are now ultimatelycash-limited. Hospitals now have a vested interest in helping to manageGPs' expenditure on medicines.
In the past, there were incentives for hospitals to serve their own
.some health
limited interests, rather than the NHS as a whole, by passing on the cost
authorities have
of medicines to primary care. Suppliers traditionally discounted the price
of medicines to hospitals in anticipation of recouping their margins fromprimary care.
GP prescribing is greatly influenced by events and decisions taken in
pharmacists to
hospitals. About 18 per cent of GP prescribing is hospital-initiated; and
establish more
40 per cent is strongly influenced by hospitals, since a GP's choices ofmedicines is likely to be guided by local consultants' treatment protocols
effective joint
(Ref. 58). Many medicines that are prescribed by hospital doctors are
continued for some years after discharge. However, three out of four GPssurveyed said that their local hospital did not take account of the impacton primary care when new medicines were introduced.
To tackle these shortcomings, some health authorities have appointed
medicines management liaison pharmacists to establish more effectivejoint working between hospitals and primary care groups or trusts(PCG/Ts); or LHGs in Wales. DTCs also have an important liaison role,and should include representatives from commissioners, GPs, PCGs andcommunity pharmacists to co-ordinate policy. Joint-care protocols shouldbe established to manage formularies and the choice of medicines. Theseneed to develop rapidly through the intermediate stage of diseasemanagement guidelines to the eventual objectives of integrated carepathways.
‘Whole system prescribing' arrangements should be examined by
all health economies, as there is evidence that this approach improves
prescribing and saves money [CASE STUDY 3].
CASE STUDY 3
Northamptonshire Prescribing Project Group
The Northamptonshire Prescribing Project Group was established at the end
of 1999 to advise on prescribing initiatives across the county. The Group
comprises representatives from hospitals, PCTs and the health authority.
The Group's work has focused on such issues as therapeutic switching of
medicines, introducing branded generic medicines, introducing original
pack dispensing and improved information about medicines when patients
are discharged from hospital.
The Group has concentrated on agreeing prescribing policies across primary
and hospital care, to avoid unnecessary therapeutic ‘switching' of medicines
when patients move between sectors.
This work has identified bankable savings of £500,000 (from a total
medicines expenditure of £60.3 million) by agreeing protocols on the use of
medicines for eight conditions in the last 18 months.
Source: Audit Commission study site
Despite such clear benefits, progress with introducing such joint
arrangements is patchy, as is shown by the development of joint
formularies [EXHIBIT 10].
Whole system reviews of medicines management practice will also
raise fundamental questions about who does what. In particular, thepractice of outpatient dispensing by hospitals should be questioned, andindeed has been challenged by the Report of the Task and Finish Groupfor Prescribing in Wales (Ref. 7).
There is a logic that says hospitals should dispense only to those
outpatients in immediate need, or where the medication is particularlyspecialised. All other outpatients are their GP's responsibility, with whomthe prescribing decision should reside, with advice following theoutpatient consultation. Such arrangements would eliminate much of theconfusion that is commonly generated when two doctors are prescribingto the same patient.
Patients' own medicines
Trusts usually ask patients to take all their medicines into hospital
with them so that an accurate medication record can be made. Patientstake some £90 million worth of GP-prescribed medicines with them intohospital each year – many of these medicines are destroyed or are notreturned when the patient is discharged (Refs. 58, 59 and 60).
If patients' medicines are checked on admission by someone who is
properly trained, their suitability for reissue can be assessed and suchwaste can be prevented. Medication should be only designated unsuitablefor re-use if:
there is insufficient quantity;
the dosage is changed;
Progress with introducing
The introduction of joint
formularies
A joint formulary covers most
The introduction of joint formularies
medicines expenditure
A joint formulary covers
specific groups of patients
A joint formulary will be
introduced in the next year
A joint formulary is under
consideration but will not be
implemented in the next year
A joint formulary
will not be considered
Source: Audit Commission acute hospitals
Number of trusts
portfolio data
medicine is stopped;
use-by dates have expired;
tablets in the container are mixed;
there is evidence of physical deterioration;
the medicine is inadequately labelled; or
the container had no label or batch number.
Observing these basic rules offers a significant quality improvement
and requires an early assessment of each patient by a pharmacist. Theyalso empower patients and reduce the confusion and errors that can occurwhen patients receive the same medicines presented and packed in threeor four different ways over the space of a few weeks.
Re-use of patients' own medicines may save money. One study found
that 77 per cent of patients' own medicines were suitable for re-use onadmission; and on receipt of the discharge prescription, 56 per cent werere-issued (the balance was not re-issued mainly because the medicationwas stopped) (Ref. 65). An annual saving of £46,000 was achieved. Anotherstudy found that 58 per cent of patients brought some of their medicinesinto hospital with them, of which 60 per cent were suitable for re-use,yielding the potential to save £37,000 a year in one trust.
Medication review on admission
.30 per cent of patients
The National Service Framework (NSF) for Older People requires that
hospitals put in place systems for medication review on admission to
had incorrect or
identify medicines-related problems. This is an area where pharmacists
have a vital role, either as provider or trainer. At some hospitals visited,30 per cent of patients had incorrect or incomplete medicines or allergies
or allergies recorded
recorded on admission. This can lead to poorer quality of care, and
on admission.
longer stays in hospital.
Medication review on admission by a pharmacist can also identify
whether an admission is due to prescribing errors or to adverse reactionsto medicines in the community. Medication review on admission can helpto identify such problems and report them back to GPs.
The public needs to be made aware of the importance of taking all
medication (including complementary therapies) into hospital so thatpatients' own medicines can be used and accurate medicine historiestaken. National co-ordination of publicity posters to support anawareness campaign would be worthwhile.
Self-administration of medicines
Patients should not be
The conventional method of giving medicines to patients in hospital is
characterised by the use of lumbering drug trolleys on the medicines
the passive recipients
round. However, the increasing number and complexity of medicines
of prescribing
means that this system can no longer support safe or efficient medicinesadministration.
decisions by
A central theme of both the NHS Plan and Improving Health in
Wales is empowering patients to take an active role in managing theirown care (Refs. 3 and 4). Patients should not be the passive recipients ofprescribing decisions by doctors – a shared approach needs to beencouraged whereby patients can learn about and take responsibility fortheir own medication (Ref. 62).
Self-administration in hospital allows patients greater independence
and enables them to participate in their own care and make decisionsabout their treatment in partnership with clinical staff. Over 80 per centof the 350 GPs surveyed supported the introduction of self-administrationof medicines by patients in hospital.
Self-administration improves patient compliance with medication
regimes and so prevents treatment failure (Refs. 63, 64 and 65). In a study ofpatients with renal failure, 18 per cent did not comply with theirmedication: 96 per cent of those who did not take their medication asrecommended died or had their transplant rejected, compared with18 per cent of the patients who did (Ref. 66). Another study found thatonly one-half of patients took their medication properly once they hadleft hospital (Ref. 67). The failure of patients and clinicians to reachconcordance about medication regimes is a major cause of increasedmorbidity and cost.
Almost all patients who self-administer prefer it because it gives them
more control. In one study, over 40 per cent of patients felt moreconfident about taking their medicines when at home, and the samenumber thought that it had increased their understanding – 90 per cent ofself-administering patients knew the purpose of their medicines comparedwith 46 per cent in a control group (Ref. 68).
Self-administration is also beneficial to patients because it:
enables the medication to do its job – patients can take analgesicswhen they are in pain, sedation when they want to sleep, and tabletsthat need to be taken before, with or after food, at the correct time;
simplifies the medicines regime – many patients, especially olderpatients, have a number of different diseases all requiring differentmedicines. The resulting polypharmacy leads to patients taking manymedicines of doubtful value (Ref. 69). Self-administration leads tosimpler and better medicine regimes because fuller assessment of allthe patient's medication is required (Ref. 70). Simplification improvescompliance with the medication regimen – the rate of non-compliancerises from 15 per cent when patients are asked to take one medicine,to 35 per cent if more than five medicines are prescribed (Ref. 71);
allows patients to practise taking medicine under supervision –including opening containers, a serious obstacle for some olderpatients; and
alerts healthcare staff to any problems the patient may experiencewith medication.
Improved compliance has quality and cost benefits, particularly by
preventing readmission – one-quarter of hospital readmissions are because
of non-compliance with medicines regimes (Ref. 72). However, progress with
implementing self-administration is variable, and there is scope to adopt
more progressive policies in some trusts [EXHIBIT 11].
The main problem associated with introducing self-administration is
the initial investment in time and money that is required. Each patientmust have his or her own lockable bedside cupboard at a cost of about£30 each. In view of the likely significant demand for these lockers fromhospitals, the NHS Purchasing and Supply Agency should considerestablishing a national contract.
Investment in staff time is also needed. In hospitals where it has been
successfully established, the change process was supported by at least onesenior nurse and one clinical pharmacist was solely allocated to the task.
Once established, self-administration in an average-sized hospital needs tomaintain most of this resource to train new staff, audit performance andensure that there is continuous improvement.
Where such investment is not forthcoming, self-administration
schemes invariably fail. Typically, they are left in limbo with the policypractised on some wards, some of the time – a recipe for confusion andincreased risk to patients.
Practice on self-administration
Self-administration of medicines by
Self-administration policies are in place
and all patients are encouraged
patients in hospital
to self-administer
Progress with implementing
Self-administration policies are in place
self-administration is variable.
but they are applied to limited
categories of patients
Self-administration will be extended
further in the next year
Extending self-administration is under
consideration, but will not happen
in the coming year
There are no plans to introduce
Source: Audit Commission acute hospitals
Number of trusts
portfolio data
Original pack dispensing
Closer co-operation across healthcare sectors will promote prescribing
and dispensing practice that minimises the cost to the NHS as a whole.
