The relationship between education and health outcomes for children and young people across England: the value of using linked administrative data.
University College London (UCL) · Academic
Expired The latest version ended on 18 April 2025. The September 2026 register still lists the agreement, but its term has passed.
- Reference
- DARS-NIC-27404-D5Z3F
- Latest version
- v3.5
- Term of latest version
- 19 April 2022 to 18 April 2025
- Start date
- Before 7 December 2018
- Data controller
- Sole Data Controller
- Commercial purposes
- No
- Sublicensing
- No
- Files released to date
- 3
Why the data was released
Objective for processing
BACKGROUND
The strong interrelationship between health and education services in relation to the health and wellbeing of children is recognised by policy makers, but evidence is lacking on how services complement or compensate for each other and there have been calls for a stronger evidence base to be developed.
The legal basis for processing personal data for this purpose data at UCL falls under Article 6(1)(e) of the General Data Protection Regulations (GDPR), i.e. a task carried out in the public interest. University College London (UCL) is a public authority and has a royal charter (see: https://www.ucl.ac.uk/governance-compliance/sites/governance_compliance/files/charter-and-statutes.pdf) which states that "The objects of the College shall be to provide education and courses of study in the fields of… Medicine and Medical Sciences, Social Sciences and Applied Sciences and… to encourage research in the said branches of knowledge and learning and to organise, encourage and
stimulate postgraduate study in such branches.". The legal basis also falls under Article 9(2)(j), processing is necessary for archiving purposes in the public interest, scientific or historical research purposes or statistical purposes.
This research is expected to have substantial public benefit by providing evidence on the quality of linkage between health and education data and by addressing relevant policy, healthcare and NHS systems questions on the association between child health and education.
This study has two purposes:
Firstly, to address the methodology for linking HES and National Pupil Data (NPD) from the Department for Education (DfE) and to address important policy and health service questions about the interrelationship of health and education for children with and without underlying chronic conditions. As part of the methodology programme of the ADRC-E, the aim is to assess the feasibility of using linked health and education administrative data to carry out such research. The research will benefit the data providers, and thereby, indirectly benefit NHS systems, by undertaking an assessment of data quality and consistency between sources and by assessing the accuracy of linkage. The results will be published to inform others (government departments and researchers) of match rates and factors associated with linkage error.
The second purpose, is to inform policy and service commissioners about associations between education risk factors and health outcomes, such as emergency hospital admissions. The hypothesis is that school attainment is associated with unplanned admissions to hospital, but this association may vary by area, type of school and individual risk factors, particularly presence of chronic conditions. Researchers need to study the whole of England in order to determine how education outcomes vary according to local authority and type of school, and what the impact is of such variation on emergency admissions to hospital.
The project combines a methodological component to evaluate linkage quality and an applied research component, which involves evaluating the association between education outcomes and emergency use of hospital services by children with and without underlying chronic conditions.
This study has three aims, namely to:
1. Evaluate linkage success between National Pupil Database (NPD), Personal Demographic Service (PDS), Hospital Episode Statistics (HES) hospital admissions data, and mortality data.
2. Evaluate the association between hospital admissions for children and adolescents with underlying chronic conditions and subsequent school achievement
3. Evaluate the association between education outcomes and subsequent use of hospital services, taking into account underlying chronic conditions.
METHOD
For this programme of research, UCL are the sole Data Controller who also process data. The Office for National Statistics (ONS) are also data processors. This programme of research uses NPD attribute data from the DfE. Agreement DR190416.03 relates to the NPD attribute data that is accessed by University College London within the ONS Secure Research Services. A separate agreement DR150701.02 relates to the NPD identifiable data that are used by NHS Digital for the linkage that facilitates the analysis of the attribute data (this has now been completed). Further details are found in ‘5b. Processing activities’
Linkage
Research from DARS-NIC-27404 also forms a baseline for evaluation of the larger linkage used in DARS-NIC-381972 ‘Assessing the impact of the COVID-19 pandemic on vulnerable children: the ECHILD-COVID study’, which is producing scientific and statistical evidence on the impact of the Covid19 pandemic on vulnerable children and families.
Linkage has been conducted by NHS Digital using identifiers supplied by DfE (forename, surname, date of birth, sex and postcode) captured in each school year. Identifiers were matched initially to PDS and then to HES and de-identified. UCL then received the pseudonymised HES data from NHS Digital together with a Study_ID supplied by DfE. DfE will supply de-identified NPD data together with a Study_ID.
Analyses
Using the linked data UCL will examine how the association between school achievement and hospitalisation varies according to local authority and type of school, taking into account factors at the individual level (eg chronic conditions in the health record, free school meals, ethnicity in the school record) that might affect both school achievement and emergency use of hospital services (ie. confounding factors).
UCL will examine whether low school achievement is associated with subsequent emergency admissions to hospital, and whether health problems, manifest in admissions to hospital, are associated with subsequent changes in school achievement. UCL would expect these associations to vary across the country, as local factors, such as type of school and local services, eg support for children with chronic conditions, vary between local authorities. Evidence on such risk factors will be important for generating hypotheses about how healthcare and schools can reduce adverse outcomes for children and adolescents. To evaluate variation across the country, and to have sufficient power to evaluate outcomes for children with chronic conditions at different ages and in different services, UCL need to use data for the whole country and for all children (within the age restriction) in both data sets.
Both data sets contain longitudinal data of a child’s routinely captured information in the NPD and of hospital admissions, outpatient and A&E attendance in HES and mortality data. Within HES, diagnosis and procedural variables will be required to identify unplanned admissions, and to define cohorts of children with and without chronic conditions. Information from OPD and A&E adds information on planned outpatient specialist care and the frequency of emergency hospital contacts without admission. Comparison groups, comprising those with and those without chronic conditions will be identified from the longitudinal record of hospital admissions, if possible from birth. Previous work completed by UCL has shown that chronic underlying conditions may not be recorded at every admission (for example, asthma may not be recorded when a child is admitted for an operation) and UCL have demonstrated the added value of using the whole longitudinal record.
Description of the cohorts:
In order to minimise the amount of data, UCL have restricted the data requested to four one-year cohorts. The four cohorts are:
COHORT 1. Young people cohort (born between 01/09/1990-31/08/1991 who entered reception class in September 1996):
This cohort will test the quality of linkage of data with young people receiving education up to age 18 years, and as young people become more mobile.
These young people will first be recorded in the NPD with their Key Stage 1 (KS1) from 1998 and Key Stage 2 (KS2) from 2002, and annual school census from 2001/2. UCL request NPD KS1, KS2, KS4, and KS5. They will also be captured in HES on their first hospitalisation on or after 01/04/1997 (at approximately 7 years of age or more). HES data is requested up until the most recent available period.
This cohort tests linkage with all children (state and non-state educated) who have a KS4 assessment (approximately 99% of adolescents aged 15/16). UCL will also follow up adolescents who sit KS5 (A levels). At this age they have shown high rates of emergency use of hospital for adversity related injury (self-harm, drug or alcohol misuse or violence). In this cohort, UCL can evaluate the antecedent education risk factors for such admissions.
COHORT 2. Primary-secondary school transition cohort (born between 01/09/1996-31/08/1997 who entered reception class in September 2002).
This cohort will comprise children whose educational profile can be followed from primary to secondary school and will capture health service utilisation from the early years and throughout the educational trajectory. The cohort will provide valuable information on the quality of data linkage, where there is an overlap between the time points on the main datasets (i.e. NPD and HES).
These children will be recorded in the NPD annual school census from 2001/2 and in KS1 data from 2003/4. These children enter secondary school in September 2008 and will have KS3 recorded in 2011 and KS4 recorded in 2012/13. This cohort will have annual school census data throughout the primary school years, but not all would have had a hospital admission (UCL expect around 40% to have been admitted at some point). Data on hospitalisations will be captured in HES on or after 01/04/1997 (when this cohort will be approximately 1 year of age) until the most recent data extract available.
COHORT 3. Preschool-primary school cohort (born between 01/09/1999-31/08/2000 who entered the reception class in September 2005).
This cohort will capture indicators of chronic conditions recorded in the birth record and in infancy, which is the period when the risk of admission to hospital is highest. It will also provide a complete record of primary school education. The frequent movement of children in the preschool years will present a challenge to linkage (ie. postcode changes), which UCL will seek to evaluate in this study using available HES resources, such as the Patient Demographic Service introduced in 2004. Linkage quality is expected to be less good than for Cohort 4, as identifiers in HES birth records between the cohort years. NPD data are requested up until KS4 data, which would end in 2015/16. UCL will examine the association between chronic conditions and school achievement in the cohort, accounting for chronic conditions and birth characteristics recorded in early life.
COHORT 4. Patient demographic service cohort (born between 01/09/2004-31/-8/2005 and enter reception class in September 2010)
This cohort data in HES birth episodes and PDS will be concurrent and therefore maximise the likelihood of successful linkage to the NPD (ie most children in NPD are expected to have a birth episode in HES). It should comprise a complete record of health service used from birth and early education that may be used to investigate the impact of early education/educational achievements on pre/post school hospital admissions.
NPD are requested up until KS2 data.
Processing activities
The HES data provided by NHS Digital and NPD data provided by DfE are for the one-year birth cohorts comprising records for all children specified in the following cohorts:
Cohort 1: Born between 01/09/90-31/08/91
Cohort 2: Born between 01/09/96-31/08/97
Cohort 3: Born between 01/09/99-31/08/00
Cohort 4: Born between 01/09/04-31/08/05
The linkage of identifiers was conducted separately from attribute data (clinical or education characteristics) by NHS Digital. NHS Digital transferred pseudonymised HES IDs for those who were successfully linked and were released, together with the match rank and anonymized Pupil Matching Reference (PMR) as permitted by DfE. The definition of pseudonymisation is where direct identifiers have been removed from the data extract; identifiers refer to fields such as names, sex, date of birth, full post code. UCL researchers will use the transferred HES IDs to append match status to linked records in pseudonymised HES data (previously approved as NIC-393510).
The HES pseudonymised attribute data for the four cohorts, with an indicator of match rank provided by NHS Digital, was transferred to the Office of National Statistics Secure Research Service (ONS SRS) with HES ID and anonymised PMR for linkage, including only the month and year of birth and death.
The following outline describes how identifiable and non-identifiable extracts from the data scheme were handled.
1) DfE supplied the Trusted Third Party (NHS Digital) with a list of NPD identifier variables, including name and postcode histories, alongside a study specific pseudo-identifier number (Study_ID, known as the anonymized PMR) for children in PDS.
2) NHS Digital matched the identifiers from DfE to records held in the PDS using an algorithm that prioritises the most recent post code in NPD (at the school census date). Matching to PDS data was done internally within NHS Digital, no PDS data will be disseminated to UCL.
3) The PDS identifiers were linked to HES data. HES IDs for linked cases were then transferred to the UCL safe haven for identification within the existing HES extract held by UCL (NIC-393510). The anonymised PMR from the records that NHS Digital linked were also sent to UCL.
The identifiable data supplied to NHS Digital for steps 1-3 has since been destroyed as these steps have now been completed.
