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		<title>BMC Public Health - Latest articles</title>
		<link>http://www.biomedcentral.com/bmcpublichealth/</link>
		<description>The latest articles from BMC Public Health (ISSN 1471-2458) published by 
				
				BioMed Central
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				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/161"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/160"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/159"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/158"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/157"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/156"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/155"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/154"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2458/8/153"/>			    
            
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		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/161">
            
            <title>Risk factors for incomplete vaccination and missed opportunity for immunization in rural Mozambique.</title>
			<description>Background:
Inadequate levels of immunization against childhood diseases remain a significant public health problem in resource-poor areas of the globe. Nonetheless, the reasons for incomplete vaccination and non-uptake of immunization services are poorly understood. This study aimed at finding out the reasons for non-vaccination and the magnitude of missed opportunities for vaccination in children less than two years of age in a rural area in southern Mozambique. Methods: Mothers of children under two years of age (N= 668) were interviewed in a cross-sectional study. The Road-to-Health card was utilized to check for completeness and correctness of vaccination schedule as well as for identifying the appropriate use of all available opportunities for vaccination. The chi-square test and the logistic regression were used for statistical analysis. Results: We found that 28.2% of the children had not completed the vaccination program by two years of age, 25.7% had experienced a missed opportunity for vaccination and 14.9% were incorrectly vaccinated. Reasons for incomplete vaccination were associated with accessibility to the vaccination sites, no schooling of mothers and children born at home or outside Mozambique. Conclusions: Efforts to increase vaccination coverage should take into account factors that contribute to the incomplete vaccination status of children. Missed opportunities for vaccination and incorrect vaccination need to be avoided in order to increase the vaccine coverage for those clients that reach the health facility, specially in those countries where health services do not have 100% of coverage.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/161</link>
			
			 	<dc:creator>Jagrati V. Jani, Caroline De Schacht, Ilesh V. Jani and Gunnar Bjune</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:161</dc:source>
			<dc:date>2008-05-16</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-161</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>161</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-16</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/160">
            
            <title>Implications for Registry-Based Vaccine Effectiveness Studies from an Evaluation of an Immunization Registry: A Cross-sectional Study</title>
			<description>Background:
Population-based electronic immunization registries create the possibility of using registry data to conduct vaccine effectiveness studies which could have methodological advantages over traditional observational studies.  For study validity, the base population would have to be clearly defined and the immunization status of members of the population accurately recorded in the registry.  We evaluated a city-wide immunization registry, focusing on its potential as a tool to study pertussis vaccine effectiveness, especially in adolescents.  
Methods:
We conducted two evaluations--one in sites that were active registry participants and one in sites that had implemented an electronic medical record with plans for future direct data transfer to the registry--of the ability to match patients' medical records to registry records and the accuracy of immunization records in the registry.   For each site, records from current pediatric patients were chosen randomly.  Data regarding pertussis-related immunizations, clinic usage, and demographic and identifying information were recorded; for 11-17-year-old subjects, information on MMR, hepatitis B, and varicella immunizations was also collected.  Records were then matched, when possible, to registry records.  For records with a registry match, immunization data were compared.  
Results:
Among 350 subjects from sites that were current registry users, 307 (87.7%) matched a registry record.  Discrepancies in pertussis-related data were common for up-to-date status (22.6%), number of immunizations (34.7%), dates (10.2%), and formulation (34.4%).  Among 442 subjects from sites that planned direct electronic transfer of immunization data to the registry, 393 (88.9%) would have matched a registry record; discrepancies occurred frequently in number of immunizations (11.9%), formulation (29.1%), manufacturer (94.4%), and lot number (95.1%.)  Inability to match and immunization discrepancies were both more common in subjects who were older at their first visit to the provider site.  For 11-17-year-old subjects, discrepancies were also common for MMR, hepatitis B, and varicella vaccination data.
Conclusions:
Provider records frequently could not be matched to registry records or had discrepancies in key immunization data.  These issues were more common for older children and were present even with electronic data transfer.  These results highlight general challenges that may face investigators wishing to use registry-based immunization data for vaccine effectiveness studies, especially in adolescents.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/160</link>
			
