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Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Yassin, Khaled. "Unravelling the mystery of liver diseases in Egypt : the burden of disease /." Lage : Jacobs, 2001. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=009222709&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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Plaß, Dietrich [Verfasser]. "The Burden of Disease framework – success story but necessities for adaptations: potentials and challenges when measuring the disease burden of infectious diseases and the disease burden at a sub-national level / Dietrich Plaß." Bielefeld : Universitätsbibliothek Bielefeld, 2014. http://d-nb.info/1059476282/34.

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Silva, Guilherme. "Economic disparities and intensifying burden of neglected tropical diseases." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=119615.

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This thesis examines the interaction between economic disparities and the burden of neglected tropical diseases through a multi-layered study of international agreements, mostly the Trade Related Aspects of Intellectual Property (TRIPS), the health structure in developing countries and the manner in which intellectual property rights relate to the right to health in poor countries. By shedding light to this interaction, it will be demonstrated that small attention and resources is attributed to neglected tropical diseases. The predominance of the interests of affluent economic stakeholders ove

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Parham, Rhian. "Caregiver burden in paediatric chronic kidney disease." Thesis, Canterbury Christ Church University, 2011. http://create.canterbury.ac.uk/10347/.

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Section A provides an overview of the role of family caregivers of individuals with chronic illness, and describes key conceptualisations and theories posited in the caregiver literature. This is followed by an overview of research conducted with caregivers of children with chronic kidney disease (CKD), a summary of the limitations of this research, and suggestions for future research. Section B Despite a recognised need to monitor caregiver burden in caregivers of children with CKD, there is no measurement tool currently available to meet this aim. The present research documents the developme

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Choate, Radmila. "ESTIMATING DISEASE SEVERITY, SYMPTOM BURDEN AND HEALTH-RELATED BEHAVIORS IN PATIENTS WITH CHRONIC PULMONARY DISEASES." UKnowledge, 2019. https://uknowledge.uky.edu/epb_etds/22.

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Chronic pulmonary diseases include a wide range of illnesses that differ in etiology, prevalence, symptomatology and available therapy. A common link among these illnesses is their impact on patients’ vital function of breathing, high symptom burden and significantly impaired quality of life. This dissertation research evaluates disease severity, symptom burden and health behaviors of patients with three different chronic pulmonary conditions. First, alpha-1 antitrypsin deficiency (AATD) is an inherited condition that typically is associated with an increased risk of early onset pulmonary emph

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McCormick, Natalie. "The health resource utilization and economic burden of systemic autoimmune rheumatic diseases." Thesis, University of British Columbia, 2012. http://hdl.handle.net/2429/42149.

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Background: SARDs (Systemic Autoimmune Rheumatic Diseases) are a group of rare, chronic conditions (systemic vasculitis, systemic lupus erythematosus, scleroderma, Sjogren's disease, and poly/dermatomyositis) associated with high health resource consumption. However, estimates of their healthcare burden are sparse, with most determined at tertiary centres over short periods. Studying them separately has also limited research progress. Here we grouped the SARDs, for the first time ever, to quantify their collective, longitudinal (twelve-year) burden at the population-level. Methods: A popula

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White, Sarah L. "The epidemiology of lifestyle-related and social risk factors for chronic kidney disease, and approaches to the burden of disease." Thesis, The University of Sydney, 2009. https://hdl.handle.net/2123/28217.

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Background and objectives Chronic kidney disease (CKD) refers to a progressive and irreversible loss of kidney function, the key outcomes of which are end-stage kidney disease (ESKD), requiring dialysis or a kidney transplant, or premature death typically due to cardiovascular complications. CKD is identified either by evidence of kidney damage (especially proteinuria or albuminuria) or decreased kidney function, measured according to glomerular filtration rate (GFR). Prevention of CKD, and timely intervention where disease does occur, is an emerging public health priority. However, our under

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Husain, Muhammad Jami, Simiao Chen, Michael Kuhn, Klaus Prettner, and David E. Bloom. "The macroeconomic burden of noncommunicable diseases in the United States: Estimates and projections." Public Library of Science, 2018. http://dx.doi.org/10.1371/journal.pone.0206702.

