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1.
PLoS One ; 15(10): e0239576, 2020.
Article in English | MEDLINE | ID: mdl-33113548

ABSTRACT

In the global context, health and the quality of life of people are adversely affected by either one or more types of chronic diseases. This paper investigates the differences in the level of income and expenditure between chronically-ill people and non-chronic population. Data were gathered from a national level survey conducted namely, the Household Income and Expenditure Survey (HIES) by the Department of Census and Statistics (DCS) of Sri Lanka. These data were statistically analysed with one-way and two-way ANOVA, to identify the factors that cause the differences among different groups. For the first time, this study makes an attempt using survey data, to examine the differences in the level of income and expenditure among chronically-ill people in Sri Lanka. Accordingly, the study discovered that married females who do not engage in any type of economic activity (being unemployed due to the disability associated with the respective chronic illness), in the age category of 40-65, having an educational level of tertiary education or below and living in the urban sector have a higher likelihood of suffering from chronic diseases. If workforce population is compelled to lose jobs, it can lead to income insecurity and impair their quality of lives. Under above findings, it is reasonable to assume that most health care expenses are out of pocket. Furthermore, the study infers that chronic illnesses have a statistically proven significant differences towards the income and expenditure level. This has caused due to the interaction of demographic and socio-economic characteristics associated with chronic illnesses. Considering private-public sector partnerships that enable affordable access to health care services for all as well as implementation of commercial insurance and community-based mutual services that help ease burden to the public, are vital when formulating effective policies and strategies related to the healthcare sector. Sri Lanka is making strong efforts to support its healthcare sector and public, which was affected by the coronavirus (COVID-19) in early 2020. Therefore, findings of this paper will be useful to gain insights on the differences of chronic illnesses towards the income and expenditure of chronically-ill patients in Sri Lanka.


Subject(s)
Betacoronavirus , Chronic Disease/epidemiology , Coronavirus Infections/epidemiology , Health Expenditures/statistics & numerical data , Income/statistics & numerical data , Pandemics , Pneumonia, Viral/epidemiology , Adolescent , Adult , Aged , Analysis of Variance , COVID-19 , Child , Child, Preschool , Chronic Disease/economics , Comorbidity , Coronavirus Infections/economics , Developing Countries/economics , Disabled Persons/statistics & numerical data , Ethnicity/statistics & numerical data , Family Characteristics , Female , Food/economics , Humans , Infant , Infant, Newborn , Male , Medical Indigency/statistics & numerical data , Middle Aged , Pandemics/economics , Pneumonia, Viral/economics , Poverty , SARS-CoV-2 , Socioeconomic Factors , Sri Lanka/epidemiology , Surveys and Questionnaires , Young Adult
2.
Cuad. bioét ; 30(100): 253-262, sept.-dic. 2019.
Article in Spanish | IBECS | ID: ibc-185239

ABSTRACT

El concepto de vulnerabilidad ha determinado múltiples actuaciones en el ámbito sanitario. En los últimos años este concepto ha originado diversos modelos holísticos que oscilan entre considerar la vulnerabilidad como un elemento descriptivo de una situación accidental hasta su consideración como principio orientador de la práctica médica. Se percibe la necesidad de profundizar en este fenómeno desde el punto de vista de la filosofía moral. La reflexión moral revela un desequilibrio en el binomio autonomía-dependencia, generando soluciones opuestas en la toma de decisiones. Aunque la autonomía ha fundamentado hasta ahora gran parte de la acción médica, la dependencia plantea una nueva óptica sobre la vulnerabilidad, ra-dicada en la ética del cuidado. Esta perspectiva permite superar la consideración de la vulnerabilidad como una característica, un accidente o un principio. La vulnerabilidad aparece como una dimensión intrínseca del ser humano que, lejos de alterar su dignidad o su autonomía, permite evidenciar la necesidad de los otros para alcanzar su plenitud


