scholarly journals Family Members’ Perspectives on Family and Social Support Available to Suicidal Patients, and Health Systems’ Interactions and Responses to Suicide Cases in Alberta: Protocol for a Quantitative Research Study (Preprint)

2020 ◽  
Author(s):  
Rabab M Abou El-Magd ◽  
Liana Urichuk ◽  
Shireen Surood ◽  
Daniel Li ◽  
Andrew Greenshaw ◽  
...  
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Quantitative Research ◽  
Research Study ◽  
Family Members ◽  
Future Research ◽  
System P ◽  
Ethics Research ◽  
Suicidal Thoughts And Behaviors ◽  
Care System

BACKGROUND Suicide is a major cause of preventable death globally and a leading cause of death by injury in Canada. To support people who experience suicidal thoughts and behaviors and to ultimately prevent people from dying by suicide, it is important to understand individual and familial experiences with the health care system. OBJECTIVE We present the protocol for a study, the objective of which is to explore how people who died by suicide, and their family members, interacted with the health care system. METHODS This is a quantitative research study. Data will be collected through a self-administered paper-based or online survey of the family member of patients who died by suicide. The sample size was calculated to be 385 (margin of error ±3%). RESULTS Data collection will start in October 2020 and results will be available by March 2021. We expect the results to shed light on the experiences of individuals who died by suicide and their family members with the health care system. The study has received ethical clearance from the Health Ethics Research Board of the University of Alberta (Pro00096342). CONCLUSIONS Our study may inform practice, policy, and future research. The findings may shape how members of the health care system respond to people who are at risk of suicide and their families. INTERNATIONAL REGISTERED REPORT PRR1-10.2196/19112

scholarly journals Family Members’ Perspectives on Family and Social Support Available to Suicidal Patients, and Health Systems’ Interactions and Responses to Suicide Cases in Alberta: Protocol for a Quantitative Research Study

10.2196/19112 ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. e19112
Author(s):  
Rabab M Abou El-Magd ◽  
Liana Urichuk ◽  
Shireen Surood ◽  
Daniel Li ◽  
Andrew Greenshaw ◽  
...  
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Quantitative Research ◽  
Online Survey ◽  
Research Study ◽  
Family Members ◽  
Future Research ◽  
Ethics Research ◽  
Suicidal Thoughts And Behaviors ◽  
Care System

Background Suicide is a major cause of preventable death globally and a leading cause of death by injury in Canada. To support people who experience suicidal thoughts and behaviors and to ultimately prevent people from dying by suicide, it is important to understand individual and familial experiences with the health care system. Objective We present the protocol for a study, the objective of which is to explore how people who died by suicide, and their family members, interacted with the health care system. Methods This is a quantitative research study. Data will be collected through a self-administered paper-based or online survey of the family member of patients who died by suicide. The sample size was calculated to be 385 (margin of error ±3%). Results Data collection will start in October 2020 and results will be available by March 2021. We expect the results to shed light on the experiences of individuals who died by suicide and their family members with the health care system. The study has received ethical clearance from the Health Ethics Research Board of the University of Alberta (Pro00096342). Conclusions Our study may inform practice, policy, and future research. The findings may shape how members of the health care system respond to people who are at risk of suicide and their families. International Registered Report Identifier (IRRID) PRR1-10.2196/19112

scholarly journals Family Members’ Perspectives of Health Care System Interactions With Suicidal Patients and Responses to Suicides: Protocol for a Qualitative Research Study (Preprint)

2019 ◽  
Author(s):  
Erin Bryksa ◽  
Reham Shalaby ◽  
Laura Friesen ◽  
Kirsten Klingle ◽  
Graham Gaine ◽  
...  
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Family Members ◽  
Qualitative Research Study ◽  
System P ◽  
Study Results ◽  
The Individual ◽  
Suicidal Patients ◽  
Suicidal Thoughts And Behaviors ◽  
Care System

BACKGROUND Suicide is a major cause of preventable death globally and a leading cause of death by injury in Canada. To support people who experience suicidal thoughts and behaviors and ultimately prevent people from dying by suicide, it is important to understand the individual and familial experiences with the health care system. OBJECTIVE This study aims to explore how suicide victims, and their family members, interacted with the health care system. METHODS We will invite family members of 6 to 8 suicide victims to participate in the study by sharing their perspectives on both their relative’s as well as their own interactions with the health care system. Interviews will take place in-person and will be audio recorded, transcribed, and analyzed thematically. RESULTS The results of the study are expected to be available in 12 months. We expect the results to shed light on the experiences of suicide victims and their family members with the health care system. CONCLUSIONS Our study results may inform practice, policy, and further research. They may shape how members of the health care system respond to people who are at risk of suicide and their families. INTERNATIONAL REGISTERED REPOR PRR1-10.2196/13797

scholarly journals Family Members’ Perspectives of Health Care System Interactions With Suicidal Patients and Responses to Suicides: Protocol for a Qualitative Research Study