			 	<dc:creator>Barbara E Mahon, Kimberly M Shea, Nancy N Dougherty and Anita M Loughlin</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:160</dc:source>
			<dc:date>2008-05-14</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-160</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>160</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-14</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/159">
            
            <title>Does transition from an unstable labour market position to permanent employment protect mental health?
Results from a 14-year follow-up of school-leavers.
</title>
			<description>Background:
Having secure employment, in contrast to being unemployed, is regarded as an important determinant of health. Research and theories about the negative health consequences of unemployment indicated that transition from unemployment to a paid job could lead to improved health. The objective of this study was to test the hypothesis that obtaining permanent employment after being in an unstable labour market position protects mental health. 
Methods:
A 14-year follow-up of all graduates from compulsory school in an industrial town in northern Sweden was performed at ages 16, 18, 21 and 30 years. Complete data on the cohort were collected for 1044 individuals with the aid of a comprehensive questionnaire. The response rate was 96.4%. The health measurement used in this study was the psychological symptoms analysed by multivariate logistic regression. Those who obtained permanent employment were the focus of the analysis. This group consisted of people who were in an unstable labour market position for a year or more between the ages of 25 and 29, and who had acquired a permanent job one year before and at the time of the investigation. 
Results:
After controlling for gender as well as for an indicator of health-related selection, possible confounders and mediators, an association was found between the lower probability of psychological symptoms and obtaining permanent employment (OR=0.35, 95% CI 0.19-0.63) as well as having permanent employment (OR=0.22, 95% CI 0.10-0.51).
Conclusions:
Our findings suggest that transition from an unstable labour market position to permanent employment could be health-promoting, even after controlling for possible confounders and mediators, as well as for an indicator of health-related selection. However, as there are few studies in the field, there is a need for more longitudinal studies in order to further analyse the relationship and to examine possible explanations. The policy implication of our study is that the transformation of unstable labour market positions into permanent employment could contribute to better public health.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/159</link>
			
			 	<dc:creator>Ieva Reine, Mehmed Novo and Anne Hammarstrom</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:159</dc:source>
			<dc:date>2008-05-13</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-159</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>159</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-13</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/158">
            
            <title>Timing of therapy for latent tuberculosis infection among immigrants presenting to a U.S. public health clinic: a retrospective study</title>
			<description>Background:
In the U.S. more than half of incident tuberculosis (TB) cases occur in immigrants.   Current guidelines recommend screening and treatment for latent TB infection (LTBI) within 5 years of arrival to the U.S.  This study evaluates the timing of LTBI therapy among immigrants presenting for care to a public health TB clinic.  
Methods:
Retrospective chart review of patients prescribed LTBI treatment based on medical records from Prince Georges County Health Department.  
Results:
1882 immigrants received LTBI therapy at Prince Georges County Health Department between 1999 and 2004.  417 of these patients were diagnosed with LTBI through contact investigations and were excluded from the analysis.  Among the remaining 1465 individuals, median time from arrival to the U.S. until initiation of LTBI therapy was 5 months (range 0-42.4 years).  16% of all immigrants initiated therapy more than 5 years after arrival to the U.S.  A logistic regression model using risks identified on univariate analysis revealed that referral for therapy by non-immigration proceedings was the strongest predictor of initiation of therapy more than 5 years after arrival to the U.S. Other factors associated with > 5 year U.S. residence prior to initiation of LTBI therapy included female gender (adjusted odds ratio (AOR) 1.8, 95% CI 1.2-2.6), age [greater than or equal to] 35 (AOR= 4.1, 95% 2.5-6.6), and originating from Latin American and the Caribbean (AOR= 1.9, 95% CI 1.3-3.0).   
Conclusion:
Foreign-born individuals who are not referred for LTBI therapy through immigration proceedings are less likely to receive LTBI therapy within 5 years of arrival to the U.S.  These data highlight the need to explore other mechanisms for timely LTBI screening beyond services provided by immigration.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/158</link>
			
			 	<dc:creator>Kathleen R Page, Yukari C Manabe, Akintoye Adelakun, Lynn Federline, Wendy Cronin, James D Campbell and Susan E Dorman</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:158</dc:source>
			<dc:date>2008-05-12</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-158</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>158</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-12</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/157">
            