4) UCL created four cohorts of all HES records for children born in years of cohorts 1 to 4 (admissions, critical care, A&E and OPD) and fact and date of death from the existing HES data (NIC-393510). These cohorts were transferred for linkage to the NPD data held in the ONS SRS. The deidentified, linked data are used by researchers authorised only for this project. Only month/year of birth and death were transferred to the ONS SRS, in order to account for well-established effects of month of birth on school achievement (i.e. research consistently shows that children born in September do better than children born in July/August). The anonymized PMR and metrics of the match rank of linkage provided by NHS Digital were also transferred to enable linkage with the NPD data and assessment of linkage accuracy.
5) DfE supplied ONS SRS with requested (attribute) data extracts, alongside the anonymised PMR for children in Cohorts 1 to 4. There was no identifiable information in the extract sent. This extract was placed in the ONS SRS for linkage using anonymized PMRs to the 4 HES cohorts and analyses by researchers authorized for this project.
6) The final data set that is being used for analyses within the ONS SRS. The files not contain any identifiable data. No additional record level data data will be gathered or linked to the dataset. The anonymised PMR is the only variable supplied from NPD data that is supplied by NHS Digital to UCL Data Safe Haven.
7) NHS Digital retained the identifier file of all individuals linked in NPD-PDS and PDS-HES and all the postcodes used in linkage and postcode dates for 12 months to address data queries. This data set will not contain any attribute data and will be accessible only to NHS Digital staff. This has now been destroyed.
The following methodology was proposed for the linkage by NHS Digital:
The current MIDAS algorithm will be modified to consider the 15 most recent postcodes in PDS, ranked according to distance from the date associated with the NPD postcode. For remaining unmatched NPD records, the second postcode in NPD will then be compared with PDS as above. This approach will be repeated up to a maximum of 5 postcodes in NPD or until a match is achieved with PDS. This is necessary because ignoring address changes in PDS after the school census date in NPD would increase the number of missed matches. For example, although NPD postcode might be correct in September, PDS postcode in the subsequent months until the next census is more likely to be the most recent postcode.
NHS Digital will not send confidential data to DfE.
DATA SECURITY
To maintain the physical and technical security measures, the following safeguards will be in place:
1) Data linkage: Linkage between identifiers supplied for the NPD with PDS and HES will be carried out by a Trusted Third Party (NHS Digital) . The NHS Digital team undertaking the linkage will only have access to identifiers from PDS and HES for hospital administrative data and they will receive full identifiers from DfE for NPD data. These identifiers include name, date of birth, full postcode and sex. No additional attribute data will be provided. These identifiers will be removed and replaced with the pseudonymised Study ID (anonymized PMR) and HES ID assigned to each child in the cohort before release to the UCL Safe Haven. The original file was retained by the Trusted Third Party for 12 months to address queries about the linkage accuracy. This identifier data has now been deleted by NHS Digital.
As a consequence, the UCL researchers will not have access to the identifiers and the NHS Digital team undertaking the linkage received full identifiers from DfE for NPD data (inc. name, date of birth, full post code and sex) but no additional attribute data was provided.
2) Minimising data disclosure: HES pseudonymised attribute data for the 4 cohorts was transferred into the ONS SRS for access only for the purposes of this project. De-identified linkage between HES and NPD was done by remote secure access to the SRS from the UCL safe room. UCL will minimise disclosure risks by transferring only year and month of death and birth, LSOA decile rather than rank, location defined only by area indicators (eg local authority) in the four HES cohorts transferred to the ONS SRS. During analyses, the UCL researchers will minimise the potential for deductive disclosure, by limiting the presentation of specific information that could potentially identify any individual in the cohort. Statistical disclosure control measures will be applied according to HES requirements by ONS data scientists operating within the SRS.
3) Limited access: The de-identified linked HES-NPD data will be held on the ONS SRS accessible remotely from the UCL safe haven which has restricted and monitored access. No record level data can be removed from the SRS and statistical disclosure controls are applied by ONS staff.
The project has Administrative Data Research Network (ADRN) panel approval and Research Ethics Committee (REC) approval: 17/LO/1494. Access will be restricted to named users, who are part of the study team and are accessing the data for purposes outlined in this DSA. Access to the data is via the ONS SRS environment.
4) Limiting outputs: The data analyses are conducted on the ONS Secure Research Service. Detailed individual level child data cannot leave the ONS Secure Research Service. Results of analyses can be exported by a secure encrypted transfer system, which his audited. Any outputs from analyses that are published have to meet statistical disclosure controls that prevent small sizes in accordance with NHS Digital and DfE requirements. Tabulations of aggregate data are assessed for statistical disclosure control and authorized for export by an ONS data scientist not involved in the project.
The de-identified linked HES-NPD attribute data will be held on the ONS SRS and will only be accessible remotely from the UCL Data Safe Room which has restricted and monitored access. No record level data can be removed from the ONS SRS and statistical disclosure controls are applied by ONS staff. Access will be restricted to named users, who are part of the study team and are accessing the data for the purposes outlined in this DSA. Access to the data is via the ONS SRS environment.
Office of National Statistics (ONS) and UCL have signed and maintain an organisational agreement to use the ONS Secure Research Statistics (SRS) service for the purposes of secure statistical research, signed on 21/03/2019 with an indefinite expiry date [SD10]. The only HES data stored in the ONS SRS are the 4 one-year cohorts of HES, plus the anonymised PMRs for those records that link to NPD. The HES data will include month of death and month of birth so no identifying data.
For security and resource reasons the SRS is a Managed Service. Equiniti Ltd (based in Belfast) maintains the system, on behalf of the ONS SRS. They do so through encrypted (TLS1.2) VPN tunnel and Remotely Access (RA) the SRS. All Equiniti Ltd administrators are SC cleared and have no access to any data. ONS SRS Research Support “Admin” staff only have permissions to carry out such tasks as creating users, updating patches, testing and installing software applications, arranging DR, ITHC for the SRS environment, closing SRS sessions down, i.e. all the SRS environment Admin maintenance - essentially they are “power users”. There have been no data infractions by Equiniti Ltd staff in the last 5 years of them maintaining the environment, they have been very professional.
The high level security document that Equiniti Ltd provided [SD13] states: 6.3. Service Management support for the SRS Service is provided from Equiniti offices in Belfast, all staff are SC cleared. The office hosting the SRS Desk is IS0/IEC27001 2018 certified. Equiniti Ltd nor any their staff process the data. Therefore Equinity Ltd is not considered to be a Data Processor.
The ONS SRS environment is an isolated system. It has no connectivity to the internet other than using it as a bearer to pass TLS1.2 encrypted image packages for a virtual desktop infrastructure (VDI), hosted on an accredited cloud server hosted by UKCloud Ltd on the mainland UK. A High Level Security report is available in supporting documents [SD13]. UKCloud Ltd merely host the environment, they have no access to data. Therefore CloudUK Ltd is not considered to be a Data Processor.
CLOUD SECURITY
NHS Digital security has provided assurance regarding the use of the Office of National Statistics' Secure Research Statistics service (ONS SRS), hosted by CloudUK Ltd in this application. The Office of National Statistics has submitted a selection of security documentation to support the use of cloud storage. NHS Digital Security have reviewed the documentation and provided relevant feedback, where necessary. NHS Digital are satisfied that the documentation demonstrates the level of security and governance in place.
The Office of National Statistics have supplied evidence to support:
• The use of the Data Risk Model to assess the Risk Profile Class.
• Risk Management of the use of the Cloud for this data, taking into consideration Confidentiality, Integrity and Availability.
• The use of Pseudonymisation.
• Board level involvement in the Risk Management Process evidenced through Minutes of these meetings.
• Understanding of the Shared Responsibility Model
The Office of National Statistics have a very good understanding of the security controls available to them to provide the appropriate controls to secure data in the Cloud.
Using the Cloud, benefits from the inherited controls that cannot practically be replicated locally such as Physical Controls, Resilience of Systems, Power Supplies, Communications and Geographically dispersed Data Centres within a region.
Elasticity in provisioning is also a consideration that benefits organisations in managing workloads. The Cloud provider, CloudUK, will use UK Data Centres only.
DATA ANALYSIS
Any outputs will contain only aggregated data that complies with the small number suppression rules in the HES Analysis Guide.
The analyses of the linked data set will involve the following steps. These will be concurrent with the evaluation of linkage accuracy:
i) Create inception cohorts of children
(a) defined by births (Cohorts 3 and 4)
(b) entry to primary school (Cohorts 1 and 2)
ii) Examine characteristics of linked and unlinked cohorts to determine impact of linkage error.
iii) Characterise children according to past admissions and history of chronic conditions in HES-mortality data.
iv) Determine variation in school achievement taking into account health care history and chronic condition status (based on admissions in previous years).
v) Determine association between school achievement and emergency use of hospital services taking into account individual characteristics (health care and chronic condition status, socioeconomic status) and type of school and local authority. School attainment will be used as a time dependent co-variate that is associated with, or mediates, unplanned hospital admissions.
All organisations party to this agreement must comply with the Data Sharing Framework Contract requirements, including those regarding the use (and purpose of that use) by Personnel (as defined within the Data Sharing Framework Contract i.e: employees, agents and contractors of the Data Recipient who may have access to that data).
Expected output
A range of outputs are expected from the study relating to the aims of the study to investigate the quality of linkage and address relevant policy, healthcare and NHS systems questions on the association between child health and education (in the presence or absence of chronic illness; please refer to ‘Objective for processing’ for Aims).
The data analyses are conducted on the ONS Secure Research Service. Individual level child data cannot leave the ONS Secure Research Service. All outputs will contain aggregate level data only and all small numbers will be suppressed. Outputs will be monitored for compliance with ADRN statistical output controls and the HES Analysis Guides. No potentially disclosive outputs will be shared or published.
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EXTENSION REQUEST
An extension is requested because:
Initial outputs have recently been delivered, as described in the yielded benefits. It is commonplace that editorial queries and comments will arise subsequent to publication. In addition, further papers are being written. All follow up papers will fall under existing approvals and the agreed permitted uses.
Research from DARS-NIC-27404 also forms a baseline for evaluation of the larger linkage used in DARS-NIC-381972 ‘Assessing the impact of the COVID-19 pandemic on vulnerable children: the ECHILD-COVID study’. Although DARS-NIC-381972 has initially used an identical linking methodology to DARS-NIC-27404, changes during 2021 and 2022 will include the use of NHSD’s Master Person Service (MPS) (https://digital.nhs.uk/services/master-person-service). The encrypted HESID (Study_ID) currently used in the linkage spine will also be replaced by Token Person Id (https://nhs-prod.global.ssl.fastly.net/binaries/content/assets/website-assets/publications/publications-admin-pages/methodological-changes/announcement-of-methodological-change-to-hes-v2.0.pdf). DARS-NIC-27404 is seen as essential to validate linkage and confirm methodology changes in DARS-NIC-381972 do not impact linkage results. This may involve a need to re-run analyses on the existing data in NIC-27404.
