OOIR: Observatory of International Research

Papers

(The TQCC of Health Information Management Journal is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-09-01 to 2025-09-01.)

Article	Citations
Digital health care and data work: Who are the data professionals?	15
Procedure-level data linkage to drive improvement in case ascertainment for the Australian Breast Device Registry	12
Evaluation of virtual training delivery for health information systems implementation in Canada: A qualitative study	11
IPPASOS: The first digital forensic information system in Greece	11
Comparison of comorbidities of stroke collected in administrative data, surveys, clinical trials and cohort studies	10
Predictive analytics for early detection of hospital-acquired complications: An artificial intelligence approach	7
Developing a code of ethics in health information management	7
Impact of clinical note format on diagnostic accuracy and efficiency	6
Factors influencing the use of big data within healthcare services: a systematic review	6
Costs of acute hospitalisation for stroke and transient ischaemic attack in Australia	6
Accuracy of site benchmarking in clinical quality registries of varying size	6
Professional identity and workplace motivation: A case study of health information managers	5
The applications of Australian-coded ICD-10 and ICD-10-AM data in research: A scoping review of the literature	5
Health information management students’ work-integrated learning (professional practice placements): Where do they go and what do they do?	5
Health information management professionals’ investigator involvement in research: barriers and facilitators	5
System-wide analysis of qualitative hospital incident data: Feasibility of semi-automated content analysis to uncover insights	5
Medical record-keeping training for undergraduate medical students in pre-clinical years: An experiment for program effectiveness and student satisfaction	5
The importance of SNOMED CT concept specificity in healthcare analytics	5
Enhancing registry impact: Translating registry outputs into C onsumer- F riendly I nformation (CoFI projec	4
Training and experience of coding with the World Health Organization’s International Classification of Diseases, Eleventh Revision	4
The biopsychosocial–spiritual impact on non-clinical health professionals who interact with traumatic and/or sensitive health data: A scoping review	4
Optimising data quality in a national clinical quality registry: Insights from the Australian Stroke Clinical Registry	4
Development and implementation of an institutional enhanced recovery program data process	4
Congenital anomaly registers in Australia: A national challenge	4
Impact of the ICD-11 on the accuracy of clinical coding in Korea	4

Enhancing nursing home quality through electronic health record implementation	4
Evaluation of Medical Certification of Cause of Death in Tertiary Cancer Hospitals in Northern India	4
The need for health information management professionals in Malawi health facilities	4
Are clinical registries an effective tool for hospital health services to address unwarranted clinical variation?	3
Varicella-zoster-virus-related hospital episodes increasingly coded concurrently for varicella and zoster, Australia, 2002–2021	3
The impact of digital health records systems on workflow and service efficiency in Tanzania: A systematic review and framework development	3
Awareness of, attitudes towards, and practices of health information management professionals in South Korea relating to privacy of personal health information	3
Recognising complexity: Foregrounding vulnerable and diverse populations for inclusive health information management research	3
Impact of data sources and ascertainment methods on reporting paediatric genetic condition prevalence: A scoping review	3
Alpha NSW: What would it take to create a state-wide paediatric population-level learning health system?	3
Researchers’ perceptions of the trustworthiness, for reuse purposes, of government health data in Victoria, Australia: Implications for policy and practice	3
Rare kidney disease registries: A scoping review on characteristics and lessons learnt	3