Weekly aggregated data on influenza isolated specimens are collected in TESSy since 2008
presented at the annual European Influenza Surveillance Network meeting, Stockholm, June 2015
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Description of influenza isolated specimens reported in TESSy (2008 to 2014)
1. Description of the isolation data reported in
TESSy
(2008 to 2014)
Martina Escher, Cornelia Adlhoch, Eeva Broberg and Pasi Penttinen on behalf of the EISN
European Influenza Surveillance Network Annual Meeting 2014
11 June 2015
2. • Weekly aggregated data on influenza isolated specimens (IS)
are collected in TESSy since 2008
To monitor the influenza specimens’ availability across EU/EEA
countries for
antigenic characterisation
influenza vaccine virus selection and production
Background:
Countries
TESSy
? ?
3. Objective of the analysis
• First analysis of IS data reported to TESSy to:
• evaluate the usefulness of the reported data to inform
the surveillance objectives
• describe who report and what is reported
• evaluate IS representativeness compare to other virological
influenza surveillance data reported
4. Weekly number of isolated specimens (IS)
• 6 influenza seasons: from 2008/2009 to 2013/2014
• Sentinel/non sentinel
• Virus (sub-)types
Weekly number of positive specimens (PS)
• 6 influenza seasons: from 2008/2009 to 2013/2014
• Sentinel/non sentinel
• Virus (sub-)types
Weekly number of antigenic characterised strains (ACS)
• 2 influenza seasons: 2012/2013 and 2013/2014
• Sentinel/non-sentinel pooled
• Retrospective classification in (sub-)types
Methods: influenza surveillance data used
5. Methods: indicators calculated
1. Description of IS reported
Reporting Countries
Number of isolates reported
2. IS versus PS reported
Proportion of IS over PS reported and timing
Comparison of proportions of Influenza
(sub)types reported
3. IS versus ACS reported
Reporting countries
Proportion of ACS over IS reported
Sentinel and non-sentinel
2008/09 – 2013/14
Sentinel and non-sentinel
2008/09 – 2013/14
Sentinel + non-sentinel
2012/13 – 2013/14
7. Description of reported isolates
N of
reporting
countries
N
Isolated
specime
ns
N weeks
with
reported
isolates
Median
(Range) of
weekly
reported
isolates
N of
reporting
countries
N
Isolated
specime
ns
N weeks
with
reported
isolates
Median
(Range) of
weekly
reported
isolates
2008/09 1 34 12 0 (0-6) 1 374 15 0 (0-82)
2009/10 2 96 10 0 (0-26) 8 366 21 1 (0-53)
2010/11 7 320 26 4 (0-28) 4 197 23 4 (0-41)
2011/12 7 299 24 4 (0-38) 6 477 33 8 (1-51)
2012/13 4 314 16 0 (0-48) 5 789 28 5 (0-78)
2013/14 5 85 20 2 (0-12) 5 184 29 3 (0-30)
Non sentinelSentinel
Influenza
season
8. IS versus PDS: N reported specimens and timing
Sentinel IS and PS reported, 2008 to 2014
Proportion (%) of IS over PDS reported
0.3 0.6 2.3 3.1 2.3 1.2
9. IS versus PS: proportion of influenza (sub-)types
A(NT) A(H1) A(H3) B(NL) B(Vic) B(Yam)
0 0 21 79 0 0
25 3 53 19 0 0
0 99 0 1 0 0
4 95 0 1 0 0
0 4 21 5 68 3
4 53 2 32 8 1
0 1 91 0 4 4
7 2 80 9 1 1
3 40 12 3 2 41
5 26 14 37 2 16
1 65 32 0 0 2
6 49 43 2 0 1
IS
PS
IS
IS
IS
IS
IS
PS
PS
PS
PS
PS
Influenza (sub-) type %
A B
Sentinel IS and PS reported, 2008 to 2014
10. Which conclusions can we draw?
- Less than 50% of EU/EEA countries reported isolation at least in one
season and in one system
- Behaviour in performing isolation varied between and within countries
- IS represent between 0.3% and 3.1% of the PS
- Isolation was undertaken during the whole season with a pattern
following the detections
- Proportion of (sub-)typed IS reported not always reflected that of PS..
…representativeness of the available isolates??
