Select Committee on Health Written Evidence


WRITTEN EVIDENCE

Memorandum by the Department of Health (MA1)

1.  INTRODUCTION

  1.1  Tackling Health inequalities has been a priority for the Government since coming to office in 1997 when they commissioned Sir Donald Acheson's Independent Inquiry into Inequalities in Health Report, published in 1998.

  1.2  The Acheson Inquiry Report provided a broad analysis of the social, economic and environmental determinants of health inequalities. It identified support for mothers with very young children as one of the top three priorities, highlighting the importance of:

    —  early interventions;

    —  a focus on the health of mothers and young children in addressing infant mortality; and

    —  in the long term, breaking the intergenerational cycle of health inequalities.

  1.3  Care for mother and baby throughout pregnancy and the early postnatal period can have a marked effect on the child's healthy development, and on their resilience to problems encountered later in childhood. There are many correlations between the health of mothers and their babies. For example, there are clear links between smoking in pregnancy and low birth weight, which is in turn related to poor health outcomes for a child.

  1.4  The NHS Plan, published in July 2000, set out a plan for investment and reform for the NHS. The Plan made health inequalities a priority and contained a commitment to establish the first ever national health inequalities targets. These headline targets, chosen as high level measures of progress, were announced in February 2001 in the areas of life expectancy (by geographical area) and infant mortality (by social class).

  1.5  For maternity services, this means knowing where pregnant women are and how they want and need their care delivered and configured. It means understanding the local patterns of disadvantage and exclusion; and designing services that reach out to ensure those most in need have prompt access to the support they need.

  1.6  The Maternity External Working Group of the Children's National Service Framework (NSF) is working to develop flexible models for maternity care, especially in the antenatal and postnatal period, that support and strengthen universal access; but at the same time, find new ways of providing accessible and appropriate services for hard to reach and disadvantaged women, their partners and babies.

  1.7  Overcoming inequalities in outcomes, some of which can be helped by improving access to antenatal care services is perhaps the biggest and most important challenge addressed by this NSF. We know that women from the most vulnerable groups of society often find it difficult to access, or maintain access with maternity services. We also know these groups of women have the poorest maternal and neonatal outcomes. Excluded women also tend to have a multiplicity of problems in conjunction with their pregnancy.

  1.8  The following sections detail major areas of work that the Department of Health either sponsors or knows about. Section two sets out the context of the cross Government health inequalities strategy and how this will impact on inequalities in maternal and child health. Section four describes the maternity module of the NSF that will be the main vehicle for drawing all of the areas of work together into a single coherent vision for maternity services over the next ten years. Section five of the memorandum sets out the range of services that are available for disadvantaged groups.

2.  HEALTH INEQUALITIES STRATEGY—THE CONTEXT FOR ACTION

  2.1  The Government has given a high priority to tackling the causes and consequences of health inequalities as part of its commitment to deliver social justice and economic prosperity. This includes action on poverty, social exclusion and inequality. In particular, it is committed to making substantial progress towards the eradication of child poverty to break the intergenerational cycle of health inequalities and poverty and deprivation that begins at birth and continues throughout life by reducing the number of children living in poverty by a quarter by 2004.

  2.2  Tackling health inequalities is part of this overall approach across DH, the NHS and other government departments is contributing to a wider strategy shaped by the first-ever national health inequalities targets on life expectancy and infant mortality. This includes addressing barriers and obstacles to the use of services, including health services, that will have an adverse effect on health. This will require more targeted services and programmes to address the health needs of disadvantaged areas and population groups. This includes setting new standards for service provision and quality of care through The Cancer Plan and NSFs on CHD, mental health and diabetes.

Infant mortality rates—current data

  2.3  The Government has made it a priority to tackle inequalities in infant mortality rates, and has set a target in this area (see paragraph 2.7).

  2.4  The infant mortality (by social class) target presents a high degree of challenge, and action will be needed across Government. Current data do not yet reflect on action since the setting of the target, but do indicate that for infant mortality, the gap continues to widen, confirming the difficulty of turning around long-term social trends.

  2.5  Latest data for 1999-2001 showed a continued widening of the gap between "manual" groups and the total population. Based on current trends, this gap is projected to widen further by 2010. Latest out-turn figures overlap the setting of the target, therefore it is not yet possible to comment on changes in performance since the time when the target was set (Feb 2001).

Department of Health initiatives/action

The Acheson Inquiry

  2.6  Sir Donald Acheson's Independent Inquiry into Inequalities in Health highlighted inequities in access to health care and treatment and acknowledged that communities most at risk tend to experience the least satisfactory access to the full range of service provision, the so called "inverse care law", although it did not specifically discuss inequalities in access to maternity care. The Inquiry Report recommended that providing equitable access to effective care in relation to need should be the governing principle of all policies in the NHS.