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We develop and calibrate a dynamic production function model to assess how noncommunicable diseases (NCDs) will affect U.S. productive capacity in 2015-2050. In this framework, aggregate output is produced according to a human capital-augmented production function that accounts for the effects of projected disease prevalence. NCDs influence the economy through the following pathways: 1) when working-age individuals die of a disease, aggregate output undergoes a direct loss because physical capital can only partially substitute for the loss of human capital in the production process. 2) I

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Obot, Stella S. "Health Care Disparities and Chronic Disease Burden: Policy Implications for NGOs." Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/iph_theses/88.

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The purpose of this capstone is to develop a program to address health literacy among African American adults. The social cognitive theory and the health belief model was used to create a model of an age appropriate, culturally sensitive program with a pre and post test to improve the health literacy in this population. The Community Health Literacy Improvement Program (CHIP) is a pilot program that will consist of a four week didactic intervention focused on combating prose, document, and quantitative health illiteracy. This program will be implemented through a community based nonprofit o

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Bigatti, Silvia Marcela. "Relationships between perceived burden, physical health, and health care use among spouses of people with fibromyalgia syndrome /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2000. http://wwwlib.umi.com/cr/ucsd/fullcit?p9970686.

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Adeloye, Davies Olubunmi. "Estimating the burden of selected non-communicable diseases in Africa : a systematic review of the evidence." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/21090.

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Background The burden of non-communicable diseases (NCDs) is rapidly increasing globally, and particularly in Africa, where the health focus, until recently, has been on infectious diseases. The response to this growing burden of NCDs in Africa has been affected owing to a poor understanding of the burden of NCDs, and the relative lack of data and low level of research on NCDs in the continent. Recent estimates on the burden of NCDs in Africa have been mostly derived from modelling based on data from other countries imputed into African countries, and not usually based on data originating from

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Katzenellenbogen, Judith Masha. "Use of data linkage to enhance burden of disease estimates in Western Australia : the example of stroke." University of Western Australia. School of Population Health, 2009. http://theses.library.uwa.edu.au/adt-WU2009.0117.

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[Truncated abstract] The Disability-Adjusted Life Year index, developed by the Global Burden of Disease Study, is used extensively to compare disease burden between locations and over time. While calculation of the fatal component of this measure, Years of Life Lost, is relatively straight-forward, the non-fatal component, Years Lived with Disability, is based on parameters that are challenging to estimate. This thesis pioneers the use of the Western Australian Data Linkage System to enhance epidemiological parameters underpinning Years Lived with Disability, providing, by way of illustration,

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Bugajski, Andrew A. "BIOLOGICAL, BEHAVIORAL, AND PSYCHOSOCIAL ATTRIBUTES OF INDIVIDUALS WITH COPD." UKnowledge, 2018. https://uknowledge.uky.edu/nursing_etds/36.

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The purpose of this dissertation was to evaluate the biological, behavioral, and psychosocial attributes of individuals diagnosed with chronic obstructive pulmonary disease (COPD). Specific aims were to: 1) explore the predictive power of spirometry measures for event-free survival in patients with heart failure and suspected COPD, focusing on the differences in survival between those with and without airflow limitation; 2) examine the psychometric properties of the Multidimensional Scale of Perceived Social Support (MSPSS) in patients with concomitant COPD and heart failure; and 3) test the e

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Chen, Jing, and 陈静. "Economic evaluation of community pharmacy based smoking cessation on burden of chronic obstructive pulmonary disease (COPD) in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47157252.

