Practicalguideclaudit2013 PDF

APracticalGuide
ToClinicalAudit
QPSD-D-029-1
A Practical Guide to Clinical Audit
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Reader Information
Directorate
Quality and Patient Safety
Title
Document reference number
QPSD-D-029-1
Version number
V.1
Document developed by
Quality and Patient Safety Directorate
Document approved by
National Director of Quality and Patient Safety
Approval date
August 2013
Revision date
August 2017
Quality & Patient Safety Directorate

Dr. Steevens Hospital
Dublin 8
Email: [email protected]
Contact Details:
QPSD-D-029-1
Web: www.hse.ie
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Acknowledgements
The Directorate of Quality and Patient Safety wish to acknowledge that extensive use was
made of work led by experts in the field of clinical audit in Ireland and in the United
Kingdom in the preparation of the content of this guidance document.
The following group was set up to guide document development:
The National Clinical Audit Advisory Group 2011-2012

Name
Title
Organisation
National Lead Clinical

Audit (2011)
HSE, Quality and Patient

Safety Directorate
Group Clinical Audit

Facilitator
St. Vincents Healthcare

Group
Joan Malone
Safety and Quality

Development Manager

Safety Directorate
Programme Lead
Ann Marie Lanigan
Area Manager
HSE South,
Carlow/Kilkenny/South
Tipperary
Member until
December 2011
Brian Conlon
CEO, Mater Hospital
Dublin Academic Teaching

Hospitals
Member
Colm Quigley
Consultant Physician
Wexford General Hospital
Member
Joe Clarke
Primary Care Clinical Lead
HSE
Member
Kenneth McKenzie
Post Doctoral Researcher
UCD School of Public

Health
Member
Louise Reid
Clinical Audit Development

Officer
Mid-Western Regional
Hospital, Limerick
Member
Niamh Macey
Clinical Audit Coordinator
Sligo General Hospital
Deputy Chair until

December 2011
Rosemary Ryan
Risk Manager and

Compliance Manager
Irish Public Bodies

Insurance
Member
Samantha Hughes
Team Lead, Clinical Audit

& Research Team
HSE, Dublin Mid Leinster
Member from
February 2012
Sheila O Connor
National Co-ordinator
Patient Focus
Member
Siobhan O Halloran
National Lead for Acute

Services
HSE
Member
Winifred Ryan
Head of Standards and

Guidance

Safety Directorate
Member
Ian Callanan
QPSD-D-029-1
Role
Chair
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Table of contents
Page
1 Introduction
1.1
Background
1.2
Setting the scene
1.3
Scope of document
10
2 The five stage approach to clinical audit
11
2.1
Stage 1: Planning for audit
12
2.2
Stage 2: Standard/criteria selection
22
2.3
Stage 3: Measuring performance
29
2.4
Stage 4: Making improvements
46
2.5
Stage 5: Sustaining improvements
49
2.6
Summary The five stage approach to clinical audit
52
3 Resources required to support clinical audit
53
3.1
Service provider support
53
3.2
Clinical audit facilitation
57
4 Wider considerations
58
4.1
Ethical issues
58
4.2
Issues of data protection
61
5 References
66
6 Additional resources
69
7 Glossary
71
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Appendices
Appendix one:
Clinical audit proposal proforma
Appendix two:
Clinical audit checklist
Appendix three:
Types of data
Appendix four:
Top tips for the successful development of clinical audit data

collection tools
Appendix five:
Glossary of terms in relation to descriptive statistics
Appendix six:
Presentation of data using table, graphs and charts
Appendix seven:
The clinical audit report
Appendix eight:
Twelve tips for successful clinical audit
Abbreviations
HIPE
Hospital In Patient Enquiry (Scheme)
HIQA
Health Information Quality Authority
HSE
Health Service Executive
MHC
Mental Health Commission
NCEC
National Clinical Effectiveness Committee
NHS
National Health Service
NICE
National Institute for Health and Clinical Excellence
NOCA
National Office of Clinical Audit
RCSI
Royal College of Surgeons in Ireland
SIGN
Scottish Intercollegiate Guidelines Network
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1. Introduction
1.
Introduction
1.1 Background
On 23rd September 2010, the Patient Safety First initiative was launched in response
to recommendations of the Report of the Commission on Patient Safety and Quality
Assurance Building a Culture of Patient Safety (Department of Health and Children,
2008). A key component of the Patient Safety First initiative is the National
Framework for Clinical Effectiveness. The purpose of this framework is to provide
formal structures and processes to support clinical effectiveness.
Clinical effectiveness involves a number of processes, but primary among these are:
(i) the development or adaptation and use of clinical guidelines to support
evidence-based practice; and
(ii) the use of clinical audit to improve service user care and outcomes.
National Clinical Effectiveness Committee (NCEC)
The oversight of the National Framework for Clinical Effectiveness is provided by the
National Clinical Effectiveness Committee (NCEC). The NCEC is a partnership between
key stakeholders in service user safety. The NCEC mission is to provide a framework
for national endorsement of clinical guidelines and audit to optimise service user care.
The NCEC terms of reference are to:
Apply criteria for the prioritisation of clinical guidelines and audit for the Irish health
system.
Apply criteria for quality assurance of clinical guidelines and audit for the Irish
health system.
Disseminate a template on how a clinical guideline and audit should be structured,

how audit will be linked to the clinical guideline and how and with what
methodology it should be pursued.
Recommend clinical guidelines and national audit, which have been quality assured
against these criteria, for Ministerial endorsement within the Irish health system.
Facilitate with other agencies the dissemination of endorsed clinical guidelines and
audit outcomes to front-line staff and to the public in an appropriate format.
Report periodically on the implementation of endorsed clinical guidelines.

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1. Introduction
Definition of a clinical guideline

The term clinical guideline has synonyms that may elsewhere be considered to be
broadly interchangeable. These include guideline, health guideline, clinical practice
guideline, evidence-based guideline, evidence-based guidance and guidance. For
the purpose of consistency, the NCEC utilises the term clinical guideline in its work.
The following identifies the specific meaning that should be inferred for this term:
Clinical guidelines are systematically developed statements, based on a
thorough evaluation of the evidence, to assist practitioner and patient
decisions about appropriate health care for specific clinical circumstances,
across the entire clinical spectrum.
Adapted from Field and Lohr (1992).
Definition of clinical audit
The term clinical audit is used to describe a process of assessing clinical practice
against standards. The Commission on Patient Safety and Quality Assurance (2008,
p.152) defined clinical audit as:
a clinically led, quality improvement process that seeks to improve patient
care and outcomes though the systematic review of care against explicit
criteria and to act to improve care when standards are not met.
The Commission further described clinical audit as involving:
the selection of aspects of the structure, processes and outcomes of care
which are then systematically evaluated against explicit criteria. If required,
improvements should be implemented at an individual, team or organisation
level and then the care re-evaluated to confirm improvements.
This description echoes the definition endorsed by the UKs National Institute for
Clinical Excellence in the seminal text Principles of Best Practice in Clinical Audit
(2002).
The Commission also recognised clinical audit as a key and essential component of
clinical governance (2008, p. 12), stating that it:
constitutes the single most important method which any healthcare
organisation can use to understand and ensure the quality of the service that
it provides.
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1. Introduction
1.2 Setting the scene

Why clinical audit?
Clinical audit is a tool which can be used to discover how well clinical care is being
provided and to learn if there are opportunities for improvement.
Clinical audit may be used to improve aspects of care in a wide variety of topics. It
can also be used in association with changes in care provision or to confirm that
current practice meets the expected level of performance.
There are many reasons to undertake clinical audit:
Clinical audit offers a way to assess and improve patient care, to uphold
professional standards and do the right thing.
Through clinical audit, healthcare staff may identify and measure areas of risk
within their service.
Regular audit activity helps to create a culture of quality improvement in the

clinical setting.
Clinical audit is educational for the participants. It involves being up to date with
evidence based good practice.
It offers an opportunity for increased job satisfaction.

It is increasingly seen as an essential component of professional practice.
It can improve the quality and effectiveness of healthcare.
Current drivers for clinical audit in the Irish Health Service (this list is not exhaustive).
The National Standards for Safer Better Healthcare (HIQA, June 2012) are an
important driver for participation in audit at all levels of healthcare. Monitoring and
evaluation of performance by developing and implementing clinical audits and
implementing improvements based on audit findings is required under these
National Standards. In the future this will be reinforced by licensing legislation.
The Quality Framework for Mental Health Services in Ireland (MHC, 2007) lists
clinical audit as a mechanism through which healthcare staff can demonstrate a
clinical governance system in compliance with Standard 8.3.
Professional regulatory bodies, for example, the Medical Council of Ireland and An
Bord Altranais, endorse audit as a mechanism for improving the quality and
effectiveness of healthcare.
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1. Introduction
As part of the enactment of Section 11 of the Medical Practitioner Act 2007,

participation in clinical audit is now required for all registered medical
practitioners. Since May 2011, medical practitioners must be enrolled in a
professional competence scheme and engage in professional competence
activities. All registered medical practitioners should engage in clinical audit, and
at a minimum participate in one audit exercise annually. The Act recommends that
practitioners spend a minimum of one hour per month in audit activity.
Clinical Audit in radiological practices is a legal requirement set out under

Statutory Instrument 478 (2002), of the European Communities Regulations. This
currently places a requirement on service providers to engage an external auditor,
appointed by the HSE, to audit radiological practice every five years.
Although not currently a legal requirement, many Health and Social Care
Professional Bodies endorse audit as a way of measuring the quality of healthcare,
for example, The Chartered Society of Physiotherapy and The College of
Occupational Therapists.
The Commission on Patient Safety and Quality Assurance (2008) recognised

clinical audit as a key and essential component of clinical governance, which
should be at the heart of clinical practice. The Commission also recommended that
all health practitioners should actively participate in clinical audit in compliance
with national standards and priorities.
The National Clinical Programmes Checklist for Clinical Governance developed by

the HSE Quality and Patient Safety Directorate (HSE, 2011) identifies a structured
programme of clinical audit as an integral component of clinical governance and
continuous quality improvement for the clinical care programmes. In order to
ensure that the quality of care provided meets defined standards, a comprehensive
system of clinical audit is required to support clinicians in identifying where
standards are being maintained and where improvements are needed.
The HSE Quality and Patient Safety Clinical Governance Development: an

assurance check for service providers (HSE, 2012) identifies having a structured
programme of clinical audit which is monitored for appropriateness and
effectiveness on an annual basis (including participation in national audits) as a
corporate responsibility of the Board/CEO or equivalent.
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1. Introduction
1.3
Scope of document
What is this document and who is it for?

The aim of this document is to support healthcare staff in understanding the concept
and processes of clinical audit, to support best practice in clinical audit and improve
awareness of clinical audit as an essential and integral component of clinical practice.
To this end, this document provides a practical guide to the methodology of clinical
audit. This document is primarily for all healthcare staff involved in or who have an
interest in carrying out clinical audit.
What does it cover?
This document describes:
The five step approach to clinical audit.

Resources required to support clinical audit.
Wider considerations (ethical issues/data protection/confidentiality).
This document also provides links to useful resources should more detailed
information be required.
What does it not cover?
Although mentioned, it is not the aim of this document to define the management of
or organisational structures required for clinical audit (locally or nationally).
The National Office of Clinical Audit (NOCA) oversees the running of national clinical
audits. This document does not define the methodologies and governance structures
employed by NOCA.
In addition, this document does not describe how to develop a clinical guideline.
NCEC and other relevant resources to support Clinical Guideline Development Groups
are available on the NCEC website www.patientsafetyfirst.ie
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2. The five stage approach to clinical audit
2.
The five stage approach to clinical audit
Clinical audit is a cyclical process which can be outlined in five stages:

Stage 1
Planning for audit
Stage 2
Standard/criteria selection
Stage 3
Measuring performance
Stage 4
Making improvements
Stage 5
Sustaining improvements
Each stage of the clinical audit cycle must be undertaken to ensure that an audit is
systematic and successful.
Figure 1 The clinical audit cycle
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2.1
Stage 1 Planning for audit
If a clinical audit is to be successful in identifying

areas of excellence or areas for improvement, it
requires effective planning and preparation. The
amount of planning and preparation will depend on the
specific circumstances of each audit.
For example, an individual healthcare professional
wishing to carry out an audit may not need to involve other stakeholders in the audit
process. This is especially true if external support and resources are not required to
carry out the audit or to support any subsequent changes in practice. On the other
hand, when a multidisciplinary team are working together on an audit there will be
greater need for planning to ensure a successful outcome for the audit.
Planning for audit can be described in three main steps:
Planning for audit
Step 1: Involving stakeholders
Step 2: Determining the audit topic
Step 3: Planning the delivery of audit fieldwork
Step 1: Involving stakeholders
All relevant stakeholders should be given the opportunity to contribute to the clinical
audit. A common question asked is which should come first: deciding on the topic for
audit or involving stakeholders? Ashmore, Ruthven and Hazelwood (2011a)
recommend that stakeholders should be involved from the beginning of the clinical
audit cycle through to completion. However, the answer to the question of which
should come first will depend on individual circumstances and the driver(s) for
carrying out the clinical audit.
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Anyone involved in providing or receiving care can be

considered a stakeholder in clinical audit. Therefore, to
determine who should be involved in deciding on the
topics and objectives of audit, it is necessary to
identify:
Who is involved in the delivery of care?

Who is in receipt of, uses or benefits from the care
or service?
Who has the authority to support implementation of any identified changes?

