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2.
Hosp Case Manag ; 22(4): 43-4, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24697136

ABSTRACT

Tampa General Hospital has created a fund that case managers can use to pay for post-discharge services for unfunded patients when there is no other option. Case managers can use the fund to pay for home health services, a short stay in a skilled nursing facility, or other post-discharge services to free beds for other patients. Case managers and social workers huddle with the treatment team every day and identify challenging patients early in the stay. The case management and social work team tries to identify family or other community support that can help care for undocumented patients after discharge.


Subject(s)
Case Management , Financial Support , Medical Indigency/economics , Florida , Hospitals, General , Organizational Case Studies
4.
Laryngoscope ; 123(9): 2142-7, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23842787

ABSTRACT

OBJECTIVES/HYPOTHESIS: This study was designed to describe the implementation, utilization, and outcomes of an otolaryngology clinic for indigent patients employing a novel design. STUDY DESIGN: Pilot study. METHODS: A tertiary-care academic otolaryngology department partnered with a nonprofit outpatient clinic for indigent patients in order to provide free subspecialty consultation services. A novel format was utilized in which the department provided on-site, scheduled outpatient multidisciplinary consultation on weekends, staffed by volunteer health care providers and ancillary staff. A review of the program was conducted using prospectively collected data. Clinic design, staffing, utilization, and feasibility were described, along with demographic and clinical data for all patients participating in the clinic from October 2010 through January 2012. RESULTS: Five clinics were held over 15 months, totaling 74 patient visits, with positive feedback regarding accessibility and quality of services provided. A total of 60 procedures were performed, including audiograms, endoscopies, otologic procedures, biopsies and/or excisions. The estimated value of medical services that were provided was $37,302. Four potentially life-threatening conditions were newly diagnosed. Twenty patients received conclusive evaluation and treatment at the time of their first visit. Eighteen patients required further subspecialty treatment and/or surgery that could not be provided in the outpatient setting, and were referred appropriately. CONCLUSIONS: The partnership between an academic otolaryngology department and a nonprofit clinic provided free on-site consultation for indigent patients. Such an arrangement is feasible, well utilized, and successful in delivering comprehensive specialized services to indigent patients who lack traditional access to medical care.


Subject(s)
Ambulatory Care Facilities/organization & administration , Health Plan Implementation/organization & administration , Health Services Accessibility/organization & administration , Medical Indigency/statistics & numerical data , Otorhinolaryngologic Diseases/therapy , Academic Medical Centers , Adolescent , Adult , Aged , Feasibility Studies , Female , Humans , Male , Medical Indigency/economics , Michigan , Middle Aged , Organizations, Nonprofit/organization & administration , Otolaryngology/organization & administration , Otorhinolaryngologic Diseases/diagnosis , Pilot Projects , Poverty , Program Development , Program Evaluation , Risk Assessment , Treatment Outcome , Young Adult
5.
West Afr J Med ; 32(1): 14-8, 2013.
Article in English | MEDLINE | ID: mdl-23613289

ABSTRACT

BACKGROUND: An equitable health care system that responds to the needs of its people is important to break the cycle of poverty and ill-health. However, rising health care cost, and the preponderance of user fees to finance health care have often limited access to needed health services. STUDY DESIGN: A cross-sectional descriptive study design was employed, using a pretested, semi-structured, interviewer-administered questionnaire. RESULTS: The study was carried out among 188 respondents. Majority (88.2%) of the respondents were within the age-group 20-49 years, about two-thirds 63.8% were married and about half (42.8%) had family size between 5 and 9. The study revealed that about a quarter (26.1%) experienced hardship in settling their medical bills. While one-third (31.1%) had to sell their assets, about half (45.2%) had to secure loan while 16.6% had to resort to begging because of hardship encountered in settling the medical bills. Furthermore, of those who sold theirs asset; 46.2% sold their farmlands, 38.5% sold a piece of land, while 16.3% sold their vehicles. CONCLUSION: This study has revealed that inhabitants of Samaru community experience hardship in settling their medical bills. Consequently, innovative strategies like deferment of payment and fee exemption, enrolling into community-based health insurance schemes as well as voluntary contributory health insurance schemes etc need to be considered, in order to alleviate the hardship in settling the medical bills.


