Orientador: Carmem Maria Casquel Monti Juliani / Banca: Silvia Cristina Mangini Bocchi / Banca: Moneda Oliveira Ribeiro / Resumo: Enquanto Supervisora Técnica da área da saúde da Fundação CASA, o interesse pela temática surgiu em decorrência da preocupação com o direito à saúde, garantido por lei. O objetivo da pesquisa foi compreender a percepção da equipe de saúde da Fundação CASA (médicos, enfermeiros e auxiliares de enfermagem) sobre o funcionamento do sistema de referência e contra referência da rede pública de saúde, quando se faz necessário o encaminhamento do adolescente. A metodologia, de caráter qualitativo, utilizou a fenomenologia. As entrevistas áudio-gravadas foram realizadas entre maio e agosto de 2007, após assinatura do termo de consentimento livre e esclarecido. Após as etapas de transcrição, redução e compreensão fenomenológica foram evidenciadas os temas e as categorias e. As categorias são: o acesso ao atendimento à saúde pelo SUS, a condição de ser adolescente em conflito com a lei, o direito à saúde e a organização dos serviços de saúde. Os achados mostram a importância do desenvolvimento de pactuações com os municípios, exigindo maiores responsabilidades dos serviços na formulação de políticas de saúde vinculadas ao adolescente, assim como deve ocorrer para qualquer cidadão. Isto implica, na necessidade de propostas de gestão e melhoria da organização conforme diretrizes e princípios do Sistema Único de Saúde. / Abstract: As a health care Technical Supervisor for CASA Foundation, the interest in this topic arose from the concern about the right to health care, which is warranted by law. This study aimed at understanding the perception of the health care team working for CASA Foundation (physicians, nurses and nursing auxiliaries) as regards the functioning of the referral and contra referral system of the public health care network when adolescents' referral is required. The qualitative methodology was used based on phenomenology. The audio-taped interviews were conducted from May to August, 2007 after a free and informed consent document was signed by the participants. Following the transcription, reduction and phenomenological comprehension phases, the topics and categories were shown. The categories are: access to health care through the Unified Health Care System (SUS), the condition of being an adolescent in conflict with the law, the right to health care and the organization of health care services. The findings show the importance of developing agreements among municipalities, requiring greater liability from services in the formulation of health care policies for adolescents, similarly to what should occur for any other citizen. This implies the need for management proposals and organization improvement according to guidelines and principles of the Unified Health Care System. / Mestre

Orientador: Flavio Cesar de Sa / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas / Made available in DSpace on 2018-08-06T20:56:49Z (GMT). No. of bitstreams: 1 Assis_ArineCamposdeOliveira_M.pdf: 36295524 bytes, checksum: a4bb7ffe71271cf13afcda1ca78f2374 (MD5) Previous issue date: 2006 / Resumo: A Saúde como direito é uma prerrogativa da Constituição vigente no Brasil, que nasceu intrinsecamente ligada à idéia de que os homens têm direitos inalienáveis decorrentes de sua condição humana. No entanto, milhares de cidadãos brasileiros fazem uma leitura reducionista, entendendo-a como restrita ao acesso à consulta médica, realizada de forma imediata nos diversos Serviços de Saúde. Um dos fatos paradigmáticos desta cultura instituída é a tradicional superlotação dos Pronto-Socorros com pacientes portadores de casos de baixa complexidade clínica, passíveis de resolução em outros serviços de menor complexidade, que será tomada como objeto deste estudo. O ponto de partida foi o questionamento sobre quais fatores seriam condicionantes e moduladores desta configuração de demanda, optando por uma abordagem do problema numa perspectiva simbólica, tendo o estudo por objetivo compreender os significados que os usuários atribuem às suas necessidades de procura por algum cuidado em caráter de urgência. O caminho percorrido para chegar aos resultados foi o Método Qualitativo utilizando-me dos conceitos de urgência e emergência, articulados ao Modelo Teórico das Representações Sociais. Foi realizada uma investigação em um Pronto-Socorro Hospitalar em quatro Unidades Básicas de Saúde do município de Campinas, utilizando-se como instrumento entrevistas semi-estruturadas com usuários e profissionais de saúde. O material foi analisado através da Análise temática, evidenciando que o usuário constrói representações sociais sobre o urgente, que são histórica e culturalmente construídas, e muitas vezes conflitantes com o Paradigma Biomédico, tornando-se