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Characterizing treatment pathways at scale using the OHDSI network
DC Field | Value | Language |
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dc.contributor.author | Hripcsak, G | - |
dc.contributor.author | Ryan, PB | - |
dc.contributor.author | Duke, JD | - |
dc.contributor.author | Shah, NH | - |
dc.contributor.author | Park, RW | - |
dc.contributor.author | Huser, V | - |
dc.contributor.author | Suchard, MA | - |
dc.contributor.author | Schuemie, MJ | - |
dc.contributor.author | DeFalco, FJ | - |
dc.contributor.author | Perotte, A | - |
dc.contributor.author | Banda, JM | - |
dc.contributor.author | Reich, CG | - |
dc.contributor.author | Schilling, LM | - |
dc.contributor.author | Matheny, ME | - |
dc.contributor.author | Meeker, D | - |
dc.contributor.author | Pratt, N | - |
dc.contributor.author | Madigan, D | - |
dc.date.accessioned | 2018-05-04T00:24:05Z | - |
dc.date.available | 2018-05-04T00:24:05Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 0027-8424 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/14800 | - |
dc.description.abstract | Observational research promises to complement experimental research by providing large, diverse populations that would be infeasible for an experiment. Observational research can test its own clinical hypotheses, and observational studies also can contribute to the design of experiments and inform the generalizability of experimental research. Understanding the diversity of populations and the variance in care is one component. In this study, the Observational Health Data Sciences and Informatics (OHDSI) collaboration created an international data network with 11 data sources from four countries, including electronic health records and administrative claims data on 250 million patients. All data were mapped to common data standards, patient privacy was maintained by using a distributed model, and results were aggregated centrally. Treatment pathways were elucidated for type 2 diabetes mellitus, hypertension, and depression. The pathways revealed that the world is moving toward more consistent therapy over time across diseases and across locations, but significant heterogeneity remains among sources, pointing to challenges in generalizing clinical trial results. Diabetes favored a single first-line medication, metformin, to a much greater extent than hypertension or depression. About 10% of diabetes and depression patients and almost 25% of hypertension patients followed a treatment pathway that was unique within the cohort. Aside from factors such as sample size and underlying population (academic medical center versus general population), electronic health records data and administrative claims data revealed similar results. Large-scale international observational research is feasible. | - |
dc.language.iso | en | - |
dc.subject.MESH | Antidepressive Agents | - |
dc.subject.MESH | Antihypertensive Agents | - |
dc.subject.MESH | Databases, Factual | - |
dc.subject.MESH | Depression | - |
dc.subject.MESH | Diabetes Mellitus, Type 2 | - |
dc.subject.MESH | Electronic Health Records | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hypertension | - |
dc.subject.MESH | Hypoglycemic Agents | - |
dc.subject.MESH | Internationality | - |
dc.subject.MESH | Medical Informatics | - |
dc.subject.MESH | Practice Patterns, Physicians' | - |
dc.title | Characterizing treatment pathways at scale using the OHDSI network | - |
dc.type | Article | - |
dc.identifier.pmid | 27274072 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941483/ | - |
dc.contributor.affiliatedAuthor | 박, 래웅 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1073/pnas.1510502113 | - |
dc.citation.title | Proceedings of the National Academy of Sciences of the United States of America | - |
dc.citation.volume | 113 | - |
dc.citation.number | 27 | - |
dc.citation.date | 2016 | - |
dc.citation.startPage | 7329 | - |
dc.citation.endPage | 7336 | - |
dc.identifier.bibliographicCitation | Proceedings of the National Academy of Sciences of the United States of America, 113(27). : 7329-7336, 2016 | - |
dc.identifier.eissn | 1091-6490 | - |
dc.relation.journalid | J000278424 | - |
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