            <title>Malaria treatment in the retail sector: knowledge and practices of drug sellers in rural Tanzania</title>
			<description>Background:
Throughout Africa, the private retail sector has been recognised as an important source of antimalarial treatment, complementing formal health services. However, the quality of advice and treatment at private outlets is a widespread concern, especially with the introduction of artemisinin-based combination therapies (ACTs). As a result, ACTs are often deployed exclusively through public health facilities, potentially leading to poorer access among parts of the population. This research aimed at assessing the performance of the retail sector in rural Tanzania. Such information is urgently required to improve and broaden delivery channels for life-saving drugs. 
Methods:
During a comprehensive shop census in the districts of Kilombero and Ulanga, Tanzania, we interviewed 489 shopkeepers about their knowledge of malaria and malaria treatment. A complementary mystery shoppers study was conducted in 118 retail outlets in order to assess the vendors' drug selling practices. Both studies included drug stores as well as general shops.
Results:
Shopkeepers in drug stores were able to name more malaria symptoms and were more knowledgeable about malaria treatment than their peers in general shops. In drug stores, 52% mentioned the correct child-dosage of sulphadoxine-pyrimethamine (SP) compared to only 3% in general shops. In drug stores, mystery shoppers were more likely to receive an appropriate treatment (OR=9.6), but at an approximately seven times higher price. Overall, adults were more often sold an antimalarial than children (OR=11.3). On the other hand, general shopkeepers were often ready to refer especially children to a higher level if they felt unable to manage the case. 
Conclusions:
The quality of malaria case-management in the retail sector is not satisfactory. Drug stores should be supported and empowered to provide correct malaria-treatment with drugs they are allowed to dispense. At the same time, the role of general shops as first contact points for malaria patients needs to be re-considered. Interventions to improve availability of ACTs in the retail sector are urgently required within the given legal framework.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/157</link>
			
			 	<dc:creator>Manuel W Hetzel, Angel Dillip, Christian Lengeler, Brigit Obrist, June J Msechu, Ahmed M Makemba, Christopher Mshana, Alexander Schulze and Hassan Mshinda</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:157</dc:source>
			<dc:date>2008-05-09</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-157</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>157</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/156">
            
            <title>The perceived impact of location privacy: a web-based survey of public health perspectives and requirements in the UK and Canada</title>
			<description>Background:
The "place-consciousness" of public health professionals is on the rise as spatial analyses and Geographic Information Systems (GIS) are rapidly becoming key components of their toolbox. However, "place" is most useful at its most precise, granular scale - which increases identification risks, thereby clashing with privacy issues. This paper describes the views and requirements of public health professionals in Canada and the UK on privacy issues and spatial data, as collected through a web-based survey.
Methods:
Perceptions on the impact of privacy were collected through a web-based survey administered between November 2006 and January 2007.  The survey targeted government, non-government and academic GIS labs and research groups involved in public health, as well as public health units (Canada), ministries, and observatories (UK). Potential participants were invited to participate through personally addressed, standardised emails.
Results:
Of 112 invitees in Canada and 75 in the UK, 66 and 28 participated in the survey, respectively. The completion proportion for Canada was 91%, and 86% for the UK. No response differences were observed between the two countries. Ninety three percent of participants indicated a requirement for personally identifiable data (PID) in their public health activities, including geographic information. Privacy was identified as an obstacle to public health practice by 71% of respondents. The overall self-rated median score for knowledge of privacy legislation and policies was 7 out of 10. Those who rated their knowledge of privacy as high (at the median or above) also rated it significantly more severe as an obstacle to research (P&lt;0.001). The most critical cause cited by participants in both countries was bureaucracy.
Conclusions:
The clash between PID requirements - including granular geography - and limitations imposed by privacy and its associated bureaucracy require immediate attention and solutions, particularly given the increasing utilisation of GIS in public health. Solutions include harmonization of privacy legislation with public health requirements, bureaucratic simplification, increased multidisciplinary discourse, education, and development of toolsets, algorithms and guidelines for using and reporting on disaggregate data.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/156</link>
			
			 	<dc:creator>Philip AbdelMalik, Maged N Kamel Boulos and Ray Jones</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:156</dc:source>
			<dc:date>2008-05-09</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-156</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>156</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/155">
            
