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1.
Sex Transm Dis ; 47(2): 71-79, 2020 02.
Article in English | MEDLINE | ID: mdl-31935206

ABSTRACT

BACKGROUND: It is well established that network structure strongly influences infectious disease dynamics. However, little is known about how the network structure impacts the cost-effectiveness of disease control strategies. We evaluated partner management strategies to address bacterial sexually transmitted infections (STIs) as a case study to explore the influence of the network structure on the optimal disease management strategy. METHODS: We simulated a hypothetical bacterial STI spread through 4 representative network structures: random, community-structured, scale-free, and empirical. We simulated disease outcomes (prevalence, incidence, total infected person-months) and cost-effectiveness of 4 partner management strategies in each network structure: routine STI screening alone (no partner management), partner notification, expedited partner therapy, and contact tracing. We determined the optimal partner management strategy following a cost-effectiveness framework and varied key compliance parameters of partner management in sensitivity analysis. RESULTS: For the same average number of contacts and disease parameters in our setting, community-structured networks had the lowest incidence, prevalence, and total infected person-months, whereas scale-free networks had the highest without partner management. The highly connected individuals were more likely to be reinfected in scale-free networks than in the other network structures. The cost-effective partner management strategy depended on the network structures, the compliance in partner management, the willingness-to-pay threshold, and the rate of external force of infection. CONCLUSIONS: Our findings suggest that contact network structure matters in determining the optimal disease control strategy in infectious diseases. Information on a population's contact network structure may be valuable for informing optimal investment of limited resources.


Subject(s)
Community Networks , Computer Simulation , Contact Tracing , Cost-Benefit Analysis , Sexual Partners/psychology , Sexually Transmitted Diseases/prevention & control , Bacterial Infections/prevention & control , Bacterial Infections/transmission , Communicable Disease Control/economics , Communicable Disease Control/methods , Community Networks/economics , Contact Tracing/methods , Contact Tracing/statistics & numerical data , Humans , Sexually Transmitted Diseases/diagnosis , Sexually Transmitted Diseases/psychology
2.
BMC Health Serv Res ; 19(1): 752, 2019 Oct 25.
Article in English | MEDLINE | ID: mdl-31653231

ABSTRACT

BACKGROUND: People living with and beyond cancer (PLC) receive various forms of specialty care at different locations and many interventions concurrently or over time. They are affected by the operation of professional and organizational silos. This results in undue delays in access, unmet needs, sub-optimal care experiences and clinical outcomes, and human and financial costs for PLCs and healthcare systems. National cancer control programs advocate organizing in a network to coordinate actions, solve fragmentation problems, and thus improve clinical outcomes and care experiences for every dollar invested. The variable outcomes of such networks and factors explaining them have been documented. Governance is the "missing link" for understanding outcomes. Governance refers to the coordination of collective action by a body in a position of authority in pursuit of a common goal. The Quebec Cancer Network (QCN) offers the opportunity to study in a natural environment how, why, by whom, for whom, and under what conditions collaborative governance contributes to practices that produce value-added outcomes for PLCs, healthcare providers, and the healthcare system. METHODS/DESIGN: The study design consists of a longitudinal case study, with multiple nested cases (4 local networks nested in the QCN), mobilizing qualitative and quantitative data and mixed data from various sources and collected using different methods, using the realist evaluation approach. Qualitative data will be used for a thematic analysis of collaborative governance. Quantitative data from validated questionnaires will be analyzed to measure relational coordination and teamwork, care experience, clinical outcomes, and health-related health-related quality of life, as well as a cost analysis of service utilization. Associations between context, governance mechanisms, and outcomes will be sought. Robust data will be produced to support decision-makers to guide network governance towards optimized clinical outcomes and the reduction of the economic toxicity of cancer for PLCs and health systems.


Subject(s)
Community Networks/organization & administration , Decision Making, Shared , Neoplasms/therapy , Community Networks/economics , Health Care Costs , Health Services Research , Humans , Institutionalization , Longitudinal Studies , Organizational Case Studies , Quebec , Research Design
3.
J Ment Health Policy Econ ; 21(2): 59-69, 2018 06 01.
Article in English | MEDLINE | ID: mdl-29961045

