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putting patients in control: An update on the implementation of patient choice in the NHS since it was introduced at the start of 2006, focusing on the experiences of patients and NHS staff.
The Local Government and Public Involvement in Health Bill received Royal Assent yesterday, heralding a fresh approach to giving people a say in their local health services. As of April, existing Patient and Public Involvement Forums and their co-ordinating body, the Commission for Patient and Public Involvement in Health (CPPIH) will be replaced with 150 Local Involvement Networks (LINks). The legislation also updates and strengthens the duty on NHS bodies to involve and consult local communities about changes to services. Backed up by £84 million over three years, LINks will make it easier for communities to influence key decisions about local health servivces and hold those services to account. Run by local people, each LINk will cover all the publically funded health and social care services in a local authority area - irrespective of who provides them. LINks will: • aim to represent everyone in the community - not just existing activists but also those not currently being heard; • have the power to investigate issues of concern, demand information, enter and view services, make reports and recommendations, and refer issues to local councillors; and • provide a one-stop-shop for the community to engage with care professionals and vice versa. In addition, the legislation changes the existing duty to consult by clarifying the notion of a ‘significant’ change to services, so that NHS bodies know when they should consult. It also gives PCTs a new statutory duty to respond to local people, explaining the activities they are undertaking as a result of patient and public feedback on their services. Health minister Ann Keen said: "We know that input from the people who use them leads to better services. Building on the work of Patients' Forums, these changes are aimed at promoting open and transparent communication between communities and the health service. By increasing the NHS's accountability to local people, we want to develop people's trust and confidence that their opinions will be heard. "If more people are going to get involved in shaping services, the process must be convenient and result in real changes. LINks will be run by local people who will be asking their communities about their views on local health services, investigating specific issues and using their powers to hold services to account. People will be able to influence key decisions about how care services are planned and run." Councillor David Rogers, Chair of the Local Government Association’s Community Well-being Board, said: "This announcement is a needed and necessary step towards ensuring local health services are publically accountable. Local Involvement Networks can offer a more integrated approach to health and social care provided sufficient support and effective scrutiny arrangements are in place. “This additional funding will give councils the green light to continue to commission the work already happening across the country to build the foundations for first class patient and public involvement in health and social care". Maggie Alexander, Director of Policy and Campaigns and Breakthrough Breast Cancer said: "Breakthrough Breast Cancer believes that patient and public involvement in shaping NHS services is vitally important. Members of Breakthrough's Campaigns & Advocacy Network have shown what a real difference they can make when they are involved in local healthcare decisions. "We hope that LINks will help the NHS engage patients and the public more in shaping local health services so that what is provided accurately reflects the needs and wishes of those it is trying to help. Only then will we move closer to a service that is genuinely patient-led - helping everyone get the best out of their NHS." Chris Brace, Director of Campaigns for the disability network RADAR, said: "Understanding and incorporating real information about peoples' needs and expectations must be at the forefront of all policies and practices in health and social care services. The Patient Forums have made great strides towards this, and the LINks principles of extending the consultation process ever-wider must be the right way forward. "We know that there are areas where some people are still left behind. The key to LINks achieving real improvement must be working with networks of voluntary organisations to place power and influence where they belong - in the hands of people with direct experience of using health and social services." Bill Freeman, Director of Development at the National Association for Voluntary and Community Action (NAVCA) said: "We welcome this announcement and strongly support the emphasis on improving local community involvement and accountability over the direction of health and social care services. Local third sector organisations have a strong track record of supporting people in their communities to have a voice and we will be encouraging them to help LINks engage with all members of the community, especially those that are seldom heard in policy making and service design.” Notes to editors • Since 2003, one of the main tools the NHS has used to listen to patients has been Patients’ Forums. Although Forums - with one attached to each health trust - have done much to help improve front-line services, they have also suffered from limitations that have stopped them being as effective as they could be. For example, Patients' Forums currently have no remit over social care services run by local authorities. • In July last year, the Department of Health published A stronger local voice: A framework for creating a stronger voice in the development of health and social services. This set out proposals for replacing Patients' Forums with LINks. www.dh.gov.uk • There will be one LINk per local authority area - 150 in total. The Government is making £84million available to support the national programme for the establishment of LINks. Most of this funding will go to local authorities. The funding that each area receives will depend on factors such as population and deprivation. Details will be announced shortly. • The Act also introduces a new requirement for PCTs and local authorities to produce a Joint Strategic Needs Assessment (JSNA) which will describe the future health and wellbeing needs of their local populations and will help local authorities and PCTs decide how best to meet those needs/provide those services through their next local area agreements. • Media enquiries to the Department of Health News Desk 020 7210 5221. General enquiries to 020 7210 4850. [ENDS]
