Monitoring equity and research policy

Small states: Economic review and basic statistics, volume 14
Commonwealth Secretariat: September 2010

This annual collection of key economic and statistical data on states with fewer than five million inhabitants is designed as a reference for economists, planners and policy-makers. The book contains fifty-four tables covering selected economic, social, demographic and Millennium Development Goal indicators culled from international and national sources and presents information unavailable elsewhere. A detailed parallel commentary on trends in Commonwealth small states, looking at growth, employment, inflation, human development, and economic policy, permits a deeper understanding of developments behind the figures. The book also includes three articles focusing on trade in services.

South African Child Gauge 2009/2010
Kibel M, Lake L, Pendlebury P and Smith C (eds): Children's Institute, University of Cape Town, May 2010

South Africa is one of only 12 countries that has failed to reduce child mortality since 1990, according to the South African Child Gauge 2009/2010, an annual review of the situation of children in the country. The review contains essays by child health experts from across the country. While South Africa is making progress towards meeting the Millennium Development Goal (MDG) target on sustainable access to safe drinking water, this has not trickled down to children: Only 64% of children have access to safe drinking water on site. Progress has been slow for access to basic sanitation, education and gender equality. On the MDG targets for reducing child hunger, HIV, tuberculosis and child mortality, South Africa is not making any progress. South Africa has also failed to submit its reports on progress in relation to implementing the United Nations Convention of the Rights of the Child – the key accountability mechanism aimed at monitoring South Africa’s progress in promoting the maximum survival and development of children. Improving child health outcomes requires concerted action from both within and outside the formal health care system. To reduce child mortality, governments should alleviate poverty and eliminate inequality, as well as improve the performance of its health services, and medical interventions should focus on prevention and encourage the participation of children.

Assessing equity in systematic reviews: Realising the recommendations of the Commission on Social Determinants of Health
Tugwell P, Petticrew M, Kristjansson E, Welch V, Ueffing E and Waters E et al: British Medical Journal 341(c4739), 13 September 2010

The Commission on Social Determinants for Health has recommended assessment of health equity effects of public policy decisions, and this study provides guidance on assessing equity for users and authors of systematic reviews of interventions. Particular challenges occur in seven components of such reviews: developing a logic model; defining disadvantage and for whom interventions are intended; deciding on appropriate study design(s); identifying outcomes of interest; process evaluation and understanding context; analysing and presenting data; and judging applicability of results. The study concludes that greater focus on health equity in systematic reviews may improve their relevance for both clinical practice and public policy making.

Casebook on ethical issues in international health research
Cash R, Wikler D, Saxena A and Capron A (eds): World Health Organization, 2009

This compilation of case studies in research ethics is designed for use by course instructors and workshop leaders. The editors argue that the use of case studies in workshops and formal courses is an especially valuable teaching tool, as students and workshop participants can grapple with ethical dilemmas and uncertainties in concrete situations. The editors have collected 64 case studies, based on episodes that have occurred in global health research throughout the world. Eight chapters comprise the cases un¬der the following titles: Defining research; Issues in study design; Harm and benefit; Voluntary informed consent; Standard of care; Obligations to participants and communities; Privacy and confidential¬ity; and Professional ethics. Each chapter begins with an introduction that outlines the issues and provides some guidance for the topics addressed in the cases, and ends with a brief annotated list of suggested readings. Questions for discussion follow each case. In each chapter there is cross-referencing to cases in other chapters.

Does South Africa need a national clinical trials support unit?
Siegfried N, Volmink J and Dhansay A: South African Medical Journal 100(9): 521–524, August 2010

No national South African institution provides a coherent suite of support, available skills and training for clinicians wishing to conduct randomised controlled trials (RCTs) in the public sector. This study assesses the need for establishing a national South African Clinical Trials Support Unit. Key informant interviews were conducted with senior decision-makers at institutions with a stake in the South African public sector clinical trials research environment. The study found that trial conduct in South Africa faces many challenges, including lack of dedicated funding, the burden on clinical load, and lengthy approval processes. Strengths include the high burden of disease and the prevalence of treatment-naïve patients. Participants expressed a significant need for a national initiative to support and enhance the conduct of public sector RCTs. Research methods training and statistical support were viewed as key. There was a broad range of views regarding the structure and focus of such an initiative, but there was agreement that the national government should provide specific funding for this purpose. In conclusion, stakeholders generally support the establishment of a national clinical trials support initiative. Consideration must be given to the sustainability of such an initiative, in terms of funding, staffing, expected research outputs and permanence of location.

