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		<title>Health Research Policy and Systems - Latest articles</title>
		<link>http://www.health-policy-systems.com</link>
		<description>The latest articles from Health Research Policy and Systems (ISSN 1478-4505) published by 
				
				BioMed Central
		</description>
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				    <rdf:li rdf:resource="http://www.health-policy-systems.com/content/6/1/7"/>			    
            
				    <rdf:li rdf:resource="http://www.health-policy-systems.com/content/6/1/6"/>			    
            
				    <rdf:li rdf:resource="http://www.health-policy-systems.com/content/6/1/5"/>			    
            
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				    <rdf:li rdf:resource="http://www.health-policy-systems.com/content/5/1/14"/>			    
            
				    <rdf:li rdf:resource="http://www.health-policy-systems.com/content/5/1/13"/>			    
            
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		<item rdf:about="http://www.health-policy-systems.com/content/6/1/7">
            
            <title>Asking the right questions: scoping studies in the commissioning of research on the organisation and delivery of health services </title>
			<description>Scoping studies have been used across a range of disciplines for a wide variety of purposes. However, their value is increasingly limited by a lack of definition and clarity of purpose. The UK's Service Delivery and Organisation Research Programme (SDO) has extensive experience of commissioning and using such studies; twenty four have now been completed.
This review article has four objectives; to describe the nature of the scoping studies that have been commissioned by the SDO Programme; to consider the impact of and uses made of such studies; to provide definitions for the different elements that may constitute a scoping study; and to describe the lessons learnt by the SDO Programme in commissioning scoping studies.
Scoping studies are imprecisely defined but usually consist of one or more discrete components; most commonly they are non-systematic reviews of the literature, but other important elements are literature mapping, conceptual mapping and policy mapping. Some scoping studies also involve consultations with stakeholders including the end users of research.
Scoping studies have been used for a wide variety of purposes, although a common feature is to identify questions and topics for future research. The reports of scoping studies often have an impact that extends beyond informing research commissioners about future research areas; some have been published in peer reviewed journals, and others have been published in research summaries aimed at a broader audience of health service managers and policymakers.
Key lessons from the SDO experience are the need to relate scoping studies to a particular health service context; the need for scoping teams to be multi-disciplinary and to be given enough time to integrate diverse findings; and the need for the research commissioners to be explicit not only about the aims of scoping studies but also about their intended uses. This necessitates regular contact between researchers and commissioners.
Scoping studies are an essential element in the portfolio of approaches to research, particularly as a mechanism for helping research commissioners and policy makers to ask the right questions. Their utility will be further enhanced by greater recognition of the individual components, definitions for which are provided. </description>
			<link>http://www.health-policy-systems.com/content/6/1/7</link>
			
			 	<dc:creator>Stuart Anderson, Pauline Allen, Stephen Peckham and Nick Goodwin</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:7</dc:source>
			<dc:date>2008-07-09</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-7</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>7</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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		<item rdf:about="http://www.health-policy-systems.com/content/6/1/6">
            
            <title>Institutional operating figures in basic and applied sciences: Scientometric analysis of quantitative output benchmarking</title>
			<description>Background:
Institutional operating figures and benchmarking systems are important features for the implementation of efficacy in basic and applied sciences. They are needed for research evaluation and funding policy. However, the current policy settings for research evaluation urgently need review since there may be imbalances present in many areas.
Methods:
The present study assessed benchmarking of research output. By the use of large data bases research output was categorized and analyzed. Specific areas of major research activity were identified by comparing publication density on different organ systems and inter- and intrafield comparison was performed for selected countries.
Results:
Novel density-equalizing mappings were constructed that illustrate trends of publication activity and identify subsets of major interest in a total of 5,527,558 published items. A dichotomy was present between Western countries such as the US, UK or Germany and Asian countries such as Japan, China or South Korea concerning research focuses.
Conclusion:
The present study is the first large scale analysis of global research activity and output over the last 50 years. The presently described assessment of operating figures at the national and international level can be used to identify single areas of research that are heavily focused. Further research on qualitative output benchmarking is needed to improve current policy settings for research evaluation.</description>
			<link>http://www.health-policy-systems.com/content/6/1/6</link>
			
