Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100374
Oscar Espinosa , Paul Rodríguez , Valeria Bejarano , Santiago León , José Luis Ortiz
Introduction
From 2021 to 2023, Colombia implemented a national policy to expand health insurance coverage for over 1.4 million Venezuelan migrants through its subsidized health insurance system, which provides universal health coverage to low-income Colombian populations. This study evaluates the cost-utility of the intervention, focusing on its health and economic returns.
Methods
We conducted a cost-utility analysis by translating government expenditure per enrolled migrant into health outcomes (QALYs/YLLs) using Colombia-specific cost-effectiveness thresholds. Health benefits were measured in quality-adjusted life years (QALYs) gained and years of life lost (YLLs) averted. Colombia-specific cost-effectiveness thresholds (CETs) were used to estimate outcomes, and an internal rate of return (IRR) analysis assessed the program's social profitability.
Results
The intervention generated an estimated 10,259 QALYs gained or 11,843 YLLs averted between 2021 and 2023. The IRR reached 27.5% when QALYs were valued at 100% of Gross Domestic Product per capita, indicating strong social returns. Women and adults aged 19–44 showed the greatest health gains, with urban areas receiving the highest benefits. This evidence demonstrates that even health policies can yield high social returns, providing a model for other countries navigating large-scale migration.
Discussion
Expanding subsidized health insurance to migrants proves to be a highly cost-effective policy. This analysis supports Colombia’s approach as a scalable and impactful model for inclusive public health aligned with universal health coverage goals.
{"title":"Health for all? A cost-utility evaluation of Colombia's policy to enroll Venezuelan migrants (2021–2023)","authors":"Oscar Espinosa , Paul Rodríguez , Valeria Bejarano , Santiago León , José Luis Ortiz","doi":"10.1016/j.jmh.2025.100374","DOIUrl":"10.1016/j.jmh.2025.100374","url":null,"abstract":"<div><h3>Introduction</h3><div>From 2021 to 2023, Colombia implemented a national policy to expand health insurance coverage for over 1.4 million Venezuelan migrants through its subsidized health insurance system, which provides universal health coverage to low-income Colombian populations. This study evaluates the cost-utility of the intervention, focusing on its health and economic returns.</div></div><div><h3>Methods</h3><div>We conducted a cost-utility analysis by translating government expenditure per enrolled migrant into health outcomes (QALYs/YLLs) using Colombia-specific cost-effectiveness thresholds. Health benefits were measured in quality-adjusted life years (QALYs) gained and years of life lost (YLLs) averted. Colombia-specific cost-effectiveness thresholds (CETs) were used to estimate outcomes, and an internal rate of return (IRR) analysis assessed the program's social profitability.</div></div><div><h3>Results</h3><div>The intervention generated an estimated 10,259 QALYs gained or 11,843 YLLs averted between 2021 and 2023. The IRR reached 27.5% when QALYs were valued at 100% of Gross Domestic Product per capita, indicating strong social returns. Women and adults aged 19–44 showed the greatest health gains, with urban areas receiving the highest benefits. This evidence demonstrates that even health policies can yield high social returns, providing a model for other countries navigating large-scale migration.</div></div><div><h3>Discussion</h3><div>Expanding subsidized health insurance to migrants proves to be a highly cost-effective policy. This analysis supports Colombia’s approach as a scalable and impactful model for inclusive public health aligned with universal health coverage goals.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"12 ","pages":"Article 100374"},"PeriodicalIF":2.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145525558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100368
Franziska Reinhardt, Imad Maatouk
While research has established links between migration and health outcomes, the role of cultural and social factors in mediating this relationship remains understudied. This study examines how family relationships, value orientations, and life satisfaction interact with migration status to influence health outcomes in Germany.
Using data from the Family Demographic Panel (FReDA), a representative German study on family relationships, we conducted multiple linear and multivariate regression analyses (n = 8939). The study employs a comprehensive set of health indicators, including both objective measures and self-reported health status.
The analyses reveal that migration status alone is not a significant predictor of health outcomes when controlling for social and cultural factors. Instead, life satisfaction and family relationships showed substantial effects on health. Both traditional and modern family values were linked to better health outcomes, showing that stable values, regardless of whether they are traditional or modern, can support health.
These findings challenge simplified assumptions about migration-health relationships and emphasize the importance of recognizing cultural values, social support systems, and psychosocial well-being as relevant factors in addressing health disparities. They also underscore the need for healthcare systems to adopt culturally sensitive approaches that consider the diverse social realities of individuals.
