Influenza Viral Infections, Respiratory Viral Infection, Severe Acute Respiratory Infection
Conditions
Keywords
sentinel surveillance
Brief summary
The Belgian Severe Acute Respiratory Infections network (BELSARI-net) was implemented during the influenza season 2011-2012 following the recommendations of the World Health Organization (WHO) to monitor severity of influenza viruses in hospitals. The network is composed of 6 hospitals throughout the country, two in each administrative region (Flanders, Wallonia and Brussels-Capital), and operates during the influenza epidemic period (from the last week of December or first/second week of January to the third/last week of April, depending on when influenza virus circulation is detected by the general population, based on the Influenza-like illness (ILI) network of general practitioners). Enrollment is performed for all cases matching the SARI case definition (based on WHO's case definition) and accepting to take part. A respiratory specimen is sampled systematically from each participant, and detailed clinico-epidemiological data, such as information on age, sex, symptoms and potential risk factors such as pregnancy or comorbidities (chronic respiratory diseases, asthma, chronic cardiovascular diseases, renal insufficiency, obesity, diabetes, hepatic or renal insufficiency, immunodeficiency, neuromuscular disease, pregnancy) is also collected. Participants are followed up during hospitalization for the occurrence of complications (detection of pneumonia based on chest radiography, development of acute respiratory distress syndrome (ARDS), requirement for respiratory assistance and/or for extracorporeal membrane oxygenation (ECMO), admission in intensive care unit (ICU)), or death (all-cause death). The current project includes all the samples received by the Belgian National Influenza Centre (NIC) during the influenza seasons 2011-2012 till 2019-2020.
Interventions
DIAGNOSTIC_TESTrespiratory specimen
nasopharyngeal swab or nasal aspiration or broncho-alveolar lavage
Sponsors
Belgian Federal Public Service, Food Chain Safety and Environment
Centre Hospitalier Universitaire Saint Pierre
AZ Sint-Jan AV
Universitair Ziekenhuis Brussel
Grand Hôpital de Charleroi
Jessa Hospital
Centre Hospitalier Universitaire UCLouvain Namur
Sciensano
Study design
Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* All pediatric and adult patients admitted to one of the 6 sentinel hospitals during the active surveillance and fulfilling the case definition of acute respiratory infection with onset within the last ten days, with history of fever or measured fever of ≥38°C, with cough and/or dyspnea, and overnight hospitalization.
Exclusion criteria
* nosocomial infection, i.e. symptoms appearing after admission
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants positive for influenza viruses | within 10 days after symptom onset | result of influenza PCR detection test (typing and subtyping) |
| Number of participants positive for non-influenza viruses | within 10 days after symptom onset (only routinely tested since influenza season 2015-2016) | results of non-influenza multiplex PCR detection test (16 targets) |
| Number of participants who died during hospitalization | from date of hospital admission until date of death during hospitalization or date of hospital exit | alive or dead |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with at least one known risk factor | on date of hospital admission | existence of co-morbidities or known risk factors among a list provided on form |
| Number of participants who experienced at least one complication | from date of hospital admission until date of death during hospitalization or date of hospital exit | occurence of complications (among a list provided on form) during hospitalisation stay |
Outcome results
None listed