• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 281
  • 68
  • 13
  • 11
  • 8
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • Tagged with
  • 477
  • 431
  • 140
  • 113
  • 77
  • 63
  • 60
  • 58
  • 57
  • 56
  • 56
  • 44
  • 42
  • 39
  • 34
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
461

Experiences of HIV positive women who utilised the PMTCT programme in one of the central hospitals in Bulawayo, Zimbabwe

Moyo, Idah 02 1900 (has links)
Text in English / This qualitative descriptive phenomenological study explored the experiences of HIV positive women utilising PMTCT services at a central hospital in Zimbabwe. Data was collected using in-depth interviews of fifteen participants. The interviews were audio recorded and transcribed verbatim. Using the Interpretive Phenomenological Analysis framework for data analysis, two super-ordinate themes emerged, namely resources for provision of PMTCT services and approaches and nature of PMTCT care. The study revealed challenges experienced by HIV positive women emanating from material, financial and human resource related constraints in the PMTCT setting. The resource challenges negatively affected access and utilisation of PMTCT services. A practice model, whose purpose is to enhance the quality and utilisation of PMTCT services, was developed and described. The model was evaluated using Chin and Krammer (2011) criteria plus a modified form of the Delphi technique. These findings have implications for effective PMTCT service provision. The key lessons learnt for programmatic improvement were that in order to provide quality and accessible PMTCT services the health care system will need to be well resourced. There is need to strengthen the health care system in line with HIV related programmatic changes. / Health Studies / D. L.itt. et Phil. (Health Studies)
462

ACUMAAF: ambiente de computação ubíqua para o monitoramento e avaliação de atividade física / ACUMAAF: ambiente de computação ubíqua para o monitoramento e avaliação de atividade física

Nunes, Douglas Fabiano de Sousa 13 June 2012 (has links)
Made available in DSpace on 2016-06-02T19:05:57Z (GMT). No. of bitstreams: 1 4452.pdf: 7806002 bytes, checksum: 03f3df43afda775ba6b11c313093d1d5 (MD5) Previous issue date: 2012-06-13 / Financiadora de Estudos e Projetos / The physical inactivity has been indicated by the World Health Organization (WHO) as one of the main risk factors for the incidence of Chronic Non-Communicable Diseases (CNCDs). Millions of deaths in the world are a result of these diseases, and this number has increased each year. In an attempt to change this scenario WHO has stimulated regular practice of physical activities, because they play an important role in preventing CNCDs. In Brazil, these activities are performed by health units which generate a large amount of data that need treatment. To deal with this problem we developed UCEMEPA, an environment that employs Ubiquitous Computing technologies and wireless communication networks, in order to monitor remotely and evaluate participants of physical activity groups in real-time. This environment automatically collects physiologic data, and provides indicators which will support and direct public policies for promoting physical activity. In this sense, UCEMEPA will contribute for the promotion of health and quality of life, and for the conduction of longitudinal studies aiming to establish correlations between the practice of physical activity and CNCDs prevention. / A inatividade física tem sido apontada pela Organização Mundial de Saúde (OMS) como um dos principais fatores de risco comportamentais responsáveis pela incidência de Doenças Crônicas Não Transmissíveis (DCNTs). Milhões de mortes no mundo são decorrentes dessas doenças e esse número vem aumentando a cada ano. Na tentativa de reverter esse quadro a OMS vem estimulando as práticas regulares de atividade física, já que estas possuem um importante papel na prevenção de DCNTs. No Brasil a promoção dessas atividades é realizada por unidades regionalizadas de saúde e geram uma grande quantidade de dados que carecem de processamento e tratamento. Em resposta a esse problema nós desenvolvemos o ACUMAAF, um ambiente que emprega tecnologias emergentes da Computação Ubíqua e redes de comunicação sem fio para monitorar e avaliar, em tempo real e a distância, participantes de grupos de atividade física. Esse ambiente coleta dados fisiológicos de forma automática e coletiva e tem como objetivo possibilitar a geração de indicadores capazes de apoiar e nortear políticas públicas de promoção de atividade física. O ACUMAAF é um ambiente computacional com contribuições para a promoção da saúde, para a promoção da qualidade de vida da população e para a realização de estudos longitudinais objetivando relacionar atividade física e a prevenção de DCNTs.
463