			 	<dc:creator>Beatrix Groneberg-Kloft, Cristian Scutaru, Carolin Kreiter, Silvana K&#246;lzow, Axel Fischer and David Quarcoo</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:6</dc:source>
			<dc:date>2008-06-13</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-6</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>6</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-13</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.health-policy-systems.com/content/6/1/5">
            
            <title>The Quality Improvement Demonstration Study: An example of evidence-based policy-making in practice</title>
			<description>Background:
Randomized trials have long been the gold-standard for evaluating clinical practice. There is growing recognition that rigorous studies are similarly needed to assess the effects of policy. However, these studies are rarely conducted. We report on the Quality Improvement Demonstration Study (QIDS), an example of a large randomized policy experiment, introduced and conducted in a scientific manner to evaluate the impact of large-scale governmental policy interventions.
Methods:
In 1999 the Philippine government proposed sweeping reforms in the National Health Sector Reform Agenda. We recognized the unique opportunity to conduct a social experiment. Our ongoing goal has been to generate results that inform health policy. Early on we concentrated on developing a multi-institutional collaborative effort. The QIDS team then developed hypotheses that specifically evaluated the impact of two policy reforms on both the delivery of care and long-term health status in children. We formed an experimental design by randomizing matched blocks of three communities into one of the two policy interventions plus a control group. Based on the reform agenda, one arm of the experiment provided expanded insurance coverage for children; the other introduced performance-based payments to hospitals and physicians. Data were collected in household, hospital-based patient exit, and facility surveys, as well as clinical vignettes, which were used to assess physician practice. Delivery of services and health status were evaluated at baseline and after the interventions were put in place using difference-in-difference estimation.
Results:
We found and addressed numerous challenges conducting this study, namely: formalizing the experimental design using the existing health infrastructure; securing funding to do research coincident with the policy reforms; recognizing biases and designing the study to account for these; putting in place a broad data collection effort to account for unanticipated findings; introducing sustainable policy interventions based on the reform agenda; and providing results in real-time to policy makers through a combination of venues.
Conclusion:
QIDS demonstrates that a large, prospective, randomized controlled policy experiment can be successfully implemented at a national level as part of sectoral reform. While we believe policy experiments should be used to generate evidence-based health policy, to do this requires opportunity and trust, strong collaborative relationships, and timing. This study nurtures the growing attitude that translation of scientific findings from the bedside to the community can be done successfully and that we should raise the bar on project evaluation and the policy-making process.</description>
			<link>http://www.health-policy-systems.com/content/6/1/5</link>
			
			 	<dc:creator>Riti Shimkhada, John W Peabody, Stella A Quimbo and Orville Solon</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:5</dc:source>
			<dc:date>2008-03-25</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-5</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>5</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-25</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.health-policy-systems.com/content/6/1/4">
            
