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Pharmacoepidemiol Drug Saf ; 28(10): 1309-1317, 2019 10.
Article in English | MEDLINE | ID: mdl-31392844

ABSTRACT

PURPOSE: Adverse event (AE) identification in social media (SM) can be performed using various types of natural language processing (NLP) and machine learning (ML). These methods can be categorized by complexity and precision level. Co-occurrence-based ML methods are rather basic, as they identify simultaneous appearance of drugs and clinical events in a single post. In contrast, statistical learning methods involve more complex NLP and identify drugs, events, and associations between them. We aimed to compare the ability of co-occurrence and NLP to identify AEs and signals of disproportionate reporting (SDR) in patient-generated SM. We also examined the performance of lift in SM-based signal detection (SD). METHODS: Our examination was performed in a corpus of SM posts crawled from open online patient forums and communities, using the spontaneously reported VigiBase data as reference data set. RESULTS: We found that co-occurrence and NLP produce AEs, which are 57% and 93% consistent with VigiBase AEs, respectively. Among the SDRs identified both in SM and in VigiBase, up to 55.3% were identified earlier in co-occurrence, and up to 32.1% were identified earlier in NLP-processed SM. Using lift in SM SD provided performance similar to frequentist methods, both in co-occurrence and in NLP-processed AEs. CONCLUSION: Our results indicate that using SM as a data source complementary to traditional pharmacovigilance sources should be considered further. Various levels of SM processing may be considered, depending on the preferred policies and tolerance for false-positive to false-negative balance in routine pharmacovigilance processes.


Subject(s)
Data Collection/methods , Drug-Related Side Effects and Adverse Reactions/epidemiology , Natural Language Processing , Pharmacovigilance , Social Media/statistics & numerical data , Adverse Drug Reaction Reporting Systems/statistics & numerical data , Datasets as Topic , Drug-Related Side Effects and Adverse Reactions/diagnosis , False Negative Reactions , False Positive Reactions , Feasibility Studies , Retrospective Studies , Sensitivity and Specificity
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