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Aim 1 (Linkage component):
i. Linkage evaluation: The first output of this study will be the evaluation of a bespoke linkage method that could be extended by NHS Digital to wider linkages of data involving postcode histories over time. UCL will publish methodological papers in peer reviewed journals reporting the evaluation of the linkage accuracy. The methodological evaluation is expected to finish two years after obtaining the data. UCL will be targeting journals such as the International Journal of Epidemiology, and PLoS One. Further UCL will share this report with NHS Digital and DfE to inform their linkage methods. UCL will publish a summary of the outputs on the ADRC-E website.
ii. UCL would expect to present findings at conferences such as the International Population Data Linkage Conference and the Administrative Data Research Network after two years from obtaining the data.
Aim 2 /3: The other outputs will address the health service and policy questions relating to the linked data i.e. the applied research component.
iii. Study findings will be disseminated through peer-reviewed academic journals, and social media including lay summaries on the ADRC-E website. UCL expect the analysis to finish three years after obtaining the data. UCL will target both health and education journals and conferences. These include the Archives of Disease in Childhood, PlosONe and Journal of Public Health, and the British Education Research Journal.
iv. Study findings will be widely disseminated through conferences and seminars such as the Public Health Science Conference, International Population Data Linkage Conference, Society for Social Medicine, Society for Longitudinal and Lifecourse Studies, the British Education Research Association Conference.
v. Relevant findings will be shared with policy makers, clinicians/health professionals, educators and parent groups particularly those with an interest in chronic conditions in accessible formats (e.g. lay summaries, videos or animations). This could include forums such as the National Children’s Bureau (NCB) Young Person and Parent group, the Great Ormond Street Hospital (GOSH) Patient Engagement group. These groups can be accessed through the joint institute of UCL Great Ormond Street Hospital Institute of Child Health, through the North Thames CLARHC (led by UCL) and through the Children’s Policy Research Unit. Lay summaries of the study findings can be published on the ADRCE website, and linked through websites for these organisations.
Feedback to the Department of Health and Department for Education will be through the Children’s Policy Research Unit.
Expected measurable benefits
UCL will evaluate whether linkage error disproportionately affects certain ethnic or disadvantaged groups, who are also at increased risk of chronic conditions requiring hospital care by comparing characteristics of children who are linked with unlinked children in HES and NPD datasets. Findings can be used to modify linkage algorithms by NHS Digital when linking non-health data via the Personal Demographic Service to HES. Such information has the potential to benefit direct health care beyond the scope of this study.
The results relating to the provision of health care will be as follows:
1. The study will inform health care services about whether certain types of schools or local authorities are associated with increased or decreased rates of emergency admissions for children with and without chronic conditions. For example, children with serious learning impairing conditions may have lower rates of emergency hospital admission if they attend a special school than if they attend a mainstream school; school type or area may affect rates of emergency admissions and A&E attendance for adversity-related conditions (eg self-harm, violence or mental health), after adjusting for underlying chronic conditions, previous admissions, age and socioeconomic factors. In this way, the study will generate hypotheses about how interventions in schools, or improved feedback from hospitals, could potentially reduce rates of emergency use of hospital services. The findings will inform preventive health strategies by local authorities and hospitals.
2. The study will provide useful information for children and their parents, which is relevant to the promotion of their health and wellbeing and relevant to clinical practice. The study will show how school achievement and absence varies between children with and without chronic conditions, across the age range and between areas. Such variation can be used to inform clinical practice by identifying potentially better practices (eg to reduce school absence for children with chronic conditions) that could be adopted more widely.
3. The study will examine whether indicators at school such as absenteeism, and school failure can identify groups of vulnerable children and young people, particularly those with chronic conditions, who could benefit from proactive or preventive healthcare input that might reduce emergency use of hospital services, and improve health and educational outcomes.
Benefits reported so far
Initial yielded benefits include:
• Linkage evaluation results shared with NHS Digital and the DfE to inform their linkage methods;
• An evaluation of whether linkage error disproportionately affects certain ethnic or groups and methodological paper published in peer reviewed journal (September 2021, https://doi.org/10.23889/ijpds.v6i1.1671);
• Findings shared with policy makers, such as the DHSC through the Children and Families Policy Research Unit (CPRU) and ECHILD Advisory Group to inform services;
• Findings shared with clinicians/health professionals, educators, such as the letter on ethnic bias in data linkage published in The Lancet Digital Health (https://doi.org/10.1016/S2589-7500(21)00081-9) and several knowledge sharing events with DHSC, DfE and research institutions:
• Findings shared more widely in accessible formats, such as the lay summary of research https://ijpds.org/news/relationships-health-education-and-social-care and the ECHILD project website (https://www.ucl.ac.uk/child-health/echild).
Datasets on the latest version
Legal basis for provision: Health and Social Care Act 2012 - s261 - 'Other dissemination of information'
| Dataset | Type of data | Sensitivity | Frequency | Confidential data |
|---|---|---|---|---|
| Civil Registrations of Death - Secondary Care Cut | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
| HES:Civil Registration (Deaths) bridge | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
| Hospital Episode Statistics Accident and Emergency (HES A and E) | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
| Hospital Episode Statistics Admitted Patient Care (HES APC) | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
| Hospital Episode Statistics Critical Care (HES Critical Care) | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
| Hospital Episode Statistics Outpatients (HES OP) | Anonymised - ICO Code Compliant | Non-Sensitive | One-Off | Does not include the flow of confidential data |
Files released
Files released counts only files released externally by DARS. Access granted in NHS England's own systems, such as its Secure Data Environment, is not included.
Patient opt-outs were not applied to any of the 3 files released under this agreement, across every version. About opt-outs
No files recorded as released under the latest version. 3 were released under earlier versions, shown in the version history.
Version history
The register lists each renewal of this agreement as a separate row. This site has 3 versions — earlier versions existed before this site's records begin.
DARS-NIC-27404-D5Z3F-v3.5 19 April 2022 to 18 April 2025
- Title
- The relationship between education and health outcomes for children and young people across England: the value of using linked administrative data.
- Commercial
- No
- Sublicensing
- No
- Datasets
- 6
- Files released
- 0
Datasets: Civil Registrations of Death - Secondary Care Cut; HES:Civil Registration (Deaths) bridge; Hospital Episode Statistics Accident and Emergency (HES A and E); Hospital Episode Statistics Admitted Patient Care (HES APC); Hospital Episode Statistics Critical Care (HES Critical Care); Hospital Episode Statistics Outpatients (HES OP)
What changed from DARS-NIC-27404-D5Z3F-v2.2
Text removed is struck through; text added is underlined. Unchanged paragraphs are summarised rather than repeated.
| Field | Was | Became |
|---|---|---|
| Start date | 2022-04-19 | |
| End date | 2025-04-18 | |
| Civil Registrations of Death - Secondary Care Cut: legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' | |
| HES:Civil Registration (Deaths) bridge: legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' | |
| Hospital Episode Statistics Accident and Emergency (HES A and E): legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' | |
| Hospital Episode Statistics Admitted Patient Care (HES APC): legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' | |
| Hospital Episode Statistics Critical Care (HES Critical Care): legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' | |
| Hospital Episode Statistics Outpatients (HES OP): legal basis | Health and Social Care Act 2012 - s261 - 'Other dissemination of information' |
Objective for processing
[2 paragraphs unchanged]
The legal basis for processing personal data for this purpose data at UCL falls under Article 6(1)(e) of the General Data Protection Regulations (GDPR), i.e. a task carried out in the public interest. University College London (UCL) is a public authority and has a royal charter (see: https://www.ucl.ac.uk/governance-compliance/sites/governance_compliance/files/charter-and-statutes.pdf) which states that "The objects of the College shall be to provide education and courses of study in the fields of… Medicine and Medical Sciences, Social Sciences and Applied Sciences and… to encourage research in the said branches of knowledge and learning and to organise, encourage and
stimulate postgraduate study in such branches.". The legal basis also falls under Article 9(2)(j), processing is necessary for archiving purposes in the public interest, scientific or historical research purposes or statistical purposes.
This research is expected to have substantial public benefit by providing evidence on the quality of linkage between health and education data and by addressing relevant policy, healthcare and NHS systems questions on the association between child health and education.
[9 paragraphs unchanged]
For this programme of research, UCL are the sole Data Controller who also process data. The Office for National Statistics (ONS) are also data processors. This programme of research uses NPD attribute data from the DfE. Agreement DR190416.03 relates to the NPD attribute data that is accessed by University College London within the ONS Secure Research Services. A separate agreement DR150701.02 relates to the NPD identifiable data that are used by NHS Digital for the linkage that facilitates the analysis of the attribute data (this has now been completed). Further details are found in ‘5b. Processing activities’
[1 paragraph unchanged]
Linkage will be conducted by NHS Digital using identifiers supplied by DfE (forename, surname, date of birth, sex and postcode) captured in each school year. Identifiers will be matched initially to PDS and then to HES and de-identified. UCL will then receive the pseudonymised HES data from NHS Digital together with a Study_ID supplied by DfE. DfE will supply de-identified NPD data together with a Study_ID.
Research from DARS-NIC-27404 also forms a baseline for evaluation of the larger linkage used in DARS-NIC-381972 ‘Assessing the impact of the COVID-19 pandemic on vulnerable children: the ECHILD-COVID study’, which is producing scientific and statistical evidence on the impact of the Covid19 pandemic on vulnerable children and families.
Linkage has been conducted by NHS Digital using identifiers supplied by DfE (forename, surname, date of birth, sex and postcode) captured in each school year. Identifiers were matched initially to PDS and then to HES and de-identified. UCL then received the pseudonymised HES data from NHS Digital together with a Study_ID supplied by DfE. DfE will supply de-identified NPD data together with a Study_ID.
[18 paragraphs unchanged]
Processing activities
Analyses for RQ1:
The HES data provided by NHS Digital and NPD data provided by DfE are for the one-year birth cohorts comprising records for all children specified in the following cohorts:
The researcher will analyse outcomes for all CYP, and compare differences in health outcomes (e.g. emergency hospital contacts, deaths) between groups classified as vulnerable or not (stratified by age group), in the years before, compared with after, COVID-19 onset. Descriptive analyses will explore whether changes post-COVID-19 reflect increased risks of contacts related to infection, mental health, adversity, or acute complications of chronic or complex health conditions for all CYP, and according to whether they had indices for vulnerability or not. The researcher will use diagnostic and procedure codes, and types of hospital contact (eg emergency/elective admission), recorded in HES, to infer whether hospital contacts are related to underlying chronic conditions. Preliminary results October 2020.
Cohort 1: Born between 01/09/90-31/08/91
Analyses for RQ2:
Cohort 2: Born between 01/09/96-31/08/97
The researcher will model expected healthcare contacts for all CYP after the onset of the COVID-19 pandemic, based on observed trajectories of healthcare contact for CYP for periods prior to the start of COVID-19. The researcher will assess potential unmet healthcare need, according to age and vulnerability status, by comparing expected vs observed healthcare contacts after COVID-19 onset. Differences between expected and observed new diagnoses and interventions, will be used to infer potential unmet need. The researcher will vary their assumptions about whether and when these healthcare needs may manifest, and whether deferred presentation is likely to be more severe. The researcher will estimate how much deferred healthcare use could add to predicted rates of healthcare contacts in the post-COVID-19 period, and potential long-term outcomes of COVID-19 restrictions. Preliminary results in Jan 2021.