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Background: Chronic Obstructive Pulmonary Disease (COPD) poses a substantial burden to Hong Kong. Smoking is the single most important risk factor for COPD. Intensive smoking cessation in COPD patients slows disease progression. Community pharmacy based smoking cessation in healthy smokers could forestall COPD onset. Each of these programs has been proven effective and cost-effective worldwide. Currently there are smoking cessation clinics in Hong Kong. But community pharmacy-based smoking cessation services are not available. The present study firstly attempts to identify the disease

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Bolden, Lois Vennesta. "Depression, anxiety, hazardous drinking, subjective burden, and rewards in family caregivers of patients with chronic liver disease." View the abstract Download the full-text PDF version (on campus access only), 2006. http://etd.utmem.edu/ABSTRACTS/2006_009_bolden_index.html.

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Thesis (Ph.D.)--University of Tennessee Health Science Center, 2006.<br>Title from title page screen (viewed on October 26, 2007 ). Research advisor: Mona Newsome Wicks, Ph.D., RN. Document formatted into pages (xii, 174 p. : ill.) Vita. Abstract. Includes bibliographical references (p. 115-132).

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Lin, Kai. "Exploring treatment burden in people with type 2 diabetes mellitus (T2DM) in primary care settings." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2024. https://ro.ecu.edu.au/theses/2814.

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Introduction Treatment burden is the perceived workload of care by individuals. The treatment burden experienced by individuals with Type 2 Diabetes Mellitus (T2DM) is a major obstacle to achieving effective healthcare outcomes. The aim of this research is to facilitate better management of treatment burden in people with T2DM in primary care settings. Methods A systematic review, encompassing narrative analysis was used to characterise the treatment burden of T2DM and critical appraisal was used to identify the appropriate patient-reported outcome measures (PROMs) for measuring this burden. T

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Schielein, Maximilian [Verfasser], and Alexander [Akademischer Betreuer] Zink. "Mental health in dermatology: addictions in psoriasis and an outlook on the psychosocial burden of chronic skin diseases / Maximilian Schielein ; Betreuer: Alexander Zink." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2021. http://d-nb.info/1232645427/34.

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Ribeiro, de Oliveira Annabella. "Towards a More Equitable Future: A Single-Dose HPV Vaccine to Reduce the Global Burden of Cervical Cancer." Scholarship @ Claremont, 2019. https://scholarship.claremont.edu/scripps_theses/1292.

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Human papillomavirus (HPV) infection currently stands as the most common sexually transmitted disease in the world. With an estimated lifetime probability of disease acquisition of 84.6% for females and 91.3% for males with at least one sexual partner, HPV is an aggressive and ubiquitous virus that affects people from all walks of life. The virus generally resolves on its own within 1 year, but successful disease progression leads to complications ranging from genital warts to anogenital cancers. Globally, there are 530,000 new cases of, and 274,000 deaths caused by, cervical cancer in females

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Rathbun, Alan M. "Depression in Rheumatoid Arthritis and an Estimation of the Bi-directional Association of Depression and Disease Burden: A Dissertation." eScholarship@UMMS, 2014. http://escholarship.umassmed.edu/gsbs_diss/699.

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Depression is a common comorbidity in rheumatoid arthritis (RA), yet it may not be adequately recognized during routine clinical care. RA symptoms may confer a risk for depression, and vice versa; depression may affect RA disease activity and response to treatment. The study aims were to compare patient- and physician-reported depression measures, evaluate the temporal bi-directional association between RA disease activity and depressive symptomology, and assess depression as a moderator of RA treatment. Patients were identified using a national RA registry sample (Consortium of Rheumatology R

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Abajobir, Amanuel Alemu, Kalkidan Hassen Abate, Cristiana Abbafati, et al. "Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016." Elsevier, 2017. http://hdl.handle.net/10150/625868.

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Background As mortality rates decline, life expectancy increases, and populations age, non-fatal outcomes of diseases and injuries are becoming a larger component of the global burden of disease. The Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) provides a comprehensive assessment of prevalence, incidence, and years lived with disability (YLDs) for 328 causes in 195 countries and territories from 1990 to 2016. Methods We estimated prevalence and incidence for 328 diseases and injuries and 2982 sequelae, their non-fatal consequences. We used DisMod-MR 2.1, a Bayesi

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Narh, Clement Tetteh [Verfasser]. "Modelling the Burden of Noncommunicable Diseases among Hospitalized Patients in Ghana = Modellierung der Krankheitslast nicht übertragbarer Krankheiten bei stationären Patienten in Ghana / Clement Tetteh Narh." Mainz : Universitätsbibliothek der Johannes Gutenberg-Universität Mainz, 2020. http://d-nb.info/1224895894/34.

