Abstract
BACKGROUND: Children born very preterm (<32 weeks of gestation) face high risks of neurodevelopmental and health difficulties compared with children born at term. Follow-up after discharge from the neonatal intensive care unit is essential to ensure early detection and intervention, but data on policy approaches are sparse.
METHODS: We investigated the characteristics of follow-up policy and programmes in 11 European countries from 2011 to 2022 using healthcare informant questionnaires and the published/grey literature. We further explored how one aspect of follow-up, its recommended duration, may be reflected in the percent of parents reporting that their children are receiving follow-up services at 5 years of age in these countries using data from an area-based cohort of very preterm births in 2011/12 (N = 3635).
RESULTS: Between 2011/12 and 22, the number of countries with follow-up policies or programmes increased from 6 to 11. The policies and programmes were heterogeneous in eligibility criteria, duration and content. In countries that recommended longer follow-up, parent-reported follow-up rates at 5 years of age were higher, especially among the highest risk children, born <28 weeks' gestation or with birthweight <1000 g: between 42.1% and 70.1%, vs. <20% in most countries without recommendations.
CONCLUSIONS: Large variations exist in follow-up policies and programmes for children born very preterm in Europe; differences in recommended duration translate into cross-country disparities in reported follow-up at 5 years of age.
| Original language | English |
|---|---|
| Journal | European Journal of Public Health |
| Volume | 34 |
| Issue number | 1 |
| Pages (from-to) | 91-100 |
| Number of pages | 10 |
| ISSN | 1101-1262 |
| DOIs | |
| Publication status | Published - 1 Feb 2024 |
Keywords
- Child
- Europe/epidemiology
- Female
- Follow-Up Studies
- Gestational Age
- Humans
- Infant
- Infant, Extremely Premature
- Infant, Newborn
- Premature Birth/epidemiology
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