Who is involved in the delivery of care?
The support of those involved in the delivery of care and their commitment to
participate is essential for any audit.
The specific responsibilities of all those involved should be clarified and agreed before
the audit commences (HSE, 2008) i.e. everyone should understand the aim of the
audit and their role in it.
The lead clinician sponsoring the audit does not necessarily need to directly participate
in the clinical audit but they should at least be aware of, and approve of, the
performance of the audit (HSE, 2008).
As the majority of clinical practice involves multi-professional teams, clinical audit
should cover the practice of the different clinical and managerial disciplines that
contribute to the relevant audit topic area. The NHS Clinical Governance Support
Team (2005) recommends that 50% of audits are multi-professional.
When preparing for clinical audit, agreement on leadership and ownership of the audit
should be reached as well as responsibility for the management of audit results and
recommendations (HSE, 2008).
Where possible, all those involved in the audit should be supportive of and committed
to change(s) shown to be necessary by the audit results and recommendations
arising.
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Who is in receipt of, uses or benefits from the

care or service?
The priorities of those receiving care can differ
significantly from those involved in the delivery of
care.
(National Institute for Clinical Excellence, 2002, p9).
When planning any clinical audit, the audit team should consider the possible benefits
of including service users in the audit process. For example, would it be beneficial to
consider their experience of receiving clinical care?
Again the NHS Clinical Governance Support Team (2005) recommends that 10% of all
audits should have active service user involvement.
Common methods of including service users in

the clinical audit process
Gathering service user feedback, for example letters of complaint.
Analysis of comments made at service user forums.
Interview with service users.
Service user surveys.
Focus groups.
Expert user groups.
Examining critical incidents.
GP liaison group.
Where service users are involved in clinical audit programmes, their roles need to be
clearly defined and appropriate support and guidance provided to enable delivery.
(This should include the provision of information and guidance in relation to data
protection requirements; See Section 4.2, pages 61-65 for further information).
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Who has the authority to support implementation

of any identified changes?
Commitment to the clinical audit process should be
sought from those with the authority to approve
changes arising from audit recommendations,
particularly if they have potential resource
consequences or implications for other service areas.
(Walsh and Spurgeon, 1997 cited in HSE, 2008, p. 10).
Stages for stakeholder involvement
Various stakeholder groups may have different roles and be involved in
different stages of the clinical audit. They can:
Contribute to decisions regarding the topics and objectives of the clinical audit.
Contribute to and/or comment on the clinical audit methodology, including the
proposed clinical audit criteria.
Assist with drafting and reviewing the project plan.

Grant permission to access service user (patient) group.
Provide support to the clinical audit team.
Act as a source for data.
Collect data.
Review cases that do not achieve the expected level of performance (when the
stakeholder is an expert).
Provide explanations as to how a care process happens currently.

Contribute to the analysis of audit findings, including analysis of problems
identified.
Assist in identification of actions to address areas requiring improvement.

Secure resources required to support change.
Monitor the implementation of agreed actions.
Contribute to the analysis of the findings of repeat measurement.
Adapted from Dixon (2009a).
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Step 2: Determining the audit topic
This is a very important step that must be given careful

consideration. Subjects for clinical audit should be
selected with a view to improving the quality or safety
of care or of service provision.
The Donabedian (1966) classification system of
structure, process and outcome can be used to focus on
areas of practice from which a topic may be selected:
Structure
Includes the:
resources required to deliver care;
environment in which care is delivered;
facilities made available (e.g. availability of single rooms);
equipment made available (e.g. resuscitation equipment);

and
documentation of policies, procedures, protocols and

guidelines.
Process
the procedures and practices implemented by staff in the

prescription, delivery and evaluation of care these may
be specific to the clinical process or service
/administrative processes.
Outcome
the effect of care received by service users as a result of

healthcare provision and the costs to the service of
providing care i.e. the result of clinical interventions.
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Prioritising possible audit topics

Selection of the audit topic needs careful thought and
planning, as clinical staff and service providers have
limited resources with which to deliver clinical audits.
Mandatory audits will take resource priority. All other
audits should therefore be prioritised to ensure that
available resources are used effectively. These audits
should focus on areas with the greatest need to
improve practice.
Questions to assist with prioritising audit topics
Is the topic concerned of high cost, volume or risk to staff or users?

Is there evidence of wide variation in clinical practice?
Is good evidence available to inform audit standards (for example, systematic
reviews or national clinical guidelines)?
Is the problem measurable against relevant standards?

Is auditing the problem likely to improve healthcare outcomes as well as process
improvements?
Is there evidence of a (serious) quality problem (for example, service user

complaints or high complication rates, adverse outcomes or poor symptom
control)?
Is the topic of key professional or clinical interest?

Are reliable sources of data readily available for data collection purposes?
Can data be collected within a reasonable time period?
Is the problem concerned amenable to change?
Is the topic pertinent to national or local initiatives or priorities?
Does the topic lend itself to the audit process, or is a different process more
appropriate (for example, root cause analysis, activity analysis or workload
analysis)?
How much scope is there for improvement, and what are the potential benefits of
undertaking this audit?
Adapted from Ashmore, Ruthven and Hazelwood (2011a).
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Other questions which can be asked include:
Have there been major changes recently?

Are there resource implications?
Levels of priority
Clinical audit activity may be managed according to
different levels of priority:
External must do audit where participation is

required due to government or regulatory requirements or as part of an
accreditation scheme. As participation in national audits is recommended in the
National Standards for Safer Better Healthcare (HIQA, June 2012), voluntary
national audits should also be considered (for example, NOCA audits).
Internal must do audit where audit topics are based on requirements of the service
providers management team in response to incidents, risk management or
complaints.
Service/directorate priorities where audit topics are based on best practice

guidelines, local policies, issues identified by professional bodies or other relevant
topics arising from issues receiving regional or national attention.
Clinician interest locally initiated audits not covered by the above but which will
contribute to the overall work of the service.
Using a scoring system to prioritise audit topics
Consideration should be given to all available audit topics and topics should be
prioritised. A scoring system can help to rank topics in order of importance.
An example of a simple scoring system is where each topic is given a score between 1
and 5 based on importance (with 1 being the lowest and 5 being the highest) on two
measures:
(i) The impact of a resulting continuous improvement plan on clinical effectiveness
and quality of care.
(ii) The importance/urgency of the audit topic.
Further examples of scoring systems for prioritising audit topics may be found at:
http://www.hqip.org.uk/assets/Downloads/Clinical-Audit-Program-Guide-andGuidance-Tools.pdf
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Clinical Audit Programme

Service providers should develop and implement a
programme for clinical audit activity. This programme
should give direction and focus with regard to how and
which clinical audit activity will be supported in the
service.
(Refer to Pages 54-55 for further information on
clinical audit programmes).
Step 3: Planning the delivery of audit fieldwork
Understanding the aims and objectives of the clinical audit

The audit team must understand the overall purpose of the audit they are to perform.
The delivery of an audit topic with no clear purpose will deliver little or no
improvement to the quality and effectiveness of clinical care.
The purpose of the audit may be outlined in the form of aims and objectives. Buttery
(1998) suggested that audit aims and objectives may be defined through the use of
verbs such as:
Improve
Increase
Enhance
Ensure
Change
For example, an audit of healthcare records might have as its overall aim:
The improvement of adherence to healthcare records policy and
procedures.
More detailed statements may be used to describe the different aspects of quality
which will be measured to show how the aim of the clinical audit will be met, for
example, an objective of the audit of healthcare records might be:
To ensure the content of the healthcare record provides an accurate
chronology of events.
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Identifying the skills and people needed to carry

out the audit
For a clinical audit to be successful and achieve its aim
and purpose, it needs to involve the right people with
the right skills from the outset. Therefore, the
identification of skills required and of individuals
possessing these skills should be a priority.
The level of skill required for a clinical audit will be dependent on the size of the audit.
Skills required for clinical audit process

Leadership, organisational and management skills.
Clinical, managerial and other service input and leadership.
Project management skills.
Change management skills.
Audit methodology expertise.
Understanding of data protection requirements.
Data collection and data analysis skills.
Facilitation skills.
Communication skills.
Interpersonal skills.
The skills outlined should be drawn from all relevant groups involved in the delivery of
care. Depending on the nature of the topic that is being audited, the audit team
should be multidisciplinary. To achieve the best possible results, all relevant staff
groups should have a degree of involvement in the performance of the clinical audit
and in the implementation of a sustainable continuous improvement programme.
For a clinical audit to be delivered effectively, all staff should be appropriately trained
and briefed with regard to their role. All team members should have:
A basic understanding of clinical audit.

An understanding of and commitment to the plans and objectives of the audit.
An understanding of what is expected of the audit team this needs to be clarified
at the outset and may be expressed in a terms of reference document.
(Ashmore, Ruthven and Hazelwood, 2011a).
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Providing the necessary structures

Appropriate structures should be in place prior to the
commencement of clinical audit work.
The clinical audit team should complete a clinical audit
proposal proforma (see Appendix one for sample
template). This ensures that all aspects of the
proposed clinical audit have been considered and that
the clinical audit will be robust and of high quality.
Completed forms along with supporting standards, audit tool and other documentation
should be submitted to the appropriate responsible clinical lead, directorate or
governance committee for consideration to ensure that the proposed audit meets the
requirements of the service provider. Whether or not formal decisions to proceed are
required will depend on local policy.
The team delivering the clinical audit should ensure that appropriate resources are
available with which to perform the audit and to implement a sustainable continuous
improvement programme. Where there is an insufficient level of resources available to
deliver an audit and a sustainable continuous improvement programme, this issue
should be raised through the appropriate governance structures as and when they
arise. The clinical audit proposal proforma should include a system for requesting any
support required for the clinical audit.
The structures should include a mechanism for the review of findings and progress
reporting to the appropriate clinical lead, directorate or governance committee. Clear
lines of accountability should be agreed at the outset of the audit.
It may be appropriate to consider and discuss the question of possible publication of
audit results via conference proceedings, poster, oral presentation or journal article at
the planning stage, particularly if the planned audit is large scale.
A timetable should be agreed for designing and carrying out the clinical audit.
A simple clinical audit checklist may also be a useful tool (see Appendix two).
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2.2
Stage 2 - Standard and criteria selection
When the audit topic has been selected, the next

essential step is to review the available evidence to
identify the standards and audit criteria against which
the audit will be conducted.
Standards should be robust and evidence based
(Potter, Fuller & Ferris, 2010).
Useful sources for standards include:
local standards in the form of evidence based guidelines;

nationally endorsed clinical guidelines;
standards and clinical guidelines from relevant quality and safety programmes,
clinical care programmes and professional bodies; and
clinical guideline development organisations such as NICE, SIGN, etc..

If national or local guidelines are not available, a literature review may be carried out
to identify the best and most up to date evidence from which audit criteria may be
generated. Access to and assistance in utilising a vast library of knowledge resources
is available through HSE library services at: www.hselibrary.ie
Section 6 of this document provides further information on relevant resources.
Defining terms
The terms standard and criterion often lead to confusion as these terms have been
used differently by various professional groups and writers across healthcare.
For some, a standard is a statement of best practice. For others, a standard is the
performance level or target for expected compliance (usually expressed as a
percentage).
Whilst recognising the confusion that has occurred, the approach taken in this guide is
consistent with the approach taken by the Health Service Executive when specifying
standards; standards are defined as structures and processes needed to identify,
assess and manage specified risks in relation to the subject area (for example,
healthcare records management, decontamination etc).
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Standard
Structures and processes needed to
identify, assess and manage specified risks
in relation to the subject area.
A standard describes and defines the quality of care to

be achieved. Each standard has a title, which
summarises the area on which that standard focuses. The standard statement which
follows explains the level of performance to be achieved. The standard statement is
expanded in the section headed criteria, with different criteria providing the detail of
what needs to be achieved for the standard to be reached.
Standard title
summarises the area on which that standard focuses.
Standard statement
explains the level of performance to be achieved.
Standard criteria
provides the detail of what needs to be achieved for the

standard to be reached.
Standard criteria
Explicit statements representing elements
of care which need to be achieved in order
for that standard to be reached.
For criteria to be valid and lead to improvements in service user care, they should be
consistent with SMART guidance:
Specific (explicit statements, not open to interpretation).