A participação de um serviço público na atenção e implementação de ações à saúde do viajante no Brasil / The participation of a public service in attention and implementation of traveler health actions in Brazil

Tânia do Socorro Souza Chaves 08 August 2014 (has links)
A medicina de viagem (MV) surgiu em resposta ao crescente deslocamento populacional, com o objetivo de prevenir os agravos à saúde relacionados às viagens. No Brasil teve inicio no final da década de 90, momento em que reformas socioeconômicas levaram a melhorias das condições de vida dos brasileiros. O Núcleo de Medicina do Viajante (NMV), do Instituto de Infectologia Emilio Ribas (IIER), foi o primeiro serviço de atenção à saúde do viajante criado na cidade de São Paulo, em maio de 2000. O presente estudo visa: descrever a população de viajantes que procuraram orientação pré-viagem no Núcleo de Medicina do Viajante (NMV) do Instituto de Infectologia Emilio Ribas (IIER) no período de janeiro de 2006 a dezembro de 2010; descrever as medidas de prevenção recomendadas em relação às doenças infecciosas; descrever as atividades de ensino realizadas e a participação do serviço na discussão de diretrizes em políticas públicas em medicina de viagem. No período estudado, 2744 viajantes procuraram orientação pré-viagem no NMV do IIER. Foram realizados 2836 atendimentos de orientação pré-viagem, 92 viajantes procuraram o serviço mais de uma vez. A faixa etária entre 18 e 34 anos (54,2%), o sexo feminino (51,1%) e grau de educação superior (75,5%) foram as principais características demográficas desses viajantes. Os destinos mais procurados foram: África (24,5%), Europa (21,2%), Ásia (16,6%) e Brasil (19,2%). O turismo (35,7%) e o trabalho (35,7%) foram os motivos de viagem mais referidos. O tempo de permanência menor ou igual a 30 dias foi referido pelos viajantes em que o objetivo de viagem foi o turismo, enquanto os viajantes que referiram o trabalho ou estudo apresentaram maior tempo de permanência (p < 0,001). O meio de transporte mais referido foi o aéreo (62,8%). Os viajantes relataram durante a consulta pré-viagem dificuldade de acesso ao serviço. As fontes de informação mais referidas foram: informação a partir de amigos, indicação por profissional da saúde e mídia eletrônica. As medidas de prevenção recomendadas variaram conforme o destino. O tratamento autoadministrado para diarreia foi mais recomendado aos viajantes com destino à Ásia. As vacinas de febre amarela, poliomielite e antimeningocócica A e C foram mais recomendadas aos viajantes com destino à África, assim como a quimioprofilaxia para malária, que foi recomendada para 26,4% dos viajantes para esse destino. A quimioprofilaxia (QPX) para malária foi recomendada em 10,3% de todas as orientações. Houve diferença com significância estatística na recomendação segundo a finalidade (p < 0,30), o destino (p < 0,001) e a duração da viagem (p < 0,001). Das 422 orientações realizadas aos viajantes com destino ao Brasil, a QPX foi recomendada somente para 30 (7,1%). Dos 2744 viajantes atendidos, 664 (24,2%) relataram pelo menos uma morbidade prévia; 66 (2,4%) eram menores de 10 anos de idade; e 157 (5,7%) tinham 60 anos ou mais. Em relação às atividades de ensino, no período do estudo, 83 médicos residentes estagiaram no NMV e foram orientadas onze monografias de conclusão de residência médica. O NMV participou de 12 reuniões para discussão de diretrizes sobre a saúde do viajante e de iniciativas como a Carta de São Paulo (documento em defesa da saúde do viajante