Tackling Health Inequalities—Consultation on a plan for delivery

  2.7  In August 2001 the Government published Tackling Health Inequalities—Consultation on a plan for delivery. The document highlighted examples of good practice and sought views on the actions needed to tackle health inequalities and to meet the national targets that were a commitment from The NHS Plan. One of the priority themes in the consultation document was the need to produce a sure foundation through a healthy pregnancy and early childhood. A follow up document, Tackling Health Inequalities: The results of the consultation exercise, published in July 2002, confirmed that there was strong support for the priorities set out, including the focus on maternity, infancy and early years.

Cross-Cutting Spending Review on health inequalities

  2.8  In summer 2002, the Government completed a Cross-Cutting Spending Review on health inequalities. This provided an opportunity for the whole Government to focus on health inequalities and establish priority areas for action to deliver the national targets. A summary of the main findings, Tackling Health Inequalities: Summary of the 2002 Cross-Cutting Review was published in November, and set out the Government's long term strategy for tackling health inequalities.

  2.9  The Review identified the priority interventions likely to make a major impact on the infant mortality target and on early years development:

    —  building on Sure Start in improve early years support in disadvantaged areas;

    —  reducing smoking in pregnancy;

    —  preventing teenage pregnancy, and tackling its causes and effects;

    —  improvements in housing conditions for children in disadvantaged areas;

    —  other forms of early interventions for the NHS, for example to increase immunisation rates and breastfeeding, improve diet, family support and education about infant sleeping position.

National health inequalities targets

  2.10  As part of the Spending Review 2002, the two national targets were combined into one overall Public Service Agreement (PSA) and this single target has also been included in the National PSA for Local Government:

    —  By 2010 reduce inequalities in health outcomes by 10% as measured by infant mortality and life expectancy at birth.

  2.11  The single target is supported by targets on life expectancy and infant mortality, revised to reflect changes in social class definitions and the abolition of Health Authorities:

    —  Starting with children under one year, by 2010 to reduce the gap in mortality by at least 10% between "routine and manual" groups and the population as a whole. [The "10%" figure is subject to review of the historic data, when available, to ensure that this target is still realistic and challenging]

    —  Starting with Local Authorities, by 2010 to reduce the gap by at least 10% between the fifth of areas with the lowest life expectancy at birth and the population as a whole.

  2.12  Tackling health inequalities is a key strand of the Government's Modernisation Programme designed to develop responsive, effective public services and action is being mainstreamed through programmes in the NHS and across Government.

Priorities and Planning Framework for the NHS, 2003-06

  2.13  The Framework, published in October 2002, described the vision for services over the three years from 2003, and how national commitments translate into priority areas and targets for the NHS and social services, and set out a summary of the new system for planning and performance management. Health inequalities have been given a high profile within the Framework, sending a clear message to the service of the importance attached to narrowing the gap in health outcomes. The Framework focuses on reducing the gap in infant mortality and life expectancy at birth, and on reducing teenage pregnancies. It contains supporting targets including:

    —  Deliver a one per centage point reduction per year in the proportion of women continuing to smoke throughout pregnancy, focussing especially on smokers from disadvantaged groups as a contribution to the national target to reduce by at least 10% the gap in mortality between "routine and manual" groups and the population as a whole by 2010, starting with children under one year.

    —  Deliver an increase of 2 per centage points per year in breast feeding initiation rate, focusing especially on women from disadvantaged groups.

    —  Achieve agreed local teenage conception reduction targets while reducing the gap in rates between the worst fifth of wards and the average by at least a quarter in line with national targets.

All-Government Delivery Plan on Health Inequalities

  2.14  The Government has recognised that health inequalities cannot be tackled by the NHS alone, but will need a concerted effort across the whole of government, working with a range of partners in the community, voluntary and business sectors.

  2.15  The Department of Health has lead work to develop an All-Government Delivery Plan on health inequalities, describing the complex health inequalities problem; the Government's strategy to tackle it; the impact in communities of programmes committed to the strategy; and how the implementation of the strategy will be managed. The main findings of the Spending Review and the health inequalities consultation have been fed into the Delivery Plan, which will be published shortly.

Progress to date

  2.16  Progress made to date includes:

    —  Reducing the number of children in poverty—there are over 400,000 fewer children in low income households since 1998

    —  improved maternal and child health care—where work on the National Service Framework for children's health and social care is well advanced, with inequalities in health and social care provision a priority

    —  improved support for child development through 439 local Sure Start programmes and related initiatives

    —  smoking througout pregnancy decreased from 23% in 1995 to 19% in 2000 in England and an increase in breast feeding initiation from 68% in 1995 to 71% in 2000 in England and Wales (although a significant social variation remains)

    —  the establishment of the Teenage Pregnancy Unit in 1999 to implement the strategy in the Social Exclusion Unit report on Teenage Pregnancy. The NHS Plan stressed the Government's commitment to reduce the rate of teenage conceptions by 15% in 2004 and by half in 2010. A third of teenage mothers aged 16-19 now participate in education, training or employment, double that since 1997

    —  falls of 9% in the under 18 conception rate and 10% in the under 16 conception rate since 1998, (the baseline year for the Teenage Pregnancy Strategy)

3.  WHY MOTHERS DIE 1997-99: THE CONFIDENTIAL ENQUIRIES INTO MATERNAL DEATHS (CEMD)

  3.1  Although very few mothers die in childbirth CEMD investigates every case in detail and is a trusted evidence base for continuous service improvement. Unlike previous CEMD reports the latest has moved from looking at purely medical issues into the wider aspects of health and inequalities. The Report is timely in that the results can feed in to the National Service Framework for Children.