In the last ten years, there has been considerable debate about thequantities of medicines issued to patients when they are discharged.
DoH guidance was that hospitals should provide a minimum of oneweek's worth of medicines to patients on discharge (and two weeks'for outpatients) (Ref. 73). But many regions drew up their own detailedguidelines, and some hospitals reduced the quantity of medicines theydispensed in order to cut costs.
Such practice served only to increase overall prescribing costs as
hospitals are able to buy some medicines at a substantial discount. It wasalso inconvenient for patients and put an added burden on primary careas each patient had to visit their GP for a repeat prescription, and thenobtain the medicine from a community pharmacist.
Co-operation between primary and secondary care is imperative
because of European Community Directive 92/27, which was
incorporated into UK law on 1st January 1999. It requires, among other
things, that all medicines supplied to patients include a patient
information leaflet (PIL) in appropriate lay language; and be labelled with
the product's batch number and expiry date.I The Directive is one of the
key drivers behind the introduction of original pack dispensing, as the
packs contain the leaflets and the expiry date. Most manufacturers supply
tablets and capsules in blister-packs for 28 days' treatment, not in bulk.
Where trusts' current arrangements limit discharge or outpatient
dispensing to one or two weeks' supply, they will have to split some packsand risk non-compliance with the law and possible prosecution.
Increasing the dispensed quantity to allow original packs to be used is theonly practical solution.
Dispensing medicines to patients in original packs (combined with
storing medication at the patient's bedside) has some important benefits,
to patients in original
and is in compliance with EU regulations:
packs has important
reduced process costs as medicines are dispensed only once;
benefits.
greater convenience for patients;
reduced GP workload at discharge;
reduced overall costs of medicines to the local health economybecause hospital prices are usually lower than those available to GPs;
having been issued with 28 days' supply on admission, most patientswill have left at least two (and on average three) weeks' supply whenthey are discharged, so allowing time for GPs to be fully informed ofany problems or changes in treatment before the patient presents fora repeat prescription;
reductions in medicine administration error rates (from 9.7 per centto 2.5 per cent at one study site);
There is an exemption for hospital inpatients in that whilst the information needs to beavailable, the PIL does not need to be physically supplied to each patient.
hospital discharge is less likely to be delayed as medicines are readilyavailable at the patient's bedside;
the opportunity for greater use of patients' own medicines as the newsystem is implemented; and
fewer interruptions to medical rounds while nurses find medicinesfrom ward stocks.
The savings to individual health economies from introducing original
pack dispensing will vary. However, work undertaken at one 1,500-bedtrust estimated an overall saving of £200,000 a year to the local healtheconomy through better procurement. Trusts will need to discuss localimplementation with their health authorities and PCG/Ts, particularlythe transfer of money from primary care to hospitals and theconsequent impact on GP budgets.
Patients are missing the quality improvement that can be derived from
original pack dispensing because some health authorities, PCTs/LHGs and
hospitals are unable to agree the reallocation of money. Currently, trusts
are not maximising their use of original packs [EXHIBIT 12].
Original pack dispensing means that hospitals take on more
responsibility for dispensing medicines that will be taken in thecommunity. This, in turn, is leading some manufacturers to review theirlong-standing practice of discounting the cost of medicines to hospitals(in anticipation of recouping their profits from community sales). Theresultant reduction in price differentiation between the hospital and thecommunity sector highlights the existing anomaly that hospitals have topay VAT on the medicines they buy, while the community sector does not.
The DoH and the National Assembly need to work with HM Customsand Excise to equalise tax treatments between the sectors and removewhat is becoming an obstacle to best prescribing practice.
Number of trusts
The proportion of trusts' total
expenditure on medication
supplied to patients in original
Not all trusts are maximising their use
of original packs.
Source: Audit Commission acute hospitals
Percentage of total medicines expenditure spent on medicines in original packs
portfolio data
The important point about the innovations described above is that
they complement each other. Progress is best achieved, therefore, when
they are introduced as part of an integrated strategy [EXHIBIT 13] and
[CASE STUDY 4].
Integrating initiatives in order to
deliver better healthcare for
patients
Initiatives need to be integrated todeliver the greatest benefit.
BETTER HEALTH OUTCOMES
LOWER COSTS
Source: Audit Commission
CASE STUDY 4
Redesign of medicines supply services at Mid-Sussex NHS Trust
Medicines supply processes have been re-engineered to enhance the role of
pharmacy technicians so that time is released for registered pharmacists to
spend on clinical pharmacy and direct patient care. The initiative sought to
tackle several problems:
prescribing errors were being made when patients were admitted to
hospital because of inadequate information (one-quarter of planned
patient admissions did not have accurate information from GPs about
their current medication);
medication and patient selection errors during medicines rounds
accounted for over one-quarter of reported medication errors;
GPs complained about the poor quality of discharge summaries;
one quarter of re-admissions of elderly care patients were known to be
due to failures surrounding medication due partly to lack of
information sent to GPs on changes in medication during inpatient
stays. An audit at Mid-Sussex found that 31 per cent of emergency
medical admissions, whose medicines were changed in hospital,
reverted to pre-admission therapy within two weeks of discharge when
the GP repeat prescribing system was used to continue treatment;
waste of inpatient medicines – if a patient moved wards, new medicines
were supplied and original medicines destroyed;
.costs were offset by
CASE STUDY 4 (cont.)
a £60,000 saving from
a 50 per cent increase in dispensary workload between 1993 and 1998;
using patients' own
little control over the timing of dispensary workload.
The trust's aim was to tackle all these problems as part of a ‘whole-system'
approach, not on a piecemeal basis. All the initiatives taken were based
upon existing good practice elsewhere.
The solution
Better use of the skills available
The role of pharmacy technicians has been developed to enable them to
assume control of the medicines supply function, thereby releasing
registered pharmacists' time to develop their role in:
reducing patient risk through active involvement in decision making
about medicines use; and
identifying and correcting weaknesses in medicines use by improving
prescription monitoring and clinical audits.
A senior technician was made responsible for all operational aspects of the
dispensary. A registered pharmacist is available, but her role is primarily to:
validate any prescriptions that arrive in the dispensary that have not
previously been validated by a ward-based pharmacist;
deal with clinical issues surrounding prescriptions; and
train and mentor technicians in patient counselling.
ii) Re-engineering the ward-based supply process
Supply processes were changed to:
use patients' own medication during inpatient stays as the ‘lever' for
initiating change;
refocus technicians' work on assessing the suitability for use of patients'
own medication for use;
provide individual de-mountable bedside patient medicines cabinets
which ‘followed the patient' during their inpatient stay;
supply medicines ready labelled for discharge to cover both inpatient
and immediate post-discharge periods; and
give GPs and community pharmacists detailed medicines information for
patients who had new medication, or who had stopped or changed
medicines during their inpatient stay.
There was an increase in costs associated with the initiative: an extra
technician was recruited, some existing staff were regraded, and patient
lockers were installed. However, these costs were offset by a £60,000 saving
from using patients' own medicines, which now account for 10 per cent of
items used in the trust. Technicians are now allied with ward-based
pharmacists and visit wards on scheduled visits to record details of patients'
medication, identifying medication that had been brought in by the patient
and medicines that the trust must supply.
CASE STUDY 4 (cont.)
The technician's record is used to supply the medicines to cover the
inpatient stay and the immediate period after discharge. These
enable more control of dispensary workflow and remove periods of
excessive activity; and
mean that the prescription chart does not leave the ward and remains
with the medical record.
Ninety per cent of patients have no change in their medication during the
latter stage of their inpatient stay and the initial supply for their discharge
is thus ready on the ward for the patient to take home.
The use of lockers has:
removed the need to re-supply medicines when a patient moves to
speeded up medicines administration rounds;
almost eliminated medicine and patient selection errors (only one
reported instance on 10 wards in the first 12 months of the initiative);
reduced the amount of medicines stored on wards and in the
The initiative also aimed to improve the quality of the information about a
patient's therapy at admission, during the inpatient stay and upon
discharge to GPs. The quality and accuracy of information at admission was
improved by having patients' own medicines available for the admitting
staff to see. The technicians' ward-prepared medicines sheet provided
dispensary staff with a full record of current therapy to refer to when
dealing with additional supply requests or other queries about a patient's
therapy. Improving the quality of information to GPs on discharge has
focused on those groups of patients that are most at risk if their treatment
reverts to that in place before admission.
The next steps
The trust is in a good position to implement patient self-medication;
patient lockers are in place and nursing staff have welcomed the fact that
medicine administration rounds are now quicker. The more effective use of
pharmacists' time also means more resources are available to train nurses in
facilitating self-administration.
The need to shift resources from non-pay to pay budgets to fund
The need to work across the whole health economy; and
The need to adopt innovation that is tried and tested, and supported
by research evidence.
The fourth strategic challenge for trust boards is to provide effective
financial planning and control.
Current annual budgeting arrangements
In many hospitals, finance directors find it impossible to produce a
balanced budget with the money available at the start of the year. Most
hospitals therefore overspend their medicines budgets [EXHIBIT 14]. In many
cases, finance directors have to rely on slippage from other budgets to
offset the overspend on medicines.
When original budgets are constantly overspent in this way, it is a
sure sign that the original budget was wrong. Medicines cost pressures
are now being made more explicit through the work of NICE, and some
trusts are working across the health economy to identify the full extent
and necessary funding of future costs pressures [CASE STUDY 5, overleaf].
Many of the proposals contained in this report require an initial
investment to improve the quality of medicines management and reducethe costs of medication errors. A characteristic of trusts that haveachieved significant progress is the willingness of the trust to transfermoney from non-pay to pay budgets. For example, investment in clinicalpharmacy services needs initial funding, but a good clinical pharmacistwill save his or her salary in the same financial year.
