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        <title>BMC International Health and Human Rights - Latest Articles</title>
        <link>http://www.biomedcentral.com/bmcinthealthhumrights/</link>
        <description>The latest research articles published by BMC International Health and Human Rights</description>
        <dc:date>2011-12-16T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/15" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/14" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/13" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/12" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/11" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/10" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/9" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/8" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1472-698X/11/7" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/15">
        <title>Perceptions and utilization of primary health care services in Iraq: findings from a national household survey  </title>
        <description>Background:
After many years of sanctions and conflict, Iraq is rebuilding its health system, with a strong emphasis on the traditional hospital-based services. A network exists of public sector hospitals and clinics, as well as private clinics and a few private hospitals. Little data are available about the approximately 1400 Primary Health Care clinics (PHCCs) staffed with doctors. How do Iraqis utilize primary health care services? What are their preferences and perceptions of public primary health care clinics and private primary care services in general? How does household wealth affect choice of services?
Methods:
A 1256 household national survey was conducted in the catchment areas of randomly selected PHCCs in Iraq. A cluster of 10 households, beginning with a randomly selected start household, were interviewed in the service areas of seven public sector PHCC facilities in each of 17 of Iraq&apos;s 18 governorates. A questionnaire was developed using key informants. Teams of interviewers, including both males and females, were recruited and provided a week of training which included field practice. Teams then gathered data from households in the service areas of randomly selected clinics.
Results:
Iraqi participants are generally satisfied with the quality of primary care services available both in the public and private sector. Private clinics are generally the most popular source of primary care, however the PHCCs are utilized more by poorer households. In spite of free services available at PHCCs many households expressed difficulty in affording health care, especially in the purchase of medications. There is no evidence of informal payments to secure health services in the public sector.
Conclusions:
There is widespread satisfaction reported with primary health care services, and levels did not differ appreciably between public and private sectors. The public sector PHCCs are preferentially used by poorer populations where they are important providers. PHCC services are indeed free, with little evidence of informal payments to providers.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/15</link>
                <dc:creator>Gilbert Burnham</dc:creator>
                <dc:creator>Connie Hoe</dc:creator>
                <dc:creator>Yuen Wai Hung</dc:creator>
                <dc:creator>Agron Ferati</dc:creator>
                <dc:creator>Allen Dyer</dc:creator>
                <dc:creator>Thamer Al Hilfi</dc:creator>
                <dc:creator>Rabia Aboud</dc:creator>
                <dc:creator>Tariq Hasoon</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:15</dc:source>
        <dc:date>2011-12-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-15</dc:identifier>
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        <prism:startingPage>15</prism:startingPage>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/14">
        <title>Evaluation of knowledge levels amongst village AIDS committees after undergoing HIV educational sessions: results from a pilot study in rural Tanzania </title>
        <description>Background:
Village AIDS committees (VAC) were formed by the Tanzanian government in 2003 to provide HIV education to their communities. However, their potential has not been realised due to their limited knowledge and misconceptions surrounding HIV, which could be addressed through training of VAC members. In an attempt to increase HIV knowledge levels and address common misconceptions amongst the VACs, an HIV curriculum was delivered to members in rural north western Tanzania.
Methods:
An evaluation of HIV knowledge was conducted prior to and post-delivery of HIV training sessions, within members of three VACs in Kisesa ward. Quantitative surveys were used with several open-ended questions to identify local misconceptions and evaluate HIV knowledge levels. Short educational training sessions covering HIV transmission, prevention and treatment were conducted, with each VAC using quizzes, role-plays and participatory learning and action tools. Post-training surveys occurred up to seven days after the final training session.
Results:
Before the training, &quot;good&quot; HIV knowledge was higher amongst men than women (p = 0.041), and among those with previous HIV education (p = 0.002). The trade-centre had a faster turn-over of VAC members, and proximity to the trade-centre was associated with a shorter time on the committee.Training improved HIV knowledge levels with more members achieving a &quot;good&quot; score in the post-training survey compared with the baseline survey (p = &lt; 0.001). The training programme was popular, with 100% of participants requesting further HIV training in the future and 51.7% requesting training at three-monthly intervals.
