Skip to main content
Official Statistics

National flu and COVID-19 surveillance report: 29 October 2026 (week 44)

Updated 29 October 2026

Applies to England

This report summarises the information from the surveillance systems which are used to monitor COVID-19 (caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)), influenza, respiratory syncytial virus (RSV) and diseases caused by other seasonal respiratory viruses in England. This report is based on data up to and including week 43 of 2026 (19 October and 25 October 2026).

Main points

The main messages of this report are:

  • influenza activity was stable across most indicators and is circulating at low levels
  • COVID-19 activity decreased and is circulating at low levels
  • respiratory syncytial virus (RSV) activity increased and is circulating at baseline levels

Summary of all respiratory virus activity

Influenza activity

Influenza activity was stable across most indicators and is circulating at low levels. Emergency department (ED) attendances for influenza-like-illness (ILI) increased and were above seasonally expected levels. The number of influenza-confirmed acute respiratory infection (ARI) incidents increased compared with the previous week.

Weekly influenza vaccine uptake for the 2026 to 2027 season is reported for the fourth time this season. Data is for week 43 (up to 25 October 2026). Influenza vaccination data was unavailable or incomplete at the time of analysis in weeks 41 and 42, and led to several cohorts not being published in week 42. This has been corrected for this week’s report (week 43), and all cohorts are included. This will be corrected retrospectively in the report for week 42. There remains an issue that affects the attribution of vaccinations by provider setting. This is not expected to affect overall vaccination uptake estimates, which are considered to remain an accurate reflection of the influenza vaccination programme.

Compared with the equivalent week last season (week 43 data, 2025 to 2026), vaccine uptake is lower among patients aged 65 years and over (53.6% vs 56.9%), patients aged 6 months to under 65 years in clinical risk groups (24.8% vs 26.2%), those aged 2 years (29.7% vs 30.8%), and those aged 3 years (29.5% vs 30.7%). Vaccine uptake is higher among pregnant women (29.1% vs 27.8%).

Indicator Trend Level [note 1] Comments
Laboratory surveillance Stable Low Influenza positivity remained stable, with a positivity rate of 6.6% compared with 6.4% on the previous Sunday
ILI general practice (GP) consultations Stable Baseline The weekly ILI consultation rate remained stable at 6.5 per 100,000 registered population in participating GP practices.
GP swabbing positivity Increasing Low In week 43, among all tested samples, 11.0% were positive for influenza, compared with 7.8% in the previous week
Hospital admissions Stable Low The overall weekly hospital admission rate for influenza hospitalisations was stable at 2.47 per 100,000 compared with 2.38 per 100,000 in the previous week
Intensive care units (ICU)/High dependency unit (HDU) admissions Increasing Low The overall weekly hospital admission rate for influenza ICU or HDU increased to 0.12 per 100,000 compared with 0.08 per 100,000 in the previous week

COVID-19 activity

COVID-19 activity decreased and is circulating at low levels. ED attendances for COVID-19-like illness decreased. The number of COVID-19 confirmed acute respiratory infections (ARI) incidents decreased compared with the previous week.

By the end of week 43 2026, 42.5% of all people aged 75 years and over in England had been vaccinated with an autumn 2026 dose. Similarly, 18.2% of all people aged under 75 years with a weakened immune system in England had been vaccinated with an autumn 2026 dose since 1 October 2026.

Indicator Trend Level [note 1] Comments
Laboratory surveillance Decreasing Low COVID-19 PCR (polymerase chain reaction) positivity in hospital settings decreased slightly with a positivity rate on the most recent Sunday of 8.3% compared with 8.8% on the previous Sunday
GP swabbing positivity Decreasing slightly Low In week 43, among all tested samples, 8.9% were positive for SARS-CoV-2, compared with 9.8% in the previous week
Hospital admissions Stable Low The overall weekly hospital admission rate for COVID-19 was stable at 2.76 per 100,000 compared with 2.65 per 100,000 in the previous week
ICU/HDU admissions Remained low Baseline The overall weekly ICU or HDU admission rate for COVID-19 remained low at 0.07 per 100,000 compared with 0.06 per 100,000 in the previous week

Respiratory syncytial virus activity

RSV activity increased and is circulating at baseline levels. ED attendances for acute bronchiolitis were stable and below seasonally expected levels.

Indicator Trend Level [note 1] Comments
Laboratory surveillance Increasing Baseline RSV positivity increased to 1.5% compared with 0.9% in the previous week.
GP swabbing positivity Increasing Baseline In week 43, among all tested samples, 0.6% were positive for RSV compared with 0.5% in the previous week
Hospital admissions Increasing Baseline The overall weekly hospital (excl ICU or HDU) admission rate for RSV increased to 0.52 per 100,000 compared with 0.31 per 100,000 in the previous week

Other viruses

Indicator Trend Level [note 1] Comments
Adenovirus Increasing Baseline Adenovirus positivity (laboratory surveillance) increased to 1.5% compared with 1.2% in the previous week
Human metapneumovirus (hMPV) Decreasing Baseline hMPV positivity (laboratory surveillance) decreased to 0.1% compared with 0.5% in the previous week
Parainfluenza Decreasing slightly Baseline Parainfluenza positivity (laboratory surveillance) decreased slightly to 2.9% compared with 3.3% in the previous week
Rhinovirus Decreasing slightly Moderate Rhinovirus positivity (laboratory surveillance) decreased slightly to 16.5% compared with 18.2% in the previous week

Note 1: these indicators use the moving epidemic method (MEM) and the mean standard deviation method (MSD) to define thresholds to determine their respective levels of activity. Further information on these methods can be found in Influenza surveillance in Europe: establishing epidemic thresholds by the Moving Epidemic Method and Setting thresholds to determine COVID-19 activity levels using the mean standard deviation (MSD) method, England, 2022 to 2024. The MEM approach is well-established for some influenza surveillance indicators, however, for other indicators both the MEM and MSD are experimental and may be subject to future revision. Influenza laboratory surveillance and GP swabbing positivity have transitioned from using MEM to using MSD. These approaches will be considered alongside expert opinion and triangulation of other data sources.