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Silva, Tatiana Detzel da. "Avaliação da sobrecarga e do ambiente familiar de pacientes com transtorno de pânico." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2013. http://hdl.handle.net/10183/76160.

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A presença de doença crônica pode ser determinante de sobrecarga familiar e interferir no ambiente. Por outro lado, os aspectos familiares podem contribuir como um fator protetor ou de risco na evolução da doença. Estudos têm avaliado a sobrecarga familiar em transtornos mentais maiores, como a esquizofrenia, mas ainda não há estudos que avaliem a sobrecarga e o ambiente familiar em relação ao transtorno de pânico (TP). O objetivo deste estudo foi comparar a sobrecarga e o ambiente de familiares de pacientes com TP e de familiares de pacientes com doenças clínicas. Também pretendeu verificar a

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Kohlmann, Sebastian [Verfasser], and Winfried [Akademischer Betreuer] Rief. "Psychological approaches to a patient-centered cardiology : somatic symptom burden, illness perceptions and supportive care needs in patients with cardiac diseases / Sebastian Kohlmann. Betreuer: Winfried Rief." Marburg : Philipps-Universität Marburg, 2013. http://d-nb.info/1033403008/34.

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Abajobir, Amanuel Alemu, Kalkidan Hassen Abate, Cristiana Abbafati, et al. "Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016." Elsevier, 2017. http://hdl.handle.net/10150/625869.

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Background Measurement of changes in health across locations is useful to compare and contrast changing epidemiological patterns against health system performance and identify specific needs for resource allocation in research, policy development, and programme decision making. Using the Global Burden of Diseases, Injuries, and Risk Factors Study 2016, we drew from two widely used summary measures to monitor such changes in population health: disability-adjusted life-years (DALYs) and healthy life expectancy (HALE). We used these measures to track trends and benchmark progress compared with ex

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Atal, Ignacio. "Cartographie globale des essais cliniques." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB071/document.

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Pour comprendre comment se construisent les connaissances sur l’effet des interventions en médecine, il est nécessaire de savoir où est faite la recherche clinique dans le monde, quelles maladies sont étudiées, et quels acteurs la mettent en place. Une vision globale du système de recherche peut aider à identifier des lacunes dans la production de connaissances et à orienter l’activité de recherche vers les priorités de santé, en particulier dans les régions où les ressources sont limitées. Dans ce travail nous avons construit des cartographies de la recherche clinique, c’est-à-dire des analys

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Eckerblad, Jeanette. "Symptom burden among people with chronic disease." Doctoral thesis, Linköpings universitet, Hälsa, Aktivitet, Vård (HAV), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-122742.

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Introduction: Chronic diseases tend to increase with old age. Older people with chronic disease are commonly suffering from conditions which produce a multiplicity of symptoms and a decreased health-related quality of life. Nurses have a responsibility to prevent, ease or delay a negative outcome through symptom management, or assist in achieving an acceptable level of symptom relief. Aim: The overall aim of the thesis was to describe different aspects of symptom burden from the perspective of community-dwelling people with chronic disease. Methods: This thesis is based upon four papers that u

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Liyanage, Thaminda. "Defining and reducing the burden of kidney disease." Thesis, The University of Sydney, 2018. http://hdl.handle.net/2123/20027.

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Background: The global burden of kidney disease continues to rise but important gaps exist in our understanding of the prevalence of CKD and its complications globally and by region. Scarcity of evidence to guide public health decisions about CKD presents a serious challenge. There is a critical need to identify patterns of disease prevalence, risk factors and potential treatments. Methods: This thesis, based on contemporary evidence, has reported various epidemiological indices in kidney disease at a global and regional level, and explored whether regional dietary patterns might be associated

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Lazzarini, Peter A. "The burden of foot disease in inpatient populations." Thesis, Queensland University of Technology, 2016. https://eprints.qut.edu.au/101526/1/Peter_Lazzarini_Thesis.pdf.

