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Information Lifecycle and Records Management Policy

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56 views40 pages

Information Lifecycle and Records Management Policy

Uploaded by

annghazali
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 40

Information Lifecycle

and Records
Management Policy
This policy describes mandatory guidance for the policies,
processes, practices, services and tools used by the organisation
to manage its information through every phase of its existence,
from creation through to destruction.
Key Words: Information, Records, Management,
Lifecycle, electronic record, retention,
disposal, transit
Version: 6

Adopted by: Trust Policy Committee

Date this version 24 August 2022


was adopted:
Name of Author: Head of Data Privacy/ Data Protection Officer

Name of Data Privacy Committee


responsible
Committee:
Please state if n/a
there is a reason
for not publishing
on website:
Date issued for August 2022
publication:
Review date: January 2025

Expiry date: 1 August 2025

Target audience: All LPT Staff

Type of Policy Clinical Non Clinical


√ √
Which Relevant CQC Regulation 17: Good Governance
Fundamental Standards?
Contents

Contents Page 2

VERSION CONTROL 4

Equality Statement 4

Due Regard 4

Definitions that apply to this policy 6

THE POLICY

1.0 Purpose 8

2.0 Summary and Key Points 8

3.0 Introduction 9

3.1 Records Management 9

3.2 Code of Practices 9

3.3 Information Security Management 10

3.4 Framework 10

4.0 Legal & Professional Obligations 11

5.0 Duties and Responsibilities 11

5.1 Corporate Body 11

5.2 Chief Executive 11

5.3 Senior Information Risk Owner 11

5.4 Caldicott Guardian 12

5.5 Head of Information Governance 12

5.6 Information Asset Owners 12

5.7 Records and Information Governance Group 12

5.8 Service Directors/Heads of Service 12

5.9 All Staff 12

5.10 Contractors & Support organisations 13

6.0 What is a record? 13

6.1 Aims of our Records Management System 13

7.0 Five Phases of the Information Lifecycle 14

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7.1 Creation & Quality 14

7.2 Using and Handling records 16

7.3 Record Closure 19

7.4 Retention 20

7.5 Appraisal 21

7.6 Disposal 23

8.0 Incidents and Lost Records 25

9.0 Information Risk 25

10.0 Research Governance 26

11.0 Monitoring and Auditing of Records Management 26

12.0 Training Needs 26

13.0 Standards/Key Performance Indicators 27

14.0 References and Bibliography 27

Appendices
Appendix 1 Training Needs 29
Appendix 2 NHS Constitution 30
Appendix 3 Stakeholders and Consultation 31
Appendix 4 Due Regard Screening 32
Appendix 5 Data Protection Impact Assessment 34
Appendix 6 Risk Assessment for Transferring/Transporting/Sending Confidential 35
Personal Data

Appendix 7 Guidance for staff carrying patient records or other confidential / 39


sensitive information off-site

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Version Control and Summary of Changes

Version Date Comments


number (description change and amendments)
February 2012
Harmonisation of policies as a result of the TCS process
3.0 Draft version
April 2012
3.1 Final Final Harmonised policy following consultation changes
February 2013 Amendments incorporated to NHSLA Monitoring section
3.2 Final
(Appendix 5)
March 2013 Further amendments incorporated to NHSLA Monitoring
3.3 Final
Section (Criteria 5.2 added to Appendix 5)
November 2013 Review as a result of implementation and NHSLA
3.4 Draft
requirements
May 2014 Final amendments following extensive consultation. Issued
3.5 Draft for approval to Records and Information Governance
Group
October 2017 Final Draft following review against revised Records
4 Management Code of Practice for Health and Social Care
issued 2016
September 2020
5 Draft Review in line with policy management
March 2022 Review following the publication of the Records
6
Management Code of Practice by NHSX December 2021

For further information contact:


Head of Data Privacy
Email: [email protected]

Equality Statement

Leicestershire Partnership NHS Trust (LPT) aims to design and implement


policy documents that meet the diverse needs of our service, population and
workforce, ensuring that none are placed at a disadvantage over others. It
takes into account the provisions of the Equality Act 2010 and promotes equal
opportunities for all. This document has been assessed to ensure that no one
receives less favourable treatment on the protected characteristics of their
age, disability, sex (gender), gender reassignment, sexual orientation,
marriage and civil partnership, race, religion or belief, pregnancy and
maternity.

Due Regard

LPT will ensure that Due regard for equality is taken and as such will
undertake an analysis of equality (assessment of impact) on existing and new
policies in line with the Equality Act 2010. This process will help to ensure
that:

• Strategies, policies and services are free from discrimination;


• LPT complies with current equality legislation;

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• Due regard is given to equality in decision making and subsequent
processes;
• Opportunities for promoting equality are identified.

Please refer to due regard assessment (Appendix 4) of this policy.

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Definitions that apply to this Policy

Access The availability of or permission to consult records

Archiving The storing of files, records, and other data for


reference and alternative backup
Authentic record A record that can be proven:
• To be what it purports to be
• To have been created, or sent by the person
purported to have created or sent it
• To have been created or sent at the time
purported
Breach of The unauthorised disclosure of personal confidential
Confidentiality information

Caldicott Guardian The person within an NHS organisation who is


responsible for the systems that protect patient data
Confidential Anything that relates to patients, staff or any other
Information information (such as contracts, tenders etc) held in
any form (such as paper or other forms like
electronic, audio) howsoever stored (such as patient
records, paper diaries, portable devices) or even
passed word of mouth. Personal identifiable
information is anything that contains the means to
identify an individual.
Corporate Records Records (other than health records) that are of, or
relating to, an organisation’s business activities
covering all functions, processes, activities and
transactions of the organisation and of its employees
Current Records Records necessary for conducting the current and on
going business of an organisation
Destruction The process of eliminating or deleting records
beyond any possible reconstruction
Disposal The implementation of appraisal and review
decisions. These comprise the destruction of records
and the transfer of custody of records (including the
transfer of selected records to an archive institution).
They may also include the movement of records from
one system to another (for example paper to
electronic)
Electronic Records Records where the information is recorded in a form
that is suitable for retrieval, processing and
communication by a digital computer
File An organised unit of documents grouped together
either for current use by the creator or in the process

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of archival arrangement, because they relate to the
same subject, activity or transaction.
Paper Records In the form of files, volumes, folders, bundles, maps,
plans etc (this list is not exhaustive)
Patient Identifiable Any piece of information which can potentially be
Information used to uniquely identify, contact, or locate a single
person or can be used with other sources to uniquely
identify a single individual.
Protective marking The process of determining security restrictions on
records. Previously called ‘classification’
Public Record Records defined in the Public Records Act 1958 or
subsequently determined as public records by The
National Archives.
Record Anything which contains information (in any media),
which has been created or gathered as a result of
any aspect of the work of NHS employees.
Records Management Filed of management responsible for the efficient and
systematic control of creation, receipt, maintenance,
use and disposition of records, including processes
for capturing and maintaining evidence of and
information about business activities and transactions
in the form of records.
Retention The duration of time for which information should be
maintained or ‘retained’, irrespective of format
Scanning
The process of transferring one document, or a
series of documents, into a form that is suitable for
retrieval, processing and communication by digital
computer.