Laboratory surveillance

Laboratory-confirmed cases

The Second Generation Surveillance System (SGSS) captures test result information for notifiable infectious diseases, including COVID-19 and influenza, from laboratories in England. The unified sample dataset (USD) stores all SARS-CoV-2 test results reported to SGSS, Respiratory DataMart and UKHSA laboratories, and is used to calculate the percentage of tests positive for SARS-CoV-2 among all SARS-CoV-2 tests conducted.

COVID-19 cases

As of 27 October 2026, there were a total of 1,847 COVID-19 cases identified in hospital settings in week 43, decreasing from 2,151 cases in the previous week.

SARS-CoV-2 (COVID-19) PCR positivity in hospital settings decreased slightly in week 43, with a rolling 7-day positivity rate of 8.3% up to Sunday 25 October 2026 compared with 8.8% for the same period on the previous Sunday.

Positivity rates were highest among those aged 85 years and over with a rolling 7-day positivity rate of 11.1% up to Sunday 25 October 2026. This has decreased compared to 13.0% in the same age group on the previous Sunday.

Figure 1. Weekly confirmed COVID-19 episodes tested in hospital settings, England.

Figure 2. Rolling 7-day positivity of tests positive for SARS-CoV-2 among all reported SARS-CoV-2 tests, England 2022 to present [note 2] [note 3]

Note 2: data from previous seasons is aligned by day.

Note 3: testing policy and practice may change over time which can impact positivity rates, therefore comparisons over time should be interpreted with caution. Notable changes in testing policy occurred during 2022 to 2023, which are outlined in the data quality report.

Figure 3. Rolling 7-day positivity of tests positive for SARS-CoV-2 among all reported SARS-CoV-2 tests by age group, England [note 4]

Note 4: the highlighted line corresponds to the age group in the subplot title, grey lines correspond to all other age groups.

Influenza cases

Influenza positivity remained stable in week 43, with a rolling 7-day positivity rate of 6.6% up to Sunday 25 October 2026. This is compared with 6.4% on the previous Sunday.

By type, influenza A positivity increased slightly in week 43, with a rolling 7-day positivity rate of 5.8% up to Sunday 25 October 2026. Influenza B positivity increased in the same week, with a rolling 7-day positivity rate of 0.3% up to Sunday 25 October 2026.

Influenza A positivity rates were highest among those aged between 5 and 11 years, with a rolling 7-day positivity rate of 16.6% up to Sunday 25 October 2026. This has increased from 11.3% in the same age group on the previous Sunday.

Influenza B positivity rates for the same period were highest among those aged between 5 and 11 years, with a rolling 7-day positivity rate of 1.8%. This has decreased from 2.3% in the same age group on the previous Sunday.

Figure 4. Rolling 7-day positivity of tests positive for influenza among all reported influenza tests, England 2022 to present [note 2]

Note 2: data from previous seasons is aligned by day.

Figure 5. Rolling 7-day positivity of tests positive for each influenza type among all reported influenza type tests, England [note 2]

Note 2: data from previous seasons is aligned by day.

Figure 6. Rolling 7-day positivity of tests positive for each influenza type among all reported influenza type tests by age group, England [note 4]

Note 4: the highlighted line corresponds to the age group in the subplot title, grey lines correspond to all other age groups.

RSV positivity

RSV swab-positivity based PCR test results reported through SGSS have been included as a pilot indicator from week 49 2025 onwards.

RSV positivity increased in week 43, with a rolling 7-day positivity rate of 1.6% up to Sunday 25 October 2026, compared with 1.1% up to the previous Sunday.

RSV positivity rates were highest in those aged between 0 and 4 years with a rolling 7-day positivity rate of 10.1% up to Sunday 25 October 2026 in week 43. This has increased from 7.8% in the same age group on the previous Sunday.

Figure 7. Rolling 7-day positivity of tests positive for RSV among all reported RSV tests in SGSS, England [note 2]

Note 2: data from previous seasons is aligned by day.

Figure 8. Rolling 7-day positivity of tests positive for RSV among all reported RSV tests in SGSS by age group, England [note 4]

Note 4: the highlighted line corresponds to the age group in the subplot title, grey lines correspond to all other age groups.

Respiratory DataMart System

Respiratory DataMart is a sentinel laboratory-based surveillance system where participating laboratories report positive and negative test results for a number of respiratory viruses from samples primarily taken in hospital. A small proportion of primary care samples are also included in this reporting.

In week 43, data is based on reporting from 9 out of the 14 sentinel laboratories.

