scholarly journals Understanding the meaning of trauma-informed care for burns health care professionals in a pediatric hospital: A qualitative study using interpretive phenomenological analysis.

Burns ◽  
2021 ◽  
Author(s):  
Megan Simons ◽  
Roy Kimble ◽  
Zephanie Tyack
Keyword(s):  
Health Care ◽  
Qualitative Study ◽  
Health Care Professionals ◽  
Phenomenological Analysis ◽  
Interpretive Phenomenological Analysis ◽  
Pediatric Hospital ◽  
Trauma Informed Care ◽  
Trauma Informed

Health-care professionals’ perceived trust in and willingness to recommend functional foods: A qualitative study

Appetite ◽  
2007 ◽  
Vol 48 (2) ◽  
pp. 241-247 ◽  
Author(s):  
Eva Landström ◽  
Birgitta Sidenvall ◽  
Ulla-Kaisa Koivisto Hursti ◽  
Maria Magnusson
Keyword(s):  
Health Care ◽  
Qualitative Study ◽  
Health Care Professionals ◽  
Functional Foods ◽  
Perceived Trust ◽  
Willingness To Recommend

The Difficulties the Caregivers of Cancer Patients Experience in the Covid-19 Pandemic

2021 ◽  
Author(s):  
Hatice KARABUGA YAKAR ◽  
Sıdıka OGUZ ◽  
Ferda KARAKAS ◽  
Hatice TEKIN ◽  
Nurullah ONER ◽  
...  
Keyword(s):  
Qualitative Study ◽  
Cancer Patients ◽  
Structured Interview ◽  
Phenomenological Analysis ◽  
Interpretive Phenomenological Analysis ◽  
Behavioural Responses ◽  
Economic Problems ◽  
Interview Technique ◽  
Diversity Sampling ◽  
Patients Experience

Abstract Purpose This is a qualitative study using interpretive phenomenological analysis to determine the difficulties experienced by caregivers of cancer patients during the Covid-19 pandemic. Methods Fourteen cancer patients were interviewed between 20 December 2020 and 20 January 2021 using maximum diversity sampling. The data were collected using semi-structured interview forms, one-on-one interviews, and online interview technique. Results The experiences of caregivers of cancer patients regarding the Covid 19 pandemic were presented under four themes, namely emotional problems, economic problems, neglect of health, and behavioural responses associated with Covid 19”. Conclusions It was found that caregivers of cancer patients were emotionally affected, faced economic difficulties, neglected their own health, and developed behavioural responses to the risk of Covid-19 during the pandemic.

scholarly journals Social and Health System Complexities Impacting on Decision-Making for Utilization of Oncology and Palliative Care in an African Context: A Qualitative Study

2019 ◽  
Vol 35 (3) ◽  
pp. 185-191 ◽  
Author(s):  
David A. Agom ◽  
Stuart Allen ◽  
Sarah Neill ◽  
Judith Sixsmith ◽  
Helen Poole ◽  
...  
Keyword(s):  
Health Care ◽  
Decision Making ◽  
Palliative Care ◽  
Qualitative Study ◽  
Health Care System ◽  
Health Care Professionals ◽  
Care Delivery ◽  
Semistructured Interview ◽  
Design Data ◽  
Care System

Background: There is a dearth of research focusing on identifying the social complexities impacting on oncology and palliative care (PC), and no study has explored how the health-care system in Nigeria or other African contexts may be influencing utilization of these services. Aim: This study explored how social complexities and the organization of health-care influenced the decision-making process for the utilization of oncology and PC in a Nigerian hospital. Methods: This qualitative study used an interpretive descriptive design. Data were collected using semistructured interview guides with 40 participants, comprising health-care professionals, patients, and their families. Thematic analysis was conducted to generate and analyze patterns within the data. Findings: Three themes were identified: dysfunctional structural organization of the health-care delivery system, service-users’ economic status, and the influence of social networks. The interrelationship between the themes result in patients and their family members decisions either to present late to the hospital, miss their clinical appointments, or not to seek oncological health care and PC. Conclusion: This article offers insights into the role of the health-care system, as organized currently in Nigeria, as “autoinhibitory” and not adequately prepared to address the increasing burden of cancer. We therefore argue that there is a need to restructure the Nigerian health-care system to better meet the needs of patients with cancer and their families as failure to do so will strengthen the existing inequalities, discourage usage, and increase mortality.

scholarly journals Trauma-informed Care: Essential Elements for Pediatric Health Care

