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https://ahro.austin.org.au/austinjspui/handle/1/31772
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | McMaster, Christopher | - |
dc.contributor.author | Chan, Julia | - |
dc.contributor.author | Liew, David F L | - |
dc.contributor.author | Su, Elizabeth | - |
dc.contributor.author | Frauman, Albert G | - |
dc.contributor.author | Chapman, Wendy W | - |
dc.contributor.author | Pires, Douglas E V | - |
dc.date | 2022 | - |
dc.date.accessioned | 2023-01-12T03:02:32Z | - |
dc.date.available | 2023-01-12T03:02:32Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Journal of Biomedical Informatics 2023; 137 | en_US |
dc.identifier.issn | 1532-0480 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/31772 | - |
dc.description.abstract | The detection of adverse drug reactions (ADRs) is critical to our understanding of the safety and risk-benefit profile of medications. With an incidence that has not changed over the last 30 years, ADRs are a significant source of patient morbidity, responsible for 5%-10% of acute care hospital admissions worldwide. Spontaneous reporting of ADRs has long been the standard method of reporting, however this approach is known to have high rates of under-reporting, a problem that limits pharmacovigilance efforts. Automated ADR reporting presents an alternative pathway to increase reporting rates, although this may be limited by over-reporting of other drug-related adverse events. We developed a deep learning natural language processing algorithm to identify ADRs in discharge summaries at a single academic hospital centre. Our model was developed in two stages: first, a pre-trained model (DeBERTa) was further pre-trained on 1.1 million unlabelled clinical documents; secondly, this model was fine-tuned to detect ADR mentions in a corpus of 861 annotated discharge summaries. This model was compared to a version without the pre-training step, and a previously published RoBERTa model pretrained on MIMIC III, which has demonstrated strong performance on other pharmacovigilance tasks. To ensure that our algorithm could differentiate ADRs from other drug-related adverse events, the annotated corpus was enriched for both validated ADR reports and confounding drug-related adverse events using. The final model demonstrated good performance with a ROC-AUC of 0.955 (95% CI 0.933 - 0.978) for the task of identifying discharge summaries containing ADR mentions, significantly outperforming the two comparator models. | en_US |
dc.language.iso | eng | - |
dc.subject | Adverse drug reactions | en_US |
dc.subject | Machine learning | en_US |
dc.subject | Natural language processing | en_US |
dc.subject | Transfer learning | en_US |
dc.title | Developing a deep learning natural language processing algorithm for automated reporting of adverse drug reactions. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Journal of Biomedical Informatics | en_US |
dc.identifier.affiliation | Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia. | en_US |
dc.identifier.affiliation | Clinical Pharmacology and Therapeutics | en_US |
dc.identifier.affiliation | Rheumatology | en_US |
dc.identifier.affiliation | The Centre for Digital Transformation of Health, University of Melbourne, Melbourne, Victoria, Australia | en_US |
dc.identifier.affiliation | School of Computing and Information Systems, University of Melbourne, Melbourne, Victoria, Australia. | en_US |
dc.identifier.doi | 10.1016/j.jbi.2022.104265 | en_US |
dc.type.content | Text | en_US |
dc.identifier.pubmedid | 36464227 | - |
dc.description.volume | 137 | - |
dc.description.startpage | 104265 | - |
local.name.researcher | Frauman, Albert G | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
crisitem.author.dept | Rheumatology | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
Appears in Collections: | Journal articles |
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