10.2196/13797 ◽  
2019 ◽  
Vol 8 (8) ◽  
pp. e13797
Author(s):  
Erin Bryksa ◽  
Reham Shalaby ◽  
Laura Friesen ◽  
Kirsten Klingle ◽  
Graham Gaine ◽  
...  
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Family Members ◽  
Qualitative Research Study ◽  
Study Results ◽  
The Individual ◽  
Suicidal Patients ◽  
Suicidal Thoughts And Behaviors ◽  
Shed Light ◽  
Care System

Background Suicide is a major cause of preventable death globally and a leading cause of death by injury in Canada. To support people who experience suicidal thoughts and behaviors and ultimately prevent people from dying by suicide, it is important to understand the individual and familial experiences with the health care system. Objective This study aims to explore how suicide victims, and their family members, interacted with the health care system. Methods We will invite family members of 6 to 8 suicide victims to participate in the study by sharing their perspectives on both their relative’s as well as their own interactions with the health care system. Interviews will take place in-person and will be audio recorded, transcribed, and analyzed thematically. Results The results of the study are expected to be available in 12 months. We expect the results to shed light on the experiences of suicide victims and their family members with the health care system. Conclusions Our study results may inform practice, policy, and further research. They may shape how members of the health care system respond to people who are at risk of suicide and their families. International Registered Report Identifier (IRRID) PRR1-10.2196/13797

scholarly journals Does higher health literacy lead to higher trust in public hospitals?

2021 ◽  
Author(s):  
Maja Bertram ◽  
Urs Steiner Brandt ◽  
Rikke Klitten Hansen ◽  
Gert Tinggaard Svendsen
Keyword(s):  
Game Theory ◽  
Health Care ◽  
Health Literacy ◽  
Health Care System ◽  
Empirical Data ◽  
Health Care Professionals ◽  
Social Groups ◽  
Public Hospitals ◽  
Future Research ◽  
Care System

Abstract Background: Does higher health literacy lead to higher trust in public hospitals? Existing literature suggests that this is the case since a positive association between the level of health literacy and the level of trust in physicians and the health care system has been shown. This study aims to challenge this assumption. Methods: Based on theoretical arguments from game theory and analysis of empirical data, we argue that the association is better described as an inversely u-shaped curve, suggesting that low and high levels of health literacy lead to a lower level of trust than a medium level of health literacy does. The empirical analysis is based on a study of the Danes’ relationship to the overall health care system. More than 6,000 Danes have been asked about their overall expectations of the health service, their concrete experiences and their attitudes to a number of change initiatives. Results: Game theory analysis show that the combined perceived cooperation and benefit effects can explain an inversely u-shaped relationship between social groups and trust in the health care system. Based on quantitative, binary regression analyses of empirical data, the lowest degree of trust is found among patients from the lowest and highest social groups, while the highest degree of trust is found in the middle group. The main driver for this result is that while patients having low health literacy perceive that the health care system is not cooperative, patients with a high level of health literacy have high expectations about the quality, which the health care system might not be able to provide. This reduces the perceived benefit from their encounter with the health care system. Conclusion: It is important that health care professionals understand that some patient groups have a higher chance of cooperation (e.g., agreeing on the choice of treatment) or defection (e.g. passing a complaint) than others. In perspective, future research should undertake further qualitative examinations of possible patient types and their demands in relation to different health care sectors, focusing specifically on the opportunities to improve the handling of different patient types.

scholarly journals Toward Comprehensive Patient-Centric Care by Integrating Digital Health Technology With Direct Clinical Contact in Australia (Preprint)

2018 ◽  
Author(s):  
Penelope Schofield ◽  
Tim Shaw ◽  
Michaela Pascoe
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Digital Health ◽  
Integrated Health Care ◽  
Care Model ◽  
Current Health ◽  
System P ◽  
Integrated Health ◽  
Integrated Health Care System ◽  
Care System

BACKGROUND There is an escalating crisis in health care, locally and internationally. The current health care model is unable to meet the increasing health care demands. OBJECTIVE The aim of this study was to reconceptualize the provision of health care to produce better outcomes at no greater cost, by placing individuals in the position of authority to direct their own care, in a personalized, integrated health care system. METHODS In this study, we used the Australian health care system as a model. We reviewed the current landscape of digital health in Australia and discussed how electronic medical records (EMRs) can be further developed into a personalized, integrated health care system. RESULTS Some components of an EMR and digital health system are already being used in Australia, but the systems are not linked. A personalized, integrated health care model that is responsive to consumer needs requires not just a passive repository of medical information; it would require a team approach, including the government, health care funders, industries, consumers and advocacy groups, health care professionals, community groups, and universities. CONCLUSIONS Implementation of a personalized, integrated health care system can result in reduced pressure on the current health care system, and it can result in the delivery of best-practice health care, regardless of location. Importantly, a personalized, integrated health care system could serve as an education platform, “upskilling” not only clinicians but also, more importantly, patients and carers by providing them with accurate information about their condition, treatment options, medications, and management strategies. By proposing personalized, integrated health care, we offer an intelligent model of health care that is ubiquitous, efficient, and continuously improving.