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This thesis examined the prevalence and factors associated with foot disease (ulcers, infections and ischaemia) in a representative Australian inpatient population. This research is the first to reveal the full extent of the foot (disease) print on our hospitals. It found firstly, that foot disease caused the hospitalisation of one in every 20 inpatients which would make it a top 10 cause of hospitalization in Australia. Secondly, it identified similar factors were associated with foot disease in both diabetes and non-diabetes inpatient populations. Finally, it recommended practical strategies

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capewell, simon. "defining and addressing the burden of coronary heart disease." Thesis, University of Liverpool, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493051.

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Malik, Iqbal Saeed. "Assessment of the inflammatory burden in coronary heart disease." Thesis, Imperial College London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542947.

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AlJuburi, Ghida. "Sickle cell and the burden of disease in England." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/28116.

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Background Sickle cell disorders (SCD) are the most common inherited blood disorders in England. Without prompt diagnosis and proper treatment, they can be a serious source of morbidity and mortality. Sickle cell diseases affect mainly black minority and ethnic populations, and have so far received relatively low priority from a health policy perspective. Antenatal and newborn screening, the development of minimum standards, antibiotic prophylaxis, comprehensive immunisations, and preventive diagnostic tests have positively influenced SCD management. There remains an unclear picture as to the

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Zhang, Yuqi. "The burden of diabetes-related foot disease: Estimating the existing burden and the impact of implementing guideline-based care on the future burden." Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/232310/1/Yuqi_Zhang_Thesis.pdf.

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This doctoral program of research systematically estimated the global disease burden of diabetes-related foot disease (DFD), investigated factors contributing to the burden, and explored cost-effective ways to reduce the burden. Through four studies, this thesis identified DFD as a comparatively large and growing cause of global and national disease burden, identified several modifiable factors that reduce ulcer healing time in a real-world cohort, and provided novel economic evidence on the cost-effectiveness of implementing guideline-based care in clinical practice to potentially reduce futu

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Carkeek, Emma Claire. "The burden of chronic respiratory disease in the Western Cape." Master's thesis, University of Cape Town, 2018. http://hdl.handle.net/11427/29663.

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Chronic respiratory disease (CRD), comprised mainly of asthma and chronic obstructive lung disease (COPD), is responsible for significant morbidity and mortality worldwide. Although asthma and COPD cannot be cured, they can be controlled using appropriate medications. Poorly controlled CRD is associated with significantly poorer quality of life and mortality for patients, an increased burden on the healthcare system, and a negative economic impact due to loss of productivity. CRD is underdiagnosed, undertreated and poorly controlled, especially in low- and middle-income countries. Improving co

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Nguyen, Van Thi Thuy Public Health &amp Community Medicine Faculty of Medicine UNSW. "Hepatitis B-related liver disease burden in Vietnam and Australia." Publisher:University of New South Wales. Public Health & Community Medicine, 2008. http://handle.unsw.edu.au/1959.4/42118.

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This thesis investigates the epidemiology of hepatitis B virus infection (HBV) and estimates HBV-related liver disease burden in Vietnam and Australia using a cross-sectional study design and mathematical modelling. A population-based seroprevalence survey was undertaken in rural Northern Vietnam. In a sample of 870 study participants, prevalence of anti-HBV core antibody (anti-HBc) and hepatitis B virus surface antigen (HBsAg) was 68.2% and 19.0%, respectively, and hepatitis B e antigen (HBeAg) was detected in 16.4% of the HBsAg-positive group. Factors associated with HBV infection (anti-HBc

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Yang, Lin, and 楊琳. "Disease burden and seasonality of influenza in subtropical Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B41508828.

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Zhou, Ying, and 周颖. "Disease burden and epidemiology of influenza among vaccine target groups." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/207181.

