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The study evaluates current characteristics and outputs of Australian clinical registries. Using a cross-sectional survey of registries listed on the ACSQHC register as of 21 September 2023, the findings cover participation, maturity, registry type, funding, data collection practices, availability, and reporting outputs. 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Objective: To assess current characteristics and outputs of clinical registries in Australia. Method: A cross-sectional survey design of Australian clinical registries listed on the Australian Commission on Safety and Quality in Health Care (ACSQHC) register as of 21 September 2023. Results: Of 107 clinical registries on the ACSQHC register that were contacted, 64 (60%) participated in the survey. Of these, 37 (58%) had been active for ⩾ 10 years, 38 (59%) were medical clinical registries and 35 (57%) received government funding. Clinical registry activities included research (92%), quality improvement (81%) and epidemiological monitoring (68%). Data were commonly patient-identifiable (64%) and collected by clinicians/staff (81%). A majority (55%) had real-time data available to contributing hospitals. Clinical registry outputs included providing data to researchers (97%), publications (83%), annual reports (69%) and site benchmarked reports (64%). Over half informed quality improvement activities (60%), monitored adherence to guidelines (59%) or informed policy or service planning (52%). Nearly half-supported clinical trials (49%), while one-fifth had integrated with government data frameworks. Conclusion: Australian clinical registries monitor health system performance across a breadth of clinical areas. A majority undertake regular public and hospital reporting and inform other quality improvement activities. Implications for health information management practice: Clinical registries interact with hospitals regarding their data collection and reporting activities. Health information management specialists have an important role in maximising registry data quality and therefore value to a wide variety of stakeholders.  \nKeywords (MeSH)  \nregistries; delivery of health care; quality improvement  \nIntroduction  \nClinical registries are continuous data collection programs that seek to prospectively enrol all individuals with a particular diagnosis, or receiving a particular procedure or service, with the aim of understanding the natural history, trends in clinical practice and patient outcomes (Gliklich et al., 2020) . Clinical registries may also be established primarily for research purposes, or to monitor high-risk treatments and provide outcome data to regulatory agencies such as the Therapeutic Goods Administration (Australian Government Department of Health, 2021) . Such data may be used to inform national regulatory approval and subsidisation decisions (Ahern et al., 2022) . Clinical quality registries (CQRs) are a type of clinical registry that has as its primary aim to monitor and report on processes and outcomes of clinical care for quality assurance and/or quality  \nimprovement purposes. When sufficiently mature, CQRs provide benchmarked reports to participating clinicians and/ or health care organisations to support shared clinical decision-making and drive clinical improvement (Australian  \n1 Monash University, Australia  \n2South Australian H","cbCaimDBHcO1xdpo","https://ap.wps.com/l/cbCaimDBHcO1xdpo","pdf",586295,"English","# Abstract\n# Introduction\n# Methods\n## Survey of Australian clinical registries\n# Results\n## Participation and registry characteristics\n## Activities and data collection\n## Outputs and impacts\n# Conclusion","[{\"question\":\"What is the main objective of the study about Australian clinical registries?\",\"answer\":\"To assess current characteristics and outputs of clinical registries in Australia.\"},{\"question\":\"How was data collected for the study?\",\"answer\":\"Through a cross-sectional survey of Australian clinical registries listed on the ACSQHC register as of 21 September 2023.\"},{\"question\":\"Which activities and outputs were most commonly supported by the registries?\",\"answer\":\"Registries commonly supported research, quality improvement, and epidemiological monitoring, and their outputs included providing data to researchers, publications, and annual or benchmarked reports. Many also informed quality improvement, guideline adherence, and policy or service planning.\"}]","Monitoring performance and improving outcomes: characteristics and outputs of Australian clinical registries | PDF",1790588076]