            <title>Sexual uses of alcohol and drugs and the associated health risks: a cross sectional study of young people in nine European cities</title>
			<description>Background:
Young people in European countries are experiencing high levels of alcohol and drug use and escalating levels of sexually transmitted infections. Individually these represent major public health priorities. Understanding of the association between sex and substance use, and specifically the strategic roles for which young people utilise substances to facilitate sexual activity, remains limited. 
Methods:
Respondent driven sampling methodology was used in nine European cities to survey 1,341 16-35 year olds representing youth and younger adults who routinely engage in nightlife. Participants self-completed questionnaires, designed to gather demographic, social, and behavioural data on historic and current substance use and sexual behaviour.
Results:
Respondents reported strategic use of specific substances for different sexual purposes. Substances differed significantly in the purposes for which each was deployed (e.g. 28.6% of alcohol users use it to facilitate sexual encounters; 26.2% of cocaine users use it to prolong sex) with user demographics also relating to levels of sexual use (e.g. higher levels of: ecstasy use by males to prolong sex; cocaine use by single individuals to enhance sensation and arousal). Associations between substance use and sex started at a young age, with alcohol, cannabis, cocaine or ecstasy use before age 16 all being associated with having had sex before the age of 16 (odds ratios, 3.47, 4.19, 5.73, 9.35 respectively). However, sexes differed and substance use under 16 years was associated with a proportionately greater increase in early sex amongst girls. Respondents' current drug use was associated with having multiple sexual partners. Thus, for instance, regular cocaine users (c.f. never users) were over five times more likely to have had five or more sexual partners in the last 12 months or have paid for sex.
Conclusions:
An epidemic of recreational drug use and binge drinking exposes millions of young Europeans to routine consumption of substances which alter their sexual decisions and increase their chances of unsafe and regretted sex. For many, substance use has become an integral part of their strategic approach to sex, locking them into continued use. Tackling substances with both physiological and psychological links to sex requires approaching substance use and sexual behaviour in the same way that individuals experience them; as part of the same social process. </description>
			<link>http://www.biomedcentral.com/1471-2458/8/155</link>
			
			 	<dc:creator>Mark A Bellis, Karen Hughes, Amador Calafat, Montse Juan, Anna Ramon, Jose A Rodriguez, Fernando Mendes, Susanne Schnitzer and Penny Phillips-Howard</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:155</dc:source>
			<dc:date>2008-05-09</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-155</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>155</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/154">
            
            <title>Tackling tuberculosis patients' internalized social stigma through patient centred care: an intervention study in rural Nicaragua
</title>
			<description>Background:
We report a patient-centered intervention study in 9 municipalities of rural Nicaragua aiming at a reduction of internalized social stigma in new AFB positive tuberculosis (TB) patients diagnosed between March 2004 and July 2005.  
Methods:
Five out of 9 municipal teams were coached to tailor and introduce patient-centered package. New TB patients  were  assigned  to  the  intervention  group  when  diagnosed  in  municipalities  implementing effectively at least TB clubs and home visits.  We  compared  the  changes  in  internalized  stigma  and  TB  treatment  outcome  in  intervention  and 
control groups. The  internalized stigma was measured  through score computed at 15 days and at 2 months of treatment. The treatment results were evaluated through classical TB program indicators. In all municipalities, we emphasized process monitoring to capture contextual factors that could influence 
package implementation, including stakeholders.   
Results:
TB clubs and home visits were effectively  implemented  in 2 municipalities after June 2004 and  in 3 municipalities after January 2005. Therefore, 122 patients were included in the intervention group and 146  in  the control group.   After 15 days,  internalized stigma scores were equivalent  in both groups. After  2  months,  difference  between  scores  was  statistically  significant,  revealing  a  decreased 
internalized stigma in the intervention group and not in the control group.    
Conclusion:
This study provides initial evidences that it is possible to act on TB patients' internalized stigma, in contexts where at least patient centered home visits and TB clubs are successfully implemented. This is important as, indeed, TB care should also focus on the TB patient's wellbeing and not solely on TB 
epidemics control.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/154</link>
			
			 	<dc:creator>Jean Macq, Alejandro Solis, Guillermo Martinez and Patrick Martiny</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:154</dc:source>
			<dc:date>2008-05-08</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-154</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>154</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/153">
            