Cohort 3: Born between 01/09/99-31/08/00
The researcher will also conduct analyses of all CYP to explore associations between inequalities (using index of multiple deprivation), ethnic group, and vulnerable vs other CYP, and outcomes measured in health care, NPD data (i.e. education and CiN/CLA) in periods before, during and after the COVID-19 pandemic. The researcher will refresh the linked NPD datasets annually in 2021 and 2022 to evaluate the longer-term impacts of COVID-19 infection and response on health, education and social care outcomes for vulnerable, compared with other CYP.
Cohort 4: Born between 01/09/04-31/08/05
To address these research questions, HES (APC, A&E, OPD, ECDS, critical care) and death registration data (HES-mortality data) provided by NHS Digital will be linked to administrative data from the National Pupil Dataset (NPD) provided by the Department for Education (DfE) to the ONS SRS. Using a pseudonymised linkage key, these datasets will be linked for all children and young people (CYP) born in England on or after 1.9.1995.
The linkage of identifiers was conducted separately from attribute data (clinical or education characteristics) by NHS Digital. NHS Digital transferred pseudonymised HES IDs for those who were successfully linked and were released, together with the match rank and anonymized Pupil Matching Reference (PMR) as permitted by DfE. The definition of pseudonymisation is where direct identifiers have been removed from the data extract; identifiers refer to fields such as names, sex, date of birth, full post code. UCL researchers will use the transferred HES IDs to append match status to linked records in pseudonymised HES data (previously approved as NIC-393510).
Linkage of identifiers from HES-mortality data and NPD will be conducted at NHS Digital which will then only transfer the pseudonymised linkage key to the UCL Data Safe Haven to flag linked records in the UCL-curated HES extract for transfer to the ONS SRS. NPD attributable data will only be available in the ONS SRS. Using the pseudonymised linkage key, linkage of pseudonymised attribute data (clinical or education characteristics) will then occur separately, at the ONS Secure Research Service (SRS). The following outline describes the complete data flow and details how identifiable and non-identifiable data extracts will be handled:
The HES pseudonymised attribute data for the four cohorts, with an indicator of match rank provided by NHS Digital, was transferred to the Office of National Statistics Secure Research Service (ONS SRS) with HES ID and anonymised PMR for linkage, including only the month and year of birth and death.
1) DfE will supply the Trusted Third Party (NHS Digital) with a list of NPD identifier variables, these identifiers include name, date of birth, full postcode and sex, alongside a study specific pseudonymised linkage key known as the anonymized Pupil Matching Reference (aPMR). The identifying variables will be used for linkage to the Personal Demographic Service (PDS) (as previously done for NIC 27404). DfE will transfer the variables for any CYP born on or after cohort inception (1.9.95).
The following outline describes how identifiable and non-identifiable extracts from the data scheme were handled.
2) NHS Digital will match the identifiers from DfE to records held in the PDS using an algorithm that makes use of the chronology of postcodes in NPD and PDS. Matching to PDS data will be done internally within NHS Digital, no PDS data will be disseminated to ONS SRS or UCL Data Safe Haven.
1) DfE supplied the Trusted Third Party (NHS Digital) with a list of NPD identifier variables, including name and postcode histories, alongside a study specific pseudo-identifier number (Study_ID, known as the anonymized PMR) for children in PDS.
3) For those CYP whose NPD identifiers were matched to PDS, onward linkage to HES-mortality data will occur within NHS Digital to link aPMRs and HES-IDs. NHS Digital will then transfer encrypted HES-IDs, aPMRs, and indicators of match rank (denoting the step at which the match to HES and PDS was made) for these linked cases to the UCL Data Safe Haven for linkage to the existing HES-mortality extract held by UCL (NIC-393510).
2) NHS Digital matched the identifiers from DfE to records held in the PDS using an algorithm that prioritises the most recent post code in NPD (at the school census date). Matching to PDS data was done internally within NHS Digital, no PDS data will be disseminated to UCL.
4) UCL will extract the HES-mortality data for all CYP born on or after 1.9.1995, using the existing HES extract (NIC 393510), and link the aPMR and match rank statistics for those CYP that were linked by NHS Digital in step (3) from NPD. The de-identified HES-mortality extract will be transferred to the ONS SRS. Only month/year of birth and death will be transferred to the ONS SRS, in order to account for well-established effects of month of birth on school achievement (i.e. research consistently shows that children born in September do better than children born in July/August). The attribute data will also include high-level categorical maternal indicators relevant to birth (e.g. parity – 0, 1, 2+ prior births), which have an important bearing on child health. These derived health indicators are created by analysing variables in our analysis files, that are covered by this DSA (e.g. diagnosis codes and baby tail) and for which we have the appropriate permissions.
3) The PDS identifiers were linked to HES data. HES IDs for linked cases were then transferred to the UCL safe haven for identification within the existing HES extract held by UCL (NIC-393510). The anonymised PMR from the records that NHS Digital linked were also sent to UCL.
5) DfE will supply ONS SRS with requested de-identified attribute data extracts, with the aPMR for all CYP born on or after 1.9.1995. The deidentified attribute NPD and HES data will be linked within the ONS SRS by the research team, using the aPMR. Data will only be used by researchers authorised for the project, with strict output controls applied by ONS SRS staff.
The identifiable data supplied to NHS Digital for steps 1-3 has since been destroyed as these steps have now been completed.
6) The final data set that will be used for analyses will remain within the ONS SRS. The files will not contain any identifiable data. No additional record level data will be gathered or linked to the dataset. The aPMR is the only variable supplied from NPD data that is supplied by NHS Digital to UCL Data Safe Haven and then to ONS SRS.
4) UCL created four cohorts of all HES records for children born in years of cohorts 1 to 4 (admissions, critical care, A&E and OPD) and fact and date of death from the existing HES data (NIC-393510). These cohorts were transferred for linkage to the NPD data held in the ONS SRS. The deidentified, linked data are used by researchers authorised only for this project. Only month/year of birth and death were transferred to the ONS SRS, in order to account for well-established effects of month of birth on school achievement (i.e. research consistently shows that children born in September do better than children born in July/August). The anonymized PMR and metrics of the match rank of linkage provided by NHS Digital were also transferred to enable linkage with the NPD data and assessment of linkage accuracy.
7) NHS Digital will retain the identifier file of all individuals linked in NPD-PDS and PDS-HES and all the postcodes used in linkage and postcode dates for 12 months to address data queries or potential linkage errors. This data set will not contain any attribute data and will be accessible only to NHS Digital staff. At the end of the 12 months, NHS Digital will confirm deletion of the data to DfE. NHS Digital will not send confidential data to DfE or UCL DSH.
5) DfE supplied ONS SRS with requested (attribute) data extracts, alongside the anonymised PMR for children in Cohorts 1 to 4. There was no identifiable information in the extract sent. This extract was placed in the ONS SRS for linkage using anonymized PMRs to the 4 HES cohorts and analyses by researchers authorized for this project.
6) The final data set that is being used for analyses within the ONS SRS. The files not contain any identifiable data. No additional record level data data will be gathered or linked to the dataset. The anonymised PMR is the only variable supplied from NPD data that is supplied by NHS Digital to UCL Data Safe Haven.
7) NHS Digital retained the identifier file of all individuals linked in NPD-PDS and PDS-HES and all the postcodes used in linkage and postcode dates for 12 months to address data queries. This data set will not contain any attribute data and will be accessible only to NHS Digital staff. This has now been destroyed.
The following methodology was proposed for the linkage by NHS Digital:
The current MIDAS algorithm will be modified to consider the 15 most recent postcodes in PDS, ranked according to distance from the date associated with the NPD postcode. For remaining unmatched NPD records, the second postcode in NPD will then be compared with PDS as above. This approach will be repeated up to a maximum of 5 postcodes in NPD or until a match is achieved with PDS. This is necessary because ignoring address changes in PDS after the school census date in NPD would increase the number of missed matches. For example, although NPD postcode might be correct in September, PDS postcode in the subsequent months until the next census is more likely to be the most recent postcode.
NHS Digital will not send confidential data to DfE.
DATA SECURITY
To maintain the physical and technical security measures, the following safeguards will be in place:
1) Data linkage: Linkage between identifiers supplied for the NPD with PDS and HES will be carried out by a Trusted Third Party (NHS Digital) . The NHS Digital team undertaking the linkage will only have access to identifiers from PDS and HES for hospital administrative data and they will receive full identifiers from DfE for NPD data. These identifiers include name, date of birth, full postcode and sex. No additional attribute data will be provided. These identifiers will be removed and replaced with the pseudonymised Study ID (anonymized PMR) and HES ID assigned to each child in the cohort before release to the UCL Safe Haven. The original file was retained by the Trusted Third Party for 12 months to address queries about the linkage accuracy. This identifier data has now been deleted by NHS Digital.
As a consequence, the UCL researchers will not have access to the identifiers and the NHS Digital team undertaking the linkage received full identifiers from DfE for NPD data (inc. name, date of birth, full post code and sex) but no additional attribute data was provided.
2) Minimising data disclosure: HES pseudonymised attribute data for the 4 cohorts was transferred into the ONS SRS for access only for the purposes of this project. De-identified linkage between HES and NPD was done by remote secure access to the SRS from the UCL safe room. UCL will minimise disclosure risks by transferring only year and month of death and birth, LSOA decile rather than rank, location defined only by area indicators (eg local authority) in the four HES cohorts transferred to the ONS SRS. During analyses, the UCL researchers will minimise the potential for deductive disclosure, by limiting the presentation of specific information that could potentially identify any individual in the cohort. Statistical disclosure control measures will be applied according to HES requirements by ONS data scientists operating within the SRS.
3) Limited access: The de-identified linked HES-NPD data will be held on the ONS SRS accessible remotely from the UCL safe haven which has restricted and monitored access. No record level data can be removed from the SRS and statistical disclosure controls are applied by ONS staff.
The project has Administrative Data Research Network (ADRN) panel approval and Research Ethics Committee (REC) approval: 17/LO/1494. Access will be restricted to named users, who are part of the study team and are accessing the data for purposes outlined in this DSA. Access to the data is via the ONS SRS environment.
4) Limiting outputs: The data analyses are conducted on the ONS Secure Research Service. Detailed individual level child data cannot leave the ONS Secure Research Service. Results of analyses can be exported by a secure encrypted transfer system, which his audited. Any outputs from analyses that are published have to meet statistical disclosure controls that prevent small sizes in accordance with NHS Digital and DfE requirements. Tabulations of aggregate data are assessed for statistical disclosure control and authorized for export by an ONS data scientist not involved in the project.
[16 paragraphs unchanged]
DATA ANALYSIS
Any outputs will contain only aggregated data that complies with the small number suppression rules in the HES Analysis Guide.