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The impact of the 2009 influenza pandemic and other recent epidemics are still being assessed. Appropriate allocation of protection and control strategies depend on accurate estimation of disease burden, with high risk groups generally being a key focus especially for distribution of influenza vaccine to maximize the disease burden prevented per vaccine when resource is limited. Therefore, better understanding the impact of influenza and control of influenza among the high risks groups with greater burden is particularly important. In this thesis, I estimated the years of life lost (YLL) assoc

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Yang, Lin. "Disease burden and seasonality of influenza in subtropical Hong Kong." Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B41508828.

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Wisneski, Jennifer Lynne. "Social Support, Gender, and Burden in Caregivers of Patients with Alzheimer's Disease." ScholarWorks, 2018. https://scholarworks.waldenu.edu/dissertations/4898.

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There are 15.9 million adults in the United States providing care to a family member diagnosed with Alzheimer's disease. Family member caregivers experience detrimental physical and mental health stress because of their caregiving role. The purpose of this study was to determine if the independent variables of marital status, perceived social support, and gender of family member caregivers of patients with Alzheimer's disease were related to the dependent variable of caregiver burden. The variables were examined through the lens of John Bowlby's attachment theory using archival data (n = 586)

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Oliveira, Priscila Natacha de. "Chronic disease burden and human capital investment: evidence from the chagas disease campaign in Brazil." reponame:Repositório Institucional do FGV, 2016. http://hdl.handle.net/10438/16587.

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Submitted by Priscila Natacha de Oliveira (priscila.natacha.oliveira@gmail.com) on 2016-06-13T11:03:01Z No. of bitstreams: 1 Thesis_Priscila_Oliveira.pdf: 431094 bytes, checksum: 412075728f1265e1624e0e3637bedff5 (MD5)<br>Approved for entry into archive by Letícia Monteiro de Souza (leticia.dsouza@fgv.br) on 2016-06-13T12:16:33Z (GMT) No. of bitstreams: 1 Thesis_Priscila_Oliveira.pdf: 431094 bytes, checksum: 412075728f1265e1624e0e3637bedff5 (MD5)<br>Made available in DSpace on 2016-06-13T12:57:01Z (GMT). No. of bitstreams: 1 Thesis_Priscila_Oliveira.pdf: 431094 bytes, checksum: 412075728f12

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Torres, Janet Shin Yi. "GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS." CSUSB ScholarWorks, 2018. https://scholarworks.lib.csusb.edu/etd/681.

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The purpose of this research was to explore the gender differences in caregiver burden in Alzheimer’s patients in the Inland Empire. Currently, there are more than half a million Californians who live with Alzheimer’s disease (Ross, Brennan, Nazareno, & Fox, 2009) and this number is expected to double over the next few years. Due to an increase in the older population and the rise of informal caregivers, the study provided insight as to how males and females perceive caregiver burden and how each gender responds to caregiver burden. This exploratory study utilized a quantitative research desig

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Jones, Ann Judith. "Parkinson's Disease, Cognitive Status and Caregiver Outcomes." Thesis, University of Canterbury. Psychology, 2013. http://hdl.handle.net/10092/8717.

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Cognitive impairment in Parkinson’s disease (PD) can impact negatively on caregivers and is associated with carer distress and feelings of burden. To investigate this relationship we examined level of burden, coping strategies, depression, anxiety and potential positive aspects of caregiving in the caregivers of 104 PD patients. The PD patients were classified as either showing normal cognition (PD-N; n=57), with mild cognitive impairment (PD-MCI; n=31) or with dementia (PD-D; n=16). The key finding was that mean Zarit burden score increased between carers of PD-N (M=14.1, SD=12.0) through to

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42

Clark, III John Davis. "Body Burden of PAHs and Cardiovascular Disease in the United States." Scholarly Repository, 2008. http://scholarlyrepository.miami.edu/oa_dissertations/141.