2019 ◽  
Vol 33 (2) ◽  
pp. 222-223
Author(s):  
Gail Hornor ◽  
Cathy Davis ◽  
Jennifer Sherfield ◽  
Kerri Wilkinson
Keyword(s):  
Health Care ◽  
Essential Elements ◽  
Pediatric Health ◽  
Pediatric Health Care ◽  
Trauma Informed Care ◽  
Trauma Informed

scholarly journals Pharyngeal carriage rates of Neisseria meningitidis in health care professionals at a tertiary university pediatric hospital

2020 ◽  
Vol 39 (9) ◽  
pp. 1703-1709
Author(s):  
Lisa-Maria Steurer ◽  
Mathias Hetzmannseder ◽  
Birgit Willinger ◽  
Peter Starzengruber ◽  
Claudia Mikula ◽  
...  
Keyword(s):  
Health Care ◽  
Neisseria Meningitidis ◽  
Health Care Professionals ◽  
Pediatric Hospital

scholarly journals ‘It’s what you do that makes a difference’ An interpretative phenomenological analysis of health care professionals and home care workers experiences of nutritional care for people living with dementia at home

2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Louise Mole ◽  
Bridie Kent ◽  
Mary Hickson ◽  
Rebecca Abbott
Keyword(s):  
Health Care ◽  
Home Care ◽  
Health Care Professionals ◽  
Interpretative Phenomenological Analysis ◽  
Phenomenological Analysis ◽  
Care Practice ◽  
Nutritional Care ◽  
Care Workers ◽  
Home Care Workers ◽  
At Home

Abstract Background People living with dementia at home are a group who are at increased risk of malnutrition. Health care professionals and home care workers, are ideally placed to support nutritional care in this vulnerable group. Yet, few, if any studies, have captured the experiences of these workers in respect of treating and managing nutritional issues. This interpretative phenomenological study aimed to explore the experiences and perceptions of the nutritional care of people living with dementia at home from the perspectives of health care professionals and home care workers. Methods Semi-structured interviews were conducted between December 2017 and March 2018, and supplemented with the use of a vignette outlining a scenario of a husband caring for his wife with dementia. Health care professionals and home care workers were purposively recruited from local care providers in the south west of England, who had experience of working with people with dementia. An Interpretative Phenomenological Analysis (IPA) approach was used throughout. Results Seven participants took part including two home care workers, a general practitioner, dietitian, occupational therapist, nurse and social worker. The time in their professions ranged from 3 to 15 years (mean = 8.9 years). Following analysis, four superordinate themes were identified: ‘responsibility to care’, ‘practice restrained by policy’, ‘in it together’, and ‘improving nutritional care’. This group of health care professionals and home care workers recognised the importance of improving nutritional care for people living with dementia at home, and felt a responsibility for it. However they felt that they were restricted by time and/or knowledge. The importance of supporting the family carer and working collaboratively was highlighted. Conclusions Health care professionals and home care workers require further training to better equip them to provide nutritional care for people living with dementia at home. Models of care may also need to be adapted to enable a more flexible and tailored approach to incorporate nutritional care. Future work in this area should focus on how health care professionals and home care workers can be better equipped to screen for malnutrition, and support changes to nutritional intake to mitigate malnutrition risk.

scholarly journals The culture of hope and ethical challenges in clinical trials: A qualitative study of oncologists and haematologists’ views

2019 ◽  
Vol 15 (1) ◽  
pp. 29-38 ◽  
Author(s):  
Tove E Godskesen ◽  
Suzanne Petri ◽  
Stefan Eriksson ◽  
Arja Halkoaho ◽  
Margrete Mangset ◽  
...  
Keyword(s):  
Health Care ◽  
Clinical Trials ◽  
Qualitative Study ◽  
Empirical Research ◽  
Health Care Professionals ◽  
Therapeutic Misconception ◽  
Ethical Challenges ◽  
Know How ◽  
Ethical Concerns ◽  
Clinical Cancer

We do not know how much clinical physicians carrying out clinical trials in oncology and haematology struggle with ethical concerns. To our knowledge, no empirical research exists on these questions in a Nordic context. Therefore, this study aims to learn what kinds of ethical challenges physicians in Sweden, Denmark and Finland (n = 29) face when caring for patients in clinical trials; and what strategies, if any, they have developed to deal with them. The main findings were that clinical cancer trials pose ethical challenges related to autonomy issues, unreasonable hope for benefits and the therapeutic misconception. Nevertheless, some physicians expressed that struggling with such challenges was not of great concern. This conveys a culture of hope where health care professionals and patients uphold hope and mutually support belief in clinical trials. This culture being implicit, physicians need opportunities to deliberately reflect over the characteristics that should constitute this culture.

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