            <title>Exploring evidence-policy linkages in health research plans: A case study from six countries</title>
			<description>The complex evidence-policy interface in low and middle income country settings is receiving increasing attention. Future Health Systems (FHS): Innovations for Equity, is a research consortium conducting health systems explorations in six Asian and African countries: Bangladesh, India, China, Afghanistan, Uganda, and Nigeria. The cross-country research consortium provides a unique opportunity to explore the research-policy interface. Three key activities were undertaken during the initial phase of this five-year project. First, key considerations in strengthening evidence-policy linkages in health system research were developed by FHS researchers through workshops and electronic communications. Four key considerations in strengthening evidence-policy linkages are postulated: development context; research characteristics; decision-making processes; and stakeholder engagement. Second, these four considerations were applied to research proposals in each of the six countries to highlight features in the research plans that potentially strengthen the research-policy interface and opportunities for improvement. Finally, the utility of the approach for setting research priorities in health policy and systems research was reflected upon. These three activities yielded interesting findings. First, developmental consideration with four dimensions &#8211; poverty, vulnerabilities, capabilities, and health shocks &#8211; provides an entry point in examining research-policy interfaces in the six settings. Second, research plans focused upon on the ground realities in specific countries strengthens the interface. Third, focusing on research prioritized by decision-makers, within a politicized health arena, enhances chances of research influencing action. Lastly, early and continued engagement of multiple stakeholders, from local to national levels, is conducive to enhanced communication at the interface. The approach described has four main utilities: first, systematic analyses of research proposals using key considerations ensure such issues are incorporated into research proposals; second, the exact meaning, significance, and inter-relatedness of these considerations can be explored within the research itself; third, cross-country learning can be enhanced; and finally, translation of evidence into action may be facilitated. Health systems research proposals in low and middle income countries should include reflection on transferring research findings into policy. Such deliberations may be informed by employing the four key considerations suggested in this paper in analyzing research proposals.</description>
			<link>http://www.health-policy-systems.com/content/6/1/4</link>
			
			 	<dc:creator>Shamsuzzoha B Syed, Adnan A Hyder, Gerald Bloom, Sandhya Sundaram, Abbas Bhuiya, Zhang Zhenzhong, Barun Kanjilal, Oladimeji Oladepo, George Pariyo, David H Peters and Future Health Systems: Innovation for Equity</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:4</dc:source>
			<dc:date>2008-03-11</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-4</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>4</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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		<item rdf:about="http://www.health-policy-systems.com/content/6/1/3">
            
            <title>From inclusion to independence &#8211; Training consumers to review research</title>
			<description>Health and medical research invariably impacts on the lives of everyday people. Organisations in the developed world are increasingly involving the public in health research projects, and research governance structures and processes. The form the involvement takes varies, as does the level of involvement, from individuals, to groups, to the wider community. Lay community members can be trained to independently review health and medical research, and wider societal involvement in funding decisions, can be effectively fostered. The theoretical foundation, design and development of a task based consumer-training program, including a number of enabling factors to support the success of such training are presented. This work is likely to be of value to those planning to train consumers in technical or complex areas.</description>
			<link>http://www.health-policy-systems.com/content/6/1/3</link>
			
			 	<dc:creator>Carla Saunders, Afaf Girgis, Phyllis Butow, Sally Crossing and Andrew Penman</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:3</dc:source>
			<dc:date>2008-03-09</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-3</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>3</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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		<item rdf:about="http://www.health-policy-systems.com/content/6/1/2">
            
            <title>Freedom and need: The evolution of public strategy for biomedical and health research in England</title>
			<description>The optimal support of health-related research and development with public money is a complex challenge. Over the last century, policy makers in England have conceived and implemented a variety of models, ranging from independent, curiosity driven research to needs-based state commissions, and promoting different bodies to oversee scientific work. This paper traces these approaches, identifies the principles that drove them, and discusses their role in shaping policy for publicly funded health research, up to the recent launch of a new research strategy by the Department of Health.</description>
			<link>http://www.health-policy-systems.com/content/6/1/2</link>
			
			 	<dc:creator>Miriam Shergold and Jonathan Grant</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:2</dc:source>
			<dc:date>2008-01-29</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-2</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>2</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-01-29</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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		<item rdf:about="http://www.health-policy-systems.com/content/6/1/1">
            
            <title>Why national health research systems matter</title>
			<description>-</description>
			<link>http://www.health-policy-systems.com/content/6/1/1</link>
			
			 	<dc:creator>Stephen R Hanney and Miguel A Gonz&#225;lez Block</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2008, 6:1</dc:source>
			<dc:date>2008-01-11</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-6-1</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>1</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-01-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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		<item rdf:about="http://www.health-policy-systems.com/content/5/1/14">
            