Conclusions:
In this setting, a series of HIV training sessions for VACs demonstrated encouraging results, with increased HIV knowledge levels following short educational sessions. Further work is required to assess the success of VAC members in disseminating this HIV education to their communities, as well as up-scaling this pilot study to other regions in Tanzania with different misconceptions.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/14</link>
                <dc:creator>Elizabeth Epsley</dc:creator>
                <dc:creator>Benjamin Nhandi</dc:creator>
                <dc:creator>Alison Wringe</dc:creator>
                <dc:creator>Mark Urassa</dc:creator>
                <dc:creator>Jim Todd</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:14</dc:source>
        <dc:date>2011-12-13T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-14</dc:identifier>
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        <prism:startingPage>14</prism:startingPage>
        <prism:publicationDate>2011-12-13T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/13">
        <title>An approach to addressing governance from a health system framework perspective </title>
        <description>As countries strive to strengthen their health systems in resource constrained contexts, policy makers need to know how best to improve the performance of their health systems. To aid these decisions, health system stewards should have a good understanding of how health systems operate in order to govern them appropriately. While a number of frameworks for assessing governance in the health sector have been proposed, their application is often hindered by unrealistic indicators or they are overly complex resulting in limited empirical work on governance in health systems. This paper reviews contemporary health sector frameworks which have focused on defining and developing indicators to assess governance in the health sector. Based on these, we propose a simplified approach to look at governance within a common health system framework which encourages stewards to take a systematic perspective when assessing governance. Although systems thinking is not unique to health, examples of its application within health systems has been limited. We also provide an example of how this approach could be applied to illuminate areas of governance weaknesses which are potentially addressable by targeted interventions and policies. This approach is built largely on prior literature, but is original in that it is problem-driven and promotes an outward application taking into consideration the major health system building blocks at various levels in order to ensure a more complete assessment of a governance issue rather than a simple input-output approach. Based on an assessment of contemporary literature we propose a practical approach which we believe will facilitate a more comprehensive assessment of governance in health systems leading to the development of governance interventions to strengthen system performance and improve health as a basic human right.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/13</link>
                <dc:creator>Inez Mikkelsen-Lopez</dc:creator>
                <dc:creator>Kaspar Wyss</dc:creator>
                <dc:creator>Don de Savigny</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:13</dc:source>
        <dc:date>2011-12-02T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-13</dc:identifier>
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        <prism:startingPage>13</prism:startingPage>
        <prism:publicationDate>2011-12-02T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/12">
        <title>Compulsory Drug Detention Center Experiences among a Community-Based Sample of Injection Drug Users in Bangkok, Thailand</title>
        <description>Background:
Despite Thailand&apos;s official reclassification of drug users as &quot;patients&quot; deserving care and not &quot;criminals,&quot; the Thai government has continued to rely heavily on punitive responses to drug use such as &quot;boot camp&quot;-style compulsory &quot;treatment&quot; centers. There is very little research on experiences with compulsory treatment centers among people who use drugs. The work reported here is a first step toward filling that gap.
Methods:
We examined experiences of compulsory drug treatment among 252 Thai people who inject drugs (IDU) participating in the Mitsampan Community Research Project in Bangkok. Multivariate logistic regression was used to identify factors independently associated with a history of compulsory treatment experience.
Results:
In total, 80 (31.7%) participants reported a history of compulsory treatment. In multivariate analyses, compulsory drug detention experience was positively associated with current spending on drugs per day (adjusted odds ratio [AOR] = 1.86; 95%CI: 1.07 - 3.22) and reporting drug planting by police (AOR = 1.81; 95%CI: 1.04 - 3.15). Among those with compulsory treatment experience, 77 (96.3%) reported injecting in the past week, and no difference in intensity of drug use was observed between those with and without a history of compulsory detention.