  3.2  Adverse pregnancy outcomes for both mother and child are strongly linked to vulnerability, social exclusion and deprivation. The latest CEMD found the maternal death rate amongst excluded women to be 20 times higher than for women in the highest two social classes, and problems with severe complications of pregnancy are also more common for these women. These findings are similar to those in other developed countries. Whilst maternal deaths are, fortunately, extremely rare they represent the tip of the iceberg of women who survive severe complications of pregnancy which may have long lasting physical and emotional consequences. Here again these poor maternal outcomes have been shown, in many cases, to be increased in women from the same vulnerable communities.

  3.3  Children born to women from the more vulnerable groups also experience problems with pre-term labour, intrauterine growth restriction, low birth weight, low levels of breast feeding and higher levels of neonatal complications.

  3.4  Socio-economic deprivation is associated with less effective health care service use and poor health status and other factors which adversely influence pregnancy outcomes, such as drug abuse, also correlate with social deprivation. Underlying factors which impact on maternal and child health also include smoking, poor nutrition and obesity.

  3.5  The CEMD report showed over one-fifth of the women who died did not receive adequate care, in that they first sought care, or "booked", late in their pregnancy or found it difficult to attend for regular care. In the vast majority of cases these women were not actively followed up when they failed to re-attend the clinic. 20% of the women who died "booked" after 20 weeks of gestation. Virtually all had multiple indicators of social exclusion and a disproportionate number were also from non-white ethnic groups. Hospital Episode Statistics (HES) data show that in general, women from non-white ethnic groups are twice as likely to "book" later than 20 weeks of gestation. Late "bookers" constitute about 8% of the white pregnant population and 17% of the non-white pregnant population.

  3.6  This new knowledge has underpinned the work of the Pre-Birth and Inequalities Sub Groups of the NSF, and formed the basis for the inequalities delivery priority element and the need for early antenatal booking.

4.  NATIONAL SERVICE FRAMEWORK FOR CHILDREN

  4.1  The general NSF programme is part of an overall Government programme to improve quality and drive up standards of services within a framework of explicit national standards. This includes addressing fundamental inequalities in access to services.

  4.2  The NHS Plan set out a vision of a service designed around the patient. To achieve that vision the NHS is undergoing radical change, supported by a major programme of investment and reform. Within this, various strands of work are currently being taken forward to improve maternity services. The most fundamental to this process is the development of the Children's National Service Framework (NSF) which will include a module on maternity service provision.

  4.3  Announced in February 2001, the Children's NSF highlights this Government's commitment to high quality maternity services for all. In the new architecture of the NHS the setting of national standards through the NSF will be the most effective way of ensuring consistency of service provision to all groups of women, including those who use the current services least, and quality in a devolved health care system; whilst at the same time continuing to allow local health systems to develop a "best fit".

  4.4  The aim of the maternity module of the Children's NSF is to define standards that will enable childbearing women and babies to achieve optimum health and wellbeing. The maternity module will develop national standards of care to cover the provision of antenatal, delivery (intrapartum) and postnatal services; and will look at how to make maternity services more flexible, accessible and appropriate for all, including the socially disadvantaged.

  4.5  Developing the maternity module is the Maternity External Working Group (EWG) which is co-chaired by Heather Mellows the Junior Vice-President of the Royal College of Obstetricians and Gynaecologists and Meryl Thomas honorary Vice-President of the Royal College of Midwives. Members are drawn from a wide range of backgrounds including medical and midwifery professionals, research experts and user groups. Further information on the NSF is available at http://www.doh.gov.uk/nsf/children

  4.6  The EWG's work is being taken forward through five sub groups.

    —  Pre-birth.

    —  Birth.

    —  Post-birth & baby.

    —  Inequalities and access.

    —  User involvement.

  4.7  The Department considers it vital that as many as possible of the stakeholder groups, with an interest in the maternity services, are given the opportunity to input to this important exercise and this is reflected in the sub group membership.

  4.8  This information is set out in Getting the right start: The National Service Framework for Children, Young People and Maternity Services—Emerging Findings published on 10 April 2003. This report sets out the overall direction of travel for the NSF, prior to its publication in 2004, to help local health communities planning and improving services. This report is available on the following website address www.doh.gov.uk/nsf/children/gettingtherightstart

Care pathways

  4.9  The NSF will promote the use of flexible care pathways to deliver high quality equitable services. Care pathways have emerged in the past decade as an important technique for continuous quality improvement in healthcare and are increasingly seen as a key NHS resource for implementing an NSF. Care pathways formalise protocols and guidelines into direct, individual women centred care. The emphasis is on the woman (and her unborn child) being at the centre of the process rather than some one to whom services "just happen" in a haphazard or uncoordinated way. They can be used to describe the routine progression of a woman through the antenatal period as well as illustrating tracer conditions or situations which can be used to illustrate how the standards will be implemented in particular circumstances.