ABSTRACT

BACKGROUND: Somatoform disorders are highly prevalent mental disorders causing impairment and large economic burden. In order to improve the diagnosis and management of affected patients, a health care network for somatoform disorders (Sofu-Net) was implemented in primary care. AIMS OF THE STUDY: The aim of the study was to determine the cost-effectiveness of a stepped, collaborative and coordinated health care network for somatoform and functional disorders (Sofu-Net) compared with regular primary care physician (PCP) practices in German primary care from a societal perspective. METHODS: This study was part of a 6-month controlled, prospective, non-randomized, observer-blinded cluster cohort trial. Participants were recruited from 33 PCP practices in Hamburg, Germany. The health care network was a collaboration of PCPs, psychotherapists, inpatient clinics and a specialized outpatient clinic. Participants in the control group received usual care. A cost-effectiveness analysis, using treatment response as measure of effectiveness, was performed. Uncertainty in cost-effectiveness was analyzed using cost-effectiveness acceptability curves. RESULTS: In total, n=218 patients (n=119 patients in the intervention group and n=99 patients in the control group) were included in the study. At 6 months, patients within the Sofu-Net group did not differ significantly from the control group with regard to costs (533; standard error 941) and treatment response (--10.3%). For Sofu-Net, the probability of being cost-effective at a willingness-to-pay (WTP) of 10,000 per additional response to treatment was only 31%. DISCUSSION: Sofu-Net is unlikely to be cost-effective. Even for high WTP, the probability of cost-effectiveness was low. The results were robust to variation of costs included in the analysis as well as when only complete cases were included in the analysis. The most important limitations of the study were that randomization could not be established at patient level and at practice level and that the study design did not allow measurement of costs at baseline. CONCLUSION: Patients with severe somatic symptoms did not benefit from the health care network. Sofu-Net might have reduced costs in patients with moderate somatic symptoms. IMPLICATIONS FOR FURTHER RESEARCH: Owing to the limitations and due to a short follow-up of this study, further cost-effectiveness analyses with high methodological quality and a follow-up of at least one year are needed in order to produce results that are more reliable.


Subject(s)
Community Networks/economics , Cost-Benefit Analysis/economics , Interdisciplinary Communication , Intersectoral Collaboration , Somatoform Disorders/economics , Somatoform Disorders/therapy , Adult , Aged , Cohort Studies , Female , Germany , Humans , Male , Middle Aged , Patient Health Questionnaire , Primary Health Care/economics , Prospective Studies , Quality Improvement/economics , Single-Blind Method , Somatoform Disorders/diagnosis
4.
Healthc Q ; 20(4): 43-47, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29595427

ABSTRACT

Patients returning to the community after surgery often experience a disconnect when transitioning from hospital to community home care. Many receive little organized/planned care following discharge sometimes resulting in unplanned expensive care in hospital emergency departments and inpatient readmissions. Trillium Health Partners, a large community/teaching hospital, in partnership with community care provider Saint Elizabeth Health Care, designed and implemented a seamless "bundled care program" for cardiac surgery patients extending from hospitalization to 30 days after discharge. With a risk/gain sharing model, the bundled care program enabled a novel integrated clinical patient care model. This included integrated care coordinators embedded within the hospital team, 24/7 patient phone line, integrated medical records and a tracking board that enabled performance monitoring and improvement. Evaluation results revealed: a 16% reduction in post-operative length of stay; a 38% reduction in readmission rates; and a 13% decrease in total system cost per patient, together with markers of improved patient experience.


Subject(s)
Academic Medical Centers/organization & administration , Community Networks/organization & administration , Heart Diseases/surgery , Patient Care Bundles/methods , Academic Medical Centers/economics , Community Networks/economics , Emergency Service, Hospital/statistics & numerical data , Heart Diseases/economics , House Calls , Humans , Length of Stay/statistics & numerical data , Ontario , Patient Care Bundles/economics , Patient Readmission/statistics & numerical data , Patient Satisfaction , Quality Assurance, Health Care , Telemedicine
5.
Gene Ther ; 24(9): 547-550, 2017 09.
Article in English | MEDLINE | ID: mdl-28467403

ABSTRACT

There are many challenges in conducting rare disease research. The conditions are often poorly understood, small patient populations are dispersed around the world, and there are limited funding opportunities. Patient groups can serve as a key partner in overcoming these challenges, as they understand the impact of rare conditions on patients' lives. This gives patient groups valuable scientific insights into the disease. This can be used to create research strategies, address research bottlenecks and directly fund research that appropriately addresses patient needs. Patient groups can also play a critical role in recruiting and retaining patients for clinical trials, which reduces time and resource waste. By partnering with patient groups, research teams can improve efficiency of research and best meet the needs of patients. Researchers can also play an important role in building and supporting patient groups to unlock these benefits.