estas diferenças, elementos significativos na configuração da demanda e na dinâmica de funcionamento de serviços de saúde. Os resultados evidenciaram que, dos 38 (trinta e oito) pacientes entrevistados, doze (31,5%) referiram algum nível de gravidade em seus problemas, e os critérios utilizados para justificar a gravidade sentida foram principalmente as repercussões na autonomia para realização de suas atividades e a intensidade da dor. Entretanto, quando abordados em relação ao conceito de urgência e emergência, trinta e cinco pacientes os entendiam como sinônimos, sem expressarem-se claramente sobre os significados, embora os relacionando fortemente a acidentes de trânsito, ocorrências em vias públicas, traumas em geral na maior parte dos relatos, e muito pouco à intercorrências clínicas, evidenciando um distanciamento dos critérios utilizados pelos profissionais para definição de graus diferenciados de urgência para os problemas clínicos apresentados pelos pacientes. As questões levantadas a partir dos resultados apontam para a necessidade de rever a dimensão em que os interesses, necessidades, valores, atitudes e crenças da população estão sendo considerados como elementos norteadores de ações de planejamento na área da Saúde. Ressalta-se ainda a importância do desenvolvimento de mecanismos de gestão que incorporem a subjetividade das relações entre as expressões individuais e coletivas do saber leigo e os saberes estruturados da clínica e epidemiologia, articuladas a um amplo desenvolvimento de ações de educação em saúde, além de uma legitimação e integração qualificada da demanda espontânea ao conjunto de ações nas Unidades Básicas de Saúde, para que se viabilizem como efetiva porta de entrada, garantindo acesso às diferentes necessidades apresentadas pela população / Abstract: Health as a right is a prerogative of the actual Constitution in Brazil, which was born intrinsically linked on to the idea that men have inalienable rights recurring of the human being condition. However, thousands of Brazilian citizens make a reduced reading, understanding it as restricted to the access to the medical consultation, carried through in an immediate form in the several services of health. One of the paradigmatic facts of this instituted culture is the traditional super capacity of the Emergency Department with patients carrying cases of low clinical complexity, passable of resolution in other services of smaller complexity, which will be taken as object of this study. The starting point was the questioning on which factors would be conditioners and modulators of this configuration of demand, opting to a boarding of the problem in a symbolic perspective, having for objective of the study to understand the meanings that the users attribute to their necessities of search for some care in a state of urgency. The covered way to arrive at the results was the Qualitative Method using the urgency concepts and emergency, articulated to the theoretical Model of the Social Representations. An inquiry was carried through in an Emergency Department Hospital and four Basic Units of Health in the city of Campinas, using as instruments interviews half-structuralized with users and professionals of health. The material was analyzed through the Thematic Analysis, evidencing that the user constructs social representations on the urgent, which are historical and culturally constructed, and many times conflicting with the Biomedical Paradigm, becoming these differences, significant elements in the configuration of the demand and in the dynamics of functioning of the health services. The results evidenced that, of the 38 (thirty eight) patients interviewed, twelve (31,5%) related some level of gravity to their problems, and the used criteria to justify the sensible gravity was mainly the repercussions in the autonomy for the accomplishment of their activities and the intensity of pain. However, when asked about the relation of the concepts of urgency and emergency, thirty five patients understood them as synonymous, without expressing themselves clearly on the meanings, even though relating them strongly to the traffic accidents, occurrences in public ways, traumas in general in the biggest part of the stories, and very little to the clinical intercurrences, evidencing a gap on the criteria used by the professionals as a definition of different degrees of urgency for the clinical problems presented by the patients. The questions that were raised from the results point to the necessity to review the dimension where the interests, necessities, values, attitudes and beliefs of the population are being considered as guiding elements of action in planning in the Health area. It should be still highlighted the importance of the development of management mechanisms that incorporate the subjectivity of the relations between the individual and collective expressions of the common knowledge and the structuralized knowledge of the clinic and the epidemiology, articulated to an ample development of actions in the health education, besides a legitimization and a qualified integration of the spontaneous demand to the set of actions in the Basic Units of Health, so that they are made possible as an effective opening door, guaranteeing access to the different necessities presented by the population / Mestrado / Saude Coletiva / Mestre em Saude Coletiva

