The Public Health Agency (PHA) has integrated influenza, respiratory syncytial virus (RSV) and COVID-19 reporting into this report to provide a single overview of the epidemiology of these infections in Northern Ireland (NI), along with the number of respiratory care home outbreaks, hospital admissions and occupancy, and deaths. It offers references to additional sources of information for further details.
Virology surveillance
Episodes of influenza, RSV and COVID-19
The number of new influenza episodes increased in week 50, with 708 unique episodes identified. There were 476 episodes reported in week 49. The number of new RSV episodes decreased in week 50, with 193 unique episodes identified; 218 episodes were reported in week 49 (Figure 2.1).
Influenza and RSV episode rates by age groups are shown in (Figure 2.2). The highest influenza episode rate in week 50 was in the 0-4 age group (143.3 per 100,000 population). Similarly, the highest RSV episode rate was in the 0-4 age group (131.8 per 100,000 population).
Influenza and RSV episode rates across local government districts (LGD) are shown in (Figure 2.3). Ards and North Down had the highest influenza episode rate in week 50 (56.2 per 100,000 population). Belfast had the highest RSV episode rate (18.0 per 100,000 population).
The number of new COVID-19 episodes remained stable in week 50, with 63 episodes identified compared to 59 in week 49 (Figure 2.1).
COVID-19 episode rates by age groups are shown in (Figure 2.2). The highest COVID-19 episode rate in week 50 was in the 75+ age group (21.8 per 100,000 population).
COVID-19 episode rates across LGD are shown in (Figure 2.3). Ards and North Down had the highest COVID-19 episode rate in week 50 (8.5 per 100,000 population).
Supplementary tables of key figures are shown at the end of this bulletin.
Testing and positivity (%)
In week 50 there were 2,451 total influenza tests, 722 of which were positive (29.5% positivity). This is an increase from week 49 (22.5% positivity) (Figure 2.4).
There were 1,432 total RSV tests, 198 of which were positive (13.8% positivity). This is a decrease from week 49 (16.8% positivity) (Figure 2.4).
There were 2,401 COVID-19 tests, 70 of which were positive (2.9% positivity). This is a decrease from week 49 (3.2% positivity) (Figure 2.4).
Supplementary tables of key figures are shown at the end of this bulletin.
Influenza subtyping
Of the 708 new influenza episodes identified in week 50, 244 were typed as Flu A(H1), nine were Flu A(H3), 443 were Flu A (not subtyped) and 12 were Flu B (Figure 2.5).
Sentinel surveillance
Sentinel surveillance plays a role in monitoring and understanding the spread and impact of respiratory viruses like influenza and COVID-19 in the community. It involves a systematic and targeted approach to collect data from a geographical representative subset of GP practices (~18% population representative) to provide information about virus activity across NI.
In week 50, 39 samples were positive for influenza from 64 samples submitted for testing (60.9% positivity) to the Regional Virus Laboratory (RVL). 29 were typed as Flu A(H1), eight were Flu A (not subtyped) and two were Flu B. Three samples were positive for RSV from 64 samples submitted for testing (4.7% positivity). Two samples were positive for COVID-19 from 64 samples submitted for testing (3.3% positivity) (Table 1).
Total sentinel cases of influenza, RSV and COVID-19 by age group for the previous year are shown in (Figure 2.6), (Figure 2.7) and (Figure 2.8), and cumulatively for the 2024/25 influenza season in Table 2.
Supplementary tables of key figures are shown at the end of this bulletin.