The concept of vulnerability has determined multiple actions in the health field. In recent years, this concept has originated various holistic models that oscillate between considering vulnerability as a descriptive element of an accidental situation until it is considered a guiding principle of medical practice. The need to deepen this phenomenon from the point of view of moral philosophy is perceived. The moral reflection reveals an imbalance in the binomial autonomy-dependence, generating opposite solutions in decision-making. Although autonomy has so far supported much of the medical action, the dependency raises a new perspective on vulnerability, rooted in the ethics of care. This perspective allows us to overcome the consideration of vulnerability as a characteristic, an accident or a principle. Vulnerability appears as an intrinsic dimension of the human being that, far from altering its dignity or autonomy, makes it possible to demonstrate the need of others to reach their fullness


Subject(s)
Humans , 34658 , Bioethics , Health Status , Minority Groups , Minority Health/ethics , Poverty , Principle-Based Ethics , Vulnerable Populations , Risk Groups , Personal Autonomy , Dependent Ambulation/ethics , Medical Indigency , Social Responsibility
3.
Int J Psychiatry Med ; 52(3): 245-254, 2017 05.
Article in English | MEDLINE | ID: mdl-29065810

ABSTRACT

This article describes a novel inter-professional curriculum designed to address the needs of homeless patients in a Midwestern region of the United States which has high rates of poverty. The curriculum is intended for healthcare trainees coming from undergraduate pre-medical programs, nursing, pharmacy, social work, clinical psychology, medical school and post-graduate medical training in family medicine, medicine-pediatrics, and psychiatry. The clinical component is specifically designed to reach destitute patients and the curriculum is structured to reverse commonly held myths about homelessness among the trainees, thereby improving their Homelessness Information Quotient, the ability to more fully understand homelessness. Participants across all disciplines and specialties have shown greater empathy and helper behavior as determined by qualitative measures. Learners have also developed a greater understanding of health-care systems allowing them to more consistently address social determinants of health identified by the authors as their Disparity Information Quotient. This article outlines the process of initiating a homeless service program, a curriculum for addressing common myths about homelessness and the effective use of narrative methods, relational connections, and reflective practice to enable trainees to process their experience and decrease burnout by focusing on the value of altruism and finding meaning in their work.


Subject(s)
Education, Medical, Continuing/methods , Education, Medical, Graduate/methods , Ill-Housed Persons/psychology , Altruism , Curriculum , Delivery of Health Care , Emotional Intelligence , Humans , Medical Indigency/psychology , United States
4.
Community Dent Oral Epidemiol ; 45(5): 389-397, 2017 10.
Article in English | MEDLINE | ID: mdl-28425612

ABSTRACT

OBJECTIVES: This systematic review examines the evidence on the effectiveness of programmes that aim to improve the oral health of Indigenous populations worldwide, as well as presents a qualitative analysis to explore the design and implementation of these initiatives. METHODS: MEDLINE and EMBASE were searched. Studies were included if they described an oral health programme for an Indigenous population in any country worldwide. A thematic synthesis of the qualitative findings was undertaken for each study's results and discussion sections. RESULTS: Nineteen studies were included. Sixteen studies reported positive results, twelve of which reported statistically significant findings. Three themes regarding design and implementation emerged from the qualitative analysis: (i) elements of successful programmes, (ii) challenges and barriers to successful interventions and (iii) suggestions for improvements. CONCLUSIONS: Successful programmes considered cultural appropriateness in their design-including extensive community engagement before, during and after implementation to enhance ownership of, and thus participation in the programme. Collaborative approaches were seen as an advantage, not only with Indigenous communities, but also with local health providers and organizations, with particular emphasis on incorporation into existing services. Challenges included low community participation, unstable funding and staffing issues. In addition, future programmes should also incorporate advocacy and community development, focus on changes to public policy, utilize evidence-based interventions that include traditional models of health, attempt to secure a stable funding base, target strategies to ensure staff retention and develop interventions that target the multilevel causes of general and oral health. This review provides an evidence base that can aid in the successful design, implementation and sustainability of oral health programmes for Indigenous people in the future.