Transit The movement of items from one place to another

Due Regard Having due regard for advancing equality involves:


• Removing or minimising disadvantages suffered by
people due to their protected characteristics.
• Taking steps to meet the needs of people from
protected groups where these are different from the
needs of other people.
• Encouraging people from protected groups to
participate in public life or in other activities where
their participation is disproportionately low.

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1.0. Purpose of the Policy
This Policy reflects the requirements of the Records Management Code of Practice
2021 which sets out a framework for consistent and effective records management
based on established standards.

This policy is an important component in guiding employees on security of personal


identifiable information and the use of information in accordance with relevant
legislation, such as Data Protection and Freedom of Information Laws.

This policy relates to all clinical and non-clinical operational records held in any
format by the organisation. These include:

• All administrative records (e.g. Personnel, estates, financial and accounting


records; notes associated with complaint-handling); and Human resource
files
• All patient health records (for all specialties and including private patients,
x-ray and imaging reports, registers, etc)

2.0. Summary and Key Points


This document sets out Leicestershire Partnership NHS Trust’s mandatory standards
for the information and records used by the organisation to manage its information,
held in whatever format, through every phase of its existence from creation to
destruction.

The Records Management Policies and procedures form part of the organisations
information lifecycle management, together with other processes, such as records
inventory, secure storage, records audit etc.

Supplementary documents relating to specific areas of records management within


the Trust but aligned to this policy include the following:

Electronic Health Records Policy (including management)


Clinical Document Scanning Policy
Data Protection and Information Sharing
Information Security and Risk
Data Protection Impact Assessment Policy and Procedure
Individual Information Rights

Aligns to:
➢ The Public Records Act 1958;
➢ Data Protection Legislation (currently UK GDPR/DPA 2018);
➢ The Freedom of Information Act 2000;
➢ The Common Law Duty of Confidentiality;
➢ The NHS Confidentiality Code of Practice
➢ Records Management Code of Practice, 2021

Page 8 of 40
➢ Care Quality Commission Outcomes Framework
➢ Caldicott2 Review, 2013
➢ National Data Guardian Standards
➢ NHS LA Risk Management Standards
➢ Information Security Management: NHS Code of Practice
➢ All professional bodies: HCPC,GMC, NMC

Describes processes and responsibilities for


➢ Record Creation, keeping and maintenance;
➢ Record Quality;
➢ Record disclosure and transfer;
➢ Record retention and disposal;
➢ Record storage, archiving and scanning

Is designed to support all staff, ensuring that records of all types are properly
controlled, tracked, accessed and made available for use and eventually archived or
otherwise disposed of appropriately.

3.0. Introduction
An Information Lifecycle and Records Management Policy is a high level document
which sets out the Organisations policy towards the management of its information.

3.1 Records Management is the process by which an organisation manages all


aspects of records whether internally or externally generated and in any format or
media type, from their creation, all the way through their lifecycle to their eventual
disposal

3.2 Code of Practice


The Records Management Code of Practice 2021 was published by the NHSX for
the Department of Health (DH) as a guide to the required standards of practice in the
management of records for those who work within or under contract to NHS
organisations in England. It is based on current legal requirements and professional
best practice.

The Trust’s records are its corporate memory, providing evidence of actions and
decisions and representing a vital asset to support daily functions and operations.
Records support policy formation and managerial decision-making, protect the
interests of the organisation and the rights of patients, staff and members of the public.
They support consistency, continuity, efficiency and productivity and help deliver safe
and effective services in consistent and equitable ways.

Information (records) management, through proper control of the content, storage and
volume of records, reduces vulnerability to legal challenge or financial loss and
promotes best value in terms of human and space resources through greater
coordination of information and storage systems.

The Trust has adopted this information lifecycle and records management policy and
is committed to ongoing improvement of its records management functions as it
Page 9 of 40
believes that it will gain a number of organisational benefits from doing so. These
include:

• More efficient use of physical and electronic storage space;


• More efficient use of staff time;
• Improved control of valuable information resources;
• Compliance with legislation and standards; and
• Reduced costs

The Trust also believes that its internal management processes will be improved by
the greater availability of information that will accrue by the recognition of records
management as a designated yet integrated corporate function.

3.3 Information Security Management

The guidance contained within the Information Security Management: NHS Code of
Practice and its related materials applies to NHS information assets of all types
(including the records of NHS patients treated on behalf of the NHS in the private
healthcare sector)
These information assets may consist of:

• digital or hard copy patient health records


• digital or hard copy administrative information
• digital or printed X-rays, photographs, slides and imaging reports, outputs
and images

• digital media (including data tapes, CD-ROMS, DVDs, USB disc drives,
removable memory sticks

• computerised records, including those that are processed in networked,


mobile or standalone systems

• email, text and other message types.

3.4 Framework
This document sets out a framework within which the staff responsible for managing
the organisation’s records can develop specific guidance and procedures to ensure
that records are managed and controlled effectively, and at best value, commensurate
with legal, operational and information needs.

4.0. Legal and Professional Obligations

All NHS records are Public Records under the Public Records Acts. The organisation
will take actions as necessary to comply with the legal and professional obligations
set out in the Records Management Code of Practice, in particular:

• The Public Records Act 1958;


• The Data Protection Act 2018;
• The Retained General Data Protection Regulation (EU) 2016/679 – UK GDPR

Page 10 of 40
• Access to Health Records Act 1990
• The Freedom of Information Act 2000;
• Health and Social Care Act 2008
• Environmental Information Regulations 2004
• The Common Law Duty of Confidentiality;
• The NHS Confidentiality Code of Practice 2003
• National Patient Safety Agency (NPSA) – Use of the NHS Number 2008
• Records Management Code of Practice 2021

And any new legislation affecting records management as it arises.

Staff who are registered to a Professional body, such as the General Medical
Council (GMC), Nursing and Midwifery Council (NMC) or Health and Care
Professionals Council (HCPC) will be required to record keeping standards defined
by their registrant body. This is designed to guard against professional misconduct
and to provide high quality care in line with the requirements of professional bodies.

5.0. Duties within the Organisation

5.1 The organisation as a Corporate Body


The organisation recognises that it has a specific corporate responsibility for records
management. All contracts of employment must contain record keeping standards as
laid out in this policy and in guidelines produced by regulatory bodies.

The organisation must have robust systems and processes that ensure that records
are fit for purpose, are stored securely, are readily available when needed and are
destroyed in compliance with the retention and destruction schedule at the end of the
cycle of the particular record.

The Trust Board has a legal responsibility for Trust policies and for ensuring that
they are carried out effectively.

5.2 Chief Executive


The Chief Executive has overall responsibility for records management in the
organisation. As accountable officer, the Chief Executive is responsible for the
management of the organisation and for ensuring appropriate mechanisms are in
place to support service delivery and continuity. Records management is key to this
as it will ensure appropriate, accurate information is available as required.