{"title":"Beyond individual integration: Family systems, social support networks and living environment as health determinants among migrants in Germany","authors":"Franziska Reinhardt, Imad Maatouk","doi":"10.1016/j.jmh.2025.100368","DOIUrl":"10.1016/j.jmh.2025.100368","url":null,"abstract":"<div><div>While research has established links between migration and health outcomes, the role of cultural and social factors in mediating this relationship remains understudied. This study examines how family relationships, value orientations, and life satisfaction interact with migration status to influence health outcomes in Germany.</div><div>Using data from the Family Demographic Panel (FReDA), a representative German study on family relationships, we conducted multiple linear and multivariate regression analyses (<em>n</em> = 8939). The study employs a comprehensive set of health indicators, including both objective measures and self-reported health status.</div><div>The analyses reveal that migration status alone is not a significant predictor of health outcomes when controlling for social and cultural factors. Instead, life satisfaction and family relationships showed substantial effects on health. Both traditional and modern family values were linked to better health outcomes, showing that stable values, regardless of whether they are traditional or modern, can support health.</div><div>These findings challenge simplified assumptions about migration-health relationships and emphasize the importance of recognizing cultural values, social support systems, and psychosocial well-being as relevant factors in addressing health disparities. They also underscore the need for healthcare systems to adopt culturally sensitive approaches that consider the diverse social realities of individuals.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"12 ","pages":"Article 100368"},"PeriodicalIF":2.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145473343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100367
Joshua A.N. van Apeldoorn , Julie S. Jansen , Eva L. Liefhebber , Özgül Uysal-Bozkir , Edanur Sert , Ralf E. Harskamp , Charles Agyemang , Edo Richard , Eric P. Moll van Charante
Objectives
First-generation Turkish migrants in the Netherlands face higher cardiovascular risk and are disproportionately affected by cardiovascular disease (CVD) compared to the Dutch host population. To improve prevention in primary care, we explored their views and preferences on cardiovascular prevention.
Design
We conducted a qualitative study by interviewing first-generation Turkish migrants in The Netherlands. Semi-structured interviews and focus groups, conducted in Dutch or Turkish, were analyzed using thematic analysis.
Results
We conducted 26 individual interviews and two sex-stratified focus group sessions. Participants were aware of CVD risk factors and related health hazards but struggled to adopt a healthy lifestyle, as family obligations, household responsibilities, and work often took precedence over personal health. All participants identified language barriers as a significant challenge, but opinions varied on whether it was necessary for GPs to understand Turkish culture. Some felt this was unnecessary, viewing GPs primarily as medical decision-makers or intermediaries for referrals to other (para)medics, with lifestyle advice outside their professional scope. They emphasized that GPs should ask openly about lifestyle rather than assuming that behaviours associated with a Turkish cultural background play a role.
Conclusions
First-generation Turkish migrants in the Netherlands were aware of CVD risk, but personal responsibilities posed challenges in adopting a healthy lifestyle. Although views on the importance of GPs understanding Turkish culture varied, participants agreed that GPs should ask openly about lifestyle rather than assuming cultural relevance in cardiovascular prevention.
{"title":"First-generation Turkish immigrants' views and preferences on cardiovascular disease prevention in primary care - a qualitative study in the Netherlands","authors":"Joshua A.N. van Apeldoorn , Julie S. Jansen , Eva L. Liefhebber , Özgül Uysal-Bozkir , Edanur Sert , Ralf E. Harskamp , Charles Agyemang , Edo Richard , Eric P. Moll van Charante","doi":"10.1016/j.jmh.2025.100367","DOIUrl":"10.1016/j.jmh.2025.100367","url":null,"abstract":"<div><h3>Objectives</h3><div>First-generation Turkish migrants in the Netherlands face higher cardiovascular risk and are disproportionately affected by cardiovascular disease (CVD) compared to the Dutch host population. To improve prevention in primary care, we explored their views and preferences on cardiovascular prevention.</div></div><div><h3>Design</h3><div>We conducted a qualitative study by interviewing first-generation Turkish migrants in The Netherlands. Semi-structured interviews and focus groups, conducted in Dutch or Turkish, were analyzed using thematic analysis.</div></div><div><h3>Results</h3><div>We conducted 26 individual interviews and two sex-stratified focus group sessions. Participants were aware of CVD risk factors and related health hazards but struggled to adopt a healthy lifestyle, as family obligations, household responsibilities, and work often took precedence over personal health. All participants identified language barriers as a significant challenge, but opinions varied on whether it was necessary for GPs to understand Turkish culture. Some felt this was unnecessary, viewing GPs primarily as medical decision-makers or intermediaries for referrals to other (para)medics, with lifestyle advice outside their professional scope. They emphasized that GPs should ask openly about lifestyle rather than assuming that behaviours associated with a Turkish cultural background play a role.