The analyses of the linked data set will involve the following steps. These will be concurrent with the evaluation of linkage accuracy:
i) Create inception cohorts of children
(a) defined by births (Cohorts 3 and 4)
(b) entry to primary school (Cohorts 1 and 2)
ii) Examine characteristics of linked and unlinked cohorts to determine impact of linkage error.
iii) Characterise children according to past admissions and history of chronic conditions in HES-mortality data.
iv) Determine variation in school achievement taking into account health care history and chronic condition status (based on admissions in previous years).
v) Determine association between school achievement and emergency use of hospital services taking into account individual characteristics (health care and chronic condition status, socioeconomic status) and type of school and local authority. School attainment will be used as a time dependent co-variate that is associated with, or mediates, unplanned hospital admissions.
All organisations party to this agreement must comply with the Data Sharing Framework Contract requirements, including those regarding the use (and purpose of that use) by Personnel (as defined within the Data Sharing Framework Contract i.e: employees, agents and contractors of the Data Recipient who may have access to that data).
Expected output
[1 paragraph unchanged]
The data analyses are conducted on the ONS Secure Research Service. Individual level child data cannot leave the ONS Secure Research Service.
All outputs will contain aggregate level data only and all small numbers
[16 words unchanged]
HES Analysis Guides. No potentially disclosive outputs will be shared or published.
The project in this application/agreement is expected to finish three years after obtaining the data.
--------------------------
EXTENSION REQUEST
An extension is requested because:
Initial outputs have recently been delivered, as described in the yielded benefits. It is commonplace that editorial queries and comments will arise subsequent to publication. In addition, further papers are being written. All follow up papers will fall under existing approvals and the agreed permitted uses.
Research from DARS-NIC-27404 also forms a baseline for evaluation of the larger linkage used in DARS-NIC-381972 ‘Assessing the impact of the COVID-19 pandemic on vulnerable children: the ECHILD-COVID study’. Although DARS-NIC-381972 has initially used an identical linking methodology to DARS-NIC-27404, changes during 2021 and 2022 will include the use of NHSD’s Master Person Service (MPS) (https://digital.nhs.uk/services/master-person-service). The encrypted HESID (Study_ID) currently used in the linkage spine will also be replaced by Token Person Id (https://nhs-prod.global.ssl.fastly.net/binaries/content/assets/website-assets/publications/publications-admin-pages/methodological-changes/announcement-of-methodological-change-to-hes-v2.0.pdf). DARS-NIC-27404 is seen as essential to validate linkage and confirm methodology changes in DARS-NIC-381972 do not impact linkage results. This may involve a need to re-run analyses on the existing data in NIC-27404.
--------------------------
[8 paragraphs unchanged]
Benefits reported
Not stated in the previous version; added here.
Initial yielded benefits include:
• Linkage evaluation results shared with NHS Digital and the DfE to inform their linkage methods;
• An evaluation of whether linkage error disproportionately affects certain ethnic or groups and methodological paper published in peer reviewed journal (September 2021, https://doi.org/10.23889/ijpds.v6i1.1671);
• Findings shared with policy makers, such as the DHSC through the Children and Families Policy Research Unit (CPRU) and ECHILD Advisory Group to inform services;
• Findings shared with clinicians/health professionals, educators, such as the letter on ethnic bias in data linkage published in The Lancet Digital Health (https://doi.org/10.1016/S2589-7500(21)00081-9) and several knowledge sharing events with DHSC, DfE and research institutions:
• Findings shared more widely in accessible formats, such as the lay summary of research https://ijpds.org/news/relationships-health-education-and-social-care and the ECHILD project website (https://www.ucl.ac.uk/child-health/echild).
Unchanged: Expected measurable benefits.
DARS-NIC-27404-D5Z3F-v2.2 1 July 2019 to 31 January 2022
- Title
- The relationship between education and health outcomes for children and young people across England: the value of using linked administrative data.
- Commercial
- No
- Sublicensing
- No
- Datasets
- 6
- Files released
- 2
Datasets: Civil Registrations of Death - Secondary Care Cut; HES:Civil Registration (Deaths) bridge; Hospital Episode Statistics Accident and Emergency (HES A and E); Hospital Episode Statistics Admitted Patient Care (HES APC); Hospital Episode Statistics Critical Care (HES Critical Care); Hospital Episode Statistics Outpatients (HES OP)
What changed from DARS-NIC-27404-D5Z3F-v1.2
Text removed is struck through; text added is underlined. Unchanged paragraphs are summarised rather than repeated.
| Field | Was | Became |
|---|---|---|
| Start date | 2019-07-01 | |
| Civil Registrations of Death - Secondary Care Cut: sensitivity | Non-Sensitive |
Objective for processing
[2 paragraphs unchanged]
This study has two purposes. Firstly, to address the methodology for linking HES and national pupil data (NPD) from the Department for Education and to address important policy and health service questions about the interrelationship of health and education for children with and without underlying chronic conditions. As part of the methodology programme of the ADRC-E, the aim is to assess the feasibility of using linked health and education administrative data to carry out such research. The research will benefit the data providers, and thereby, indirectly benefit NHS systems, by undertaking an assessment of data quality and consistency between sources and by assessing the accuracy of linkage. The results will be published to inform others (government departments and researchers) of match rates and factors associated with linkage error.
This study has two purposes:
Firstly, to address the methodology for linking HES and National Pupil Data (NPD) from the Department for Education (DfE) and to address important policy and health service questions about the interrelationship of health and education for children with and without underlying chronic conditions. As part of the methodology programme of the ADRC-E, the aim is to assess the feasibility of using linked health and education administrative data to carry out such research. The research will benefit the data providers, and thereby, indirectly benefit NHS systems, by undertaking an assessment of data quality and consistency between sources and by assessing the accuracy of linkage. The results will be published to inform others (government departments and researchers) of match rates and factors associated with linkage error.
[3 paragraphs unchanged]
1. Evaluate linkage success between National Pupil Database (NPD), Personal Demographic Service (PDS),
Hospital Episode Statistics (HES)
hospital admissions
data (HES)
data,
and mortality data.
[2 paragraphs unchanged]
Methods
METHOD
[4 paragraphs unchanged]
UCL will examine whether low school achievement is associated with subsequent emergency
[109 words unchanged]
whole country and for all children (within the age restriction) in both
datasets.
data sets.
Both
datasets
data sets
contain longitudinal data of a child’s routinely captured information in the NPD
[116 words unchanged]
UCL have demonstrated the added value of using the whole longitudinal record.
[1 paragraph unchanged]
In order to minimise the amount of data, UCL have restricted the data requested to four one-year cohorts.
The four cohorts are:
The four cohorts are:
[12 paragraphs unchanged]
Processing activities
Data Flows
Analyses for RQ1:
The HES data to be provided by NHS Digital and NPD data provided by DfE are for the one-year birth cohorts comprising records for all children specified in the following cohorts:
The researcher will analyse outcomes for all CYP, and compare differences in health outcomes (e.g. emergency hospital contacts, deaths) between groups classified as vulnerable or not (stratified by age group), in the years before, compared with after, COVID-19 onset. Descriptive analyses will explore whether changes post-COVID-19 reflect increased risks of contacts related to infection, mental health, adversity, or acute complications of chronic or complex health conditions for all CYP, and according to whether they had indices for vulnerability or not. The researcher will use diagnostic and procedure codes, and types of hospital contact (eg emergency/elective admission), recorded in HES, to infer whether hospital contacts are related to underlying chronic conditions. Preliminary results October 2020.
Cohort 1: Born between 01/09/90-31/08/91
Analyses for RQ2:
Cohort 2: Born between 01/09/96-31/08/97
The researcher will model expected healthcare contacts for all CYP after the onset of the COVID-19 pandemic, based on observed trajectories of healthcare contact for CYP for periods prior to the start of COVID-19. The researcher will assess potential unmet healthcare need, according to age and vulnerability status, by comparing expected vs observed healthcare contacts after COVID-19 onset. Differences between expected and observed new diagnoses and interventions, will be used to infer potential unmet need. The researcher will vary their assumptions about whether and when these healthcare needs may manifest, and whether deferred presentation is likely to be more severe. The researcher will estimate how much deferred healthcare use could add to predicted rates of healthcare contacts in the post-COVID-19 period, and potential long-term outcomes of COVID-19 restrictions. Preliminary results in Jan 2021.
Cohort 3: Born between 01/09/99-31/08/00
The researcher will also conduct analyses of all CYP to explore associations between inequalities (using index of multiple deprivation), ethnic group, and vulnerable vs other CYP, and outcomes measured in health care, NPD data (i.e. education and CiN/CLA) in periods before, during and after the COVID-19 pandemic. The researcher will refresh the linked NPD datasets annually in 2021 and 2022 to evaluate the longer-term impacts of COVID-19 infection and response on health, education and social care outcomes for vulnerable, compared with other CYP.
Cohort 4: Born between 01/09/04-31/08/05
To address these research questions, HES (APC, A&E, OPD, ECDS, critical care) and death registration data (HES-mortality data) provided by NHS Digital will be linked to administrative data from the National Pupil Dataset (NPD) provided by the Department for Education (DfE) to the ONS SRS. Using a pseudonymised linkage key, these datasets will be linked for all children and young people (CYP) born in England on or after 1.9.1995.
The linkage
Linkage
of identifiers
from HES-mortality data and NPD
will be conducted
separately from
at NHS Digital which will then only transfer the pseudonymised linkage key to the UCL Data Safe Haven to flag linked records in the UCL-curated HES extract for transfer to the ONS SRS. NPD attributable data will only be available in the ONS SRS. Using the pseudonymised linkage key, linkage of pseudonymised
attribute data (clinical or education characteristics)
by NHS Digital
will then occur separately, at the ONS Secure Research Service (SRS). The following outline describes the complete data flow
and
pseudonymised before release to the UCL Safe Haven for analyses (the definition of pseudonymisation is where direct identifiers have been removed from the
details how identifiable and non-identifiable
data
extract; identifiers refer to fields such as names, sex, date of birth, full post code). UCL researchers
extracts
will
receive only pseudonymised HES data and pseudonymised NPD data (without sensitive variables, ie no date of birth or date of death).
be handled:
The following outline describes how identifiable and non-identifiable extracts from the data scheme will be handled.
1) DfE will supply the Trusted Third Party (NHS Digital) with a list of NPD identifier variables, these identifiers include name, date of birth, full postcode and sex, alongside a study specific pseudonymised linkage key known as the anonymized Pupil Matching Reference (aPMR). The identifying variables will be used for linkage to the Personal Demographic Service (PDS) (as previously done for NIC 27404). DfE will transfer the variables for any CYP born on or after cohort inception (1.9.95).
1) NHS Digital will create four cohorts of all HES records for children born in years of cohorts 1 to 4 (admissions, critical care, A&E and OPD and fact and date of death. Only month/year of death will be released to UCL, not full date of death. UCL request month of birth for each child in order to account for well-established effects of month of birth on school achievement (ie research consistently shows that children born in September do better than children born in July/August).
2) NHS Digital will match the identifiers from DfE to records held in the PDS using an algorithm that makes use of the chronology of postcodes in NPD and PDS. Matching to PDS data will be done internally within NHS Digital, no PDS data will be disseminated to ONS SRS or UCL Data Safe Haven.