Subject(s)
Financing, Personal/economics , Health Expenditures , Medical Indigency/economics , Adult , Cross-Sectional Studies , Health Care Surveys , Humans , Middle Aged , Nigeria , Poverty , Socioeconomic Factors , Urban Population , Young Adult
6.
BMC Health Serv Res ; 12: 23, 2012 Jan 27.
Article in English | MEDLINE | ID: mdl-22284934

ABSTRACT

BACKGROUND: This study examines health-related "hardship financing" in order to get better insights on how poor households finance their out-of-pocket healthcare costs. We define hardship financing as having to borrow money with interest or to sell assets to pay out-of-pocket healthcare costs. METHODS: Using survey data of 5,383 low-income households in Orissa, one of the poorest states of India, we investigate factors influencing the risk of hardship financing with the use of a logistic regression. RESULTS: Overall, about 25% of the households (that had any healthcare cost) reported hardship financing during the year preceding the survey. Among households that experienced a hospitalization, this percentage was nearly 40%, but even among households with outpatient or maternity-related care around 25% experienced hardship financing.Hardship financing is explained not merely by the wealth of the household (measured by assets) or how much is spent out-of-pocket on healthcare costs, but also by when the payment occurs, its frequency and its duration (e.g. more severe in cases of chronic illnesses). The location where a household resides remains a major predictor of the likelihood to have hardship financing despite all other household features included in the model. CONCLUSIONS: Rural poor households are subjected to considerable and protracted financial hardship due to the indirect and longer-term deleterious effects of how they cope with out-of-pocket healthcare costs. The social network that households can access influences exposure to hardship financing. Our findings point to the need to develop a policy solution that would limit that exposure both in quantum and in time. We therefore conclude that policy interventions aiming to ensure health-related financial protection would have to demonstrate that they have reduced the frequency and the volume of hardship financing.


Subject(s)
Health Expenditures , Health Services Accessibility/economics , Medical Indigency/economics , Rural Health/economics , Analysis of Variance , Family Characteristics , Financing, Personal/economics , Financing, Personal/methods , Health Care Surveys , Health Services Accessibility/statistics & numerical data , Humans , India , Logistic Models , Medical Indigency/statistics & numerical data , Poverty Areas , Residence Characteristics , Rural Health/statistics & numerical data
8.
Nurs Econ ; 28(5): 323-9, 2010.
Article in English | MEDLINE | ID: mdl-21158253

ABSTRACT

Annual costs paid by families for intravenous infusion of home parenteral nutrition (HPN) health insurance premiums, deductibles, co-payments for health services, and the wide range of out-of-pocket home health care expenses are significant. The costs of managing complex chronic care at home cannot be completely understood until all out-of-pocket costs have been defined, described, and tabulated. Non-reimbursed and out-of-pocket costs paid by families over years for complex chronic care negatively impact the financial stability of families. National health care reform must take into account the long-term financial burdens of families caring for those with complex home care. Any changes that may increase the out-of-pocket costs or health insurance costs to these families can also have a negative long-term impact on society when greater numbers of patients declare bankruptcy or qualify for medical disability.


Subject(s)
Deductibles and Coinsurance/economics , Financing, Personal/economics , Income/statistics & numerical data , Parenteral Nutrition, Home/economics , Bankruptcy/economics , Chronic Disease , Cost of Illness , Crohn Disease/economics , Crohn Disease/psychology , Crohn Disease/therapy , Family/psychology , Female , Health Care Reform/economics , Health Care Surveys , Humans , Long-Term Care/economics , Male , Medical Indigency/economics , Middle Aged , Nursing Administration Research , Parenteral Nutrition, Home/psychology , Quality of Life/psychology , Socioeconomic Factors
9.
J Palliat Med ; 13(8): 941-4, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20712463

ABSTRACT

OBJECTIVE: To gather pilot data on the economic impact of terminal illness on families and on the feasibility of training caregivers as a method of stemming illness-related poverty. DESIGN: Exploratory, descriptive study involving semistructured interviews with patient and caregiver dyads. SETTING: Pallium India Palliative Care Clinic in Trivandrum, Kerala, India. PARTICIPANTS: Eleven patient-caregiver dyads (22 individual participants) visiting Pallium India in 2008. METHODS: Trained interviewers conducted face-to-face interviews consisting of 114 questions with the patient and caregiver separately. Questions covered topics of economic impact of illness on household, family, and individual. Questions included if the illness had so impacted families that they needed to sell assets or significantly reduce work and/or schooling. RESULTS: All families reported that patients were obliged to give up work as a result of illness. In seven families, the caregiver also had to change work habits. All respondents stated illness had forced them to sell assets. Ten households reported that their children were obliged to miss school due to the illness. All respondents indicated they would use trained caregivers to help with the care burden if available. Nine respondents thought that use of trained caregivers would have reduced or prevented some of the household's illness-related change. Nine caregivers said they would be interested in becoming a trained caregiver. CONCLUSION: These data indicate that a definitive study would be feasible and would reveal how much assistance caregiver training could lend to household socio-economic resilience.