Number of trusts
Comparison of trusts' outturn
expenditure on medicines and
One in three trusts overspent their2000/01 medicines budgets by more
than 10 per cent.
11% to 15% 16% to 20% 21% to 25%
Percentage overspend 2000/01 (original budget vs. outturn)
Source: Audit Commission acute hospitalsportfolio data
CASE STUDY 5
Identifying future medicines cost pressures
To improve annual budget-setting at Salford Hospitals, directorate pharmacists and their clinical colleagues prepare
an assessment of future medicines cost pressures and develop a planned approach to the introduction of new
medicines in consultation with health authorities and local PCG/Ts.
The assessment identifies existing medicines that have an identified change in use or a change in clinical practice
that will generate future cost pressures.
Arrangements for in-year cost pressures are agreed between commissioners and providers on the basis of ‘shared-
Example of medicines cost pressures 2000/01 – Salford Hospitals NHS Trust
HARD TO AVOID
Microbial resistance
IV Administration
Pre-made syringes/minibags EL(97)52
DVT and PE Homecare
Low molecular weight heparins to reduce bed stay
Trigeminal Neuralgia
Anaemia in dialysis
Erythropoietin – virement
Ribavirin and Interferon alpha
PCTA/stent medicines
Clopidogrel – Cardiology
PCTA/stent medicines
Abciximab – Cardiology
Glycoprotein iib/iiia blockers – NICE guidance
Chimeric monoclonal antibodies
Muscle relaxation
Total IV anaesthesia
Specialist medicines
Mirena – unlicensed use
Premature infants
Palivizumab – prevention of RSV
Urology – CA bladder
BCG for irrigation
Source: Salford Hospitals NHS Trust
Procurement
Pharmacists need to.
A number of regional contracts for medicines between the NHS
Purchasing and Supply Agency (PASA) (and its predecessors) and
work closely with PASA
suppliers has long been established. These cover about 60 per cent of
and the procurement
product lines and seek to aggregate NHS purchasing power.
professionals in their
However, regional contracts have, to some extent, been weakened by
hospitals renegotiating them in order to gain short-term price advantage.
trusts to develop
Suppliers have in all probability anticipated the likelihood of local
re-negotiations when making tender offers to the NHS.
with key suppliers.
A Ministerial letter sent to trusts in January 2001 makes clear the
Government's view about procurement in England. It wants:
procurement and supplies issues are to be considered regularly bytrust boards;
more of trusts' non-pay expenditure, including medicines, are to becovered in a cohesive strategy; and
a united NHS front presented to suppliers – contracts established bythe PASA should be adhered to, not ignored or re-negotiated.
For medicines that are not covered by regional contracts, pharmacists
in both English and Welsh trusts have a strong track-record of working inconsortia, using their purchasing power and commitment to contractvolume to reduce prices.
100. However, while prices are strongly controlled, there is patchy
performance in other aspects of supply: hospitals in London are currentlyexperiencing particularly poor performance from wholesalers in terms oflate deliveries and partially-filled orders, although in Wales wholesalerperformance is much better. Across the country, there are also fewexamples of the use of consignment stocks or of using suppliers to helpwith management information on performance and use.
101. Pharmacists need to build on their procurement expertise and work
closely with PASA and the procurement professionals in their trusts todevelop strategic partnerships with key suppliers. These arrangementsshould seek to ensure that both buyers and sellers work together to takeadvantage of the significant opportunities that exist to reduce process andtransaction costs in the whole medicines supply chain.
102. Greater use of technology would also reduce process costs. Work by
PASA has found that moving from manual to electronic updating ofcontract details in hospitals reduces the time taken for this task from20 staff days a year to two.
103. Both the Association of the British Pharmaceutical Industry and PASA
are aware of the opportunities to improve service standards and reducetotal supply chain costs, and should work with trusts to deliver them.
104. However, as previously noted, it is not known how much of the
variation in prescribing activity between hospitals is explained bydifferences in the age and medical condition of the patients treated. Thecurrent absence of any arrangement to aggregate local data associatedwith prescribing, purchasing and supplying medicines to a national levelwill limit the effectiveness of NHS procurement in general and thepotential benefits offered by e-commerce in particular.
Obstacles to Progress and How to
Overcome Them
In order to meet the strategic challenges presented by the
medicines management agenda, hospitals need to elevate
the status of some pharmacy services to focus their attention
on patient care, address staff recruitment and retention
problems, and invest in computer technology to reduce
risk to patients.
105. Three main obstacles need to be overcome in order to meet the
strategic challenges that are described in the previous chapter. They are:
the current low status of some hospital pharmacy services;
staff recruitment and retention problems; and
the need to introduce computer technology.
106. The importance of the pharmacist's role needs greater recognition
The status of
outside the profession, especially at board level; and sometimes within the
Attitudes outside the profession
107. Research evidence that supports innovation is overwhelming in areas
pro-active care on admission;
re-engineering supply through the use of original pack dispensing;
medication review clinics;
better use of pharmacy technicians;
development of pro-active clinical pharmacy services;
self-administration of medicines by patients;
pharmacist prescribing; and
the use of IT and automation.
108. But not enough trust boards have acted on this evidence and
.trust boards often
considered sufficiently the link between medicines management and
appoint new consultants
effective clinical governance.
without reference to
109. There is also a tendency to regard pharmacy merely as another
support service, rather than one that is absolutely vital to the quality of
the effect that their
patient care. For example, trust boards often appoint new consultants
without reference to the effect that their additional workload will have onpharmacy services.
will have on pharmacy
110. At the hospitals visited, auditors reviewed the background papers
making the case to trust boards for the appointment of consultants, but inonly one case out of twenty was there explicit reference to the impact thatthe new consultant would have on the demand for pharmacy services.
111. The NHS is seeking to recruit 7,500 new consultants and 20,000
nurses as part of the NHS Plan (Ref. 3). It is important that boards makeprovision for the impact that they will have on pharmacy services.
112. Medicines management is so vital to the quality of patient care that
its status, and the status of hospital chief pharmacists, need to bereviewed in many hospitals. At the hospitals visited, greatest progress indelivering the strategic challenges outlined in this report had beenachieved where the head of the pharmacy service held a positionequivalent to that of a clinical director.
113. The introduction of directors of pharmacy would also open up greater
career opportunities further down the organisational hierarchy and wouldhelp to reverse the exodus of pharmacists from the hospital service.
Attitudes within the profession
114. Attitudes also need to change within the profession. In some
pharmacy services, there is an inherent conservatism and a need to‘market' pharmacy positively to senior management. If trusts are tooptimise the use of medicines, pharmacy needs to be a core clinicalfunction.
115. Excellent pharmacy services are characterised by:
a chief pharmacist with the necessary strategic vision and politicalskills to ensure that pharmacy services are given due prominence withits key ‘customers';
pharmacists with the necessary skills of persuasion and negotiation, tomanage working relationships with their clinical colleagues; and
recognition by the trust board that pharmacy is first and foremost aclinical service.
116. The introduction of the four-year master's degree for pharmacists will
improve the quality of clinical education, but developing management andinfluencing skills also needs attention, both at a professional level andthrough on-the-job training and coaching.
117. The Royal Pharmaceutical Society of Great Britain (RPSGB) also has
a major role to play in equipping a new generation of pharmacists forenhanced clinical and managerial roles. The Society therefore shouldreview the adequacy of its current support for hospital pharmacists'education and training; continuing professional development; professionalcompetence and performance; and its workforce planning arrangements.
Staffing
118. The number of hospital pharmacy staff has increased by 25 per cent
in the last five years. Most of the increase is due to a growth in pharmacy
technicians [EXHIBIT 15].
119. Despite these increases, 15 per cent of pharmacy posts are still
vacant.I One-half of the hospitals in the UK are unable to provide all their
intended pharmacy services because of staff shortages (Ref. 74). Overcoming
these shortages in the short-term is unlikely – supply has been curtailed
by increasing the length of pharmacy undergraduate courses to four years.
In 2000/01, there were very few new pharmacy graduates going on to
take their pre-registration training year, so in 2001/02 there will be very
few newly qualified pharmacists.
120. The effect of these continued shortages is exacerbated by growing
demand for pharmacy staff:
demand for pharmacists from outside the hospital sector;
increases in demand from traditional workload areas;
increases in demand from new services; and
the need to increase pharmacy operating hours.
Demand for pharmacists from outside the hospital sector
121. Demand for pharmacists has been increased by the requirement that
all PCG/Ts or LHGs have a pharmaceutical adviser. There is also demandfrom private sector pharmacies, particularly the supermarket chains, someof whom are able to attract pharmacists because of better pay andconditions.
National hospital pharmacy vacancy survey 1999, conducted by the NHS PharmacyEducation and Development Committee.
WTE staff numbers
Whole time equivalent staff
employed in hospital pharmacies
The number of hospital pharmacystaff has increased by about 25 percent in the last five years.
Headcount at 30 September
Source: Audit Commission analysis of data
supplied by the DoH
Increases in demand from traditional service areas
122. The number of inpatient episodes has increased by about 10 per cent
in the last five years, and the number of prescriptions written per patienthas also increased. This has had an effect on traditional pharmacyservices, such as dispensing.
Demand from new services
123. Workload pressures also stem from the demand to extend
pharmacists' clinical roles (Ref. 75). For example, in outpatient services,there are demands for pharmacists to run anticoagulant clinics andtherapeutic drug monitoring clinics. Pharmacists are also assumingresponsibility for managing inpatient anticoagulation and aspects of doseadjustment for some shared care medicines.
