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Conceptual Understandings of Early Intervention Practice: Synergistic Relationships
Clare Carroll,
Jane Sixsmith
Posted: 16 April 2025
A Markov Chain Model of Population Growth with an Application in Assessing Healthcare Demand: Kazakhstan Case Study
Berik Koichubekov,
Nazgul Omarbekova,
Khamida Abdikadirova,
Azamat Kharin,
Bauyrzhan Omarkulov,
Meruyert Mukhanova
Posted: 16 April 2025
The Multifactorial Determinants of Tuberculosis Mortality: A Global Comprehensive Epidemiological Analysis and Framework for Disease Elimination
Richard Murdoch Montgomery
Posted: 16 April 2025
"A Comprehensive Review of Women's Exposure to Gender-Based Violence in Timor-Leste: Insights Applied from Feminist, Intersectionality, and Health Determinants Theory"
Marcelo Amaral Amaral Mali,
Nelson Martins,
Nivia de Pina Sarmento Seran,
Perpetua Ana Mery Laot,
Benigna Veneranda Amaral,
Filipe de Neri Machado,
Livia Natalia Maria Guterres Babo,
Noel Gama Soares
Posted: 15 April 2025
Geopolitical Instability and Maternal Health: Assessing the Impact on Obstetric Fistula Prevalence and Care in Low‐ and Middle‐Income Countries
Sohier Elneil,
Gayathri Delanerolle,
Mohammad Haddadi,
Imran Morhason-Bello,
Lauri Romanzi
Posted: 14 April 2025
Racial and Ethnic Disparities in Emergency Medical Transport: A Comparative Analysis of Trauma Admissions at a County Hospital and Academic Health Center in a Major U.S. City
Fezaan Kazi,
Ajay Patel,
Ali H Sualeh,
Jeff Guo,
Ahsan Siddiqui,
Ammaar Basher,
Mohamed A Zaazoue,
Muqsit Buchh,
Varun Rao,
Jamie Bradbury
Posted: 11 April 2025
Confidence in Network Meta-Analysis of Occupational Hazards and Burnout Risk Among Public Health Inspectors
Ioannis Adamopoulos,
Antonios Valamontes
Posted: 09 April 2025
Balancing Costs and Clinical Outcomes: A Cost-effectiveness Study of PICC Types Across Chinese Healthcare Settings
Jia Xu,
Renan C. Castillo,
Hossein Zare,
Herng-Chia Chiu,
Xia Yan
Posted: 07 April 2025
Fundamental Flaws in Collecting and Interpreting Covid Data: ‘Covidisation’ of “Regular Deaths” in USA
Jan Charles Biro
Posted: 31 March 2025
Development of a Multilayer Transdermal Patch Platform Based on Electrospun Nanofibers for the Delivery of Caffeine
Jorge Teno,
Zoran Evtoski,
Cristina Prieto,
Jose Lagaron
Posted: 31 March 2025
Accessibility of Tourist Attractions for People with Disabilities as a Factor in the Development of Inclusive Tourism. Example of Swietokrzyskie Region – Poland
Klaudia Chwaja,
Błażej Chwaja,
Iwona Marczak,
Zygmunt Kruczek
Posted: 27 March 2025
Measuring Hospital Performance Using the EGIPSS Model: Lessons Learned from Ten Hospitals in the Kadutu Health Zone in the Democratic Republic of Congo
Hermès Karemere,
Samuel Lwamushi Makali,
Innocent Batumike,
Serge Kambale
Posted: 26 March 2025
A Pilot Observational Study of the Development and Utilization of a Psychotherapy Incorporating Horses Program at a Veterans Health Administration Medical Center
William R Marchand,
Elena Nazarenko,
Ryan Lackner,
Amir Ramezani,
Amber Martinson,
Amy Hartquist,
Lisa Finnell,
Dylan Taplin
Posted: 21 March 2025
Nurturing Leaders in Community-Based, Primary Healthcare Services for People with Disabilities in Low and Middle Income Countries
Roy McConkey
The health and social care needs of children and adults with disabilities are often neglected in many low and middle income countries. International opinion favours the creation of community-based supports rather than the institutional and clinic-based care that has dominated to date. However models of care that are reliant on community leadership have been slow to develop within and across less affluent countries. Moreover, the managerial models inherent in institutional based care are likely to be inadequate in such settings. The study aimed to explore the leadership qualities required in initiating and sustaining community-based