In week 43, 4,070 respiratory specimens reported through the Respiratory DataMart System were tested for influenza. There were 258 positive samples for influenza: 179 influenza A (not subtyped), 11 influenza A (H3N2), 51 influenza A (H1N1)pdm09, and 19 influenza B. Overall, influenza positivity increased slightly to 6.3% in week 43 compared with 5.9% in the previous week.

In week 43, 4,952 respiratory specimens reported through the Respiratory DataMart System were tested for SARS-CoV-2. There were 376 positive samples for SARS-CoV-2. SARS-CoV-2 positivity remained stable at 7.6% compared with 7.3% in the previous week, with the highest positivity in those aged between 65 and 79 years at 10.0%.

RSV positivity increased to 1.5%, with the highest positivity in those aged under 5 years at 8.3%.

Adenovirus positivity increased to 1.5%, with the highest positivity in those aged under 5 years at 5.1%.

Human metapneumovirus (hMPV) positivity decreased to 0.1%, with the highest positivity in those aged between 15 and 44 years at 0.4%.

Parainfluenza positivity decreased slightly to 2.9%, with the highest positivity in those aged between 5 and 14 years at 11.3%.

Rhinovirus positivity decreased slightly to 16.5%, with the highest positivity in those aged under 5 years at 29.1%.

DataMart data is provisional and subject to retrospective updates.

Figure 9a. Respiratory DataMart weekly percentage of tests positive for influenza, SARS-CoV-2, RSV and rhinovirus, England [note 5]

Note 5: shading represents 95% confidence intervals.

Figure 9b. Respiratory DataMart weekly percentage of tests positive for adenovirus, hMPV and parainfluenza, England [note 5]

Note 5: shading represents 95% confidence intervals.

Figure 10. Respiratory DataMart weekly cases by influenza subtype, England

Figure 11. Respiratory DataMart weekly percentage testing positive for RSV by season, England

Figure 12. Respiratory DataMart weekly percentage testing positive for RSV by age, England [note 4]

Note 4: the highlighted line corresponds to the age group in the subplot title, grey lines correspond to all other age groups.

SARS-CoV-2 lineages

This section is updated fortnightly. Data below was last updated in the week 43 report.

UKHSA conducts genomic surveillance of SARS-CoV-2 lineages.

This section provides an overview of circulating lineages in England, derived from data on sequenced PCR-positive SARS-CoV-2 samples in SGSS.

The prevalence of UKHSA-designated lineages among sequenced cases is presented in Figure 13.

To account for reporting delays, we report the proportion of lineages within COVID-19 cases that have had a sequenced positive sample between 14 September 2026 and 27 September 2026.

Of those sequenced in this period:

  • 25.9% was classified as TA.1
  • 18.9% was classified as ST.1
  • 9.8% was classified as RF.5
  • 8.4% was classified as XFZ.4.1
  • 6.3% was classified as RF.5.4.1
  • 5.6% was classified as TK.1
  • 4.2% was classified as XFG
  • 3.5% was classified as NB.1.8.1
  • 3.5% was classified as RV.2.1
  • 2.8% was classified as RV.1.3
  • 2.8% was classified as SB.1.1

Note that low sequencing numbers, especially within the latest reporting period, will impact the accuracy of the prevalence estimates. These most recent figures should therefore be interpreted with caution.

Note that lineages will be grouped independently from their parent lineage once they reach sufficient prevalence, and may be re-grouped into their parent lineage if their prevalence subsequently falls. The data quality report contains more information on lineage groupings.

Figure 13. Prevalence of SARS-CoV-2 lineages amongst available sequenced cases for England from 13 October 2025 to 11 October 2026

Influenza virus characterisation

Analysis of viruses from primary and secondary care shows that circulating A(H1N1)pdm09 viruses show low genetic diversity and all belong to clade D.3.1.1.

Observations published from the WHO influenza vaccine composition meeting (VCM) in September 2026 suggest low reactivity of some viruses within the D.3.1.1 subclade with post-infection ferret antisera raised against A/Missouri/11/2025 (H1N1)pdm09-like virus – the A(H1N1)pdm09 component in 2026 Southern and 2026/2027 Northern Hemisphere cell- and egg-based influenza vaccines - and human sera post-vaccination with the Southern Hemisphere vaccine 2026.

It is not yet clear how vaccine effectiveness against clinical disease may be affected by these observations. Vaccines typically still provide protection against severe clinical disease when drifted strains are seen with only a modest reduction in effectiveness.

The characterisation of circulating A(H3N2) viruses shows that A(H3N2) viruses are currently showing low genetic diversity. All sequenced viruses to date belong to genetic subclade K.

To date, only a small number of influenza B viruses have been detected, which show some genetic diversity.

Genetic characterisation

Between week 35 2026 (week ending 30 August 2026) and week 43 2026 (week ending 25 October 2026), the UKHSA respiratory virus unit (RVU) has genetically characterised 297 seasonal influenza viruses, and identified 184 influenza A(H1N1)pdm09 viruses, 86 influenza A(H3N2) viruses, and 27 influenza B viruses. Details of the characterised viruses by subtype are shown in Tables 1, 2 and 3. The RVU has confirmed by genome sequencing the detection of live attenuated influenza vaccine (LAIV) viruses in 11 influenza A/B positive samples, collected from children aged between 2 and 16 years.