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Polycyclic aromatic hydrocarbons (PAHs) are environmental and occupational carcinogens that are produced by the incomplete combustion of organic material, such as from the burning of tobacco, coal, and petroleum products. In addition to causing cancer, exposure to PAHs is hypothesized to contribute to atherosclerosis and to lead to increased incidence rates of cardiovascular disease in populations. Considering the number of deaths attributable to tobacco smoke exposure, ambient air pollution, and occupational hazards, PAHs may be a significant contributor to the prevalence of cardiovascular

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Galesanu, Roxana Gabriela. "The multisystemic burden of chronic obstructive pulmonary disease: a longitudinal study." Thesis, Université Laval, 2010. http://www.theses.ulaval.ca/2010/27205/27205.pdf.

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Arellanes-Amador, Yvonne. "Caregiver burden in the Latino family." CSUSB ScholarWorks, 2006. https://scholarworks.lib.csusb.edu/etd-project/3094.

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The study focused on the attitudes and beliefs regarding perceived and actual burden experienced by Latino caregivers and their use of formal support services. It also looked at the needs of Latino caregivers and explored their beliefs about why they had taken on the caregiver role, the responsibilities the role entailed, and coping skills used by these caregivers. Participants were obtained from two Alzheimer's caregiver support groups in the East Los Angeles area, and an adult day health care center in the high desert area of San Bernardino county. The author used both qualitative interviews

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Anderson, Cristina L. (Cristina Lee). "Caregiver Personality as a Contributing Factor in Caregiver Burden." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc500270/.

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Personality characteristics of spousal and adult children and active potential caregivers of persons with Alzheimer's Disease were studied in order to better predict caregiver burden and aspects of well-being. Contrary to prediction, no differences were found between spouse and adult children active caregivers on measures of well-being. Additionally, adult children potential caregivers indicated feeling less control over their lives than spouse potential caregivers. When social desirability was controlled, active caregivers reported greater fluctuations in affect than did potential caregivers.

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Wei, Jade Wei. "Disparities in the burden of stroke in China and its relevance to emerging economies." Thesis, The University of Sydney, 2011. https://hdl.handle.net/2123/28922.

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With an estimated 5.7 million deaths from stroke each year, stroke is the second leading cause of mortality worldwide. However, there are significant disparities in the burden of chronic, non-communicable diseases such as stroke across the world. Whilst rates of stroke and cardiovascular disease have remained relatively stable or have been declining over the past 10 years in developed countries, recent demographic transitions and economic developments have resulted in developing countries witnessing an escalation in the rates of these diseases that now top lists of leading causes of deat

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Backlund, Emma, and Felicia Lilja. "Livspartnerns upplevelse av att leva med en partner med demenssjukdom." Thesis, Umeå universitet, Institutionen för omvårdnad, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-117249.

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Background: In Sweden, eight percent of all people by the age of 65 years or older have a dementia disease. The healthy spouse received or unconsciously took the role as caregiver in the home which could cause psychological and physical stress. Therefore it is important that nurses have good understanding of how the healthy spouses experience their life situation. Aim: The aim of this study was to describe spouses´experiences of living with a partner with dementia disease. Methods: This literature study was performed with a qualitative method. Nine scientific articles have been quality checked

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Bergman, Amber Joy. "Dyadic spousal experiences of Alzheimer's disease marital satisfaction, caregiver burden, and coping /." [Ames, Iowa : Iowa State University], 2008.

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Norström, Fredrik. "The burden of celiac disease and the value of having it diagnosed." Doctoral thesis, Umeå universitet, Epidemiologi och global hälsa, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-54058.

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Background: Celiac disease is a chronic disease characterized by intolerance to gluten. It is considered a public health problem affecting about 1% of Western populations, but, with most cases still undiagnosed. A glutenfree diet is the only effective treatment for the disease. Objectives: To investigate the burden of celiac disease and the value of having it diagnosed. Additionally, the implications for a potential future celiac disease mass screening are discussed. Methods: A questionnaire was sent during 2009 to 1,560 randomly selected adult members of the Swedish Society for Coeliacs, in e

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Wang, Xiling, and 王锡玲. "Extension of disease burden modeling from seasonal influenza to 2009 pandemic influenza." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206724.

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