supports. Face-to-face interviews were conducted with a purposeful sample of 16 leaders of projects in Africa, Asia and South America. They included people with sensorial, physical and intellectual disabilities as well as non-disabled leaders of local and national projects plus others whose leadership was at a regional or international level. Two main questions were addressed: what are the qualities required to function as a community leaders and how can these qualities be nurtured in low resourced settings. Thematic content analysis identified three core themes: first, personal qualities such as empathy with an understanding of the personal circumstances of persons in need of support, second, communicating clearly the vision and values informing their work, and thirdly, building and mobilising community support from families and neighbours. The nurturing of leadership comes through mentoring and coaching, the empowerment of others, networking opportunities and the development of inter-personal and communication skills. These themes were commonly expressed across the 16 leaders from all the participating nations and at all levels of responsibility which validates their universality. The findings are in marked contrast to current practices in health and social care that have valued professional expertise over lived experience, knowledge and technical skills over compassion and empathy, and the provision of person-centred ‘treatments’ over developing community and personal self-reliance. Nonetheless the challenges involved in establishing and sustaining new styles of leadership are many and will not be quickly resolved.
The health and social care needs of children and adults with disabilities are often neglected in many low and middle income countries. International opinion favours the creation of community-based supports rather than the institutional and clinic-based care that has dominated to date. However models of care that are reliant on community leadership have been slow to develop within and across less affluent countries. Moreover, the managerial models inherent in institutional based care are likely to be inadequate in such settings. The study aimed to explore the leadership qualities required in initiating and sustaining community-based supports. Face-to-face interviews were conducted with a purposeful sample of 16 leaders of projects in Africa, Asia and South America. They included people with sensorial, physical and intellectual disabilities as well as non-disabled leaders of local and national projects plus others whose leadership was at a regional or international level. Two main questions were addressed: what are the qualities required to function as a community leaders and how can these qualities be nurtured in low resourced settings. Thematic content analysis identified three core themes: first, personal qualities such as empathy with an understanding of the personal circumstances of persons in need of support, second, communicating clearly the vision and values informing their work, and thirdly, building and mobilising community support from families and neighbours. The nurturing of leadership comes through mentoring and coaching, the empowerment of others, networking opportunities and the development of inter-personal and communication skills. These themes were commonly expressed across the 16 leaders from all the participating nations and at all levels of responsibility which validates their universality. The findings are in marked contrast to current practices in health and social care that have valued professional expertise over lived experience, knowledge and technical skills over compassion and empathy, and the provision of person-centred ‘treatments’ over developing community and personal self-reliance. Nonetheless the challenges involved in establishing and sustaining new styles of leadership are many and will not be quickly resolved.
