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1.
Healthcare (Basel) ; 12(3)2024 Jan 23.
Article in English | MEDLINE | ID: mdl-38338175

ABSTRACT

OBJECTIVE: In the age of digital transformation, there is a need for a sustainable information management vision in health. Understanding the accumulation of health information management (HIM) knowledge from the past to the present and building a new vision to meet this need reveals the importance of understanding the available scientific knowledge. With this research, it is aimed to examine the scientific documents of the last 40 years of HIM literature with a holistic approach using science mapping techniques and to guide future research. METHODS: This study used a bibliometric analysis method for science mapping. Co-citation and co-occurrence document analyses were performed on 630 academic publications selected from the Web of Science core collection (WoSCC) database using the keyword "Health Information Management" and inclusion criteria. The analyses were performed using the R-based software Bibliometrix (Version 4.0; K-Synth Srl), Python (Version 3.12.1; The Python Software Foundation), and Microsoft® Excel® 2016. RESULTS: Co-occurrence analyses revealed the themes of personal health records, clinical coding and data quality, and health information management. The HIM theme consisted of five subthemes: "electronic records", "medical informatics", "e-health and telemedicine", "health education and awareness", and "health information systems (HISs)". As a result of the co-citation analysis, the prominent themes were technology acceptance, standardized clinical coding, the success of HISs, types of electronic records, people with HIM, health informatics used by consumers, e-health, e-mobile health technologies, and countries' frameworks and standards for HISs. CONCLUSIONS: This comprehensive bibliometric study shows that structured information can be helpful in understanding research trends in HIM. This study identified critical issues in HIM, identified meaningful themes, and explained the topic from a holistic perspective for all health system actors and stakeholders who want to work in the field of HIM.

2.
Int J Risk Saf Med ; 27(1): 11-21, 2015.
Article in English | MEDLINE | ID: mdl-25766063

ABSTRACT

BACKGROUND: The goal of this study was to measure an adverse event rate and determine the potential usefulness of the Institute for Healthcare Improvement's Global Trigger Tool (GTT). Besides using the GTT to measure the adverse event rate, a comparison was also made with the internal Voluntary Reporting Notification System (VRNS) to identify and compare the strengths and weaknesses of the two approaches. METHOD: Retrospective data were collected from reported patient safety incidents covering a one-year period at Duzce University Hospital, Turkey. Using a range of selection criteria, a total of 219 patient records were selected and then reviewed by a trained GTT team, to investigate the positive triggers in the content of the patient records. RESULTS: It was determined that adverse events per 1000 patient days totalled 80.72. Adverse events per 100 admissions were 29.39, and the rate of admissions with adverse events was 16.67%. The comparison between the GTT and the VRNS showed that the GTT is 19 times more sensitive than the VRNS in the adverse event evaluation process. CONCLUSION: This is the first published study of the rate of adverse events in a Turkish healthcare setting using the GTT. It was found that the GTT was applicable in this setting, yielding more accurate measurement of the adverse event rate. However, the content of the GTT should be adjusted regarding the standards and documentations used in the Turkish healthcare system to be more useful.


Subject(s)
Patient Safety , Quality Indicators, Health Care/organization & administration , Safety Management/organization & administration , Adolescent , Adult , Aged , Aged, 80 and over , Female , Hospital Administration , Humans , Male , Medical Errors/prevention & control , Middle Aged , Quality Indicators, Health Care/classification , Retrospective Studies , Turkey , Young Adult
3.
Brain Dev ; 26(2): 137-8, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15036435

ABSTRACT

Congenital factor X deficiency is a rare autosomal recessive disorder that usually presents with variable bleeding tendency, prolonged prothrombin time and partial thromboplastin time. Therefore, it may be misdiagnosed as hemorrhagic disease of the newborn. Factor X level should be investigated for the definite diagnosis. We first report a new family whose two infants presented with severe intracranial bleeding at different times and were found to have congenital factor X deficiency. Plasma replacement therapy was not found to be efficacious in these infants. In conclusion, a possible factor X deficiency should be considered when a newborn presents with intracranial bleeding.


Subject(s)
Diagnostic Errors/prevention & control , Factor X Deficiency/complications , Factor X Deficiency/diagnosis , Intracranial Hemorrhages/diagnosis , Intracranial Hemorrhages/etiology , Brain/diagnostic imaging , Brain/pathology , Brain/physiopathology , Brain Edema/diagnostic imaging , Brain Edema/etiology , Brain Edema/pathology , Factor X/metabolism , Factor X Deficiency/congenital , Fatal Outcome , Female , Humans , Infant , Infant, Newborn , Intracranial Hemorrhages/physiopathology , Male , Plasma Exchange , Siblings , Tomography, X-Ray Computed , Treatment Failure
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