</div></div><div><h3>Conclusions</h3><div>First-generation Turkish migrants in the Netherlands were aware of CVD risk, but personal responsibilities posed challenges in adopting a healthy lifestyle. Although views on the importance of GPs understanding Turkish culture varied, participants agreed that GPs should ask openly about lifestyle rather than assuming cultural relevance in cardiovascular prevention.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"12 ","pages":"Article 100367"},"PeriodicalIF":2.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145227176","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100303
Silvia Loi , Peng Li , Mikko Myrskylä
The weathering hypothesis implies that there is an interaction between age and race or ethnicity that results in marginalized groups experiencing a more rapid decline in health than the dominant groups. This hypothesis has been tested mostly focusing on racial and ethnic health inequalities, while less is known about weathering by immigration background. This paper aims at contributing to this strand of research by addressing four research questions: is the health of immigrants declining at a faster pace over the life-course, compared to non-immigrants? Do higher levels of education protect immigrants from accelerated ageing compared to non-immigrants? How do income and marital status affect the health trajectories of immigrants and non-immigrants? How do these patterns vary by sex? We use longitudinal survey data to estimate healthy ageing trajectories of immigrants and non-immigrants over the life-course, in the German context. We examine the roles of education, income, and marital status, separately for men and women. We find that immigrants, and especially immigrant women, have a faster health decline than non-immigrants; that high education is linked to higher levels of health, but does not protect immigrants from ageing in poorer health compared to non-immigrants; and that health disparities between immigrants and non-immigrants persist over the life-course net of the socio-economic controls, which appear to be secondary to other unobserved determinants.
{"title":"Unequal weathering: How immigrants’ health advantage vanishes over the life-course","authors":"Silvia Loi , Peng Li , Mikko Myrskylä","doi":"10.1016/j.jmh.2025.100303","DOIUrl":"10.1016/j.jmh.2025.100303","url":null,"abstract":"<div><div>The weathering hypothesis implies that there is an interaction between age and race or ethnicity that results in marginalized groups experiencing a more rapid decline in health than the dominant groups. This hypothesis has been tested mostly focusing on racial and ethnic health inequalities, while less is known about weathering by immigration background. This paper aims at contributing to this strand of research by addressing four research questions: is the health of immigrants declining at a faster pace over the life-course, compared to non-immigrants? Do higher levels of education protect immigrants from accelerated ageing compared to non-immigrants? How do income and marital status affect the health trajectories of immigrants and non-immigrants? How do these patterns vary by sex? We use longitudinal survey data to estimate healthy ageing trajectories of immigrants and non-immigrants over the life-course, in the German context. We examine the roles of education, income, and marital status, separately for men and women. We find that immigrants, and especially immigrant women, have a faster health decline than non-immigrants; that high education is linked to higher levels of health, but does not protect immigrants from ageing in poorer health compared to non-immigrants; and that health disparities between immigrants and non-immigrants persist over the life-course net of the socio-economic controls, which appear to be secondary to other unobserved determinants.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"11 ","pages":"Article 100303"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143101960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100324
Suhaila Halasa , Reema Safadi , Dua' Al-Maharma , Manar Nabolsi , Jennifer Dohrn , Muayyad Ahmad
Breastfeeding initiation and exclusivity are essential in reducing maternal and neonatal mortality and morbidity rates. Employing the Health Belief Model as a framework, this cross-sectional survey aimed to identify influencing factors and barriers to exclusive breastfeeding among 523 eligible Syrian refugee mothers living in Jordan. Of these, 35.8 % practiced exclusive breastfeeding and 36.9 % initiated breastfeeding within the first hour of birth. The logistic regression model showed that prior breastfeeding experience (OR = 5.06, p < 0.001, 95 % CI: 2.17–11.82), maternal satisfaction with feeding method (OR = 3.58, p < 0.001, 95 % CI: 1.89–6.76), medical insurance (OR = 1.74, p = 0.015, 95 % CI: 1.11–2.73), birth method (OR = 1.69, p = 0.034, 95 % CI: 1.04–2.73) and infant gender (OR= 0.64, p = 0.05, 95 % CI: 0.41–0.99) significantly influenced exclusive breastfeeding rates.