Measurable.
Achievable (of a level of acceptable performance agreed with stakeholder).
Relevant (related to important aspects of care).
Theoretically sound or timely (evidence based).
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Criteria can be classified as:
Structure criteria
(What is needed), refers to those resources

that are required to deliver care, including
the numbers of staff and skill mix, current
knowledge, skills and attitudes, materials
and drugs, equipment and physical space.
Process criteria
(What is done), refers to the actions and decisions taken by

healthcare professionals together with users and includes
communications, assessments and prescription of surgical and
other therapeutic interventions. The importance of process criteria
is determined by the extent to which poor design and/or non
adherence with processes in place influences care quality.
Outcome criteria
(What is expected to happen as a result), refers to the expected

outcomes of care. Increasingly the measurement of outcomes of
care is being seen as the most appropriate measure of
effectiveness.
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Measuring care
The measurement of compliance against criteria of care
is at the heart of clinical audit. In order to compare
actual care with care that should be provided, each
audit criterion should have an expected level of
performance or target assigned to it (Ashmore,
Ruthven and Hazelwood, 2011a).
Target/level of performance
A defined level or degree of expected compliance with audit criteria;

may be expressed in percentage or proportion of cases.
Selecting and developing appropriate performance levels

Audit criteria should consist of measurable statements of what should be happening
with explicit and quantifiable performance levels. These performance levels or targets
may be expressed as percentages.
There are a number of ways to set targets for compliance, including discussion and
development of a consensus opinion among audit team members and relevant
stakeholders and benchmarking against national rates.
Three factors should be taken into account and assessed when setting targets. These
factors are clinical importance, practicability and acceptability. The expected level of
performance or target can range from 0% (the criterion is something that must never
be done) to 100% (the criterion is something that must always be adhered to).
Clinical Importance
Where a criterion is critical to the safety of service users, targets may be set at 100%
or 0%, for example, a clinical audit relating to safe administration of medication could
have a target of 100% for the following criterion medication is not administered to a
service user with a known allergy to the medication.
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Practicability
However where clinical importance is not as significant,
resources required to fulfil the target performance level
should be considered and an acceptable performance
level (one which is seen as both reasonable and
attainable by those delivering and receiving care) should
be identified, for example, in a clinical audit relating to
the time frame within which service users should be seen
in a particular outpatient clinic, a target of 90% may be
deemed appropriate.
Acceptability
An optimum level of performance is set when the best care possible is identified given
the resources available and normal conditions of care-giving. This will lie somewhere
between the minimal acceptable level of care and the highest possible level of care
(possible under ideal conditions, with no restrictions on resources).
Inclusion/exclusion criteria
In order to ensure that the audit sample is representative of the target population and
to collect data which is fit for purpose, it is necessary to define what information
should be collected and what information should not be collected.
Inclusion criteria
Identify a target population to whom a clinical guideline

is intended to apply.
Exclusion criteria
Define areas outside the remit of the clinical guideline.
Many evidence based clinical guidelines identify inclusion and exclusion criteria.
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Example 1
In a clinical audit on compliance with the clinical
guideline NICE CG 52 (NICE, 2007) Drug misuse: opioid
detoxification, the following inclusion/exclusion criteria
apply:
Inclusion criteria:
Adults and young people who are dependent on

opiates, who have been identified as suitable for a detoxification programme and
who have made an informed decision to take part in a detoxification programme.
Exclusion criteria:
Adults and young people whose primary drug of misuse is a non-opiate.

Adults and young people who misuse alcohol, where the primary diagnosis and
focus of intervention is alcohol misuse.
Adults and young people who misuse other prescription drugs (for example,
benzodiazepines).
Adults and young people who misuse solvents (for example, aerosols and glue) or
other street drugs (for example, LSD [lysergic acid diethylamide]).
Adults and young people prescribed opiates and related drugs for therapeutic
purposes unrelated to substance misuse.
Example 2
In a clinical audit on compliance with clinical guideline NICE CG61 (NICE, 2008)
Irritable bowel syndrome in adults: diagnosis and management in primary care, the
following apply:
Inclusion criteria:
Adults (18 years and over) who present to primary care with symptoms suggestive
of irritable bowel syndrome (IBS).
Exclusion criteria:
Adults with other gastrointestinal disorders such as non-ulcer dyspepsia, coeliac

disease or inflammatory bowel disease.
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Exceptions
There may be a justifiable reason why some cases from
the identified sample may not comply with specific audit
criterion. In such cases the sample is not included in the
data analysis.
Exceptions
An exception is a clinically acceptable reason or

circumstance for not complying with specific
criteria (Dixon, 2009a).
Consensus on exceptions should be agreed before the start of the audit.

Example 1
The criterion involves treatment with a specific medication.
Possible exceptions:
There is a contra-indication to the medication.

Treatment had to be stopped due to side effects of medication.
Patient choice the patient declines this course of treatment.
Care should be taken that an exception is not a failure to comply with standard. For
example, patient choice may mask the fact that the patient was not given sufficient
information about risks and benefits to confidently agree to treatment (UH Bristol
Clinical Audit Team, 2009a).
Example 2
An audit on compliance with the previously referenced NICE CG61 Irritable bowel
syndrome in adults could have the following criterion and exceptions:
Criterion:
Percentage of service users with irritable bowel syndrome (IBS) advised how to
adjust their doses of laxative or anti-motility agent according to the clinical
response.
Exceptions:
Service users with IBS who are not using laxative or anti-motility agent.
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2.3
Stage 3 Measuring performance
This stage may be described in steps as follows:

Step 1: Data collection
Step 2: Data analysis
Step 3: Drawing conclusions
Step 4: Presentation of results
Step 1: Data
collection
Collection of
relevant data
about current
practice in
order to
facilitate
comparison.
Step 2: Data
analysis
Convert a
collection of
facts (data) into
useful
information in
order to identify
the level of
compliance with
the agreed
standard.
Step 3:
Drawing
conclusions
Identify the
reasons why
the standard
was not met.
Step 4:
Presentation of
results
Maximise the
impact of the
clinical audit on
the audience in
order to
generate
discussion and
to stimulate and
support action
planning.
Step 1: Data collection

The overall objective of clinical audit is to improve the quality of care and outcomes
by measuring current practice against best practice. When the standards against
which the audit will be conducted have been identified, the next step in the audit
process is the collection of relevant data about current practice in order to facilitate
comparison.
It is important that data collected in the course of any clinical audit is precise and
pertinent to the audit being performed. To ensure that data is collected appropriately,
there are a number of details which need to be established at the outset. These are:
The user group to be included, with inclusion/exclusion criteria defined.

The consent required to access user group information.
The healthcare professionals involved in the service users care.
The time period over which the criteria apply.
The analysis to be performed.
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Resources should be used effectively to collect the

minimum amount of data necessary to achieve the
audit objectives. Resource utilisation decisions should
be made at the outset of the audit and revised, if
appropriate, during the audit process. Due cognisance
should be given to data protection requirements. (See
section 4.2, pages 61-65 for further information).
Planning data collection
Before data collection commences, a structured approach should be taken to the
identification of relevant data and to ensuring that the data collection process is
efficient, effective and accurate.
Questions to assist when preparing for

data collection
What type of data do I need to collect (quantitative and/or qualitative)?
What data items will need to be used to show whether or not
performance levels have been met for each standard?
What data sources will be used to find the data?

Will a data collection tool need to be designed?
Will I need to collect data prospectively and/or retrospectively?
What size is the target population and will I need to take a sample?
How long will data be collected (manually and/or electronically)?
How long will it take to collect the required amount of data?
Who will be collecting the data?
How will I ensure data quality?
Adapted from Ashmore, Ruthven and Hazelwood (2011b).
Data type
The type of data required is dependent on the audit question and objectives. The aim
of data collection is to enable comparison of current practice against the audit
standard; therefore the type of data collected must facilitate this comparison.
Appendix three of this document provides further information on data type and
classification.
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Data items
All data collected must be relevant to the aims and
objectives of the audit. It is equally important that each
data item is adequate and not excessive for the purpose
of measurement of practice against the relevant audit
criteria. Collection of data which is not required for the
purposes of measurement provides little or no benefit, is
more time consuming and may infringe compliance with
information governance requirements and practices.
(See section 4.2, pages 61-65 for more information).
When standards of best practice, audit criteria, expected compliance rates and known
exceptions have been identified, definitions and instructions for data collection should
be compiled. This involves defining terms in the audit criteria and known exceptions
for data collection purposes and also defining where evidence should be obtained.
Sources of data
The source of data for an audit should be specified and agreed by the audit team. The
source specified should provide the most accurate and complete data as readily as
possible.
Where possible, relevant, routinely collected raw data from existing sources should be
used for the purposes of the clinical audit as this avoids duplication of information and
work and allows for repeated data collection and re-audit with minimum effort.
Examples of such sources are clinical information systems, service user records, HIPE
and observation of practice.
However, such records may be incomplete. Collection of data from several sources
may overcome this problem. The audit may only need data specific to the question at
hand and as a result the collection of new data is necessary. In such cases, only data
relevant to the audit is collected rather than collecting a large amount of data and
then deciding what is needed.
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Data collection tool

The following principles should apply when a data
collection tool is being developed (for example,
data collection forms or questionnaire):
The data to be collected should be relevant to

the objectives and criteria for the audit and the
expected performance levels.
Acronyms, jargon and technical terms should be avoided.

Definition of terms used should be included where necessary (involves
defining terms in the audit criteria and known exceptions).
There should be space to record exceptions.

Questions should be episode-specific i.e. relate to a specific episode of care.
Closed questions should be used, these should be clearly worded and contain no
ambiguity i.e. clarify the format for the answer (for example, date: day/month/yr).
Limit the use of free text or open questions to clinical audits with qualitative
elements as free text is difficult to code and analysis is very time consuming.
Filters should be used in order to make the process of completing the tool as quick
and efficient as possible, for example, if Yes, go to question four.
Data items should be presented in a logical order i.e. the tool should not require the
person collecting or analyzing the data to skip backwards and forwards.
Appendix four of this document provides further tips for the successful development
of clinical audit collection tools.
Data collection strategy
A data collection strategy should be decided following consideration of the audit topic
and objectives. Factors affecting selection of a data collection strategy for a clinical
audit include:
Feasibility in terms of resources and time frame to implement the data collection
strategy.
What data collection strategy is most likely to result in complete and reliable data?
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Retrospective data collection

Retrospective data is collected after completion of
treatment/care to service users.
Advantages include:
The data already exists and may be gathered quickly.

The possibility of identifying all service users meeting
the inclusion criteria may be increased; however, this
is dependent on being able to identify relevant service
users through coding or other records systems.
However, such data can quickly become out of date and the data available may not be
complete and accurate.
Concurrent/prospective data collection (looking forward)
Concurrent data is collected while treatment/care is being provided. Prospective audit
involves planning the recording of data on care which will be provided. The terms
concurrent and prospective are sometimes used interchangeably. If the data required
is not routinely collected, a prospective or concurrent audit should be undertaken.
Disadvantages to prospective data collection include:
Time is required to collect the data.

When data is collected concurrent with patient care, there is a potential for bias will clinical practice be affected by the knowledge that an audit is ongoing?
Deciding on a population or a sample
In order to decide on a population or a sample, it is first necessary to define the
population of concern (target population). A population can be defined as including all
the service users, events, cases, situations or items on which the audit is focused. A
sample is a part of the population of interest.
In order to determine which is suitable for the purposes of the clinical audit, the
following should be considered:
The audits inclusion/exclusion criteria (in order to identify the relevant population).
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Timeframe/time interval, for example, the previous

year, the next three months - is the time period
from which cases are to be drawn appropriate for
the objectives of the audit?
The size of the population.

What resources are available for the audit?
Whether sampling or population is most appropriate?
What sample selection method should be employed?
Sample selection methods
It is often not possible or necessary to gather data on all service users, events or
items for audit purposes; therefore sampling is often required. It is important that any
sample selected is representative of the population under examination. There are
numerous sampling methods which may be used; however random sampling and
convenience sampling tend to be the most commonly used methods.
The simplest form of random sampling involves selecting service users at random
from an overall population listing, for example every 3rd, 6th case etc. The Hospital Inpatient Enquiry System (HIPE) offers this facility (HSE, 2008). Random number
generation can also be used.
Convenience sampling is sometimes used as a simple and effective way of carrying
out a sample survey. It involves choosing the nearest and most convenient persons to
act as respondents; it therefore does not produce findings that can be taken to be
representative, for example, the first 10 cases presenting after a specific time.
Interval sampling is often determined by a time period. For example, all cases in a
specific timeframe.
Sample size
Clinical audit is not research. It is about evaluating compliance with standards rather
than creating new knowledge, therefore sample sizes for data collection are often a
compromise between the statistical validity of the results and pragmatic issues around
data collection i.e. time, access to data, costs.
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When determining the number of sample subjects,

consideration should be given to the level of assurance
required from audit results and any constraints which
may impact upon the audit.
For many audit topics, a small amount of data may be
sufficient for the purposes of the audit; however, if a
contentious issue is being audited a larger sample size
may be required.
The sample size should be sufficient to generate meaningful results.

Where necessary the sample should allow for adjustment for case mix.
The clinical audit should use pre-existing data sets where possible.
The sample should be small enough to allow for speedy data collection but large
enough to be representative. In some audits the sample will be time driven and in
others it will be numerical.
If the data collection takes too long, interest will be lost and data completeness will
suffer.
In numerical audits, the number of cases selected should reflect the commonness
of the condition or therapy, but should be of reasonable number to draw
subsequent conclusions.
In time based audits one to three months should be adequate for the majority of
audits.
(NHS Clinical Governance Support Team, 2005).
A credible sample of subjects should be agreed with stakeholders. If the audit intends
to include the perspective of service users, the aim should be to ensure that the
sample of service users recruited to the audit is as representative of the relevant
population as possible. In addition, different audit techniques might be needed to
engage the views of different groups.
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How should data be collected (manually and/or

electronically)?
The most appropriate method for data collection
should be utilised, for example, pocket PCs or
paper based audits. As clinical audit records must
be retained for five years (National Hospitals
Office, 2007), electronic storage is optimal.
How long should it take to collect the required amount of data?
The time period chosen depends on the number of cases that are treated on a daily
basis and the number needed to make a confident judgment of the care provided.
(NICE, 2002).
Timeframe for data collection is influenced by:
The sample (size and population).
Inclusion and exclusion criteria.
Target date for audit completion.
Who collects the data?