elaborado por acadêmicos e profissionais de saúde participantes do SUS). Da criação da Sociedade Brasileira de Medicina de Viagem e da criação do Comitê Estadual de Saúde do Viajante, pela Secretaria de Estado da Saúde de São Paulo. Essas atividades foram passos decisivos para corroborar a implementação de políticas públicas em saúde do viajante no Brasil / Travel medicine (TM) arose in response to the growing population displacement and its objective is the prevention of health problems related to travel. Began in Brazil in the in the late 1990s, at which socioeconomic reforms have led to improvements in of life of Brazilians. Travel Medicine Center (TMC) at \"Instituto de Infectologia Emilio Ribas\" (IIER) was the first health of traveler service created in São Paulo city in May 2000. The present study aims: to describe the traveler population who sought pre-travel guidance in TMC at IIER from January 2006 to December 2010; to describe the recommended preventive measures to travelers concerned with infectious diseases; to describe the teaching activities performed and the service involvement in debating guidelines about public policies in travel medicine. In the time period studied, a total of 2744 travelers sought pre-travel guidance in TMC of IIER, but 2836 assistances were provided for pre-trip orientation since 92 travelers sought the service more than once. The age group between 18-34 years (54.2%), female (51.1%), and university level degree (75.5%) were the main demographic characteristics. The more popular destinations were: Africa (24.5%), Europe (21.2%), Asia (16.6%) and Brazil (19.2%). Tourism (35.7%) and work (35.7%) were the main purposes of trip for travelers. For tourism purpose travelers would stay 30 or less days, while for work or study they stayed for a longer time (p <0,001). Commercial air travel was the preferred alternative (62.8%). The main sources of information were friends, health professionals, and electronic media. The recommended preventive measures varied according to the destination. The self-treatment for diarrhea was more recommended for travelers to Asia. Vaccination against yellow fever, polio, and anti-meningococcal (A and C) was more recommended for travelers to Africa, as well as chemoprophylaxis (CP) of malaria was recommended for 26.4% of travelers to the same country. The CP of malaria was indicated for 10.3% of all assistances. There was statistically significant difference in the recommendation according to purpose (p < 030), destination (p < 0.001) and trip duration (p < 0.001). From 422 assistances to travelers to Brazil, CP was only recommended for 30 (7.1%) travelers. From the 2744 travelers assisted, 664 (24.2%) reported at least one previous morbidity; 66 (2.4%) were under age 10; and 157 (5.7%) were 60 years or older. During the research period and relating to study activities, 83 residents were interns in TMC, and eleven monographs for completion of the Medical Residency were supervised. TMC participated in 12 meetings to discuss guidelines in travel medicine, and participated in initiatives such as \"Carta de São Paulo\" (a document in defense of traveler health prepared by academics and health professionals participating in the Unified Health System); in the institution of the Brazilian Society of Travel Medicine, and of the São Paulo State Travel Medicine Committee by the Secretariat for Health of São Paulo State. These were decisive steps to support implementation of public policies in traveler health in Brazil
464