Subject(s)
Patient Participation/economics , Rare Diseases/economics , Research Support as Topic/economics , Community Networks/economics , Community Networks/organization & administration , Humans , Rare Diseases/psychology , Research Support as Topic/organization & administration , Societies/economics , Societies/organization & administration
6.
Malar J ; 16(1): 277, 2017 07 05.
Article in English | MEDLINE | ID: mdl-28679378

ABSTRACT

BACKGROUND: Ghana has developed two main community-based strategies that aim to increase access to quality treatment for malaria, diarrhoea and suspected pneumonia: the integrated community case management (iCCM) and the community-based health planning and services (CHPS). The aim of the study was to assess the cost-effectiveness of these strategies under programme conditions. METHODS: A cost-effectiveness analysis was conducted. Appropriate diagnosis and treatment given was the effectiveness measure used. Appropriate diagnosis and treatment data was obtained from a household survey conducted 2 and 8 years after implementation of iCCM in the Volta and Northern Regions of Ghana, respectively. The study population was carers of children under-5 years who had fever, diarrhoea and/or cough in the last 2 weeks prior to the interview. Costs data was obtained mainly from the National Malaria Control Programme (NMCP), the Ministry of Health, CHPS compounds and from a household survey. RESULTS: Appropriate diagnosis and treatment of malaria, diarrhoea and suspected pneumonia was more cost-effective under the iCCM than under CHPS in the Volta Region, even after adjusting for different discount rates, facility costs and iCCM and CHPS utilization, but not when iCCM appropriate treatment was reduced by 50%. Due to low numbers of carers visiting a CBA in the Northern Region it was not possible to conduct a cost-effectiveness analysis in this region. However, the cost analysis showed that iCCM in the Northern Region had higher cost per malaria, diarrhoea and suspected pneumonia case diagnosed and treated when compared to the Volta Region and to the CHPS strategy in the Northern Region. CONCLUSIONS: Integrated community case management was more cost-effective than CHPS for the treatment of malaria, diarrhoea and suspected pneumonia when utilized by carers of children under-5 years in the Volta Region. A revision of the iCCM strategy in the Northern Region is needed to improve its cost-effectiveness. Long-term financing strategies should be explored including potential inclusion in the National Health Insurance Scheme (NHIS) benefit package. An acceptability study of including iCCM in the NHIS should be conducted.


Subject(s)
Community Networks/economics , Diarrhea/therapy , Malaria/therapy , Pneumonia/therapy , Architectural Accessibility/economics , Child, Preschool , Cost-Benefit Analysis , Cross-Sectional Studies , Diarrhea/diagnosis , Diarrhea/economics , Family Characteristics , Ghana , Health Services Accessibility/economics , Health Services Accessibility/standards , Humans , Infant , Malaria/diagnosis , Malaria/economics , Pneumonia/diagnosis , Pneumonia/economics , Sensitivity and Specificity , Universal Health Insurance/economics , Universal Health Insurance/standards
7.
Global Health ; 13(1): 2, 2017 01 13.
Article in English | MEDLINE | ID: mdl-28086925

ABSTRACT

BACKGROUND: Mental illnesses are the largest contributors to the global burden of non-communicable diseases. However, there is extremely limited access to high quality, culturally-sensitive, and contextually-appropriate mental healthcare services. This situation persists despite the availability of interventions with proven efficacy to improve patient outcomes. A partnerships network is necessary for successful program adaptation and implementation. PARTNERSHIPS NETWORK: We describe our partnerships network as a case example that addresses challenges in delivering mental healthcare and which can serve as a model for similar settings. Our perspectives are informed from integrating mental healthcare services within a rural public hospital in Nepal. Our approach includes training and supervising generalist health workers by off-site psychiatrists. This is made possible by complementing the strengths and weaknesses of the various groups involved: the public sector, a non-profit organization that provides general healthcare services and one that specializes in mental health, a community advisory board, academic centers in high- and low-income countries, and bicultural professionals from the diaspora community. CONCLUSIONS: We propose a partnerships model to assist implementation of promising programs to expand access to mental healthcare in low- resource settings. We describe the success and limitations of our current partners in a mental health program in rural Nepal.


Subject(s)
Community Networks/economics , Developing Countries/economics , Mental Disorders/economics , Public-Private Sector Partnerships/economics , Developing Countries/statistics & numerical data , Health Personnel/education , Health Services Accessibility/economics , Health Services Accessibility/standards , Humans , Mental Disorders/therapy , Mental Health Services/supply & distribution , Nepal , Rural Population/statistics & numerical data
8.
Afr J AIDS Res ; 16(4): 355-363, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29132285

ABSTRACT

This paper reports on the health and psychosocial impacts of a programme designed to economically empower female caregivers of orphans and vulnerable children (OVC). The results presented are from a cohort of 492 female caregivers who participated in savings groups and were responsible for 887 OVC. The data showed that the caregivers had increased earnings, borrowed more, repaid their loans, and expanded their businesses. Important health impacts were found for both the caregivers and the OVC. Access to health care increased and the proportion of OVC and caregivers who reported being too ill to take part in daily activities decreased. Results showed that WORTH savings group members increased their financial resources and used them to improve the wellbeing of OVC in their care. The economic and social empowerment had a positive impact on child protection, child wellbeing and health.


