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Can we identify the prevalence of perinatal mental health using routinely collected health data?: A review of publicly available perinatal mental health data sources in England.
Masefield, Sarah; Willan, Kathryn; Darwin, Zoe; Blower, Sarah; Nekitsing, Chandani; Dickerson, Josie.
Afiliación
  • Masefield S; Department of Health Sciences, Faculty of Sciences University of York York UK.
  • Willan K; Bradford Institute for Health Research Bradford Teaching Hospitals NHS Foundation Trust Bradford UK.
  • Darwin Z; Bradford Institute for Health Research Bradford Teaching Hospitals NHS Foundation Trust Bradford UK.
  • Blower S; Department of Allied Health Professions, Sport and Exercise, School of Human and Health Sciences University of Huddersfield Huddersfield UK.
  • Nekitsing C; Department of Health Sciences, Faculty of Sciences University of York York UK.
  • Dickerson J; Department of Health Sciences, Faculty of Sciences University of York York UK.
Learn Health Syst ; 8(1): e10374, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38249845
ABSTRACT

Introduction:

Perinatal mental health (PMH) conditions affect around one in four women, and may be even higher in women from some ethnic minority groups and those living in low socioeconomic circumstances. Poor PMH causes significant distress and can have lifelong adverse impacts for some children. In England, current prevalence rates are estimated using mental health data of the general population and do not take sociodemographic variance of geographical areas into account. Services cannot plan their capacity and ensure appropriate and timely support using these estimates. Our aim was to see if PMH prevalence rates could be identified using existing publicly available sources of routine health data.

Methods:

A review of data sources was completed by searching NHS Digital (now NHS England), Public Health England and other national PMH resources, performing keyword searches online, and research team knowledge of the field. The sources were screened for routine data that could be used to produce prevalence of PMH conditions by sociodemographic variation. Included sources were reviewed for their utility in accessibility, data relevance and technical specification relating to PMH and sociodemographic data items.

Results:

We found a PMH data 'blind spot' with significant inadequacies in the utility of all identified data sources, making it impossible to provide information on the prevalence of PMH in England and understand variation by sociodemographic differences.

Conclusions:

To enhance the utility of publicly available routine data to provide PMH prevalence rates requires improved mandatory PMH data capture in universal services, available publicly via one platform and including assessment outcomes and sociodemographic data.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prevalence_studies / Risk_factors_studies Idioma: En Revista: Learn Health Syst Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prevalence_studies / Risk_factors_studies Idioma: En Revista: Learn Health Syst Año: 2024 Tipo del documento: Article