Table 1. Total sentinel tests and positivity for Influenza, RSV and COVID-19, current week
|
|
|
Total Tests
|
Total Positives
|
Positivity (%)
|
2024 - 50
|
Influenza
|
64
|
39
|
60.94
|
2024 - 50
|
RSV
|
64
|
3
|
4.69
|
2024 - 50
|
COVID-19
|
64
|
2
|
3.12
|
Table 2. Total sentinel cases of Influenza, RSV and COVID-19 by age group, Week 40 - current week, 2024/25
|
|
0-4
|
5-14
|
15-44
|
45-64
|
65-74
|
75+
|
Total
|
Flu A (H1)
|
4
|
9
|
35
|
18
|
4
|
0
|
70
|
Flu A (H3)
|
1
|
0
|
2
|
0
|
2
|
0
|
5
|
Flu A (not subtyped)
|
3
|
1
|
9
|
4
|
0
|
0
|
17
|
Flu B
|
0
|
0
|
6
|
1
|
0
|
0
|
7
|
RSV
|
15
|
2
|
4
|
4
|
1
|
1
|
27
|
COVID-19
|
0
|
0
|
3
|
1
|
2
|
7
|
13
|
Non-sentinel surveillance
Non-sentinel surveillance is the monitoring of respiratory viruses from virology data collected from settings such as hospitals and GPs (excluding the sentinel GPs). This provides information about virus activity across NI.
In week 50, 685 samples were positive for influenza from 2,391 samples submitted for testing to laboratories across NI (28.7% positivity). 233 were typed as Flu A(H1), 11 were Flu A(H3), 433 were Flu A (not subtyped) and eight were Flu B. 195 samples were positive for RSV from 1,369 samples submitted for testing (14.2% positivity). 68 samples were positive for COVID-19 from 2,345 samples submitted for testing (2.9% positivity). (Table 3).
Total non-sentinel cases of influenza, RSV and COVID-19 by age group for the previous year are shown in (Figure 2.6), (Figure 2.7) and (Figure 2.11), and cumulatively for the 2024/25 influenza season in Table 4.
Supplementary tables of key figures are shown at the end of this bulletin.
Table 3. Total non-sentinel tests and positivity for Influenza, RSV and COVID-19, current week
|
|
|
Total Tests
|
Total Positives
|
Positivity (%)
|
2024 - 50
|
Influenza
|
2,391
|
685
|
28.65
|
2024 - 50
|
RSV
|
1,369
|
195
|
14.24
|
2024 - 50
|
COVID-19
|
2,359
|
68
|
2.88
|
Table 4. Total non-sentinel cases of Influenza, RSV and COVID-19 by age group, Week 40 - current week, 2024/25
|
|
0-4
|
5-14
|
15-44
|
45-64
|
65-74
|
75+
|
Total
|
Flu A (H1)
|
145
|
66
|
96
|
111
|
75
|
155
|
648
|
Flu A (H3)
|
13
|
8
|
10
|
7
|
3
|
3
|
44
|
Flu A (not subtyped)
|
284
|
162
|
182
|
171
|
98
|
206
|
1,103
|
Flu B
|
16
|
6
|
8
|
3
|
0
|
1
|
34
|
RSV
|
913
|
28
|
28
|
38
|
47
|
74
|
1,128
|
COVID-19
|
55
|
13
|
84
|
164
|
175
|
490
|
981
|
SARS-CoV-2 variants
XEC is a recombinant lineage of KS.1.1 and KP.3.3 (both of which are JN.1 sub-lineages). The KP.3 and other KP lineages are descended from JN.1 sub-lineages, and they are now reported separately from JN.1 to illustrate the evolving genomic epidemiology. For the week commencing 25th November 2024, XEC accounted for 60% of all sequenced samples, JN.1 20% with KP and KP.3 10%, respectively. Due to small numbers of samples sequenced, the level of confidence in precision of the estimate is low, and the percentages of each variant may change as further results become available. A more detailed COVID-19 Genomics Bulletin containing a further breakdown of sub-lineages is reported here. Technical information is published by UKSHA on some specific KP variants online here with a commentary on them here.
Parent lineages displayed are subject to change based on lineages under monitoring by the UKHSA horizon scanning team.
Recombinant refers to any recombinant lineage, starting “X”, that does not fall under the parent lineage of a defined variant.
Primary care surveillance
Consultation rates for influenza/influenza-like-illness (‘flu/FLI’)
The general practice (GP) flu/FLI consultation rate during week 50 was 21.2 per 100,000 population. This is an increase from week 49 (13.3 per 100,000 population). Rates increased to moderate activity levels (20.5 to <47.4 per 100,000 population) (Figure 3.1).