Table 1. Number of influenza A H1N1(pdm09) viruses characterised by genetic analysis at the UKHSA Respiratory Virus Unit since week 35 2026

Clade Subclade Detections
5a.2a.1 D.3.1.1 184

Table 2. Number of influenza A(H3N2) viruses characterised by genetic analysis at the UKHSA Respiratory Virus Unit since week 35 2026

Clade Subclade Detections
2a.3a.1 K 86

Table 3. Number of influenza B viruses characterised by genetic analysis at the UKHSA Respiratory Virus Unit since week 35 2026

Clade Subclade Detections
V1A.3a.2 C.3.1 1
V1A.3a.2 C.5.6 18
V1A.3a.2 C.5.6.1 8

Antigenic characterisation

UKHSA RVU performs antigenic characterisation of influenza A(H1N1)pdm09, influenza A(H3N2) and influenza B viruses using haemagglutination inhibition (HI) assays. Data from these assays are used to compare how similar the currently circulating influenza viruses are to the strains included in seasonal influenza vaccines, and to monitor for changes in circulating influenza viruses. Similarity of currently circulating influenza strains to vaccine strains is defined as having an antibody titre within 4-fold when compared with reference viruses representative of the vaccine strain. Antigenic characterisation of viruses in the current reporting period is underway.

  • A(H1N1)pdm09: 5 A(H1N1)pdm09 viruses have been antigenically characterised and 3 were similar to reference viruses representative of the A/Missouri/11/2025 (H1N1)pdm09-like Northern Hemisphere 2026/27 (H1N1)pdm09 vaccine strains.

  • A(H3N2): 6 A(H3N2) viruses have been antigenically characterised and 6 were similar to reference viruses representative of the A/Darwin/1454/2025 (H3N2)-like and A/Darwin/1415/2025 (H3N2) like Northern Hemisphere 2026/27 (H3N2) vaccine strains.

Influenza virus antiviral susceptibility surveillance

Influenza positive samples are screened for mutations in the virus neuraminidase (NA) and the cap-dependent endonuclease of the polymerase acidic protein (PA) genes known to confer neuraminidase inhibitor (oseltamivir and zanamivir) or baloxavir resistance, respectively. Results from this surveillance are given in table 4. There have been five detections with mutations related to reduced susceptibility/resistance to oseltamivir and/or reduced susceptibility to baloxavir.

Table 4. Oseltamivir, zanamivir and baloxavir marboxil antiviral susceptibility results of influenza positive samples tested at UKHSA-RVU since week 35 of 2026 using whole genome sequencing

Subtype Interpretation Detections Relevant mutations (in gene) Antiviral use if known
H1N1pdm09 Normal inhibition (oseltamivir and zanamivir) 179 None (NA) Not applicable
H1N1pdm09 Normal susceptibility (baloxavir marboxil) 172 None (PA) Not applicable
H1N1pdm09 Highly reduced inhibition (oseltamivir) <5 H275Y (NA) <5
H3N2 Normal inhibition (oseltamivir and zanamivir) 86 None (NA) Not applicable
H3N2 Normal susceptibility (baloxavir marboxil) 84 None (PA) Not applicable
H3N2 Reduced susceptibility (baloxavir marboxil) <5 E23K (PA) 0
B Victoria Normal inhibition (oseltamivir and zanamivir) 27 None (NA) Not applicable
B Victoria Normal susceptibility (baloxavir marboxil) 25 None (PA) Not applicable

Community surveillance

Acute respiratory infection incidents (ARI)

Data is presented on viral ARI incidents in different settings that are reported to UKHSA health protection teams (HPTs).

Reporting practices are known to vary between seasons and between regions. Any interpretation of temporal and regional trends should consider the likelihood of differences in reporting of ARI incidents over time and between regions.

There were 112 new ARI incidents reported in week 43 in England. These included:

  • 101 incidents from care homes, of which 24 were due to SARS-CoV-2, 17 were due to influenza A, 4 were due to other pathogens, 3 were due to influenza (no type information available) and 3 were due to multiple pathogens. No pathogen was reported in 50 incidents

  • 4 incidents from hospitals, of which 3 were due to influenza A and 1 was due to SARS-CoV-2

  • 4 incidents from educational settings, of which 2 were due to influenza (no type information available) and 1 was due to other pathogens. No pathogen was reported in 1 incident

  • 1 incident from prisons, of which 1 was due to SARS-CoV-2

  • 2 incidents from other settings, of which 1 was due to SARS-CoV-2 and 1 was due to influenza (no type information available)

Figure 14. Number of ARI incidents by setting, England

Figure 15. Number of ARI incidents in all settings by virus type, England

Syndromic surveillance

Syndromic surveillance collects data from various healthcare sources where presentations are classified by patterns of symptoms compatible with specific infections. In some settings, the syndromic diagnosis can be supplemented by (rapid) testing. In this report, ED attendances are displayed. Further details and data from other syndromic surveillance systems can be found in the syndromic surveillance weekly summaries.

During the week ending on 25 October 2026, ED attendances for acute respiratory infections increased and were similar to seasonally expected levels. ED attendances for COVID-19-like illness decreased. ED attendances for influenza-like illness increased and were above seasonally expected levels. ED attendance for acute bronchiolitis (a syndrome related to RSV infection) remained stable and below seasonally expected levels.

Daily NHS 111 acute respiratory infection triaged calls remained stable. GP in-hours consultation rates for COVID-19 like consultations decreased, and other respiratory infection indicators remained stable. GP out-of-hours daily contacts for acute bronchitis/bronchiolitis increased but remained below seasonally expected levels overall.