Subject(s)
Caregivers/economics , Caregivers/psychology , Child, Orphaned , Community Networks/economics , Vulnerable Populations , Adolescent , Adult , Cohort Studies , Eswatini , Female , Humans , Income , Longitudinal Studies , Middle Aged , Power, Psychological , Young Adult
9.
J Aging Soc Policy ; 29(1): 20-34, 2017.
Article in English | MEDLINE | ID: mdl-27195447

ABSTRACT

This study examined experiences of 156 informal caregivers of older adults who transitioned to the community through the Connecticut Money Follows the Person (MFP) Rebalancing Demonstration after prolonged nursing home stays. Caregiver burden, positive aspects of caregiving, depressive symptoms, anxiety, and comparative subjective stress were examined in relation to caregiver demographics and care receiver characteristics with a cross-sectional survey. Caregivers reported low burden, depressive symptoms, and anxiety, and fairly high levels of positive aspects of caregiving and satisfaction with community services. Most caregivers were less stressed compared to the time the care recipient was in, or before they entered, a nursing home. Live-in caregivers experienced more positive aspects of caregiving, but adult children reported higher burden than other caregivers. Unmet service needs also increased caregiver burden. Programs like MFP are a viable option with broadly positive outcomes from a caregiver's perspective. Enthusiasm for increasing access to community care is growing for older adults who otherwise would reside in nursing homes for extended periods. Identifying unmet service needs and needs for targeted functional support could further enhance caregiver experiences and contribute to the successful transition of older adults to the community.


Subject(s)
Caregivers , Community Networks/economics , Nursing Homes/economics , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Personal Satisfaction
10.
Milbank Q ; 94(3): 597-625, 2016 09.
Article in English | MEDLINE | ID: mdl-27378581

ABSTRACT

POLICY POINTS: At age 65, the average man and woman can respectively expect 1.5 years and 2.5 years of requiring daily help with "activities of daily living." Available services fail to match frail elders' needs, thereby routinely generating errors, unreliability, unwanted services, unmet needs, and high costs. The number of elderly Medicare beneficiaries likely to be frail will triple between 2000 and 2050. Low retirement savings, rising medical and long-term care costs, and declining family caregiver availability portend gaps in badly needed services. The financial simulation reported here for 4 diverse MediCaring Communities shows lower per capita costs. Program savings are substantial and can improve coverage and function of local supportive services within current overall Medicare spending levels. CONTEXT: The Altarum Institute Center for Elder Care and Advanced Illness has developed a reform model, MediCaring Communities, to improve services for frail elderly Medicare beneficiaries through longitudinal care planning, better-coordinated and more desirable medical and social services, and local monitoring and management of a community's quality and supply of services. This study uses financial simulation to determine whether communities could implement the model within current Medicare and Medicaid spending levels, an important consideration to enable development and broad implementation. METHODS: The financial simulation for MediCaring Communities uses 4 diverse communities chosen for adequate size, varying health care delivery systems, and ability to implement reforms and generate data rapidly: Akron, Ohio; Milwaukie, Oregon; northeastern Queens, New York; and Williamsburg, Virginia. For each community, leaders contributed baseline population and program effect estimates that reflected projections from reported research to build the model. FINDINGS: The simulation projected third-year savings between $269 and $537 per beneficiary per month and cumulative returns on investment between 75% and 165%. CONCLUSIONS: The MediCaring Communities financial simulation demonstrates that better care at lower cost for frail elderly Medicare beneficiaries is possible within current financing levels. Long-term success of the initiative will require reinvestment of Medicare savings to bolster nonmedical supportive services in the community. Successful implementation will necessitate waiving certain regulations and developing new infrastructure in pilot communities. This financial simulation methodology will help leadership in other communities to project fiscal performance. Since the MediCaring Communities model also achieves the Centers for Medicare and Medicaid Services' vision for care for frail elders (better care, healthier people, smarter spending) and since these reforms can proceed with limited waivers from Medicare, willing communities should explore implementation and share best practices about how to achieve fundamental service delivery changes that can meet the challenges of a much older population in the 21st century.