The findings revealed that breastfeeding practices do not align with WHO recommendations, emphasizing the crucial role of healthcare providers in supporting breastfeeding mothers during crises. It is essential to consider the unique circumstances and cultural backgrounds of refugees when evaluating their needs for developing breastfeeding programs. International health organizations, like the UNHCR, and host country policymakers should prioritize access to antenatal and postnatal counseling services and health insurance for mothers and children during crises.
母乳喂养的开始和专一性对于降低孕产妇和新生儿死亡率和发病率至关重要。采用健康信念模型作为框架,这项横断面调查旨在确定生活在约旦的523名符合条件的叙利亚难民母亲纯母乳喂养的影响因素和障碍。其中,35.8%实行纯母乳喂养,36.9%在出生后一小时内开始母乳喂养。logistic回归模型显示,既往母乳喂养经历(OR = 5.06, p <;0.001, 95% CI: 2.17-11.82),产妇对喂养方式的满意度(OR = 3.58, p <;0.001, 95% CI: 1.89-6.76)、医疗保险(OR= 1.74, p = 0.015, 95% CI: 1.11-2.73)、分娩方法(OR= 1.69, p = 0.034, 95% CI: 1.04-2.73)和婴儿性别(OR= 0.64, p = 0.05, 95% CI: 0.41-0.99)显著影响纯母乳喂养率。调查结果显示,母乳喂养做法不符合世卫组织的建议,强调了卫生保健提供者在危机期间支持母乳喂养母亲方面的关键作用。在评估难民制定母乳喂养计划的需求时,必须考虑他们的独特情况和文化背景。难民署等国际卫生组织和东道国决策者应优先考虑在危机期间为母亲和儿童提供产前和产后咨询服务和健康保险。
{"title":"Breastfeeding practices and exclusive breastfeeding among syrian refugee mothers in Jordanian Host Communities","authors":"Suhaila Halasa , Reema Safadi , Dua' Al-Maharma , Manar Nabolsi , Jennifer Dohrn , Muayyad Ahmad","doi":"10.1016/j.jmh.2025.100324","DOIUrl":"10.1016/j.jmh.2025.100324","url":null,"abstract":"<div><div>Breastfeeding initiation and exclusivity are essential in reducing maternal and neonatal mortality and morbidity rates. Employing the Health Belief Model as a framework, this cross-sectional survey aimed to identify influencing factors and barriers to exclusive breastfeeding among 523 eligible Syrian refugee mothers living in Jordan. Of these, 35.8 % practiced exclusive breastfeeding and 36.9 % initiated breastfeeding within the first hour of birth. The logistic regression model showed that prior breastfeeding experience (OR = 5.06, <em>p</em> < 0.001, 95 % CI: 2.17–11.82), maternal satisfaction with feeding method (OR = 3.58, <em>p</em> < 0.001, 95 % CI: 1.89–6.76), medical insurance (OR = 1.74, <em>p</em> = 0.015, 95 % CI: 1.11–2.73), birth method (OR = 1.69, <em>p</em> = 0.034, 95 % CI: 1.04–2.73) and infant gender (OR= 0.64, <em>p</em> = 0.05, 95 % CI: 0.41–0.99) significantly influenced exclusive breastfeeding rates.</div><div>The findings revealed that breastfeeding practices do not align with WHO recommendations, emphasizing the crucial role of healthcare providers in supporting breastfeeding mothers during crises. It is essential to consider the unique circumstances and cultural backgrounds of refugees when evaluating their needs for developing breastfeeding programs. International health organizations, like the UNHCR, and host country policymakers should prioritize access to antenatal and postnatal counseling services and health insurance for mothers and children during crises.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"11 ","pages":"Article 100324"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143768138","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100334
Akindele Abimibayo Adeoya
Objective
Health literacy (HL) is the ability to access, understand, evaluate, and apply health information for well-being. However, comparisons between domestic and international students remain limited. This study aims to investigate HL among Japanese and international university students in Japan and explore the factors that influence it.