  4.10  The use of these pathways should thus result in the same standard of care being provided for all women, and more importantly, if given or explained to the woman will enable her to understand exactly who and, what may be required to provide or offer additional services to her should the need arise and where these still exist.

  4.11  The development of a particular pathway will involve a multidisciplinary approach with agreement with all those likely to be involved in providing care. Pregnant women may require care from a variety of sources or professionals, provided through clinical or social networks. Knowing which path to follow, and who is responsible for providing what, will help to reduce clinical variation, eliminate duplication of services, maintain quality care and adherence to clinical or other guidelines and give professionals agreed control over the care of the delivery process.

Open Forum Events

  4.12  The User Involvement Sub Group held two Open Forum meetings in Leeds and London (January 2003) for people who have used maternity services and now act as representatives for their local community. Speaking at the events were women with disabilities who had been recent users of maternity services.

  4.13  Issues addressed at the events included the changes needed to improve maternity care and postnatal services for women and their families, how a broad range of parents and user representatives can best contribute to the planning and monitoring of maternity services in the future and examples of good practice in listening to users and using their views to change the way that care is delivered. The issues discussed at the events are being fed into the developing maternity module at the NSF.

  4.14  Following the Open Forum events the User Involvement Sub Group is also developing a database of good practice initiatives that improve the quality of local maternity services in any or all of the following ways: improving access to maternity services, increasing user involvement, reducing health inequalities, improving public health. These will be included in the NSF and will be useful for those developing local services.

Inequalities and Access Sub Group

  4.15  This sub group will ensure that the maternity module addresses all areas of inequalities for all groups of women including those who find it hard to access services. This group has identified that there are two dimensions to inequality that must be addressed. How do services find the hard to reach and how do these services respond when these women do attend? Care needs to be individual and personal for each woman. Carers should not make assumptions about a woman's needs from her appearance, ability to communicate and her past history. This sub group will examine existing models of good practice. Staff in NHS maternity services cannot be expected to know about every service available from every agency in great detail. However the NSF will act as a signpost to enable them to refer vulnerable women to other professional, voluntary groups and agencies who have a specialist interest.

  4.16  It is also clear to all sub groups that they must and will address inequalities throughout their own considerations and topic areas. Models of postnatal care that are working for some "hard to reach" communities have been developed by local Sure Start programmes and we are seeking more information on reasons for non-attendance at antenatal appointments and pressing for generic solutions in the NSF. For example care pathways that describe the journey of a pregnant woman through the services whatever her circumstances.

5  SERVICES FOR DISADVANTAGED GROUPS

A.   Minority Ethnic Groups

  5.1  The CEMD report highlighted the fact that women from ethnic minority groups appear to be at greater (twice) the risk of a maternal death. There are many issues affecting minority ethnic groups. Some of these are poor health outcomes, for example Pakistani women are more likely to have a stillbirth or a death in infancy and Somali women are more likely to have a low birth weight baby. Other issues include the attitudes of NHS staff and cultural expectations. Some women's cultural expectations will require exclusively female care staff; others may prefer to have care led by a doctor rather than a midwife.

  5.2  The NHS Plan has signalled to the service the need to become more responsive to black and minority ethnic communities and to provide services which take account of their religious, cultural and linguistic requirements.

  5.3  Access to maternity can be a problem for this group. Out of the cases investigated in the CEMD report more than 25% of women from ethnic communities either contacted the maternity services for the first time when they were more than five months pregnant or missed four or more routine appointments. Some were also newly arrived in the UK. Access to care was also an issue for the disadvantaged white women and this is a general issue that will need to be addressed in the forthcoming NSF.

  5.4  There are a number of reports, including Mothers in Exile produced by the Maternity Alliance, highlighting the need for NHS staff to be aware of cultural differences and the need to provide culturally sensitive, non-judgmental services that meet the needs of the woman and her family. The findings of these reports are being considered by the maternity module of the Children's NSF.

  5.5  The NHS Plan recognises the need to tackle disadvantage in all its forms, including the specific health needs of specific groups including minority ethnic groups. The NHS will shape its services around the need and preferences of individual patients, their families and their carers, including challenging racial discrimination. Furthermore, the Race Relations Act, as amended 2000, places a duty of public authorities to promote race equality. Public authorities must have due regard to the need to eliminate unlawful racial discrimination, promote equality of opportunity; and promote good relations between people of different racial groups. Delivery on the Race Relations Act is a core part of the Department's vision of equality and fair treatment for patients and staff. Achieving sustainable improvements in health and services for black and minority ethnic people is an integral and vital aspect of the Department's programme of investment and reform.

