E. Segundo, M. Far, C.I. Rodríguez-Casado, J.M. Elorza, J. Carrere-Molina, R. Mallol-Parera, M. Aragón
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引用次数: 0
Abstract
Background
Large-scale clinical databases containing routinely collected electronic health records (EHRs) data are a valuable source of information for research studies. For example, they can be used in pharmacoepidemiology studies to evaluate the effects of maternal medication exposure on neonatal and pediatric outcomes. Yet, this type of studies is infeasible without proper mother–child linkage.
Methods
We leveraged all eligible active records (N = 8,553,321) of the Information System for Research in Primary Care (SIDIAP) database. Mothers and infants were linked using a deterministic approach and linkage accuracy was evaluated in terms of the number of records from candidate mothers that failed to link. We validated the mother–child links identified by comparison of linked and unlinked records for both candidate mothers and descendants. Differences across these two groups were evaluated by means of effect size calculations instead of p-values. Overall, we described our data linkage process following the GUidance for Information about Linking Data sets (GUILD) principles.
Results
We were able to identify 744,763 unique mother–child relationships, linking 83.8 % candidate mothers with delivery dates within a period of 15 years. Of note, we provide a record-level category label used to derive a global confidence metric for the presented linkage process. Our validation analysis showed that the two groups were similar in terms of a number of aggregated attributes.
Conclusions
Complementing the SIDIAP database with mother–child links will allow clinical researchers to expand their epidemiologic studies with the ultimate goal of improving outcomes for pregnant women and their children. Importantly, the reported information at each step of the data linkage process will contribute to the validity of analyses and interpretation of results in future studies using this resource.
期刊介绍:
The Journal of Biomedical Informatics reflects a commitment to high-quality original research papers, reviews, and commentaries in the area of biomedical informatics methodology. Although we publish articles motivated by applications in the biomedical sciences (for example, clinical medicine, health care, population health, and translational bioinformatics), the journal emphasizes reports of new methodologies and techniques that have general applicability and that form the basis for the evolving science of biomedical informatics. Articles on medical devices; evaluations of implemented systems (including clinical trials of information technologies); or papers that provide insight into a biological process, a specific disease, or treatment options would generally be more suitable for publication in other venues. Papers on applications of signal processing and image analysis are often more suitable for biomedical engineering journals or other informatics journals, although we do publish papers that emphasize the information management and knowledge representation/modeling issues that arise in the storage and use of biological signals and images. System descriptions are welcome if they illustrate and substantiate the underlying methodology that is the principal focus of the report and an effort is made to address the generalizability and/or range of application of that methodology. Note also that, given the international nature of JBI, papers that deal with specific languages other than English, or with country-specific health systems or approaches, are acceptable for JBI only if they offer generalizable lessons that are relevant to the broad JBI readership, regardless of their country, language, culture, or health system.