            <title>Housing, income support and mental health: Points of disconnection</title>
			<description>There exists a disconnection between evolving policies in the policy arenas of mental health, housing, and income support in Canada. One of the complexities associated with analysing the intersection of these policies is that federal, provincial, and municipal level policies are involved. Canada is one of the few developed countries without a national mental health policy and because of the federal policy reforms of the 1970s, the provincial governments now oversee the process of deinstitutionalization from the hospital to the community level. During this same period the availability of affordable housing has decreased as responsibility for social housing has been transfered from the federal government to the provincial and/or municipal levels of government. Canada also stands alone in terms of being a developed nation without national housing policy instead what is considered "affordable" housing is partially dependant upon individuals' personal economic resources. As well, over the past decade rates of income supports have also been reduced. Psychiatric survivors have long been identified as being at risk for homelessness, with the disconnection existing between housing, income and mental health policies and the lack of a national policy in any of these policies areas further contributing to this risk.</description>
			<link>http://www.health-policy-systems.com/content/5/1/14</link>
			
			 	<dc:creator>Cheryl Forchuk, Libbey Joplin, Ruth Schofield, Rick Csiernik, Carolyne Gorlick and Katherine Turner</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2007, 5:14</dc:source>
			<dc:date>2007-12-12</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-5-14</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>5</prism:volume>
					
			
							
					<prism:startingPage>14</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-12-12</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.health-policy-systems.com/content/5/1/13">
            
            <title>Comparative health systems research in a context of HIV/AIDS: lessons from a multi-country study in South Africa, Tanzania and Zambia</title>
			<description>Comparative, multi-country research has been underutilised as a means to inform health system development. South-south collaboration has been particularly poor, even though there have been clearly identified benefits of such endeavours. This commentary argues that in a context of HIV/AIDS, the need for regional learning has become even greater. This is because of the regional nature of the problem and the unique challenges that it creates for health systems. We draw on the experience of doing comparative research in South Africa, Tanzania and Zambia, to demonstrate that it can be useful for determining preconditions for the success of health care reforms, for affirming common issues faced by countries in the region, and for developing research capacity. Furthermore, these benefits can be derived by all countries participating in such research, irrespective of differences in capacity or socio-economic development.</description>
			<link>http://www.health-policy-systems.com/content/5/1/13</link>
			
			 	<dc:creator>Suraya Dawad and Nina Veenstra</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2007, 5:13</dc:source>
			<dc:date>2007-10-30</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-5-13</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>5</prism:volume>
					
			
							
					<prism:startingPage>13</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-10-30</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.health-policy-systems.com/content/5/1/12">
            
            <title>Participation and argument in legislative debate on statewide smoking restrictions</title>
			<description>Background:
In this paper we review the relationship between participation in legislative hearings, the use of ideological arguments, and the strength of public health legislation using a theoretical construct proposed by E. E. Schattschneider in 1960. Schattschneider argued that the breadth and types of participation in a political discussion could change political outcomes.
Methods:
We test Schattschneider's argument empirically by reviewing the efforts of six states to pass Clean Indoor Air Acts by coding testimony given before legislators, comparing these findings to the different characteristics of each state's political process and the ultimate strength of each state's legislation.
Results:
We find that although greater participation is associated with stronger legislation, there is no clear relationship between the use and type of ideological arguments and eventual outcomes.
Conclusion:
These findings offer validation of a long-standing theory about the importance of political participation, and suggest strategies for public health advocates seeking to establish new legislation.</description>
			<link>http://www.health-policy-systems.com/content/5/1/12</link>
			
			 	<dc:creator>Dorie E Apollonio, Peggy Lopipero and Lisa A Bero</dc:creator>
			
			<dc:source>Health Research Policy and Systems 2007, 5:12</dc:source>
			<dc:date>2007-10-22</dc:date>
			<dc:identifier>doi:10.1186/1478-4505-5-12</dc:identifier>
			
			
							
					<prism:publicationName>Health Research Policy and Systems</prism:publicationName>
					
			
							
					<prism:issn>1478-4505</prism:issn>
					
			
							
					<prism:volume>5</prism:volume>
					
			
							
					<prism:startingPage>12</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-10-22</prism:publicationDate>
					

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