Select Committee on Health Written Evidence


APPENDIX 47

Memorandum by National Perinatal Epidemiology Unit (MS 56)

  The National Perinatal Epidemiology Unit (NPEU) was established at Oxford University by the Department of Health in 1978 and is one of several Department of Health Research Policy Units in England. The NPEU undertakes research about pregnancy, childbirth and newborn babies, as well as long term outcomes for babies and mothers. The Department of Health provides over 50% to the Unit's annual income, the remainder coming from a variety of externally funded research projects. Funding of this post comes from the Unit "envelope" of money from the Department of Health and is available until December 2005. In 2004 the Unit will undergo its quinquennial review when a programme of work will be presented to the Department of Health for the period 2006-10.

THE COLLECTION OF DATA FROM MATERNITY UNITS

  The collection of data from maternity units is of key importance in the provision of a quality service in maternity care. Current data collection is poor. Maternity care providers use a variety of different electronic systems for collecting routine data and then find it difficult to use. As a consequence, there is no incentive to ensure that the data is entered accurately, so that even if the completeness of the "maternity tail" data can be increased, the quality of the data being collected may be so poor that it makes the data meaningless.

CAESAREAN SECTION RATES

  One consequence of the lack of accurate and comprehensive routine data about maternity care is that the National Sentinel Caesarean Section Audit had to be undertaken to answer pressing but basic questions about the incidence of caesarean section in the UK and the reasons for the recent increase. If routine data sources had been reliable much of this audit could have been achieved using routine data sources at a fraction of the cost and time. Similarly, if government wishes to continue to monitor trends in the caesarean section rate over time, further audits will need to be repeated as routine data sources are still not adequate to answer these basic questions.

  In addition, the collection of routine data underpins another of the committees questions which relates to staffing levels and training and the impact of these on the type of birth a woman has and the health of her baby. In order for meaningful data to be collected on the type of birth a woman has, routine data sources need to be accurate. In addition, the "linking" of mothers birth details to early or later child health is currently not possible. It is also currently not possible to monitor child health using routine data sources.

  If the influence of quality of care on mother and baby outcomes is to be monitored in a meaningful way, it is essential that (a) routine data collected from maternity units is standardised, (b) the systems used to collect the data are compatible with each other throughout the country, (c) the data is checked regularly for quality and completeness and (d) that there is an incentive for trusts to provide accurate and timely data to the Office of National Statistics. Equally important, however, is that data are collated, analysed and the findings fed back to clinicians in a timely and meaningful way. If the individuals providing the data do not benefit from its collection in a tangible way, then it will be extremely difficult to maintain quality and completeness.

  The NPEU has undertaken or is currently undertaking a number of studies which may be helpful to the committee. These are:

IN RELATION TO COMMUNICATION

  Reports from a study about stillbirth and infant death:

  Rowe R, Garcia J, Macfarlane A, Davidson L. (1999) Communication Issues in Stillbirth and Infant Death: a Review of Communications within the CESDI Framework. National Perinatal Epidemiology Unit, Oxford.

  Rowe R, Garcia J, Macfarlane A, Davidson L. (2001) Does poor communication contribute to stillbirths and infant deaths? a review. Journal of Public Health Medicine; 23(1): 23-34

ORGANISATION OF CARE

  Reports for a DH-funded study of maternity care organisation:

  (1)  Report on the Research Colloquium, June 2000.

  (2)  National survey of maternity care organisation, England 2001 A report to the Department of Health, July 2001.

  (3)  Research directions: a briefing paper for the Department of Health, 2002.

INEQUALITIES IN MATERNITY

  Barriers to care for low-income childbearing women. This is a Community Fund project involving NPEU and Maternity Alliance which is nearing completion. Reports which may be relevant include:

    —  Summary of evidence about existing inequalities in maternal and child health in England.

    —  Response to DH consultation "Tackling Health Inequalities: consultation on a plan for delivery" (November 2001).

    —  Paper submitted to Public Health—Social and ethnic inequalities in access to prenatal screening and diagnosis in the UK: a systematic review (April 2002).

    —  Paper submitted to J Public Health Medicine—Social class, ethnicity and attendance for antenatal care in the United Kingdom: a systematic review.

    —  Draft paper—Anti-smoking interventions: taking account of the views of low-income childbearing women for UK policy and practice.

    —  Draft report—Access to care for very disadvantaged childbearing women. This reports on 16 projects across England aimed at women in three categories—refugees and asylum seekers, women at risk of domestic violence and women from non-English speaking backgrounds. It uses the projects as case-studies to draw out lessons about the particular needs of those categories of women and to look for common themes.

    —  Draft reports—evidence of effectiveness of interventions aimed at limiting the impact of poverty and disadvantage on the health of mothers and babies. Topics covered: breastfeeding, immunisation, social support, preventing teen pregnancy, nutrition and smoking.

February 2003


 
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