Figure 16a. Daily emergency department attendances for acute respiratory infection nationally, England [note 6]

Note 6: 7-day moving average is adjusted for bank holidays. Grey columns show weekends and bank holidays.

Figure 16b. Daily emergency department attendances for acute respiratory infection by age group, England [note 7]

Note 7: the coloured line is the 7-day moving average by age group. Grey lines show the other age groups. The y-axis shows daily attendances. It is adjusted for bank holidays.

Figure 17a. Daily emergency department attendances for COVID-19-like illness nationally, England [note 6]

Note 6: 7-day moving average is adjusted for bank holidays. Grey columns show weekends and bank holidays.

Figure 17b. Daily emergency department attendances for COVID-19-like illness by age group, England [note 7]

Note 7: the coloured line is the 7-day moving average by age group. Grey lines show the other age groups. The y-axis shows daily attendances. It is adjusted for bank holidays.

Figure 18a. Daily emergency department attendances for ILI nationally, England [note 6]

Note 6: 7-day moving average is adjusted for bank holidays. Grey columns show weekends and bank holidays.

Figure 18b. Daily emergency department attendances for ILI by age group, England [note 7]

Note 7: the coloured line is the 7-day moving average by age group. Grey lines show the other age groups. The y-axis shows daily attendances. It is adjusted for bank holidays.

Figure 19a. Daily emergency department attendances for acute bronchiolitis nationally, England [note 6]

Note 6: 7-day moving average is adjusted for bank holidays. Grey columns show weekends and bank holidays.

Figure 19b. Daily emergency department attendances for acute bronchiolitis by age group, England [note 7]

Note 7: the coloured line is the 7-day moving average by age group. Grey lines show the other age groups. The y-axis shows daily attendances. It is adjusted for bank holidays.

Primary care surveillance

Primary care surveillance is undertaken in collaboration with the Royal College of General Practitioners (RCGP) Research and Surveillance Centre (RSC), using a national sentinel surveillance system of around 2,000 GP practices covering over 20 million registered patients of all ages across England. More information on the methodology can be found in the data quality report.

RCGP clinical indicators (England)

The weekly ILI consultation rate through the RCGP surveillance remained stable at 6.5 per 100,000 registered population in participating GP practices in week 43. This rate is in the baseline activity level (Figure 20). By age group, the highest rates were seen in those aged under 1 year (8.3 per 100,000), and those aged between 1 and 4 years (7.4 per 100,000).

The lower respiratory tract infections (LRTI) consultation rate remained stable at 81.6 per 100,000 in week 43 compared with 81.9 per 100,000 in the previous week.

Further details are available in the weekly RSC communicable and respiratory disease report for England.

Figure 20. RCGP ILI consultation rates per 100,000, all ages, England

MEM thresholds are based on data from the 2018 to 2019 season to the 2025 to 2026 season. Note the 2019 to 2020, 2020 to 2021 and 2021 to 2022 seasons have been removed.

RCGP sentinel swabbing scheme in England

From week 40 2025, the RCGP sentinel swabbing scheme testing capability has been expanded to the UKHSA Bristol laboratory in addition to the UKHSA Colindale laboratory. Samples sent to Colindale are tested for influenza A and B, RSV A and B, SARS-CoV-2, hMPV, adenovirus, seasonal coronavirus and enterovirus/rhinovirus while samples sent to Bristol are tested for influenza A and B, RSV and SARS-CoV-2.

653 samples were taken in week 43 2026 through the GP sentinel swabbing, 482 were tested and 128 tested positive (Figure 21). Starting from week 40 2025, samples with more than 7 days between the sample collection date and the symptom onset date have been excluded.

In week 43 2026, influenza positivity was 11.0%, SARS-CoV-2 positivity was 8.9%, and RSV positivity was 0.6%. Of the 482 samples tested, 29.3% were from the South West. Due to proximity to one of the testing laboratories, samples from the South West tend to be tested more rapidly than those from other parts of the country; therefore, the latest week’s data may not be fully representative of the country as a whole and should be interpreted with caution.

In week 42 2026, influenza positivity was 7.8%, SARS-CoV-2 positivity was 9.8%, RSV positivity was 0.5%, adenovirus positivity was 1.7%, hMPV positivity was 0.0%, seasonal coronavirus positivity was 2.6%, and enterovirus/rhinovirus positivity was 23.1%. In week 42 2026, 858 samples were tested for influenza, SARS-CoV-2 and RSV only, and a further 235 samples were tested for an extended panel of respiratory viruses. As testing and reporting schedules differ between pathogens, denominators vary and estimates for the most recent week may be subject to revision.

Due to the number of samples which have not yet been categorised, data should be interpreted with caution when compared with previous weeks. The weekly positivity is not calculated when the number of samples with a result is fewer than 50.

Figure 21. Number of samples tested for respiratory viruses in England by week, GP sentinel swabbing scheme [note 8] [note 9]

Note 8: unknown category corresponds to samples with no result yet.

Note 9: Due to proximity to one of the testing laboratories, samples from the South West tend to be tested more rapidly than those from other parts of the country; therefore, the latest week’s data may not be fully representative of the country as a whole and should be interpreted with caution.