B.   Refugees and Asylum seekers

  5.6  Persons with an outstanding application for asylum in the UK are entitled to full use of the NHS without charge. This includes maternity services.

  5.7  Asylum applicants may apply for support and accommodation from the National Asylum Support Service (NASS). If accommodation is required, asylum applicants are dispersed to available accommodation around the UK. The Home Office is responsible for asylum and NASS support applications.

  5.8  Pregnant asylum applicants may be in a particularly vulnerable condition. They may have undertaken a long journey while pregnant; the pregnancy may have been the result of rape in their country of origin; they may not be able to speak English; they are unlikely to have family/friends around them for support; and their future in the UK may not be certain. For these reasons and others, pregnant asylum applicants commonly show signs of psychological distress.

PMS

  5.9  Many PCTs have set up PMS (Personal Medical Services) pilots. PMS is an alternative model of primary care provision that has been developed by the Government to allow flexible use of funding to provide care for vulnerable populations such as asylum seekers. Many successful models are now in existence around the country of PMS pilots providing dedicated services to asylum seekers. PMS practices often act as a first point of contact for asylum seekers requiring healthcare on arrival in a city.

Induction Centres

  5.10  The Government is developing a network of induction centres, where asylum seekers will stay for short periods upon arrival in the UK, before they are dispersed around the country. As part of the induction process, asylum seekers will receive a health assessment. This will identify health needs at an early stage so that appropriate care/treatment can be commenced as soon as possible and enable health factors to be played into the dispersal process. The first induction centre is up and running in East Kent, others will follow over the coming year.

DH Guidance

  5.11  Caring for asylum applicants in all contexts can be challenging for frontline health staff. The Department of Health is developing, with the Refugee Council, a resource pack for the NHS and social services that will include reference to maternity services. The pack will be launched in the summer.

Translated resources

  5.12  Providing adequate interpreting and translation services for asylum applicants is challenging for local health organisations—particularly in view of the huge variety of languages spoken by many of those entering the UK. To help offset this challenge the Department of Health are working with HARPweb (www.harpweb.org.uk) on translated web based health resources. At the moment a "multi-lingual" appointment card is available at this site to download in over 30 languages. Plans are also afoot to provide a range of other translated materials which will include leaflets on vaccines & immunisations, child protection/abuse, domestic violence and breast feeding/bottle feeding/weaning.

Extra Payments

  5.13  Families receiving social security benefits, specifically Income Support or an income based Jobseeker's Allowance, are eligible to receive milk tokens which can be exchanged for infant formula. However, asylum seekers do not receive milk tokens because they are not eligible for social security benefits (destitute asylum seekers are supported by NASS). In appreciation of this, on 5 November 2002 the Home Secretary announced that additional payments would be made to pregnant women and children aged under three in receipt of support by NASS. Pregnant women and children aged 1-3 now receive an additional payment of £3 per week. Babies under 1 will receive an additional £5 per week.

  5.14  In addition, asylum seekers may be able to access formula milk free or at reduced prices through local schemes operated by community clinics or hospital services. A pilot scheme has been launched in Lambeth, Southwark and Lewisham that aims to provide sterilising equipment and one year's free access to formula milk for HIV-infected women experiencing financial hardship. Asylum-seeking mothers are just one of the vulnerable groups that will be helped by the scheme.

C.   Those who do not speak English as their first language

  5.15  The CEMD report highlighted the dangers of using family members to act as translators. Translation services were not available to many ethnic minority women and in some instances children were used and key items of information were lost because the woman felt unable to pass on intimate personal health or personal concerns to her health care workers. Women may also need to be put in touch with voluntary organisations that provide the sort of social network that will assist and support them when they are pregnant. The provision of translation services is an enormous challenge for those areas of the country with few ethnic communities. The maternity module of the NSF will address this issue.

The work of NHS Direct

  5.16  NHS direct is doing much work in this area. Each call centre has a contract with an interpreting service provider, ensuring that callers who do not speak English as their first language can have a telephone interpreter present during their consultation, whether the consultation is with a nurse for a symptomatic caller, or with a Health Information Advisor. The interpreting service provides interpreters in whatever language is required, and the service is available 24 hours a day, seven days a week.

  5.17  Call centre staff have desktop access to a comprehensive computerised health information database that contains detailed records of all health information resources held at site level. These resources include topics such as maternity service access, information on pregnancy and care of the newborn, and conditions and treatment of particular relevance to babies and young children. Parents, carers and any other callers can request relevant resources to be read out over the telephone, or to be posted to them, and information will be made available in languages other than English when ever it is possible to source it from trusted information providers. Information can also be made available in formats other than print, including, for example in Braille or on audio tape. All patient information is subject to quality assessment. In addition, each site has comprehensive information in the database, backed up by information on nhs.uk, on local health and social care services, including statutory and voluntary service provision. Callers can be provided with details of all general and specialist services, and this would include maternity services and other provision for pregnant women, parents, and babies and small children.

