Establishment of a sentinel surveillance network for sexually transmissible infections and blood borne viruses in Aboriginal primary care services across Australia: the ATLAS project

Male Native Hawaiian or Other Pacific Islander Australian Aboriginal and Torres Strait Islander Peoples anzsrc-for: 4205 Nursing anzsrc-for: 0807 Library and Information Studies Community Networks sexually transmissible infection 0302 clinical medicine Medicine and Health Sciences reporting anzsrc-for: 42 Health Sciences Surveillance 3 Good Health and Well Being Blood-borne Virus Health Services 4203 Health Services and Systems 3. Good health anzsrc-for: 4203 Health Services and Systems surveillance Female Public aspects of medicine RA1-1270 Infection 0305 other medical science anzsrc-for: 1117 Public Health and Health Services Research Article Adult Adolescent Sexually Transmitted Diseases anzsrc-for: 1110 Nursing anzsrc-for: 4206 Public health 610 primary care 03 medical and health sciences Health Services, Indigenous Humans first peoples Primary Care Aboriginal and Torres Strait Islander Blood-Borne Infections First Peoples Primary Health Care 9. Industry and infrastructure Australia 42 Health Sciences blood-borne virus and the Centre of Research Excellence in Aboriginal Sexual Health investigator group 15. Life on land 2719 Health Policy Indigenous Reporting bloodborne virus Sexually Transmissible Infection Sentinel Surveillance
DOI: 10.1186/s12913-020-05388-y Publication Date: 2020-08-20T07:04:44Z
ABSTRACT
Abstract Background Sexually transmissible infection (STI) and blood-borne virus (BBV) diagnoses data are a core component of the Australian National Notifiable Diseases Surveillance System (NNDSS). However, the NNDSS data alone is not enough to understand STI and BBV burden among priority population groups, like Aboriginal and Torres Strait Islander people, because it lacks testing, treatment and management data. Here, we describe the processes involved in establishing a STI and BBV sentinel surveillance network representative of Aboriginal Community-Controlled Health Services (ACCHS)—known as the ATLAS network—to augment the NNDSS and to help us understand the burden of disease due to STI and BBV among Aboriginal and Torres Strait Islander peoples. Methods Researchers invited participation from ACCHS in urban, regional and remote areas clustered in five clinical hubs across four Australian jurisdictions. Participation agreements were developed for each clinical hub and individual ACCHS. Deidentified electronic medical record (EMR) data relating to STI and BBV testing, treatment and management are collected passively from each ACCHS via the GRHANITEtm data extraction tool. These data are analysed centrally to inform 12 performance measures which are included in regular surveillance reports generated for each ACCHS and clinical hub. Results The ATLAS network currently includes 29 ACCHS. Regular reports are provided to ACCHS to assess clinical practice and drive continuous quality improvement initiatives internally. Data is also aggregated at the hub, jurisdictional and national level and will be used to inform clinical guidelines and to guide future research questions. The ATLAS infrastructure can be expanded to include other health services and potentially linked to other data sources using GRHANITE. Conclusions The ATLAS network is an established national surveillance network specific to Aboriginal and Torres Strait Islander peoples. The data collected through the ATLAS network augments the NNDSS and will contribute to improved STI and BBV clinical care, guidelines and policy program-planning.
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