124. Supplying medicines under patient group directions, as set out in the
NHS Plan, will enhance the role of pharmacists in the multi-disciplinaryclinical team, both as trainers and as clinicians (Ref. 3). Studies have shownthat pharmacist involvement produces benefits in patient outcomes,improves the quality of doctors' prescribing and saves money (Ref. 76). Aswell as taking these steps, trusts should anticipate possible changes to theMedicines Act that will allow pharmacists to act as full independentprescribers.
125. Schemes such as pharmacist prescribing will force pharmacists away
from their traditional, re-active model of prescription review to adopting
a more pro-active role. Currently, pharmacists spend a significant amount
of time annotating patients' prescription charts. However, these
interventions take place, on average, 48 hours after the patient has been
given their medication [EXHIBIT 16] (Ref. 77). Since some errors are potentially
life-threatening, it is clear that a pro-active approach would be safer for
patients. However, introducing pro-active rather than re-active pharmacy
services will place further demands on pharmacists' time.
Category of error
Average time between prescription
and identification/correction of a
There are significant delays betweenprescription errors and intervention.
Average hours between prescription and intervention
Source: Ref. 77
126. On all fronts, pharmacy services should be asked to provide a more
.an extension of service
pro-active approach. Prescriptions should be reviewed on or as soon after
hours is unavoidable if
admission as possible; reviews of patients' own medicines are needed; and
hospitals are to deliver
there is a growing demand for pharmacy involvement in dischargeplanning (Ref. 78).
all aspects of
127. The clinical role of pharmacists will further increase with the likely
growth of pharmacist prescribing (expected following the provisions of
the 2001 Health and Social Care Act) (Ref. 79).
128. The quality of patient care and cost-effectiveness of medicines use can
be achieved by enhancing the role of the clinical pharmacist in the multi-disciplinary team. Enhancing their role would also reduce the workloadof doctors in training. Such schemes have been found to improve thequality of doctors' prescribing, as well as saving money (Ref. 80).
The need to extend pharmacy operating hours
129. Finally, workload demands are placed on pharmacy services by the
need to move away from the traditional model of a 9 to 5, Monday toFriday service.
130. Extending the pharmacy service's operating hours makes sense given
the time of day when prescriptions are written. Up to one-half of
inpatient prescriptions are written outside the traditional 9 to 5 weekday
working hours [EXHIBIT 17]; over the weekend, 77 per cent of
prescriptions are written outside the traditional three-hour Saturday
service (9am–12 noon) (Ref. 81). Thus, an extension of service hours is
unavoidable if hospitals are to deliver all aspects of pharmaceutical care
uniformly to all patients.
131. Moving to a 24-hour, seven days a week service would be impractical
in most hospitals on cost grounds. However, extending ward-basedservices into the early evening and at weekends appears logical.
132. The pattern of hospital work also means that adequate arrangements
must be in place for on-call medicines information services. Theopportunities afforded by computer technology should enable more ofthese services to be provided off-site and out of hours in order tominimise cost.
The time of day that prescriptions are written
Prescriptions are written around the clock.
Number of items dispensed
Pharmacy open
Pharmacy closed
Time of day
Discharge medication
Source: Audit Commission (surveys from four study sites, based on the research model in ref. 81)
Tackling staff shortages
133. Trusts can tackle staff shortages by investing a sustained effort in the
introducing more flexible working patterns;
re-engineering pharmacy services;
redesigning and enriching jobs;
introducing automation;
providing administrative support; and
reviewing make or buy decisions.
Introducing more flexible working patterns
134. Some trusts need to offer more attractive remuneration packages and
flexible working conditions to attract and retain pharmacists. Womenmake up 68 per cent of the pharmacy workforce and 70 per cent of themare under 40 years old (Ref. 82). Delivering the NHS's Improved WorkingLives Directive is highly important to meet their needs (Ref. 83).
Re-engineering pharmacy services
135. The principal objective of a re-engineered service is to put pharmacists
closer to patients as this is where they add the greatest value. Trusts
should review the tasks that are being undertaken by pharmacists with a
view to ensuring that this objective is met, while activities like dispensing
are automated. Revision and expansion of the pharmacy technician and
pharmacy assistant roles need to play a major part in this strategy,
provided that proper competency assessments are established and adhered
to [BOX I].
136. The role of the pharmacy technician is now so pivotal to hospital
pharmacy services that the RPSGB should consider the formal registrationof pharmacy technicians.
Job design and enrichment
137. Studies of staff turnover have found that there is wide and
unexplained variation in turnover between trusts in similar geographiclocations (Ref. 84). Although local and national economic factors play theirpart, more than one-half of the variation is explained by differences inthe way that trusts manage their staff. At the trusts visited, it was notablethat while most reported recruitment and retention problems, those atthe leading edge of medicines management practice reported that theirservices were not adversely affected by recruitment and retentionproblems.
Main roles in pharmacy services
Pharmacists' key roles
Pharmacy technicians' key roles
Regular top-up service to wards
Prescribing (once the provisions
Clinical pharmacy services
of the Health & Social Care Act
within agreed guidelines
Dispensary and aseptic support
Procurement of medicines
Services that could be supported by
Clinical governance
All aspects of supply and
non-pharmacy staff
Preparing guidelines of clinical
dispensing of medicines
Business planning
Educating for concordance
Performance management
Checking patients' own
Some aspects of procurement
Reviewing whole health
Pharmacy assistant key roles
Services that could be supported by
economy prescribing
Supply of medicines – inpatient
Running certain clinics
and stock dispensing (with
Medicines information services
checking by a pharmacy
138. Enriching the work of technicians is particularly important if staff are
to be retained. Some pharmacy services make extensive use of pharmacytechnicians to undertake work that was hitherto the preserve of registeredstaff, such as procurement, supply and dispensing functions. Universitycourses are also now available to train technicians in clinical pharmacyroles.
Robotic systems release
139. Staff can also be released through automated dispensing. Robotic
systems release staff for patient-centred services, and reduce dispensing
staff for patient-centred
errors [CASE STUDY 6] (Ref. 85).
services, and reduce
140. Few trusts are likely to have the capital or the expertise to invest in
these systems, and there seems little sense in trusts individually specifyingdifferent systems. Economy of scale, and standardisation of systems andbarcodes, could be achieved if the DoH and the National Assemblyjointly commissioned a national specification for automated dispensing.
The provision of earmarked funds to roll-out the introduction of thesesystems to all large acute hospitals might also be considered in light of theimprovements they offer.
CASE STUDY 6
Wirral Hospitals NHS Trust's robotic dispensing system
Wirral Hospital installed a robotic dispensing system in January 2001, at a
cost of £300,000. The business case was approved by the board on the
grounds that the system would reduce dispensing error rates and release
staff to manage medicines at ward level.
Items are bar-coded and selected for dispensing via remote terminals. The
systems covers 77 per cent of medicines items, handling mainly items in
whole containers.
The system dispenses between 900 and 1,200 items each day.
The benefits of the system include:
dispensary turnaround times have been reduced;
reported dispensing errors reduced from 19 per 100,000 to 7 per
ordering processes are simplified;
improved reliability of service;
more efficient use of staff – three whole time equivalent pharmacy
technicians have been released to support direct patient care;
reduced staff down time;
potential use of consignment stocking;
70 per cent less shelving needed; and
floor space required has been reduced by one-half.
141. Some managerial and administrative tasks that are undertaken by
qualified pharmacists could be undertaken equally well by non-clinicalstaff. General managers and administrative staff should be used for tasksthat they can perform, such as business planning, performance review anddata management.
Make or buy decisions
142. The DoH's Controls Assurance Standards for Medicines Management
acknowledges that aseptic dispensing is an increasing and demandingactivity for pharmacy services (Ref. 1). Some NHS manufacturing capacityis also needed to provide medicines that are not commercially available.
However, boards should always consider whether collaboration withother trusts for the provision of common aseptically prepared items andmanufacturing is a viable alternative to individual trusts investing in theseservices. Such collaboration may be a way to release pharmacy staff andcapital for investment in other activities.
143. Computerised prescribing linked with electronic health records will
radically alter the way in which care is provided and will deliversignificant improvements in the quality of patient care (Ref. 86). Theintroduction of these systems, which ultimately need to be accessible byprimary care and other hospitals, is vital to provide access to commonclinical data. It is one of the biggest challenges currently facing the NHS.
144. The Information for Health strategy expects 35 per cent of trusts to
have installed electronic patient record systems (including the reporting ofresults and prescribing) by 2002, and all trusts by 2005 (Ref. 87). Thestrategy provided £60 million (about £600,000 for an average healthauthority) to which a further £250 million is provided in the NHS Plan.
However, the funds are not ringfenced, so some trusts have spent lessbecause of competing priorities and deficits, and generally progress isextremely slow.
145. These systems have been introduced in only a few hospitals. Two
trusts that have introduced them successfully share a number of common
attributes [CASE STUDY 7].
CASE STUDY 7
Introducing electronic patient records – Burton on Trent Hospitals and Wirral Hospitals
and are therefore more prepared
Providing the capacity to deliver
A major source of risk and
to take managerial risk. The sheer
avoidable costs in hospitals stems
size and organisational complexity
Both organisations created
from inadequate patient records.
of the larger teaching trusts may
managerial slack to invest in the
Patient care is jeopardised by
make informal networking and
change process. Both projects were
inaccurate, illegible or lost paper
commitment building difficult.
led by small, multidisciplinary
records; professionals' time is
There was extraordinary stability in
project boards of 5 or 6 individuals.
wasted and errors in diagnosis and
key personnel at both trusts. Wirral
Large, representative working
treatment are made because
kept the same chief executive and
parties were avoided. The project
accurate information is not
chief pharmacist throughout the
boards were professionally-led, not
available at the time decisions are
1990s; Burton also had the same
dominated by finance or technical
chief pharmacist, and promoted
The technology to deliver electronic
their medical director into the chief
Change takes time
patient records (EPR) in hospitals
executive's post when it became
There was an acceptance in both
has been around for more than 10
vacant. Both retained the same
organisations that change would
years but few hospitals have been
core of lead consultants. This
take a significant amount of time
successful in managing the changes
consistency is regarded as vital in
because the work involved re-
that are necessary to implement
maintaining direction and ensuring
engineering the way that doctors,
high priority for EPR
nurses and other clinicians work.