Posted: 13 March 2025
A Perspective on Economic Barriers and Disparities to Access Hormone Replacement Therapy in Low and Middle-Income Countries (MARIE-WP2d)
Gayathri Delanerolle,
Snehal Ghosh,
Paula Briggs,
Peter Phiri,
Julie Taylor,
Vindya Pathiraja,
Tharanga Mudalige,
Yassine Bouchareb,
Heitor Cavalini,
Sharron Hinchliff
Background Women globally spend a significant portion of their lives experiencing perimenopausal and menopausal symptoms, which can severely affect their quality of life. Hormone Replacement Therapy (HRT) has proven effective in alleviating symptoms such as hot flushes, sleep disturbances, and mood disorders. However, disparities in access to HRT exist, especially in low- and middle-income countries (LMICs), where socioeconomic factors and healthcare availability may limit treatment access.AimWe aimed to explore economic barriers and disparities to access to HRT across Brazil, Ghana, Malaysia, Nepal, Nigeria and Sri Lanka. Methods An exploratory study was conducted using publicly available data from national healthcare databases, pharmacies, and hospital formularies from Brazil, Ghana, Malaysia, Nepal, Nigeria, and Sri Lanka. The availability and cost of common HRT medicines, including oral and transdermal therapies, were analysed alongside of surgical procedures. Affordability was assessed by comparing the cost of a two-month HRT supply to the number of days of minimum wage work required to cover the cost. Additionally, Gross National income (GNI) per capita was also collected to contextualise these findings.Findings The availability of HRT medicines varied widely across the six countries, with Brazil and Nigeria offering a broader range of options compared to Ghana and Nepal. Pricing disparities were significant, with the cost of medicines such as the Mirena Coil requiring over 21 days of minimum wage work in Brazil and more than 260 days in Nigeria for Angeliq. Affordability remained a critical issue across LMICs, with high out-of-pocket costs restricting access to essential menopausal treatments.Conclusion This study reveals substantial economic barriers to accessing HRT in LMICs, driven by high costs and limited availability. Healthcare policy reforms to improve access and affordability of HRT in these regions are urgently needed. These findings can inform strategies to reduce healthcare inequalities and enhance women’s health outcomes globally.
Background Women globally spend a significant portion of their lives experiencing perimenopausal and menopausal symptoms, which can severely affect their quality of life. Hormone Replacement Therapy (HRT) has proven effective in alleviating symptoms such as hot flushes, sleep disturbances, and mood disorders. However, disparities in access to HRT exist, especially in low- and middle-income countries (LMICs), where socioeconomic factors and healthcare availability may limit treatment access.AimWe aimed to explore economic barriers and disparities to access to HRT across Brazil, Ghana, Malaysia, Nepal, Nigeria and Sri Lanka. Methods An exploratory study was conducted using publicly available data from national healthcare databases, pharmacies, and hospital formularies from Brazil, Ghana, Malaysia, Nepal, Nigeria, and Sri Lanka. The availability and cost of common HRT medicines, including oral and transdermal therapies, were analysed alongside of surgical procedures. Affordability was assessed by comparing the cost of a two-month HRT supply to the number of days of minimum wage work required to cover the cost. Additionally, Gross National income (GNI) per capita was also collected to contextualise these findings.Findings The availability of HRT medicines varied widely across the six countries, with Brazil and Nigeria offering a broader range of options compared to Ghana and Nepal. Pricing disparities were significant, with the cost of medicines such as the Mirena Coil requiring over 21 days of minimum wage work in Brazil and more than 260 days in Nigeria for Angeliq. Affordability remained a critical issue across LMICs, with high out-of-pocket costs restricting access to essential menopausal treatments.Conclusion This study reveals substantial economic barriers to accessing HRT in LMICs, driven by high costs and limited availability. Healthcare policy reforms to improve access and affordability of HRT in these regions are urgently needed. These findings can inform strategies to reduce healthcare inequalities and enhance women’s health outcomes globally.
Posted: 13 March 2025
Implementing a Clinical Research Database Management System in an Academic Institute: Lessons Learned
Janete Quelhas-Santos,
Daniela Santos,
Hadassa Santos,
Diogo Nogueira-Leite,
António Soares,
Ricardo Cruz Correia
Clinical research is a cornerstone of medical advancement, requiring efficient data management and coordination across multiple stakeholders. This study explores the implementation of a digital research management system at the Faculty of Medicine of the University of Porto (FMUP) to address the challenges posed by its extensive and diverse clinical research portfolio. Given the institution's need to centralize research activities, improve efficiency, and ensure regulatory compliance, the CR-Digital project was launched to integrate a comprehensive database management system. Over a two-year period, FUNDANET was selected and implemented due to its adaptability to FMUP’s research framework, its ability to enhance collaboration, and its alignment with legal and financial requirements. The implementation process was structured into seven key phases, with the primary challenge being the alignment of diverse departmental objectives and preferences. These ranged from ensuring seamless interoperability with electronic health records to meeting the usability needs of researchers and administrators. Despite these complexities, FUNDANET successfully provided a robust platform encompassing digital research management, clinical study tools, and advanced data analytics, streamlining research workflows and optimizing decision-making processes. This study highlights the lessons learned during the system’s deployment, demonstrating the importance of selecting adaptable technological solutions, fostering stakeholder engagement, and implementing structured change management strategies. The insights gained from this project can inform other institutions seeking to modernize their clinical research infrastructure, ultimately contributing to more efficient, transparent, and data-driven research environments.