Orientador: Sergio Resende Carvalho / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas / Made available in DSpace on 2018-08-22T20:19:23Z (GMT). No. of bitstreams: 1 Souza_TadeudePaula_D.pdf: 1730036 bytes, checksum: ad2e6eaf302e19e0eb38612d993b23d5 (MD5) Previous issue date: 2013 / Resumo: Neste trabalho problematizamos o desafio de cumprimento do direito universal ao acesso em saúde para usuários de álcool e outras drogas no Brasil. Para isso apresentamos alguns vetores que interferem na produção de saúde para esta população. A análise destes vetores (de ordem política, histórica e subjetiva) nos conduziu a composição de um método de pesquisa situado no encontro entre a genealogia e a cartografia. Analisar os desafios do campo da saúde nos conduziu a necessidade de compreender alguns vetores construídos historicamente e ao mesmo tempo nos conduziu a necessidade de avaliar como estes vetores se atualizam no contemporâneo. Assim, o empreendimento de fazer uma genealogia das drogas nos conduziu a diferentes diagramas de saber-poder construídos historicamente. O empreendimento de fazer uma cartografia das drogas nos aproximou ao mesmo tempo dos movimentos atuais das políticas sobre drogas no cenário brasileiro e das experiências concretas vividas nas redes de saúde. Nesse ultimo caso propomos uma aproximação com as metodologias de avaliação participativa e interventiva no intuito de avaliar a rede de atenção a usuário de álcool e outras drogas do município de Campinas - SP. A trajetória de pesquisa de campo partiu das analises dos agentes redutores de danos, profissionais de saúde que acessam usuários de drogas em situação de rua. Além destes aspectos cabe ressaltar o trabalho conceitual que propôs uma análise histórica do conceito de universalidade e dos diferentes sentidos que ele pode assumir / Abstract: In this paper we problematize the challenge of fulfilling the right to universal access to health care services by alcohol and other drugs users in Brazil. To do that, we present some factors that interfere with the health status of these persons. The analysis of these factors (of political, historical and subjective order) led us to compose a research method located in the intersection of genealogy and cartography. Analyzing the challenges in the health field led us to the need to understand how these factors were historically constructed and at the same time how they are contemporary updated. Thus, the endeavor of making a genealogy of drugs led us to different knowledge-power diagrams that were historically constructed. At the same time, the endeavor of mapping the drugs brought us together to the current moves of drug policies in the Brazilian scenario as well as to the concrete experiences performed in mental health services. As to these latter, we propose an approach to participatory and intervention evaluation methodologies in order to evaluate the health care services network offered to alcohol and other drugs users in Campinas - SP. The path of this field research departs from the analysis made by some harm-reduction agents or healthcare workers who approach homeless drug users in street outreach practices, as well as the analytical perspective adopted in this paper derives from their experience. Besides these aspects it is worth noting the conceptual work that proposed a historical analysis of the different meanings that the concept of universality can take on / Doutorado / Política, Planejamento e Gestão em Saúde / Doutor em Saude Coletiva

"Although the number of new infections has dramatically decreased during the last ten years, portraying this country [Uganda] as the 'AIDS miracle', the number of people already infected and progressing to AIDS is increasing. Acces to anti-retroviral (ARV) drugs, as well as to medicines for treatment of opportunistic infections (TOI), is essential for people living with HIV/AIDS (PLWHA) to enjoy their right to life and health. Although access to these essentail medicines forms part of the core content of the right to health, which states should be able to provide irrespective of their available resources, slightly more than half of the people in need in Uganda were accessing them in June 2005. Of 63,896 PLWHA accessing ARVs, still 