5.3 Senior Information Risk Owner


The Senior Information Risk Owner (SIRO) is an Executive Director of the
organisations Board. As SIRO they are expected to understand how the strategic
business goals of the organisation may be impacted by information risks and act as
an advocate for information risk on the Board. They have an essential role in
ensuring that identified information security risks are followed up and incidents
managed. The role is supported by the organisations Head of Data Privacy (the
individual responsible for records management), Information Asset Owners and the
Caldicott Guardian.

5.4 Caldicott Guardian

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The organisation’s Caldicott Guardian has a particular responsibility for reflecting
patients’ interests regarding the use of patient identifiable information. They are
responsible for ensuring patient identifiable information is shared in an appropriate
and secure manner.

5.5 Head of Data Privacy


The Head of Data Privacy is responsible for the overall development and
maintenance of records management practices throughout the organisation, in
particular for drawing up guidance for good records management practice

5.6 Information Asset Owners


Information Asset Owners (IAOs) are accountable to the SIRO and provide
assurance that information risk is being managed effectively for those information
assets that they have been assigned ownership. They will be assisted in their role by
staff acting as Information Asset Administrators (IAAs). These roles are generally
fulfilled by Service Directors

5.7 Data Privacy Committee


This Committee is responsible for ensuring that the records management strategy
and policy are implemented. It advises on clinical records management issues
maintaining standards by:

• Identifying areas where improvements could be made


• Reporting performance standards
• Monitor compliance with the standards, legislation, policies and procedures
relating to the management of records
• Approving locally devised methods of recording information e.g. the
development of a standard format/design for clinical records

Its remit also includes:

• Ensuring record collection activities are rationalised by encouraging users to


share records and the information they contain (subject to Data Protection and
agreed confidentiality guidelines)
• Publicise and promote the local guidelines by supporting the implementation of
a formal training programme to launch and support the guidelines and the
inclusion of records management in induction training and staff handbooks.

5.8 Service Directors and Heads of Service


are responsible for local records management .Heads of Departments/ Professional
leads within the organisation have overall responsibility for the management of
records generated by their activities, i.e. ensuring that records controlled within their
unit are managed in a way which meets the aims of the organisation’s Records
Management policies.

5.9 All Staff


All staff within the organisation, whether clinical or administrative, who create,
receive and use records have records management responsibilities. In particular all
staff must ensure that they keep appropriate records of their work in the organisation
and manage those records in keeping with this policy and with any guidance
subsequently produced.

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All staff are provided with information on Information Governance standards during
induction and are expected to familiarise themselves with organisational policy in
relation to these issues. New starters are required to complete Data Security
Awareness Level 1 training within 6 weeks of their commencement with the Trust.

All staff must have an understanding of the key requirements of laws and guidelines
concerning records, in particular those relating to confidentiality, data protection and
access to information including under the Freedom of Information Act 2000. All staff
and those carrying out functions on behalf of the organisation have a duty of
confidence to patients and a duty to support professional ethical standards of
confidentiality. The duty of confidence continues even after the death of the patient
or after an employee or contractor has left the NHS. Unauthorised disclosure of
information may lead to a complaint against the organisation or a disciplinary action
against a member of staff for a breach of confidentiality.

5.10 Contractors and support organisations


Service Level Agreements and contracts must include responsibilities for information
governance and records management as appropriate.

6.0 What is a record?

The ISO standard, ISO 15489-1:2016 Information and documentation - Records


management 8, defines a record as ‘information created, received, and maintained
as evidence and information by an organisation or person, in pursuance of legal
obligations or in the transaction of business’.

Section 205 of the Data Protection Act 2018 defines a health record as a record
which:

• Consists of data concerning health;


• Has been made by or on behalf of a health professional in connection with the
diagnosis, care or treatment of the individual to whom the data relates.

6.1 Aims of our Records Management System

The design and implementation of record keeping systems (DIRKS) is a manual


which led to the creation of ISO 15489-1:2016 Information and documentation –
Records Management. This standard focuses on the business principles behind
records management and how organisations can establish a framework to enable a
comprehensive records management programme.

The aims of our Records Management System are to ensure that:

• Records are available when needed – from which the organisation is able to
form a construction of activities or events that have taken place
• Records can be accessed – records and the information within them can be
located and displayed in a way consistent with its initial use, and that the
current version is identified where multiple versions exist

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• Records can be interpreted – the context of the record can be interpreted:
who created or added to the record and when, during which business
process, and how the record is related to other records
• Records can be trusted – the record reliably represents the information that
was actually used in, or created by, and its integrity and authenticity can be
demonstrated
• Records can be maintained through time – the qualities of availability,
accessibility, interpretation and trustworthiness can be maintained for as long
as the record is needed, perhaps permanently, despite changes of format
• Records are secure - from unauthorised or inadvertent alteration or erasure,
that access and disclosure are properly controlled and audit trails will track all
use and changes. To ensure that records are held in a robust format which
remains readable for as long as the records are required
• Records are retained and disposed of appropriately – using consistent
and documented retention and disposal procedures, which include provision
for appraisal and the permanent preservation of records with archival value
• Staff are trained – so that all staff are made aware of their responsibilities for
record –keeping and records management.

7.0 The 5 Phases of the Information Lifecycle

The records lifecycle, or the information lifecycle, is a term that describes a


controlled regime in which information is managed from the point that it is created to
the point that it is either destroyed or permanently preserved as being of historical or
research interest. This can be seen diagrammatically in Figure 1.

This policy covers the details for each of these phases and the obligations of the
Trust’s employees’ under this policy. This policy covers the obligations of all
organisations employed by the Trust, all organisations contracted to the Trust and
any organisation, or third party that shares Person Confidential Data (PCD) with the
Trust.

7.1 Declaring a Record - Creation

Within a record keeping system, there must be a method of deciding:


• What is a record
• What needs to be kept

This process is known as ‘declaring a record’. This is normally done at the point that it
is created but it can also happen at a later date.

The process of declaring a record must be clear to staff. A declared record is then
managed in a way that will fix it in an accessible format until it is appraised for further
value or disposed of, according to the retention policy adopted.

Some activities will be pre-defined as creating a record that needs to be kept, such as
a health record or the minutes and papers of board meetings. Other records will need
to fulfil criteria as being worth keeping, such as unique instances of a business
document or email.

Page 14 of 40
Figure 1 – The Records/Information Lifecycle

Characteristics of authoritative records

ISO 15489-1:2016 Information and documentation - Records management,30


published by the International Organization for Standardization (ISO), describes the
characteristics that will enable records to be authentic, reliable, integral and usable
throughout their lifecycle.

Record How to evidence


characteristic

Authentic It is what it purports (claims) to be

To have been created or sent by the person purported to have


created or sent it and

To have been created or sent at the time purported.

Reliable Full and accurate record of the transaction/activity or fact

Created close to the time of transaction/activity

Created by individuals with direct knowledge of the facts or by


instruments routinely involved in the transaction /activity.

Integrity Complete and unaltered

Protected against unauthorised alteration

Alterations after creation can be identified as can the persons


making the changes.

Useable Located, retrieved, presented and interpreted

Page 15 of 40
The context can be established through links to other records in
the transaction/activity.