Subject(s)
Community Networks/economics , Delivery of Health Care/economics , Frail Elderly , Medicare , Program Development , Aged , Community Networks/statistics & numerical data , Cost Savings , Efficiency, Organizational/economics , Female , Health Care Reform , Humans , Male , Models, Organizational , United States
11.
Am J Public Health ; 106(1): 45-8, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26562110

ABSTRACT

Recent changes in policymaking, such as the passage of the Patient Protection and Affordable Care Act, have ushered in a new era in community health partnerships. To investigate characteristics of effective collaboration between hospitals, their parent systems, and the public health community, with the support of major hospital, medical, and public health associations, we compiled a list of 157 successful partnerships. This set was subsequently narrowed to 12 successful and diverse partnerships. After conducting site visits in each of the partnerships' communities and interviews with key partnership participants, we extracted lessons about their success. The lessons we have learned from our investigation have the potential to assist others as they develop partnerships.


Subject(s)
Community Networks/organization & administration , Hospital Administration , Public Health Administration , Public-Private Sector Partnerships/organization & administration , Community Networks/economics , Cooperative Behavior , Humans , Interinstitutional Relations , Organizational Case Studies , Patient Protection and Affordable Care Act , Program Evaluation , Public-Private Sector Partnerships/economics , United States
12.
Matern Child Health J ; 20(5): 968-73, 2016 May.
Article in English | MEDLINE | ID: mdl-27013517

ABSTRACT

PURPOSE: Infant mortality reduction in the U.S. has been addressed predominantly through clinical approaches. While these efforts have reduced the infant mortality rate overall, they have not reduced disparities between different racial/socioeconomic groups. To address the interrelated social, economic and environmental factors contributing to infant mortality, a place-based approach is needed to complement existing initiatives and clinical practices. DESCRIPTION: Best Babies Zone (BBZ) is an early attempt to put life course theory into practice, taking a place-based approach to reducing infant mortality by aligning resources, building community leadership, and transforming educational opportunities, economic development, and community systems in concentrated neighborhoods. BBZ is currently in three neighborhoods: Price Hill (Cincinnati, OH), Hollygrove (New Orleans, LA), and Castlemont (Oakland, CA). Assessment In its first 4 years, each BBZ crafted resident-driven strategies for decreasing the root causes of toxic stress and poor birth outcomes. To address resident priorities, BBZ sites experimented with tools from other fields (like design thinking and health impact assessment), and emphasized existing MCH strategies like leadership development. Early challenges, including shifting from traditional MCH interventions and addressing health equity, point to areas of growth in implementing this approach in the maternal and child health field. CONCLUSION: BBZ aims to elevate local voice and mobilize multiple sectors in order to address the social determinants of infant mortality, and other initiatives working to improve MCH outcomes can learn from the successes and challenges of the first 4 years of BBZ in order to bring life course theory into practice.


Subject(s)
Community Networks/organization & administration , Health Status Disparities , Infant Mortality , Maternal-Child Health Centers/organization & administration , Social Determinants of Health , California , Child , Community Networks/economics , Female , Health Impact Assessment , Humans , Infant , New Orleans , Ohio , Pilot Projects , Pregnancy , Pregnancy Outcome/ethnology , Public Health/methods , Socioeconomic Factors
13.
J Postgrad Med ; 62(3): 170-2, 2016.
Article in English | MEDLINE | ID: mdl-27241808

ABSTRACT

BACKGROUND: The Innovative Mobile-phone Technology for Community Health Operation (ImTeCHO) is a mobile-phone application that helps Accredited Social Health Activists (ASHAs) in complete registration through the strategies employed during implementation that is linking ASHAs' incentives to digital records, regular feedback, onsite data entry, and demand generation among beneficiaries. OBJECTIVE: To determine the proportion of pregnancies, deliveries, and infant deaths (events) being registered through the ImTeCHO application against actual number of events in a random sample of villages. MATERIALS AND METHODS: Five representative villages were randomly selected from the ImTeCHO project area in the tribal areas of Gujarat, India to obtain the required sample of 98 recently delivered women. A household survey was done in the entire villages to enumerate each family and create a line-listing of events since January 2014; the line-listing was compared with list of women registered through the ImTeCHO application. The proportion of events being registered through the ImTeCHO application was compared against the actual number of events to find sensitivity of the ImTeCHO application. RESULT: A total of 844 families were found during household enumeration. Out of actual line-listing of pregnancies (N = 39), deliveries (N = 102), and infant deaths (N = 5) found during household enumeration, 38 (97.43%), 101 (99.01%), and 5 (100%) were registered by ASHAs through the ImTeCHO application. CONCLUSION: The use of mobile-phone technology and strategies applied during the ImTeCHO implementation should be upscaled to supplement efforts to improve the completeness of registration.