83.5 percent are paying the medicines out of their pockets. This is despite the fact that Uganda receives funds from various sources, among which Global Fund to Fight AIDS, Tuberculosis and Malaria (GF) and the US President's Emergency Plan for AIDS Relief (PEPFAR). Although the cost of ARV treatment in Uganda has dramatically decreased since 1997, the price of treatment remains still unaffordable for most Ugandans. ... This study comprises five chapters. The present chapter exposes the problem, the objectives of the study and the research questions, reviews the literature available on the subject, outlines the study's structure, proposes a methodology and points out the study's limitations and relevance. Chapter two sets out the international legal framework of the study. It oulines the scope of the right of PLWHA to access to essential treatment under different international instruments of relevance for Uganda and its connection with other human rights. The chapter also assesses the implications of this right for state and non-state actors. Chapter three sets out the national legal, policy and judicial framework. It explores the action taken by the various branches of the government in addressing the international obligations with regard to access essential treatment. This chapter will also look at the role played by other relevant stakeholders in the realisation of this right in Uganda. Chapter four analyses the various obstacles that impede the realisation of this right at national level, taking into account the globalisation process, the political situation of Uganda, as well as other socio-economic factors. Chapter five provides the final conclusions and recommends legal, judicial and administrative channels towards the realisation of the right to access essential treatment for OLWHA in Uganda." -- Introduction. / Thesis (LLM (Human Rights and Democratisation in Africa)) -- University of Pretoria, 2005. / [Prepared under the supervision of] Dr. Ben Kiromba Twinomugisha, Makerere University / http://www.chr.up.ac.za/academic_pro/llm1/dissertations.html / Centre for Human Rights / LLM

This research explores final year dental students’ knowledge and attitudes towards the treatment and management of patients with Intellectual and Developmental Disabilities (I/DD) as related to variations in the dental practices in Special Health Care Needs (SHCN) training they received. A quantitative, non-experimental study was conducted, employing survey data collection methods, to address descriptive, comparative, and correlational questions. One cohort, Class 2020, attended extramural rotations in specialized clinics for patients with I/DD and in-person lecture concerning this topic. However, due to the COVID-19 pandemic and its health-related restrictions, another cohort, Class 2021, did not have the same opportunity as rotations were cancelled and the lecture was prerecorded and viewed online. Responses from a 35-item survey, distributed through an online platform, were obtained from both cohorts (n= 14 for Class 2020; n= 19 for Class 2021), addressing descriptive, comparative, and correlational research questions. Results revealed higher levels of knowledge and more positive perceptions of the program from Class 2020, the group that received clinical guidance, than Class of 2021. Analysis revealed positive relationships between students’ confidence levels and whether they had examined, assisted, or treated patients with I/DD. Associations were also found between students’ confidence and willingness to treat patients with I/DD. Although only correlational, this study’s findings suggest ways to foster students’ confidence and induce positive attitudes in dental school graduates that are likely to improve equitable access to healthcare for those with I/DD.

Oral health is strongly correlated to systemic health in the United States. Dental professionals play a significant role in addressing the oral health and prevention of disease for populations in the United States. Because many areas in the United States lack access to dental care, the federal government considers dental hygienists part of the solution. It is now paying attention to restrictive dental hygiene scope of practice rules in each state. State dental boards, comprised mainly of dentists, make these rules based on their perception of dental hygienists' lack of education. This study explored fourth-year dental students' perceptions of the dental hygienist's education and scope of practice. This research found that while dental students felt that the dental hygienist would be a positive addition to their future practices, they did not wholly understand the rigors of dental hygiene education. In addition, dental schools may need to educate on the differences between direct and general supervision.