In addition to the above, employees should consider the following when creating
information:

• What they are recording and how it should be recorded;


• Why they are recording it;
• How to validate information (with the staff, patient or carers or against other
records) to ensure they are recording the correct data;
• How to identify and correct errors and how to report errors if they find them;
• The use of information; staff should understand what the records are used for
and therefore why timeliness, accuracy and completeness of recording is so
important; and
• How to update information and how to add in information from other sources
• Tracking & Retrieval System for paper based records

7.2 Using and handling records

All information must be used consistently, only for the intentions for which it was
intended and never for individual employee’s personal gain or purpose. If in doubt
employees should seek guidance from the SIRO or, for health records, the Caldicott
Guardian.

7.2.1 Organising records

The organisation must have a means of physically or digitally organising records.


This is often referred to as a file plan or business classification scheme. In its most
basic form, a business classification scheme is a list of activities (for example,
finance or HR) arranged by business functions but most often linked to the
organisations hierarchical structure.

At the simplest level, the business classification scheme can be anything from an
arrangement of files and folders on a network to an Electronic Document Records
Management System (EDRMS). The important element is the naming convention
which is logical and can be followed by staff.

Classification schemes should try to classify by function first. Once the functional
classification has been selected, the scheme can be further refined to produce a
classification tree based on function, activity and transaction, for example:

Function: Corporate Governance


Activity: Board minutes and associated papers
Transaction: April 2020 – March 2021

7.2.2 Applying security classification

The NHS has developed a protective marking scheme for records it creates. It is
based on the Cabinet Office ‘Government Security Classifications’ defined protective

Page 16 of 40
marking scheme which is used by both central and local government. Under the
NHS Protective Marking Scheme 2014, patient information is classed as ‘NHS
Confidential’.

Unauthorised disclosure or misuse of information contained in records constitutes a


serious breach of conduct that may lead to disciplinary action, and is also a criminal
offence under Section 170 of the Data Protection Act 2018. Staff must guard against
breaches of confidentiality by protecting information from improper disclosure and
use at all times.

The Data Protection Act 2018, Professional Codes of Conduct, Human Rights Act
1998, administrative law and common law duty of confidentiality all place
responsibility on everyone to maintain confidentiality of personal information.
(‘Confidentiality: NHS Code of Practice’ provides further guidance and applies to all
NHS employees)

Basic principles that should be adhered to are as follows:

• Records should never be left in a position where unauthorised persons can


obtain access to them (including computer screens left on but unattended)
• Only staff who are authorised to access patient/service users records as part
of their duties in or associated to the provision of care and treatment, or in
carrying out audit and governance duties, are permitted to do so. The content
of records should not be communicated with persons not authorised to receive
them. They may be discussed on a need to know basis only to provide care
and treatment to the patient/service user.
• Correspondence between the organisation and staff/patient/service users
about staff/patient/service users should be clearly marked ‘NHS Confidential’
to ensure confidentiality.

7.2.3 Information Sharing

National policy developments, the White Paper Our Health, Our Care, Our Say’,
highlights the need for health and social care to work together to provide seamless
services to patients wherever the need arises. This has important implications for
sharing information between health and social care. This was confirmed within the
Health & Social Care Act 2012, the Caldicott 2 Review (To Share or Not to Share)
and the National Data Guardian update to the Caldicott Principles (See Data
Protection and Information Sharing Policy for more details).

As an NHS organisation, we increasingly need to seek assurances that our social


care partners apply the equivalent information security standards to their own
information assets and vice versa. Where cross-boundary NHS information sharing
arrangements are required, the implementation of relevant and consistent standards
for information security management provides the basis that underpins trust and
confidence in these partnership arrangements.

Person confidential data will be shared in line with legislation, national guidance and
documented information sharing agreements which have been agreed through the
Trusts Information Governance processes.

Page 17 of 40
7.2.4 Tracking & Retrieval System
When paper records are retrieved or removed for any reason from the file storage
system, their removal and subsequent return should be recorded using a robust
tracking system. As a minimum it should include:

• The unique identifier (NHS Number in the case of clinical records)


• A description of the item
• The name of the individual requesting and the reason for the request
• The person or department to whom it is being sent
• The date of transfer
• The date of return
• The signature and printed name of the person returning the file

In order to provide an effective retrieval service, it is essential that the movement of


all patient records are recorded either on an electronic system; on a suitable
database for manual tracking systems.

Electronic tracking of records through a PAS or Secure Tracking through the off-site
storage supplier should be used to record and monitor movement of records, where
staff have access to it. Where these systems are not used, the transfer of information
slips/tracking record slips should be used, particularly where there are site to site
transfers using the portering service.

7.2.5 Transporting of Records

Paper records

The mechanism for transferring information from one organisation to another should
also be tailored to the sensitivity of the material contained within the records and the
media on which they are held.

Health records or other confidential information for transportation between LPT


sites/departments or to other health organisations within the Local Health
Community must be enclosed in sealed bags /envelopes/designated secure boxes
and labelled appropriately i.e. Confidential, and sending location included in order to
aid return. For specific situations of extreme sensitivity e.g. child protection, a further
statement should be added stating ‘to be opened by addressee only’.

Records must be carried between sites/departments by authorised staff only.


Authorised staff may include:

• Appropriate member of staff


• Internal transport systems – Portering Service
• Authorised courier service
• Off-site records storage supplier
• Special Delivery by Royal Mail

Where external courier services are used to transfer staff/patient/service user


records between health organisations, a formal contract needs to be put in place

Page 18 of 40
including ensuring that the documents are transported in sealed envelopes. The
contract should include confidentiality issues. A schedule of documents should be
presented to the courier for signature which should be cross-checked by the
organisation receiving the records.

Employees must not send health records by first class mail. Appendix 6 sets out
a risk assessment process to assist in making the decision about the appropriate
transport mechanism and media.

Records should not be left unattended in transit at any time. When carried in a car
they must be locked in the boot.

Only in exceptional circumstances may records be taken home by a member


of staff to work on. Where this is necessary, a risk assessment should be undertaken
and arrangements put in place to ensure that they are kept secure. Evidence of this
risk assessment should be held locally by the service, with authorisation from the lead
for the service. Staff who do will be responsible for the security and confidentiality of
the records (See Information Security and Risk Policy and Appendix 7 – Guidance for
Staff carrying records off site).

Transporting records from LPT premises requires vigilance and the principles
of confidentiality must be maintained.

Electronic Records

In line with the level of security around the transfer and transport of paper records,
electronic records require the same level of sensitive handling.

Where there are requests for records to be sent to other organisations, individuals or
agencies (including solicitors and the Police), these request should be handled by
the Data Privacy Team under a Request for Information. The Subject Access
Request Standard operating Procedure outlines the detail of what needs to be done.

In the rare occasion where a staff member is requested to send clinical


documentation or electronic records, they are requested, in the first instance, to
contact the Data Privacy Team ([email protected]) for advice and support.

7.3 Record Closure

Information held in records should be closed (i.e. made inactive and transferred to
secondary storage) as soon as they have ceased to be in active use, other than for
reference purposes. An indication that a file of paper records or folder of electronic
records has been closed should be shown on the record itself as well as noted in the
index or database of files/folders. Where possible, information on the intended
disposal of electronic records should be included in the metadata when the
information is created.