The procurement processes alone
took two years. This commitment at
Both EPR projects were pump-
board level helped to insulate the
Unlike most NHS trusts, Burton and
primed with additional ear-marked
change processes from competing
Wirral have avoided significant
funds – Wirral was a first wave, and
organisational change over the last
Burton a second wave Resource
10 years – there has been no
Management Initiative site.
significant merger activity.
Both projects had clear milestones,
‘Marketing' the system objectives
breaking the project down into
Both trusts have a comparative
manageable pieces. Both trusts
organisational simplicity – both are
In both trusts, the systems were
rolled their projects out on to
geographically isolated with clear
designed and ‘marketed' to
wards where they expected the
catchment populations, referral
improve the process of patient care,
most support from the staff
lines into primary care and links
not to save money. The benefits
involved, and both were willing to
with their health authorities. This
were described in terms of reduced
retreat and retrench in the face of
has created an environment that to
patient risk and improved clinical
some extent insulates both trusts
audit. Although there are
from ‘politicisation', competition
secondary financial benefits,
and some would say outside
through reduced process costs and
Both trusts (perhaps by virtue of
better use of medicines, these
the ‘scientific' management style of
benefits were never seen as central
Both trusts are of a manageable
doctors and pharmacists) collected
to either project. This approach
size. Some hold the view that
baseline data on key indicators to
helped to ensure professional
change is easier in organisations of
demonstrate benefits and calibrate
this scale, because senior people
the success of the new systems.
can ‘see across the organisation'
Data included measuring (reduced)
CASE STUDY 7 (cont.)
medication errors, speed of test
delivered – once paper systems are
results, discharge delays, and
abandoned there is no ‘going back.'
On the evidence of this case study,
additional time spent with patients.
This places a premium (and cost) on
the key ingredients that lead to
Collecting the baseline data helped
training new staff. Temporary staff
success in implementing EPR are:
to maintain commitment to the
– particularly locum doctors – are
staff and organisational
projects at board level, and to
unable to work without full
demonstrate their value in the face
training in the systems. Potential
insulating the change process;
of competing priorities.
new consultants are asked to
confirm at interview that they
accepting that change takes
Making change stick
would work with EPRs and EP, and
Introducing EPR and electronic
are not appointed if they are
collecting data to calibrate
prescribing (EP) radically changes
the way that patient care is
146. Computer technology is not an optional extra but a fundamental part
of the modernisation agenda on which to build other changes required bythe NHS Plan and Improving Health in Wales, including theimplementation of effective clinical governance (Refs. 3 and 4). Technology isalso the way to release scarce pharmacy resources into direct patient care
Percentage of total time
How pharmacists' time is spent
Pharmacists in trusts with automated
dispensing and electronic prescribingsystems are able to devote more time
to direct patient care.
With automated
automated dispensing
and electronic prescribing
Clinical activity
Travelling from pharmacy to wards
Supply of medicines
Prescription monitoring and adaptation
Source: Ref 92
147. Achieving the targets that are set out in the Information Management
and Technology (IM and T) strategy in respect of electronic healthrecords and electronic prescribing systems is a tall order given the currentstate of development in most trusts (Ref. 88). Only one in three executivedirectors surveyed said that their trusts had clear plans to introduce thesesystems. On current progress it is likely that less than 10 per cent of trustswill meet the 2005 deadline.
148. Urgent action is needed to put the IM and T strategy back on course.
A standard national system for coding medicines across the NHS isrequired to support the introduction of electronic prescribing andelectronic health records. Earmarked funds and expertise should beconsidered, as well as central guidance on systems specifications, screenlayouts and coding structures. Such a centralised approach would preventunnecessary duplication of effort, provide economy of scale inprocurement and would make working with the NHS in this area a moreattractive proposition to suppliers of IT and software systems.
Urgent action is needed
149. As well as the significant cost of the computers and software, the
introduction of new systems will fundamentally alter the way that
to put the IM and T
doctors, nurses and pharmacists work together to deliver patient care.
strategy back
Many trusts will need support and guidance in the organisationaldevelopment aspects of introducing these new technologies.
on course.
150. The cost of introducing IT and software to deliver electronic health
records and electronic prescribing systems to a typical hospital is in theregion of £2 million, with £500,000 annual running costs. Much of themoney needed is already available in the provisions of the IM and Tstrategy, and its investment would be recouped quickly by eliminating alarge proportion of the £500 million spent each year on treating patientswho are harmed by medication errors and adverse reactions.
151. A strongly centralised strategy runs directly counter to the
government's philosophy of decentralisation, expressed in Shifting theBalance of Power within the NHS (Ref. 89). Nevertheless, it is an optionthat merits urgent and serious consideration.
The Way Forward
Urgent action and investment are needed in many hospitals
to bring medicines management arrangements up to the
level of the best. The risks of not acting are substantial, both
in terms of the quality of patient care and the costs to the
NHS. Maintaining the status quo is not a viable option.
The NHS Plan
152. The main principles that underpin the NHS Plan are to:
re-shape care around the patient;
improve quality; and
make better use of NHS staff.
153. Pharmacy in the Future – Implementing the NHS Plan covers issues
that are relevant to medicines management (Ref. 9). It envisages some
radical shifts in job design [BOX J] and support for medicines management
Principal responsibilities in medicines management implied by the NHS Plan
NEW MODEL (?)
Diagnose disease state
Supply the therapy
Nurses (under guidelines)
Administer the therapy
The relevance of the NHS Plan to medicines management
NHS PLAN COMMITMENT
RELEVANCE TO MEDICINES MANAGEMENT
The ‘expert patient' programme will be
Argues for greater use of patients' own medicines; and
extended – NICE will publish patient-friendly
versions of clinical guidelines
Breaking down the barriers between staff
Qualified nurses, midwives, therapists and pharmacists will
(£10m for increased nurse prescribing)
be empowered to undertake a broader range of clinical tasks, including for some prescribing medicines and for the majority supplying medicines under Patient Group Directions
Integrated electronic patient records are very important to improving the quality of medicines management services – for example, improving links across healthcare organisations
£140m to ensure that all professional staff are
Presents an opportunity to increase the skills of
supported in keeping their skills up-to-date and
administrative staff and technicians and so release
to provide access to learning for all NHS staff
pharmacists for professional work
without a professional qualification
£30m to boost childcare
One-half of all hospital pharmacists are women. Family-friendly policies would ease recruitment and retention problems
What should trust
154. Action is required on several fronts to deliver better medicines
management. The DoH has much to do in delivering the agenda set out in
boards do?
Building a Safer NHS for Patients, and the IM and T strategy (Refs. 6 and 88).
The pharmaceutical supply industry, too, should also be taking a morepro-active role: it shares the same interests as the NHS in ensuring theefficacy of medicines; in eliminating unnecessary supply-chain costs; andin improving patients' compliance with medication.
155. But this report has been mainly about what trust boards must do. It is
important not to underestimate the scale of the task that they face indelivering the agenda that is described in this report. This is not through alack of desire or interest but due to the time and staff required to leadand implement the changes.
.trust boards will need
156. The list of recommendations provides a challenging agenda for
change. A systematic approach needs to be taken by each trust. They need
to invest in computer
to compare their current position against the recommendations of this
systems and automation
report, then prioritise actions, plan, and monitor the outcomes. It is adaunting agenda, where a significant investment of money and effort is
in order to release
needed to secure progress. But the risks of not acting are substantial, both
pharmacy staff
in terms of the quality of patient care and the costs to the NHS.
resources into direct
157. In particular, trust boards will need to invest in computer systems and
automation in order to release pharmacy staff resources into direct
patient services.
patient services. Investment in training and development will also beneeded to increase the knowledge base in order to provide comprehensiveclinical pharmacy services.
The DoH medicines
158. The DoH has emphasised its commitment to the importance of
medicines management through the dissemination of its framework. The
framework will indicate to trust boards where progress is needed locally
in the following areas:
senior management commitment;
financial control;
policy on the use of medicines;
primary care interface;
prescribing influence; and
risk management.
159. A preliminary review of the framework returns suggests that, of the
seven areas, senior management commitment is the one where significantimprovement is needed.
160. Over the coming months, returns from the medicines management
framework will be analysed in conjunction with returns to the AuditCommission's acute hospitals portfolio. The DoH should consider usingthis exercise to enable identification of Beacon Sites for medicinesmanagement. These trusts should then be funded to run open days thatare aimed at board members. Dissemination of good practice in this wayneeds to be encouraged. A mechanism to make readily available advice,guidance and the experience of achieving the goals stated in this reportwould be beneficial to trusts.
Local audits
161. The Commission has collected quantitative data about acute
hospitals' medicines management arrangements. Where analysis highlightsshortcomings, the Commission's auditors will recommend in-depthreviews as part of their performance management audit. Auditors willthen tailor the findings and recommendations of this report to localcircumstances.
162. Local audits will supplement the DoH initiative and generate much-
needed attention to raising the profile of medicines management. Alltrusts and health authorities should consider auditors' recommendationsin the context of their overall responsibilities for clinical governance.
The terminology used in these recommendations is aimed at England; however, they are
broadly consistent with the recommendations that are made in the the National
Assembly's Report of the Task and Finish Group on Prescribing (Ref. 7).