Clinical research is a cornerstone of medical advancement, requiring efficient data management and coordination across multiple stakeholders. This study explores the implementation of a digital research management system at the Faculty of Medicine of the University of Porto (FMUP) to address the challenges posed by its extensive and diverse clinical research portfolio. Given the institution's need to centralize research activities, improve efficiency, and ensure regulatory compliance, the CR-Digital project was launched to integrate a comprehensive database management system. Over a two-year period, FUNDANET was selected and implemented due to its adaptability to FMUP’s research framework, its ability to enhance collaboration, and its alignment with legal and financial requirements. The implementation process was structured into seven key phases, with the primary challenge being the alignment of diverse departmental objectives and preferences. These ranged from ensuring seamless interoperability with electronic health records to meeting the usability needs of researchers and administrators. Despite these complexities, FUNDANET successfully provided a robust platform encompassing digital research management, clinical study tools, and advanced data analytics, streamlining research workflows and optimizing decision-making processes. This study highlights the lessons learned during the system’s deployment, demonstrating the importance of selecting adaptable technological solutions, fostering stakeholder engagement, and implementing structured change management strategies. The insights gained from this project can inform other institutions seeking to modernize their clinical research infrastructure, ultimately contributing to more efficient, transparent, and data-driven research environments.
Posted: 10 March 2025
Rehabilitation Needs Are Growing in Brazil and Across Its Regions, Including the Underserved: Secondary Analysis of the Global Burden of Disease Study
Rogério Olmedija de Araújo,
Tiótrefis Gomes Fernandes,
Tiago Silva Jesus
Posted: 06 March 2025
How Screen Time Affects Greek Schoolchildren’s Eating Habits and Sleep?
Irene Chrysovalantou Votsi,
Antonios E. Koutelidakis
Background: Television (TV), video games, PC and devices such as tablets and smart phones have become part of everyday life at an ever-younger age. Increased screen time correlates with unhealthy eating habits and reduced sleep duration among children. Methods: 374 children aged 9-12 years and their parents (n=159), from 3 schools in Lemnos and 5 schools in Thessaloniki, Greece, took part in this cross-sectional study. The children completed the KIDMED score and a questionnaire about their physical activity, time spent watching TV, PC and playing electronic games, the frequency of cooking or shopping with their parents, the frequency of eating fast food and soft drinks. Statistical analysis was performed with SPSSS-29.0, using One Way ANOVA, T-test, Cross Tabulation, Reliability Statistics, Bivariate, Bonferoni, Post-hoc, Kolmogorov – Smirnov and Pearson chi-square. Results: There was a statistically significant difference between soft drinks consumption and hours of television viewing (p=0.03). A statistically significant difference detected between television (p=0,024), video games (p=0,028), all screen categories (p=0,011) and fast-food consumption. The more hours children spent in front of screens, the less adherence they had to the Mediterranean Diet. Sleep hours and screen time were correlated (p=0.002). Conclusions: The results suggest that screen time seem to be interrelated and affect children’s eating behaviors and sleep duration. The study concluded that the longer the screen time the unhealthier dietary habits and lifestyle profile have schoolchildren. Future research should focus on reducing screen time, as a means of improving dietary patterns, sleeping and potentially reducing childhood obesity.