Implications of a national immunization registry an alliance to win the race for the future care and accuracy of pediatric immunization

Patail, Shoaib Chotoo 01 January 2004 (has links)
This project examines the role of immunization registries and their effect on a health care delivery system. Recent efforts to attain coverage of child populations by recommended vaccines have included initiatives by federal and state agencies, as well as private foundations, to develop and implement statewide community-based childhood immunization registries.
465

Evaluation of immunization coverage among 0 to 24 month old children in Dzimauli Village, Vhembe District, South South

Nyathi, Emmanuel Mzwakhe 16 July 2015 (has links)
MPH / Department of Public Health
466

Hepatitis C Virus Screening in Federally Qualified Health Centers in Rural Appalachia

Olanrewaju, Folawiyo S, Falodun, Ayotola, Jawla, Muhammed, Vanhook, Patricia, McKenzie, Stacey 12 April 2019 (has links)
The prevalence of Hepatitis C Virus (HCV) in the US is estimated at 3.5 million with 18,153 deaths in 2016. It is the most common bloodborne infection, with a higher age-adjusted mortality rate than Hepatitis B Virus or Human Immunodeficiency Virus. Without treatment, nearly 1.1 million people will die from HCV by 2060. About 41,200 new cases of HCV were reported in 41 states in the US in 2016. The reported cases of acute HCV in 2016 is 2.3 per 100,000 in Tennessee, which is more than twice the national goal set by Healthy People 2020. This is a descriptive study to ascertain the HCV prevalence and usefulness of screening in medical outreach settings (MO) compared to indigent healthcare clinics (IHC) in northeast Tennessee. This study period was from April 2017 – February 2019. Participants (n=250), were adults, who engaged in routine, opt-out HCV testing at 4 IHC and 3 MO sites in the Tri-Cities, TN region. During the screening, demographic information- age, gender, race- were collected and the de-identified data were analyzed using Statistical Analysis System (SAS 9.3) to perform a descriptive analysis. Also, several discrete Chi-Square tests of independence between the demographic variables, screening locations, and HCV antibody prevalence was conducted. A total of 250 clients were screened for HCV. The majority of clients screened were non-Hispanic whites 228 (91.20%); females 136 (54.40%); young adults 131 (52.40%) and at IHC clinics 187 (74.80%). Screening showed HCV antibody prevalence of 14.8%. The majority of positive cases were non-Hispanic whites 36 (97.30%; P=0.1561); females 19 (51.35%; P=0.6867) and young adults 23 (62.16%; P=0.286). The prevalence at the IHC clinics and MO settings were 36 (97.30%; P=0.0006) and 1(2.70%) respectively. This analysis shows the higher yield of targeted HCV screening at IHC clinics. Focused HCV screening is critical in the era of opioid epidemic, particularly when direct-acting antiviral agents (DAAs) which offer a Sustained Virologic Response (SVR) rate of more than 90% are available. The use of case control or cohort study designs to establish causality is recommended for improving focused HCV screening.
467

Integrating indigenous and scientific knowledge in community-based early warning system development for climate-related malaria risk reduction in Mopani District of South Africa

Ramutsa, Brenda Nyeverwai January 2020 (has links)
PhD (Geography) / Department of Geography and Geo-Information Sciences / Malaria is a climate-change concatenated biological hazard that may, like any other natural hazard, can lead to a disaster if there is a failure in handling emergencies or risks. A holistic solution for malaria mitigation can be provided when indigenous knowledge is complemented with scientific knowledge. Malaria remains a challenge in South Africa and Limpopo province is the highest burdened malaria-endemic region. Specifically, Vhembe District is the highest burdened followed by Mopani District (Raman et al., 2016). This research sought to mitigate malaria transmissions in Mopani District through the integration of indigenous and scientific knowledge. The study was carried out in Mopani District of South Africa and 4 municipalities were involved. These are Ba-Phalaborwa, Greater Tzaneen, Greater Letaba, and Maruleng. A pragmatism philosophy was adopted hence the study took a mixed approach (sequential multiphase design). Data was collected from 381 selected participants through in-depth interviews, a survey and a focus group discussion. Participants for the in-depth interviews were obtained through snowballing and selected randomly for the survey, while for the focus group discussion purposive sampling was used. The study applied constructivist grounded theory to analyze qualitative data and to generate theory. Statistical Package for Social Sciences version 23.0 was used for quantitative data. Based on empirical findings, it was concluded that temperature and rainfall among other various factors exacerbate malaria transmission in the study area. Results of the study also show that people in Mopani District predict the malaria season onset by forecasting rainfall using various indigenous knowledge based indicators. The rainfall indicators mentioned by participants in the study were used in the developed early warning system. An Early warning system is an essential tool that builds the capacities of communities so that they can reduce their vulnerability to hazards or disasters. In the design of the system, Apache Cordova, JDK 1.8, Node JS, and XAMPP software were used. The study recommends malaria management and control key stakeholders to adopt the developed early warning system as a further mitigation strategy to the problem of malaria transmission in Mopani District. / NRF
468

Upplevelsen av att använda ett digitalt motivationsprogram för en hälsosam och hållbar livsstil hos personer med diabetes typ 2 eller prediabetes