For the Department of Health and the National Assembly for Wales
The establishment of standard nation-wide definitions and categories of
1 medication errors and ‘near-misses' should be an early priority for the new
National Patient Safety Agency. Trusts should be required to adopt such systems
as part of their clinical governance arrangements and should report progress in
their annual reports, as well as reporting along the lines proposed in Building a
Safer NHS (Ref. 6).
Following agreement of standard definitions and categories of medication
2 errors, base-line audits should be undertaken with central funding at a
representative sample of hospitals to calibrate the current situation in order that
improvement targets can be set and their achievement monitored. Work should
prioritise specialties with the highest likely risk.
National co-ordination of publicity posters should be considered to encourage
3 patients to take their medicines into hospital with them.
The DoH and the National Assembly need to work with HM Customs and Excise
4 to equalise tax treatments between hospital and community sectors and thus
remove what is becoming an obstacle to best prescribing practice.
The DoH and the National Assembly should commission a specification for
5 automated dispensary systems and consider the provision of earmarked funds to
roll-out the introduction of these systems to all trusts.
A standard national system for the coding of medicines and barcodes should be
6 introduced across the whole of the NHS to support the development of
electronic prescribing systems and automated dispensing systems.
(Paragraphs 140 and 148)
Earmarked funds should be made available to enable trusts to comply with the
7 targets that are set in the NHS IM and T strategy (Ref. 88). Central guidance on
systems specification and screen layouts should be considered.
Trusts' medicines management framework returns should be analysed in
8 conjunction with returns to the Audit Commission's acute hospitals portfolio. The
DoH and the National Assembly should consider using this exercise to enable the
identification of Beacon Sites for medicines management. These trusts should
then be funded to run open days aimed at board members.
For the Royal Pharmaceutical Society of Great Britain
The RPSGB should review the adequacy of its current support for hospital
9 pharmacists' education and training; continuing professional development;
professional competence and performance; and its workforce planning
The RPSGB should consider introducing the formal registration of pharmacy
For the NHS Purchasing and Supply Agency
PASA should consider establishing a national contract for the supply of patients'
11 medicines lockers.
(Paragraph 80).
PASA should work with trusts and with the Association of the British
12 Pharmaceutical Industry to examine and eliminate supply chain costs and
improve wholesaler and supplier performance where necessary.
(Paragraphs 101 to 103)
For NHS trust boards
Trust boards should use the DoH's Medicines Management Framework in
13 conjunction with the Audit Commission's diagnostic to review medicines
management arrangements and develop local action plans (Ref. 2).
Medicines formularies should be agreed that are linked to joint care
14 arrangements, clinical guidelines and NICE guidance.
Medicines management groups and DTCs should be made formally accountable
15 to the trust board or to the clinical governance committee.
Risk management arrangements should be reviewed and ‘fair blame' and ‘near
16 miss' reporting systems introduced.
(Paragraphs 44 to 45)
Trust boards and senior managers should seek regular assurance that actual
17 clinical practice reflects agreed protocols – in particular, the practice of making-
up aseptic preparations on hospital wards should be stopped.
Lead clinicians should ensure that the induction programme of all clinical staff
18 provides adequate coverage of policies on prescribing practice, medicines
administration and incident reporting. Monitoring of competencies in
prescription and administration of medicines should be given high priority.
(Paragraphs 47 and 48)
Trusts should undertake reviews of pharmacy staffing levels and consider
19 whether there are adequate resources to:
(i) provide for all aspects of clinical pharmacy services;
(ii) meet the demands of the NHS Plan in respect of new consultants and nurse
(iii) take patients' medication histories; and
(iv) support dispensing for discharge schemes.
(Paragraphs 56 and 132)
Arrangements should be introduced for the use of patients' own medicines in
(Paragraphs 68 to 69)
Trust boards should call for a position statement on progress towards introducing
21 self-administration of medicines and providing the necessary staff resource to
maximise implementation.
(Paragraphs 72 to 82)
Original pack dispensing should be introduced in all appropriate areas
22 immediately, using Department of Health guidance. Re-packaging of medicines
from bulk should be stopped, wherever possible.
(Paragraphs 85 to 88)
The annual Service and Financial Framework round should include an assessment
23 of future cost pressures from medicines, and a risk-sharing approach agreed
between commissioners and providers.
(Paragraph 94 and Case study 5)
Transfer of money from non-pay to pay budgets should be considered in order to
24 fund investment in pharmacy services.
Wherever possible, trusts should use PASA contracts for medicines.
25 (Paragraphs 96 to 98)
Pharmacists should work with procurement professionals in the development of
26 strategic partnerships with the main suppliers.
Trusts should introduce electronic updating of supplier contract details.
27 (Paragraph 102)
Trust boards should always consider the impact on pharmacy services when
28 appointing new consultants.
(Paragraph 111).
The role of chief pharmacist should be elevated to the equivalent of a clinical
29 director and should be a member of the trust's management executive.
A review of pharmacy operating hours should be undertaken.
30 (Paragraph 130)
Recruitment and retention policies and practice should be reviewed to provide
31 competitive working flexibilities and remuneration packages for pharmacists.
Primary and secondary care should work together to consider limiting the
32 practice of outpatient dispensing.
(Paragraphs 64 and 65)
Original pack dispensing should be introduced immediately.
33 (Paragraphs 95 to 97)
Appendix 1
NHS bodies
Addenbrooke's Hospital
Association of the British Pharmaceutical Industry
Airedale Hospitals and Health Authority
Birmingham Children's Hospital
Centre for Practice and Policy, School of Pharmacy,University of London
Blackpool Victoria Hospitals
Department of Health
Burton Hospitals
Glaxo, SmithKline
Cardiothoracic Centre, Liverpool
National Prescribing Centre
East Riding NHS Trust and Health Authority
NHS Purchasing and Supply Agency
George Eliot Hospital
Royal College of Nursing
Guy's and St Thomas's
Royal Pharmaceutical Society of Great Britain
John Radcliffe Hospital,
Kettering Hospital
Manchester Children's Hospital
Mid-Sussex NHS Trust
Milton Keynes Hospitals
North Birmingham Mental Health Trust
North Cheshire Hospitals
North Staffordshire Hospitals
Northumbria Healthcare
Plymouth Hospitals
Salford Hospitals
South Warwickshire General Hospitals
United Lincolnshire NHS Trust
University Hospital of Wales
Regional meetings of chief pharmacists in Wales, WestMidlands, South-East and London regions
Appendix 2
The following individuals have supported the study team with advice and
Sue Ashwell
Kettering Hospitals NHS Trust
Derbyshire Royal Infirmary NHS Trust
Keith Farrar
Wirral Hospitals NHS Trust
John Farrell
Department of Health
North Staffordshire NHS Trust
Royal Salford Hospitals NHS Trust
Department of Health
Deputy Chief Pharmacist, Department of Health
Queen's Medical Centre, Nottingham
Royal Pharmaceutical Society of Great Britain
Mike Pollard
North East Wales NHS Trust
Keith Ridge
Department of Health
University Hospital of Wales
David Scott
John Radcliffe Hospital, Oxford
Chelsea and Westminster Hospital NHS Trust
Wirral Hospitals NHS Trust
Mike Spencer
University Hospital of Wales
Vic Standing
North Western Regional Pharmaceutical Advisor
NHS Purchasing and Supply Agency
Debra Walker
National Prescribing Centre
Chief Pharmacist, National Assembly for Wales
The work was undertaken principally by conducting observational
reviews and audits at the organisations visited, by seeking expert opinion,and by analysing data and literature from secondary sources.
In addition, the Commission has collected data from all acute hospitaltrusts on aspects of their performance in delivering effective medicinesmanagement.
Controls Assurance Standards for Medicines
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2. Department of Health, Medicines Management Framework, 2001
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5. Department of Health, An Organisation with a Memory, The Stationery
6. Department of Health, Building a Safer NHS for Patients, The Stationery
7. National Assembly for Wales, Report of the Task and Finish Group on
Prescribing, 2000
8. Department of Health, HSC(99)/143, Review of NHS Procurement
9. Department of Health, Pharmacy in the Future, The Stationery Office,
10. Department of Health, National Service Framework for Older People,
The Stationery Office, 2001
11. Health Survey for England 1998, Vol 1: Findings
12. Cunningham G et al, Drug-related problems in elderly patients admitted
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13. Mannesse CK et al, Adverse drug reactions in elderly patients as a
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14. Mannesse CK et al, Contribution of adverse drug reactions to hospital
admission of older patients. Age and Ageing, 2000; 29:35–39
15. Royal Pharmaceutical Society of Great Britain, National Sentinel Clinical
Audit of Evidence-Based Prescribing for Older People, Royal College ofPhysicians, 2000
16. Duggan C et al, Reducing adverse prescribing discrepancies following
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17. Duffin et al, An investigation into medication changes initiated in general
practice after patients are discharged from hospital. PharmaceuticalJournal, 1998; 261(Suppl.):R32
18. Miller EFR et al, The development and validation of a hospital
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elderly patients, Gerontology, 1999; 45:220–226
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22. Koren G, Barzilay Z, Greenwald M, Tenfold errors in administration of
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24. Phillips DP et al, Increase in US medication error deaths between 1983
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25. Ferner RE, Whittington RM, Coroner's cases of death due to errors in
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26. Bates DW, Cullen DJ, Laird N, Petersen LA, Small SD, Servi D et al,
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27. Vincent C et al, Adverse events in British hospitals: preliminary
retrospective record review. British Medical Journal, 2001; 322:517–519
28. Department of Health, The Prevention of Intrathecal Medication Errors,
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30. Alberti KGMM, Medical errors: a common problem, British Medical
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32. Orton DI and Cruzelier JH, Adverse changes in mood and cognitive
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Journal, 2001; 322:563
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36. Cousins D, Presentation to the European Association of Hospital
Pharmacy Congress, Amsterdam, March 2001
37. Leape LL, Brennan TA, Laird N, Lawthers AG, Localio AR, Barnes BA
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38. Bates DW, Cullen DJ, Laird N, Petersen LA, Small SD, Servi D et al,
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39. Ferner RE, Errors in prescribing and giving drugs. Journal of the Medical
Defence Union, 1992; 8:60–63
40. Leape LL, Bates DW, Cullen DJ, Cooper J, Demonaco HJ, Gallivan T
et al, Systems analysis of adverse drug events. Journal of the AmericanMedical Association, 1995; 274: 35–43
41. Lesar TS, Briceland L, Stein DS, Factors related to errors in medication
prescribing. Journal of the American Medical Association, 1997; 277:312–317
42. Bates DW, Boyle DL, Vander Vliet M, Schneider J, Leape L, Relationship
between medication errors and adverse drug events. Journal of GeneralInternational Medicine, 1995; 10:199–205
43. Wyatt J, Walton R, Computer based prescribing: improves decision
making and reduces costs. British Medical Journal, 1995; 311:1181–1182
44. Schiff GD, Rucker TD, Computerized prescribing: building the electronic
infrastructure for better medication usage. Journal of the AmericanMedical Association, 1998; 279:1024–1029
45. Johnston ME, Langton KB, Haynes RB, Mathieu A, Effects of computer-
based clinical decision support systems on clinician performance andpatient outcome: a critical appraisal of research. Archive of InternationalMedicine, 1994; 120:135–142
46. Evans RS, Classen DC, Pestotnik SL, Lundsgaarde HP, Burke JP,
Improving empiric antibiotic selection using computer decision support.