  5.18  NHS Direct is seeking to improve access to information for those who do not speak English as their first language by establishing an Ethnic Health Information Resource Centre at one site, which will hold stocks of all materials available in languages other than English. In addition, they are reviewing their interpreting and translations service provision, and will be moving to commissioning one national contract for this service, thereby achieving economies of scale and improved quality assurance and training standards. The Department has commissioned consultants to undertake a review of effective service delivery models for providing translation and interpreting support services. The review will assist NHS Direct in developing a tender specification for its national contract and provide a basis for considering how to ensure wider service improvement.

D.   Poverty

  5.19  The effects of poverty on maternal health are well documented. Poor diet and nutrition can lead to low birthweight babies and poor maternal outcomes. Lack of access to public transport can make it extremely difficult for some women to attend antenatal appointments particularly if they have other young children to look after. Loss of income from missing work to attend such appointments can have a dire effect on poor families' budgets.

Reform of Welfare Food Scheme

  5.20  Proposals to reform the 63 year old Welfare Food Scheme were recently put out for consultation following the NHS Plan commitment to reform the Scheme by 2004. The proposals reflect the evidence of the 1999 Committee on Medical Aspects of Food and Nutrition Policy (COMA) scientific review that recommended broadening the nutritional basis of the Scheme in order to ensure that mothers and children in poverty have access to a healthy diet. The proposals also aim to provide increased support for breastfeeding. A report on the responses to consultation will be published in March 2003.

  5.21  It is proposed that the reformed scheme be renamed "Healthy Start" and will come into effect in 2004. In line with the Government's commitment to tackling health inequalities the reformed scheme would provide better nutrition and greater choice in a healthy diet for over 800,000 people in low income families—making the most effective use of the £142 million funding each year in England, Scotland and Wales.

Sure Start

  5.22  Sure Start demonstrates the Government's commitment to deliver the best start in life for every child, better opportunities for parents, affordable, good quality childcare, stronger and safer communities and a cornerstone in the Government's commitment to halve child poverty by 2010. The first Sure Start programme, which was announced in 1998, has worked by bringing together early education, childcare, health and family support to give a sure start to young children living in disadvantaged areas. The Government invested £452 million in Sure Start during the period 1999-2000 to 2001-02. The Spending Review in July 2000 announced an extra £580 million for Sure Start over the period April 2001 to March 2004. This includes £60 million to extend Sure Start to pregnant women and their partners, from the time of conception rather than birth.

E.   Homeless

  5.23  The NHS seeks to offer all patients, ordinarily resident in the UK—including the homeless who so wish, access to free treatment by a GP. This is important for women of childbearing age. A GP is usually the first point of contact when a woman becomes pregnant and the GP acts as a gateway to other services. The Department reminded GPs, in the monthly GP newsletter for February 2003, that a patient does not need to have a permanent address to register for services.

Action to increase access to health care services for homeless people

  5.24  Personal Medical Service Contracts are improving access to primary care by helping the homeless register with GPs. Currently around 86 pilot schemes have the homeless listed as one of their priority objectives. Substantial service improvements are provided across these schemes, particularly with regard to access. Plans are in place for some of the schemes to extend surgeries and clinics, appointment times and consultation times. Closer liaison with Social Services and other stakeholders is also planned.

  5.25  Local Development Schemes (LDS) provide financial support which enables PCTs to use their power to tailor GP contracts to take account of the special needs of particular client groups—eg the homeless. Model LDS schemes were published in 1999 in HSC 1999/107.

  5.26  NHS Walk in Centres are also a key player in the drive to improve access to primary care. Patients can receive immediate, high quality NHS walk in treatment and advice, without having to register, which is of particular benefit for the homeless. Many Walk in Centres are tackling inequalities through nurses developing good relationships with support workers and undertaking outreach work with the homeless to inform what services they can access at the Centre. The national evaluation report published in July on the University of Bristol website showed that they are safe, popular, improved access and reached a different population from traditional general practice. There are currently 42 Walk in Centres in England covering 11 million people.

F  Domestic Violence

  5.27  Violence against women encompasses physical, sexual, emotional and psychological abuse. It is rarely an isolated event and can escalate in severity and frequency during pregnancy. In the context of obstetric care it can cause recurrent miscarriage, stillbirths and maternal deaths. Women who suffer violence are also far less likely to attend for routine antenatal care. It is difficult to ascertain the prevalence of domestic violence as it remains largely unrecognised but the last report of the Confidential Enquiries into Maternal Deaths (CEMD) estimated that about 30% of domestic violence starts during pregnancy and existing abuse often intensifies when a woman is pregnant. As a result, the CEMD has advocated routine questioning about domestic violence during pregnancy, a recommendation the DH is taking seriously.