Subject(s)
Community Health Services/organization & administration , Community Networks/organization & administration , Delivery of Health Care/methods , Rural Health Services/organization & administration , Telemedicine , Cluster Analysis , Community Networks/economics , Cross-Sectional Studies , Female , Government Programs , Humans , India , Infant , Infant Mortality , Infant, Newborn , Maternal Health , Maternal Mortality , Maternal-Child Health Services , Pregnancy , Program Evaluation , Rural Population
14.
J Public Health Manag Pract ; 22(2): 164-74, 2016.
Article in English | MEDLINE | ID: mdl-25783004

ABSTRACT

CONTEXT: Achieving meaningful population health improvements has become a priority for communities across the United States, yet funding to sustain multisector initiatives is frequently not available. One potential source of funding for population health initiatives is the community benefit expenditures that are required of nonprofit hospitals to maintain their tax-exempt status. OBJECTIVE: In this article, we explore the importance of nonprofit hospitals' community benefit dollars as a funding source for population health. DESIGN: Hospitals' community benefit expenditures were obtained from their 2009 IRS (Internal Revenue Service) Form 990 Schedule H and complemented with data on state and local public health spending from the Association of State and Territorial Health Officials and the National Association of County & City Health Officials. Key measures included indicators of hospitals' community health spending and governmental public health spending, all aggregated to the state level. Univariate and bivariate statistics were used to describe how much hospitals spent on programs and activities for the community at large and to understand the relationship between hospitals' spending and the expenditures of state and local health departments. RESULTS: Tax-exempt hospitals spent a median of $130 per capita on community benefit activities, of which almost $11 went toward community health improvement and community-building activities. In comparison, median state and local health department spending amounted to $82 and $48 per capita, respectively. Hospitals' spending thus contributed an additional 9% to the resources available for population health to state and local health departments. Spending, however, varied widely by state and was unrelated to governmental public health spending. Moreover, adding hospitals' spending to the financial resources available to governmental public health agencies did not reduce existing inequalities in population health funding across states. CONCLUSIONS: Hospitals' community health investments represent an important source for public health activities, yet inequalities in the availability of funding across communities remain.


Subject(s)
Community Networks/economics , Economics, Hospital/statistics & numerical data , State Government , United States Public Health Service/economics , Humans , Organizations, Nonprofit/economics , Tax Exemption/trends , United States , United States Public Health Service/statistics & numerical data
15.
HEC Forum ; 28(2): 153-67, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26055879

ABSTRACT

Ethics networks have emerged over the last few decades as a mechanism for individuals and institutions over various regions, cities and states to converge on healthcare-related ethical issues. However, little is known about the development and nature of such networks. In an effort to fill the gap in the knowledge about such networks, a survey was conducted that evaluated the organizational structure, missions and functions, as well as the outcomes/products of ethics networks across the country. Eighteen established bioethics networks were identified via consensus of three search processes and were approached for participation. The participants completed a survey developed for the purposes of this study and distributed via SurveyMonkey. Responses were obtained from 10 of the 18 identified and approached networks regarding topic areas of: Network Composition and Catchment Areas; Network Funding and Expenses; Personnel; Services; and Missions and Accomplishments. Bioethics networks are designed primarily to bring ethics education and support to professionals and hospitals. They do so over specifically defined areas-states, regions, or communities-and each is concerned about how to stay financially healthy. At the same time, the networks work off different organizational models, either as stand-alone organizations or as entities within existing organizational structures.


Subject(s)
Bioethics/trends , Community Networks/trends , Ethicists/supply & distribution , Bioethics/education , Community Networks/economics , Community Networks/supply & distribution , Ethics Committees/organization & administration , Humans , Surveys and Questionnaires , United States
16.
Prev Sci ; 16(1): 158-67, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24706195

ABSTRACT

This study is a longitudinal investigation of the Promoting School-community-university Partnerships to Enhance Resilience (PROSPER) partnership model designed to evaluate the level of sustainability funding by community prevention teams, including which factors impact teams' generation of sustainable funding. Community teams were responsible for choosing, implementing with quality, and sustaining evidence-based programs (EBPs) intended to reduce substance misuse and promote positive youth and family development. Fourteen US rural communities and small towns were studied. Data were collected from PROSPER community team members (N = 164) and prevention coordinators (N = 10) over a 5-year period. Global and specific aspects of team functioning were assessed over six waves. Outcome measures were the total funds (cash and in-kind) raised to implement prevention programs. All 14 community teams were sustained for the first 5 years. However, there was substantial variability in the amount of funds raised, and these differences were predicted by earlier and concurrent team functioning and by team sustainability planning. Given the sufficient infrastructure and ongoing technical assistance provided by the PROSPER partnership model, local sustainability of EBPs is achievable.