The storage of closed, or non-current records awaiting disposal should follow


accepted standards relating to environment, security and physical organisation of
files.

Page 19 of 40
For digital records, a system may already be set up whereby records no longer
required for current business are stored (such as a dedicated network drive or space
on a drive). Records should be moved there keeping operational space free for
current cases or work. This will also restrict unnecessary access to non-current
personal and sensitive data.

7.4 Retention

It is a fundamental requirement that the organisation’s records are retained for a


minimum period of time for legal, operational, research and safety reasons. The
length of time for retaining records will depend on the type of record and its
importance to the organisation’s business functions.

The organisation has adopted the retention periods set out in the Records
Management Code of Practice 2021. A separate guidance document setting out
these retention periods is available.

All information needs to be maintainable through time. The qualities of availability,


accessibility, interpretation and trustworthiness must be maintained for as long as
the information is needed, perhaps permanently, despite changes in format. The use
of standardised filenames and version control methods should be applied
consistently throughout the life of the information.

7.4.1 Storage of Records

All manual and electronic records in the organisation must be appropriately stored
and retained in accordance with recommended retention periods

Paper: Wherever possible the Trusts direction of travel is to move to digital records.
The original paper guarantees the authenticity of the record. However, it can be hard
to audit access to the record, depending on where it is stored, because paper
records do not have automatic audit logs.

Digital: digital records offer many advantages over paper records. They can be
accessed simultaneously by multiple users, take up less physical storage space and
enable activities to be carried out more effectively.

Digital information must be stored in such a way that throughout the lifecycle it can
be recovered in an accessible format in addition to providing information about those
who have accessed the record.

The movement and location of records should be controlled to ensure that a record
could be easily retrieved at any time, that any outstanding issues can be dealt with,
and that there is an auditable trail of record transactions.

Records must always be kept securely with appropriate security measures in place
to prevent loss, unauthorised access and modification, but a balance needs to be
achieved between security and accessibility. Storage accommodation for current
records should be clean and tidy, and it should prevent damage to the records.

Page 20 of 40
Equipment used for active records should provide storage which is safe from
unauthorised access and for paper records storage, this also includes meeting fire
regulations, but which allows maximum accessibility to the information
commensurate with its frequency of use. The following factors must be taken into
account:
• Compliance with health and safety regulations
• Degree of security required
• Users needs
• Type of records to be stored
• Size and quantity of record
• Usage and frequency of retrievals
• Ergonomics, space, efficiency and price.

Electronic records/documents in shared folders


Where electronic records/documents are stored on a network shared folder, it is
important that the naming of the folders are clear in order that their contents are easily
identifiable/retrievable (as outlined in 7.2.1); the access to the folders should be
restricted to those who require access and not left with open access (contact with LHIS
service desk for support with this).

Clinical documents/records should not be stored outside of the clinical record unless
they are too large to be uploaded or attached but where this is the case the secure
cloud storage or LPT Clinical Drive should be used as a preference. Alternatively a
separate clearly marked and restricted access folder created and referenced in the
clinical record.

7.4.2 Records in Patient/Service Users’ Homes

In some circumstances records may be stored at the patient/service user’s home,


e.g. nursing care plans. They must be returned to the base when no longer in use.
Stored records should be made safe whenever they are left unattended. Ideally they
should be protected by additional security such as being locked up and keys made
available to authorised staff only. However, confidentiality of records left in the
patient/service user’s home is the responsibility of the patient/service user and they
must be informed of this.

7.5 Appraisal

The process of deciding what to do with records when their business use has ceased
and the minimum retention period has been reached. No record or series can be
automatically destroyed or deleted.

Appraisal will be defined in a separate Standard Operating Procedure and any


decisions documented and linked to a mandate to act. Any changes to the status of
records must also be reflected in the Trusts’ Record of Processing Activity (ROPA).

When appraising records that have come to the end of their minimum retention
period, the following should be considered:

Page 21 of 40
• Ongoing use: The may be a reason to keep the record for longer than the
minimum retention period for care, legal or audit reasons. In these cases
extensions can be set provided it is justified and approved.

• Classification of diseases (based on ICD-10 code): Some health conditions


lend themselves towards longer, or extended retention periods.

• Operational Delivery: The way a service was delivered may have been
transformative at the time, which may justify an extended retention or long-term
archival preservation.

• The way care is delivered: The records may be reflective of health or care policy
at the time.

• Series Growth: If records are part of a series that will be added to (type of record
as opposed to additional content) there may need to be a consideration of space.
For example, continued expansion of a series of records that has a very low recall
rate, continued retention would be harder to justify.

• Recall rates: If a series of records is routinely accessed to retrieve records, then


there must be justification for extending the retention period due to ongoing use.
Whereas for a series with very low recall rate would be harder to justify.

• Historical value: If the record has potential historical or social value (for example,
innovative new service or treatment or care delivery method) then consideration
may be considered for retaining longer. In these circumstances it is worth
engaging with the Trusts Records Exploitation Manager to have early contact with
the local Place of Deposit (PoD). They normally do not accept records before 20
years retention has passed, unless there are exceptional circumstances for early
transfer.

• Previous Deposits: The records held may be a continuous series that has
historically been accessioned by a local PoD. It is important to find out what has
historically been accessioned so that a series of records remains complete. It is
likely that records that add to an already accessioned series will continue to be
taken by the PoD.

Digital records can be appraised if they are:

• Arranged in an organised filing system

• Differentiated by the year of creation

• Organised by the year of closure

• Clear about the subject of the record

Page 22 of 40
If digital record have been organised in an effective classification scheme or
electronic record system, this process is made easier. Decisions can then be applied
to an entire class of records rather than reviewing each record in turn.

There will be one of three outcomes from appraisal:

Destroy / delete

To keep for a longer period

To transfer to a place of deposit appointed under the Public Records Act 1958.

All appraisal decision need to be justified, follow documented Trust guidance and be
documented and approved by the Data Privacy Committee or delegated sub-group.

7.6 Disposal

It is particularly important under freedom of information legislation that the disposal


of records, is undertaken in accordance with clearly established policies which have
been formally adopted by the Trust and which are enforced by properly trained and
authorised staff. No information can be destroyed if it is the subject of a request
under the Data Protection Act 2018 and/or the Freedom of Information Act 2000.

7.6.1 Permanent Destruction / Deletion

It is important to keep accurate records of destruction and appraisal decisions.


Destruction implies a permanent action. For electronic records ‘deletion’ may be
reversed and may not meet the standard as the information can/may be able to be
recovered or reversed.

Paper records: Records may contain sensitive or confidential information. It is


therefore vital that confidentiality is safeguarded at every stage and that the method
used to destroy records is fully effective and secures their complete illegibility and
inability to be reconstructed. Any records that have been identified for destruction
must be destroyed as soon as possible after they are eligible in accordance with
approved Trust procedures and using Contractors and methods authorised by the
Trust.

The Destruction provider must provide a certification of destruction for the bulk
destruction of records. This certification must be linked to a list of records, so that the
Trust has clear evidence that particular records have been destroyed.