Depending on the audit, data may be collected by more than one person or different
people may be responsible for completing different data sets. There should be no
confusion over terminology. A definition should be provided for each data item so that
it is collected consistently (inter-rater reliability). In addition, everyone involved in
data collection should know and understand who is responsible for the various
elements including what, how and where the data is to be recorded.
Ensuring data quality
Data can be said to be of good quality when it does what it is needed to do. There
should be clear definitions for each data item to be collected to ensure that data
collectors have a good understanding of what, how and when data needs to be
collected. There should also be routine data quality checks to minimise the occurrence
of reporting and input errors.
(Health Information and Quality Authority, 2010).
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Pilot
Before collecting the data for the full audit sample, a
pilot should be considered. Piloting a planned audit
and its methodology can provide evidence as to
whether the proposed methodology is feasible. Potter,
Fuller & Ferris (2010) suggest pilot testing of a 10%
sample of the planned sample size has the potential to
save a great deal of time.
A pilot may:
reveal problems such as a data collection tool which is difficult to understand or to

complete; or
be used in order to identify themes in answers provided to open questions on data

collection forms and these in turn can be reformed as tick-box options for ease of
analysis.
Step 2: Data analysis
Data collection is only part of the process of measuring performance, in order to

compare actual practice and performance against the agreed standards, the clinical
audit data must be collated and analysed. The basic aim of data analysis is to convert
a collection of facts (data) into useful information in order identify the level of
compliance with the agreed standard.
Collation of clinical audit data
Collation of data involves the gathering together of all data collected during the period
of the audit. This may involve transferring the data collected from the data collection
tool onto summary sheets (manual data collection) or onto a spreadsheet or database
(manual or electronic data collection) for interpretation. When electronic files are
used, service user data should be recorded anonymously with the use of a unique
identifier and files should be password protected.
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Coding of data
Use of a data coding sheet or a coding manual may
assist if data is to be entered onto a spreadsheet or a
database for analysis. This is where a simple numeric
code is assigned to all the possible answers for each
question in the data set.
A number of variables (characteristics) may be measured
for each subject, for example, in the case of a person;
variables could include gender, age and ethnicity.
A variable such as age may be entered directly into a database, however for variables
such as gender or ethnicity it is necessary to identify a coding system. For example,
in the case of gender, 1 may be assigned for male and 2 for female, similarly if one
question requires a yes or no answer, 1 may be assigned for yes and 2 for no. In
the case of questions such as ethnicity, each ethnic group is allocated a different
number and the appropriate number is entered onto the spreadsheet/database.
When a coding manual is used, a clear consistent coding scheme should be used,
including codes for missing or unavailable data. 9 is the universal code for missing
data or 99 if options are higher than 9. Where free text is used, code the text
information by category wherever possible, for example, disease groups, therapeutic
drug groups. A key question to ask is whether an independent person could review
the spreadsheet, understand it and draw the same conclusions from their own
independent analysis.
Organisation of clinical data
Once the data is collated, it needs to be organised in a logical way to enable analysis.
This may involve preparing tables of data, grouping the data, for example, waiting
time <1hour, 1- 4hours, > 4hours or summarising using descriptive statistics.
Checking/interpreting the data
Interpretation of data involves looking for patterns in the data sets. Inconsistent or
missing data should be reviewed as errors in data collection or transfer may have
occurred. It may be necessary to check back to the original records to identify errors.
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Type of data analysis

The main aim of data analysis is to answer the questions
posed by the audit objectives; highlighting areas of
good practice and areas that require particular
attention or improvement. It is often necessary to
perform basic calculations on the raw data collected in
order to get results from which conclusions can be
arrived. The type of data analysis depends on the type of
information collected. This can range from simple averages
and percentages to sophisticated statistical techniques.
For the majority of audits, complex statistical analysis is not necessary or appropriate.
A simple, clear and concise analysis which can be easily understood by everyone
involved in the provision of care is required in order to stimulate change.
For the single healthcare professional carrying out an audit with a small dataset, a
pen, paper and calculator may be all that is required to carry out a simple analysis.
Alternatively a spreadsheet program such as Microsoft Excel may be a useful tool.
By using this program it is possible to perform the calculations required and to
produce tables, charts and graphs for presenting and comparing information in a
simple, easy to understand format.
Calculating compliance with clinical audit criteria
The basic requirement of an audit is to identify whether or not performance levels
have been reached. This requires working out the percentage of cases that have met
each audit criterion. In order to calculate the percentage it is necessary to identify
both the total number of applicable cases for a criterion (the denominator) and the
total number within the denominator group that met the criterion (the numerator).
The percentage is then calculated by
Numerator
dividing the numerator by the denominator
and multiplying the answer by 100.
100
Denominator
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The most important factor in preventing errors when

calculating the percentage of cases that have met the
audit criterion is ensuring identification of the correct
denominator.
The denominator is the total number of cases to which
the audit criterion applies.
This figure is obtained by subtracting cases meeting any agreed
exceptions for a particular criterion (refer to Stage 2, page 28) from the total number
of cases which meet each of the inclusion criteria and none of the exclusion criteria.
Example
Using the previously referenced clinical guideline NICE CG61 (NICE, 2008) Irritable
bowel syndrome in adults; diagnosis and management in primary care:
Audit Criterion:
Percentage of service users with irritable bowel syndrome (IBS) advised how to
adjust their doses of laxative or anti-motility agent according to the clinical
response.
The total number of cases to which this audit criterion applies, is identified by
determining the number of cases which may be included/excluded in the audit sample
using the inclusion/exclusion criteria below and then subtracting any case which
meets the agreed exception:
Inclusion criteria Adults (18 years and over) who present to primary care with
symptoms suggestive of irritable bowel syndrome (IBS).
Exclusion criteria Adults with other gastrointestinal disorders such as non-ulcer

dyspepsia, coeliac disease or inflammatory bowel disease.
Agreed exception Service users with IBS who are not using laxative or anti-motility
agent.
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Descriptive statistics
Descriptive statistics may be used to describe the
basic quantitative (numerical) features of data in a
study.
A descriptive statistic reduces lots of data into a
simpler more understandable summary.
The nature of the audit topic and the data measured will determine which type of
descriptive statistic will be most useful for presentation of information.
Useful descriptive statistics include information on the distribution of data, the mean
or average, median, mode and measures of dispersion i.e. the range and standard
deviation.
More elaborate statistical manipulation is possible but not necessary in any clinical
audit effecting change is more important.
Appendix five contains a glossary of terms relating to descriptive statistics.
Displaying data
To facilitate the drawing of conclusions from analysed data, the data should be
displayed in the simplest, clearest and most effective way possible. There are many
different ways of displaying data, through comparing data from one area against data
from another area to comparing results against expected level of performance or
current audit results against previous audit results.
Please refer to Step 4, Presentation of results (pages 44-45), for further information
on effective data display and presentation.
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Step 3: Drawing conclusions

After results have been compiled and the data has
been analysed against the standards, the final step
in the process (where applicable), is to identify the
reasons why the standard was not met.
In order to understand the reason for failure to achieve
compliance with clinical audit criteria, the audit team should
carefully review all findings. Individual cases where care is not consistent with criteria
should be reviewed to find any cases which may still represent acceptable care.
Cases of unacceptable care should then be reviewed in order for the team to:
Clearly identify and agree on areas for improvement identified by the clinical audit.
Analyse the areas for improvement to identify what underlying, contributory or
deep-rooted factors are involved.
There must be a clear understanding of the reasons why performance levels are not
being reached to enable development of appropriate and effective solutions. There are
a number of tools that can be utilised to facilitate a root cause analysis, including
process mapping, the five whys and cause and effect diagrams (fishbone
diagramming).
Process mapping
This involves mapping out each step of a process in sequence so that areas for
improvement can be identified. Process maps are an effective way to identify
constraints and ineffective or unnecessary process steps.
The five whys
Involves repeatedly asking the question why? in order to drill down further into an
issue which can lead to the cause of the problem. The reason for any problem can
often lead to another question. Asking why five times is only a guide as depending on
the issue, the question may be asked a lesser or greater number of times before
reaching the origin of the problem. This process can be used independently or as part
of a cause and effect diagram.
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Cause and effect (fishbone) diagramming

This is a graphic problem solving tool that can be
used to explore and display the possible causes for
effects or problems. It can be used to structure a
brainstorming session as it can help to sort ideas
into various useful categories.
A problem or an effect is written at the head of the fish,
then a common set of major categories of causative factors
are written on diagonal lines branching from the main arrow, the bones.
Examples include people, procedures, materials, equipment and environment. In
order to develop the various categories, it is necessary to think in terms of each major
step in the process.
A list of possible causes for each category should be generated through brainstorming
by asking the question why does this happen? in relation to each cause. The causes
and sub-causes are then listed on branch bones (branching off from the main
branch/cause). This will highlight relationships among the causes. It is necessary to
keep asking why? until a useful level of detail is reached and an appropriate solution
may be developed.
By establishing the reasons why performance levels for specific criteria were not met,
the team are then enabled to discuss/lead discussions around recommendations for
improvements.
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Step 4: Presentation of results
The aim of any presentation of results should be to

maximise the impact of the clinical audit on the
audience in order to generate discussion and to
stimulate and support action planning.
There are various different methods for the
presentation of clinical audit results including:
Visual presentations, for example, posters which are useful ways of

reaching as many stakeholders as possible. Data can also be presented
visually using tables, charts and graphs in both written and verbal presentations
(for example, through using presentation software like Microsoft PowerPoint).
Written reports for submission to the relevant clinical lead, directorate or

governance committee.
Verbal presentations at relevant meetings.

Visual presentation of data
To facilitate the drawing of conclusions from analysed data, the data should be
displayed in the simplest, clearest and most effective way possible. Reading or
listening to lots of facts and figures is not always an effective way to convey
information and may prove difficult for an audience to interpret and understand the
information being conveyed. Visual methods can make the point much stronger than
just describing the data.
Data graphics are a good way of communicating this information to others. The most
commonly used form of data graphics in clinical audit are tables, graphs and charts.
When deciding on which form of data graphics to use, consideration of the following
may be helpful:
What information is to be communicated?

Who is the audience?
What might prevent them from understanding this information?
Appendix six of this document contains further information on the presentation of data
using tables, graphs and charts.
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Written Reports
An audit report should be written as soon as all audit
data has been analysed. Graphical analysis should be
used to visually demonstrate audit results.
The audit report should outline the purpose of the audit,
the criteria measured, the actual performance achieved
and a comparison of actual performance against the
selected best practice benchmarks or high quality evidence
based standards of care.
The report should clearly identify:
Areas for improvement, for example, unrecorded practice, practice not occurring,
poor levels of service user satisfaction.
Causes, for example, poor documentation, inadequate staffing, training and

practice issues.
Needed improvements, for example, the introduction of a structured assessment

pro-forma for service users with asthma so that all relevant service user data and
examination findings are checked.
Information explaining why some cases do not meet the required standards.
Relevant, meaningful and useful information that will help to identify and address
issues arising from the audit.
Appendix seven contains further information on the clinical audit report.
In compliance with Data Protection legislation, unless presentation of clinical audit
results are confined to the clinical care team, only irrevocably anonymised data should
be disclosed.
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2.4
Stage 4 Making improvements
The purpose of performing clinical audit is to assess

the degree to which the clinical services offered comply
with the accepted evidence based practice standard.
Clinical audit results may show areas of excellent or
notable practice and this should be acknowledged. For
such audits there should be an explicit statement saying no
further action required in the audit summary report and a rationale why re-audit is
not required.
Clinical audit results may also identify areas for improvement where the required
standards are not being met.
Ashmore, Ruthven and Hazelwood (2011c) identify clinical audit as a change process,
stating:
audit that simply measures but does not drive change to address problems
identified, is not good audit. All good audit projects must include a programme
of change activity and post-identification of the findings from audit, to ensure
necessary changes happen.
The clinical audit group should interpret and discuss the findings in order to clarify the
areas where action is required so as to improve the quality of clinical care and its
outcomes. Where audit has shown that there are serious concerns regarding the
practice of an individual, these should be conveyed immediately to the audit sponsor,
who should inform the manager of the service for urgent action.
All audit reports should be shared with the service, specifically with the relevant Head
of Department, Head of Service and Governance Group. Where audits are instigated
by a particular committee/group, reports should be submitted to the committee/group
for review and action.
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Change is often the most difficult part of the audit.