Subject(s)
Attitude to Health , Caregivers , Cost of Illness , Family , Poverty , Terminal Care , Absenteeism , Adult , Caregivers/education , Caregivers/psychology , Employment/economics , Employment/psychology , Family/psychology , Family Characteristics , Feasibility Studies , Female , Humans , Income/statistics & numerical data , India , Male , Medical Indigency/economics , Medical Indigency/psychology , Middle Aged , Pilot Projects , Poverty/economics , Poverty/prevention & control , Surveys and Questionnaires , Terminal Care/economics , Terminal Care/psychology
11.
Healthc Financ Manage ; 63(9): 72-4, 76, 78 passim, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19743652

ABSTRACT

Steps that Grady Health System in Atlanta undertook in transforming its revenue cycle include: Conducting a complete revenue cycle assessment. Enhancing staff skill levels and customer service techniques--and holding staff. accountable for errors. Automating processes that previously were performed manually. Validating applications for financial assistance electronically. Screening for Medicare/Medicaid eligibility among self-pays.


Subject(s)
Economics, Hospital/organization & administration , Efficiency, Organizational/economics , Medical Indigency/economics , Automation , Georgia , Organizational Case Studies
12.
Track Rep ; (24): 1-6, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19343833

ABSTRACT

Almost 72 million working-age Americans--18-64 years old--live with chronic conditions, such as diabetes, asthma or depression. In 2007, almost three in 10, or more than 20 million people with chronic conditions, lived in families with problems paying medical bills--a significant increase from 21 percent in 2003, according to a new national study by the Center for Studying Health System Change (HSC). While problems paying medical bills are especially acute and still rising for uninsured people with chronic conditions (62%), medical-bill problems also are significant and growing among people with private insurance and higher incomes. For the more than 20 million chronically ill adults with medical bill problems in 2007, one in four went without needed medical care, half put off care and more than half went without a prescription medication because of cost concerns.


Subject(s)
Chronic Disease/economics , Cost of Illness , Health Services Accessibility/economics , Medical Indigency/statistics & numerical data , Medically Uninsured/statistics & numerical data , Obesity/economics , Adult , Female , Health Benefit Plans, Employee , Health Services Accessibility/trends , Humans , Insurance Coverage , Male , Managed Care Programs , Medical Indigency/economics , Medical Indigency/trends , Middle Aged , United States , Young Adult
13.
Transcult Psychiatry ; 46(1): 86-106, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19293281

ABSTRACT

Antidepressant uses have been rising rapidly over the past decades. Two main theories have been advanced to explain this. One claims that socio-economic change causes a global rise of depressive illness. The other holds that European and North American corporations are aggressively marketing antidepressants to expand their global reach. Both theories assume that multinational capitalism drives rising depression rates. Based on ethnographic data from India, this article shows that antidepressants are increasingly used in this country as well, but for reasons than have been little explored yet. Taking fluoxetine (Prozac) as the main example, it is argued that the spread of antidepressants in India is ;unlicensed' by Euro-American corporations in at least three ways: (i) drug marketing is driven by Indian generic producers; (ii) fluoxetine is given by practitioners who have no license to do so; and (iii) knowledge of fluoxetine is spread through unlicensed ;floating' prescriptions that patients take from one prescriber to another.