Records that do not contain personal information or confidential material can be


destroyed in a less secure manner (such as confidential waste bins that do not
provide certificates of destruction). If there is any doubt, material should be treated
as confidential and evidentially destroyed.

Page 23 of 40
Do not use the domestic waste or put records in rubbish bins that will go to
the tip because the confidential material remains accessible to anyone that
finds it.

Digital records/media: Destruction implies a permanent action. For digital records


‘deletion’ may not meet ISO 27001 standard as the information can or may be able
to be recovered or reversed. Destruction of digital information is therefore more
challenging.

One element of records management is concerned with accounting for information,


so any destruction of hard assets, like computers, hard drives and backup tapes,
must be auditable in respect of the information they hold. An electronic records
management system will retain a metadata stub which will show what has been
destroyed.

The Information Commissioner’s Office (ICO) guidance ‘Deleting Personal Data’1


sets out that information is deleted from a live environment and cannot be readily
accessed then this will suffice to remove information for the purposes of Data
Protection Law.

Electronic systems vary in their functionality. They may have the ability to
permanently delete records from the system or not. Where a record has reached its
retention period and has been approved for destruction, then the record should be
deleted if the system allows. A separate record should be kept of what record has
been deleted.

If a system does not allow permanent deletion, then all reasonable efforts must be
made to remove the record from normal daily use. It should be marked in such a way
that anyone accessing the record can recognise that it is dormant or archived.

7.6.2 Digital Records, Digital Continuity, Digital Preservation and Forensic


Readiness

Digital information presents a unique set of issues which must be considered and
overcome to ensure that records remain authentic and reliable, retaining their
integrity and usability. Digital continuity refers to the process of maintaining digital
information in such a way that the information will continue to be available, as
needed, despite advances in digital technology. Digital preservation ensures that
digital information of continuing value remains accessible and usable. Refer to The
Digital Preservation Coalition handbook when considering issues associated with
retaining digital records for long periods of time and well as the Trusts’ Information
Security and Risk Policy section on IG Forensic Readiness

1
https://ico.org.uk/media/for-%20organisations/documents/1475/deleting_personal_data.pdf

Page 24 of 40
.

8.0 Incidents and Lost records

This section predominantly relates to paper records/documents.

Any incident or near miss relating to a breach in the security regarding use, storage,
transportation or handling of records must be reported using the organisation’s
Incident recording system.

A serious breach of security e.g. major theft or fire must be managed in accordance
with the same Policy in relation to it being a Serious Untoward Incident.

A lost record is defined as any record that cannot be located within 10 working days
of first attempt to access the record or any record that has been stolen from a known
place, for example, the boot of a car. Any suspected thefts must be reported to the
Police.

The organisation’s Caldicott Guardians must be informed immediately of any loss or


misplacement of any document that is used to record patient information, including
diaries, or organisational business. When all efforts to locate the record have been
exhausted, an incident form must be completed giving clear details of all actions
including:
• When and where the record was last seen, with date known
• If stolen, from where and Police Incident Number
• Actions taken to locate file

It is the responsibility of the line manager, liaising with and taking advice as
necessary from the Data Privacy Team, to investigate such incidents and identify
any learning points that must be implemented in order to prevent a recurrence.

9.0 Information Risk

Threats to NHS data shall be appropriately identified and based upon robust risk
assessments and risk management arrangements in line with the organisations risk
management strategy and policy, and shall be managed and reviewed regularly to
ensure:

• protection against unauthorised access or disclosure


• that the integrity and value of information is maintained
• that information is only available to authorised personnel as when it is
required.

The organisation will ensure adequate audit provision, based upon robust risk
management arrangements, ensuring the continuing effectiveness of NHS
information security management arrangements.

In particular, the organisation will set out its commitment to create, maintain and
manage the security of its key information assets (including its records) and other
external information resources that it depends upon, and documents its principle
activities in this respect.

Page 25 of 40
Also see the Information Security and Risk Policy for more detailed guidance.

10.0 Research Governance

Any research, as opposed to audit, undertaken using patient records must first have
had Research Ethics Approval as part of the Research Governance Framework. For
advice on your proposed project and requests for information from other
organisations, please contact the organisations Research lead.

11.0 Training needs

There is a need for training identified within this policy. In accordance with the
classification of training outlined in the Trust Learning and Development Strategy this
training has been identified as mandatory training.

At least 95% of all staff, including new starters, locums, temporary, students and
staff contracted to work in the organisation must have completed their annual Data
Security Awareness Level One training in the period 1 April to 31 March. A record of
the training will be recorded on uLearn.

The information button against the title of the module ’NHS Data Security
Awareness Level 1’ on uLearn identifies who the training applies to, the update
frequency and learning outcomes.

There is also a recommendation for additional non-mandatory subject specific


training where roles involve the management of requests to access health records.

The governance group responsible for monitoring the training is Trust’s Data Privacy
Committee.

12.0 Monitoring Compliance and Effectiveness

Evidence for Responsible Frequency


Minimum Process for
Ref Self- Individual / of
Requirements Monitoring
assessment Group monitoring
All new starters Section 5.9 Monthly Data Privacy Quarterly
complete Data Mandatory Committee
Security training
Awareness Level Report
1 training within 6
weeks of
commencement
Unauthorised use Section 7.2.2 Incident Data Privacy Quarterly
of disclosure Reporting – Committee
constitutes and Caldicott
offence Report

Page 26 of 40
Evidence for Responsible Frequency
Minimum Process for
Ref Self- Individual / of
Requirements Monitoring
assessment Group monitoring
There should be Section 7.2.4 Incident Data Privacy Quarterly
a tracking Reporting – Committee
mechanism in Caldicott
place for Report
movement and
transfer of paper
records
Incidents of lost Section 8.0 Incident Data Privacy Quarterly
records are Reporting – Committee
reported Caldicott
Report

13.0 Standards/Performance Indicators

TARGET/STANDARDS KEY PERFORMANCE INDICATOR


Data Protection and Security Toolkit All records are appropriately stored or archived

14.0 References and Bibliography

This policy was drafted with reference to the following:

National and Legal requirements

NHSX Records Management Code of Practice 2021

National Data Guardian Standards

Data Protection and Security Toolkit

Data Protection/Privacy Law

Freedom of Information Act 2000

Trust Policy

Data Security and Protection Strategic Framework

Data Protection and Information Sharing Policy

Freedom of Information Policy

Electronic Health Records Policy (including management)

Page 27 of 40
Individual Information Rights Policy

Information Security and Risk Policy


Data Protection Impact Assessment Policy and Procedure

Page 28 of 40
Appendix 1
Training Needs Analysis

Training Required YES ✓ NO

Training topic: Data Security Awareness Level 1

✓ Mandatory (must be on mandatory training register)


Type of training:
☐ Role specific
(see study leave policy)
☐ Personal development

✓ Adult Mental Health & Learning Disability Services


✓ Community Health Services
Division(s) to which the
✓ Enabling Services
training is applicable:
✓ Families Young People Children
✓ Hosted Services
All Staff including temporary, contract and students
Staff groups who require
the training:

Regularity of Update
Annually
requirement:
Who is responsible for
eLearning through ULearn
delivery of this training?
Have resources been
Yes
identified?
Has a training plan been
Yes
agreed?