2) DfE will supply UCL Safe Haven with requested (attribute) data extracts, alongside the study specific pseudo-identifier number (Study_ID) for children in Cohort 1 – 4. There will be no identifiable information on the extract sent to UCL.
3) For those CYP whose NPD identifiers were matched to PDS, onward linkage to HES-mortality data will occur within NHS Digital to link aPMRs and HES-IDs. NHS Digital will then transfer encrypted HES-IDs, aPMRs, and indicators of match rank (denoting the step at which the match to HES and PDS was made) for these linked cases to the UCL Data Safe Haven for linkage to the existing HES-mortality extract held by UCL (NIC-393510).
3) DfE will supply the Trusted Third Party (NHS Digital) with a list of NPD identifier variables, including name and postcode histories, alongside a study specific pseudo-identifier number (Study_ID) for children in Cohort 1 – 4.
4) UCL will extract the HES-mortality data for all CYP born on or after 1.9.1995, using the existing HES extract (NIC 393510), and link the aPMR and match rank statistics for those CYP that were linked by NHS Digital in step (3) from NPD. The de-identified HES-mortality extract will be transferred to the ONS SRS. Only month/year of birth and death will be transferred to the ONS SRS, in order to account for well-established effects of month of birth on school achievement (i.e. research consistently shows that children born in September do better than children born in July/August). The attribute data will also include high-level categorical maternal indicators relevant to birth (e.g. parity – 0, 1, 2+ prior births), which have an important bearing on child health. These derived health indicators are created by analysing variables in our analysis files, that are covered by this DSA (e.g. diagnosis codes and baby tail) and for which we have the appropriate permissions.
4) NHS Digital will match the identifiers from DfE to records held in the PDS using an algorithm that prioritises the most recent post code in NPD (at the school census date). Matching to PDS data will be done internally within NHS Digital, no PDS data will be disseminated to UCL.
5) DfE will supply ONS SRS with requested de-identified attribute data extracts, with the aPMR for all CYP born on or after 1.9.1995. The deidentified attribute NPD and HES data will be linked within the ONS SRS by the research team, using the aPMR. Data will only be used by researchers authorised for the project, with strict output controls applied by ONS SRS staff.
The following methodology is proposed for the linkage by NHS Digital:
6) The final data set that will be used for analyses will remain within the ONS SRS. The files will not contain any identifiable data. No additional record level data will be gathered or linked to the dataset. The aPMR is the only variable supplied from NPD data that is supplied by NHS Digital to UCL Data Safe Haven and then to ONS SRS.
The current MIDAS algorithm will be modified to consider the 15 most recent postcodes in PDS, ranked according to distance from the date associated with the NPD postcode. For remaining unmatched NPD records, the second postcode in NPD will then be compared with PDS as above. This approach will be repeated up to a maximum of 5 postcodes in NPD or until a match is achieved with PDS. This is necessary because ignoring address changes in PDS after the school census date in NPD would increase the number of missed matches. For example, although NPD postcode might be correct in September, PDS postcode in the subsequent months until the next census is more likely to be the most recent postcode.
7) NHS Digital will retain the identifier file of all individuals linked in NPD-PDS and PDS-HES and all the postcodes used in linkage and postcode dates for 12 months to address data queries or potential linkage errors. This data set will not contain any attribute data and will be accessible only to NHS Digital staff. At the end of the 12 months, NHS Digital will confirm deletion of the data to DfE. NHS Digital will not send confidential data to DfE or UCL DSH.
NHS Digital will not send confidential data to DfE.
The de-identified linked HES-NPD attribute data will be held on the ONS SRS and will only be accessible remotely from the UCL Data Safe Room which has restricted and monitored access. No record level data can be removed from the ONS SRS and statistical disclosure controls are applied by ONS staff. Access will be restricted to named users, who are part of the study team and are accessing the data for the purposes outlined in this DSA. Access to the data is via the ONS SRS environment.
5) NHS Digital will create two HES – NPD data files. Each file will contain the pseudo-id provided by NPD (Study_ID) and pseudo-id provided by HES (HESID). All individuals within the relevant cohorts 1-4 age range, whether they are linked or unlinked (i.e. appear in both HES and NPD or just one dataset) will be assigned a HESID, and those matched to NPD will be assigned the study-ID transferred from DfE. These pseudo- anonymised files will be transferred to the UCL Safe Haven to be accessed by the researcher. These files will not be provided to DfE.
Office of National Statistics (ONS) and UCL have signed and maintain an organisational agreement to use the ONS Secure Research Statistics (SRS) service for the purposes of secure statistical research, signed on 21/03/2019 with an indefinite expiry date [SD10]. The only HES data stored in the ONS SRS are the 4 one-year cohorts of HES, plus the anonymised PMRs for those records that link to NPD. The HES data will include month of death and month of birth so no identifying data.
The HES-Mortality/PDS-NPD Matched Assessment File will contain linkage details of the matches between NPD and PDS using the pseudo-study id for each of the data sets i.e. HESID and Study_ID. It will indicate the match rank at linkage with NPD (i.e. the first, second or third etc. running of the modified MIDAS algorithm). The file will not contain any postcodes or other identifiers.
For security and resource reasons the SRS is a Managed Service. Equiniti Ltd (based in Belfast) maintains the system, on behalf of the ONS SRS. They do so through encrypted (TLS1.2) VPN tunnel and Remotely Access (RA) the SRS. All Equiniti Ltd administrators are SC cleared and have no access to any data. ONS SRS Research Support “Admin” staff only have permissions to carry out such tasks as creating users, updating patches, testing and installing software applications, arranging DR, ITHC for the SRS environment, closing SRS sessions down, i.e. all the SRS environment Admin maintenance - essentially they are “power users”. There have been no data infractions by Equiniti Ltd staff in the last 5 years of them maintaining the environment, they have been very professional.
The second file will contain attribute data. This contains the HES records for the matched HES-Mortality/PDS - NPD records and the unmatched HES records for patients in cohorts 1-4. All records will contain a HESID and those matched to NPD will also contain a Study-ID.
The high level security document that Equiniti Ltd provided [SD13] states: 6.3. Service Management support for the SRS Service is provided from Equiniti offices in Belfast, all staff are SC cleared. The office hosting the SRS Desk is IS0/IEC27001 2018 certified. Equiniti Ltd nor any their staff process the data. Therefore Equinity Ltd is not considered to be a Data Processor.
6) NHS Digital will retain the identifier file of all individuals linked in NPD-PDS and PDS-HES and all the postcodes used in linkage and postcode dates for 12 months to address data queries. This data set will not contain any attribute data and will be accessible only to NHS Digital staff.
The ONS SRS environment is an isolated system. It has no connectivity to the internet other than using it as a bearer to pass TLS1.2 encrypted image packages for a virtual desktop infrastructure (VDI), hosted on an accredited cloud server hosted by UKCloud Ltd on the mainland UK. A High Level Security report is available in supporting documents [SD13]. UKCloud Ltd merely host the environment, they have no access to data. Therefore CloudUK Ltd is not considered to be a Data Processor.
7) The two HES-NPD files will be transferred to the UCL Data Safe Haven from NHS Digital for analysis by the UCL team. The pseudo Study IDs attached to NPD data supplied by DfE, attached to the matched HES-NPD records assessment file supplied by NHSD, and attached to the unmatched and matched HES attribute records, will be used to create the final dataset that will be used for analyses within the UCL Safe Haven. The files will not contain any identifiable data. No additional record level data data will be gathered or linked to the dataset.
CLOUD SECURITY
Data security
NHS Digital security has provided assurance regarding the use of the Office of National Statistics' Secure Research Statistics service (ONS SRS), hosted by CloudUK Ltd in this application. The Office of National Statistics has submitted a selection of security documentation to support the use of cloud storage. NHS Digital Security have reviewed the documentation and provided relevant feedback, where necessary. NHS Digital are satisfied that the documentation demonstrates the level of security and governance in place.
To maintain the physical and technical security measures, the following safeguards will be in place:
The Office of National Statistics have supplied evidence to support:
1) Data linkage: Linkage will be carried out by a Trusted Third Party (NHS Digital) following the separation principle. The NHS Digital team undertaking the linkage will only have access to identifiers from the HES team for hospital administrative data and receive full identifiers from DfE for NPD data. These identifiers include name, date of birth, full postcode and sex. No additional attribute data will be provided. These identifiers will be removed and replaced with the pseudonymised Study ID and HESID assigned to each child in the cohort before release to the UCL Safe Haven for access by the researchers. The original file will be retained by the Trusted Third Party for 12 months to address queries about the linkage accuracy.
• The use of the Data Risk Model to assess the Risk Profile Class.
As a consequence, the UCL researcher will not have access to the identifiers and NHS Digital will at no point have access to NPD attribute data.
• Risk Management of the use of the Cloud for this data, taking into consideration Confidentiality, Integrity and Availability.
2) Minimising data disclosure: During analyses, the UCL researchers will minimise the potential for deductive disclosure, by limiting the presentation of specific information that could potentially identify any individual in the cohort. Statistical disclosure control measures will be applied according to HES requirements. UCL have minimised disclosure risks by requesting: only month of death and month of birth, LSOA decile rather than rank, location defined only by area indicators (eg local authority), and UCL will allocate a pseudo-id for school.
• The use of Pseudonymisation.
3) Limited access: The data will be held on a secure server at University College London. The project has ADRN panel approval and REC approval: 17/LO/1494. Access will be restricted to named users, who are notified to the i) data providers, the ii) secure server operators, and who are contractually part of iii) the study team and have signed a data user agreement with all three parties. The users must also be accredited as data users (meaning they have been trained in governance and confidentiality) by the UK Administrative Data Research Network (ADRN adrn.ac.uk). All users have university contracts that stipulate compliance with data governance. This means that the researcher can be dismissed from their post if they fail to comply with data governance requirements. Access to the data is via a remote login that requires a physical authentication system as well as a password (i.e. double authentication).
• Board level involvement in the Risk Management Process evidenced through Minutes of these meetings.
4) Limiting outputs: The data analyses are conducted on the UCL data safe haven. Detailed individual level child data cannot leave the UCL Safe Haven (i.e. secure server) except by a secure encrypted transfer system, as that would be in breach of data sharing agreements. It is used to export results of analyses and can be audited. Any outputs from analyses that are published have to meet statistical disclosure controls that prevent small cell sizes in accordance with NHSD requirements. Tabulations of aggregate data are assessed for statistical disclosure control and authorised for export by a data scientist not involved with the analysis who has delegated exporting rights authorised by the Principal Investigator of the project. No de-identified death registration data will leave the UCL safe setting.
• Understanding of the Shared Responsibility Model
Data Analysis
The Office of National Statistics have a very good understanding of the security controls available to them to provide the appropriate controls to secure data in the Cloud.
The record-level HES-mortality data will only be accessed by staff with contracts at UCL who have been trained and authorised to access the UCL safe haven. Any outputs will contain only aggregated data that complies with the small number suppression rules in the HES Analysis Guide.
