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Pharmaceutical Medicine

, Volume 32, Issue 1, pp 31–37 | Cite as

A Case Study of the Incremental Utility for Disease Identification of Natural Language Processing in Electronic Medical Records

  • Lisa S. WeissEmail author
  • Xiaofeng Zhou
  • Alexander M. Walker
  • Ashwin N. Ananthakrishnan
  • Rongjun Shen
  • Rachel E. Sobel
  • Andrew Bate
  • Robert F. Reynolds
Short Communication
  • 98 Downloads

Abstract

Background

Information exists as unstructured medical text in healthcare databases. Such information is not routinely considered in safety surveillance but typically relies solely on structured (coded) data. Natural language processing (NLP) may allow the capture of concepts from unstructured data and thus enhance safety surveillance capability.

Objectives

We sought to assess the added contribution of unstructured data extracted from medical text by NLP for detecting acute liver dysfunction (ALD) in patients with inflammatory bowel disease (IBD).

Methods

Using a previously developed rule, we evaluated structured and unstructured NLP-extracted terms from a commercially available electronic medical record (EMR) system. The rule was intended to identify ALD diagnosis and timing of onset and was the result of three iterations of rule development using 150 ALD candidate cases. We evaluated the performance of the rule with or without NLP among all candidate cases and among 50 new cases with clinical adjudication.

Results

NLP terms were necessary for the diagnosis of 9% of cases and for ruling out 3% of false-positive cases. Inclusion of NLP terms led to an identification of an additional  9% of ALD-onset dates, with consequent earlier recognition in 5%.

Conclusions

NLP-derived terms in one large commercially available EMR system modestly improved the sensitivity and specificity in the identification of ALD and identified earlier onset.

Notes

Compliance with Ethical Standards

All patient and provider information was provided in the form of non-identifying study code numbers. The work did not require institutional review board approval.

Funding

This work was conducted using Pfizer, Inc., internal funds and under a research contract between Pfizer and World Health Information Science Consultants (AW and AA).

Conflicts of Interest

LSW, XZ, RS, RES, AB and RR are employees and may be shareholders of Pfizer, Inc. AW has worked under contract with Optum, which owns Humedica (whose data resource is being studied). AA has received consulting fees or honoraria for serving on scientific advisory boards for Abbvie, Takeda, and Merck. The views expressed herein are those of the authors and do not necessarily represent those of Pfizer, Inc.

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Copyright information

© Springer International Publishing AG, part of Springer Nature 2017

Authors and Affiliations

  • Lisa S. Weiss
    • 1
    Email author
  • Xiaofeng Zhou
    • 1
  • Alexander M. Walker
    • 2
  • Ashwin N. Ananthakrishnan
    • 3
  • Rongjun Shen
    • 1
  • Rachel E. Sobel
    • 1
  • Andrew Bate
    • 1
  • Robert F. Reynolds
    • 1
  1. 1.Epidemiology, Research and Development, Worldwide Safety and RegulatoryPfizerNew YorkUSA
  2. 2.WHISCONNewtonUSA
  3. 3.Division of Gastroenterology, Crohn’s and Colitis CenterMassachusetts General HospitalBostonUSA

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