OOIR: Observatory of International Research

Papers

(The median citation count of Health Information Management Journal is 1. 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 2022-06-01 to 2026-06-01.)

Article	Citations
Evaluation of virtual training delivery for health information systems implementation in Canada: A qualitative study	18
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	14
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	10
Developing a code of ethics in health information management	9
Costs of acute hospitalisation for stroke and transient ischaemic attack in Australia	8
Automating cancer registries: Pearls and pitfalls	8
Predictive analytics for early detection of hospital-acquired complications: An artificial intelligence approach	8
Data professionals in healthcare: Who they are and what they do	7
Accuracy of site benchmarking in clinical quality registries of varying size	7
Factors influencing the use of big data within healthcare services: a systematic review	7
Impact of clinical note format on diagnostic accuracy and efficiency	7
The applications of Australian-coded ICD-10 and ICD-10-AM data in research: A scoping review of the literature	7
Medical record-keeping training for undergraduate medical students in pre-clinical years: An experiment for program effectiveness and student satisfaction	6
Health information management professionals’ investigator involvement in research: barriers and facilitators	6
Professional identity and workplace motivation: A case study of health information managers	5
Enhancing nursing home quality through electronic health record implementation	5
System-wide analysis of qualitative hospital incident data: Feasibility of semi-automated content analysis to uncover insights	5
Digitising health history: The creation, function and implementation of the Norwegian Health Archives Registry	5
ICD-11 in Canada: Leveraging crosswalks to evaluate adoption, impact and transition strategies	5
Health information management students’ work-integrated learning (professional practice placements): Where do they go and what do they do?	5
Enhancing registry impact: Translating registry outputs into C onsumer- F riendly I	5
Development and implementation of an institutional enhanced recovery program data process	4
Optimising data quality in a national clinical quality registry: Insights from the Australian Stroke Clinical Registry	4

Evaluation of Medical Certification of Cause of Death in Tertiary Cancer Hospitals in Northern India	4
A scientometric review of health data sharing for secondary use: Insights, frontiers and the path ahead	4
The need for health information management professionals in Malawi health facilities	4
The importance of SNOMED CT concept specificity in healthcare analytics	4
Congenital anomaly registers in Australia: A national challenge	3
The biopsychosocial–spiritual impact on non-clinical health professionals who interact with traumatic and/or sensitive health data: A scoping review	3
Rare kidney disease registries: A scoping review on characteristics and lessons learnt	3
The impact of digital health records systems on workflow and service efficiency in Tanzania: A systematic review and framework development	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
Exploring maturity of electronic medical record use among allied health professionals	2
Digital hospital evaluation scale: A scale-development research study	2
Is source data verification a valid tool to improve data quality of tumour documentation data? A critical assessment	2
Use of family planning information by primary healthcare clinic managers in South Africa	2
Concordance between ICD-10-AM clinical coding and SARS-CoV-2 PCR testing for COVID-19 in Australian hospitals	2
From data collection to downstream data use: Malaysia’s experience with ICD-11	2
Monitoring performance and improving outcomes: characteristics and outputs of Australian clinical registries	2
The Australian and New Zealand Massive Transfusion Registry: An innovation focusing on data collection, standardisation and interoperability between healthcare systems	2
Researchers’ perceptions of the trustworthiness, for reuse purposes, of government health data in Victoria, Australia: Implications for policy and practice	2
Erratum to “A documentary analysis of Victorian Government health information assets’ websites to identify availability of documentation for data sharing and reuse in Australia”	2
Are clinical registries an effective tool for hospital health services to address unwarranted clinical variation?	2
A fiscally sound, evidenced-based solution to conquering the complexity of physician billing guidelines: A physician-centric note template	2
Perceptions of Portuguese medical coders on the transition to ICD-10-CM/PCS: A national survey	2
Performance of ICD-10-AM codes for quality improvement monitoring of hospital-acquired pneumonia in a haematology-oncology casemix in Victoria, Australia	2
Health information manager competency standards and their application to final-year, work-integrated learning (professional practice) project descriptions and learning outcomes	2
Varicella-zoster-virus-related hospital episodes increasingly coded concurrently for varicella and zoster, Australia, 2002–2021	2
Attaining consensus on a core dataset for upper limb lymphoedema using the Delphi method: A foundational step in creating a clinical support system	2
Clinical staff members’ awareness of the security and privacy components of hospital health information governance in Kumasi, Ghana	2
Minimum dataset for the development of the National Haemophilia Registry	2
Defining career success: A cross-sectional analysis of health information managers’ perceptions	2
Comparison of the Victorian emergency minimum dataset (VEMD) human intent coding descriptor to medical records in discriminating suicide attempts for emergency presentations to Eastern Health Psychiat	2
Demystifying environmental health-related diseases: Using ICD codes to facilitate environmental health clinical referrals	1
Rethinking ICD-11 training: Why and how	1
Risk prediction model for early detection of urinary tract infection in a hospital setting in Australia	1
Empowering educators: AI literacy as a catalyst for competency-based health information training	1
Enhancing the quality of medicine handover at hospital discharge: a priority setting workshop	1
Early-career pathways in health information management: A comparison of graduates’ position titles and knowledge-skill domains using two classificatory methodologies	1
ICD-11 “by the people for the people”: The open feedback proposal platform	1
Developing a minimum dataset for smart aged care service platforms in China	1
Digital competencies for health service managers and health service implications for Australia	1
Challenges and successes in implementing an integrated electronic patient record (HIVE) at the Manchester University National Health Service Foundation Trust, England: 1000+ legacy systems, 10 hospita	1
Applying the hospital administrative data quality scoring tool in 15 countries	1
Information system support for case-based knowledge formation in social welfare: a cross-sectional study	1
Workforce survey of Australian health information management graduates, 2017–2021: A 5-year follow-on study	1
Junior doctors’ perspectives on the hospital discharge process: A qualitative study exploring preparation of discharge summaries and medication reconciliation	1
BORN to be validated: Assessing agreement between Ontario’s birth registry and CIHI-DAD	1
Evaluating the use of new and advanced technologies in a population-based cancer registry	1
Attitudes towards data access and sharing health data for research: a case study of Australian data custodian perspectives	1
Regulatory framework for health information systems in Ethiopia: A qualitative document analysis	1
The positive predictive value of ICD-10-AM S06.0~ concussion codes for mild traumatic brain injury	1

Satisfaction and usability of e-referral among physicians and health information management technicians in Muscat Governorate, Oman	1
Clinically meaningful categorisation of ICD-10-AM (Australian modification)	1
Automated data collection in cancer care: State of play among registries in the United Kingdom and Europe	1
For-profit versus non-profit cybersecurity posture: breach types and locations in healthcare organisations	1
Analysis of data items and gaps in Australia’s national mental health services activity and capacity data collections for integrated regional service planning	1
Concordance between coding sources of burn size and depth across Australian and New Zealand specialist burn services	1
Exploration of the role of health information managers in the world of clinical registries	1
The health information management workforce: Looking to the future	1
Localisation of an assessment tool for disease registry software	1
Medical record-keeping educational interventions for medical students and residents: a systematic review	1
System interoperability and data linkage in the era of health information management: A bibliometric analysis	1
Using personal health records for medication continuity during transition of care: An observational study	1
Telepsychiatry readiness assessment at the Department of Psychiatry, Dr. Soeharto Heerdjan Hospital, Indonesia	1