Svedberg, Therese January 2023 (has links)
Bakgrund: Icke smittsamma sjukdomar, som diabetes typ 2, är en stor och ökande utmaning för ett hållbart samhälle. Diabetes typ 2 går att förebygga och behandla genom hälsosamma levnadsvanor. Digitala motivationsprogram som använder sig av beteendemodeller har visat sig vara kostnadseffektiva interventioner för att förbättra levnadsvanor. Vid utveckling av dessa tjänster är användarens behov viktigt för att få reda på vilka faktorer som bidrar till ett långsiktigt användande. Syfte: Syftet med studien var att undersöka hur personer med diabetes typ 2 och prediabetes upplevde användandet av en evidensbaserad digital tjänst som stödjer hälsosamma levnadsvanor. Metod: Studien var en kvalitativ explorativ studie där semistrukturerade intervjuer användes för att samla in data. Data analyserades med en kvalitativ induktiv innehållsanalys med fokus på det manifesta innehållet. Resultat: Resultatet visade på vikten av att det digitala motivationsprogrammet var användarvänligt för att optimera stöd för hälsosamma vanor och för att innehållet i det skulle nå fram till användaren. Appen upplevdes innehålla många uppskattade funktioner som stödjer möjligheten till mer hälsosamma vanor. Flera av funktionerna skulle ha haft ett högre användarvärde om de varit anpassade efter målgruppen och om användarvänligheten förbättrades. Slutsats: För att möjliggöra stöd till hälsosamma vanor behöver digitala motivationsprogram vara användarvänliga och anpassade efter den tänkta målgruppen. Genom att optimera tjänsten utifrån användarens upplevelse kan evidensbaserade digitala motivationsprogram bidra till att förbättra folkhälsan. Fler studier behövs för att studera vad som främjar långsiktigt användande och långtidseffekter. / Background: Non-communicable diseases, such as type 2 diabetes, are a major and increasing challenge for a sustainable society. Type 2 diabetes can be prevented and treated through healthy lifestyle habits. Digital motivational programs using behavioral models have been shown to be cost-effective interventions to improve lifestyle habits. When developing these programs, the user's needs are important in order to find out which factors contribute to long-term use. Purpose: The aim of the study was to explore how people with diabetes type 2 and prediabetes experienced the use of an evidence-based digital service that supports healthy lifestyle habits. Method: A qualitative explorative design was applied where semi-structured interviews were used to collect data. The data was analyzed with a qualitative inductive content analysis with a focus on the manifest content. Results: The result showed the importance of the digital motivation program being user-friendly in order to optimize support for healthy lifestyle habits and for its content to reach the user. The app was perceived to contain many appreciated features that support the possibility of healthy lifestyle habits. Several of the functions would have had a higher user value if they had been adapted to the target group and if the user-friendliness had been improved. Conclusion: To enable support for healthy lifestyle habits, digital motivation programs need to be user-friendly and adapted to the intended target group. By optimizing the program based on the user's experience, evidence-based digital motivation programs can contribute to improving public health. More studies are needed to explore what promotes long-term use and long-term effects.
469

Place de l’autonomisation dans l’observance thérapeutique des maladies chroniques non transmissibles au Cameroun : le cas des diabétiques et des hypertendus