When the audit team have developed the
recommendations, decisions should be made on how
changes can be introduced and monitored. Results
should be used in conjunction with feedback and local
consensus to change clinical practice and to improve
standards.
Priorities for action should be identified and these should be
clearly documented. All audits should be accompanied by a quality
improvement plan in order to achieve the required improvements in practice.
Quality improvement plans (QIPs)
Quality improvement plans can be developed to address those areas requiring
improvement. It is important that improvement tasks or actions outlined in the QIP
relate to local and national priorities or targets and the service providers own
available resources. QIPs should also be integrated into the existing management
system of the service provider to monitor implementation.
Quality improvement plans should be time limited with clear milestones and concrete
recommendations. Responsibilities for implementing tasks or actions should be clearly
allocated to staff who carry the necessary authority to effect such change. Sometimes,
QIPs and associated actions or tasks are beyond the scope or domain of individuals. In
these cases, the support and backing of the service is fundamental to the success of
the audit.
Note: There may not be QIPs against every standard; priorities should be identified,
for example, through risk assessment to identify areas of highest risk. Risks
identified as a result of clinical audit should be submitted for inclusion on the
appropriate risk register. The governance committee should be responsible for
escalating those high and very high risks up the line for possible inclusion in
higher level risk registers, for example, hospital, regional or national risk
registers.
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Writing quality improvement plans
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2.5
Stage 5 Sustaining improvements
The audit cycle is a continuous process. A complete audit

cycle as described by Ashmore, Ruthven and
Hazelwood (2011d, p.93):
ideally involves two data collections and a
comparison of one with the other, following
implementation of change after the first data collection,
in order to determine whether the desired
improvements have been made. Further cycles may be
necessary if performance still fails to attain the levels set at the outset of the
audit. At this stage there may be justification for adjusting the desired
performance levels in the light of the results obtained.
Where quality improvement plans are put in place, monitoring should be performed to
ensure plans are implemented as agreed and within the agreed timeframe.
Clinical leads and/or managers who agree to implement quality improvement plans
are accountable for the delivery of quality improvement plans and sustaining quality
improvement. A summary report of progress should be submitted through the
appropriate lines of responsibility at regular intervals.
The appropriate governance committee is responsible for monitoring and reporting the
progress of implementation through the reporting structure. The progress of any
quality improvement plan associated with an audit should be formally assessed at
regular intervals and appropriate actions to be taken should be determined where
progress is not being maintained.
Where plans have not been implemented, a rapid re-audit is recommended to ensure
that changes have indeed improved practice and to ascertain whether further audit
procedures are required in the short term.
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Performance indicators
Performance indicators can be used to monitor
improvements as a result of quality improvement
activities. A small number of key performance
indicators may be developed for each quality
improvement programme to monitor implementation of
the improvement plans.
A red, amber and green traffic light system can be used to
monitor implementation status. This system can also be used to measure
the impact of change on practice when performing rapid re-audits.
Evaluating audit quality
It is recommended that the quality of an audit programme is evaluated as part of the
wider quality and risk management agenda (NICE, 2002). Service providers should
assess their structures, processes, outcomes and resources for audit activities. All
clinical audits should be conducted in a manner that complies with legislation,
guidance and service provider policies relating to confidentiality and data protection.
Dissemination and celebrating success
Completion of an audit cycle will usually result in improvements in practice. This
should be communicated to all stakeholders.
A successful audit in one service may be transferable to other parts of the service.
Completed audits should be shared locally via the most appropriate mechanisms,
including department quality and safety meetings, journal club meetings, the intranet,
newsletters and local conferences and seminars. Consideration should also be given to
sharing clinical audit work regionally and nationally through relevant journals,
conferences and other media.
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Remember to close the loop by re-auditing

Audit is a continuous cycle. If following an initial audit it
is found that desired performance levels are not being
reached, and a programme of change activity has been
put in place; then the audit should be repeated to show
whether the changes implemented have improved care or
whether further changes are required. This cycle is repeated
until the desired performance levels are being achieved.
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2.6
Summary The five stage approach to

clinical audit
The Stages of Clinical Audit

Stage 1 - Planning for audit
Involving stakeholders
Determining the audit topic
Planning the delivery of audit fieldwork
Stage 2 Standard and criteria selection
Identification of standards and audit criteria
Selecting and developing appropriate performance levels
Inclusion/exclusion criteria
Exceptions
Stage 3 - Measuring performance
Data collection
Data analysis measure actual performance against standard
Drawing conclusions
Presentation of results
Stage 4 Making improvements
Development of quality improvement plans (QIPs)
Stage 5 Sustaining improvements
Monitoring the quality improvement plan
Performance indicators
Dissemination and celebrating success
Remember - close the loop - re-audit
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3. Resources required to support clinical audit
3.
Resources required to support clinical audit
3.1
Service provider support
For clinical audit to be effective it requires commitment and support throughout the
service including senior management. Clinical audit should be seen to be recognised
as a valued activity and should be included as a priority in service planning.
Recommendation 7.8 of the Report of the Commission on Patient Safety and Quality
Assurance Building a Culture of Patient Safety (2008, P. 161) states:
Every healthcare facility should develop and implement an Annual Clinical Audit
Forward Plan as part of its annual planning and delivery cycle for clinical audit
activities and the facility's safety and quality governance framework. This Plan
should reflect the national, service, team and individual audit requirements on
the facility. It should be the responsibility of the Clinical Leader, with
accountability for safety and quality at Board level, to ensure that the Plan is
developed and implemented with effective clinical engagement and reported to
the Board of the facility.
A.
Clinical audit strategy
A clinical audit strategy is an operational action plan primarily aimed at those with
responsibility for overseeing the direction and development of clinical audit within the
service. For example, divisional/service/department leads or committees/steering/
governance groups.
Clinical audit strategies should begin with a statement of the service providers
commitment to the process of clinical audit and to delivering the objectives set out in
the strategy.
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A clinical audit strategy should:
Be a time-limited document, i.e. covering a period of one or more years.
Connect clinical audit with the service providers governance and assurance
systems and its corporate objectives.
Provide a medium to long term vision for the development of clinical audit for
example, 3 -5 years.
Set out a number of service objectives for the period covered by the strategy.
Healthcare Quality Improvement Partnership (2012).
Progress in delivering the plan and meeting objectives should be monitored on a

regular basis. The plan should be revised and updated annually.
Clinical audit strategies should be supported and underpinned by a clinical audit
policy.
B.
Clinical audit policy
A clinical audit policy should set out the procedure for the conduct of clinical audit
within the service outlining standards which should be met, processes and procedures
to be followed and how different issues are to be addressed.
The target audience of a clinical audit policy should be everyone involved in the
clinical audit process.
C.
Clinical audit programme
Each service provider should have a programme for clinical audit. This is a plan which
specifies what clinical audits will be carried out over the course of the programme
duration (usually annually). It should give direction and focus with regard to how and
which clinical audit activity will be supported in the service.
It should be based on the service providers priorities for clinical audit (see section on
prioritising audit topics and levels of priority on pages 17-18 of this document).
Acknowledging that the audit cycle includes re-audit, a proportion of topics for reaudit should also be included in the annual audit plan.
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As with all plans, the clinical audit programme is subject to change as priorities in
service provision change. Any changes to the clinical audit plan should be
communicated to all stakeholders.
Resources to support the delivery of a clinical audit programme

Clinical audit committee with members who can provide expertise and
experience with clinical audit.
Clinical audit support staff who can provide advice and training and refer to other
available resources.
Clinical and educational leads.
Healthcare records manager and staff who can facilitate access to service user
records.
Information systems access and advice.
Training available related to the clinical audit process and how to design and
carry out clinical audits.
Advice on how to handle ethical issues related to clinical audits.
Templates for planning and reporting on clinical audits.
Advice on the technical aspects of carrying out a clinical audit.
Access to reference materials on clinical audit.
Technical support for clinical audit including a database of clinical audits.
Adapted from Dixon and Pearse (2011).
Proposed audit programmes should be discussed at a meeting of relevant
stakeholders (dependant on whether the programme pertains to a particular clinical
service or the service in its entirety).
D.
Clinical audit leads
There are different levels of clinical audit lead, for example, at service, divisional or
speciality level. At service level the clinical audit leads responsibility is to organise,
develop, improve and support the performance of clinical audit within the service
whereas the role of the lead for a specific clinical audit is to provide leadership in the
completion of the clinical audit.
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E.
Fostering a culture which is supportive of clinical audit
Requirements of a culture supportive of clinical audit:
A common vision of the benefits and resource requirements of clinical audit among
managers and staff.
A service wide strategy with clear lines of responsibility and accountability.

An overall plan for clinical audit comprising of a comprehensive structured
programme aimed at nurturing effective clinical audits.
Leadership and direction of audit programmes including a designated lead whose

responsibility is to organise, develop, improve and support the performance of
clinical audit within the service.
Strategy and planning in audit programmes.

Resources and support for audit programmes.
Monitoring and reporting of audit activity.
Commitment to, participation in and high levels of clinical audit activity which by its
nature and impact is seen by its participants to be involving and relevant and thus
fosters positive attitudes to further participation.
F.
Practical supports for clinical audit
Provision of practical supports for clinical audit includes the provision of the following:
Policies, procedures, protocols and guidelines (PPPGs) in relation to clinical audit

which provide a vision of the goals and purposes of clinical audit within the service
and defining how a clinical audit should be undertaken.
Effective training in clinical audit methods.

Dedicated staff to provide expertise and/or advice on audit design and analysis, for
example, clinical audit facilitators.
Practical mechanisms to make data collection easier such as good quality

information systems and support from service information departments and
information specialists.
Allocated (protected) time for clinical audit.

Support for required changes identified by the clinical audit process.
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3.2
Clinical audit facilitation
Service providers should assess whether additional clinical audit support staff are
required to provide hands on help and advice on the design of projects.
Clinical audit facilitators can provide support in all aspects of clinical audits, including:
Project planning.
Proforma design.
Spreadsheet/database design.
Data checking and entry.
Data analysis.
Presentation design.
Report writing.
Action planning.
Clinical audit facilitators should have skills in study design, data collection, computing,
and statistical analysis. The training needs of clinical audit facilitators should be
recognised and resources should be made available in order to facilitate their
attendance at appropriate courses.
In relation to clinical audit, the aim of clinical governance is to support changes to
improve practice identified by the clinical audit process through ensuring the
engagement of senior management and senior clinicians in the process of oversight of
audit thus providing the leadership and managerial commitment which is required for
successful clinical audit practice.
Clinical audit can provide the required evidence to show how well a service is meeting
a desired standard of clinical care and providing quality care to service users. It can
also demonstrate the effectiveness of implemented changes and leadership.
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4. Wider considerations
4.
Wider considerations
Consideration also needs to be given to ethical and data protection issues in relation
to clinical audit.
4.1
Ethical issues
A.
What is ethics?
Ethics is the inquiry into the morality of an action. There should be consideration of
ethical principles in relation to all aspects of clinical care including clinical audit.
Clinical audit should be conducted within an ethical framework, i.e. the clinical audit
process should:
Respect each service users right to make choices concerning their own lives.
Benefit service users and not cause harm.
Treat all service users fairly.
At a practical level, this means ensuring service users and staff confidentiality and
ensuring that data is collected and stored appropriately (UH Bristol Clinical Audit
Team, 2009b).
No clinical audit should examine the work of another professional or speciality without
their knowledge. All those whom the audit will directly affect should be informed of
and if possible, involved in, the audit.
Service users should be approached in a sensitive and respectful manner and it should
be explained that they are not obliged to be part of the audit and declining to take
part will not affect care in any way.
Service users should be assured about the confidentiality of any responses given (for
example, anonymisation of data) and the length of time for which their personal
information will be held.
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Anyone conducting an audit that involves direct contact with service users for
interview or to request completion of a questionnaire should give a full written
explanation to the service user, in relevant language, as to the purpose of the audit.
Clinical audits involving questionnaires posted to service users homes should be
accompanied by a written explanation of the purpose of the questionnaire/audit along
with an identified contact name and number (usually the audit lead or an audit
facilitator). While encouraging participation for improvement purposes, the letter
should also state that recipients are under no obligation to take part in the audit and
that declining to take part will not affect their care in any way.
The name and the telephone number of a contact point should be given in case any
questions/issues arise in connection with the questionnaire. No consent form is
required for questionnaires as consent will be deemed to have been given if the
service user returns the questionnaire.
Where there is a possibility that the audit may be intrusive to service users, for
example, in cases where a service user is asked to complete a questionnaire or
undergo an interview which may involve asking sensitive questions, those involved in
managing the audit should seek ethical advice.
B.
Is ethical review required for clinical audit?
Previously decisions regarding whether an activity required ethical review related

directly to whether the activity was classed as clinical audit or research. If an activity
was classed as clinical audit it was automatically deemed not to require ethical review,
whereas research proposals required ethical review and approval. However due to the
many similarities between clinical audit and clinical research the boundaries between
them can be blurred. As a result, Wade (2005) recommends that Decisions about the
need for ethical review should be based on the morality of all actions rather than
arbitrary distinctions between audit and research.
Guidance from the Irish Council of Bioethics (2004) suggests that clinical audits do not
require the approval of the Research Ethics Committee. This guidance assumes that
audit never involves disturbance to the service user beyond that required for normal
clinical management.
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Possible screening questions to determine if ethical review may be required are

outlined in the following table:
Will the proposed clinical audit:

Infringe on the rights of any service user or risk breaching their confidentiality or
privacy?
Pose any risk for or burden on a service user beyond those of his or her routine
care?
Involve any clinically significant departure from usual clinical care?
Gather any information about any service user other than information that is
ordinarily collected as part of providing routine care for the patient?
Collect data directly from any service user and if so could the activity subject a
service user to more than a minimal burden or risk if it requests sensitive
information or is time consuming?
Collect or disclose any data that could be used to identify any service user or
healthcare professional?
Have someone carrying out the activity who does not normally have access to
service users records? People who normally have access to service user records
include clinical staff providing direct patient care and staff employed to support
clinical audit when a duty of confidentiality is included in their job descriptions.
Involve a potential conflict of obligation to individual or all service users such as
if the activity involves a trade-off between cost and quality?
Involve the use of any untested clinical or systems intervention or testing a
hypothesis?
Allocate any interventions differently among groups of service users or staff, for
example, in implementing a change in practice?
Adapted from Dixon, N. (2009b).
If the audit team is concerned about the ethicality of their audit, ethical advice should
be sought.
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4.2
Issues of data protection
A.
Data protection responsibilities
Legislation around data protection and service user record confidentiality must be
complied with when performing clinical audits. The Data Protection Acts 1988 & 2003
provide the legislative basis for the approach of the Office of the Data Protection
Commissioner with regard to personal data across all sectors of society - public,
private and voluntary.
B.
Data protection principles
Anyone processing personal data must comply with the eight rules of data protection
in line with the Data Protection Acts, 1988 and 2003:
Obtain and process information fairly.