Methods
This cross-sectional study used both the English and Japanese versions of the 47-item European Health Literacy Survey Questionnaire (HLS-EU-Q47). Using convenience sampling, a total of 1366 university students across six regions in Japan who provided informed consent participated in this self-administered, online-based survey. Descriptive statistics, t-tests, ANOVA and multiple regression were conducted as appropriate at a 0.05 alpha level using JMP statistical software (version 17.0.0)
Results
The results revealed that 60 % and 32 % of participants had inadequate and problematic HL, respectively, indicating that 92 % of all students had limited HL. International students exhibited better HL than Japanese university students (p < 0.0001), a difference that remained after adjusting for sociodemographic and educational factors (β = 3.39, 95 % confidence interval = 2.83 – 3.95, p < 0.0001). The competency of “appraising” within the healthcare domain presented the greatest challenge for international students, whereas “understanding” within the disease prevention domain was most difficult for Japanese students. Furthermore, the results indicated a strong association between HL and sociodemographic factors such as age, level of study, marital status, and religious affiliation. In contrast, health literacy showed an inverse association with economic status, program of study and parental education level. There was an observable trend between improved Japanese language proficiency and improved HL among international students.
Conclusion
International students in Japan demonstrated better HL than Japanese university students. Educational institutions must take a more proactive role in fostering HL for all students through general health education and peer-to-peer programs to create a more informed, healthy, and productive student community.
{"title":"Exploring health literacy among Japanese and international university students in Japan: A comparative cross-sectional study","authors":"Akindele Abimibayo Adeoya","doi":"10.1016/j.jmh.2025.100334","DOIUrl":"10.1016/j.jmh.2025.100334","url":null,"abstract":"<div><h3>Objective</h3><div>Health literacy (HL) is the ability to access, understand, evaluate, and apply health information for well-being. However, comparisons between domestic and international students remain limited. This study aims to investigate HL among Japanese and international university students in Japan and explore the factors that influence it.</div></div><div><h3>Methods</h3><div>This cross-sectional study used both the English and Japanese versions of the 47-item European Health Literacy Survey Questionnaire (HLS-EU-Q47). Using convenience sampling, a total of 1366 university students across six regions in Japan who provided informed consent participated in this self-administered, online-based survey. Descriptive statistics, <em>t</em>-tests, ANOVA and multiple regression were conducted as appropriate at a 0.05 alpha level using JMP statistical software (version 17.0.0)</div></div><div><h3>Results</h3><div>The results revealed that 60 % and 32 % of participants had inadequate and problematic HL, respectively, indicating that 92 % of all students had limited HL. International students exhibited better HL than Japanese university students (<em>p</em> < 0.0001), a difference that remained after adjusting for sociodemographic and educational factors (β = 3.39, 95 % confidence interval = 2.83 – 3.95, <em>p</em> < 0.0001). The competency of “appraising” within the healthcare domain presented the greatest challenge for international students, whereas “understanding” within the disease prevention domain was most difficult for Japanese students. Furthermore, the results indicated a strong association between HL and sociodemographic factors such as age, level of study, marital status, and religious affiliation. In contrast, health literacy showed an inverse association with economic status, program of study and parental education level. There was an observable trend between improved Japanese language proficiency and improved HL among international students.</div></div><div><h3>Conclusion</h3><div>International students in Japan demonstrated better HL than Japanese university students. Educational institutions must take a more proactive role in fostering HL for all students through general health education and peer-to-peer programs to create a more informed, healthy, and productive student community.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"11 ","pages":"Article 100334"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143894949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100341
Neila Gross , Maia C. Tarnas , Rashmina J. Sayeeda , Carly Ching , David Flynn , Muhammad H Zaman
Background
Infectious disease research is essential for disease prevention and management within refugee camps and informal settlements. The objective of this study is to identify the characteristics of existing infectious disease research in these settings and to assess stated research challenges, ethical considerations, and studied interventions within these studies.
Methods
This is a systematic review of forty primary studies focused on infectious disease research conducted among displaced populations. Included studies are published in English between 1995 and 2023. Three databases were searched, PubMed, Embase, and Web of Science, and this review was registered with PROSPERO (CRD42023461567). The risk of bias of the studies was assessed using the Mixed Methods Appraisal Tool.
Results
85 % of studies (n = 34) researched an intervention for infectious disease prevention or control and 70 % of studies (n = 28) were randomized controlled trials. 75 % of studies were located in Bangladesh (n = 15) or Pakistan (n = 15). 40 % of studies focused on diarrheal diseases (n = 16) and 28 % on malaria (n = 11). Common identified research challenges included population mobility, limited external validity, and low recruitment. No studies included the community in the initial study conception or investigated the research impact on the community. Community involvement was often through community health workers (45 %). Of the 18 studies that studied a resource-based intervention, 20 % explicitly noted that the intervention was unsustainable.
