Article Types

Research

Experiencing racism in health care: the mental health impacts for Victorian Aboriginal communities

Objectives: To examine experiences of racism in health settings and their impact on mental health among Aboriginal Australians. Design, setting and participants: A cross-sectional survey of experiences of racism and mental health was conducted in two metropolitan and two rural Victorian local government areas (LGAs) between 1 December 2010 and 31 October 2011. Participants included 755 Aboriginal Australians aged over 18 years who had resided in the relevant LGA for at least a year. The response rate across all LGAs was 99%. Main outcome measures: Being above or below the threshold for high or very high psychological distress on the Kessler Psychological Distress Scale. Results: 221 participants reported experiences of racism in health settings in the past 12 months. The results suggested that people experiencing racism in health settings (OR, 4.49; 95% CI, 2.28–8.86) and non-health settings (OR, 2.66; 95% CI, 1.39–5.08) were more likely than people who did not experience racism to be above the threshold for high or very high psychological distress. Conclusions: Experiencing interpersonal racism in health settings is associated with increased psychological distress over and above what would be expected in other settings. This finding supports the rationale for improving cultural competency and reducing racism as a means of closing the health gap between Aboriginal and other Australians. Capitalising on this investment will require explicitly evaluating the impact of these initiatives on reducing patient experiences of racism.

Margaret A Kelaher BSc, PhD · Angeline S Ferdinand BA, MPH · Yin Paradies PhD

13 10503

Follow-up of Indigenous-specific health assessments - a socioecological analysis

Despite an increase in uptake of health assessments, delivery of Indigenous-specific follow-up care is lagging

Jodie Bailie BA, GradDipEd · Gill H Schierhout PhD · Margaret A Kelaher PhD · Alison F Laycock BFA, BEd · Nikki A Percival BSc, MPH · Lynette R O’Donoghue · Tracy L McNeair BA, MPH · Amal Chakraborty · Barbara D Beacham BSocSc, MCDM, CertBT · Ross S Bailie MB ChB, MPhil, MD

13 00256

The cost-effectiveness of primary care for Indigenous Australians with diabetes living in remote Northern Territory communities

Objective: To evaluate the costs and health outcomes associated with primary care use by Indigenous people with diabetes in remote communities in the Northern Territory. Design, setting and participants: A population-based retrospective cohort study from 1 January 2002 to 31 December 2011 among Indigenous NT residents ≥ 15 years of age with diabetes who attended one of five hospitals or 54 remote clinics in the NT. Main outcome measures: Hospitalisations, potentially avoidable hospitalisations (PAH), mortality and years of life lost (YLL). Variables included disease stage (new, established or complicated cases) and primary care use (low, medium or high). Results: 14 184 patients were eligible for inclusion in the study. Compared with the low primary care use group, the medium-use group (patients who used primary care 2–11 times annually) had lower rates of hospitalisation, lower PAH, lower death rates and fewer YLL. Among complicated cases, this group showed a significantly lower mean annual hospitalisation rate (1.2 v 6.7 per person [P < 0.001]) and PAH rate (0.72 v 3.64 per person [P < 0.001]). Death rate and YLL were also significantly lower (1.25 v 3.77 per 100 population [P < 0.001] and 0.29 v 1.14 per person-year [P < 0.001], respectively). The cost of preventing one hospitalisation for diabetes was $248 for those in the medium-use group and $739 for those in the high-use group. This compares to $2915, the average cost of one hospitalisation. Conclusion: Improving access to primary care in remote communities for the management of diabetes results in net health benefits to patients and cost savings to government.

Susan L Thomas DrPH · Yuejen Zhao BM, MBiostat, PhD · Steven L Guthridge MB BS, MTH, FAFPHM · John Wakerman MB BS, MTH, FAFPHM

13 11316

High chlamydia positivity rates in Indigenous people attending Australian sexual health services

High, increasing chlamydia rates highlight need for better prevention and screening programs for Indigenous people

Catherine C O’Connor DrPH, FAChSHM, MB BS(Hons) · Hammad Ali MB BS, MPH · Rebecca J Guy BAppSc, MAppEpi, PhD · David J Templeton MB ChB, PhD, FAChSHM · Christopher K Fairley PhD, FRACP, FAChSHM · Marcus Y Chen MB BS, PHD, FAChSHM · Bridget M Dickson · Lewis J Marshall MB BS, FAChSHM, FAFPHM · Andrew E Grulich MB BS, PhD, MScEpid · Margaret E Hellard MB BS, FRACP, PHD · John M Kaldor PhD · Basil Donovan MB BS, MD, FAChSHM · James S Ward BA

13 10875

A national study of the processes and outcomes of paediatric formulary applications in Australia

Paediatric hospitals are making decisions about drugs based on poor evidence and incomplete documentation

Yashwant K Sinha MB BS(Hons), FRACP, PhD · Jonathan C Craig MB ChB, FRACP, PhD · Peter G Barclay BPharm, DipHospPharm · Hugh Miller BScPharm(Hons), DipHospPharm(Admin), GradCertMan · Sean C Turner BPharm, MSc, DipClinPharm · Joseph P Whitehouse BPharm(Hons) · Jo-anne E Brien BPharm, BS(Pharm), PharmD

13 11138
Women's health Research 21 April 2014 Free

Emergency contraception in Australia: the desired source of information versus the actual source of information

Fewer women receive information and counselling about emergency contraception from their GP

Danielle Mazza MD, FRACGP · Christopher M Harrison BPsych(Hons), MSocHlth · Angela J Taft BA, MPH, PhD · Helena C Britt BA, PhD · Melissa Hobbs RN, MPH, PhD · Kay Stewart BPharm(Hons), PhD · Safeera Hussainy BPharm(Hons), PhD, GCHE · Bianca R Brijnath BA(Hons), PhD

13 10983

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