Flu/FLI consultation rates by age groups are shown in Table 5. The highest rate in week 50 was seen in the 0-4 year old age group (31.0 per 100,000 population).
Flu/FLI consultation rates by Health and Social Care Trust (HSCT) are shown in Table 6. The highest rate in week 50 was seen in the South Eastern Trust (27.6 per 100,000 population).
Since the beginning of the COVID-19 pandemic, the offer of uptake of GP consultations has changed. As a result, consultation rates in the most recent period are unlikely to be directly comparable to pre-pandemic and pandemic years.
The baseline MEM threshold for Northern Ireland is 10.1 per 100,000 population for 2024-25. Low activity is 10.1 to <20.5, moderate activity 20.5 to <47.4, high activity 47.4 to <68.5 and very high activity is >68.5 per 100,000 population.
Table 5. Flu/FLI consultation rates per 100,000 population, by age groups, over a six week period
|
|
0-4
|
5-14
|
15-44
|
45-64
|
65-74
|
75+
|
Total
|
2024 - 45
|
2.81
|
1.13
|
4.95
|
4.92
|
3.57
|
5.28
|
4.26
|
2024 - 46
|
5.63
|
3.40
|
5.07
|
4.37
|
3.06
|
3.52
|
4.40
|
2024 - 47
|
10.32
|
5.29
|
5.92
|
4.74
|
5.60
|
6.45
|
5.77
|
2024 - 48
|
16.90
|
6.80
|
6.76
|
9.47
|
5.60
|
5.86
|
7.80
|
2024 - 49
|
16.91
|
15.86
|
13.16
|
14.57
|
10.18
|
7.62
|
13.33
|
2024 - 50
|
31.02
|
17.75
|
21.73
|
24.05
|
11.71
|
19.33
|
21.18
|
Table 6. Flu/FLI consultation rates per 100,000 population, by Health and Social Care Trust, over a six week period
|
|
Belfast
|
Northern
|
Western
|
Southern
|
South Eastern
|
Northern Ireland
|
2024 - 45
|
3.08
|
4.20
|
6.36
|
3.51
|
4.69
|
4.26
|
2024 - 46
|
4.62
|
3.82
|
3.76
|
3.51
|
6.62
|
4.40
|
2024 - 47
|
7.69
|
2.48
|
6.65
|
5.14
|
8.00
|
5.77
|
2024 - 48
|
5.49
|
6.10
|
7.52
|
10.98
|
9.66
|
7.80
|
2024 - 49
|
15.60
|
9.54
|
14.17
|
14.25
|
14.07
|
13.33
|
2024 - 50
|
18.90
|
16.79
|
19.95
|
24.53
|
27.59
|
21.18
|
Consultation rates for acute respiratory infection (ARI)
The GP ARI consultation rate during week 50 was 206.0 per 100,000 population. This is an increase from week 49 (190.5 per 100,000 population) (Figure 3.2).
ARI consultation rates by age groups are shown in Table 7. The highest rate in week 50 was seen in the 0-4 age group (1,065.1 per 100,000 population).
ARI consultation rates by HSCT are shown in Table 8. The highest rate in week 50 was seen in the Western Trust (231.0 per 100,000 population).