Discussion
While guidelines for conducting research in displaced settings exist, there are gaps in their utilization. We identified a disconnect between where displaced individuals reside and where research is conducted, as well as a prioritization of particular infectious diseases. Researchers identified numerous challenges in conducting research in these settings, though the community was rarely involved in the research. Context-specific considerations and community involvement are vital in research with displaced communities.
{"title":"Infectious disease research in forcibly displaced populations: A systematic review in low- and middle-income host countries","authors":"Neila Gross , Maia C. Tarnas , Rashmina J. Sayeeda , Carly Ching , David Flynn , Muhammad H Zaman","doi":"10.1016/j.jmh.2025.100341","DOIUrl":"10.1016/j.jmh.2025.100341","url":null,"abstract":"<div><h3>Background</h3><div>Infectious disease research is essential for disease prevention and management within refugee camps and informal settlements. The objective of this study is to identify the characteristics of existing infectious disease research in these settings and to assess stated research challenges, ethical considerations, and studied interventions within these studies.</div></div><div><h3>Methods</h3><div>This is a systematic review of forty primary studies focused on infectious disease research conducted among displaced populations. Included studies are published in English between 1995 and 2023. Three databases were searched, PubMed, Embase, and Web of Science, and this review was registered with PROSPERO (CRD42023461567). The risk of bias of the studies was assessed using the Mixed Methods Appraisal Tool.</div></div><div><h3>Results</h3><div>85 % of studies (<em>n</em> = 34) researched an intervention for infectious disease prevention or control and 70 % of studies (<em>n</em> = 28) were randomized controlled trials. 75 % of studies were located in Bangladesh (<em>n</em> = 15) or Pakistan (<em>n</em> = 15). 40 % of studies focused on diarrheal diseases (<em>n</em> = 16) and 28 % on malaria (<em>n</em> = 11). Common identified research challenges included population mobility, limited external validity, and low recruitment. No studies included the community in the initial study conception or investigated the research impact on the community. Community involvement was often through community health workers (45 %). Of the 18 studies that studied a resource-based intervention, 20 % explicitly noted that the intervention was unsustainable.</div></div><div><h3>Discussion</h3><div>While guidelines for conducting research in displaced settings exist, there are gaps in their utilization. We identified a disconnect between where displaced individuals reside and where research is conducted, as well as a prioritization of particular infectious diseases. Researchers identified numerous challenges in conducting research in these settings, though the community was rarely involved in the research. Context-specific considerations and community involvement are vital in research with displaced communities.</div></div><div><h3>Funding</h3><div>Wellcome Trust (Contract Number C-010,656).</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"12 ","pages":"Article 100341"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144534638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2024.100297
Rodrigo Puentes , María Alejandra Dünner , Natalia T. Santis-Alay , Mario E. Soto-Marchant , Cecilia Canales , Janepsy Díaz
Background
International migrants are central to HIV research, but comparative data on their infection rates versus resident populations, including in Chile, are scarce. This study compares HIV incidence rates between international migrants and Chileans.
Methods
A longitudinal study was conducted. Crude and standardized rates of new HIV infections reported by the Institute of Public Health of Chile (ISP) were calculated for the period 2013 to 2022, using data from public and private health facilities nationwide. Population estimates for international migrants and Chileans were obtained from the National Institute of Statistics (INE) and the National Migration Service (SERMIG). Rates were adjusted for age and sex using the direct method.
Results
A total of 51,513 validated new HIV infections were analyzed, of which 14,936 (29.0 %) occurred in international migrants and 36,577 (71.0 %) in Chileans. International migrants showed an increase in incidence rates between 2013 and 2022 (adjusted rate from 22.6 [95 % CI: 18.3 – 27.0] to 115.6 [95 % CI: 110.5 – 120.7] new HIV infections per 100,000 population). Throughout the study period, the ratio of adjusted incidence rates between international migrants and Chileans increased from 1.0 [95 % CI: 0.9 – 1.2] to 7.6 [95 % CI: 7.2 – 8.0].
Conclusions
HIV incidence rates were higher in international migrants than in Chileans and increased over the study period. This may be influenced by various exogenous factors, including social determinants of health and the COVID-19 pandemic. It is crucial to focus on HIV diagnosis, prevention, and control strategies for international migrants in Chile.