Departmental initiatives/action

  5.28  In taking this strand of work forward, the Department has recently agreed programme funding for a pilot project to introduce routine questioning on domestic violence during the antenatal period. The University of the West of England and the North Bristol NHS Trust is undertaking this pilot. 80 midwives have been recruited to the study. Outcomes of the Bristol Pilot will be fully evaluated. DH will look closely at emerging findings and consider national roll out as part of the maternity element of the Children's National Service Framework. In the longer term, the maternity module could provide opportunities to extend routine questioning to other areas of the NHS, eg A&E.

  5.29  Prior to this, the Department published "Domestic Violence: A Resource Manual for Health Care Professionals" (March 2000). The Manual gives comprehensive advice and guidance to all health professionals and managers for dealing with domestic violence, including routine questioning of patients. Individual Trusts and Health Authorities are being encouraged to use the Manual in developing their local domestic violence policies and protocols. The Department is funding the Women's Aid Federation of England (WAFE) to help raise awareness of domestic violence and to help implement the Manual in the NHS. A baseline survey of Health Authorities, Trusts and PCGs/Ts in 2000-01 on the extent to which they have policies, protocols and guidelines for good practice indicated some progress over the past few years. For example, over half of all Health Authorities has a designate member of staff for domestic violence issues. DH will look closely at the findings of the latest survey and consider what further steps need to be taken.

  5.30  The Department is also providing funding to the Maternity Alliance Educational and Research Trust to develop training materials for health professionals. Based on women's views and experiences the materials will help health professionals to support their clients who are experiencing domestic violence during pregnancy and early parenthood.

G.   Travellers

  5.31  The CEMD Report found that a disproportionate number of women from the traditional travelling community died in pregnancy or after childbirth. Their relationships with service providers can be strained by mutual distrust and suspicion and this can have a detrimental effect on the health services they receive and influence the take up of services. The maternity module of the Children's NSF will examine how to make services more accessible for this group.

  5.32  The Department of Health is funding the Maternity Alliance (2003-04 £23,700 2004-05 £16,000) to undertake a project on Service take up. The project will work with gypsy and traveller groups, consult with women and with health professionals and produce guidance on service delivery and information materials to encourage these women to make better use of the maternity services.

  5.33  The Department of Health is also funding the organisation Action on Pre-Eclampsia (APEC)—£9,450 for the Pre-Eclampsia Advice for Travellers and Gypsies Project. This project will provide an easy to understand leaflet aimed at travellers and gypsies together with a pamphlet designed for use by community health workers and support groups involved in their welfare. The leaflet will provided information on the signs and symptoms of the condition and where help can be sought.

H.   Mental health

  5.34  The occurrence of mental ill health at or around childbirth is common and any type of disorder may occur postnatally and about twenty are described. The most common is postnatal depression and the most serious puerperal psychosis.

  5.35  It is important to distinguish between the relatively normal occurrence of the "baby blues" and postnatal depression. Baby blues usually occur shortly after childbirth and while they are potentially very distressing to the mother and her family, tend to be self-limiting, short-lived and mild in nature. Estimates of prevalence range from 26-85% depending on how the condition is assessed.

  5.36  Postnatal depression usually begins in the first 12 weeks after birth although it can be emerge any time in the first year. Quoted prevalence rates vary between 10 and 15%, 3 to 5% meet the criteria for depression.

  5.37  Puerperal psychosis is a serious disorder in which depression or mania occurs in the first six weeks after birth; onset is often in the first week postpartum. About two per 1,000 women delivered are admitted to hospital with the condition. There is a greater risk of recurrence of puerperal psychosis and psychotic relapses may also occur postpartum in women who have existing psychotic illnesses such as schizophrenia. Estimates suggest that two per 1,000 of women delivered will be suffering from severe, chronic or enduring mental illness.

  5.38  The women's mental health strategy consultation document that was published in Autumn 2002, highlights that is likely that having a mental health practitioner in each specialist mental health service with an interest in perinatal mental health will lead to the improvement of local service provision, both at primary and specialist level. They could help to develop a community-based multi-disciplinary/multi-agency perinatal mental health service, working in partnership with local communities to build capacity for early identification, support and treatment. This could be underpinned by a care pathway approach for all pregnant women from the booking-in phase, covering mental health promotion, early intervention for vulnerable mothers and follow-up. Care plans for mothers in contact with specialist mental health services should specifically address needs related to their pregnancy.

  5.39  The Implementation Framework for the Strategy that will help services better address the needs of women across a wide range of services will be published in the summer.

  5.40  With regard to more specialised services that, by their very nature, are provided from relatively few providers, PCTs will increasingly have collaborative commissioning arrangements. This will enable them to pool expertise and ensure sufficient dedicated capacity to develop effective health needs assessments, and plan and secure delivery of services. In addition, there is the flexibility within the NHS of making referrals into the private sector if, in the judgement of clinicians and commissioners, an individual's needs warrant this, and the service is an appropriate one. The National Director for Mental Health, Professor Appleby, is leading a review of provision of all specialised mental health care, including Perinatal Psychiatric Services (Mother and Baby Units) and will make recommendations within the next year.

