Sciensano & Influenza

Last updated on 29-5-2019 by Admin Drupal

In most cases influenza is a benign illness but for elderly people, pregnant women and people with chronic diseases, the complications of flu can be dangerous. Vaccination remains the best way of preventing the complications of flu and hospitalisation.

Surveillance of influenza, a public health issue

The intensity and severity of influenza varies year on year and depends on: 

  • the viral strains in circulation
  • the vulnerability and sensitivity of the population to these viruses.

As it is very contagious, influenza must be closely watched to assess whether it poses a danger for public health

What does Sciensano do?

Sciensano is the reference body in Belgium with regard to the surveillance of the flu and accommodates 2 teams: 

The 2 teams work together and manage a surveillance network of general practitioners and hospitals for permanent assessment of the intensity and severity of the epidemic and its impact on the population.

Finally, the Vaccine and Blood Product Quality Department is the Belgian Official Medicines Control Laboratory (OMCL), which is responsible for the quality control of the influenza vaccines before they can be placed on the European market. 

Describe the development of influenza 

Every week a network of 150 general practitioners report to Sciensano the number of consultations for the influenza syndrome and for acute respiratory infections.

These clinical data are collected throughout the year and make it possible to follow the development of influenza week after week.

By comparing the data of one year with that of the preceding years, Sciensano can determine the beginning and duration of an epidemic, as well as its intensity. 

Identify the viruses in circulation 

During the flu season (from week 40 of one year to week 20 of the next year), a systematical virological surveillance of respiratory samples is organised.

Every week the doctors also send samples of respiratory secretions (swabs) collected from a selection of patients with the influenza syndrome to Sciensano.

Sciensano's National Reference Centre (NRC) for influenza virus analyses these samples to identify and characterise the different viruses in circulation responsible for the influenza. 

Assess the severity of the epidemic and its impact on the population

It is only after the epidemic has occurred that Sciensano can estimate its impact and severity.

According to the clinical data collected and the viruses detected by the hospital network, Sciensano also analyses the complications relating to the influenza.

Epidemic threshold

The epidemic threshold makes it possible to declare the onset of an epidemic. It specifies the number of consultations per 100,000 inhabitants per week following which it may be considered that there is an epidemic.

Every year the European Centre for Disease and Control (ECDC) calculates the epidemic threshold for each country and each region on the basis of the figures for the previous 5 years.

According to the Moving Epidemic Method the curves are divided into three periods: pre-epidemic, epidemic and post-epidemic.

By comparing the epidemic periods for each curve, Sciensano determines the start of an epidemic according to the number of visits per week to the doctor for the influenza syndrome.

Control of vaccines for influenza

Sciensano is the Belgian Official Medicines Control Laboratory (OMCL) and is responsible for the quality control of the influenza vaccines before they can be placed on the European market. This control is carried out by the OMCL, independently of the vaccine manufacturer and for each batch separately. This control consists on the one hand of a critical review of the production data and quality analyses carried out by the vaccine manufacturer and on the other hand of additional analyses carried out by an OMCL. Thus, the Vaccine and Blood Product Quality Department performs various laboratory analyses according to the European Official Control Authority Batch Release (OCABR) guidelines. In addition, the Department also checks whether the production and quality data of the vaccine manufacturer are in conformity with the specifications as approved and recorded in the registration dossier. If a batch complies with all the quality criteria, the Department issues a certificate to the manufacturer, the so-called EU batch release certificate, and the vaccine may enter the European market.

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