{"title":"Rate estimation and trend analysis of new HIV infections among the international migrant population in Chile from 2013 to 2022","authors":"Rodrigo Puentes , María Alejandra Dünner , Natalia T. Santis-Alay , Mario E. Soto-Marchant , Cecilia Canales , Janepsy Díaz","doi":"10.1016/j.jmh.2024.100297","DOIUrl":"10.1016/j.jmh.2024.100297","url":null,"abstract":"<div><h3>Background</h3><div>International migrants are central to HIV research, but comparative data on their infection rates versus resident populations, including in Chile, are scarce. This study compares HIV incidence rates between international migrants and Chileans.</div></div><div><h3>Methods</h3><div>A longitudinal study was conducted. Crude and standardized rates of new HIV infections reported by the Institute of Public Health of Chile (ISP) were calculated for the period 2013 to 2022, using data from public and private health facilities nationwide. Population estimates for international migrants and Chileans were obtained from the National Institute of Statistics (INE) and the National Migration Service (SERMIG). Rates were adjusted for age and sex using the direct method.</div></div><div><h3>Results</h3><div>A total of 51,513 validated new HIV infections were analyzed, of which 14,936 (29.0 %) occurred in international migrants and 36,577 (71.0 %) in Chileans. International migrants showed an increase in incidence rates between 2013 and 2022 (adjusted rate from 22.6 [95 % CI: 18.3 – 27.0] to 115.6 [95 % CI: 110.5 – 120.7] new HIV infections per 100,000 population). Throughout the study period, the ratio of adjusted incidence rates between international migrants and Chileans increased from 1.0 [95 % CI: 0.9 – 1.2] to 7.6 [95 % CI: 7.2 – 8.0].</div></div><div><h3>Conclusions</h3><div>HIV incidence rates were higher in international migrants than in Chileans and increased over the study period. This may be influenced by various exogenous factors, including social determinants of health and the COVID-19 pandemic. It is crucial to focus on HIV diagnosis, prevention, and control strategies for international migrants in Chile.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"11 ","pages":"Article 100297"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11759548/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143048124","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100323
Victoria Sophie Boettcher, Frank Neuner
Objective
Social support has been associated with the mental health of refugees. However, little is known about the characteristics and effects of social support in this group. The aim of this study was to investigate the protective role of social support, specifically through the perceived opportunity to confide in someone. We hypothesized that the opportunity to confide would have a moderating influence on the dose-effect relationship between trauma exposure and PTSD symptoms.
Methods
Clinical face-to-face interviews were conducted with 65 adult refugees who were living in the north-east of North Rhine-Westphalia. Interpreters (Arabic, Farsi, Kurmancî) were present if necessary. Interviews included a detailed assessment of traumatic event types, PTSD symptoms (assessed via the PTSD Checklist for DSM-5 (PCL-5)), and social support experienced by the participants.
Results
The multiple hierarchical regression analysis revealed a significant moderation of the perceived opportunity to confide on the association of number of traumatic event types reported and PTSD symptomatology. For refugees with limited trauma exposure, opportunity to confide was associated with lower PTSD symptoms. Most confidants were located within the countries of reception, while contacts in the home countries were less often identified as protective.
Conclusions
Social support, in particular the opportunity to confide, seems to act as a buffering factor up to a certain number of experienced traumatic event types. Specialized interventions may be necessary for people with a high trauma load and / or high symptom level.
{"title":"Posttraumatic stress among refugees: The moderating effect of perceived social support","authors":"Victoria Sophie Boettcher, Frank Neuner","doi":"10.1016/j.jmh.2025.100323","DOIUrl":"10.1016/j.jmh.2025.100323","url":null,"abstract":"<div><h3>Objective</h3><div>Social support has been associated with the mental health of refugees. However, little is known about the characteristics and effects of social support in this group. The aim of this study was to investigate the protective role of social support, specifically through the perceived opportunity to confide in someone. We hypothesized that the opportunity to confide would have a moderating influence on the dose-effect relationship between trauma exposure and PTSD symptoms.</div></div><div><h3>Methods</h3><div>Clinical face-to-face interviews were conducted with 65 adult refugees who were living in the north-east of North Rhine-Westphalia. Interpreters (Arabic, Farsi, Kurmancî) were present if necessary. Interviews included a detailed assessment of traumatic event types, PTSD symptoms (assessed via the PTSD Checklist for DSM-5 (PCL-5)), and social support experienced by the participants.</div></div><div><h3>Results</h3><div>The multiple hierarchical regression analysis revealed a significant moderation of the perceived opportunity to confide on the association of number of traumatic event types reported and PTSD symptomatology. For refugees with limited trauma exposure, opportunity to confide was associated with lower PTSD symptoms. Most confidants were located within the countries of reception, while contacts in the home countries were less often identified as protective.</div></div><div><h3>Conclusions</h3><div>Social support, in particular the opportunity to confide, seems to act as a buffering factor up to a certain number of experienced traumatic event types. Specialized interventions may be necessary for people with a high trauma load and / or high symptom level.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"11 ","pages":"Article 100323"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143760179","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.jmh.2025.100342
Chrissy PB Moonen , Christian JPA Hoebe , Casper DJ den Heijer , Jill Buursma , Marita ILS Werner , Ymke J Evers , Nicole HTM Dukers-Muijrers
Background
Migrant men who have sex with men (mMSM) carry a disproportionate burden of sexually transmitted infections (STIs) yet encounter unique barriers to accessing sexual healthcare. This qualitative study explored mMSM’s and professionals’ perspectives regarding mMSM’s personal, social and structural barriers and facilitators to Dutch sexual healthcare access and outreach strategies.
