scholarly journals Organisational views on health care access for hauā (disabled) Māori in Murihiku (Southland), Aotearoa New Zealand: A mixed methods approach

2018 ◽  
Vol 46 (2) ◽  
pp. 51-66
Author(s):  
Leigh Hale ◽  
Katrina Bryant ◽  
Aimee Ward ◽  
Amy Falloon ◽  
Aroha Montgomery ◽  
...  
Author(s):  
Paul George Holland ◽  
Ozan Nadir Alakavuklar

The purpose of this study is to understand whether the seeking of legitimacy from Maori communities by Aotearoa New Zealand energy companies is a historical consistent practice or a result of a proposal of privatization. Corporate Social Responsibility (CSR) reports of four different State Owned Enterprises are analyzed longitudinally beginning from 2008 to 2013 with a mixed methods approach. It is found that the NZ energy sector doesn't have a common approach in how it communicates with Maori stakeholders but rather that each organization tailors its interaction with Maori communities based on the circumstances each individual organization is in. The study contributes to research concerning the use of content related to Maori and Maori indigenous values in CSR communication as well as to that research investigating how organizations respond to potential threats to their legitimacy through the use of CSR communication in Aotearoa New Zealand context.


Author(s):  
Jennifer White ◽  
Dominic Cavenagh ◽  
Julie Byles ◽  
Gita Mishra ◽  
Leigh Tooth ◽  
...  

Author(s):  
Isabel Goicolea ◽  
Dean Carson ◽  
Miguel San Sebastian ◽  
Monica Christianson ◽  
Maria Wiklund ◽  
...  

2021 ◽  
Vol 14 (1) ◽  
pp. 100967 ◽  
Author(s):  
Anne Ordway ◽  
Chris Garbaccio ◽  
Michael Richardson ◽  
Kathe Matrone ◽  
Kurt L. Johnson

2014 ◽  
Vol 6 (1) ◽  
pp. 7 ◽  
Author(s):  
Amanda Wheeler ◽  
Brian McKenna ◽  
Dominic Madell

INTRODUCTION: Literature suggests that good quality health care access can have a positive impact on the health of people with serious mental illness (SMI), but literature relating to patterns of access by this group is equivocal. AIM: This study was designed to explore health care access patterns in a group of people with SMI and to compare them with a general New Zealand population group, in order for health providers to understand how they might contribute to positive health outcomes for this group. METHODS: The study surveyed 404 mental health consumers aged 18–65 years receiving care from one district health board in Auckland about their patterns of health care access. Results were compared with those from the New Zealand Health Survey of the general population. RESULTS: Findings suggest that the SMI consumer respondents had poorer physical health than the general population respondents, accessed health care services in more complex ways and were more particular about who they accessed for their care than the general population respondents. There was some concern from SMI consumers around discrimination from health care providers. The study also suggested that some proactive management with SMI consumers for conditions such as metabolic syndrome was occurring within the health care community. DISCUSSION: The first point of access for SMI consumers with general health problems is not always the family general practitioner and so other health professionals may sometimes need to consider the mental and physical health of such consumers in a wider context than their own specialism. KEYWORDS: General practice; health services accessibility; mental disorders; mental health; primary health care


Author(s):  
P Phimphasone-Brady ◽  
J Chiao ◽  
L Karamsetti ◽  
A Sieja ◽  
R Johnson ◽  
...  

Abstract The COVID-19 pandemic has rapidly altered ambulatory health care delivery and may have worsened disparities in health care access. To assess the telehealth implementation experiences of ambulatory personnel in different disciplines and their perspectives on potential telehealth disparities, and to make recommendations for more equitable telehealth delivery. We used a convergent parallel mixed-methods design. Clinic managers from geriatric medicine, internal medicine, and psychiatry e-mailed a survey to clinicians and staff regarding experiences with telehealth care delivery. Quantitative survey responses were analyzed with Fisher’s Exact tests. Qualitative responses were coded thematically. Recommendations were categorized by type of implementation strategy. Quantitative and qualitative findings on telehealth disparities were merged in a joint data display. Respondents (n = 147, 57% response rate) were distributed across three specialties: 66% internal medicine, 19% psychiatry, and 14% geriatric medicine. Prior to 2020, 77% of clinicians had never delivered telehealth services. By Spring 2020, 78% reported conducting more than half of clinic visits by telehealth. Among clinicians, 52% agreed/strongly agreed that rapid telehealth implementation exacerbated access to care disparities to: older adult patients, those with limited internet access, and those needing interpretation services. Staff expressed similar difficulties with telehealth set-up especially for these patients. To improve telehealth equity, clinicians recommended to: (i) change infrastructure; (ii) train and educate stakeholders; and (iii) support clinicians. Clinicians and staff reported specific subpopulations had challenges in accessing telehealth visits. To avoid perpetuating telehealth access disparities, further co-discovery of equitable implementation strategies with patients and clinics are urgently needed.


2015 ◽  
Vol 38 (2) ◽  
pp. 178-187 ◽  
Author(s):  
Barry John Milne ◽  
Karl Parker ◽  
Jessica McLay ◽  
Martin von Randow ◽  
Roy Lay-Yee ◽  
...  

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