En mars 2020, l’Organisation mondiale de la santé déclare une pandémie mondiale de SARS-CoV-2. Rapidement, le gouvernement du Québec décrète l’état d’urgence sanitaire alors que la métropole de la province, Montréal, se voit affligée de la plus forte prévalence du virus lors de la première vague. La vulnérabilité et les iniquités antérieurement documentées sont potentialisées parmi les populations migrantes et plus spécifiquement pour celles vivant sans assurance médicale. Selon les données les plus récentes, 50 000 à 70 000 personnes vivent sans couverture médicale au Québec. Déjà, avant la pandémie, les personnes migrantes sans assurance médicale (MSAM) étaient confrontées à des barrières culturelles, linguistiques, économiques lorsqu’elles se présentaient dans le réseau public de santé. Ce mémoire de maîtrise vise à documenter les enjeux sociaux, de santé et d’accès aux soins au Québec, plus spécifiquement à Montréal pour la population MSAM dans le contexte de la COVID-19. Une analyse thématique des entretiens semi-dirigés menés auprès de personnes MSAM (n=19) est supportée par le cadre des déterminants sociaux de santé (Gautier et al.,2020). Quatre thèmes émergents de l’analyse seront présentés: Perceptions et attentes par rapport aux politiques (1), Précarité des conditions de vie et de travail : la position sociale déterminante avant et durant la pandémie (2), Stratégies d’adaptation (et leurs limites) pour prévenir les menaces à la santé (3) intraitables institutions de santé en pandémie de COVID-19 (Ou comment les institutions accentuent-elles les barrières d’accès aux soins?) (4). Les résultats de ce projet de recherche mettent en lumière des difficultés et des défis, potentiellement productrices d’ISS, auxquelles ont dit faire face les personnes MSAM durant les premières vagues de la pandémie. Des recommandations sont adressées aux décideurs et aux institutions de santé afin de favoriser l’inclusion des personnes MSAM dans la société québécoise. Celles-ci touchent notamment des politiques et des programmes pour améliorer leur accessibilité aux soins de santé et aux programmes sociaux en temps de pandémie et même au-delà. / In March 2020, WHO declares a global SARS-CoV-2 pandemic. Quickly, the Quebec government declared a state of health emergency while the metropolis of the province, Montreal, was afflicted with the highest prevalence of the virus during the first wave. Vulnerability and previously documented inequities are growing among migrant populations and more specifically for those living without medical insurance. According to the most recent data, 50,000 to 70,000 people live without medical coverage in Quebec. Already before the pandemic, uninsured migrants faced cultural, linguistic and economic barriers when they entered the public health network. This master's thesis aims to document the health and social challenges that they are facing in the context of COVID-19, in Quebec Province, specifically in Montreal. A thematic analysis of the semi-structured interviews conducted with uninsured migrants (n = 19) is supported by the social determinants of health framework (Gautier et al., 2020). Three emerging themes of the analysis will be presented: Precarious living and working conditions: Four emerging themes of the analysis will be presented: Perceptions and expectations in relation to policies (1), precarious living and working conditions: the decisive social position before and during the pandemic (2), adaptation strategies (and its limits) to prevent threats to health (3) Intractable health structures in the COVID-19 pandemic (or how to accentuate the barriers to access to care?) (4). The results of this research project shed light on the difficulties and challenges, potentially producing ISS, that uninsured migrants said they faced during the first waves of the pandemic. Recommendations are addressed to decision-makers and health institutions in order to promote the inclusion of uninsured migrants in Quebec. These relate to policies and programs to improve their accessibility to health care and social programs in times of pandemic and even beyond.