Conclusion:
These findings raise concerns about the current approach to compulsory drug detention in Thailand. Exposure to compulsory drug detention was associated with police abuse and high rates of relapse into drug use, although additional research is needed to determine the precise impact of exposure to this form of detention on future drug use. More broadly, compulsory &quot;treatment&quot; based on a penal approach is not consistent with scientific evidence on addressing drug addiction and should be phased out in favor of evidence-based interventions.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/12</link>
                <dc:creator>Joanne Csete</dc:creator>
                <dc:creator>Karyn Kaplan</dc:creator>
                <dc:creator>Kanna Hayashi</dc:creator>
                <dc:creator>Nadia Fairbairn</dc:creator>
                <dc:creator>Paisan Suwannawong</dc:creator>
                <dc:creator>Ruth Zhang</dc:creator>
                <dc:creator>Evan Wood</dc:creator>
                <dc:creator>Thomas Kerr</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:12</dc:source>
        <dc:date>2011-10-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-12</dc:identifier>
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        <prism:startingPage>12</prism:startingPage>
        <prism:publicationDate>2011-10-20T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/11">
        <title>Health-care seeking behaviour among persons with diabetes in Uganda: an interview study. </title>
        <description>Background:
Healthcare-seeking behaviour in patients with diabetes mellitus (DM) has been investigated to a limited extent, and not in developing countries. Switches between different health sectors may interrupt glycaemic control, affecting health. The aim of the study was to explore healthcare-seeking behaviour, including use of complementary alternative medicine (CAM) and traditional healers, in Ugandans diagnosed with DM. Further, to study whether gender influenced healthcare-seeking behaviour.
Methods:
This is a descriptive study with a snowball sample from a community in Uganda. Semi-structured interviews were held with 16 women and 8 men, aged 25-70. Data were analysed by qualitative content analysis.
Results:
Healthcare was mainly sought among doctors and nurses in the professional sector because of severe symptoms related to DM and/or glycaemic control. Females more often focused on follow-up of DM and chronic pain in joints, while males described fewer problems. Among those who felt that healthcare had failed, most had turned to traditional healers in the folk sector for prescription of herbs or food supplements, more so in women than men. Males more often turned to private for-profit clinics while females more often used free governmental institutions.
Conclusions:
Healthcare was mainly sought from nurses and physicians in the professional sector and females used more free-of-charge governmental institutions. Perceived failure in health care to manage DM or related complications led many, particularly women, to seek alternative treatment from CAM practitioners in the folk sector. Living conditions, including healthcare organisation and gender, seemed to influence healthcare seeking, but further studies are needed.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/11</link>
                <dc:creator>Katarina Hjelm</dc:creator>
                <dc:creator>Fortunate Atwine</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:11</dc:source>
        <dc:date>2011-09-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-11</dc:identifier>
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                <prism:publicationName>BMC International Health and Human Rights</prism:publicationName>
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        <prism:startingPage>11</prism:startingPage>
        <prism:publicationDate>2011-09-26T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/10">
        <title>Access to primary healthcare services for the Roma population in Serbia: a secondary data analysis.</title>
        <description>Background:
Serbia has proclaimed access to healthcare as a human right. In a context wherein the Roma population are disadvantaged, the aim of this study was to assess whether the Roma population are able to effectively access primary care services, and if not, what barriers prevent them from doing so. The history of the Roma in Serbia is described in detail so as to provide a context for their current vulnerable position.
Methods:
Disaggregated data were analyzed from three population groups in Serbia; the general population, the Roma population, and the poorest quintile of the general population not including the Roma. The effective coverage framework, which incorporates availability, affordability, accessibility, acceptability, and effectiveness of health services, was used to structure the secondary data analysis. Acute respiratory infection (ARI) in children less than five years of age was used as an example as this is the leading cause of death in children under 5 years old in Serbia.
