Abstract

BackgroundMany women with hyperglycaemia in pregnancy do not receive care during and after pregnancy according to standards recommended in international guidelines. The burden of hyperglycaemia in pregnancy falls disproportionately upon Indigenous peoples worldwide, including Aboriginal and Torres Strait Islander women in Australia. The remote and regional Australian context poses additional barriers to delivering healthcare, including high staff turnover and a socially disadvantaged population with a high prevalence of diabetes.MethodsA complex health systems intervention to improve care for women during and after a pregnancy complicated by hyperglycaemia will be implemented in remote and regional Australia (the Northern Territory and Far North Queensland). The Theoretical Domains Framework was used during formative work with stakeholders to identify intervention components: (1) increasing workforce capacity, skills and knowledge and improving health literacy of health professionals and women; (2) improving access to healthcare through culturally and clinically appropriate pathways; (3) improving information management and communication; (4) enhancing policies and guidelines; (5) embedding use of a clinical register as a quality improvement tool. The intervention will be evaluated utilising the RE-AIM framework at two timepoints: firstly, a qualitative interim evaluation involving interviews with stakeholders (health professionals, champions and project implementers); and subsequently a mixed-methods final evaluation of outcomes and processes: interviews with stakeholders; survey of health professionals; an audit of electronic health records and clinical register; and a review of operational documents. Outcome measures include changes between pre- and post-intervention in: proportion of high risk women receiving recommended glucose screening in early pregnancy; diabetes-related birth outcomes; proportion of women receiving recommended postpartum care including glucose testing; health practitioner confidence in providing care, knowledge and use of relevant guidelines and referral pathways, and perception of care coordination and communication systems; changes to health systems including referral pathways and clinical guidelines.DiscussionThis study will provide insights into the impact of health systems changes in improving care for women with hyperglycaemia during and after pregnancy in a challenging setting. It will also provide detailed information on process measures in the implementation of such health system changes.

Highlights

  • Many women with hyperglycaemia in pregnancy do not receive care during and after pregnancy according to standards recommended in international guidelines

  • A complex health systems intervention to improve care for women during and after a pregnancy complicated by hyperglycaemia will be implemented in remote and regional Australia

  • Previous work of the Partnership has included improvements in antenatal service delivery for women with hyperglycaemia in pregnancy in the Northern Territory [26] and the establishment of the Diabetes in Pregnancy (DIP) Clinical Register [27]. Building on this previous work we have developed a multi-component health systems intervention to improve care for women across regions of northern Australia during and after a pregnancy complicated by hyperglycaemia

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Summary

Introduction

Many women with hyperglycaemia in pregnancy do not receive care during and after pregnancy according to standards recommended in international guidelines. The burden of hyperglycaemia in pregnancy falls disproportionately upon Indigenous peoples worldwide, including Aboriginal and Torres Strait Islander women in Australia. An estimated 16.9%, or 21.4 million, live births around the world are complicated by hyperglycaemia each year [7] This burden falls disproportionately upon Indigenous women globally [8, 9]. The consequences of hyperglycaemia in pregnancy contribute substantially to the epidemic of diabetes, and to the 10-year gap in life expectancy between Aboriginal and Torres Strait Islander peoples and non-Indigenous Australians [16, 17]. To address disparities in health outcomes between Aboriginal and Torres Strait Islander and non-Indigenous Australians, there is an urgent need to reduce risk as early as possible in the life course

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