Keep it only for one or more specified, explicit and lawful purposes.
Use and disclose it only in ways compatible with these purposes.
Keep it safe and secure.
Keep it accurate, completed and up to date.
Ensure it is adequate, relevant and not excessive.
Retain it for no longer than is necessary for the purpose or purposes.
Give a copy of his/her personal data to that individual on request.
C.
Data protection guidelines
Data Protection Guidelines on research in the Health Sector (Data Protection

Commissioner, 2007, P.12) states:
Given the fundamental role played by clinical audit in patient care, implied consent
is normally all that is required when the audit could likely be of benefit to that
patient. Implied consent will also be considered as sufficient in those cases where
no direct benefit is likely to accrue to the patient concerned and where the audit is
to be carried out by the health facility itself.
However, the Data Protection Acts provides an exemption from obtaining consent
from the service user for processing for statistical, research or scientific purposes
carried out by the data controller itself (i.e. the treating healthcare professional
/service provider) where there are no disclosures of personal data to any outside third
parties.
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Where access to service user identifiable information is not accompanied by explicit

consent, the Data Protection Acts require that access is necessary for medical
purposes; and access is only given to:
a health professional; or
a person who, in the circumstances, owes a duty of confidentiality to the

service user that is equivalent to that which would exist if that person were a
health professional.
Exceptions to the healthcare professions duty of

confidentiality to the service user:
Where a service user gives explicit consent to the disclosure of information to
third parties.
When disclosure is required by or under any enactment or by a rule of law or
order of a court.
When disclosure is necessary to protect the vital interests of the service user or
of another individual (consent should be obtained if possible in such situations).
Data Protection Acts, 1988 and 2003.
Other exceptions provided for in legislation include:
Health (Provision of information) Act 1997 allows for provision of information to
the National Cancer Registry without the consent of the service users concerned.
Infection Diseases Regulations (1981 and 2011) set out legal obligations to
disclose details of notifiable diseases with or without consent.
D.
Guidance regarding consent requirements for clinical audit
In general, clinical audit does not require informed consent (HSE, 2013). Members of
a healthcare team (or their support staff, for example, clinical audit staff) delivering
direct care to a service user can perform a review of service user data without
consent. However, it is good practice to inform service users that as part of normal
care processes personal data may be used for audit and quality improvement
purposes and also about the importance of the clinical audit function within the
service. This may be achieved through informing service users through a statement of
information practices or leaflets or posters which are clearly displayed/made available
by the service provider (HIQA, October 2012).
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Consent is not required where the personal health information is irrevocably

anonymised by the data controller prior to disclosing to a third party. Care must be
taken to ensure that the service user is completely unidentifiable even when the data
is anonymised. (See section F, pages 64-65 for further information.)
Where a clinical audit is carried out by persons who are not involved in service user
care (i.e. persons who are external to the data controller (the service provider)),
informed consent is required to enable such persons to access personal data.
If a service user gives consent to the disclosure of records to third parties, the health
professional ensures they understand the consequences of such disclosure, what will
be disclosed, the reasons for the disclosure and the consequences of giving consent.
Service users healthcare records are only disclosed in accordance with the conditions
of their consent. Service users have the right to withdraw consent to disclosure of
their healthcare records /information at any time.
E.
Confidentiality and access to service user health information
The audit methodology should be designed so that the confidentiality of personal

health information is not compromised. When reporting on clinical audits, data is
completely anonymised in every case. No link between audit conclusions, service
users or healthcare staff should be possible.
All staff must make every effort to preserve the confidentiality of personal health
information and ensure that they work within the requirements of the Data Protection
Acts 1988 and 2003:
Data is only accessible by appropriately authorised staff on a need-to-know basis.

Data collection sheets containing any personal identifiable information should only
be kept for the length of time they are absolutely required (for the purposes of the
audit). Once they are no longer required, they should be destroyed immediately.
Raw data is anonymised before it is entered into a computer database.

Data is checked to ensure confidentiality and accuracy.
No service user identifiable information is stored on a computer with raw data.
Anonymised data sheets/questionnaires should be kept only for as long as is
necessary and destroyed as soon as all information has been retrieved from the
questionnaires.
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Any waste material that contains personal, private or confidential information

should be eliminated in a manner which ensures that privacy rights and
confidentiality obligations are not compromised.
There should be a designated point of storage for data in current use. This should
be a locked filing cabinet, to comply with data protection requirements.
All data should be stored together i.e. the physical raw data, the first data input
into the computer, any subsequent analysis, and the final draft.
The data must be archived, so that it remains available throughout the subsequent
phases of the clinical audit and for five years afterwards.
Archived clinical audits should be stored on a secure computer.

All computers are password protected.
All devices used to store data are encrypted (for example, laptops and USB
devices).
If laptops are removed from the work location, the person responsible for that
laptop must ensure that it is secure at all times.
The service provider should have a central location for the storage of final audit
reports (both in hard and soft copy). It is also recommended that a log be
maintained for traceability purposes of the reports and where they are at any given
time.
All data recorded for audit purposes should be made anonymous by appropriately
authorised individuals before being made available for review and consideration by
others.
F.
Anonymisation of data
The anonymisation of data involves removal of all data elements that could be used to
identify an individual, for example, name or healthcare record number. It is
recommended that service user data be anonymised before it is accessed for clinical
audit purposes:
Irrevocable anonymisation of personal data puts it outside data protection

requirements as the data can no longer be linked to an individual and therefore
cannot be considered to be personal data.
Where service user data is anonymised, there is no need from a data protection
perspective to seek consent for the use of the data for clinical audit purposes.
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However, care needs to be taken when rendering data anonymous, as depending on

the nature of the illness and the profile of the service user, there may be instances in
which the data may actually still be identifiable. Where this might possibly be the
case, an extra effort should be made to further remove any potential identifying
information. Where this is not possible it would be advisable to either refrain from
using the identifiable information or seek the consent of the person for such use.
Equally, it is recognised that in some instances where there is a need to link episodes
of care and prevent duplication of data; information may need to be capable of being
matched or linked. This can be achieved through appropriate pseudonymisation (e.g.,
use of initials, coding) methods without the need to retain all identifying
characteristics with the data.
Pseudonymisation (or reversible anonymisation) involves the use of a coding
system, for example, allocating individuals with unique, reference numbers. The lookup list from which the true identities may be obtained is then held securely and only
accessed by authorised persons for specific, pre-defined purposes. Similar to the
advice in relation to anonymisation, where pseudonymisation methods are used, it is
recommended that extra efforts, beyond use of initials etc, be incorporated where a
condition is particularly rare. Unique identifying numbers should also be given to
healthcare professional that may be involved in the audits. Individuals should not be
named in any of the reports.
In certain cases where anonymising data may be impractical and detrimental to the
clinical audit, such as during the ongoing data collection to prevent duplication of data
collection, the audit team must ensure that the data is kept purely for the purposes of
analysis by those directly involved in the management of the clinical audit. Identifiable
data must not be transferred to third parties without the permission of the service
user.
Further data protection information and advice is available from the Office of the Data
Protection Commissioner website www.dataprotection.ie. At the time of writing this
document, a Health Information Bill is being drafted. It is likely, when enacted, that it
will contain a number of provisions around the governance of personal health
information.
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5. References
5.
References
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and organisation of clinical audit. In Burgess, R. (ed) NEW Principles of Best Practice
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Radcliffe Medical Press, pp 23-58.
Ashmore, S., Ruthven, T., and Hazelwood, L. (2011b). Stage 2: Measuring
performance. In Burgess, R. (ed) NEW Principles of Best Practice in Clinical Audit.
Healthcare Quality Improvement Partnership (HQIP). Abingdon, Radcliffe Medical
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Ashmore, S., Ruthven, T., and Hazelwood, L. (2011c). Stage 3: Implementing change.
In Burgess, R. (ed) NEW Principles of Best Practice in Clinical Audit. Healthcare Quality
Improvement Partnership (HQIP). Abingdon, Radcliffe Medical Press,pp 81-92.
Ashmore, S., Ruthven, T., and Hazelwood, L. (2011d). Stage 4: Sustaining
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Data Protection Commissioner (2007). Data Protection Guidelines on research in the
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Department of Health and Children (2008) Building a Culture of Patient Safety. Report
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Dixon N. (2009a). Getting Clinical Audit Right to Benefit Patients. Romsey: Healthcare
Quality Quest.
Dixon, N. (2009b). Ethics and Clinical Audit and Quality Improvement A Guide for
NHS Organisations. London: Healthcare Quality Improvement Partnership.
Dixon, N. and Pearse, M. (2011). Guide for clinical audit leads. Healthcare Quality
Improvement Partnership. Available at: http://www.hqip.org.uk/assets/Guide-forclinical-audit-leads-21-Mar-11.pdf
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5. References
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Performance Indicators and Minimum Data Sets to Monitor Healthcare Quality
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Health Information and Quality Authority (June 2012). National Standards for Safer
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Health Information and Quality Authority (October 2012). Guidance on information
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Health (Provision of Information) Act 1997. Available from:
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Health Service Executive (2011). National Clinical Programmes: Checklist for Clinical
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Health Service Executive (2012). Quality and Patient Safety Clinical Governance
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ocs/clingovassurancecheckFeb2012.pdf
Health Service Executive (2013). National Consent Policy. Available from:
http://www.hse.ie/eng/about/Who/qualityandpatientsafety/Advocacy/National_Conse
nt_Advisory_Group
Healthcare Quality Improvement Partnership (2012). Template for Clinical Audit
Strategy. Available from: http://www.hqip.org.uk/template-policy-strategy
Infectious Diseases (Maintenance) Regulations 1981. Available from:
Infectious Diseases (Amendment) Regulations 2011. Available from:
Irish Council of Bioethics (2004). Guidance on Operational Procedures for Research
Ethics Committees. Irish Council of Bioethics, Dublin.
Medical Practitioner Act 2007. Available from: http://www.irishstatutebook.ie
Mental Health Commission (2007). Quality Framework for Mental Health Services in
Ireland. Available at:
http://www.mhcirl.ie/Standards_Quality_Assurance/Quality_Framework.pdf
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5. References
National Hospitals Office (2007). Code of Practice for Healthcare Records Management
Version 2.0 Part 5: Retention and Disposal Schedule. Available at:
http://www.hse.ie/eng/services/Publications/services/Hospitals/NHO_Code_of_Practic
e_for_Healthcare_Records_Management_Version_2_0.pdf
National Institute for Clinical Excellence (2002). Principles for Best Practice in Clinical
Audit. Abingdon, Radcliffe Medical Press. Available at:
http://www.nice.org.uk/niceMedia/pdf/BestPracticeClinicalAudit.pdf
National Institute for Health and Clinical Excellence (2007). Drug misuse: opioid
detoxification (CG52). Available from: http://www.nice.org.uk/CG52
National Institute for Health and Clinical Excellence (2008). Irritable bowel syndrome
(CG61). Available from: http://www.nice.org.uk/CG61
Statutory Instrument No. 478 of 2002. European Communities (Medical Ionising
Radiation Protection) Regulations 2002. Available from:
NHS Clinical Governance Support Team (2005). A Practical Handbook for Clinical
Audit. Available at:
http://www.wales.nhs.uk/sites3/Documents/501/Practical_Clinical_Audit_Handbook_v
1_1.pdf
Potter, J., Fuller, C., and Ferris, M (2010). Local clinical audit: handbook for
physicians. Healthcare Quality Improvement Partnership. Available at:
http://www.hqip.org.uk/assets/Guidance/Local-clinical-audit-handbook-forphysicians-August-2010-FINAL.pdf
UH Bristol Clinical Audit Team (2009a). How to: Set an Audit Aim, Objectives &
Standards. Available at: http://www.uhbristol.nhs.uk/files/nhsubht/4%20How%20to%20Aim%20Objectives%20and%20Standards%20v3.pdf
UH Bristol Clinical Audit Team (2009b). How to: Apply Ethics to Clinical Audit.
Available at:
http://www.uhbristol.nhs.uk/files/nhs-ubht/10%20How%20To%20Ethics%20v3.pdf
Wade, DT (2005). Ethics, audit, and research: all shades of grey. British Medical
Journal, 330:468-73.
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6. Additional resources
6.
Additional resources
Additional reading
G Johnston, I Crombie, E Alder, H Davies, and A Millard. (2000). Reviewing audit:
barriers and facilitating factors for effective clinical audit. Quality in Health Care. 9(1):
2336. Available at: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1743496/
A series of helpful clinical audit guides have been produced by the University Hospital
Bristol Clinical Audit team and can be accessed at:
http://www.uhbristol.nhs.uk/for-clinicians/clinicalaudit/how-to-guides
The Health Information and Quality Authority has published a useful guide for frontline health and social care staff about the importance of data quality as part of the
process of providing safe and effective services. This can be accessed at:
http://www.hiqa.ie/publications/what-you-should-know-about-data-quality-guidehealth-and-social-care-staff
Professional bodies and organisations offering support for clinical audit
http://www.patientsafetyfirst.gov.ie/
This website outlines ongoing patient safety initiatives and activities in Ireland
including progress of the 12 project groups which are driving the implementation
of recommendations from the Commission on Patient Safety and Quality
Assurance.
http://www.hseland.ie/tohm/default.asp
Health Service Executive online resource for learning and development. Register
for clinical audit e-learning programme.
http://www.hselibrary.ie/
Developed and maintained by a team of librarians across the Health Service
Executive, this library website provides a gateway for HSE employees to access
local HSE library resources to support clinical audit.
http://www.noca.ie/
The National Office of Clinical Audit (NOCA). Established in 2012, NOCA will
design, develop and implement national clinical audit programmes in order to
improve patient outcomes and promote patient safety in hospitals.
http://www.icgp.ie/audit
Irish College of General Practitioners website. Provides specific guidance and tools
for clinical audit in general practice.
http://gain-ni.org/
Guidelines and Audit Implementation Network (GAIN). Promotes good clinical audit
practice in Northern Ireland through commissioning of regional guidelines and
audits, dissemination of audit results and the publication and facilitation of
implementation of regional guidelines.
http://www.hqip.org.uk/
Healthcare Quality Improvement Partnership (HQIP) provides guidance and
support for clinical audit in England and Wales.
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6. Additional resources
Sources of clinical guidelines