Subject(s)
Community Networks/economics , Community-Institutional Relations/economics , Family Health , Health Promotion/organization & administration , Program Evaluation/economics , Public Health , Adult , Child , Evidence-Based Practice , Female , Humans , Iowa , Longitudinal Studies , Male , Pennsylvania
17.
Gesundheitswesen ; 77(3): 206-12, 2015 Mar.
Article in German | MEDLINE | ID: mdl-25625796

ABSTRACT

Health-care service provider networks are regarded as an important instrument to overcome the widely criticised fragmentation and sectoral partition of the German health-care system. The first part of this paper incorporates health-care service provider networks in the field of health-care research. The system theoretical model and basic functions of health-care research are used for this purpose. Furthermore already established areas of health-care research with strong relations to health-care service provider networks are listed. The second part of this paper introduces some innovative options for reimbursing health-care service provider networks which can be regarded as some results of network-oriented health-care research. The origins are virtual budgets currently used in part to reimburse integrated care according to §§ 140a ff. SGB V. Describing and evaluating this model leads to real budgets (capitation) - a reimbursement scheme repeatedly demanded by SVR-Gesundheit (German governmental health-care advisory board), for example, however barely implemented. As a final step a direct reimbursement of networks by the German sickness fund is discussed. Advantages and challenges are shown. The development of the different reimbursement schemes is partially based on models from the USA.


Subject(s)
Biomedical Research/economics , Community Networks/economics , Financing, Government/economics , Health Maintenance Organizations/economics , Health Services/economics , Reimbursement Mechanisms/economics , Financing, Government/methods , Germany , Models, Economic
18.
Matern Child Health J ; 18(2): 380-8, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23456413

ABSTRACT

To describe the efforts of a community-based maternal and child health coalition to integrate the life course into its planning and programs, as well as implementation challenges and results of these activities. Jacksonville-Duval County has historically had infant mortality rates that are significantly higher than state and national rates, particularly among its African American population. In an effort to address this disparity, the Northeast Florida Healthy Start Coalition embraced the life course approach as a model. This model was adopted as a framework for (1) community needs assessment and planning; (2) delivery of direct services, including case management, education and support in the Magnolia Project, its federal Healthy Start program; (3) development of community collaborations, education and awareness; and, (4) advocacy and grass roots leadership development. Implementation experience as well as challenges in transforming traditional approaches to delivering maternal and child health services are described. Operationalizing the life course approach required the Coalition to think differently about risks, levels of intervention and the way services are organized and delivered. The organization set the stage by using the life course as a framework for its required local planning and needs assessments. Based on these assessments, the content of case management and other key services provided by our federal Healthy Start program was modified to address not only health behaviors but also underlying social determinants and community factors. Individual interventions were augmented with group activities to build interdependence among participants, increasing social capital. More meaningful inter-agency collaboration that moved beyond the usual referral relationships were developed to better address participants' needs. And finally, strategies to cultivate participant advocacy and community leadership skills, were implemented to promote social change at the neighborhood-level. Transforming traditional approaches to delivering maternal and child health services and sustaining change is a long and laborious process. The Coalition has taken the first steps; but its efforts are far from complete. Based on the agency's initial implementation experience, three areas presented particular challenges: staff, resources and evaluation. The life course is an important addition to the MCH toolbox. Community-based MCH programs should assess how a life course approach can be incorporated into existing programs to broaden their focus, and, potentially, their impact on health disparities and birth outcomes. Some areas to consider include planning and needs assessment, direct service delivery, inter-agency collaboration, and community leadership development. Continued disparities for people of color, despite medical advances, demand new interventions that purposefully address social inequities and promote advocacy among groups that bear a disproportionate burden of infant mortality. Successful transformation of current approaches requires investment in staff training to garner buy-in, flexible resources and the development of new metrics to measure the impact of the life course approach on individual and programmatic outcomes.