Figure 22. Percentage of detected respiratory viruses among samples with completed testing for each virus in England by week, GP sentinel swabbing scheme [note 9]

Note 9: Due to proximity to one of the testing laboratories, samples from the South West tend to be tested more rapidly than those from other parts of the country; therefore, the latest week’s data may not be fully representative of the country as a whole and should be interpreted with caution.

Figure 23. Percentage of detected respiratory viruses among samples with completed testing for each virus in England by age group, GP sentinel swabbing scheme, week 40 to week 43 [note 9]

Note 9: Due to proximity to one of the testing laboratories, samples from the South West tend to be tested more rapidly than those from other parts of the country; therefore, the latest week’s data may not be fully representative of the country as a whole and should be interpreted with caution.

Figure 24. Weekly positivity for SARS-CoV-2, influenza and RSV in England, GP sentinel swabbing scheme [note 5] [note 9]

Note 5: shading represents 95% confidence intervals.

Note 9: Due to proximity to one of the testing laboratories, samples from the South West tend to be tested more rapidly than those from other parts of the country; therefore, the latest week’s data may not be fully representative of the country as a whole and should be interpreted with caution.

Secondary care surveillance

COVID-19 hospital and ICU or HDU admissions

Surveillance of COVID-19 hospitalisations to all levels of care and admissions to intensive care units (ICU) or high dependency units (HDU) are both mandatory, with data required from all acute NHS trusts in England.

SARI Watch data is provisional and subject to retrospective updates. ICU or HDU admission rates may also be affected by lags from admission to hospital to an ICU or HDU ward. Rates are presented per 100,000 trust catchment population.

COVID-19 hospitalisations for all levels of care in week 43 2026 based on 90 NHS trusts in England were as follows:

  • the overall weekly hospital admission rate for COVID-19 remained stable at 2.76 (compared with 2.65 per 100,000 in the previous week)

  • hospital admission rates for COVID-19 were highest in the North East region (increasing to 4.26 per 100,000 compared with 3.31 in the previous week). See the supplementary graphs and data file for regional breakdowns

  • the highest hospital admission rate for COVID-19 was in those aged 85 years and over (slightly decreasing to 25.02 per 100,000 compared with 27.20 in the previous week)

COVID-19 ICU-HDU admissions in week 43 2026 based on 75 NHS trusts in England were as follows:

  • the overall ICU or HDU rate for COVID-19 remained low at 0.07 per 100,000 (compared with 0.06 per 100,000 in the previous week). Note that with low rates in critical care, small random fluctuations may occur

  • ICU or HDU admission rates for COVID-19 were highest in the South West region (increasing to 0.10 per 100,000 compared with 0.03 in the previous week). See the supplementary graphs and data file for regional breakdowns

  • the highest ICU or HDU admission rate for COVID-19 was in those aged between 55 and 64 years (increasing to 0.19 per 100,000 compared with 0.13 in the previous week)

Figure 25. Weekly overall COVID-19 hospital admission rates per 100,000 trust catchment population reported through SARI Watch mandatory surveillance, England

Figure 26. Weekly hospital admission rate by age group for new COVID-19 positive cases reported through SARI Watch mandatory surveillance, England [note 10]

Note 10: the highlighted line corresponds to the most recent 2026 to 2027 season, grey lines correspond to the previous 2025 to 2026 season.

Figure 27. Weekly overall COVID-19 ICU or HDU admission rates per 100,000 trust catchment population reported through SARI Watch mandatory surveillance, England

Figure 28. Weekly ICU or HDU admission rate by age group for new COVID-19 positive cases reported through SARI Watch mandatory surveillance, England [note 10]

Note 10: the highlighted line corresponds to the most recent 2026 to 2027 season, grey lines correspond to the previous 2025 to 2026 season.

Influenza hospital and ICU or HDU admissions

From the 2026 to 2027 season, surveillance of influenza hospitalisations to all levels of care was expanded to all acute NHS trusts in England as a pilot initiative. Previously this was a sentinel collection involving a small network of contributing NHS trusts. Surveillance of admissions to ICU or HDU for influenza is mandatory with data required from all acute NHS trusts in England.

SARI Watch data is provisional and subject to retrospective updates. Rates are presented per 100,000 trust catchment population.

Influenza hospitalisations to all levels of care in week 43 2026 based on 52 NHS trusts in England were as follows:

  • the overall weekly hospital admission rate for influenza hospitalisations was stable at 2.47 per 100,000 compared with 2.38 per 100,000 in the previous week

  • this rate is in the low impact range (2.15 to less than 7.13 per 100,000)

  • hospital admission rates for influenza were highest in those aged 85 years and over (12.78 per 100,000)

  • see the respiratory virus section of the data dashboard for regional breakdowns

  • there were 588 new hospital admissions for influenza (532 influenza A (subtype unknown), 23 influenza A(H1N1)pdm09, 16 influenza A(H3N2), and 17 influenza B)

Influenza ICU or HDU admissions in week 43 2026 based on 90 NHS trusts in England were as follows:

  • the overall weekly hospital admission rate for influenza ICU or HDU increased to 0.12 per 100,000 compared with 0.08 per 100,000 in the previous week

  • this rate is in the low impact range (0.09 to 0.27 per 100,000)

  • see the respiratory virus section of the data dashboard for regional breakdowns

  • there were 49 new ICU or HDU admissions for influenza (39 influenza A (subtype unknown), 6 influenza A(H1N1)pdm09, 1 influenza A(H3N2), and 3 influenza B)

Figure 29. Weekly overall influenza hospital admission rates per 100,000 trust catchment population with MEM thresholds, reported through SARI Watch surveillance, England

Figure 30. Weekly influenza hospital admissions by influenza type, reported through SARI Watch surveillance, England

Figure 31. Weekly hospital admission rate by age group for new influenza reported through SARI Watch surveillance, England [note 10]

Note 10: the highlighted line corresponds to the most recent 2026 to 2027 season, grey lines correspond to the previous 2025 to 2026 season.