Mogueo, Amélie 05 1900 (has links)
Introduction : Les maladies chroniques non transmissibles (MCNT) tuent chaque année près de 41 millions de personnes au monde, ce qui représente 71% du taux de mortalité mondiale. Le taux d’accroissement de ces maladies est plus élevé en Afrique Sub-Saharienne (ASS) comparativement au reste des pays du monde. Le Cameroun n’est pas en reste avec 35% du taux de mortalité attribuable aux MCNT dont l’hypertension artérielle (HTA) et le diabète de type 2 (DT2) qui sont en tête de liste, avec une prévalence de 32,1% et de 5,8% respectivement. L'HTA et le DT2 sont des maladies chroniques, coûteuses pour les patients et leurs familles qui supportent généralement seuls les coûts de traitement au Cameroun, compte tenu de l'insuffisance ou l’absence d'un système d'assurance maladie. De plus, ce qui est scientifiquement bien défini n’est pas toujours socialement/culturellement acceptable ou ne donne pas lieu à des changements de comportements attendus. Il en résulte une prépondérance de la non-observance des plans thérapeutiques par les patients. Il est donc urgent de mettre en œuvre des interventions à faible coût/efficacité axées sur les patients, qui leur permettent de mieux contrôler et de gérer leur maladie. Les interventions basées sur l’autonomisation des patients et de leurs familles, en plus d’améliorer la qualité des soins de santé, seraient utiles pour assurer l’observance des patients. Elles favoriseraient un meilleur contrôle de leurs paramètres biochimiques et physiques ainsi qu’une amélioration de leur mode de vie, notamment quand il s’agit des MCNT comme l’HTA et le DT2. L’objectif de la présente recherche est d’explorer les obstacles et facilitateurs de l’autonomisation des patients atteints de DT2 ou HTA au niveau individuel, organisationnel et systémique selon le point de vue et l’expérience de différents acteurs du système de soins camerounais. Méthodologie : Pour réaliser cette recherche, nous avons utilisé différentes méthodes de collecte et d’analyse des données. Nous avons d’abord réalisé́ une revue systématique avec méta-analyse pour identifier les interventions basées sur l’autonomisation des patients et leur efficacité dans le contrôle du DT2 en ASS. Nous avons utilisé les données issues de la revue systématique et d’autres écrits scientifiques pour développer un cadre conceptuel intégré multiniveau, adapté à notre contexte d’étude, le Cameroun. Nous avons ensuite eu recours à une étude qualitative multiniveau. Cette étude réalisée sur le terrain était une étude de cas unique à trois niveaux d’analyse imbriquée (macro, méso, micro). Pour explorer les barrières et les facilitateurs à l’autonomisation des patients, des entrevues semi-structurées ont été réalisées avec les patients (n = 23 participants) et leurs familles (n = 17 participants), les professionnels de la santé (six infirmiers/infirmières, deux médecins généralistes, et quatre médecins spécialistes) et les décideurs politiques (deux décideurs institutionnels et six décideurs centraux). Un groupe de discussion a été réalisé avec les patients préalablement interviewés (six participants). Des observations non participantes des consultations (n = 29) dans les bureaux des médecins spécialistes et des dispensations des services et soins de santé (n = 7) dans les salles d’hospitalisation ont été faites. Puis, des documents en rapport avec la prise en charge des patients diabétiques et hypertendus (n = 9) ont été analysés. Nous avons analysé ces données qualitatives à l'aide d'analyses thématiques et lexicométriques. Résultats: La revue systématique avec méta-analyse nous a permis de mettre en exergue l’efficacité des interventions basées sur l’autonomisation des patients en Afrique subsaharienne dans le contrôle du DT2 via l’amélioration de la glycémie et de la pression artérielle. Cette étude soutient les conclusions selon lesquelles les interventions à long terme et les interventions liées aux habitudes de vie seraient les plus efficaces dans l'amélioration du contrôle de la glycémie et de la pression artérielle. Cette efficacité était surtout liée à la fréquence des rencontres, au soutien à l’éducation des patients et à la participation active d’une équipe multidisciplinaire. L’étude multiniveau réalisée à l’hôpital de district de santé de Byiem-Assi (HDSB) au Cameroun a révélé que les facteurs exerçant une influence sur l'autonomisation des patients dans le contrôle de la maladie, identifiés par les différents participants à l’étude étaient similaires dans le même groupe de participants, et variaient beaucoup d’un groupe de participants à l’autre (ex : patients versus professionnels de la santé). Les participants identifiaient majoritairement les facteurs aux niveaux individuels et organisationnels, comparés à ceux du niveau central ou national, très peu ou pas connus des patients et leurs familles. Parallèlement, les décideurs politiques semblaient méconnaitre plusieurs facteurs au niveau individuel qui influencent l’autonomisation des patients. Les facteurs présents au niveau central, bien que peu nombreux et moins connus par les patients et leurs familles ainsi que certains professionnels de la santé, étaient généralement à l’origine des facteurs d’ordre individuel et organisationnel. Les facteurs identifiés par les patients étaient principalement liés à l'autogestion de la maladie. Il s’agissait des facteurs directement liés à la gestion de la maladie, identifiés au niveau individuel, en rapport avec les habitudes