Indigenous health equity in health register ascertainment and data quality: a narrative review
Health registers play an important role in monitoring distribution of disease and quality of care; however, benefit is limited if ascertainment (i.e., the process of finding and recruiting people on to a register) and data quality (i.e., the accuracy, completeness, reliability, relevance, and timeliness of data) are poor. Indigenous peoples experience significant health inequities globally, yet health data for, and about, Indigenous peoples is often of poor quality. This narrative review, published in the International Journal for Equity in Health, aimed to identify perceived barriers for the ascertainment of Indigenous peoples on health registers, and collate strategies identified and used by health registers to support comprehensive ascertainment and high-quality data for Indigenous peoples.
Using vignettes about racism from health practice in Aotearoa to generate anti‐racism interventions
Racism is a key modifiable determinant of health that contributes to health inequities in Aotearoa and elsewhere. Experiences of racism occur within the health sector for workers, patients and their whānau (extended family) every day. This paper, published in Health & Social Care in the Community, uses stories of racism from nurses – reworked into vignettes – to examine the dynamics of racism to generate possible micro, meso and macro anti-racism interventions.