Levels and trends in child mortality, 1990-2009
You D, Jones G, Hill K, Wardlaw T and Chopra M: The Lancet 376(9745): 931–933, 18 September 2010

According to this article, the latest estimates of under-five mortality from the United Nations Inter-agency Group for Child Mortality Estimation (IGME) show a one-third decline at the global level of under-five mortality rates from 89 deaths per 1000 livebirths in 1990 to 60 in 2009. Over the same period, the total number of under-five deaths has decreased from 12.4 million in 1990 to 8.1 million in 2009. The article argues that this constitutes evidence that progress on child mortality is being made across all regions of the world, with many regions having reduced the under-five mortality rate by 50% or more. With only five years left until the 2015 deadline to achieve the Millennium Development Goals (MDGs), progress needs to be accelerated. These IGME estimates are the latest available information on child mortality to provide a basis for assessing progress and reaching consensus for action.

Overview of research activities associated with the World Health Organization: Results of a survey covering 2006/07
Terry RF and Rijt TV: Health Research Policy and Systems 8(25), 6 September 2010

This paper presents the first comprehensive effort to provide an overview of the research associated with the World Health Organization (WHO) headquarters in 2006/07. Information was obtained by questionnaire and interviews with senior staff operating at WHO headquarters in Geneva. The paper found that 45% of WHO permanent staff are involved with health research and the WHO's approach to research is predominantly focused on policy, advocacy, health systems and population based research. The Organization principally undertakes secondary research using published data and commissions others to conduct this work through contracts or research grants. This approach is broadly in line with the stated strategy of the Organization. The researchers note that the difficulty in undertaking this survey highlights the complexity of obtaining an organisation-wide assessment of WHO’s research activity in the absence of common standards for research classification, methods for priority setting and a mechanism across WHO, or within the governance of global health research more generally, for managing a research portfolio. As the rollout of the WHO strategy on research for health proceeds, the researchers expressed hope that similar exercises will be undertaken at the WHO Regional Offices and in support of capacity building of national health research systems within Member States.

Access to Medicine Index 2010
Access to Medicine Foundation: 2010

The Access to Medicine Index independently assesses how individual pharmaceutical companies perform in promoting universal access to essential medicines, and may be used as a tool in improving performance. The 2010 ranking reveals important progress, if only because companies have shown far greater willingness to open up. The Index unveils improvements research and development, and pricing, but also shows that the industry as a whole still has a long way to go, according to Wim Leereveld, the Index's founder. The Access to Medicine Index ranks 20 of the world's largest pharmaceutical companies on their efforts to make sure that medicines are made for, and reach, people in developing countries. The Index encourages drug companies to compete and offers investors and others a way to compare their social responsibility records.

Global Forum for Health Research, Forum 2009: Innovating for the Health of All
Jupp S: MEDICC Review 12(3): 5–7, July 2010

This article discuss the work of the Global Forum, a global body of health decision-makers that focuses on questions of equity, advocating for more research to address the health problems of those most in need – essentially the poor and marginalised –and providing evidence to support greater investments in neglected areas. Since the Forum’s previous conference in 2009, the article notes that a paradigm shift has taken place from ‘health research’ to ‘research for health’. This new approach promotes greater understanding among all stakeholders of the impact on health of policies, programmes, processes, actions or events originating from other sectors. It also is intended to assist in developing interventions that will help prevent or mitigate any adverse impact on health and contribute to the achievement of health equity. While the number of resources, actors and efforts to address the health problems of the poor have grown signifi cantly in recent years, the range of health challenges faced by low- and middle-income countries has expanded considerably, demanding a more extensive research portfolio. Challenges include countries that are not on track to reaching the Millennium Development Goals, rising rates of chronic non-communicable diseases in low- and middle-income countries, urbanisation, demographic shifts, climate change, food security, the threat of pandemics, and the global financial crisis.

Making the web work for scientific research
Science Online London, 16 August 2009

In preparation for the Science Online London 2010 Conference, which will be held from 3-4 September 2010 in London, United Kingdom, this video provides information on how the web is changing the way researchers conduct, communicate, share, and evaluate their work. The video is a panel discussion with Jimmy Watson, Stephen Friend and John Wilbanks, which is moderated by Tim O’Reilly. Some of the topics they talk about will also be discussed at Science Online London, such as new platforms for collaboration, networking and sharing research.

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