Subject(s)
Community Networks/organization & administration , Health Plan Implementation/organization & administration , Health Status Disparities , Maternal-Child Health Centers/organization & administration , Social Determinants of Health , Black or African American/statistics & numerical data , Case Management/organization & administration , Case Management/standards , Community Networks/economics , Community Networks/standards , Cooperative Behavior , Female , Financing, Government , Florida , Health Plan Implementation/economics , Health Plan Implementation/methods , Humans , Infant , Infant Mortality/ethnology , Infant Mortality/trends , Infant Welfare/economics , Infant Welfare/ethnology , Maternal-Child Health Centers/economics , Maternal-Child Health Centers/standards , Organizational Case Studies , Pregnancy , Pregnancy Outcome/ethnology , Social Marketing , United States
19.
Matern Child Health J ; 18(2): 413-22, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23595565

ABSTRACT

National experts are calling for more integrated approaches such as the life course perspective to reduce health disparities and achieve greater health equity. The translation and application of the life course perspective is therefore of great interest to public health planners, policy makers and funders to promote community-wide improvements in maternal and child health. However, few organizations have applied the life course perspective in designing strategic funding initiatives. For over three decades, Wisconsin has observed persistent racial disparities in birth outcomes. This complex public health issue led to the development of the Lifecourse Initiative for Health Families, a regional multi-million dollar funding initiative created and supported by the Wisconsin Partnership Program of the University of Wisconsin School of Medicine and Public Health (Created by the UW SMPH from an endowment following the conversion of Blue Cross Blue Shield United of Wisconsin, the Partnership Program makes investments in research, education, and public health and prevention initiatives that improve health and reduce health disparities in the state.). Over a 2-year period, the program funded four collaboratives to adopt a life course perspective and develop strategic plans for improving African American birth outcomes. The Twelve-point plan to close the black-white gap in birth outcomes provided the framework for the planning process. Despite the conceptual challenges, the life course perspective was embraced by the collaboratives, challenged community assumptions on the root causes of poor birth outcomes and provided a unifying funding construct for organizing and planning complementary individual-level interventions with social and physical environmental change strategies. These integrated and complimentary approaches provide a long-term opportunity to address the persistent racial birth outcome disparity in Wisconsin.


Subject(s)
Family Health/ethnology , Health Status Disparities , Infant Mortality/ethnology , Preconception Care/standards , Pregnancy Outcome/ethnology , Prenatal Care/standards , Racism/psychology , Social Determinants of Health , Black or African American/statistics & numerical data , Community Networks/economics , Community Networks/organization & administration , Community Networks/standards , Family Health/economics , Fathers , Female , Financial Support , Humans , Infant , Infant Mortality/trends , Male , Organizational Case Studies , Preconception Care/economics , Preconception Care/organization & administration , Pregnancy , Pregnancy Outcome/economics , Prenatal Care/economics , Prenatal Care/organization & administration , Public-Private Sector Partnerships/economics , Public-Private Sector Partnerships/organization & administration , Stress, Psychological/complications , Stress, Psychological/ethnology , Stress, Psychological/etiology , Wisconsin/epidemiology
20.
J Community Health ; 39(4): 633-45, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24370600

ABSTRACT

Smokefree policies (SFPs) have diffused throughout the US and worldwide. However, the development of SFPs in the difficult policy environment of tobacco-producing states and economies worldwide has not been well-explored. In 2007, Tennessee, the third largest tobacco producer in the US, enacted the Non-Smoker Protection Act (NSPA). This study utilizes the multiple streams model to provide understanding of why and how this policy was developed by triangulating interviews with key stakeholders and legislative debates with archival documents. In June 2006, the Governor unexpectedly announced support for SFP, which created a window of opportunity for policy change. The Campaign for Healthy and Responsible Tennessee, a health coalition, seized this opportunity and worked with the administration and the Tennessee Restaurant Association to negotiate a comprehensive SFP, however, a weaker bill was used by the legislative leadership to develop the NSPA. Although the Governor and the Tennessee Restaurant Association's support generated an environment for 100% SFP, health groups did not fully capitalize on this environmental change and settled for a weak policy with several exemptions. This study suggests the importance for proponents of policy change to understand changes in their environment and be willing and able to capitalize on these changes.


Subject(s)
Agriculture/economics , Community Networks/organization & administration , Public Health Administration/legislation & jurisprudence , Smoke-Free Policy/legislation & jurisprudence , Tobacco Industry/economics , Agriculture/history , Agriculture/legislation & jurisprudence , Archives , Attitude to Health , Community Networks/economics , Community Networks/legislation & jurisprudence , History, 20th Century , History, 21st Century , Humans , Interviews as Topic , Models, Organizational , Organizational Case Studies , Politics , Public Facilities/economics , Public Facilities/legislation & jurisprudence , Public Health Administration/economics , Public Health Administration/methods , Restaurants/economics , Restaurants/legislation & jurisprudence , Smoke-Free Policy/economics , Smoke-Free Policy/history , State Government , Tennessee , Tobacco Industry/history , Tobacco Industry/legislation & jurisprudence , Workplace/legislation & jurisprudence
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