Using the Cloud, benefits from the inherited controls that cannot practically be replicated locally such as Physical Controls, Resilience of Systems, Power Supplies, Communications and Geographically dispersed Data Centres within a region.
The analyses of the linked dataset will involve the following steps. These will be concurrent with the evaluation of linkage accuracy:
Elasticity in provisioning is also a consideration that benefits organisations in managing workloads. The Cloud provider, CloudUK, will use UK Data Centres only.
i) Create inception cohorts of children:
(a) defined by birth (Cohorts 3 and 4)
(b) entry to primary school (Cohorts 1 and 2)
ii) Examine characteristics of linked and unlinked cohorts to determine impact of linkage error.
iii) Characterise children according to past admissions and history of chronic conditions in HES-mortality data.
iv) Determine variation in school achievement taking into account health care history and chronic condition status (based on admissions in previous years).
v) Determine association between school achievement and emergency use of hospital services taking into account individual characteristics (health care and chronic condition status, socioeconomic status) and type of school and local authority. School attainment will be used as a time dependent covariate that is associated with, or mediates, unplanned hospital admissions.
All organisations party to this agreement must comply with the Data Sharing Framework Contract requirements, including those regarding the use (and purposes of that use) by “Personnel” (as defined within the Data Sharing Framework Contract ie: employees, agents and contractors of the Data Recipient who may have access to that data).
Unchanged: Expected output, Expected measurable benefits.
Objective for processing
BACKGROUND
The strong interrelationship between health and education services in relation to the health and wellbeing of children is recognised by policy makers, but evidence is lacking on how services complement or compensate for each other and there have been calls for a stronger evidence base to be developed.
This study has two purposes:
Firstly, to address the methodology for linking HES and National Pupil Data (NPD) from the Department for Education (DfE) and to address important policy and health service questions about the interrelationship of health and education for children with and without underlying chronic conditions. As part of the methodology programme of the ADRC-E, the aim is to assess the feasibility of using linked health and education administrative data to carry out such research. The research will benefit the data providers, and thereby, indirectly benefit NHS systems, by undertaking an assessment of data quality and consistency between sources and by assessing the accuracy of linkage. The results will be published to inform others (government departments and researchers) of match rates and factors associated with linkage error.
The second purpose, is to inform policy and service commissioners about associations between education risk factors and health outcomes, such as emergency hospital admissions. The hypothesis is that school attainment is associated with unplanned admissions to hospital, but this association may vary by area, type of school and individual risk factors, particularly presence of chronic conditions. Researchers need to study the whole of England in order to determine how education outcomes vary according to local authority and type of school, and what the impact is of such variation on emergency admissions to hospital.
The project combines a methodological component to evaluate linkage quality and an applied research component, which involves evaluating the association between education outcomes and emergency use of hospital services by children with and without underlying chronic conditions.
This study has three aims, namely to:
1. Evaluate linkage success between National Pupil Database (NPD), Personal Demographic Service (PDS), Hospital Episode Statistics (HES) hospital admissions data, and mortality data.
2. Evaluate the association between hospital admissions for children and adolescents with underlying chronic conditions and subsequent school achievement
3. Evaluate the association between education outcomes and subsequent use of hospital services, taking into account underlying chronic conditions.
METHOD
Linkage
Linkage will be conducted by NHS Digital using identifiers supplied by DfE (forename, surname, date of birth, sex and postcode) captured in each school year. Identifiers will be matched initially to PDS and then to HES and de-identified. UCL will then receive the pseudonymised HES data from NHS Digital together with a Study_ID supplied by DfE. DfE will supply de-identified NPD data together with a Study_ID.
Analyses
Using the linked data UCL will examine how the association between school achievement and hospitalisation varies according to local authority and type of school, taking into account factors at the individual level (eg chronic conditions in the health record, free school meals, ethnicity in the school record) that might affect both school achievement and emergency use of hospital services (ie. confounding factors).
UCL will examine whether low school achievement is associated with subsequent emergency admissions to hospital, and whether health problems, manifest in admissions to hospital, are associated with subsequent changes in school achievement. UCL would expect these associations to vary across the country, as local factors, such as type of school and local services, eg support for children with chronic conditions, vary between local authorities. Evidence on such risk factors will be important for generating hypotheses about how healthcare and schools can reduce adverse outcomes for children and adolescents. To evaluate variation across the country, and to have sufficient power to evaluate outcomes for children with chronic conditions at different ages and in different services, UCL need to use data for the whole country and for all children (within the age restriction) in both data sets.
Both data sets contain longitudinal data of a child’s routinely captured information in the NPD and of hospital admissions, outpatient and A&E attendance in HES and mortality data. Within HES, diagnosis and procedural variables will be required to identify unplanned admissions, and to define cohorts of children with and without chronic conditions. Information from OPD and A&E adds information on planned outpatient specialist care and the frequency of emergency hospital contacts without admission. Comparison groups, comprising those with and those without chronic conditions will be identified from the longitudinal record of hospital admissions, if possible from birth. Previous work completed by UCL has shown that chronic underlying conditions may not be recorded at every admission (for example, asthma may not be recorded when a child is admitted for an operation) and UCL have demonstrated the added value of using the whole longitudinal record.
Description of the cohorts:
In order to minimise the amount of data, UCL have restricted the data requested to four one-year cohorts. The four cohorts are:
COHORT 1. Young people cohort (born between 01/09/1990-31/08/1991 who entered reception class in September 1996):
This cohort will test the quality of linkage of data with young people receiving education up to age 18 years, and as young people become more mobile.
These young people will first be recorded in the NPD with their Key Stage 1 (KS1) from 1998 and Key Stage 2 (KS2) from 2002, and annual school census from 2001/2. UCL request NPD KS1, KS2, KS4, and KS5. They will also be captured in HES on their first hospitalisation on or after 01/04/1997 (at approximately 7 years of age or more). HES data is requested up until the most recent available period.
This cohort tests linkage with all children (state and non-state educated) who have a KS4 assessment (approximately 99% of adolescents aged 15/16). UCL will also follow up adolescents who sit KS5 (A levels). At this age they have shown high rates of emergency use of hospital for adversity related injury (self-harm, drug or alcohol misuse or violence). In this cohort, UCL can evaluate the antecedent education risk factors for such admissions.
COHORT 2. Primary-secondary school transition cohort (born between 01/09/1996-31/08/1997 who entered reception class in September 2002).
This cohort will comprise children whose educational profile can be followed from primary to secondary school and will capture health service utilisation from the early years and throughout the educational trajectory. The cohort will provide valuable information on the quality of data linkage, where there is an overlap between the time points on the main datasets (i.e. NPD and HES).
These children will be recorded in the NPD annual school census from 2001/2 and in KS1 data from 2003/4. These children enter secondary school in September 2008 and will have KS3 recorded in 2011 and KS4 recorded in 2012/13. This cohort will have annual school census data throughout the primary school years, but not all would have had a hospital admission (UCL expect around 40% to have been admitted at some point). Data on hospitalisations will be captured in HES on or after 01/04/1997 (when this cohort will be approximately 1 year of age) until the most recent data extract available.
COHORT 3. Preschool-primary school cohort (born between 01/09/1999-31/08/2000 who entered the reception class in September 2005).
This cohort will capture indicators of chronic conditions recorded in the birth record and in infancy, which is the period when the risk of admission to hospital is highest. It will also provide a complete record of primary school education. The frequent movement of children in the preschool years will present a challenge to linkage (ie. postcode changes), which UCL will seek to evaluate in this study using available HES resources, such as the Patient Demographic Service introduced in 2004. Linkage quality is expected to be less good than for Cohort 4, as identifiers in HES birth records between the cohort years. NPD data are requested up until KS4 data, which would end in 2015/16. UCL will examine the association between chronic conditions and school achievement in the cohort, accounting for chronic conditions and birth characteristics recorded in early life.
COHORT 4. Patient demographic service cohort (born between 01/09/2004-31/-8/2005 and enter reception class in September 2010)
This cohort data in HES birth episodes and PDS will be concurrent and therefore maximise the likelihood of successful linkage to the NPD (ie most children in NPD are expected to have a birth episode in HES). It should comprise a complete record of health service used from birth and early education that may be used to investigate the impact of early education/educational achievements on pre/post school hospital admissions.
NPD are requested up until KS2 data.
Expected output
A range of outputs are expected from the study relating to the aims of the study to investigate the quality of linkage and address relevant policy, healthcare and NHS systems questions on the association between child health and education (in the presence or absence of chronic illness; please refer to ‘Objective for processing’ for Aims).
All outputs will contain aggregate level data only and all small numbers will be suppressed. Outputs will be monitored for compliance with ADRN statistical output controls and the HES Analysis Guides. No potentially disclosive outputs will be shared or published. The project in this application/agreement is expected to finish three years after obtaining the data.
Aim 1 (Linkage component):
i. Linkage evaluation: The first output of this study will be the evaluation of a bespoke linkage method that could be extended by NHS Digital to wider linkages of data involving postcode histories over time. UCL will publish methodological papers in peer reviewed journals reporting the evaluation of the linkage accuracy. The methodological evaluation is expected to finish two years after obtaining the data. UCL will be targeting journals such as the International Journal of Epidemiology, and PLoS One. Further UCL will share this report with NHS Digital and DfE to inform their linkage methods. UCL will publish a summary of the outputs on the ADRC-E website.
ii. UCL would expect to present findings at conferences such as the International Population Data Linkage Conference and the Administrative Data Research Network after two years from obtaining the data.
Aim 2 /3: The other outputs will address the health service and policy questions relating to the linked data i.e. the applied research component.
iii. Study findings will be disseminated through peer-reviewed academic journals, and social media including lay summaries on the ADRC-E website. UCL expect the analysis to finish three years after obtaining the data. UCL will target both health and education journals and conferences. These include the Archives of Disease in Childhood, PlosONe and Journal of Public Health, and the British Education Research Journal.
iv. Study findings will be widely disseminated through conferences and seminars such as the Public Health Science Conference, International Population Data Linkage Conference, Society for Social Medicine, Society for Longitudinal and Lifecourse Studies, the British Education Research Association Conference.
v. Relevant findings will be shared with policy makers, clinicians/health professionals, educators and parent groups particularly those with an interest in chronic conditions in accessible formats (e.g. lay summaries, videos or animations). This could include forums such as the National Children’s Bureau (NCB) Young Person and Parent group, the Great Ormond Street Hospital (GOSH) Patient Engagement group. These groups can be accessed through the joint institute of UCL Great Ormond Street Hospital Institute of Child Health, through the North Thames CLARHC (led by UCL) and through the Children’s Policy Research Unit. Lay summaries of the study findings can be published on the ADRCE website, and linked through websites for these organisations.
Feedback to the Department of Health and Department for Education will be through the Children’s Policy Research Unit.
DARS-NIC-27404-D5Z3F-v1.2 7 December 2018 to 31 January 2022
- Title
- The relationship between education and health outcomes for children and young people across England: the value of using linked administrative data.