de vie des patients et sur lesquels ils pouvaient exercer un certain contrôle. Les facteurs au niveau organisationnel / hospitalier étaient plus ciblés par les membres de la famille, à l’exemple de long temps d’attente, indirectement liés à la gestion de la maladie par les patients et sur lesquels ils n’avaient aucun contrôle. L’implication des patients et leurs familles dans le processus de prise de décision et les supports à l’autogestion de la maladie aidaient ces derniers à mieux s’approprier leur rôle dans le contrôle de la maladie et à être responsables de leurs actions, et ultimement à développer un fort sentiment de cohérence. Cette étude met en exergue le rôle important que jouent les membres de la famille dans le développement de l’autonomisation des patients pour un meilleur contrôle de l’HTA et du DT2. Les facteurs identifiés par les professionnels de la santé étaient principalement liés à la prestation des services et soins de santé au niveau organisationnel et à l'autogestion de la maladie au niveau individuel. Les décideurs politiques étaient principalement axés sur les politiques / programmes élaborés au niveau central du ministère de la Santé et sur la prestation de services et soins de santé au niveau organisationnel. L’implication des professionnels de la santé dans le processus de prise de décision pour la prestation des services et soins de santé contribuait à promouvoir leur sentiment d'appropriation et de responsabilité sur ce qu'ils faisaient pour aider leurs patients à développer leurs capacités d'autogestion pour mieux contrôler leur maladie. Conclusion : A notre connaissance, cette étude est une première au Cameroun et dans l’ensemble des pays de l’ASS. Elle intègre les différents niveaux du système de soins avec la participation de différents acteurs pour l’exploration des facteurs qui contribuent ou pas à l’autonomisation des patients. Bien que les interventions axées sur la modification des facteurs au niveau individuel soient essentielles, il est nécessaire de développer aussi des interventions ciblant les obstacles organisationnels et politiques au développement de l’autonomisation des patients. Les interventions ciblant simultanément ces facteurs à plusieurs niveaux peuvent être plus efficaces que les interventions à un seul niveau. Le cadre conceptuel intégré que nous avons développé est une véritable contribution pour l’avancement de la science et pour le développement et la mise en œuvre des interventions futures de lutte contre les MCNT telles que l’HTA et le DT2. Dans l'ensemble, les résultats de cette thèse seront importants pour les cliniciens, les chercheurs, les patients et les décideurs politiques directement ou indirectement impliqués dans la prévention et le contrôle de l’HTA et du DT2 au Cameroun ainsi que dans des contextes similaires aux pays à revenu faible ou intermédiaire. / Background: Chronic noncommunicable diseases (CNCDs) kill nearly 41 million people worldwide each year, accounting for 71% of the global mortality rate. The rate of growth of these diseases is higher in Sub-Saharan Africa (SSA) compared to the rest of the world. In Cameroon, 35% of the mortality rate is attributable to CNCDs; hypertension (HTN) and type 2 diabetes (T2D) on the top of the list with the prevalence of 32.1% and 5.8%, respectively. HTN and T2D are long-term management diseases, financially draining for patients and their families generally bearing treatment costs in Cameroon, given the inadequate or non-existence of a health insurance system. Furthermore, what is scientifically known is not always socially or culturally acceptable or results in expected behavioural changes. This has resulted in a preponderance of patients’ being non-adherent to therapeutic plans. Thus, there is an urgent need to implement cost-effective patient-based interventions that empower patients to control and manage their own disease. Interventions based on patient empowerment have shown that, in addition to improving the quality of health care are necessary for patient adherence, allowing them to better control their biochemical and physical parameters as well as their lifestyle, especially when it comes to CNCDs such as HTN and T2D that patients are likely to deal with for the rest of their lives. The objective of this research is to explore the potential barriers and facilitators to patient empowerment at the individual, organizational, and systemic levels from the perspective and experience of different actors in the Cameroonian health care system. Method: For this thesis, we used different methods of data collection and analysis. We first conducted́ a systematic review and meta-analysis to identify patient empowerment-based interventions and their effectiveness in controlling T2D in sub-Saharan Africa. We did the literature review to develop an integrated multi-level conceptual framework adapted to our study context in Cameroon. The qualitative study that followed was a single case study with entailing three levels of embedded analysis within the primary healthcare district hospital (PHCDH) in Cameroon (macro, meso, micro). To explore barriers and facilitators to the development of patient empowerment, semi-structured interviews were conducted with patients (n = 23 participants) and their families (n = 17 participants), health professionals (six nurses, two general practitioners, four specialists) and policy makers (two institutional decision makers, six central decision makers). A focus group was conducted