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. 2014 Jun 5;14:564. doi: 10.1186/1471-2458-14-564

Table 2.

Protocol specificities between coordinating sites

Characteristic Valencia, Spain St. Petersburg, Russia Moscow, Russia Turkey France
Hospitals
5 health care district general hospitals
1 infectious disease hospital, 1 children’s city hospital, 1 children’s infectious disease hospital
1 infectious disease hospital
7 general hospitals
5 university hospitals
Screening ward
Emergency
Emergency and 3 selected wards
Paediatric, mixed, pregnancy, adults
Emergency and 7 selected wards
Emergency and >20 selected wards
Screening diagnosis
Admission diagnosis associated with influenza infection; clinical symptoms of ILI
Clinical symptoms of ILI
Admission diagnosis associated with influenza inflection; clinical symptoms of ILI
Clinical symptoms of ILI
Signs of respiratory illness for <7 days
Recruited by
Full-time trained nurses
Doctors
Doctors, nurses, heads of wards
Doctors
Doctors, clinical researchers, nurses
Additional exclusion criteria
Outside catchment area
-
-
-
Not affiliated with social security
Study start criteria
2 consecutive weeks with ≥2 cases
Week with ≥5 laboratory-confirmed influenza cases using national surveillance data
Week with ≥5 laboratory-confirmed influenza cases using national surveillance data
Not defineda
Defined by the national surveillance system
Study end criteria
2 consecutive weeks with no cases
Week with no laboratory-confirmed influenza cases
Week with no laboratory-confirmed influenza cases
Not defineda
Defined by the national surveillance system
Actual study period (epidemiological weeks) 2013-01 – 2013-15 2013-03 – 2013-22 2013-02 – 2013-21 2013-01 – 2013-14 2012-51 – 2013-16

aStudy period not defined because it was a pilot study. Cases of ILI were reported between epidemiological weeks 1 and 14 of 2013.

Dashes indicate no additional exclusion criteria.