Methods
A qualitative study was conducted using semi-structured interviews with 15 mMSM (aged ≥16) and 10 professionals from various organisations working with mMSM. mMSM were recruited via sexual health nurses at three STI clinics of a Dutch Public Health Service and flyers; professionals via email, flyers, and the project team’s network. Transcripts were analysed thematically using deductive and inductive coding by two researchers, ensuring intercoder agreement.
Results
Key facilitators for sexual healthcare access included supportive social networks, in-person consultations, and culturally and LGBTQ+-sensitive staff. Main barriers involved fear of stigma rooted in cultural and religious beliefs, limited awareness of available services, and language-related challenges. Suggested outreach strategies included dating app advertisements, short multilingual videos, and translated posters in venues frequented by mMSM (e.g., bars and schools). Notably, most participants accessed services through personal referrals, underlining the importance of including social networks in outreach strategies.
Conclusions
Addressing personal, social and structural barriers while enhancing facilitators contributes to more inclusive and equitable sexual healthcare services. Besides, increasing reach of mMSM through the dissemination of tailored information via social networks, digital platforms, and community settings further supports this objective. These findings inform strategies aimed at reducing health disparities and contribute to broader STI, HIV, and hepatitis prevention goals.
{"title":"Perspectives of migrant men who have sex with men and professionals on personal, social and structural barriers and facilitators to sexual healthcare access and outreach strategies: A qualitative study","authors":"Chrissy PB Moonen , Christian JPA Hoebe , Casper DJ den Heijer , Jill Buursma , Marita ILS Werner , Ymke J Evers , Nicole HTM Dukers-Muijrers","doi":"10.1016/j.jmh.2025.100342","DOIUrl":"10.1016/j.jmh.2025.100342","url":null,"abstract":"<div><h3>Background</h3><div>Migrant men who have sex with men (mMSM) carry a disproportionate burden of sexually transmitted infections (STIs) yet encounter unique barriers to accessing sexual healthcare. This qualitative study explored mMSM’s and professionals’ perspectives regarding mMSM’s personal, social and structural barriers and facilitators to Dutch sexual healthcare access and outreach strategies.</div></div><div><h3>Methods</h3><div>A qualitative study was conducted using semi-structured interviews with 15 mMSM (aged ≥16) and 10 professionals from various organisations working with mMSM. mMSM were recruited via sexual health nurses at three STI clinics of a Dutch Public Health Service and flyers; professionals via email, flyers, and the project team’s network. Transcripts were analysed thematically using deductive and inductive coding by two researchers, ensuring intercoder agreement.</div></div><div><h3>Results</h3><div>Key facilitators for sexual healthcare access included supportive social networks, in-person consultations, and culturally and LGBTQ+-sensitive staff. Main barriers involved fear of stigma rooted in cultural and religious beliefs, limited awareness of available services, and language-related challenges. Suggested outreach strategies included dating app advertisements, short multilingual videos, and translated posters in venues frequented by mMSM (e.g., bars and schools). Notably, most participants accessed services through personal referrals, underlining the importance of including social networks in outreach strategies.</div></div><div><h3>Conclusions</h3><div>Addressing personal, social and structural barriers while enhancing facilitators contributes to more inclusive and equitable sexual healthcare services. Besides, increasing reach of mMSM through the dissemination of tailored information via social networks, digital platforms, and community settings further supports this objective. These findings inform strategies aimed at reducing health disparities and contribute to broader STI, HIV, and hepatitis prevention goals.</div></div>","PeriodicalId":34448,"journal":{"name":"Journal of Migration and Health","volume":"12 ","pages":"Article 100342"},"PeriodicalIF":3.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144557291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}