The independent inquiry into access to healthcare for people with learning disabilities has invited written information from professionals, people with learning disabilities, their carers, families and all others with an interest in ensuring adults and children with learning disabilities receive appropriate treatment in the NHS. Information about how to respond to the call for evidence is available at: www.iahpld.org.uk (opens new window) About the Inquiry The Secretary of State for Health established an Independent Inquiry into Access to Healthcare for People with Learning Disabilities on 31 May 2007 to identify the action needed to ensure adults and children with learning disabilities receive appropriate treatment in acute medical (hospital) care and general primary care (not specialist learning disability or mental health services). The establishment of the Inquiry follows the publication of Death by Indifference by Mencap and the Disability Rights Commission’s formal investigation into health inequalities experienced by people with learning disabilities and people with mental health problems. The Inquiry is chaired by Sir Jonathan Michael MB, BS; FRCP:(Lond); FKC, who is the Deputy Managing Director of BT Health and formerly the Chief Executive of Guy's and St Thomas' NHS Foundation Trust and University Hospitals Birmingham NHS Trust. Sir Jonathan is supported by two panels: a panel of experts on health and social care services: Mr Chris Davies CBE, Consultant in Social Care/Lead Advisor, Social Services Agency, Wales Mr Len Fenwick CBE, Chief Executive, Newcastle upon Tyne Hospitals NHS Foundation Trust Prof Sheila Hollins, President, Royal College of Psychiatrists Prof Jim Mansell, Professor of Applied Psychology of Learning Disability, Tizard Centre, University of Kent Dr John Moxham, Medical Director, King’s College Hospital NHS Foundation Trust Ms Anne Norman, Professional Adviser for Learning Disabilities, Royal College of Nursing Ms Joan Saddler, Chair, Waltham Forest Primary Care Trust and a panel of people with learning disabilities who have experience of using health services: Mr Paul Adeline, Training advisor at St George's, University of London Ms Michelle Chinery, Independent consultant and former co-chair of the Learning Disability Task Force Ms Jackie Downer MBE, Campaigner and advocate for the rights of people with learning disabilities Ms Karen Flood, Independent consultant and co-chair of the National Forum of People with Learning Disabilities Mr Fahad Matabdin, Self-advocate and campaigner for the rights of people with learning disabilities Mr Michael Ratcliffe, Independent consultant and member of the National Forum of People with Learning Disabilities The Inquiry held two workshops with carers of people with learning disabilities in October 2007 to ensure that their views are fed into its work. It will also take careful account of any information that The Parliamentary and Health Service Ombudsman shares as she undertakes an independent investigation of the six cases highlighted in Death by Indifference. The Inquiry aims to report in June 2008.
Key Findings • There are around 86 volunteers within Wirral PCT. They operate from 5 sites, and within the community. The volunteers assist with the provision of 12 different services. • The volunteers spend an average of 6.11 hours a week volunteering. • This suggests an economic value for volunteering within the PCT of £313,461 a year. • The costs to the PCT of supporting volunteers are approximately £32,359 • For every £1 spent supporting volunteering, £9.69 of value can be said to have been created. • Volunteers tend to be female (73%) and retired, only 5 (15%) respondents were aged under 55 • The most popular reason for volunteering at Wirral PCT is “to give something back” (39%) • Volunteers are happy with the support they receive. 94% are aware of what is expected of them. 91% know who to contact if problems arise. 81% get support whenever they need it. • 81% of volunteers feel that patients value their contribution. 78% feel that staff value their contribution. • Less than half the volunteers have access to training that is relevant to their task description. Those that do receive training are happy with the quality of provision • Some Volunteers noted that there is too much red tape involved in volunteering. This relates especially to the recruitment and selection process. • The main benefits of volunteering to the volunteer are feeling good about oneself as a result of helping others. • A small number of volunteers (4 of the 5 aged under 55) felt that volunteering improved their prospects of finding paid employment. All those who have volunteered at Teddy Bears play group in the past have progressed into paid employment, usually in the childcare sector. • Volunteering has a positive impact on perceptions of physical health for one in four volunteers, and mental health for 29% of the volunteers. • Volunteering is particularly important for 87% of respondents in helping volunteers make new friends. • 76% of paid staff feel that volunteers enhance the Trust’s reputation in the community, and 81% feel that the volunteers are good ambassadors for the Trust. • In general staff are happy with the contribution of the volunteers. 87% are satisfied with the amount of services they provide. 93% are satisfied with the quality of services provided by volunteers. • 61% of staff feel volunteers enable staff to concentrate on service provision. • There is no significant opposition to using volunteers in the PCT from those staff responding to the survey. • 87% of staff recognise that by working closely with volunteers, they are able to provide a better level of service. • Mothers attending Teddy Bears play group would like to see more volunteers taking on more roles. • Staff involved with Teddy Bears recognise that without volunteers the service could not continue • The volunteers at Teddy Bears play a part in providing a cost effective service to the local community, in partnership with the PCT and local church.