Archive of International Medicine, 1994; 154:878–884
47. Pestotnik SL, Classen DC, Evans RS, Burke JP, Implementing antibiotic
practice guidelines through computer-assisted decision-support: clinicaland financial outcomes. Archive of International Medicine, 1996;124:884–890
48. Evans RS, Pestotnik SL, Classen DC, Clemmer TP, Weaver LK, Orme JF
et al, A computer-assisted management program for antibiotics and otheranti-infective agents. New England Journal of Medicine, 1998;338:232–238
49. Shojania KG, Yokoe D, Platt R, Fiskio J, Ma'luf N, Bates DW, Reducing
vancomycin use utilizing a computer guideline: results of a randomizedcontrolled trial. Journal of the American Medical InformationAssociation, 1998; 5:554–562
50. Bates DW, Leape LL, Cullen DJ, Laird N, Petersen LA, Teich JM et al,
Effect of computerized physician order entry and a team intervention onprevention of serious medication errors. Journal of the American MedicalAssociation, 1998; 280:1311–1316
51. Raschke RA, Gollihare B, Wunderlich TA, Guidry JR, Leibowitz AI,
Peirce JC et al, A computer alert system to prevent injury from adversedrug events: development and evaluation in a community teachinghospital. Journal of the American Medical Association, 1998;280:1317–1320
52. The Way Forward for Hospital Pharmacy Services, Department of
53. Bond et al, Clinical pharmacy services and hospital mortality rates,
Pharmacotherapy, 1999; 19: 556–564
54. Leape L et al, Pharmacist participation on physician rounds and adverse
incidents in intensive care units, Journal of the American MedicalAssociation, 1999; 282(3):267–270
55. Stevenson N, MSc thesis, Liverpool John Moores University, 1998
56. Stephens MJ et al, Managing medicines: the optimising drug value
approach, Hospital Pharmacist, October 2000, Vol 7, 256–259
57. Fitzpatrick RW et al, A comprehensive system for managing medicines in
secondary care, Pharmaceutical Journal, 2001; 266:585–588
A Prescription for Improvement – Towards more
Rational Prescribing in General Practice, Audit Commission/HMSO,1994
59. Bowden JE, Reissuing patients' medicines – a step to seamless care.
Pharmaceutical Journal, 1993, 251:356
60. Dobrzanski S, Reidy F, The pharmacist as a discharge medication planner
in surgical patients. Pharmaceutical Journal, 1993; HS53–HS56
61. Campbell D et al, Waste not, want not, Health Service Journal, 24 August
62. HSC 2000/01:LAC (2001) Intermediate Care, Department of Health,
63. Lowe C et al, Effects of self-medication programme on knowledge of
drugs and compliance with treatment in elderly patients, British MedicalJournal, 1995; 310:1229–1231
64. Wood SI, Calvert RT, Acomb C, Kay EA, A self-medication scheme for
elderly patients improves compliance with their medication regimens.
International Journal of Pharmacy Practice, 1992; 1:240–1
65. Foster H, Mclean KA, Giles R, Franklin G, Auckland J, Neal KR et al,
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drugs and compliance with treatment in elderly patients, British MedicalJournal, 1995; 310:1229–1231
69. Wade B and Finlayson J, Drugs and the elderly, Nursing Mirror, 1983;
70. Bream S, Teaching the elderly about drugs. Nursing Times, 1985;
71. Koltun A and Stone G, Past and current trends in patient noncompliance
research, The Journal of Compliance in Healthcare, 1986;1,(1), 22
72. Ausburn L, Patient compliance with medication regimes, Advances in
Behavioural Medicines, 1981; Vol 1
73. NHS Management Executive, Responsibility for Prescribing Between
Hospitals and GPs, EL(91)127, Department of Health, 1991
74. National hospital pharmacy vacancy survey 1999, conducted by the NHS
Pharmacy Education and Development Committee
75. Royal College of Physicians, Hospital Doctors Under Pressure: New
Roles for the Healthcare Workforce, 2000
76. Hughes DS et al, Collaborative medicines management: pharmacist
prescribing, Pharmaceutical Journal; 263:170–172
77. Farrar KT, Stoddart M, Slee AL, Clinical pharmacy and re-active
prescription review – time for a change? Pharmaceutical Journal 1998;260:759–61
78. Cousins DH, Luscombe DK, A New Model for Hospital Pharmacy
Practice, Pharmaceutical Journal, l996; 256:347–51
79. Health and Social Care Act, The Stationery Office, 2001
80. Sayers D et al, Collaborative medicines management: pharmacist
prescribing, Pharmaceutical Journal, 1999; 263:170–172
81. Slee AL, Farrar KT, What are Normal Working Hours for Hospital
Pharmacy? Pharmaceutical Journal, 1998; 260:923–5
82. Department of Health, Pharmacy Workforce and Training Report, 1997
83. Department of Health, Improved Working Lives Directive, 2001
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Turnover in NHS Trusts, Audit Commission, 1997
85. Bates DW et al, Using IT to reduce rates of medication errors in hospitals,
British Medical Journal, 2000; 320:788–791
86. Ford NG, Curtis C, Paul R, The Use of Electronic prescribing as part of a
system to provide medicines management in secondary care. BritishJournal of Hospital Care, 2000; 17:26–28
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88. Abu Zayed L et al, Time spent on drug supply activities in UK hospitals,
American Journal of Health Systems Pharmacy, 2000; 57:2006–7
89. Department of Health, Shifting the Balance of Power within the NHS,
Index References are to paragraph numbers, except in the case of boxes and case studies (page numbers)
8, 19, 23, 90, 140, 154, 160
controls assurance framework
Complementary therapies
Adverse reactions to
Controls Assurance Standards
Computer technology
Box B (p12),
for Medicines Management
Box D (p19)
guidance on preventing
centralised strategy
medication errors
Ageing population
14; Box B (p12)
medicines management
Anti-coagulant clinics
Drug monitoring clinics
appointment by trust boards 109–11
Anti-retroviral medicines
Drugs and Therapeutics
clinical freedom
Committees (DTCs)
impact on demand for
Case Study 1 (p16)
pharmacy services
influence on GP prescribing
Aseptic preparations
Association of the British
reviews of prescribing practice
Pharmaceutical Industry
Cost discounts on medicines
Efficacy of medicines 6, 22, 26, 53, 154
Audit Commission
Electronic patient records (EPR)
Automated dispensing
Costs of medicines
143, 144, 147, 148, 150;
Box I (p50)
management 11–9
Case Study 7 (pp53–4)
107, 135, 139–40, 157
Electronic prescribing (EP)
computer technology
52, 147, 148, 150;
consequences of undeveloped
Case Study 7 (pp53–4)
future medicines cost pressures
Case Study 5 (p40)
European Community
Case Study 6 (p51)
Information for Health strategy 144
Beacon Sites for medicines
litigation claims
Expiry dates of medicines
medicines for patients on
discharge 83–4,
Case Study 4 (pp36–8)
recent increases
savings from original pack
Building a Safer NHS for Patients
Financial planning
dispensing 87–8
current annual budgeting
savings from re-use of patients'
arrangements 93–5
Case Study 7 (pp53–4)
future costs pressures
systematic reviews
overspending on medicines
variations between hospitals
procurement of medicines 9, 96–104
Box D (p19)
Financial targets
Chest pain clinics
Definition of medicines
Flexible working patterns
Chief Medical Officer
Box A (p5)
evidence-based 28
Delays in supplying medicines
Future developments in
Clinical governance
Dispensing errors
Case Study 6 (p51)
medicines management
approach to quality assurance
role in medicines
Doctors' prescribing
management 21–32,
Clinical negligence litigation
caused by doctors'
NHS Purchasing and Supply
inexperience 39–40
80, 96, 98, 101–3
caused by inadequate
agenda for change
Health and Social Care Act 2001
Case Study 4 (pp36–8)
need to review medicines
caused by unsatisfactory
management arrangements
prescriptions or patients'
HM Customs and Excise
Box F (p24)
role in medicines management 21–4,
definitions and categories
strategic challenges
DoH guidance on prevention
Iatrogenic disease
Box D (p19)
32–5; Box D (p19)
Non-clinical staff
Importance of medicines
improvement targets
Non-formulary medicines
management in healthcare
investigation of
North Staffordshire Hospitals
Improved Working Lives
Case Study 1 (p16),
pharmacist's role in reducing
Case Study 2 (p27)
reduced by electronic prescribing 52
Improving Health in Wales
Northamptonshire Prescribing
Case Study 3 (p29)
Medication histories
Induction and training
Medication regimes
medicines supplied by
Information for Health strategy
Case Study 4 (pp36–8)
Medication review on admission
Information Management and
mistakes made by
Technology (IM and T) strategy 147,
training in prescribing
Information systems
Mental health teams
Intravenous medicines
Mid-Sussex NHS Trust
Case Study 4 (pp36–8)
19, 107, 147–50
Obstacles to improving medicines
Monitoring of medicines
management arrangements
Organisation with a Memory,
Morbidity in hospitals
Job design and enrichment
Box H (p26)
153; Box J (p57)
Original pack dispensing
Multiple conditions
16; Box B (p12)
107; Case Study 3 (p29)