Table 7. ARI consultation rates per 100,000 population, by age groups, over a six week period
|
|
0-4
|
5-14
|
15-44
|
45-64
|
65-74
|
75+
|
Total
|
2024 - 45
|
692.67
|
100.38
|
83.92
|
96.79
|
126.35
|
143.23
|
128.74
|
2024 - 46
|
817.97
|
146.09
|
78.61
|
93.13
|
129.37
|
152.53
|
138.76
|
2024 - 47
|
994.26
|
191.78
|
92.73
|
103.69
|
131.93
|
142.53
|
161.07
|
2024 - 48
|
1,107.62
|
219.72
|
105.74
|
124.79
|
156.33
|
182.87
|
186.31
|
2024 - 49
|
1,055.90
|
204.30
|
118.44
|
130.99
|
154.28
|
211.53
|
190.45
|
2024 - 50
|
1,065.09
|
230.80
|
126.15
|
151.38
|
199.05
|
203.81
|
206.04
|
Table 8. ARI consultation rates per 100,000 population, by Health and Social Care Trust, over a six week period
|
|
Belfast
|
Northern
|
Western
|
Southern
|
South Eastern
|
Northern Ireland
|
2024 - 45
|
133.84
|
118.34
|
152.39
|
110.31
|
136.58
|
128.74
|
2024 - 46
|
151.86
|
122.53
|
169.48
|
115.91
|
143.48
|
138.76
|
2024 - 47
|
163.05
|
163.36
|
186.24
|
135.74
|
161.16
|
161.07
|
2024 - 48
|
187.15
|
200.31
|
210.48
|
151.84
|
182.66
|
186.31
|
2024 - 49
|
189.85
|
195.74
|
204.46
|
163.99
|
201.44
|
190.45
|
2024 - 50
|
196.00
|
208.70
|
231.04
|
184.33
|
216.57
|
206.04
|
Mortality surveillance
Medical certificate of cause of death for respiratory-associated deaths
The NI Statistics and Research Agency (NISRA) provides the weekly number of respiratory-associated deaths and the proportion of all-cause registered deaths (by week of death registration, not by week of death).
Respiratory-associated deaths include those that are attributable to influenza, other respiratory infections or their complications. This includes “bronchiolitis, bronchitis, influenza or pneumonia” keywords recorded on the death certificate.
In week 50, 100 respiratory associated deaths out of 387 all-cause deaths were reported (25.8%). This is higher to the same period in 2023/24 (84 respiratory associated deaths out of 374 all-cause deaths, 22.5%) (Figure 6.1).
Excess Mortality
NISRA use the UK-wide methodology to report on excess deaths as advised by the Office for National Statistics (ONS) which can be found online here.
EuroMOMO is a European mortality monitoring activity, aiming to detect and measure excess deaths related to seasonal influenza, pandemics and other public health threats. Reports on excess deaths can be found online here.
Methods
Presentation of data
Unless otherwise stated, data are presented using epidemiological weeks (a standardised method of counting weeks [Monday-Sunday] to allow for the comparison of data year after year). This is dependent on the data available. The data included in this report are the most up to date data available at the time of the report; however, this is subject to change as the data are subject to ongoing quality assurance.
Virology surveillance
All virology data provided here are preliminary. Virology data for prior weeks, as included in this or future bulletins, are subject to updates based on laboratory returns received after the last report was produced. The current bulletin offers the most current information available.
Rates per 100,000 population are calculated using the NISRA 2021 Mid-Year Population Estimates.
Episodes of infection
Influenza
Influenza episodes are defined by a rolling 42-day (6-week) period from the date of the first positive test result (utilising any test method, including PCR and Point of Care Tests, or source of sample, including hospital, GP, other source), with the episode beginning with the earliest positive specimen date. Subsequent positive specimen dates for the same individual within 42 days of the last are included in the one episode. Positive specimens for the same individual more than 42 days after the last are counted in a separate episode.
RSV
RSV episodes are defined by a rolling 14-day (2-week) period from the date of the first positive test result (utilising any test method, including PCR and Point of Care Tests, or source of sample, including hospital, GP, other source), with the episode beginning with the earliest positive specimen date. Subsequent positive specimen dates for the same individual within 14 days of the last are included in the one episode. Positive specimens for the same individual more than 14 days after the last are counted in a separate episode.
COVID-19
COVID-19 episodes are defined by a rolling 90-day period between positive test results (any test method, sourced from the NI COVID-19 combined testing register), with the episode beginning with the earliest positive specimen date. Subsequent positive specimen dates for the same individual within 90 days of the last are included in the one episode. Positive specimens for the same individual more than 90 days after the last are counted in a separate episode.
Testing and positivity (%)
Influenza, RSV and COVID-19
Instead of utilising an episode-based approach, the data is analysed on an epidemiological week basis. Within each epidemiological week, an individual is limited to one influenza test, whether positive or negative. If an individual tests positive for influenza during a specific epidemiological week and subsequently tests positive again within the same week, the second positive test is not counted. Regardless of whether it occurs before or after a negative test within the same epidemiological week, a positive test always takes precedence and is recorded. Similarly, only the first test of multiple negative results is counted for each individual within any given epidemiological week. This helps prevent the double-counting of tests, particularly for individuals who may be hospitalised and routinely tested.