Results:
Roma children were significantly more likely to experience an ARI than either the general population or the poorest quintile of the general population, not including the Roma. All three population groups were equally likely to not receive the correct treatment regime of antibiotics. An analysis of the factors that affect quality of access to health services reveal that personal documentation is a statistically significant problem; availability of health services is not an issue that disproportionately affects the Roma; however the geographical accessibility and affordability are substantive issues that disproportionately affect the Roma population. Affordability of services affected the Roma and the poorest quintile and affordability of medications significantly affected all three population groups. With regards to acceptability, mothers from all three population groups are equally likely to recognize the importance of seeking treatment.
Conclusions:
The Roma should be assisted in applying for personal documentation, the geographical accessibility of clinics needs to be addressed, and the costs of healthcare visits and medications should be reviewed. Areas for improvement specific to ARI are the costs of antibiotics and the diagnostic accuracy of providers. A range of policy recommendations are outlined.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/10</link>
                <dc:creator>Leanne Idzerda</dc:creator>
                <dc:creator>Orvill Adams</dc:creator>
                <dc:creator>Jonathan Patrick</dc:creator>
                <dc:creator>Ted Schrecker</dc:creator>
                <dc:creator>Peter Tugwell</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:10</dc:source>
        <dc:date>2011-08-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-10</dc:identifier>
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                <prism:publicationName>BMC International Health and Human Rights</prism:publicationName>
        <prism:issn>1472-698X</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>10</prism:startingPage>
        <prism:publicationDate>2011-08-18T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/9">
        <title>Efficacy of integrated school based de-worming and prompt malaria treatment on helminths-Plasmodium falciparum co-infections: A 33 months follow up study</title>
        <description>Background:
The geographical congruency in distribution of helminths and Plasmodium falciparum makes polyparasitism a common phenomenon in Sub Saharan Africa. The devastating effects of helminths-Plasmodium co-infections on primary school health have raised global interest for integrated control. However little is known on the feasibility, timing and efficacy of integrated helminths-Plasmodium control strategies. A study was conducted in Zimbabwe to evaluate the efficacy of repeated combined school based antihelminthic and prompt malaria treatment.
Methods:
A cohort of primary schoolchildren (5-17 years) received combined Praziquantel, albendazole treatment at baseline, and again during 6, 12 and 33 months follow up surveys and sustained prompt malaria treatment. Sustained prompt malaria treatment was carried out throughout the study period. Children&apos;s infection status with helminths, Plasmodium and helminths-Plasmodium co-infections was determined by parasitological examinations at baseline and at each treatment point. The prevalence of S. haematobium, S. mansoni, STH, malaria, helminths-Plasmodium co-infections and helminths infection intensities before and after treatment were analysed.
Results:
Longitudinal data showed that two rounds of combined Praziquantel and albendazole treatment for schistosomiasis and STHs at 6 monthly intervals and sustained prompt malaria treatment significantly reduced the overall prevalence of S. haematobium, S. mansoni, hookworms and P. falciparum infection in primary schoolchildren by 73.5%, 70.8%, 67.3% and 58.8% respectively (p &lt; 0.001, p &lt; 0.001, p &lt; 0.001, p &lt; 0.001 respectively). More importantly, the prevalence of STH + schistosomes, P. f + schistosomes, and P. f + STHs + schistosomes co-infections were reduced by 68.0%, 84.2%, and 90.7%, respectively. The absence of anti-helminthic treatment between the 12 mth and 33 mth follow-up surveys resulted in the sharp increase in STHs + schistosomes co-infection from 3.3% at 12 months follow up survey to 10.7%, slightly more than the baseline level (10.3%) while other co-infection combinations remained significantly low. The overall prevalence of heavy S. haematobium, S. mansoni and hookworms infection intensities were significantly reduced from: 17.9-22.4% to 2.6-5.1%, 1.6-3.3% to 0.0% and 0.0-0.7% to 0.0% respectively.