Where will completion of ✓ ULearn


this training be recorded? ☐ Other (please specify)

How is this training going to Monthly manager reports with overarching oversight by Data
be monitored? Privacy Committee

Page 29 of 40
Appendix 2

The NHS Constitution

The NHS will provide a universal service for all based on clinical need, not
ability to pay. The NHS will provide a comprehensive range of services

Shape its services around the needs and preferences of individual



patients, their families and their carers

Respond to different needs of different sectors of the population ✓

Work continuously to improve quality services and to minimise errors ✓

Support and value its staff ☐

Work together with others to ensure a seamless service for patients ✓

Help keep people healthy and work to reduce health inequalities ✓

Respect the confidentiality of individual patients and provide open



access to information about services, treatment and performance

Page 30 of 40
Appendix 3

Stakeholders and Consultation

Key individuals involved in developing the document


Name Designation

Circulated to the following individuals for comment


Name Designation
Members of Data Privacy Committee
Dr Avinash Hiremath Medical Director/Caldicott Guardian
Sharon Murphy Executive Director of Finance &
Performance/SIRO

Page 31 of 40
Appendix 4

Due Regard Screening Template

Section 1
Name of activity/proposal Information Lifecycle and Records
Management Policy
Date Screening commenced
Directorate / Service carrying out the Enabling/Data Privacy
assessment
Name and role of person undertaking Sam Kirkland, Head of Data Privacy
this Due Regard (Equality Analysis)
Give an overview of the aims, objectives and purpose of the proposal:
AIMS:
The purpose of the document is to promote good practice and consistency of information being
collected, managed and used within Leicestershire Partnership NHS Trust (LPT). The principles of
records management practices are embedded in national guidance and Law

OBJECTIVES:
To provide staff with a framework within which they can operate, taking into account the safety,
security and integrity of the information and records that they hold for all service users

Section 2
Protected Characteristic If the proposal/s have a positive or negative impact
please give brief details
Age Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Disability Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Gender reassignment Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Marriage & Civil Partnership Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Pregnancy & Maternity Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Race Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Religion and Belief Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Sex Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust

Page 32 of 40
Sexual Orientation Positive – the policy covers the expectations for the
management and handling of all information held by the
Trust
Other equality groups?
Section 3
Does this activity propose major changes in terms of scale or significance for LPT?
For example, is there a clear indication that, although the proposal is minor it is likely
to have a major affect for people from an equality group/s? Please tick appropriate
box below.
Yes No
High risk: Complete a full EIA starting click Low risk: Go to Section 4.
here to proceed to Part B ✓
Section 4
If this proposal is low risk please give evidence or justification for how you
reached this decision:
The Policy is written in line with national guidance and the legal framework for the
management and handling of information, which does not discriminate

Signed by reviewer/assessor Sam Kirkland Date 08/03/22


Sign off that this proposal is low risk and does not require a full Equality Analysis
Head of Service Signed Date

Page 33 of 40
Appendix 5

DATA PRIVACY IMPACT ASSESSMENT SCREENING

Data Privacy impact assessment (DPIAs) are a tool which can help organisations identify the
most effective way to comply with their data protection obligations and meet Individual’s
expectations of privacy.
The following screening questions will help the Trust determine if there are any privacy issues
associated with the implementation of the Policy. Answering ‘yes’ to any of these questions is
an indication that a DPIA may be a useful exercise. An explanation for the answers will assist
with the determination as to whether a full DPIA is required which will require senior
management support, at this stage the Head of Data Privacy must be involved.

Name of Document: Information Lifecycle and Records Management Policy

Completed by: Sam Kirkland


Job title Head of Data Privacy Date: 08/03/22
Screening Questions Yes /
No Explanatory Note
1. Will the process described in the document involve No
the collection of new information about individuals?
This is information in excess of what is required to
carry out the process described within the document.
2. Will the process described in the document compel No
individuals to provide information about them? This is
information in excess of what is required to carry out
the process described within the document.
3. Will information about individuals be disclosed to No
organisations or people who have not previously had
routine access to the information as part of the
process described in this document?
4. Are you using information about individuals for a No
purpose it is not currently used for, or in a way it is
not currently used?
5. Does the process outlined in this document involve No
the use of new technology which might be perceived
as being privacy intrusive? For example, the use of
biometrics.
6. Will the process outlined in this document result in No
decisions being made or action taken against
individuals in ways which can have a significant
impact on them?
7. As part of the process outlined in this document, is No
the information about individuals of a kind particularly
likely to raise privacy concerns or expectations? For
examples, health records, criminal records or other
information that people would consider to be
particularly private.
8. Will the process require you to contact individuals No
in ways which they may find intrusive?
If the answer to any of these questions is ‘Yes’ please contact the Data Privacy Team via
[email protected]
In this case, adoption of a procedural document will not take place until review by the Head of Data
Privacy.
Data Privacy approval name: Sam Kirkland, Head of Data Privacy

Date of approval 08/03/22

Acknowledgement: This is based on the work of Princess Alexandra Hospital NHS Trust

Page 34 of 40
Appendix 6

Risk Assessment for Transferring/Transporting/Sending Confidential


Personal Data

All NHS organisations work to a Code of Conduct for handling patient-identifiable


information. Working to the same Code of Conduct helps ensure a more unified
approach across NHS organisations to the way NHS staff handle, store, transfer and
work with patient information. This also helps ensure compliance with the Data
Protection Legislation.

The NHS holds large amounts of confidential information about you, members of
your family, friends, and colleagues; but the vast majority of this information will be
about strangers, most of whom you are unlikely to meet. This information is classed
as Patient Confidential Data (PCD). The information belongs to the patients. Their
information should be treated with as much respect and integrity as you would like
others to treat your own information. It is your responsibility to protect that
information from inappropriate disclosure and to take every measure to ensure that
patient-identifiable information is not made available to unauthorised persons.

Breaches of confidentiality are a serious matter. Non-compliance with this code may
result in disciplinary action being taken. No employee shall knowingly misuse any
information or allow others to do so.

What is meant by the transfer of patient confidential data?

The transfer of patient confidential data, by whatever means, can be as simple as:
• taking a document and giving it to a colleague;
• making a telephone call;
• sending a email;
• passing on information held on computer, for example confidential clinical
information held on patient records.

In all cases, however simple or complicated, the Caldicott Principles (Figure 1) must
be adhered to in order to ensure that patient-identifiable information is not disclosed
inappropriately.

Page 35 of 40
Figure 1 Caldicott Principles

1. Justify the purpose.


2. Don’t use patient-identifiable information unless it is absolutely
necessary.
3. Use the minimum necessary patient-identifiable information.
4. Access to patient-identifiable information should be on a strict need
to know basis.
5. Everyone should be aware of their responsibilities.
6. Understand and comply with the law.
7. The duty to share information can be as important as the duty to
protect patient confidentiality
8. Inform service users and patients about how their information is
used

ENSURING CONFIDENTIALITY

Information transfer principles

It is imperative that the utmost care is exercised when transferring PCD. To this end
written documents as well as email should be used with care. When internal courier
post or public mail is used, it is essential to confirm that the addressee details are
correct. The basic rule is that in all circumstances where PCD is shared, by whatever
method, the items transferred should be restricted to a minimum. Only essential
items of information should be included. Other items should be omitted or blocked
out before transmission.