Subject(s)
Dental Care , Global Health , Health Promotion/methods , Medical Indigency , Oral Health , Cultural Competency , Health Services Accessibility , Health Services Needs and Demand , Humans , Qualitative Research
7.
J Dent Educ ; 80(10): 1180-1187, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27694291

ABSTRACT

Community-based clinical rotations in rural areas expose dental students to diverse patient populations, practice models, and career opportunities as well as rural culture. The aims of this study at West Virginia University were to determine the best predictors of rural practice, assess the predictive validity of students' intention to practice in a rural area before and after their rural rotations, and evaluate the relationship between students' intention to practice in a rural area and intention to provide care for indigent patients. Online survey data were submitted pre- and post-rural clinical rotation by 432 of 489 dental students over the study period 2001-12, yielding an 88% response rate. In 2013, practice addresses from the West Virginia Board of Dentistry were added to the student database. The results showed that significant predictors of rural practice site were intended rural practice choice, rural hometown, and projected greater practice accessibility for indigent patients. The likelihood of students' predicting they would choose a rural practice increased after completion of their rural rotations. After the rotations, students predicted providing greater accessibility to indigent patients; these changes occurred for those who changed their predictions to rural practice choice after the rotations and those who subsequently entered rural practice. The dental students with a rural background or a greater service orientation were also more likely to expect to enter a rural practice and actually to do so after graduation. These findings suggest that dental school curricula that include rural rotations may increase students' sensitivity to issues of indigent patients and increase students' likelihood of rural practice choice.


Subject(s)
Attitude of Health Personnel , Dental Health Services , Medical Indigency , Professional Practice Location , Rural Health Services , Students, Dental , Career Choice , Forecasting , Self Report , United States
8.
Aust Nurs Midwifery J ; 23(11): 15, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27532097
9.
Neurosurg Focus ; 41(1): E4, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27364257

ABSTRACT

The Civil War era was an age-defining period in the history of the United States of America, the effects of which are still seen in the nation today. In this era, the issue of head injury pervaded society. From the president of the United States, Abraham Lincoln, to the officers and soldiers of the Union and Confederate armies, and to the population at large, head injury and its ramifications gripped the nation. This article focuses on 3 individuals: Major General John Sedgwick, First Lieutenant Alonzo Cushing, and Harriet Tubman, as examples of the impact that head injury had during this era. These 3 individuals were chosen for this article because of their lasting legacies, contributions to society, and interesting connections to one another.


Subject(s)
American Civil War , Craniocerebral Trauma/history , Military Personnel/history , Black or African American/history , Craniocerebral Trauma/epidemiology , Craniocerebral Trauma/psychology , History, 19th Century , History, 20th Century , Humans , Medical Indigency/history , Social Work/history , United States/epidemiology
10.
Del Med J ; 88(3): 73-4, 2016 Mar.
Article in English | MEDLINE | ID: mdl-27215043
11.
Otolaryngol Head Neck Surg ; 155(2): 197-8, 2016 08.
Article in English | MEDLINE | ID: mdl-27221569

ABSTRACT

Many young people look forward to volunteering abroad and overlook the ample volunteer opportunities at home. There are several advantages to volunteering at home: you help people in your own community; you can make a long-term commitment; and you have continuity of care for your patients. There are >1200 free clinics in the United States whose main goal is to provide care to the indigent population. These free clinics are always looking for volunteers with specialized medical training. This article reviews the medically related and unrelated volunteer opportunities available in the United States. Volunteering at home is a worthwhile experience, and I encourage the otolaryngology community to explore these opportunities.


Subject(s)
Medical Indigency , Otolaryngology , Volunteers , Health Services Accessibility , Health Services Needs and Demand , Humans , United States
12.
CMAJ ; 188(8): 563, 2016 May 17.
Article in English | MEDLINE | ID: mdl-27067819
15.
Matern Child Health J ; 20(6): 1280-7, 2016 06.
Article in English | MEDLINE | ID: mdl-27017228

ABSTRACT

Objectives To examine retention of Medicaid coverage over time for children in the child welfare system. Methods We linked a national survey of children with histories of abuse and neglect to their Medicaid claims files from 36 states, and followed these children over a 4 year period. We estimated a Cox proportional hazards model on time to first disenrollment from Medicaid. Results Half of our sample (50 %) retained Medicaid coverage across 4 years of follow up. Most disenrollments occurred in year 4. Being 3-5 years of age and rural residence were associated with increased hazard of insurance loss. Fee-for-service Medicaid and other non-managed insurance arrangements were associated with a lower hazard of insurance loss. Conclusions for Practice A considerable number of children entering child environments seem to retain Medicaid coverage over multiple years. Finding ways to promote entry of child welfare-involved children into health insurance coverage will be critical to assure services for this highly vulnerable population.