DH INFORMATION READER BOX Policy Estates HR/Workforce Commissioning Management IM & T Planning Finance Clinical Social care/partnership working Document purpose Policy Gateway reference 9087 Title Healthy Weight, Healthy Lives: a Cross-Government Strategy for England Author Cross-Government Obesity Unit, Department of Health and Department of Children, Schools and Families Publication date 23 January 2008 Target audience PCT CEs, Directors of PH, Local Authority CEs, Directors of Adult SSs, Directors of HR Circulation list NHS Trust CEs, SHA CEs, Care Trust CEs, Foundation Trust CEs, Medical Directors, Directors of Nursing, Directors of Adult SSs, PCT PEC Chairs, NHS Trust Board Chairs, Special HA CEs, Directors of Finance, Allied Health Professionals, GPs, Communications Leads, Directors of Children’s SSs, Voluntary Organisations/ NDPBs Description This cross-government strategy is the first step in a sustained programme to support people to maintain a healthy weight. It will be followed by a public annual report that assesses progress, looks at the latest evidence and trends, and makes recommendations for further action. Cross reference N/A Superseded documents N/A Action required N/A Timing N/A Contact details Cross-Government Obesity Unit Room 708, Wellington House Waterloo Road, London SE1 8UG www.dh.gov.uk/obesity For recipient’s use © Crown copyright 2008 First published January 2008 Produced by COI for the Department of Health and the Department for Children, Schools and Families The text of this document may be reproduced without formal permission or charge for personal or in-house use. www.dh.gov.uk/publications
The Council of Ethnic Minority Voluntary Sector Organisations (CEMVO) is a national infrastructure registered charity established in 1999. We act as an advocate and expert advisor and are committed to the social regeneration of disadvantaged minority ethnic (ME) communities in England, Scotland and Wales. CEMVO aims to strengthen and support the Minority Ethnic voluntary and community sector by building and enhancing their capacity and by contributing to policy debates through the development of key areas of research. We work towards securing the social regeneration of ME communities by securing more resources and developing the management capacity within the sector. As a way of providing a voice for ME communities, CEMVO develops key areas of research in relation to ME issues to lobby government and other agencies on policy issues. We also develop the ME voluntary and community sector by actively promoting networking and the sharing of best practice within the sector to increase social capital and address concerns facing ME communities in health, education, income and housing. CEMVO welcomes the opportunity to comment on the position of volunteering in health, and hope that thee comments will make a positive contribution to the work being undertaken by Baroness Neuberger. 1. What is the extent and variety of the volunteering that already happens in the health service? CEMVO’s experience of delivering our National Health Service Volunteering programme demonstrates that this is something that is very varied. We currently engage with 40 hospitals in the South West, North East and North West of England. All these hospitals are situated in inner city and diverse communities, and our work indicates that there is sadly a great variation in both extent and variety of volunteering opportunities. This has a direct impact on some of the most marginalised communities in society today. Our experience, for example indicates that volunteering is an activity which is generally not mainstreamed within the core business of running a hospital, and is a function, which we believe would benefit from greater recognition as for example, Human Resources. We also believe that there is scope for greater innovation in relation to the creation and development of volunteering opportunities, which would in turn attract more diverse candidates to volunteering. We would therefore state the following: • The extent of volunteering in the health services in our opinion is a matter which would benefit from a mapping exercise in order to establish an accurate picture of the current state of affairs. For example, patterns of volunteering in this sector indicate that this is an activity which is not necessarily accessible, flexible, enabling, and representative of our diverse communities.
Volunteers across the NHS- Improving the Patient experience and creating a patient-led service publication
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