When transferring paper documents, including records, which contain PCD, make
sure “NHS CONFIDENTIAL” is marked in a prominent place on the front of the
envelope. Ensure that the address of the recipient is correct and clearly stated, using
the following format and using window envelopes:

• Name;
• designation (job title);
• department;
• organisational address.

Write a return address on the back of the envelope (if using a plain envelope).

If PCD is to be sent in carrier (internal) envelopes, the envelope must be sealed and
marked “NHS CONFIDENTIAL”. Internal mail should still be properly named and
addressed, e.g. not just to "Mary from Medical Records".

Page 36 of 40
Do not pass documents containing PCD to other colleagues by leaving them on a
secretary's desk or in an "IN" tray. Always ensure that the information is in a sealed
envelope addressed to the recipient and clearly marked “NHS CONFIDENTIAL”.

Transfer between hospital sites, clinics, community bases etc.

You should always ensure that a secure system for transferring care records (or
other personal information that identifies individuals) between sites is used, referring
to this guidance.

Only authorised personnel may assist in the transfer of patient records where an
office, department or practice is moving premises from one site to another. This must
be done under the guidance of an authorised employee/employees of the relevant
organisation.

Transfer between departments on site

Where there is an internal system for transferring confidential information (e.g.


routine portering transfer) in place, this may be used to transport records between
departments. Alternatively, appropriate special arrangements may need to be made
for information required urgently (e.g. non-routine portering transfer). In either
situation, the information must be correctly packaged and labelled as detailed earlier.
Depending upon circumstances, it may be more appropriate and expedient to
transport the information personally. If this is the preferred option, do not leave any
information visible inside the car; ensure that it is locked away securely in the boot.

It is not appropriate for unpackaged information to be handed to another person for


delivery simply because she/he is going to the destination department.

If you have any specific questions regarding transferring patient records, contact the
assigned Data Privacy Team or line manager for further guidance.

Risk associated with sending patient identifiable information out of the


organisation

Risks related to Some Suggested Controls


transporting/transferring patient
information

Sending appointment letters out to Confirm numbers


patients with no clinical details
Use of Royal Mail

Provide return address (PO Box for


mental health services)

Page 37 of 40
Sending referrals to external agency Use of agreed format outlining
with clinical information included proportionate amount of detail

What is the preferred method of


sending to the agency/organisation?

Can you keep a copy of the information


sent?

How do you obtain receipt to referral?

Consider use of secure online


form/sending via secure email

Sending detailed report including Do you know who the report should go
medical conditions and outcomes of to i.e. named individual?
treatment
Can the information be password
protected?

Does the receiving


organisation/individual have a secure
email address?

Is the receiving organisation/individual


local?

Do you need to be able to track the


journey of the report?

Consider using secure email/Arrange to


hand deliver/ Recorded Delivery mail
where no tracking required/Special
Delivery

Page 38 of 40
Appendix 7

GUIDANCE FOR STAFF CARRYING PATIENT RECORDS OR OTHER


CONFIDENTIAL / SENSITIVE INFORMATION OFF-SITE

Who is this guidance for?

Any staff of the organisation including temporary, agency or


bank staff and staff under contract, who are transporting confidential, sensitive or
personally identifiable information themselves.

It does not apply to transportation by porters, internal or external mail, or transport of


records between hospitals by ambulances or couriers.

What is covered?

This includes, but is not limited to, any patient records, sensitive financial, estates or
personnel records, contracts, and confidential information relating to GP and other
independent contractor practices. This information is hereafter called ‘records’ in the
remainder of the guidance. If in any doubt talk to your line manager

Are formats other than paper covered?

➢ Any hard copy format is covered. For guidance on electronic records you are
strongly advised to read the Secure Email Guidance for Sending PCD. You
can also refer to the Information Security and Risk Policy.

➢ At local induction managers need to make clear to the individual what records
they can take off-site and what, if anything, should never be removed without
prior permission. This should ensure clarity of understanding and also that the
individual does not need to get approval for individual records.

➢ No records should be removed from base unless they are needed for work.

➢ It is recognised that healthcare professionals may find it necessary to remove


patient’s health records or other related clinical documentation from their
base, to facilitate their daily practice of seeing patients in community setting.
To reduce the risk of loss of such records and to reduce the risk of breaches
of confidentiality there are various considerations to be made, based on best
practice. Only those records required for the patients being seen in the
community should be removed. Ideally, records should not be removed for
general administration purposes, e.g. writing reports. There should be a trace
or booking out reference kept at the base from which records have been
removed.

➢ It is important that other staff know where the records have gone. Use the
tracking system in place. If one does not exist then discuss creating one with
your line manager. This does not have to be complex.

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➢ Records/clinical documentation should be transported from the office in
suitable covers or containers so that they are protected and not in danger of
being dropped or damaged. They should be handled carefully when being
loaded or unloaded. Vehicles must be fully covered so that records are
protected from exposure to weather, wind, excessive light and other risks
such as theft.

➢ Records/clinical documentation should not usually be left unattended in cars.


However, it is acceptable to do so if there is a definite risk that they will be
viewed by unauthorised personnel, damaged or stolen if they are taken into
the building. Risk assess the situation and use your professional judgement to
decide whether it will be safer to take the records into the house or to leave
them in the car. If left in the car the records should be placed in a locked car
boot out of sight, with the car alarm on if there is one.

➢ Cars should be parked in a secure and well-lit location.

➢ At the end of a working shift records it is best practice to return the records to
the base office.

➢ If the member of staff does not return to base at the end of a shift,
records/clinical documentation must be removed from the car and care taken
to ensure that members of the family or visitors cannot gain access. Ideally,
records should be stored and carried in a secure case and kept out of sight.
Staff should ensure that they place the secure case in a cupboard or similar,
as soon as they enter the house. If they do not have a secure case, notes
should be stored in a locked cupboard or cabinet with access only by the
member of staff.

➢ If the staff member is involved in a road traffic accident / incident which


necessitates the car being left on the roadside or taken to a garage, records
should be removed if possible. If this is not possible the police should be
informed that confidential records/clinical documentation are in the car. The
line manager and/or On-Call manager should be contacted and made aware
of the situation. They should ensure that an incident form is completed and do
whatever they can to help retrieve the records.

➢ If a member of staff’s car is stolen or broken into and records/clinical


documentation stolen, the police should be informed, the line manager and/or
on-call manager should be contacted immediately and an Incident form
completed.

➢ Staff should not attempt to remove records/clinical documentation from a


burning car. The emergency services should be informed that records are in
the car. The line manager and/or on-call manager should be contacted
immediately and an incident form completed.

It is inappropriate to work on records whilst travelling by public transport or in any


non-NHS, non-secure environment e.g. cafes

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