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Cost of Illness Associated With Influenza in the UK

The Cost of Illness Associated With Influenza in the UK

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01521416
Enrollment
1
Registered
2012-01-30
Start date
2011-06-30
Completion date
2013-04-30
Last updated
2013-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Influenza

Keywords

Illness, Influenza, Cost, UK

Brief summary

The objective of this study is to describe the burden associated with influenza in the UK, from both primary and secondary care perspectives, and to stratify the burden by the annual degree of mismatch between predicted and actual virus strains.

Detailed description

This is a retrospective, cross sectional, exploratory, observational study using database analysis and therefore there is no patient or user group involvement.

Interventions

OTHERData collection

Data of patients diagnosed with acute respiratory illness is extracted from General Practice Research Database (GPRD), Hospital Episode Statistics (HES), the Health Protection Agency (HPA), Office of National Statistics (ONS), and National Health Service (NHS) Reference Costs, during the period January 21st 2001 and March 31st 2009 inclusive. All analyses of primary care data (GPRD) and separately for secondary care (HES) data will be repeated for all eligible patients, and the subset of patients with a linkage to additional data (HES, ONS). All analysis including secondary care data will be restricted to the subset of patients with linked HES data. Estimates of average burden per patient and total burden in the UK will be performed. Burden is defined as both resource use and cost. Annual incidence and burden will be calculated.

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female patients coded within the database as having acute respiratory events that could be related to an infection between 2001 and 2009. * Patients must have a minimum of 14 days observation before and after the index event to permit the capturing of complications attributable to influenza.

Exclusion criteria

Not Applicable

Design outcomes

Primary

MeasureTime frame
Incidence of influenza-related events in High Risk groupsOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Incidence of complications and exacerbationsOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Incidence of influenza-related eventsOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Number of confirmed influenza infectionsOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Assessment of resource useOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Evaluation of patient outcomes, treatments and costs (type and duration)Over the study time period (from January 21st 2001 to March 31st 2009 inclusive)
Cause of deathsOver the study time period (from January 21st 2001 to March 31st 2009 inclusive)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026