Impact of revised @BAPM_Official
extreme preterm framework: risk based approach to provision of survival focused care for babies born at 22 weeks’ gestation in England and Wales 2018-2019 vs 2020-2021.
Published @BMJMedicine today ⬇️ https://t.co/wYVrW9krQ9
Please have a read of our (open access!) paper: Two-year neurodevelopmental data for preterm infants born over an 11-year period in England and Wales, 2008–2018: a retrospective study using the National Neonatal Research Database, published in @ADC_BMJ https://t.co/QRnw5KBk8G
The PARCA-R is a validated parent-completed questionnaire used for developmental screening, now captured in the NNRD. We hope that practicality of this tool will improve completeness of standardised assessments sufficiently for use of this routinely recorded data for research
Here's your weekly reminder that 10 years ago the NHS was the best healthcare system on the planet, ranked number 1 by the @commonwealthfnd. The NHS crisis is due to a decade of Tory underfunding and criminal grade neglect. We don't need a new system, we need a new govt.
#SOSNHS
Paediatricians speak for children; they need our advocacy more than ever now; read “Message to the new prime minister (whoever this might be)” in @ADC_BMJ @EUperinatal @NeonatalUpdate @BAPM_Official @RCPCHtweets https://t.co/TzZfnAvkWf
Linkage of routinely collected datasets offers tremendous potential for research on improving future outcomes of babies born preterm. But what do parents of preterm babies, adults born preterm and professionals think of data linkage? We undertook a study to explore their views 🧵
This study forms a part of @neoWONDER20 : Neonatal Whole Population data linkage to improve lifelong outcomes of preterm babies. Watch this co-produced video explaining complex data linkage steps: https://t.co/yoayFxhlSs