- Commercial
- No
- Sublicensing
- No
- Datasets
- 6
- Files released
- 1
Datasets: Civil Registrations of Death - Secondary Care Cut; HES:Civil Registration (Deaths) bridge; Hospital Episode Statistics Accident and Emergency (HES A and E); Hospital Episode Statistics Admitted Patient Care (HES APC); Hospital Episode Statistics Critical Care (HES Critical Care); Hospital Episode Statistics Outpatients (HES OP)
Objective for processing
Background
The strong interrelationship between health and education services in relation to the health and wellbeing of children is recognised by policy makers, but evidence is lacking on how services complement or compensate for each other and there have been calls for a stronger evidence base to be developed.
This study has two purposes. Firstly, to address the methodology for linking HES and national pupil data (NPD) from the Department for Education and to address important policy and health service questions about the interrelationship of health and education for children with and without underlying chronic conditions. As part of the methodology programme of the ADRC-E, the aim is to assess the feasibility of using linked health and education administrative data to carry out such research. The research will benefit the data providers, and thereby, indirectly benefit NHS systems, by undertaking an assessment of data quality and consistency between sources and by assessing the accuracy of linkage. The results will be published to inform others (government departments and researchers) of match rates and factors associated with linkage error.
The second purpose, is to inform policy and service commissioners about associations between education risk factors and health outcomes, such as emergency hospital admissions. The hypothesis is that school attainment is associated with unplanned admissions to hospital, but this association may vary by area, type of school and individual risk factors, particularly presence of chronic conditions. Researchers need to study the whole of England in order to determine how education outcomes vary according to local authority and type of school, and what the impact is of such variation on emergency admissions to hospital.
The project combines a methodological component to evaluate linkage quality and an applied research component, which involves evaluating the association between education outcomes and emergency use of hospital services by children with and without underlying chronic conditions.
This study has three aims, namely to:
1. Evaluate linkage success between National Pupil Database (NPD), Personal Demographic Service (PDS), hospital admissions data (HES) and mortality data.
2. Evaluate the association between hospital admissions for children and adolescents with underlying chronic conditions and subsequent school achievement
3. Evaluate the association between education outcomes and subsequent use of hospital services, taking into account underlying chronic conditions.
Methods
Linkage
Linkage will be conducted by NHS Digital using identifiers supplied by DfE (forename, surname, date of birth, sex and postcode) captured in each school year. Identifiers will be matched initially to PDS and then to HES and de-identified. UCL will then receive the pseudonymised HES data from NHS Digital together with a Study_ID supplied by DfE. DfE will supply de-identified NPD data together with a Study_ID.
Analyses
Using the linked data UCL will examine how the association between school achievement and hospitalisation varies according to local authority and type of school, taking into account factors at the individual level (eg chronic conditions in the health record, free school meals, ethnicity in the school record) that might affect both school achievement and emergency use of hospital services (ie. confounding factors).
UCL will examine whether low school achievement is associated with subsequent emergency admissions to hospital, and whether health problems, manifest in admissions to hospital, are associated with subsequent changes in school achievement. UCL would expect these associations to vary across the country, as local factors, such as type of school and local services, eg support for children with chronic conditions, vary between local authorities. Evidence on such risk factors will be important for generating hypotheses about how healthcare and schools can reduce adverse outcomes for children and adolescents. To evaluate variation across the country, and to have sufficient power to evaluate outcomes for children with chronic conditions at different ages and in different services, UCL need to use data for the whole country and for all children (within the age restriction) in both datasets.
Both datasets contain longitudinal data of a child’s routinely captured information in the NPD and of hospital admissions, outpatient and A&E attendance in HES and mortality data. Within HES, diagnosis and procedural variables will be required to identify unplanned admissions, and to define cohorts of children with and without chronic conditions. Information from OPD and A&E adds information on planned outpatient specialist care and the frequency of emergency hospital contacts without admission. Comparison groups, comprising those with and those without chronic conditions will be identified from the longitudinal record of hospital admissions, if possible from birth. Previous work completed by UCL has shown that chronic underlying conditions may not be recorded at every admission (for example, asthma may not be recorded when a child is admitted for an operation) and UCL have demonstrated the added value of using the whole longitudinal record.
Description of the cohorts:
In order to minimise the amount of data, UCL have restricted the data requested to four one-year cohorts.
The four cohorts are:
Cohort 1. Young people cohort (born between 01/09/1990-31/08/1991 who entered reception class in September 1996):
This cohort will test the quality of linkage of data with young people receiving education up to age 18 years, and as young people become more mobile.
These young people will first be recorded in the NPD with their Key Stage 1 (KS1) from 1998 and Key Stage 2 (KS2) from 2002, and annual school census from 2001/2. UCL request NPD KS1, KS2, KS4, and KS5. They will also be captured in HES on their first hospitalisation on or after 01/04/1997 (at approximately 7 years of age or more). HES data is requested up until the most recent available period.
This cohort tests linkage with all children (state and non-state educated) who have a KS4 assessment (approximately 99% of adolescents aged 15/16). UCL will also follow up adolescents who sit KS5 (A levels). At this age they have shown high rates of emergency use of hospital for adversity related injury (self-harm, drug or alcohol misuse or violence). In this cohort, UCL can evaluate the antecedent education risk factors for such admissions.
Cohort 2. Primary-secondary school transition cohort (born between 01/09/1996-31/08/1997 who entered reception class in September 2002).
This cohort will comprise children whose educational profile can be followed from primary to secondary school and will capture health service utilisation from the early years and throughout the educational trajectory. The cohort will provide valuable information on the quality of data linkage, where there is an overlap between the time points on the main datasets (i.e. NPD and HES).
These children will be recorded in the NPD annual school census from 2001/2 and in KS1 data from 2003/4. These children enter secondary school in September 2008 and will have KS3 recorded in 2011 and KS4 recorded in 2012/13. This cohort will have annual school census data throughout the primary school years, but not all would have had a hospital admission (UCL expect around 40% to have been admitted at some point). Data on hospitalisations will be captured in HES on or after 01/04/1997 (when this cohort will be approximately 1 year of age) until the most recent data extract available.
Cohort 3. Preschool-primary school cohort (born between 01/09/1999-31/08/2000 who entered the reception class in September 2005).
This cohort will capture indicators of chronic conditions recorded in the birth record and in infancy, which is the period when the risk of admission to hospital is highest. It will also provide a complete record of primary school education. The frequent movement of children in the preschool years will present a challenge to linkage (ie. postcode changes), which UCL will seek to evaluate in this study using available HES resources, such as the Patient Demographic Service introduced in 2004. Linkage quality is expected to be less good than for Cohort 4, as identifiers in HES birth records between the cohort years. NPD data are requested up until KS4 data, which would end in 2015/16. UCL will examine the association between chronic conditions and school achievement in the cohort, accounting for chronic conditions and birth characteristics recorded in early life.
Cohort 4. Patient demographic service cohort (born between 01/09/2004-31/-8/2005 and enter reception class in September 2010)
This cohort data in HES birth episodes and PDS will be concurrent and therefore maximise the likelihood of successful linkage to the NPD (ie most children in NPD are expected to have a birth episode in HES). It should comprise a complete record of health service used from birth and early education that may be used to investigate the impact of early education/educational achievements on pre/post school hospital admissions.
NPD are requested up until KS2 data.
Expected output
A range of outputs are expected from the study relating to the aims of the study to investigate the quality of linkage and address relevant policy, healthcare and NHS systems questions on the association between child health and education (in the presence or absence of chronic illness; please refer to ‘Objective for processing’ for Aims).
All outputs will contain aggregate level data only and all small numbers will be suppressed. Outputs will be monitored for compliance with ADRN statistical output controls and the HES Analysis Guides. No potentially disclosive outputs will be shared or published. The project in this application/agreement is expected to finish three years after obtaining the data.
Aim 1 (Linkage component):
i. Linkage evaluation: The first output of this study will be the evaluation of a bespoke linkage method that could be extended by NHS Digital to wider linkages of data involving postcode histories over time. UCL will publish methodological papers in peer reviewed journals reporting the evaluation of the linkage accuracy. The methodological evaluation is expected to finish two years after obtaining the data. UCL will be targeting journals such as the International Journal of Epidemiology, and PLoS One. Further UCL will share this report with NHS Digital and DfE to inform their linkage methods. UCL will publish a summary of the outputs on the ADRC-E website.
ii. UCL would expect to present findings at conferences such as the International Population Data Linkage Conference and the Administrative Data Research Network after two years from obtaining the data.
Aim 2 /3: The other outputs will address the health service and policy questions relating to the linked data i.e. the applied research component.
iii. Study findings will be disseminated through peer-reviewed academic journals, and social media including lay summaries on the ADRC-E website. UCL expect the analysis to finish three years after obtaining the data. UCL will target both health and education journals and conferences. These include the Archives of Disease in Childhood, PlosONe and Journal of Public Health, and the British Education Research Journal.
iv. Study findings will be widely disseminated through conferences and seminars such as the Public Health Science Conference, International Population Data Linkage Conference, Society for Social Medicine, Society for Longitudinal and Lifecourse Studies, the British Education Research Association Conference.
v. Relevant findings will be shared with policy makers, clinicians/health professionals, educators and parent groups particularly those with an interest in chronic conditions in accessible formats (e.g. lay summaries, videos or animations). This could include forums such as the National Children’s Bureau (NCB) Young Person and Parent group, the Great Ormond Street Hospital (GOSH) Patient Engagement group. These groups can be accessed through the joint institute of UCL Great Ormond Street Hospital Institute of Child Health, through the North Thames CLARHC (led by UCL) and through the Children’s Policy Research Unit. Lay summaries of the study findings can be published on the ADRCE website, and linked through websites for these organisations.
Feedback to the Department of Health and Department for Education will be through the Children’s Policy Research Unit.
Register history
When this agreement appeared in, or was edited in, each monthly edition of the register. Built by comparing every edition this site holds, the earliest of which is July 2021.
-
July 2021 —
already listed in the earliest edition this site holds, so it may be older. 2 versions: DARS-NIC-27404-D5Z3F-v1.2, DARS-NIC-27404-D5Z3F-v2.2
-
July 2022
1 version added: DARS-NIC-27404-D5Z3F-v3.5
-
December 2022
Register-wide edit DARS-NIC-27404-D5Z3F-v1.2, DARS-NIC-27404-D5Z3F-v2.2 — Datasets: legal basis: “
s261(1) and” taken out. Made to 639 agreements in this edition, so it is reported once, on the changes page, and not counted as an amendment of this agreement.
Cite this page
NHS England (2026) Data Uses Register, September 2026 edition, agreement DARS-NIC-27404-D5Z3F, “The relationship between education and health outcomes for children and young people across England: the value of using linked administrative data.”. Read via NHS Data Access Explorer (unofficial), https://healthdatauses.uk/agreements/dars-nic-27404-d5z3f/ (accessed [date]).
This address stays the same, but the page is rebuilt with each monthly edition, so the citation names the edition it shows. Every edition's data is kept in the facts store.
Source: datausesregister_september2026.xlsx, September 2026 edition of the NHS England Data Uses Register. Search that workbook for DARS-NIC-27404-D5Z3F to see the original rows.