www.patientsafetyfirst.ie
National Clinical Effectiveness Committee (NCEC).
www.nice.org.uk
National Institute for Clinical Excellence (NICE).
www.sign.ac.uk
Scottish Intercollegiate Guideline Network (SIGN).
www.guideline.gov
National Guideline Clearinghouse (USA) is a public resource for evidence-based clinical
practice guidelines.
Some clinical guidelines contain audit criteria and targets for compliance based on the
guidelines key recommendations, for example National Clinical Guideline 1 National
Early Warning Score (NEWS). Available at: http://www.patientsafetyfirst.ie
Other clinical guidelines are accompanied by support tools for clinical audit, including
NICE CG 52 (NICE 2007) Drug misuse: opioid detoxification and NICE CG61 (NICE,
2008) Irritable bowel syndrome in adults: diagnosis and management in primary
care used as examples in this document.
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7. Glossary of terms and definitions
7.
Glossary of terms and definitions
Audit criterion
The measurement of compliance against criteria of care is at the heart of clinical
audit. An audit criterion is a criterion of care with an expected level of performance
or target assigned to it.
Clinical audit
Clinical audit is a clinically led, quality improvement process that seeks to improve
patient care and outcomes though the systematic review of care against explicit
criteria and to act to improve care when standards are not met.
Clinical governance
Clinical governance is the system through which healthcare teams are accountable for
the quality, safety and satisfaction of patients in the care they have delivered. For
health care staff this means; specifying the clinical standards you are going to deliver
and showing everyone the measurements you have made to demonstrate that you
have done what you set out to do. Further information on clinical governance is
available at: http://www.hse.ie/go/clinicalgovernance/
Clinical guidelines
Clinical guidelines are systematically developed statements, based on a thorough
evaluation of the evidence, to assist practitioner and patient decisions about
appropriate healthcare for specific clinical circumstances, across the entire clinical
spectrum.
Data controller
Refers to a person who, either alone or with others, controls the contents and use of
personal data.
Data item
A single unit of data for which the definition and permissible values are specified by
means of a set of attributes.
Data quality
Refers to data that is accurate, valid, reliable, relevant, legible, timely and complete.
Data set
A group of data items.
GP liaison group
An individual or group tasked with improving communication between primary and
secondary care providers.
Health Information and Quality Authority (HIQA)
Reporting directly to the Minister for Health, this independent organisation has legal
power and responsibility for improving the quality, safety and value of health and
social care services in Ireland. HIQA has responsibility across health and social care
services (excluding mental health) for setting standards, monitoring and inspecting
the quality and safety of service provision, providing guidance on health information
and carrying out health technology assessments.
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Healthcare Quality Improvement Partnership (HQIP)

Body funded by the English Department of Health to promote best practice in clinical
audit and to re-invigorate audit activity.
Key Performance Indicators (KPI)
Performance Indicators are specific and measurable elements of practice that can be
used to assess quality of care. Indicators are quantitative measures of structures,
processes or outcomes that may be correlated with the quality of care delivered by
the healthcare system.
National Clinical Effectiveness Committee (NCEC)
A partnership between key stakeholders in service user safety in the Irish health
system. The aim of the committee is to provide a framework for national
endorsement of clinical guidelines and audit to optimise patient care, within the health
system, both public and private.
National clinical guideline
A guideline that meet specific quality assurance criteria and has been mandated by
the designated national body National Clinical Effectiveness Committee (NCEC).
National Institute for Health and Clinical Excellence (NICE)
The National Institute for Health and Clinical Excellence was established as a Special
Health Authority by the UK Department of Health and is one of the key elements of
the NHS in England and Wales. It was set up to reduce variation in the availability and
quality of treatments and care in the National Health Service. Its principal role is to
provide authoritative, robust and reliable guidance on best practice procedure.
National Office of Clinical Audit (NOCA)
The National Office of Clinical Audit was established in 2012 through the collaboration
of the HSEs Quality and Patient Safety Directorate and Clinical Strategy and
Programmes Directorate together with the Royal College of Surgeons in Ireland
(RCSI) and the College of Anaesthetists. Its role is to design, develop and implement
national clinical audit programmes in order to improve patient outcomes and promote
patient safety in hospitals. The RCSI is responsible for the administration and
operation of NOCA on behalf of the HSE.
Personal data
Data relating to a living individual who is or can be identified either from the data or
form the data in conjunction with other information that is in, or is likely to come into,
the possession of the data controller.
Sample
Some of the service users, events, cases, situations or items that are drawn from the
population on which the audit is focused (a sub-set of the population).
Service
Anywhere health or social care is provided. Examples include but are not limited to:
acute hospitals, community hospitals, district hospitals, health centres, dental clinics,
GP surgeries, home care, etc.
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Service provider
Any person, organisation, or part of an organisation delivering healthcare or social
care services as described in the Health Act 2007 Section 8(1)(b)(i)(ii).
Service user
The term service user is used in general throughout this document, but occasionally
the term patient is used where it is more appropriate. The term service user
includes:
People who use health and social care services as patients.
Carers, parents and guardians.
Organisations and communities that represent the interests of people who use
health and social care services.
Members of the public and communities who are potential users of health services
and social care interventions.
Stakeholder
A person, group, organisation, or system who affects or can be affected by an
organisations actions. Health service providers stakeholders, for example, include its
service users, employees, healthcare staff, government, insurers, industry and the
community.
Standard
Standards are defined as structures and processes needed to identify, assess and
manage specified risks in relation to the subject area (for example, healthcare records
management, decontamination etc).
Standard criteria
The standard statement is expanded in the section headed criteria, with different
criteria providing the detail of what needs to be achieved for the standard to be
reached.
Statement of information practices
A document, clearly displayed and accessible to all staff and service users that sets
out what information the service collects, how it is used, with whom it is shared and
for what purpose, the safeguards that are in place to protect it and how service users
can access information held about them.
Target/level of performance
A defined level or degree of expected compliance with audit criteria; may be
expressed in percentage or proportion of cases.
Target population
All of the service users, events, cases, situations or items on which the standard or
audit is focused. A population can range from a very small limited number to a large
or infinite number.
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Appendix one
Appendix one
Sample template for clinical audit proposal proforma
Name
Department
Title
Contact details
Audit title
Is this a re-audit?
Yes
No
If Yes, have previous audits actions been implemented?
Why are you proposing to conduct this audit?
Why was this topic chosen?
What standards will you be auditing against? Please attach a copy of the relevant standard(s) to the
submission
Describe the audit tool you intend to use? Please attach a copy of the audit tool to the submission
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Appendix one
Please tick additional reasons (if any) for carrying out this audit:
Patient centeredness
Professional development
High volume activity
Service improvement
High risk activity
Re-audit
Risk management
High cost activity

Policy/guideline recommendation
Specify if:
Local
National
Other, please state:

_____________________________________________________________________
Each audit should satisfy all of the following:
It should aim to improve patient care.

It should be multidisciplinary where possible.
It should have support within your department, including a willingness to implement
changes.
Data Protection legislation.
Yes
Have all the potential stakeholders been identified?

List relevant stakeholders by name
No
Are these stakeholders

aware of this audit?
Has a literature search been undertaken?
Yes
No
Yes
No
Yes
No
Yes
No
Yes
No
Sample size:
date
Length of time to audit and target completion date:

I confirm that all data collection/storage will comply
with (insert name of service provider) ICT policies:
Yes
The final section of the clinical audit proposal submission will depend on the resources/supports
available within the service i.e. request for assistance with carrying out the clinical audit, who has
the authority to approve performance of the audit etc.
Signed:
Signed:
Audit lead
Date received:
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Audit sponsor
Date discussed:
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Appendix two
Appendix two
Clinical audit checklist

Stage 1 :
Plan for audit
Stage 2 :
Select
standard/criteria
Stage 3 :
Measure
performance
Stage 4 :
Make
improvements
Step 1
Involve stakeholders
Step 2
Determine the audit topic
Step 3
Plan the delivery of audit fieldwork
Step 1
Identify standard (evidence based)
Step 2
Identify audit criteria - measurable statements

of what should be happening
Step 3
Set targets/expected performance levels
Step 4
Agree acceptable exceptions (if appropriate)
Checklist
()
Steps
Step 1
Collect data
Step 2
Analyse data
Step 3
Draw conclusions
Step 4
Present results
Checklist
()
Steps
Step 1
Share audit report
Step 2
Review areas for improvement and agree

priorities for action
Step 3
Identify appropriate interventions
Step 4
Develop quality improvement plan (if required)
Step 6
Identify:
- persons responsible for each task / action
- reasonable timescale for completion
- how and when progress will be measured
Ensure that change is supported by those with
the necessary authority to effect such change
Checklist
()
Steps
Step 1
Step 2
Step 3
QPSD-D-029-1
Checklist
()
Steps
Step 5
Stage 5 :
Sustain
improvements
Checklist
()
Steps
Monitor implementation of changes

Report on progress of implementation as
required
Re-audit to ensure changes have improved
practice and decide if further audit procedures
are required
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Appendix three
Appendix three Types of data

There are different types of data and each type can be described in different ways.
Data may be quantitative (sometimes referred to as objective or hard data) which is
concerned with numerical or specific data, for example, age, gender, length of stay.
Data may be qualitative which is usually descriptive i.e. concerned with words rather
than numbers (sometimes referred to as subjective or soft data), for example,
comments on questionnaires. Qualitative data may sometimes be represented in a
quantitative form (i.e. 8 out of 10 people) or responses may be themed into
different categories (for example, levels of satisfaction with care).
The table below provides further information on how data may be classified.
Table 1 Classification of data
Type of data
Level of measurement
Categorical
Data which can be
sorted into
separate (distinct)
categories , where
each subject in a
sample can only fit
in one category
Quantitative/
numerical
(Interval/ratio)
(NB units of
measurement
used)
Nominal
Data in separate categories
which have no inherent
order (numerical
relationship)
Some nominal data will only
have two categories
Ordinal
Data in separate categories
which have an inherent
order/relationship. Can be
counted and ordered but not
measured.
Discrete arise from a
count or a scale
(usually whole numbers)
Continuous measurement
(can, in theory, take any
value in a range, although
necessarily recorded to a
predetermined degree of
precision)
Examples
Examples of
presentation
methods
Eye colour, ethnicity,

diagnosis, level of
satisfaction
Pie chart/Bar chart
Gender: Male/Female
Answers options:
Yes/No
Usually expressed as a
ratio or % rather than
graphically
Job grade, age groups

1-5, 6-10 etc
Pie chart/Bar chart
Number of nonattendees at a clinic.

(ratio)
Level of satisfaction,
rated from 1 to 10
(ratio)
Temperature C/F (no
absolute zero)
(interval)
Histogram
Histogram, Scatter
graph
Age, weight, Hb level,

length of stay. (ratio)
Interval/ratio data: Data recorded on a scale with equal distances between points.
Data can be continuous or discrete. Interval data cannot be multiplied or divided. Data
at ratio level has an additional quality of an 'absolute zero' and numbers are multiples
of one another. Therefore temperature (in C or F) is measured at interval level. Age,
height, etc are at ratio level. Ratio data can be multiplied and divided because not
only is the difference between 1 and 2 the same as between 3 and 4, but also that 4
is twice as much as 2.
(Adapted from: http://hsc.uwe.ac.uk/dataanalysis/quantIssuesTypes.asp)
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Appendix four
Appendix four
Top tips for the successful development of clinical

audit data collection tools
Developed by the Irish Clinical Audit Network 2006
Validity
As in research, the data collection tool should have a high level of validity i.e. it
collects the data that it purports to collect. This is why it is important to start with
clear clinical audit objectives and use evidence-based standards from the outset.
Reliability
As in research, the data collection tool should have a high level of reliability, i.e.
different personnel collecting the data will record the exact same or highly similar data
using the tool.
Inter-rate reliability: If data is being collected by many personnel it is important that a
check is made to ensure that inter-rater reliability is high.
Sequencing
Data collection questions should flow logically based on the sequence of events in the
data source i.e. patient records etc. If feedback is sought from service users or staff
members questions should be worded clearly and follow the same basic principles
used in developing research interview schedules.
Quantitative versus qualitative clinical audit data collection
Clinical audits can use either quantitative or qualitative data to meet the clinical audit
objectives.
The majority of clinical audits focus on quantitative data. Data collection tools of
this type should ensure that clear closed questions are used i.e. Yes/No,
Documented/Not documented etc.
Where qualitative data is required it is necessary to develop data collection
questions for use in interviews/focus groups or via questionnaire.
Drafting closed questions
When drafting closed questions:
use mutually exclusive options, for example Yes/No; Male/Female
include an option for all responses, for example Yes/No/Dont know/Not applicable
where appropriate, give more than two options, for example, 4 or 6 (an even
number is better as this may assist selection of the middle option as a default).
Reliability tends to rise as the number of options rise.
Presentation
Ensure that the data collection tool is present in such a way that it is visually
appealing to those collecting the data:
Use standard fonts.
Ensure that the font size is readable.
Do not overcrowd each page ensure that there is space for recording all relevant
information and additional comments.
Comments
Ensure that there is sufficient space for including comments during data collection
Include the date of data collection
Ensure that the date of data collection is recorded clearly on each data collection
sheet. This is particularly helpful when data is collected over an extended timeframe.
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Appendix four
Include data collection site
Include the name (or unique ID code) for the data collection site. This is helpful if data
is being collected on several sites or wards etc and will make comparison of data
across sites more efficient.
Include data collector
Include the name of the data collector on each data collection tool. This is particularly
helpful when data is been collected on different site or if issues arise at a later stage.
Ensure confidentiality
It is best practice to ensure that each data collection tool does not include the name
of the relevant service user or healthcare professional. A unique ID code should be
used. This unique ID can link to a separate list of names/case record numbers etc that
should be stored securely and used only in accordance with all relevant data privacy
regulations.
Include data collection instructions
Instructions for collecting the data or using specific codes should be included on each
data collection tool. This is helpful if there are several data collectors. These
instructions might include items such as: Where to find the specific data or any special
instructions regarding the location of data, different codes.
Pilot the data collection tool
Always pilot the data collection tool using a small number of cases.
This will help:
highlight any difficulties relating to sequencing;
identify missing data items; and
identify unclear data collection questions or instructions.
Code each data collection item
Ensure that each item on the data collection tool is numbered/coded so in order to
maximise the efficiency of data entry and analysis.
Keep it simple
Do not collect data that is not required:
Avoid the I might as well collect this information too now that I have the notes
open syndrome.
Dont re-invent the wheel!
Check if there is another clinical audit data collection tool that can be used directly or
one that requires a minor amount of modification. It is usually less time-consuming to
develop a data collection tool than search and adapt tools already available.
Beware! Do not fall into the trap of buying off-the-shelf data collection tools that
promise the earth. Most of them cant.
Quality control
It is useful for a percentage of data collection records to be checked to ensure data
accuracy.
Sharing best practice
Increase the clinical audit knowledge base - share good data collection tools and good
audit proposal schedule.
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Appendix five
Appendix five
Glossary of terms in relation to descriptive statistics
Analysis of free-text data