Because of evidence of regional variation in health and healthcare use, this thesis used health equity and access to care theory to examine regional differences in access to primary care, using survey- as well as secondary data in four empirical studies. First, a systematic literature review was used to categorize forms and reasons for regional healthcare shortages and access barriers, with a particular focus on rural areas. After information extraction from the selected studies and a thematic content analysis, the forms and causes identified in the literature were grouped and discussed. Following the literature-based review of these thematic foundations, a study was then designed to evaluate patient-reported access to primary care in exemplary German regions and assess empirical differences in rural vs. urban populations. This allowed the importance to patients of different access dimensions to be evaluated. For a subgroup of study participants with multidisciplinary care needs, care coordination failures and the supportive role of the general practitioner as a primary point of access was investigated. Finally, regional factors that are associated with variations in need, health, and utilisation beyond individual health determinants were identified, and placed on different regional framework conditions. These health-related factors were summarised in a regional deprivation measure and small-scale regions in Germany were differentiated by their regional deprivation by the main dimensions (material, social, ecological). Finally, their association to regional health outcomes were cross-sectionally estimated. To reduce unwarranted access variation, while also taking the patient perspective (by region) into account, the thesis concludes with a chapter on implications. Here, concepts for regional and multidimensional access monitoring, as well as further regulatory measures in capacity and distribution planning of primary care, are discussed.:Content Tables ........................................................................................................................... V Figures ....................................................................................................................... VI Abbreviations ........................................................................................................... VII 1. Background and research objectives .................................................................. 9 1.1. Health equity and access to health care ........................................................ 10 1.2. Regional variation as a contradiction to the equity principle ....................... 16 1.3. Reducing unwarranted regional variation in health care .............................. 20 1.4. Research objectives and thesis structure ...................................................... 24 References ............................................................................................................... 28 Legal sources .......................................................................................................... 33 2. Rural health care shortages and access barriers ............................................. 34 3. Regional access and satisfaction with primary care........................................ 35 Appendix 3 .............................................................................................................. 36 4. Access to primary care and outpatient care coordination .............................. 48 4.1. Introduction .................................................................................................. 49 4.2. Background ................................................................................................... 51 4.2.1. The patient perspective of care coordination ......................................... 51 4.2.2. Coordinating mechanisms ..................................................................... 52 4.3. Methods ........................................................................................................ 55 4.3.1. Data collection and sample .................................................................... 55 4.3.2. Measures ................................................................................................ 55 4.3.3. Data analysis .......................................................................................... 58 4.4. Results .......................................................................................................... 59 4.5. Discussion and limitations ............................................................................ 62 4.6. Implications .................................................................................................. 65 References ............................................................................................................... 69 Appendix 4 .............................................................................................................. 73 5. Area deprivation and its impact on health ....................................................... 76 6. Summary of implications ................................................................................... 77 6.1. Establishing a framework to assess primary care access and performance .. 77 6.2. Strengthening patient involvement in health care structure planning .......... 81 6.3. Strengthening access to GPs as outpatient care coordinators ....................... 84 6.4. Including regional deprivation factors in health care structure planning ..... 86 References ............................................................................................................... 90