Joint working arrangements
role of liaison pharmacists
limits of supply
National Assembly for Wales
Outdated medicines management
Length of stay in hospital
National Institute for Clinical
Excellence (NICE)
Outpatient dispensing
Litigation claims costs
Box K (p57)
Local audits of medicines
National Patient Safety Agency
management 161–2
National Service Framework
Local health authorities (LHGs) 31, 61,
Packaging of medicines
for Older People 19, 70; Box B (p12)
Box G (p25)
7, 74, 124, 146, 152–62
Patient information leaflet (PIL)
action by trust boards
DoH medicines management
Patients' own medicines
Make or buy decisions
framework 158–60
savings from re-use of
Medication errors 3, 5–7, 19, 25, 32–56
Case Study 4 (pp36–8)
152; Box J (p57)
cause of adverse publicity for
relevance to medicines
Box E (p23)
Box K (p57)
Pharmaceutical supply industry
Primary care groups (PCGs)
Robotic dispensing
and trusts (PCTs)
Case Study 6 (p51)
Procurement of medicines 19, 96–104,
Royal Pharmaceutical Society of
education and training
Great Britain (RPSGB)
exodus from hospital service
electronic updating of contract
four-year master's degree
Government's view
as key members of clinical
5, 53-4, 124, 128;
late deliveries and partially-filled
Salford Hospitals
Case Study 5 (p40)
Box I (p50)
Self-administration of
liaison role between hospitals
57, 73–82, 107;
and primary care
regional contracts
Case Study 4 (pp36–8)
55, 107, 125, 127;
strategic partnerships with
benefits to patients
Case Study 2 (p27)
failures of some schemes
united NHS front to suppliers
investment in time and money
quality control role
wholesaler performance
role in medical review on
Proton pump inhibitors
for older people
Box B (p12)
Psychiatric conditions
women pharmacists
Senior management commitment 158,
Pharmacy assistants
135; Box I (p50)
Shifting the Balance of Power
Pharmacy in the Future –
within the NHS (DoH)
Implementing the NHS
Quality assurance
7, 21, 22, 25, 38,
Shortcomings in medicines
management arrangements
Pharmacy operating hours
Quality of healthcare
Spinal injections
Pharmacy technicians
Quality standards and targets
for medicines management
Case Study 4 (pp36–8);
Box C (p15)
Staffing 118–51
Box I (p50)
automation 139–40
Queen's Medical Centre,
Polypharmacy 78;
Case Study 2 (p27)
computer technology
Postcode lottery
demand from new services
Prescribing practice
demand for pharmacists outside
for hospital patients on
Readmission to hospital
discharge 83–4,
extension of pharmacy
Case Study 4 (pp36–8)
Recent trends in medicines
variations between hospitals
management 11–8
increase in hospital pharmacy
Prescription monitoring
Review of medicines management
increased demand from
traditional service areas
costs passed from hospitals
job design and enrichment
integrating initiatives
changing the culture
make or buy decisions
joint working arrangements
induction and training
managerial support
with secondary care
minimising medication errors
need for flexible working
medication review on admission 70–2
pharmacist's role in reducing
original pack dispensing
medication errors
re-engineering of pharmacy
patients' own medicines
redesigning processes
services 135–6;
Box I (p50)
Case Study 4 (pp36–8)
role of clinical pharmacy in
recruitment and retention
and secondary care 6, 20, 57–82, 85;
Box B (p12)
seriousness of problem
reviews of levels by trusts
self-administration of
use of computer technology to
medicines 73–82
vacancies in pharmacy services
variations in turnover
Status of pharmacy services
attitudes outside the
profession 107–13
attitudes within the profession
a clinical service
conservatism in pharmacy
hospital chief pharmacists
Task and Finish Group in Wales 19, 31,
Toxicity of medicines
Traditional ways of working
Box D (p19)
VAT on medicines
8, 19, 90, 100, 140
Whole system prescribing
arrangements 62,
Case Study 3 (p29)
Wirral Hospitals NHS Trust
Case Study 6 (p51),
Case Study 7 (pp53–4)
Workload pressures 3, 33, 44, 109, 123
The Audit Commission has produced a number of reports covering related issues.
Acute Hospital Portfolio
Goods for your Health
Review of National Findings
Improving Supplies Management in
for Day Surgery
NHS Trusts
This review, the fourth in a new series
The proper management of supplies is
from the Audit Commission, summarises
vital to the smooth running of NHS trusts.
the results from the Commission's national
Moreover, substantial amounts of money
survey of all day surgery units in England
are involved: a typical trust spends
and Wales. It examines current day
between one-fifth and one-quarter of its
surgery performance, the progress made
annual revenue expenditure on supplies.
since the Commission's last review in 1998,
The results of this study indicate that
and the scope for further improvement in
better management could release at least
the management and use of day
£150 million over the next three years.
surgery units.
Goods for your Health makes
2001, ISBN 1862403139, £10, stock code HNR2594
recommendations as to how this can be
achieved.
National Report, 1996, ISBN 1862400024, £15,
stock code HNR1170
Education, Training and
Development for Healthcare
Acute Hospital Portfolio
Staff in NHS Trusts
This report explores the methods that
Review of National Findings for
trusts can adopt to help them to
Accident and Emergency Services
proactively manage education, training
The second report in the Audit
and development for their staff, from
Commission's Acute Hospital Portfolio
creating an organisation-wide training
series reviews the national findings of the
and learning culture, through to setting
Audit Commission's survey on A&E
up effective support systems to make it
services. It compares waiting times across
a reality. The study focuses on nurses,
departments and against national
midwives, health visitors, allied health
standards. It also examines the workloads
professionals, scientific and technical
of nurses and doctors.
staff and healthcare staff without a
2001, ISBN 1862403090, £10, stock code HNR1877
professional qualification.
National Report, 2001, ISBN 1862402701, £20,
stock code HNR1519
To order further copies, or a full catalogue of Audit Commission Publications, please
contact Audit Commission Publications, PO Box 99, Wetherby, LS23 7JA.
Telephone 0800 502030.
A SPOONFUL OF SUGAR
Medicines management in hospitals encompasses the entire
way in which medicines are selected, procured, delivered,
prescribed, administered and reviewed in order to optimise
the contribution that medicines make to producing informed
and desired outcomes of patient care.
Managing the way that medicines are used in hospitals is
the business of all clinical staff and it directly affects most
patients. It is a strategic issue fundamental to the way that
hospitals work, to the quality of patient care and to the
delivery of the NHS Plan and Improving Health in Wales
This report sets out a number of recommendations to help to
optimise the use of medicines. The Department of Health and
the National Assembly for Wales have important leadership
roles to play in supporting new technology and providing
a framework for risk management. But there is much that
hospitals must do, both in terms of placing medicines
management at the heart of their clinical governance
responsibilities, and by introducing innovations that are
accepted good practice. Patients too have a central part
to play – at present only one-half of them take their
medicines as recommended by their doctor.
Further copies are available from:
The report will be of interest to patients, to all healthcare
Audit Commission Publications,
professionals who work in hospitals, to executive and
TIONAL REPOR
non-executive board members, to service commissioners,
Telephone: 0800 502030
policy makers, and to the supply industry.
STOCK CODE: HNR2623
£20.00 net
Audit Commission1 Vincent Square, London SW1P 2PNTelephone: 020 7828 1212 Fax: 020 7976 6187www.audit-commission.gov.uk
Source: http://www.jac.co.uk/files/A_spoonful_of_sugar.pdf
Comparison of ebastine to cetirizine in seasonal allergic rhinitis in adults
Comparison of ebastine to cetirizine in seasonal allergic rhinitis in adultsPierre Gehanno, MD*; Clothilde Bremard-Oury, MD†; and Philippe Zeisser, MD† Background: Second-generation histamine H1-receptor antagonists are accepted antagonist with no anticholinergic or first-line systemic therapy for seasonal allergic rhinitis. Ebastine is a new histamine
Degenerative myelopathy in a bernese mountain dog with a novel sod1 missense mutation
Case ReportJ Vet Intern Med 2011;25:1166–1170 F.A. Wininger, R. Zeng, G.S. Johnson, M.L. Katz, G.C. Johnson, W.W. Bush, J.M. Jarboe, An 8-year-old female spayed Bernese Mountain Dog sociation with a protein concentration of 30mg/dL and (BMD) presented to the Bush Veterinary Neurology no nucleated cells. Magnetic resonance imaging of the Service (BVNS) for paraparesis. The dog had been seen