The Neonatal Register SNQ contains information on newborn infants admitted to neonatal care, and longitudinal follow-up data for selected high-risk patients assessed at 2 and 5½ years of age.
The mission for SNQ is to provide data to professionals, administrators and families that can stimulate quality improvement and research. The information gathered in SNQ forms an important foundation for the quality improvement work that is continuously carried out in Swedish neonatal care. The information in the register illustrates how interventions and outcomes vary over time and across the country, and how these variations affect the results of the neonatal care system and the children’s future health.
Total volume of the register in October 2019: over 200,000 admissions.
Note: Variable lists are updated on a regular basis and should therefore be seen as preliminary. For the latest version, please contact the registry.
Category: Paediatrics, obstetrics and gynaecology
Certification level: 1
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