Figure 32. Weekly overall influenza ICU or HDU admission rates per 100,000 trust catchment population with MEM thresholds, reported through SARI Watch mandatory surveillance, England

Figure 33. Weekly influenza ICU or HDU admissions by influenza type, reported through SARI Watch mandatory surveillance, England

Figure 34. Weekly ICU or HDU admission rate by age group for new influenza cases, reported through SARI Watch mandatory surveillance, England [note 10]

Note 10: the highlighted line corresponds to the most recent 2026 to 2027 season, grey lines correspond to the previous 2025 to 2026 season.

RSV hospital admissions

Surveillance of respiratory syncytial virus (RSV) hospitalisations (excluding ICU or HDU admissions) is based on data from a small sentinel network of acute NHS trusts in England submitting data voluntarily. Trusts submit weekly aggregate counts of new RSV admissions and these are summed and converted to rates per 100,000 trust catchment population by linking to catchment populations of participating trusts in that week.

SARI Watch data is provisional and subject to retrospective updates. Please refer to the data quality report for details on the new trust catchment population for calculating rates. The new denominator has also been applied retrospectively to the 2024 to 2025 and 2025 to 2026 seasons for consistency. The data quality report includes further details on SARI Watch RSV data and other collections.

RSV hospitalisations, excluding ICU or HDU admissions, in week 43 2026 were based on 17 sentinel NHS trusts in England:

  • the overall weekly hospital admission rate for RSV increased to 0.52 per 100,000 (compared with 0.31 per 100,000 in the previous week)

  • in children aged under 5 years, the hospitalisation rate for RSV increased to 6.56 per 100,000 (compared with 4.25 per 100,000 in the previous week)

  • in adults aged 75 years and over, the hospitalisation rate for RSV increased to 0.74 per 100,000 (compared with 0.31 per 100,000 in the previous week). Broken down further, rates were 0.40 per 100,000 in those aged between 75 and 84 years, and 1.66 per 100,000 in those aged 85 years and over in week 43

RSV ICU or HDU admissions in week 43 2026 were based on 17 sentinel NHS trusts in England:

  • the overall weekly ICU or HDU admission rate for RSV remained low at 0.01 per 100,000 (compared with 0.00 per 100,000 in the previous week)

Figure 35. Weekly overall hospital admission rates (excluding ICU or HDU) of RSV positive cases per 100,000 population reported through SARI Watch sentinel surveillance, England [note 11]

Note 11: surveillance commenced from week 40 in the 2023 to 2024 season. In subsequent seasons this was from week 36. As the surveillance will conclude in week 12 in the 2026 to 2027 season, the time series is truncated to week 12 for consistency across all seasons.

Figure 36. Weekly hospital admission rates (excluding ICU or HDU) of RSV positive cases per 100,000 population in those aged under 5 years and aged over 75 years reported through SARI Watch sentinel surveillance, England [note 11]

Note 11: surveillance commenced from week 40 in the 2023 to 2024 season. In subsequent seasons this was from week 36. As the surveillance will conclude in week 12 in the 2026 to 2027 season, the time series has been truncated to week 12 for consistency across all seasons.

Figure 37. Weekly hospital admission rates (excluding ICU or HDU) by age group for RSV cases reported through SARI Watch sentinel surveillance, England [note 10]

Note 10: the highlighted line corresponds to the most recent 2026 to 2027 season, grey lines correspond to the previous 2025 to 2026 season.

ECMO admissions

Surveillance of extracorporeal membrane oxygenation (ECMO) admissions is based on data from severe respiratory failure (SRF) centres in the UK. Refer to the data quality report for additional information.

SARI Watch data is provisional and subject to retrospective updates (the figure below may vary from those presented in previous reports). Please note that time series data from week 26 2026 is from SRF units in England only until further notice.

There were 2 new ECMO admissions reported in week 43 2026 in adults:

  • one was due to influenza (1 influenza A(H1N1)pdm09)

  • one was due to a suspected ARI

Figure 38. Laboratory-confirmed ECMO admissions in adults (COVID-19, influenza and non-COVID-19 confirmed) to severe respiratory failure centres in the UK [note 12]

Note 12: The other group includes other viral, bacterial or fungal ARI, suspected ARI, non-infection (such as asthma, primary cardiac and trauma) and sepsis of non-respiratory origin.

Vaccine coverage

COVID-19 vaccine uptake in England

Cumulative data up to the end of week 43 2026 (Sunday 25 October 2026) was extracted from the Immunisation Information System (IIS). Data is extracted on the next working day following the end of reporting week (Monday 26 October 2026). Age is calculated as age on date of extraction.

Data is provisional and subject to change following further validation checks. Any changes to historic figures will be reflected in the most recent publication.