with patients (six participants), non-participant observations of consultations (n = 29) and health care delivery (n = 7), and document reviews related to the management of diabetic and hypertensive patients (n = 9). We analyzed these qualitative data using thematic and lexicometric analysis. Results: The systematic review and meta-analysis supports the findings that interventions based on patient empowerment may improve glycemia (HbA1c) and blood pressure of patients with T2D in SSA. The long-term and lifestyle interventions appeared to be the most effective interventions for glycemic control. Effectiveness that was mainly related to the frequency of meetings, the support for patient education and the active participation of a multidisciplinary team. The multilevel study conducted at the PHCDH in Cameroon revealed that factors influencing the development of patient empowerment in disease control identified by the different participants were similar within the same group and different between groups. There was a preponderance of factors identified at the individual and organizational levels, compared to factors identified at the central level. While patients and families knew very little about the central level factors, at the same time, policy makers seemed to be unaware of several factors at the individual level that influence the development of patient empowerment. The factors present at the central level were generally trigger those identified at the individual and organizational levels. Factors identified by patients were mainly associated with disease self-management. Present at the individual healthcare system level, they were related to patients' lifestyles, over which they could exercise some control. Factors at the organizational/hospital level were more targeted by family members, such as long waiting times, which were indirectly related to the patients' management of the disease and over which they had no control. Involving patients and their families in the decision-making process and providing them with supports for self-management of the disease helped them to have a sense of ownership and responsibility over what they are doing which leads to a sense of empowerment. This study further emphasizes the important role that family members called "caregivers" play in the development of patient empowerment in the disease-control process. Factors identified by health professionals were mainly related to the delivery of health care and services at the organizational level and to self-management of the disease at the individual level. Policy makers were mainly focused on policies/programs developed at the central level of the ministry of health and on the delivery of health care and services at the organizational level. Involving health care professionals in the decision-making process for the delivery of health care services tended to increase their sense of ownership and responsibility over what they were doing to help their patients develop self-management skills to better control their disease. Conclusion: To our knowledge, no prior study to this exists in Cameroon and in SSA countries that integrates the different levels of the health care system with different participants to explore the factors that contribute or not to the development of patient empowerment. While interventions focused on changing patient-level factors are essential, there is a need for more interventions addressing organizational and political barriers to the development of patient empowerment. Interventions simultaneously targeting these multilevel factors may be more effective than single-level interventions. The integrated conceptual framework we have developed is a real contribution to the advancement of science and to the development and implementation of future interventions for CNCDs such as HTN and T2D. Overall, the results of this thesis will be important for clinicians, researchers, patients, and policy makers directly or indirectly involved in the prevention and control of HTN and T2D in Cameroon as well as in similar settings in low- and middle-income countries.
470

Innate Immune Memory and the Host Response to Infection

Sherwood, Edward R., Burelbach, Katherine R., McBride, Margaret A., Stothers, Cody L., Owen, Allison M., Hernandez, Antonio, Patil, Naeem K., Williams, David L., Bohannon, Julia K. 15 February 2022 (has links)
Unlike the adaptive immune system, the innate immune system has classically been characterized as being devoid of memory functions. However, recent research shows that innate myeloid and lymphoid cells have the ability to retain memory of prior pathogen exposure and become primed to elicit a robust, broad-spectrum response to subsequent infection. This phenomenon has been termed innate immune memory or trained immunity. Innate immune memory is induced via activation of pattern recognition receptors and the actions of cytokines on hematopoietic progenitors and stem cells in bone marrow and innate leukocytes in the periphery. The trained phenotype is induced and sustained via epigenetic modifications that reprogram transcriptional patterns and metabolism. These modifications augment antimicrobial functions, such as leukocyte expansion, chemotaxis, phagocytosis, and microbial killing, to facilitate an augmented host response to infection. Alternatively, innate immune memory may contribute to the pathogenesis of chronic diseases, such as atherosclerosis and Alzheimer's disease.

Page generated in 0.0511 seconds