<p>This thesis comprises three essays that empirically investigate important issues in two areas of health economics: physician labour supply and health insurance policy interventions.</p> <p>In the first essay, gendered associations between family status and physician labour supply are explored in the Canadian labour market, where physicians are paid according to a common fee schedule and have substantial discretion in setting their hours of work. Data from 1991 to 2006 show no gender difference in physician labour supply after controlling for family status. Male and female physicians have statistically indistinguishable hours of work when never married and without children. Married male physicians, however, have higher market hours than unmarried male physicians and parenthood either increases their hours or leaves them unchanged. In contrast, married female physicians have lower market hours than unmarried physicians and parenthood substantially lowers market hours. Little change over time in these patterns is observed for males, but for females two offsetting trends are observed: the magnitude of the marriage-hours effect declined, whereas that for motherhood increased. Preferences and/or social norms induce substantially different labour market outcome across the sexes. In terms of work at home, the presence of children is associated with higher hours for male physicians, but for females the hours increase is at least twice as large. A male physician’s spouse is much less likely to be employed in the presence of children, and if employed, has lower market hours in the presence of children. In contrast, a female physician’s spouse is more likely to be employed in the presence of children, and if employed, has slightly lower market hours in the presence of children. Both male and female physicians have lower hours of work when married to another physician.</p> <p>This second essay examines the impacts of a mandatory, universal prescription drug insurance program on health care utilization and health outcomes in a public health care system with free physician and hospital services. Beginning in 1997, all residents of the province of Quebec, Canada, were required by law to have drug insurance coverage. Under this program, all persons under age 65 who are eligible for a private plan are required to join that plan, while the public prescription drug insurance plan covers all Quebecers who are not eligible for a private plan. Using the National Population Health Survey from 1994 to 2003, we find that the mandatory program substantially increased drug coverage among the general population. The program also increased medication use and general practitioner visits but had little effect on specialist visits and hospitalization. Findings from quantile regressions suggest that there was a large improvement in the health status of less healthy individuals. Further analysis by pre-policy drug insurance status and the presence of chronic conditions reveals a marked increase in the probability of taking medication and visiting a general practitioner among the previously uninsured and those with a chronic condition. We also find evidence of positive health gains among the chronically ill.</p> <p>The third essay examines the impact of delisting routine eye exam services on patient eye care utilization and on providers’ labour market outcomes in a public health care system. Beginning in the early 1990s, provincial governments in Canada started to de-insure routine eye examinations from the basket of publicly funded health care services. We exploit delisting policy changes across Canadian provinces to estimate the impact of delisting from the supply- and demand-sides. Demand side analysis using the National Population Health Survey and Canadian Community Health Survey data suggests that the delisting of eye exams for the working age population decreased the probability of using eye care among this population group. However, the number of visits among those who continued to use eye care services was not affected. We also find suggestive evidence that the delisting policies targeted at the working age population were associated with increased eye care utilization among the elderly patients. Using the optometrist sample from the Canadian census data we find that the delisting of eye exams decreased optometrists’ weekly work hours while raised their annual work weeks. There was no statistically significant effect on optometrists’ income.</p> / Doctor of Philosophy (PhD)

Tusentals människor tvingas fly sina hemländer på grund av bland annat krig, förföljelse och våld. Under 2015 migrerade 60 miljoner vuxna och barn och ungdomar under 18 år. Syfte: Att beskriva den orala hälsan hos flyktingbarn. Metod: Allmän litteraturstudie. Litteratursökningen utfördes i tre databaser: CINAHL, DOSS och MEDLINE. Totalt valdes 16 vetenskapliga artiklar som var publicerade mellan åren 2014–2023. Resultat: Resultatet visar att de mest förekommande orala sjukdomarna bland flyktingbarn är karies och gingivit. Riskfaktorer för den orala hälsan identifieras som tillgång till tandvård och munhygienartiklar, socioekonomisk status och kost. Barn på flykt under en längre tid anses vara mer benägna att ha högre antal kariesskador jämfört med de motsvarande barnen på flykt under en kortare tid. Slutsats: Karies och gingivit är de mest förekommande orala sjukdomarna hos flyktingbarn. Riskfaktorerna som svårigheter med tillgång till tandvård och munhygiensartiklar, kost och socioekonomisk status är vanligt förekommande vilket påverkar förekomsten av karies och gingivit. / Thousands of people are forced to flee their home countries because of war, persecution and violence. In 2015, 60 million adults, children and adolescents under the age of 18 emigrated. Aim: To describe the oral health of refugee children. Method: Literature review. The literature search was performed in three databases. 16 scientific articles were selected that were published between 2014-2023. Results: The results show that the most prevalent oral diseases among refugee children are caries and gingivitis. Risk factors for oral health are identified as access to dental care and oral hygiene items, socioeconomic status and diet. Children on the move for a longer period of time are considered to be more likely to have higher rates of dental caries compared to their counterparts on the move for a shorter period of time. Conclusion: Dental caries and gingivitis are the most common oral diseases in refugee children. Risk factors such as difficulties in accessing dental care and oral hygiene products, diet and socioeconomic status are common and influence the prevalence of caries and gingivitis.