Conclusion:
Biannual Integrated school based antihelminthic and sustained prompt malaria treatment has a potential to reduce the burden of helminths-plasmodium co-infections in primary school children. In areas of stable malaria transmission, active case finding is recommended to track and treat asymptomatic malaria cases as these may sustain transmission in the community.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/9</link>
                <dc:creator>Nicholas Midzi</dc:creator>
                <dc:creator>Sekesai Mtapuri-Zinyowera</dc:creator>
                <dc:creator>Davison Sangweme</dc:creator>
                <dc:creator>Noah Paul</dc:creator>
                <dc:creator>Godfrey Makware</dc:creator>
                <dc:creator>Munyaradzi Mapingure</dc:creator>
                <dc:creator>Kimberly Brouwer</dc:creator>
                <dc:creator>James Mudzori</dc:creator>
                <dc:creator>Gibson Hlerema</dc:creator>
                <dc:creator>Vivian Chadukura</dc:creator>
                <dc:creator>Francisca Mutapi</dc:creator>
                <dc:creator>Nirbhay Kumar</dc:creator>
                <dc:creator>Takafira Mduluza</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:9</dc:source>
        <dc:date>2011-06-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-9</dc:identifier>
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        <prism:startingPage>9</prism:startingPage>
        <prism:publicationDate>2011-06-22T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/8">
        <title>Health and human rights of women imprisoned in Zambia</title>
        <description>Background:
The healthcare needs and general experience of women in detention in sub-Saharan Africa are rarely studied and poorly understood.
Methods:
A mixed-methods study was conducted including in-depth interviews with 38 adult female prisoners and 21 prison officers in four Zambian prisons to assess the health and human rights concerns of female detainees. Key informant interviews with 46 officials from government and non-governmental organizations and a legal and policy review were also conducted.
Results:
Despite special protection under international and regional law, incarcerated women&apos;s health needs&#8211;including prenatal care, prevention of mother-to-child transmission of HIV, and nutritional support during pregnancy and breastfeeding&#8211;are not being adequately met in Zambian prisons. Women are underserved by general healthcare programs including those offering tuberculosis and HIV testing, and reported physical and sexual abuse conducted by police and prison officers that could amount to torture under international law.
Conclusions:
There is an urgent need for women&apos;s healthcare services to be expanded, and for general prison health campaigns, including HIV and tuberculosis testing and treatment, to ensure the inclusion of female inmates. Abuses against women in Zambian police and prison custody, which violate their rights and compromise their health, must be halted immediately.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/8</link>
                <dc:creator>Katherine Todrys</dc:creator>
                <dc:creator>Joseph Amon</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:8</dc:source>
        <dc:date>2011-06-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-8</dc:identifier>
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                <prism:publicationName>BMC International Health and Human Rights</prism:publicationName>
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        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2011-06-22T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/7">
        <title>&apos;The girl with her period is the one to hang her head&apos; Reflections on menstrual management among schoolgirls in rural Kenya</title>
        <description>Background:
The onset of menstruation is a landmark event in the life of a young woman. Yet the complications and challenges that can accompany such an event have been understudied, specifically in resource-poor settings. As interventions aim to improve female attendance in schools, it is important to explore how menstruation is perceived and navigated by girls in the school setting. This research conveys rural Kenyan schoolgirls&apos; perceptions and practices related to menstruation
Methods:
Data were collected at six rural schools in the Nyanza Province of Western Kenya. Using focus group discussions, in-depth interviews, and field notes from observations, researchers collected information from 48 primary schoolgirls and nine teachers. Systematic analysis began with a reading of transcripts and debriefing notes, followed by manual coding of the narratives.
Results:
Focus group discussions became opportunities for girls to share thoughts on menstruation, instruct one another on management practices and advise one another on coping mechanisms. Girls expressed fear, shame, distraction and confusion as feelings associated with menstruation. These feelings are largely linked to a sense of embarrassment, concerns about being stigmatized by fellow students and, as teachers explained, a perception that the onset of menstruation signals the advent of a girl&apos;s sexual status. Among the many methods for managing their periods, girls most frequently said they folded, bunched up or sewed cloth, including cloth from shirts or dresses, scraps of old cloth, or strips of an old blanket. Cloth was reported to frequently leak and cause chafing, which made school attendance difficult particularly as the day progressed. Attitudes and practices of girls toward menstruation have been arranged into personal, environmental and behavioural factors.