scholarly journals THE LEVEL OF DECENTRALIZATION IMPACT ON THE BULGARIAN SOCIAL HEALTH CARE COMPETITIVENESS

2019 ◽  
Vol 5 (15) ◽  
pp. 1251-1258
Author(s):  
Venelin Terziev ◽  
Stoyanka Petkova ◽  
GEORGİEVA GEORGİEVA
Keyword(s):  
Health Care ◽  
Theoretical Model ◽  
Health Care System ◽  
Measurement System ◽  
Social Health ◽  
Performance Measurement System ◽  
Future Research ◽  
Health Care Managers ◽  
Care Managers ◽  
Care System

One of the most significant characteristics on which the Bulgarian social health care system competitiveness depends is the level of decentralization. In this study the authors explain a methodology for estimating the level of decentralization by using the knowledge of the so-called performance measurement system (PMS). The established theoretical model is tested among health care managers in 78 sub-divisional units randomly chosen among the Bulgarian health care system – facilities and hospitals. There have been made several conclusions that could be a base for future research and discussion. Keywords: competitiveness, impact, level of decentralization, Bulgarian health care system.

scholarly journals Traditional Birth Attendants in Samoa: Integration With the Formal Health System

2012 ◽  
Vol 2 (1) ◽  
pp. 5-11 ◽  
Author(s):  
Caroline S. E. Homer ◽  
Tauaitala Lees ◽  
Pelenatete Stowers ◽  
Fulisia Aiavao ◽  
Annabel Sheehy ◽  
...  
Keyword(s):  
Health Care ◽  
Health System ◽  
Health Care System ◽  
Maternity Care ◽  
Significant Proportion ◽  
Traditional Birth Attendant ◽  
Safe Motherhood ◽  
Future Research ◽  
Health Providers ◽  
Care System

A traditional birth attendant (TBA) is a person who assists the mother during childbirth and who initially acquired her skills by delivering babies herself or through apprenticeship to other TBAs. In many parts of the world, TBAs continue to provide a significant proportion of maternity care during pregnancy, birth, and the postpartum period. In Samoa, TBAs are recognized part of both the formal and informal health care system. The aim of this research was to examine the contribution that TBAs made in the provision of maternity care in Samoa. A descriptive study was undertaken, and 100 TBAs who had attended more than 400 births a year were interviewed as part of a broader Safe Motherhood Needs Assessment.The findings highlighted that although TBAs can work in collaboration with individual health providers or facilities or be integrated into the health system, TBAs were often practicing autonomously within their communities, independent of collaborative links. This study showed that formal recognition and registration of TBAs would improve the recording of births and augment their partnership to the formal health care system. This formal registration process has since been implemented to improve monitoring and evaluation and assist future research with this important group.

Enabling Technologies and Challenges for the Future of Ubiquitous Health The Interoperability Framework

2010 ◽  
pp. 596-622 ◽  
Author(s):  
Donald W. M. Juzwishin
Keyword(s):  
Health Care ◽  
Web 2.0 ◽  
Health Care System ◽  
Care Delivery ◽  
Future Research ◽  
Health Care Reforms ◽  
High Performing ◽  
Web 3.0 ◽  
System Interoperability ◽  
Care System

Web 2.0 and Web 3.0 emerge at a time when health care reforms are stymied. Current barriers to an effectively functioning health care system are linked to the historical, political and social institutions and processes that are preventing health system interoperability causing issues with access (to service and information), continuity of care, safety and the assessment of program delivery. An interoperability framework, identifying citizens, providers, policy makers and researchers is developed and related to the improvement of understanding, access, trust, discourse, and practice for the purpose of moving toward a high performing health care system. Web 2.0 and Web 3.0 offer great promise as an eHealth platform to synergistically catalyze significant improvements to health care delivery, however, caution is advised about uncritical adoption. Barriers to progress and opportunities for advancement are identified and questions for future research are posited.

scholarly journals Pharmacist-led medication non-adherence intervention: reducing the economic burden placed on the Australian health care system

2019 ◽  
Vol Volume 13 ◽  
pp. 853-862 ◽  
Author(s):  
Rachelle Louise Cutler ◽  
Andrea Torres-Robles ◽  
Elyssa Wiecek ◽  
Barry Drake ◽  
Naomi Van der Linden ◽  
...  
Keyword(s):  
Health Care ◽  
Health Care System ◽  
Economic Burden ◽  
Australian Health ◽  
System P ◽  
Adherence Intervention ◽  
Care System
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