Autumn 2026 campaign

The autumn 2026 data reported below covers any dose administered from 1 October 2026 (ISO Week 40) provided there is at least 20 days from the previous dose. Eligible groups for the campaign are defined in the Green Book chapter on COVID-19. By the end of week 43 2026 (week ending 25 October 2026) 42.5% (2,529,022 / 5,951,685) of all people aged 75 years and over, and 18.2% (274,866 / 1,514,192) of all people aged under 75 years with a weakened immune system, who are living and resident in England had been vaccinated with an autumn 2026 dose since 1 October 2026 (Figure 39).

Figure 39. Cumulative weekly COVID-19 vaccine uptake by target group in England [note 13]

Note 13: the month is taken from the Monday of an international organisation for standardisation (ISO) week.

For data on the real-world effectiveness of the COVID-19 vaccines, please see the epidemiology of COVID-19 in England reports.

For COVID-19 management information on the number of COVID-19 vaccinations provided by the NHS in England, please see the COVID-19 vaccinations webpage.

For UK COVID-19 daily vaccination figures and definitions, please see the Vaccinations section of the UK COVID-19 dashboard.

Influenza vaccination

Influenza vaccine uptake in GP patients

Weekly vaccine uptake data is provisional.

Influenza vaccination is reported by GP practice through the ImmForm website. ImmForm provides a secure online platform for vaccine uptake data collection for several immunisation surveys, including the seasonal influenza vaccine uptake collection. Details can be found at sources of surveillance data for influenza, COVID-19 and other respiratory viruses.

For the 2026 to 2027 season’s vaccination programme, as in the previous 2 seasons, children and pregnant women have been eligible since 1 September. For this current season and the previous 2 seasons (2026 to 2027, 2025 to 2026 and 2024 to 2025 seasons respectively), adult groups (excluding pregnant women) were eligible from 1 October, rather than 1 September as in previous seasons. See the Timing section of the annual flu letter for more information.

Up to the end of week 43 of 2026 (Sunday 25 October 2026), the provisional proportion of people in England who had received an influenza vaccine this season in targeted groups was as follows:

Adults (98.6% of GP practices reporting through ImmForm):

  • 24.8% in those aged under 65 years in a clinical risk group

  • 29.1% in all pregnant women

  • 53.6% in all those aged over 65 years

Children (98.7% of GP practices reporting):

  • 29.7% in children aged 2 years

  • 29.5% in children aged 3 years

Figure 40. Cumulative weekly influenza vaccine uptake by target group in England [note 14] [note 15]

Note 14: on 26 November 2026, monthly vaccine uptake data will be published for the first time this season, which covers influenza vaccinations given between 1 September and 31 October 2026 for GP patients, school-aged children and frontline healthcare workers.

Note 15: influenza vaccination data was unavailable or incomplete at the time of analysis in weeks 41 and 42, and led to several cohorts not being published in week 42. A subsequent investigation has found that a dataflow issue affected analysis in week 42, which resulted in artificially low vaccine uptake in both the unpublished cohorts and, to a lesser extent, the published pregnancy data. This issue was corrected for all reports from week 43 onwards, and all cohorts are now included. The report for week 42 will be corrected shortly. The investigation also found that vaccinations administered in pharmacies are currently being recorded using non-specific vaccination setting codes, meaning pharmacy vaccinations cannot be reliably distinguished from those administered in general practices, unlike in previous seasons. As a result, some pharmacy vaccinations are likely to be misclassified as general practice, artificially increasing the vaccination activity reported for general practices and reducing the activity reported for pharmacies. This issue affects the attribution of vaccinations by provider setting but is not expected to affect overall vaccination uptake estimates, which are considered to remain an accurate reflection of the influenza vaccination programme.

International updates

For further information on the global respiratory virus situation see the World Health Organization (WHO) Global respiratory virus weekly updates.

For further information on respiratory viruses in Europe see the European Respiratory Virus Surveillance Summary (ERVISS).

For further information on respiratory viruses in the Americas see Pan American Health Organization Influenza, SARS-CoV-2, RSV and other respiratory viruses.

For further information on respiratory viruses in the United States of America see Centers for Disease Control and Prevention respiratory virus activity levels.

For further information on respiratory viruses in Canada see the Canadian respiratory virus surveillance report.

For further information on respiratory viruses in Australia see Australian Respiratory Surveillance Reports.

Data sources and methodology

For additional information regarding data sources, see the data quality report.

Background information

National flu and COVID-19 surveillance reports: 2025 to 2026 season

Weekly national flu reports (historic)

Influenza in the UK, annual epidemiological reports

Epidemiology of COVID-19 in England

Weekly all-cause mortality surveillance report

UKHSA data dashboard

RCGP virology dashboard

Further information and contact details

Feedback and contact information

To provide feedback and for all queries relating to this document, contact respdsr.enquiries@ukhsa.gov.uk

Official statistics

Our statistical practice is regulated by the Office for Statistics Regulation (OSR). OSR sets the standards of trustworthiness, quality and value in the Code of Practice for Statistics that all producers of official statistics should adhere to.

You are welcome to contact us directly by emailing respdsr.enquiries@ukhsa.gov.uk with any comments about how we meet these standards.

Alternatively, you can contact OSR by emailing regulation@statistics.gov.uk or via the OSR website.

UKHSA is committed to ensuring that these statistics comply with the Code of Practice for Statistics. This means users can have confidence in the people who produce UKHSA statistics because our statistics are robust, reliable and accurate. Our statistics are regularly reviewed to ensure they support the needs of society for information.