Background: Television (TV), video games, PC and devices such as tablets and smart phones have become part of everyday life at an ever-younger age. Increased screen time correlates with unhealthy eating habits and reduced sleep duration among children. Methods: 374 children aged 9-12 years and their parents (n=159), from 3 schools in Lemnos and 5 schools in Thessaloniki, Greece, took part in this cross-sectional study. The children completed the KIDMED score and a questionnaire about their physical activity, time spent watching TV, PC and playing electronic games, the frequency of cooking or shopping with their parents, the frequency of eating fast food and soft drinks. Statistical analysis was performed with SPSSS-29.0, using One Way ANOVA, T-test, Cross Tabulation, Reliability Statistics, Bivariate, Bonferoni, Post-hoc, Kolmogorov – Smirnov and Pearson chi-square. Results: There was a statistically significant difference between soft drinks consumption and hours of television viewing (p=0.03). A statistically significant difference detected between television (p=0,024), video games (p=0,028), all screen categories (p=0,011) and fast-food consumption. The more hours children spent in front of screens, the less adherence they had to the Mediterranean Diet. Sleep hours and screen time were correlated (p=0.002). Conclusions: The results suggest that screen time seem to be interrelated and affect children’s eating behaviors and sleep duration. The study concluded that the longer the screen time the unhealthier dietary habits and lifestyle profile have schoolchildren. Future research should focus on reducing screen time, as a means of improving dietary patterns, sleeping and potentially reducing childhood obesity.
Posted: 04 March 2025
Effective for Whom? A Review of Psychological and Social Intervention Recommendations in European Dementia Care Guidelines, Through the Lenses of Social Health and Intersectionality
David Neal,
Sara Laureen Bartels,
Saloua Berdai Chaouni,
Thais Caprioli,
Adelina Comas-Herrera,
Rabih Chattat,
Ana Diaz,
Rose-Marie Droes,
Thomas Faulkner,
Simone Anna Felding
In dementia care, access to effective psychosocial interventions is often addressed by evidence-based guidelines for care providers. However, it is unclear if current guidelines consider personal characteristics that may impact intervention effectiveness. This study investigates if, and within what framing, dementia care guidelines in Europe address what is effective and for whom. A review of 47 guidelines from 12 European countries was conducted. Content analysis focused on: i) if guidelines recommended specific psychosocial interventions, and how guidelines referred to ii) social health, iii) intersection of social positioning, and iv) inequities in care or outcomes. Thirty-five guidelines (74%) recommended specific psychosocial interventions. Around half referenced aspects of social health and of intersectionality. Thirteen guidelines (28%) referenced inequities. Social health was not explicitly recognised as a mechanism of psychosocial interventions. Only age and comorbidity were consistently considered to impact interventions’ effectiveness. Inequities were acknowledged to arise from within-country regional variations and individual economic status but not linked to (intersectional) individual societal positions such as sex and/or gender, sexuality, and/or religion. Results between European countries were heterogeneous. Current guidelines offer little insight into what works for whom. Policymakers and guideline developers should work with researchers, generating and translating evidence into policy.
In dementia care, access to effective psychosocial interventions is often addressed by evidence-based guidelines for care providers. However, it is unclear if current guidelines consider personal characteristics that may impact intervention effectiveness. This study investigates if, and within what framing, dementia care guidelines in Europe address what is effective and for whom. A review of 47 guidelines from 12 European countries was conducted. Content analysis focused on: i) if guidelines recommended specific psychosocial interventions, and how guidelines referred to ii) social health, iii) intersection of social positioning, and iv) inequities in care or outcomes. Thirty-five guidelines (74%) recommended specific psychosocial interventions. Around half referenced aspects of social health and of intersectionality. Thirteen guidelines (28%) referenced inequities. Social health was not explicitly recognised as a mechanism of psychosocial interventions. Only age and comorbidity were consistently considered to impact interventions’ effectiveness. Inequities were acknowledged to arise from within-country regional variations and individual economic status but not linked to (intersectional) individual societal positions such as sex and/or gender, sexuality, and/or religion. Results between European countries were heterogeneous. Current guidelines offer little insight into what works for whom. Policymakers and guideline developers should work with researchers, generating and translating evidence into policy.
Posted: 28 February 2025
Knowledge, Attitudes, and Practices of Learners Towards COVID-19 Guidelines in Bushbuckridge Local Municipality, Mpumalanga Province
Riborn Sibuyi,
Bumani Solomon Manganye,
Gudani Goodman Mukoma
Posted: 27 February 2025
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