Accuracy of using automated methods for detecting adverse events from electronic health record data: a research protocol

被引:17
|
作者
Rochefort, Christian M. [1 ,2 ,3 ]
Buckeridge, David L. [2 ,3 ]
Forster, Alan J. [4 ,5 ]
机构
[1] McGill Univ, Fac Med, Ingram Sch Nursing, Montreal, PQ H3A 2A7, Canada
[2] McGill Univ, McGill Clin & Hlth Informat Res Grp, Montreal, PQ H3A 1A3, Canada
[3] McGill Univ, Fac Med, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ H3A 1A2, Canada
[4] Ottawa Hosp, Res Inst, Ottawa, ON, Canada
[5] Ottawa Hosp, Ottawa, ON K1Y 4E9, Canada
来源
IMPLEMENTATION SCIENCE | 2015年 / 10卷
基金
加拿大健康研究院;
关键词
Adverse events; Electronic health record; Acute care hospital; Automated detection; Natural language processing; Patient safety; Data warehouse; HOSPITAL-ACQUIRED PNEUMONIA; BLOOD-STREAM INFECTION; SURVEILLANCE; CARE; INDICATORS; QUALITY; FALLS; PREVENTION; GUIDELINES; VALIDITY;
D O I
10.1186/s13012-014-0197-6
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Adverse events are associated with significant morbidity, mortality and cost in hospitalized patients. Measuring adverse events is necessary for quality improvement, but current detection methods are inaccurate, untimely and expensive. The advent of electronic health records and the development of automated methods for encoding and classifying electronic narrative data, such as natural language processing, offer an opportunity to identify potentially better methods. The objective of this study is to determine the accuracy of using automated methods for detecting three highly prevalent adverse events: a) hospital-acquired pneumonia, b) catheter-associated bloodstream infections, and c) in-hospital falls. Methods/design: This validation study will be conducted at two large Canadian academic health centres: the McGill University Health Centre (MUHC) and The Ottawa Hospital (TOH). The study population consists of all medical, surgical and intensive care unit patients admitted to these centres between 2008 and 2014. An automated detection algorithm will be developed and validated for each of the three adverse events using electronic data extracted from multiple clinical databases. A random sample of MUHC patients will be used to develop the automated detection algorithms (cohort 1, development set). The accuracy of these algorithms will be assessed using chart review as the reference standard. Then, receiver operating characteristic curves will be used to identify optimal cut points for each of the data sources. Multivariate logistic regression and the areas under curve (AUC) will be used to identify the optimal combination of data sources that maximize the accuracy of adverse event detection. The most accurate algorithms will then be validated on a second random sample of MUHC patients (cohort 1, validation set), and accuracy will be measured using chart review as the reference standard. The most accurate algorithms validated at the MUHC will then be applied to TOH data (cohort 2), and their accuracy will be assessed using a reference standard assessment of the medical chart. Discussion: There is a need for more accurate, timely and efficient measures of adverse events in acute care hospitals. This is a critical requirement for evaluating the effectiveness of preventive interventions and for tracking progress in patient safety through time.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Accuracy of using automated methods for detecting adverse events from electronic health record data: a research protocol
    Christian M Rochefort
    David L Buckeridge
    Alan J Forster
    Implementation Science, 10
  • [2] Accuracy and generalizability of using automated methods for identifying adverse events from electronic health record data: a validation study protocol
    Christian M. Rochefort
    David L. Buckeridge
    Andréanne Tanguay
    Alain Biron
    Frédérick D’Aragon
    Shengrui Wang
    Benoit Gallix
    Louis Valiquette
    Li-Anne Audet
    Todd C. Lee
    Dev Jayaraman
    Bruno Petrucci
    Patricia Lefebvre
    BMC Health Services Research, 17
  • [3] Accuracy and generalizability of using automated methods for identifying adverse events from electronic health record data: a validation study protocol
    Rochefort, Christian M.
    Buckeridge, David L.
    Tanguay, Andreanne
    Biron, Alain
    D'Aragon, Frederick
    Wang, Shengrui
    Gallix, Benoit
    Valiquette, Louis
    Audet, Li-Anne
    Lee, Todd C.
    Jayaraman, Dev
    Petrucci, Bruno
    Lefebvre, Patricia
    BMC HEALTH SERVICES RESEARCH, 2017, 17
  • [4] Feasibility of Electronic Health Record-Based Triggers in Detecting Dental Adverse Events
    Kalenderian, Elsbeth
    Obadan-Udoh, Enihomo
    Yansane, Alfa
    Kent, Karla
    Hebballi, Nutan B.
    Delattre, Veronique
    Kookal, Krisna Kumar
    Tokede, Oluwabunmi
    White, Joel
    Walji, Muhammad F.
    APPLIED CLINICAL INFORMATICS, 2018, 9 (03): : 646 - 653
  • [5] Detection of Pharmacovigilance-Related Adverse Events Using Electronic Health Records and Automated Methods
    Haerian, K.
    Varn, D.
    Vaidya, S.
    Ena, L.
    Chase, H. S.
    Friedman, C.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2012, 92 (02) : 228 - 234
  • [6] Using electronic medical record data to report laboratory adverse events
    Miller, Tamara P.
    Li, Yimei
    Getz, Kelly D.
    Dudley, Jesse
    Burrows, Evanette
    Pennington, Jeffrey
    Ibrahimova, Azada
    Fisher, Brian T.
    Bagatell, Rochelle
    Seif, Alix E.
    Grundmeier, Robert
    Aplenc, Richard
    BRITISH JOURNAL OF HAEMATOLOGY, 2017, 177 (02) : 283 - 286
  • [7] Methods for Detecting Pediatric Adverse Drug Reactions From the Electronic Medical Record
    Joyner, Lydia M.
    Alicea, Leah A.
    Goldman, Jennifer L.
    Suppes, Sarah L.
    Tillman, Emma M.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2021, 61 (11): : 1479 - 1484
  • [8] Novel Methods of Adverse Event Detection Using Electronic Health Record Data: A Critical Review of the Literature
    Rochefort, Christian M.
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2014, 23 : 126 - 126
  • [9] Data Mining on Large Health Record Databases for Detecting Adverse Reactions: Which Events to Monitor?
    Trifiro, G.
    Pariente, A.
    Polimeni, G.
    Miremont-Salame, G.
    Catania, M. A.
    Salvo, F.
    David, A.
    Moore, N.
    Caputi, A. P.
    Sturkenboom, M.
    van der Lei, J.
    Fourrier-Reglat, A.
    DRUG SAFETY, 2008, 31 (10) : 904 - 904
  • [10] Data Mining on Large Health Record Databases for Detecting Adverse Reactions: Which Events to Monitor?
    G. Trifiro’
    A. Pariente
    G. Polimeni
    G. Miremont-Salame’
    M. A. Catania
    F. Salvo
    A. David
    N. Moore
    A. P. Caputi
    M. Sturkenboom
    J. van der Lei
    A. Fourrier-Reglat
    Drug Safety, 2008, 31 : 885 - 885