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The effect of hospital location and ethnicity on stroke care access and outcomes in New Zealand
Doctoral Thesis   Open access

The effect of hospital location and ethnicity on stroke care access and outcomes in New Zealand

Stephanie Gabriele Thompson
Doctor of Philosophy - PhD, University of Otago
University of Otago
2022
Handle:
https://hdl.handle.net/10523/12733

Abstract

Stroke stroke care access urban/non-urban outcomes best practice stroke care health equity
Background International research has shown that patients treated at non-urban hospitals and those from ethnic minority groups experience poorer access to best practice stroke care interventions. Much of this previous research has focussed on access to acute stroke care, with fewer studies investigating access to post-acute care. Evidence has shown that ethnic minority groups have poorer post-stroke outcomes compared to Europeans, however, it is less clear whether patients treated at non-urban hospitals also experience worse outcomes. In New Zealand there has been limited research on either of these topics, however, departures from best practice care have previously been accepted for smaller, non-urban hospitals. Over the past decade, there has been a lot of work undertaken to improve stroke care in New Zealand, however, it remains unknown whether best practice stroke care access is equitable and outcomes equal for all patients. Aims The aims of this research were to investigate whether hospital location (urban/non-urban) or ethnicity have an impact on access to best practice stroke care or patient outcomes in New Zealand. In addition, the research aimed to gain an understanding of consumer (patient, carer/family member) and health worker perspectives of stroke care in New Zealand and identify barriers to accessing best practice care. Methods This programme of research consisted of four interconnected studies beginning with an online survey investigating stroke service provision in New Zealand stroke hospitals (n=28), with a particular focus on urban/non-urban differences in care delivery. Two prospective studies, run concurrently, involved 2,379 patients admitted to hospital with stroke between May and October 2018. Data on stroke interventions provided across the care continuum, up to three months following admission, were collected. Outcomes were captured at three months, and for a sub-set of patients at six and 12 months. An online mixed methods survey was conducted to explore consumer [patient (n=41), carer/family member (n=12)] and health worker (n=41) perspectives of stroke care, and barriers to accessing best practice stroke care in New Zealand. Results Patients treated at non-urban hospitals had poorer access to a number of components of best practice stroke care and had poorer outcomes across several domains, including functional outcome, mortality and vascular and stroke recurrence, up to 12 months post stroke. By ethnicity, many components of best practice stroke care were accessed equally, and for some components there was enhanced provision. Of concern, the provision of cultural care for Māori and Pacific patients was found to be sub-optimal. Despite generally equal access to stroke care, non-Europeans had poorer functional outcomes at three, six and 12 months, and Māori specifically were more likely to have a poor functional outcome at three and 12 months and were more likely to have died by 12 months. Ethnicity was not identified by consumers as a barrier to accessing care, whereas ‘geographic inequities’ was one of the access barrier themes identified. Consumers generally rated stroke care in New Zealand higher than health workers, but both groups agreed that there was variability in care by stage of treatment, with improvements required particularly post discharge. Discussion Patients treated at non-urban hospitals had reduced access to key stroke interventions across the entire care continuum, and this was associated with poorer outcomes up to 12 months post stroke. Non-Europeans had equal access to many components of best practice stroke care, however, despite this, had poorer outcomes compared to Europeans. This points to inequitable access for non-Europeans to best practice stroke care and suggests that enhanced provision of care is required to achieve truly equitable access and equal outcomes. Perceptions of stroke care differed between consumers and health workers. Post-discharge follow-up and geographic equity were identified as key areas for improvement, with telehealth a likely strong enabler.
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