I.   Learning Disabilities

  5.41  The number of people with learning disabilities who are forming relationships and having children has steadily increased over the last 20 years. Parents with learning disabilities are amongst the most socially and economically disadvantaged groups. They are more likely than other parents to make heavy demands on child welfare services and have their children looked after by the local authority. People with learning disabilities can be good parents and provide their children with a good start in life, but may require considerable help to do so. This requires children and adult social services teams to work closely together to develop a common approach. Social services departments have a duty to safeguard the welfare of children, and in some circumstances a parent with learning disabilities will not be able to meet their child's needs. However, we believe this should not be the result of agencies not arranging for appropriate and timely support. The maternity module of the NSF will address the individual needs of these women.

  5.42  The Government White Paper Valuing People: A New Strategy for Learning Disability for the twenty-first Century (2001) is based on four key principles—rights, independence, choice and inclusion. It includes a section on parents with a learning disability. Support for disabled parents, including those with learning disabilities, is patchy and underdeveloped as confirmed in the Social Services Inspectorate inspection "A Jigsaw of Services." In 2002 the DH published good practice guidance on health action plans and health facilitation—key elements of the Valuing People White Paper strategy for reducing the health inequalities faced by people with learning disabilities.

Government funded projects

Maternity Alliance "Parents with Learning Disabilities" Section 64 project

  5.43  Maternity Alliance is in receipt of Section 64 project grant totalling £71,000 over three years (1999 to 2002). This project is linked to an earlier three-year initiative "Right From The Start" which sought to gather information on ways the maternity services could adapt to meet the needs of parents with learning disabilities. The project included the production of an information guide on effective resources such as benefits, housing and so forth, and aimed for the following specific outcomes (1) cross disciplinary work facilitated in the field of learning difficulties (2) increasing awareness of health professionals' of the needs of parents with learning difficulties (3) better maternity care and support for parents with learning difficulties.

Change North

  5.44  Change North recently received a Department of Health grant to produce a booklet for people with learning disabilities entitled "Planning a Baby".

J.   Physical Disabilities

  5.45  Disabled people, when choosing to become parents, often face negative attitudes, an inaccessible environment and support which is inappropriate. The maternity module of the NSF will take into account the needs of women and their families with disabilities.

  5.46  The Government has made its commitment to supporting comprehensive, enforceable civil rights for disabled people and extending basic rights and opportunities in its 1997 and 2001 Manifestos.

Disability Discrimination Act (DDA) 1995

  5.47  Part III of the DDA states that from October 1999, service providers must take reasonable steps to change practices policies, or procedures that make it impossible or unreasonably difficult for disabled people to use a service. From 2004, service providers will have to take reasonable steps to remove, alter, or provide reasonable means of avoiding, physical features that make it impossible or unreasonably difficult for disabled people to use a service.

  5.48  The NHS Executive issued management guidance to NHS Trusts, Health Authorities and Primary Care Groups on implementing Part III of the DDA in July 1999. Health Authorities were asked to develop a strategy to ensure that Section 21 of the DDA was implemented across their premises including hospitals, primary care premises, health centres and clinics. Consultation with disabled people about the development of the strategy needs to be built in at all stages of the programme, including monitoring and review.

NHS Plan

  5.49  The NHS Plan commits the Department of Health to ensuring that public services are equitable and accessible for disabled people. Existing and forthcoming legislation means that DH must take action to:

    —  promote human rights and combat discrimination in all its forms;

    —  support the social and economic integration of disabled people;

    —  increase overall awareness of disability issues and promote the exchange of good practice.

  5.50  Doubly Disabled is a guide to help NHS managers and staff improve their awareness of the needs of disabled people whether they are patients, carers or employees. The guide has five sections and each includes suggestions for specific issues that may require particular attention.

6.  CONCLUSION

  6.1  The focus of the Department's work to reduce inequalities and modernise maternity services will be delivered through the development of the Maternity Module of the Children's NSF.

  6.2  The NSF will develop high quality maternity services which:

    —  reduce health inequalities and inequalities of access;

    —  are woman focused: involving users in all aspects of care and service provision;

    —  maximise normal births;

    —  meet minimum standards for all women and babies;

    —  develop the workforce's skills and competences to provide appropriate care and carer;

    —  enhance communication and teamwork between healthcare professionals and with women;

    —  facilitate maternity information and data collection;

    —  enhance women's choices.

  6.3  The maternity module of the NSF will look at how to make maternity services more flexible, accessible and appropriate by providing a package of care to meet the particular needs of the individual woman and her baby. Emphasis will be made on women's choices in the planning of not only her own care but also the planning of local maternity services.

  6.4  The Maternity Services Module of the Children's National Service Framework is being developed within the context of other Government policy initiatives and is also being developed using the best available evidence, including guidelines issued by the National Institute for Clinical Excellence and drawing on examples of existing good practice.

May 2003


 
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