Patient Centered Identification, Attribution and Ranking of Adverse Drug Events

被引:3
|
作者
Banerjee, Ritwik [1 ]
Ramakrishnan, I. V. [1 ]
Henry, Mark [2 ]
Perciavalle, Matthew [2 ]
机构
[1] SUNY Stony Brook, Comp Sci, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Sch Med, Stony Brook, NY 11794 USA
来源
2015 IEEE INTERNATIONAL CONFERENCE ON HEALTHCARE INFORMATICS (ICHI 2015) | 2015年
基金
美国国家科学基金会;
关键词
ELECTRONIC HEALTH RECORDS; PHYSICIAN ORDER ENTRY; EMERGENCY-DEPARTMENT; TEXT CLASSIFICATION; DECISION-SUPPORT; TRIGGER TOOL; MEDICATION; ALERTS; SAFETY; INFORMATION;
D O I
10.1109/ICHI.2015.8
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Adverse drug events (ADEs) trigger a high number of hospital emergency room (ER) visits. Information about ADEs is often available in online drug databases in the form of narrative texts, and serves as the physician's primary reference point for ADE attribution and diagnosis. Manually reviewing these narratives, however, is an error prone and time consuming process, especially due to the prevalence of polypharmacy. So ER health care providers, especially given the heavy volume of traffic in ERs, often either skip this step or at best do it rather perfunctorily. This causes ADEs to be missed or misdiagnosed, often leading to extensive and unnecessary testing and treatment, including hospitalization. In this paper, we present a system that automates the detection of ADEs and provides a list of suspect drugs, ranked by their likelihood of causing the patient's complaints and symptoms. The input data, i.e., medications and complaints, are obtained from triage notes that often contain descriptive language. Our application utilizes heterogeneous information sources (including drug databases) to refine and transform these descriptions as well as the online database narratives using a natural language processing (NLP) pipeline. We then employ ranking measures to establish correspondence between the complaints and the medications. Our preliminary evaluation based on actual ER cases demonstrates that this system achieves high precision and recall.
引用
收藏
页码:18 / 27
页数:10
相关论文
共 50 条
  • [1] Patient stratification and identification of adverse event correlations in the space of 1190 drug related adverse events
    Roitmann, Eva
    Eriksson, Robert
    Brunak, Soren
    FRONTIERS IN PHYSIOLOGY, 2014, 5
  • [2] Identification of Adverse Drug Events in Chinese Clinical Narrative Text
    Ge, Caixia
    Zhang, Yinsheng
    Duan, Huilong
    Li, Haomin
    UBIQUITOUS COMPUTING APPLICATION AND WIRELESS SENSOR, 2015, 331 : 605 - 612
  • [3] Analysis of adverse drug events as a way to improve cancer patient care
    Vicente-Oliveros, Noelia
    Gramage-Caro, Teresa
    Corral de la Fuente, Elena
    Delgado-Silveira, Eva
    Maria Alvarez-Diaz, Ana
    EUROPEAN JOURNAL OF HOSPITAL PHARMACY, 2024, 31 (01) : 27 - 30
  • [4] SEMI-AUTOMATED IDENTIFICATION OF POTENTIAL ADVERSE DRUG EVENTS
    Ploessnig, M.
    Schuler, J.
    Hansbauer, B.
    Stroka, S.
    Engel, T.
    Hofer-Dueckelmann, C.
    Radulescu, M.
    Adlassnig, K-P
    EHEALTH2012 - HEALTH INFORMATICS MEETS EHEALTH - VON DER WISSENSCHAFT ZUR ANWENDUNG UND ZURUCK: MOBILE HEALTH & CARE - GESUNDHEITSVORSORGE IMMER UND UBERALL, 2012, : 51 - 56
  • [5] A Clustering Framework for Patient Phenotyping with Application to Adverse Drug Events
    Bampa, Maria
    Papapetrou, Panagiotis
    Hollmen, Jaakko
    2020 IEEE 33RD INTERNATIONAL SYMPOSIUM ON COMPUTER-BASED MEDICAL SYSTEMS(CBMS 2020), 2020, : 177 - 182
  • [6] Dictionary construction and identification of possible adverse drug events in Danish clinical narrative text
    Eriksson, Robert
    Jensen, Peter Bjodstrup
    Frankild, Sune
    Jensen, Lars Juhl
    Brunak, Soren
    JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, 2013, 20 (05) : 947 - 953
  • [7] Data Mining to Generate Adverse Drug Events Detection Rules
    Chazard, Emmanuel
    Ficheur, Gregoire
    Bernonville, Stephanie
    Luyckx, Michel
    Beuscart, Regis
    IEEE TRANSACTIONS ON INFORMATION TECHNOLOGY IN BIOMEDICINE, 2011, 15 (06): : 823 - 830
  • [8] Improving attribution of adverse events in oncology clinical trials
    George, Goldy C.
    Barata, Pedro C.
    Campbell, Alicyn
    Chen, Alice
    Cortes, Jorge E.
    Hyman, David M.
    Jones, Lee
    Karagiannis, Thomas
    Klaar, Sigrid
    Le-Rademacher, Jennifer G.
    LoRusso, Patricia
    Mandrekar, Sumithra J.
    Merino, Diana M.
    Minasian, Lori M.
    Mitchell, Sandra A.
    Montez, Sandra
    O'Connor, Daniel J.
    Pettit, Syril
    Silk, Elaine
    Sloan, Jeff A.
    Stewart, Mark
    Takimoto, Chris H.
    Wong, Gilbert Y.
    Yap, Timothy A.
    Cleeland, Charles S.
    Hong, David S.
    CANCER TREATMENT REVIEWS, 2019, 76 : 33 - 40
  • [9] Electronic health records and adverse drug events after patient transfer
    Boockvar, K. S.
    Livote, E. E.
    Goldstein, N.
    Nebeker, J. R.
    Siu, A.
    Fried, T.
    QUALITY & SAFETY IN HEALTH CARE, 2010, 19 (05):
  • [10] Using technology to prevent adverse drug events in the intensive care unit
    Hassan, Erkan
    Badawi, Omar
    Weber, Robert J.
    Cohen, Henry
    CRITICAL CARE MEDICINE, 2010, 38 : S97 - S105