11. IS ACS ACS/IS % IS ACS ACS/IS %
Austria
Belgium
Bulgaria
Czech Republic 255 13
Germany
Denmark
Estonia
Greece
Spain 20
Finland
France
Hungary
Ireland
Island
Italy
Lithuania
Luxembourg
Latvia 2
Malta
Netherlands
Norway
Poland
Portugal 387
Romania 149
Sweden 78
Slovenia 38
Slovakia 380
United Kingdom 1 49
2012/2013 2013/2014
IS versus ACS:
Sentinel+non-sentinel IS and ACS reported, 2012 to 2014
• Reporting countries
• Proportion of ACS over
IS reported
IS ACS ACS/IS % IS ACS ACS/IS %
Austria 7 1
Belgium
Bulgaria 7
Czech Republic 255 217 85% 13 19 146%
Germany 289 297
Denmark 10 39
Estonia
Greece 38 15
Spain 63 20 24 120%
Finland 2
France
Hungary
Ireland 23
Island
Italy 29 16
Lithuania
Luxembourg 4
Latvia 2 106 5300% 124
Malta
Netherlands 52
Norway 7
Poland
Portugal 387 387 100% 149
Romania 22 149 56 38%
Sweden 78
Slovenia 55 38 78 205%
Slovakia 380 349 92% 47
United Kingdom 1 1767 176700% 49 665 1357%
2012/2013 2013/2014
IS ACS IS ACS
Austria 7 1
Belgium
Bulgaria 7
Czech Republic 255 217 13 19
Germany 289 297
Denmark 10 39
Estonia
Greece 38 15
Spain 63 20 24
Finland 2
France
Hungary
Ireland 23
Island
Italy 29 16
Lithuania
Luxembourg 4
Latvia 2 106 124
Malta
Netherlands 52
Norway 7
Poland
Portugal 387 387 149
Romania 22 149 56
Sweden 78
Slovenia 55 38 78
Slovakia 380 349 47
United Kingdom 1 1767 49 665
2012/2013 2013/2014
IS ACS ACS/IS % IS ACS ACS/IS %
Austria 7 1
Belgium
Bulgaria 7
Czech Republic 255 217 85% 13 19 146%
Germany 289 297
Denmark 10 39
Estonia
Greece 38 15
Spain 63 20 24 120%
Finland 2
France
Hungary
Ireland 23
Island
Italy 29 16
Lithuania
Luxembourg 4
Latvia 2 106 5300% 124
Malta
Netherlands 52
Norway 7
Poland
Portugal 387 387 100% 149
Romania 22 149 56 38%
Sweden 78
Slovenia 55 38 78 205%
Slovakia 380 349 92% 47
United Kingdom 1 1767 176700% 49 665 1357%
2012/2013 2013/2014
13. Conclusion
• Objectives for influenza IS reporting: monitoring the
influenza specimens’ availability across Europe
• Do the data reported in TESSy inform this objective?
• Is this surveillance objective needed at European level?
ECDC surveillance strategy :
“develop the quality, effectiveness and accessibility of the EU
surveillance activities while ensuring that the burden on those
contributing to these activities remains congruent with the benefits”
• Are there alternative ways to inform the objective?
• If not, should ECDC stop collecting these data?
- number of specimens processed per week;
- number of isolates obtained by subtype (i.e. A(H1), A(H3), A(H5), pandemic (H1N1)
2009, A(not subtyped) and B);
What data are reported???
Which PH information these data provide?
establishment of the WHO Global Influenza Surveillance Network (GISN).
Virological weekly data (INFLVIRWAGGR)
The objectives for virological surveillance are:
To collect and provide timely information on the distribution of types, subtypes, lineages and clades among circulating influenza viruses over the influenza season.
Early warning upon emergence of new subtypes.
To assess the start of the influenza season.
To monitor the intensity and geographic progression of influenza throughout the season
Inform public health preparedness in Europe, especially in countries not yet affected by widespread influenza epidemics, and trigger operational plans (e.g. use of antivirals and personal protective measures).
To inform WHO vaccine composition meeting.
Aggregated virological data should be reported weekly during the influenza season (week 40 to week 20 of the following year). The metadata includes information on virus detection by (sub-)type from sentinel and non-sentinel sources, number virus (sub-)types isolated by sentinel and non-sentinel sources and characterisation of viruses by genetic and antigenetic methods. In addition to influenza, respiratory syncytial virus (RSV) detections can also be reported from sentinel and non-sentinel sources (see TESSy metadata).
The characterisation data of viruses should preferably be reported via the strain-based reporting in the INFLANTIVIR record type (see Influenza antiviral susceptibility strain-based (INFLANTIVIR)). The aggregate reporting for characterisation data should only be used if the country does not have resources for strain-based reporting.
The virological data are entered in the week that the swab was taken (by week of sampling).
One virus detection corresponds to the detection of influenza in one patient, regardless of the number of specimens taken from that patient, or which technique(s) were used to detect the virus.
Case definition
Influenza and RSV case definitions are specified in the EU Commission Decision 2012/506/EU of 8 August 2012.
Population under surveillance
Virological surveillance can be either sentinel or non-sentinel. Surveillance is considered sentinel when virological testing is performed in the same population in which clinical cases are recorded and reported taking a country-wide representative collection scheme into account. The virological surveillance of laboratory-confirmed influenza and RSV in Europe uses the same primary healthcare sentinel network model as the syndromic surveillance of ILI/ARI. The catchment population of the sentinel physicians forms the main population under surveillance. Patients with ILI/ARI (or a subset of these patients) seen by a sentinel physician are swabbed according to a defined sampling protocol. The virological surveillance system also captures non-sentinel detections of influenza virus, but the non-sentinel population under surveillance is not defined in all Member States. Virological data from non-sentinel sources can be from patients presenting at outpatient or inpatient health care facilities, outbreak investigations and as part of enhanced surveillance, for example as performed by countries during the early stages of the pandemic.
Overall, 16 different countries reported isolation data for at least one season during the study period , 13 (1-7) in the sentinel and 14 (1-8) in the non-sentinel system.
However a grate variation of reporting behaviour between countries was observed.
Countries reported between 1– 334 considering the two systems
0.1% and 100% depending on the country and on the season