Subject(s)
Antidepressive Agents/therapeutic use , Capitalism , Clinical Competence , Depressive Disorder/drug therapy , Developing Countries , Drug Approval , Drug Industry , Drugs, Generic/therapeutic use , Licensure , Prescription Drugs/therapeutic use , Social Marketing , Antidepressive Agents/economics , Antidepressive Agents/supply & distribution , Brain/drug effects , Cross-Sectional Studies , Depressive Disorder/economics , Depressive Disorder/epidemiology , Depressive Disorder/ethnology , Drugs, Generic/economics , Drugs, Generic/supply & distribution , Ethics, Medical , Fluoxetine/economics , Fluoxetine/supply & distribution , Fluoxetine/therapeutic use , Humans , India , Medical Indigency/economics , Medical Indigency/ethnology , Prescription Drugs/economics , Prescription Drugs/supply & distribution , Social Change , Social Justice , Social Marketing/ethics
16.
Spine J ; 9(3): 221-4, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18468957

ABSTRACT

BACKGROUND CONTEXT: Access to care for poor/near poor patients is a concerning and growing problem within the American system of medical care. PURPOSE: The objective of this study was to examine the relationship between health insurance status and access to spine care among patients below 65 years of age eventually receiving treatment at our tertiary academic medical center. STUDY DESIGN: Descriptive study based on chart review and telephone interviews. PATIENT SAMPLE: Two groups of 64 patients each with surgical pathology of limited complexity and limited comorbidities, one with Medicaid insurance and one with private, commercial insurance. OUTCOME MEASURES: Reasons for referral, travel distance, travel time, frequency of visits, and proximity of fellowship-trained spinal surgeons. METHODS: Two groups, each with 64 consecutive spine surgical patients, were studied and compared. Group One had "Medicaid" coverage and Group Two was privately insured. All patients (both groups) were treated surgically for similar pathology of limited complexity and had limited comorbidities. They were assessed to determine the difficulties they encountered in receiving care before referral to our medical center including factors such as referral by a local provider based on insurance status alone and travel time/distance/frequency to eventually receive care at our center. The availability of local care for these patients (fellowship-trained spine surgeons in their local area) was also assessed. RESULTS: The great majority (78%) of poor/near poor patients with Medicaid coverage from counties at some distance from (and local to) our center were referred/deferred on the basis of insurance status alone given surgical problems which could have comfortably been addressed by orthopedic surgeons, neurosurgeons, or fellowship-trained spine surgeons local to the patient. This difficulty in access to care results in a significant burden (measured in time/travel/costs) for these patients. CONCLUSIONS: The poor/near poor with Medicaid insurance have less access to local spine care than those with private, commercial health insurance. The implications (from both surgeon and patient perspectives) of this dilemma are discussed.


Subject(s)
Health Services Accessibility/economics , Medical Indigency/economics , Medically Uninsured , Referral and Consultation/economics , Spinal Diseases/surgery , Humans , Insurance, Health , Medicaid , Poverty , Practice Patterns, Physicians'/economics , United States
17.
Eval Rev ; 32(6): 526-46, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18981334

ABSTRACT

We conduct an evaluation of MedShare, a program designed to enhance access to prescription drugs for indigent patients in the Greater Cincinnati area. The program expands access to drugs by providing subsidies to reduce the costs paid by patients for their prescriptions. The assumption is that by expanding access to prescription drugs, participant health outcomes as measured by quality of life improve. Although the program appears outwardly successful, we found little difference between program participants and comparison groups. We feel that these findings point to a major flaw with existing health policy: access alone is not sufficient to improve health outcomes. Too often programs are created and, provided they show outwards signs of success (e.g., enrollment and utilization), are assumed to be improving the health of the community. Our findings indicate that one must look beyond just expanding access to ensure that programs are indeed achieving their overall objectives.


Subject(s)
Health Policy , Health Services Accessibility , Health Services Needs and Demand/economics , Insurance, Pharmaceutical Services/economics , Medical Indigency/economics , Prescription Drugs/economics , Program Development , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Ohio , Patient Compliance , Pilot Projects , Psychological Tests , Psychometrics , Quality of Life/psychology , Social Support , United States , Young Adult
19.
J Pediatr Nurs ; 23(5): 386-92, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18804019

ABSTRACT

The Deficit Reduction Act of 2005 makes changes in the Medicaid program that may have a significant effect on children's health. Nurses and other health care professionals should be aware of these changes in order to monitor the impact of the legislation, guide families in the process of accessing needed services, and advocating on behalf of children and families.


Subject(s)
Child Health Services/economics , Health Services Accessibility/economics , Medicaid/economics , Benchmarking , Case Management/organization & administration , Child , Cost Control , Cost Sharing , Documentation , Eligibility Determination , Humans , Medical Indigency/economics , Organizational Innovation , Pediatric Nursing/organization & administration , Poverty/economics , Residence Characteristics , United States
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