Conclusion:
Further research on menstrual management options that are practical, sustainable and culturally acceptable must be conducted to inform future programs and policies that aim to empower young girls as they transition into womanhood. Stakeholders working within this and similar contexts must consider systematic mechanisms to explain to young girls what menstruation is and how to manage it. Providing sanitary supplies or guiding girls on how to create supplies serve as critical components for future interventions.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/7</link>
                <dc:creator>Shannon McMahon</dc:creator>
                <dc:creator>Peter Winch</dc:creator>
                <dc:creator>Bethany Caruso</dc:creator>
                <dc:creator>Alfredo Obure</dc:creator>
                <dc:creator>Emily Ogutu</dc:creator>
                <dc:creator>Imelda Ochari</dc:creator>
                <dc:creator>Richard Rheingans</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:7</dc:source>
        <dc:date>2011-06-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-7</dc:identifier>
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        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2011-06-16T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1472-698X/11/6">
        <title>&quot;If the patients decide not to tell what can we do?&quot; - TB/HIV counsellors&apos; dilemma on partner notification for HIV</title>
        <description>Background:
There is a global consensus towards universal access to human immunodeficiency virus (HIV) services consequent to the increasing availability of antiretroviral therapy. However, to benefit from these services, knowledge of one&apos;s HIV status is critical. Partner notification for HIV is an important component of HIV counselling because it is an effective strategy to prevent secondary transmission, and promote early diagnosis and prompt treatment of HIV patients&apos; sexual partners. However, counsellors are often frustrated by the reluctance of HIV-positive patients to voluntarily notify their sexual partners. This study aimed to explore tuberculosis (TB)/HIV counsellors&apos; perspectives regarding confidentiality and partner notification.
Methods:
Qualitative research interviews were conducted in the Northwest Region of Cameroon with 30 TB/HIV counsellors in 4 treatment centres, and 2 legal professionals between September and December 2009. Situational Analysis (positional map) was used for data analysis.
Results:
Confidentiality issues were perceived to be handled properly despite concerns about patients&apos; reluctance to report cases of violation due to apprehension of reprisals from health care staffs. All the respondents encouraged voluntary partner notification, and held four varying positions when confronted with patients who refused to voluntarily notify their partners. Position one focused on absolute respect of patients&apos; autonomy; position two balanced between the respect of patients&apos; autonomy and their partners&apos; safety; position three wished for protection of sexual partners at risk of HIV infection and legal protection for counsellors; and position four requested making HIV testing and partner notification routine processes.
Conclusion:
Counsellors regularly encounter ethical, legal and moral dilemmas between respecting patients&apos; confidentiality and autonomy, and protecting patients&apos; sexual partners at risk of HIV infection.This reflects the complexity of partner notification and demonstrates that no single approach is optimal, but instead certain contextual factors and a combination of different approaches should be considered. Meanwhile, adopting a human rights perspective in HIV programmes will balance the interests of both patients and their partners, and ultimately enhance universal access to HIV services.</description>
        <link>http://www.biomedcentral.com/1472-698X/11/6</link>
                <dc:creator>Barnabas Njozing</dc:creator>
                <dc:creator>Kerstin Edin</dc:creator>
                <dc:creator>Miguel San Sebastian</dc:creator>
                <dc:creator>Anna-Karin Hurtig</dc:creator>
                <dc:source>BMC International Health and Human Rights 2011, null:6</dc:source>
        <dc:date>2011-06-03T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1472-698X-11-6</dc:identifier>
                            <dc:title>HIV status partner notification dilemma</dc:title>
                            <dc:description>When confronted with HIV-positive patients who refuse to inform partners about their status, counsellors may need to consider a combination of several approaches to reach a balance between respecting the patient and safeguarding the partner.</dc:description>
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        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2011-06-03T00:00:00Z</prism:publicationDate>
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