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Hypertensive Disorders of Pregnancy - the Neonatal Burden of Disease

Active, not recruiting
Conditions
Hypertension in Pregnancy
Registration Number
NCT05015049
Lead Sponsor
Imperial College London
Brief Summary

Around one in ten women have high blood pressure in pregnancy. This is potentially serious, with risks to the woman and her baby. Whilst maternal deaths from high blood pressure in pregnancy are now rare in the UK, blood pressure problems in pregnancy still cause many stillbirths and early births. Studies have shown that women of Black and Asian backgrounds are more likely to have worse pregnancy outcomes when blood pressure problems in pregnancy develop.

This study aims to:

i) describe the burden of disease of high blood pressure in pregnancy amongst babies admitted to neonatal units on a national scale.

ii) investigate outcomes for babies born to women with high blood pressure in pregnancy admitted to UK neonatal units across maternal ethnic groups.

To complete this study, we will use the National Neonatal Research Database, which holds population-level data for all babies admitted to neonatal units (where unwell babies receive care) in the UK. We will look at records of babies admitted to neonatal units in England and Wales between 2012 and 2020. The records will include information on over half a million babies and their mothers. We will assess how many babies admitted to neonatal units were born to women who had high blood pressure in pregnancy. We will report the outcomes of these babies, and how they compare to babies born to women without high blood pressure in pregnancy. We will analyse whether outcomes for babies born to women with high blood pressure in pregnancy varies according to maternal ethnicity, and investigate what may be driving differences we find.

Detailed Description

Study Aims

This study aims to:

* quantify the proportion of all babies admitted to neonatal units born to women with a hypertensive disorder of pregnancy

* describe the national neonatal morbidity, mortality and resource use of babies admitted to neonatal units born to women with a hypertensive disorder of pregnancy

* examine ethnic disparities in neonatal outcomes of babies admitted to neonatal units born to women with hypertensive disorders of pregnancy.

The National Neonatal Research Database (NNRD)

The NNRD is an approved research database constituting real-world prospective clinical data extracted from point-of-care neonatal electronic health records with complete coverage of infants admitted for neonatal care to National Health Service (NHS) neonatal units in England and Wales (since 2012) and Scotland (since 2015). A defined data extract of approximately 450 items (the Neonatal Data Set) is transmitted quarterly to the Neonatal Data Analysis Unit at Imperial College London for data linkage and cleaning prior to entry into the NNRD. To date, the NNRD contains data for over a million babies (approximately 80,000 babies annually). High completeness and accuracy (\>95%) of neonatal data held in the NNRD has been confirmed by formal comparison with a multicentre, randomised placebo-controlled trial.

Study Design

This study is a secondary analysis of an existing national electronic health record population cohort using anonymised, routinely recorded clinical data from the National Neonatal Research Database (NNRD). There will be no new patients recruited and there will be no changes made to patient care.

The research team will work with NNRD data analysts to extract anonymised data from the NNRD. A cohort of babies born to women with a hypertensive disorder of pregnancy (HDP) will be defined based on records of maternal medical problems prior to pregnancy, obstetrics problems during pregnancy, medications given during labour and neonatal discharge diagnoses. The morbidity, mortality and health resource use of this cohort will be described in depth. This cohort will also be compared to a cohort of babies born to women without a hypertensive disorder of pregnancy. The HDP cohort will also be stratified by maternal ethnicity to investigate disparities in outcomes.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
823957
Inclusion Criteria
  • Must be born between 1st January 2012 and 31st December 2020
  • Must be admitted to and received all care in a National Health Service (NHS) neonatal unit in England or Wales
Exclusion Criteria
  • None

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of days of intensive careFrom birth to discharge or death, assessed up to 1 year

Number of days of intensive care

Primary recorded reason for neonatal unit admissionFrom birth to discharge or death, assessed up to 1 year

Primary recorded reason for neonatal unit admission

Length of stay in neonatal unitFrom birth to discharge or death, assessed up to 1 year

Length of stay in neonatal unit

Survival to discharge from neonatal careFrom birth to discharge or death, assessed up to 1 year

Survival to discharge from neonatal care

Secondary Outcome Measures
NameTimeMethod
Cause of deathFrom birth to discharge or death, assessed up to 1 year

Cause of death

Discharge weight SDS (standard deviation score)From birth to discharge or death, assessed up to 1 year

Discharge weight SDS (standard deviation score)

Birthweight centile (z-score)From birth to discharge or death, assessed up to 1 year

Birthweight centile (z-score)

General neonatal complicationsFrom birth to discharge or death, assessed up to 1 year

Brain injury on imaging, necrotising enterocolitis, sepsis, jaundice, GI perforation

Preterm complicationsFrom birth to discharge or death, assessed up to 1 year

Chronic lung disease/bronchopulmonary dysplasia, retinopathy of prematurity

Age at deathFrom birth to discharge or death, assessed up to 1 year

Age at death

Clinical diagnoses potential specific to hypertensive disorders of pregnancyFrom birth to discharge or death, assessed up to 1 year

Fetal growth restriction/intrauterine growth restriction, hypoglycaemia

Number of days of special careFrom birth to discharge or death, assessed up to 1 year

Number of days of special care

Number of days of invasive respiratory supportFrom birth to discharge or death, assessed up to 1 year

Number of days of invasive respiratory support

Survival to discharge from neonatal care without comorbidityFrom birth to discharge or death, assessed up to 1 year

Survival to discharge from neonatal care without comorbidity

Number of days of high-dependancy careFrom birth to discharge or death, assessed up to 1 year

Number of days of high-dependancy care

Number of days of non-invasive respiratory supportFrom birth to discharge or death, assessed up to 1 year

Number of days of non-invasive respiratory support

Surfactant administeredFrom birth to discharge or death, assessed up to 1 year

Surfactant administered

Surfactant administered on first dayFrom birth to discharge or death, assessed up to 1 year

Surfactant administered on first day

Transfusion of blood productsFrom birth to discharge or death, assessed up to 1 year

Transfusion of blood products

Type of feeding (number of days of each e.g. breastmilk, formula etc)From birth to discharge or death, assessed up to 1 year

Type of feeding (number of days of each e.g. breastmilk, formula etc)

Number of days nil by mouthFrom birth to discharge or death, assessed up to 1 year

Number of days nil by mouth

Line type(s)From birth to discharge or death, assessed up to 1 year

Line type(s)

Number of days of parenteral nutritionFrom birth to discharge or death, assessed up to 1 year

Number of days of parenteral nutrition

Method of feeding (number of days of each e.g. NG, breast etc)From birth to discharge or death, assessed up to 1 year

Method of feeding (number of days of each e.g. NG, breast etc)

Trial Locations

Locations (1)

Imperial College London

🇬🇧

London, United Kingdom

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