Some clinical audits include the collection of qualitative data, for example descriptive
elements such as additional comments in a questionnaire or where service users
experiences are being captured. Analysis of such data can be assisted by grouping
comments into themes or categories and can often produce ideas for improvements.
Distribution of data
Even or normal distribution is seen when most of the values in the range are close to
the average, with a smaller number closer to either extreme of the range of values. If
a graph is used to illustrate normal distribution, the graph will appear to be bell
shaped around a centre point i.e. the graph is symmetrical in appearance (the two
sides are mirror images of one another).
Skewed or non-normal distribution occurs when there are a number of extreme values
which may result in an asymmetrical curve with a long tail on one side or the other or
more than one peak i.e. not mirror images.
Mean or average
This is the most commonly used method of describing the centre of a distribution of
values. To calculate the mean, all the individual values are added together and then
divided by the number of data points (values). However, the mean can be affected by
extreme values i.e. when the values are not evenly distributed throughout the range
of values.
Median
This is the mid-point of all values in a data set when all the values are arranged in
numerical order. The median is a better measure for instances where data distribution
is skewed as it is less sensitive to extreme scores than the mean.
Mode
This is the most frequently occurring value or score in the data set. Where two or
more values are equally frequent there is more than one modal value. The mode can
be valuable where there is more than one modal value or when both mean and
median are affected by extreme values.
Range
The range is a measure of dispersion and refers to how spread out the data is. The
range states the highest and lowest values in a data set.
Standard deviation
The standard deviation is a more accurate and detailed estimate of dispersion because
a single extreme value or outlier can greatly exaggerate the range. The standard
deviation (SD) is a measure of the dispersion of values around the mean and allows
conclusions to be made about specific scores in the distribution of data. A small SD
implies that the data are mainly concentrated around the mean while a large SD
implies that the data are distributed widely.
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Appendix six
Appendix six
Presentation of data using tables, graphs and charts
Tables
The basic structure of a table is a set of columns and rows that contain the data and
usually contain either row and/or column headings to organise the data. When using
tables, the amount of information included should be kept to a reasonable level.
Various techniques can be employed to highlight certain information contained within
a table if required, for example through using bold or different coloured text or by
using a different background colour in relevant cells.
A table is generally less effective than a graph because it only shows data, whereas a
graph can be used to show an interpretation of the data, which may be easier to
understand.
Graphs and charts
A graph or chart provides for the graphical representation of one or more sets of data.
There are several different types of charts and there are no strict rules as to which
one should be used in any given circumstance. The most important thing is to use
those which illustrate the point in the clearest way possible.
Line graphs
Line graphs show sets of data points plotted over a time period and connected by
straight lines. Line graphs are useful for displaying any set of figures that need to be
shown over time and can be used to compare two or more groups compared over
time, for example a vital signs observation chart consists of a line graph.
Pie charts
Pie charts may be used for showing proportions in relation to the whole, with each
wedge representing a percentage of the total. When a different colour/shading is used
for each section, the proportions of the component parts of the whole are easily
comparable. Each pie chart can only represent one set of variables for a subject.
Bar charts
Bar charts show quantities represented by horizontal or vertical bars and are a
practical way of illustrating several categories of results at once. For each category an
individual bar is drawn to indicate the frequency or percentage of that category. There
are usually gaps between the bars to indicate that the categories are discrete. Bar
charts may be simple, grouped (comparative) or stacked/divided.
A simple bar chart sorts data into simple categories. A grouped bar chart divides data
into groups within each category and allows comparisons between individual groups
as well as between categories, therefore giving more useful information than a simple
total of all the components, for example, showing changes in results between initial
audit and re-audit. Stacked/divided bar charts show proportional relationships
between data within each bar. In addition, these bar graphs can show changes over
time. This type of bar chart illustrates both the sum of the parts and each groups
contribution to the whole.
Histograms
A vertical or horizontal bar graph whose lengths indicate quantities/relative frequency
and the width of the bars represent the various categories or data range. It differs
from the bar chart in that the bars may have differing widths, but the key feature is
that, for each rectangle, the area is proportional to the frequency represented. There
are no spaces between each bar as the data is continuous on a numerical scale.
Histograms may be used for displaying ranges, for example, height, weight.
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Appendix seven
Appendix seven
The clinical audit report
The clinical audit report should:
Be simple and clear.

Be written in plain English.
Use a structured, systematic approach, for example, IMRAD (introduction, method,
results and discussion which would include recommendations and an agreed quality
improvement plan).
Present descriptive statistics graphically where possible.
Make sense and follow a logical progression.
Be easy to understand the report should be written in such a way that it could be
understood by a colleague from a different discipline. A good report will make even
a complex issue understandable to all.
Layout of report
The audit report should follow a standard audit report template. For example:
Introduction
Explain the reasoning why the audit was undertaken.

Outline when the audit undertaken and how many people/items were surveyed.
Outline the aims and objectives of the audit.
Method and Sample
Briefly explain the method used and how the sample was chosen.
This section should include enough detail to allow anyone re-auditing to use the
same approach and methodology.
It should include: Who was involved; what type of data collection tool or scale was
used; any difficulties experienced; timescales and any expectations.
Results
There should be no commentary in this section.

Anonymity should be heeded i.e. dont refer to specific people.
Where possible use visual aids such as tables or charts. All tables and figures
should have a title and be understood without reference to the text.
Be consistent with data presentation, e.g. decimal places, percentages, format.
Discussion
This section should not contain any new data.

It should draw on the results and make careful interpretation of the findings.
Compare the results to other audits.
Discuss the strengths and weakness of the audit, are there any discrepancies?
Discuss the meaning of the findings and possible implications for health care
professionals.
Conclusion and recommendations
Use this section to summarise.

Put forward recommendations for change, for example, better documentation,
training requirements, change of practice.
Recommendations should be realistic and achievable.
Suggest areas for further works and plans for re-audit if appropriate.
QPSD-D-029-1
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Appendix seven
Quality improvement plan
The quality improvement plan is a fundamental part of the audit, without it the
audit is not effective and has just wasted time, money and effort.
The audit loop is completed by developing and implementing the quality
improvement plan, use bullet points to keep it short and to the point.
The quality improvement plan should identify the person/s responsible for each
action.
Plan a date for re-audit.
Acknowledgements
All those who helped should be mentioned.
References
Should be numbered or in alphabetical order.
Appendices
It may be appropriate to include a copy of the data collection form.
Another version of a template for a clinical audit report is provided on the next page.
QPSD-D-029-1
Page 83 of 86
Appendix seven
Sample Template for Clinical Audit Report (Version 2)

Title of Audit:
For office use: audit number
Date of report:
Re-audit date:
Department/Speciality:
Audit lead/author:
Job title:
Service provider:
Job title:
Key stakeholders:
Names:
Department/
Speciality:
Background & aim:

Say why the audit
was done. Perhaps
a problem had
been identified?
Statement of what
the project is
trying to achieve:
Standard:
Methodology:
State
Chosen
population
How sample
selected
Retrospective or
prospective
Sample size
Describe tool
used
Results:
(State the results.
Start with total
number (n=). Data
may be presented
visually (graphs,
tables)
QPSD-D-029-1
Page 84 of 86
Appendix seven
Conclusion:
(List key points
that flow from
results)
Recommendation:
(bullet point action
plan-with review
date and initials of
person in charge of
implementation)
A report must be written up for each Clinical Audit done. This is the official record of what has been done, which can be returned to in
future years.
Title
This should be the same as the title on the proforma.
Background & aim(s) of the audit (Introduction)
This is essentially narration, clarifying why the audit was done. For example, was the project prompted by an identified local problem or
concern? The background should explain the rationale for doing the audit. Summarise the evidence base for the audit topic, giving any
references at the end. If a team was convened to undertake this audit, say how this was organised and who was involved.
This will explain what the project is trying to achieve and should have been identified before the audit commenced.
Standards
Clinical audit must measure against standards, guidelines or benchmarks of some sort, these should be identified and where they come
from (the source and strength of evidence). State if the intention was to set standards at the end of the project and if so, which aspects
of care those standards pertain to.
Methodology
State the chosen population for this study (for example, "patients referred to the one-stop breast clinic for suspected cancer") and then
to say how the sample was selected the sample for the audit, specifying whether a retrospective or prospective approach was used (for
example, for a prospective audit, "the first 100 patients referred to the clinic starting from 1/10/04", or for a retrospective audit, "all
patients seen at the outpatient clinic during July "). Describe how these patients were identified, the sample size, the time period, and
clarify how this was calculated or agreed upon.
The data collection method should also be stated, for example, "Data was collected from patients' case notes using a data collection
sheet or a query was run in ICT. List who was responsible for data collection, when this was done, and mention briefly the method of
data input (if appropriate) and analysis.
Results
The number of subjects (for example, patients) included in the audit is the initial 'n' number. If data is incomplete, explain why, for
example, it might not be possible to find every set of patient notes.
How data is analysed depends upon the question/s to be answered. Ensure to include the number and percentage of cases meeting
each criteria of the standard, making it clear what number is been taken a percentage of as the 'n' number may change at different
points of the report, for example, 45/50 (90%) for criterion A and 81/90 (90%) for criterion B.
Conclusions
List the key points that flow from the audit results - use bullet points and avoid long paragraphs. Ensure conclusions are supported by
the data, or if the data points to no firm conclusions, say so - don't make claims that are not supported by the evidence. Make
objective, factual statements, not subjective ones, i.e. don't say "it is obvious that... or "clearly, what is happening is ... "
Recommendations & Quality Improvement Plan
Recommendations for change should be made. Make sure these are realistic and achievable.
A quality improvement plan (action plan) should be agreed saying what changes will be implemented, who will be responsible for
carrying them out and when this will be done. If appropriate (i.e. changes are to be made), set a date for a re-audit to complete the
audit cycle.
QPSD-D-029-1
Page 85 of 86
Appendix eight
Appendix eight
TWELVE TIPS FOR SUCCESSFUL CLINICAL AUDIT

1.
Keep audits simple
2.
Get everyone involved
3.
Determine the topic
4.
Have a plan
5.
Do not confuse clinical audit

with research
6.
Do not collect needless data
7.
Take care with statistics errors can lead to inaccurate

conclusions
8.
Close all clinical audit loops
9.
Keep data only for as long as it is needed
10. Share learning - tell everyone about your audit

11. Tell The Organisation about your audit
12. Re-audit to ensure improvement in clinical care
QPSD-D-029-1
Page 86 of 86

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APracticalGuide

A Practical Guide to Clinical Audit

Quality and Patient Safety

A Practical Guide to Clinical Audit

Document reference number

Quality and Patient Safety Directorate

National Director of Quality and Patient Safety

Quality & Patient Safety Directorate

A Practical Guide to Clinical Audit

The National Clinical Audit Advisory Group 2011-2012

National Lead Clinical

HSE, Quality and Patient

Group Clinical Audit

St. Vincents Healthcare

Safety and Quality

HSE, Quality and Patient

Ann Marie Lanigan

CEO, Mater Hospital

Dublin Academic Teaching

Wexford General Hospital

Primary Care Clinical Lead

Post Doctoral Researcher

UCD School of Public

Clinical Audit Development

Clinical Audit Coordinator

Sligo General Hospital

Deputy Chair until

Risk Manager and

Irish Public Bodies

Team Lead, Clinical Audit

HSE, Dublin Mid Leinster

National Lead for Acute

Head of Standards and

HSE, Quality and Patient

A Practical Guide to Clinical Audit

Setting the scene

2 The five stage approach to clinical audit

Stage 1: Planning for audit

Stage 2: Standard/criteria selection

Stage 3: Measuring performance

Stage 4: Making improvements

Stage 5: Sustaining improvements

Summary The five stage approach to clinical audit

3 Resources required to support clinical audit

Service provider support

Clinical audit facilitation

Issues of data protection

A Practical Guide to Clinical Audit

Clinical audit proposal proforma

Clinical audit checklist

Top tips for the successful development of clinical audit data

Glossary of terms in relation to descriptive statistics

Presentation of data using table, graphs and charts

The clinical audit report

Twelve tips for successful clinical audit

Hospital In Patient Enquiry (Scheme)

Health Information Quality Authority

Health Service Executive

Mental Health Commission