            <title>Are hygiene and public health interventions likely to improve outcomes for Australian Aboriginal children living in remote communities? A systematic review of the literature</title>
			<description>Background:
Australian Aboriginal children living in remote communities still experience a high burden of common infectious diseases which are generally attributed to poor hygiene and unsanitary living conditions. The objective of this systematic literature review was to examine the epidemiological evidence for a relationship between various hygiene and public health intervention strategies, separately or in combination, and the occurrence of common preventable childhood infectious diseases. The purpose was to determine what intervention/s might most effectively reduce the incidence of skin, diarrhoeal and infectious diseases experienced by children living in remote Indigenous communities. 
Methods:
Studies were identified through systematically searching electronic databases and hand searching.  Study types were restricted to those included in Cochrane Collaboration Effective Practice and Organisation of Care Review Group (EPOC) guidelines and reviewers assessed the quality of studies and extracted data using the same guidelines. The types of participants eligible were Indigenous populations and populations of developing countries. The types of intervention eligible for inclusion were restricted to those likely to prevent conditions caused by poor personal hygiene and poor living environments. 
Results:
The evidence showed that there is clear and strong evidence of effect of education and handwashing with soap in preventing diarrhoeal disease among children (consistent effect in four studies). In the largest well-designed study, children living in households that received plain soap and encouragement to wash their hands had a 53% lower incidence of diarrhoea (95% CI, 0.35, 0.59). There is some evidence of an effect of education and other hygiene behaviour change interventions (six studies), as well as the provision of water supply, sanitation and hygiene education (two studies) on reducing rates of diarrhoeal disease. The size of these effects is small and the quality of the studies generally poor. 
Conclusion:
Research which measures the effectiveness of hygiene interventions is complex and difficult to implement. Multifaceted interventions (which target handwashing with soap and include water, sanitation and hygiene promotion) are likely to provide the greatest opportunity to improve child health outcomes in remote Indigenous communities.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/153</link>
			
			 	<dc:creator>Elizabeth McDonald, Ross Bailie, David Brewster and Peter Morris</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:153</dc:source>
			<dc:date>2008-05-08</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-153</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>153</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2458/8/152">
            
            <title>Cancer patterns among children of Turkish descent in Germany: a study at the German Childhood Cancer Registry</title>
			<description>Background:
Cancer risks of migrants might differ from risks of the indigenous population due to differences in socioeconomic status, life style, or genetic factors. The aim of this study was to investigate cancer patterns among children of Turkish descent in Germany. 
Methods:
We identified cases with Turkish names (as a proxy of Turkish descent) among the 37,259 cases of childhood cancer registered in the German Childhood Cancer Registry (GCCR) during 1980-2005. As it is not possible to obtain reference population data for children of Turkish descent, the distribution of cancer diagnoses was compared between cases of Turkish descent and all remaining (mainly German) cases in the registry, using proportional cancer incidence ratios (PCIRs). 
Results:
The overall distribution of cancer diagnoses was similar in the two groups. The PCIRs in three diagnosis groups were increased for cases of Turkish descent: acute non-lymphocytic leukaemia (PCIR 1.23; CI (95%) 1.02-1.47), Hodgkin's disease (1.34; 1.13-1.59) and Non-Hodgkin/Burkitt lymphoma (1.19; 1.02-1.39). Age, sex, and period of diagnosis showed no influence on the distribution of diagnoses. 
Conclusions:
No major differences were found in cancer patterns among cases of Turkish descent compared to all other cases in the GCCR. Slightly higher proportions of systemic malignant diseases indicate that analytical studies involving migrants may help investigating the causes of such cancers.</description>
			<link>http://www.biomedcentral.com/1471-2458/8/152</link>
			
			 	<dc:creator>Jacob Spallek, Claudia Spix, Hajo Zeeb, Peter Kaatsch and Oliver Razum</dc:creator>
			
			<dc:source>BMC Public Health 2008, 8:152</dc:source>
			<dc:date>2008-05-07</dc:date>
			<dc:identifier>doi:10.1186/1471-2458-8-152</dc:identifier>
			
			
							
					<prism:publicationName>BMC Public Health</prism:publicationName>
					
			
							
					<prism:issn>1471-2458</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>152</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-07</prism:publicationDate>
					

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