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 2021-10-01 to 2025-10-01.)

Article	Citations
Procedure-level data linkage to drive improvement in case ascertainment for the Australian Breast Device Registry	17
Evaluation of virtual training delivery for health information systems implementation in Canada: A qualitative study	12
Digital health care and data work: Who are the data professionals?	11
Comparison of comorbidities of stroke collected in administrative data, surveys, clinical trials and cohort studies	11
IPPASOS: The first digital forensic information system in Greece	9
Predictive analytics for early detection of hospital-acquired complications: An artificial intelligence approach	8
Costs of acute hospitalisation for stroke and transient ischaemic attack in Australia	7
Developing a code of ethics in health information management	7
Accuracy of site benchmarking in clinical quality registries of varying size	6
Medical record-keeping training for undergraduate medical students in pre-clinical years: An experiment for program effectiveness and student satisfaction	6
Factors influencing the use of big data within healthcare services: a systematic review	6
Impact of clinical note format on diagnostic accuracy and efficiency	6
The applications of Australian-coded ICD-10 and ICD-10-AM data in research: A scoping review of the literature	6
Health information management students’ work-integrated learning (professional practice placements): Where do they go and what do they do?	5
Professional identity and workplace motivation: A case study of health information managers	5
System-wide analysis of qualitative hospital incident data: Feasibility of semi-automated content analysis to uncover insights	5
Optimising data quality in a national clinical quality registry: Insights from the Australian Stroke Clinical Registry	5
Health information management professionals’ investigator involvement in research: barriers and facilitators	5
Enhancing registry impact: Translating registry outputs into C onsumer- F riendly I nformation (CoFI projec	5
The importance of SNOMED CT concept specificity in healthcare analytics	4
The need for health information management professionals in Malawi health facilities	4
Congenital anomaly registers in Australia: A national challenge	4
Development and implementation of an institutional enhanced recovery program data process	4
Impact of the ICD-11 on the accuracy of clinical coding in Korea	4
Evaluation of Medical Certification of Cause of Death in Tertiary Cancer Hospitals in Northern India	4

Enhancing nursing home quality through electronic health record implementation	4
The biopsychosocial–spiritual impact on non-clinical health professionals who interact with traumatic and/or sensitive health data: A scoping review	4
Impact of data sources and ascertainment methods on reporting paediatric genetic condition prevalence: A scoping review	4
Researchers’ perceptions of the trustworthiness, for reuse purposes, of government health data in Victoria, Australia: Implications for policy and practice	3
Alpha NSW: What would it take to create a state-wide paediatric population-level learning health system?	3
The impact of digital health records systems on workflow and service efficiency in Tanzania: A systematic review and framework development	3
Digital hospital evaluation scale: A scale-development research study	3
Recognising complexity: Foregrounding vulnerable and diverse populations for inclusive health information management research	3
Are clinical registries an effective tool for hospital health services to address unwarranted clinical variation?	3
Rare kidney disease registries: A scoping review on characteristics and lessons learnt	3