The same methodology is applied when analysing RSV and COVID-19 data.
Sentinel surveillance
The Public Health Agency works with GPs to deliver a community-based surveillance programme for respiratory infections in NI. The programme provides valuable intelligence about the circulation of respiratory viruses in NI to inform health and social care system planning and preparedness. Participation involves taking nasal/throat swabs from some symptomatic patients who agree to have a swab, and who attend (in person) with ILI, ARI or suspected COVID-19. Testing is opportunistic and within 10 days of symptom onset. Swabs are tested for influenza, RSV and COVID-19 at the RVL and surveillance is year-round.
SARS-CoV-2 genomics
A subset of SARS-CoV-2 positive PCR samples are sent to sequencing laboratories in Belfast Health and Social Care Trust and Queen’s University Belfast for sequencing. On 29th November the lineage assignment algorithm was switched from PangoLEARN to UShER for lineage counts. PangoLEARN uses a machine learning algorithm, whereas UShER uses phylogenetic placement and produces fewer unassigned lineages. This switch has been applied retrospectively, therefore total counts for all lineages have been affected. A more detailed COVID-19 Genomics Bulletin containing a further breakdown of sub-lineages is reported here.
Primary care surveillance
Consultation rates for influenza/influenza-like-illness (‘flu/FLI’) and acute respiratory infection (ARI)
GP in-hours consultation data with ~95% coverage of the NI population is auto-extracted weekly from GPIP. This data includes weekly aggregate consultations for ‘flu/FLI’ and ARI, and includes weekly registered patients. The data is available for different Health and Social Care Trusts, and by age and sex.
Secondary care surveillance
Admissions and occupancy
Where it is currently possible (SHSCT and WHSCT) only admissions where the method of admission was ‘Emergency’ are counted. It is not currently possible for this report to distinguish emergency from other types of admission for SEHSCT, BHSCT and NHSCT hospital data, following the introduction of a new electronic healthcare record on 06/11/2023, 06/06/2024 and 07/11/2024 respectively. For this report, all community-acquired admissions for SEHSCT, BHSCT and NHSCT are included, which will include non-emergency admissions (which are a small minority of the total admissions reported). Work is ongoing to adapt systems to new data sources and re-instate differentiation of emergency admissions. Ongoing developmental and quality assurance work may result in adjustments to figures.
Influenza and RSV
Community-acquired influenza and RSV emergency admissions to acute hospitals are estimated by combining data from PAS and virological reports in NIHAP. Admissions are counted where there was a positive test up to seven days before admission or up to one day after admission, and the method of admission was ‘Emergency’. The number of inpatients is counted at midnight. Admissions and occupancy refer to the first admission per infection episode.
COVID-19
Community-acquired COVID-19 emergency admissions are estimated by combining data from the NI COVID-19 Combined Testing Register and hospital admission information. Admissions are counted where there was a positive PCR or lateral flow test up to 14 days before admission or up to one day after admission. The number of inpatients is counted at midnight. Admissions and occupancy refer to the first admission per infection episode, including transfers between hospitals. The method used in this report is different to that previously reported by the Department of Health’s COVID-19 dashboard, which used administrative coding to identify COVID-19 admissions.
Mortality surveillance
PHA report weekly counts of selected respiratory infection death registrations in NI, as supplied by NISRA for influenza and RSV. PHA report weekly counts of COVID-19 death registrations in NI, as published by NISRA online here. Deaths occurring in NI are registered on the NI General Register Office’s Registration System (NIROS). Provisional data on deaths registered in each week (ending on a Friday) are compiled at the end of the following week. The data presented here is based on registrations of deaths, not occurrences. The majority of deaths are registered within five days in NI. The selected respiratory infections include deaths due to influenza, bronchitis, bronchiolitis, and pneumonia. These figures may be impacted by General Registration Office closures over public holidays.