Subject(s)
Child Protective Services , Child Welfare , Medicaid/statistics & numerical data , Medically Uninsured/statistics & numerical data , Child , Child Abuse , Child Health Services/statistics & numerical data , Child, Preschool , Female , Humans , Insurance Coverage , Male , Medical Indigency/statistics & numerical data , Residence Characteristics , Rural Population , United States
18.
BMC Med ; 13: 190, 2015 Aug 18.
Article in English | MEDLINE | ID: mdl-26282128

ABSTRACT

BACKGROUND: One of the biggest obstacles to developing policies in cancer care in Southeast Asia is lack of reliable data on disease burden and economic consequences. In 2012, we instigated a study of new cancer patients in the Association of Southeast Asian Nations (ASEAN) region - the Asean CosTs In ONcology (ACTION) study - to assess the economic impact of cancer. METHODS: The ACTION study is a prospective longitudinal study of 9,513 consecutively recruited adult patients with an initial diagnosis of cancer. Twelve months after diagnosis, we recorded death and household financial catastrophe (out-of-pocket medical costs exceeding 30% of annual household income). We assessed the effect on these two outcomes of a range of socio-demographic, clinical, and economic predictors using a multinomial regression model. RESULTS: The mean age of participants was 52 years; 64% were women. A year after diagnosis, 29% had died, 48% experienced financial catastrophe, and just 23% were alive with no financial catastrophe. The risk of dying from cancer and facing catastrophic payments was associated with clinical variables, such as a more advanced disease stage at diagnosis, and socioeconomic status pre-diagnosis. Participants in the low income category within each country had significantly higher odds of financial catastrophe (odds ratio, 5.86; 95% confidence interval, 4.76-7.23) and death (5.52; 4.34-7.02) than participants with high income. Those without insurance were also more likely to experience financial catastrophe (1.27; 1.05-1.52) and die (1.51; 1.21-1.88) than participants with insurance. CONCLUSIONS: A cancer diagnosis in Southeast Asia is potentially disastrous, with over 75% of patients experiencing death or financial catastrophe within one year. This study adds compelling evidence to the argument for policies that improve access to care and provide adequate financial protection from the costs of illness.


Subject(s)
Cost of Illness , Neoplasms , Adult , Aged , Asia, Southeastern/epidemiology , Demography , Female , Health Expenditures/statistics & numerical data , Humans , Longitudinal Studies , Male , Medical Indigency , Middle Aged , Neoplasms/economics , Neoplasms/mortality , Odds Ratio , Prospective Studies , Socioeconomic Factors
19.
Rev Med Suisse ; 11(467): 735-9, 2015 Mar 25.
Article in French | MEDLINE | ID: mdl-26027205

ABSTRACT

The health status of the so-called "Roma" is usually much poorer than that of neighbouring non-Roma populations with a life expectancy gap of 5-15 years. This results from prolonged exposure to adverse determinants of health and to persistent exclusion from social and political arenas. Scientific and social research has only poorly addressed the health issues of Roma and evidences are scarce. Insufficient access to public services, including to health care and non optimal clinical practices are modifiable factors. If correctly addressed, this could contribute to reduce health disparities, including in Switzerland.


Subject(s)
Ill-Housed Persons , Roma , Tuberculosis/therapy , Vulnerable Populations , Health Services Accessibility/statistics & numerical data , Health Status Disparities , Humans , Lost to Follow-Up , Male , Medical Indigency , Poverty , Switzerland/epidemiology , Tuberculosis/diagnosis , Vulnerable Populations/ethnology , Vulnerable Populations/statistics & numerical data
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