Literature DB >> 34476768

Leveraging Case Narratives to Enhance Patient Age Ascertainment from Adverse Event Reports.

Phuong Pham1,2, Carmen Cheng3, Eileen Wu2, Ivone Kim2, Rongmei Zhang4, Yong Ma4, Cindy M Kortepeter2, Monica A Muñoz1,2.   

Abstract

INTRODUCTION: Missing age presents a significant challenge when evaluating individual case safety reports (ICSRs) in the FDA Adverse Event Reporting System (FAERS). When age is missing in an ICSR's structured field, it may be in the report's free-text narrative.
OBJECTIVES: This study aimed to evaluate the performance and assess the potential impact of a rule-based natural language processing (NLP) tool that utilizes a text string search to identify patients' numerical age from unstructured narratives.
METHODS: Using FAERS ICSRs from 2002 to 2018, we evaluated the annual proportion of ICSRs with age missing in the structured field before and after NLP application. Reviewers manually identified patients' age from ICSR narratives (gold standard) from a random sample of 1500 ICSRs. The gold standard was compared to the NLP-identified age.
RESULTS: During the study period, the percentage of ICSRs missing age in the structured field increased from 21.9 to 43.8%. The NLP tool performed well among the random sample: sensitivity 98.5%, specificity 92.9%, positive predictive value (PPV) 94.9%, and F-measure 96.7%. It also performed well for the subset of ICSRs missing age in the structured field; when applied to these cases, NLP identified age for an additional one million ICSRs (10% of the total number of ICSRs from 2002 to 2018) and decreased the percentage of ICSRs missing age to 27% overall.
CONCLUSIONS: NLP has potential utility to extract patients' age from ICSR narratives. Use of this tool would enhance pharmacovigilance and research using FAERS data.
© 2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

Entities:  

Mesh:

Year:  2021        PMID: 34476768      PMCID: PMC9136956          DOI: 10.1007/s40290-021-00398-5

Source DB:  PubMed          Journal:  Pharmaceut Med        ISSN: 1178-2595


  13 in total

1.  Completeness of serious adverse drug event reports received by the US Food and Drug Administration in 2014.

Authors:  Thomas J Moore; Curt D Furberg; Donald R Mattison; Michael R Cohen
Journal:  Pharmacoepidemiol Drug Saf       Date:  2016-02-10       Impact factor: 2.890

2.  An Evaluation of Postmarketing Reports with an Outcome of Death in the US FDA Adverse Event Reporting System.

Authors:  Kathryn Marwitz; S Christopher Jones; Cindy M Kortepeter; Gerald J Dal Pan; Monica A Muñoz
Journal:  Drug Saf       Date:  2020-05       Impact factor: 5.606

Review 3.  Use of data mining at the Food and Drug Administration.

Authors:  Hesha J Duggirala; Joseph M Tonning; Ella Smith; Roselie A Bright; John D Baker; Robert Ball; Carlos Bell; Susan J Bright-Ponte; Taxiarchis Botsis; Khaled Bouri; Marc Boyer; Keith Burkhart; G Steven Condrey; James J Chen; Stuart Chirtel; Ross W Filice; Henry Francis; Hongying Jiang; Jonathan Levine; David Martin; Taiye Oladipo; Rene O'Neill; Lee Anne M Palmer; Antonio Paredes; George Rochester; Deborah Sholtes; Ana Szarfman; Hui-Lee Wong; Zhiheng Xu; Taha Kass-Hout
Journal:  J Am Med Inform Assoc       Date:  2015-07-23       Impact factor: 4.497

Review 4.  Natural Language Processing and Its Implications for the Future of Medication Safety: A Narrative Review of Recent Advances and Challenges.

Authors:  Adrian Wong; Joseph M Plasek; Steven P Montecalvo; Li Zhou
Journal:  Pharmacotherapy       Date:  2018-07-22       Impact factor: 4.705

5.  Evaluation of Postmarketing Reports from Industry-Sponsored Programs in Drug Safety Surveillance.

Authors:  Lisa Harinstein; Dipti Kalra; Cindy M Kortepeter; Monica A Muñoz; Eileen Wu; Gerald J Dal Pan
Journal:  Drug Saf       Date:  2019-05       Impact factor: 5.606

6.  Industry Assessment of the Contribution of Patient Support Programs, Market Research Programs, and Social Media to Patient Safety.

Authors:  Jeremy Jokinen; Dominique Bertin; Bruce Donzanti; Janet Hormbrey; Valerie Simmons; Hal Li; Charles Dharmani; Karolyn Kracht; Thomas S Hilzinger; Peter Verdru
Journal:  Ther Innov Regul Sci       Date:  2019-11-04       Impact factor: 1.778

Review 7.  Natural language processing systems for capturing and standardizing unstructured clinical information: A systematic review.

Authors:  Kory Kreimeyer; Matthew Foster; Abhishek Pandey; Nina Arya; Gwendolyn Halford; Sandra F Jones; Richard Forshee; Mark Walderhaug; Taxiarchis Botsis
Journal:  J Biomed Inform       Date:  2017-07-17       Impact factor: 6.317

8.  Trends in Off-Label Drug Use in Ambulatory Settings: 2006-2015.

Authors:  Divya Hoon; Matthew T Taylor; Pooja Kapadia; Tobias Gerhard; Brian L Strom; Daniel B Horton
Journal:  Pediatrics       Date:  2019-09-16       Impact factor: 7.124

9.  Pediatric drug surveillance and the Food and Drug Administration's adverse event reporting system: an overview of reports, 2003-2007.

Authors:  Rosemary Johann-Liang; Jo Wyeth; Min Chen; Judith U Cope
Journal:  Pharmacoepidemiol Drug Saf       Date:  2009-01       Impact factor: 2.890

10.  vigiGrade: a tool to identify well-documented individual case reports and highlight systematic data quality issues.

Authors:  Tomas Bergvall; G Niklas Norén; Marie Lindquist
Journal:  Drug Saf       Date:  2014-01       Impact factor: 5.606

View more
  1 in total

1.  Challenges and opportunities for mining adverse drug reactions: perspectives from pharma, regulatory agencies, healthcare providers and consumers.

Authors:  Graciela Gonzalez-Hernandez; Martin Krallinger; Monica Muñoz; Raul Rodriguez-Esteban; Özlem Uzuner; Lynette Hirschman
Journal:  Database (Oxford)       Date:  2022-09-02       Impact factor: 4.462

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.