Literature DB >> 21418535

Assessment of electronic health information system use and need in US adult congenital heart disease centers.

Joseph B Weiss1, Andrew Grant, Ariane Marelli, Paul Khairy, Tony Maurais, Silven Rehel, Philippe Chetaille, Craig S Broberg.   

Abstract

OBJECTIVES: Efforts to improve care for adult congenital heart disease (ACHD) patients necessitates collection of accurate, detailed, longitudinal data. We sought to document what electronic health record systems are currently available at ACHD centers and to assess national interest in a uniform ACHD-focused system.
DESIGN: Directors of ACHD centers in the United States were invited to complete an online questionnaire regarding current health information systems at their institution both for general cardiology and for ACHD. Topics that were surveyed included utility and perceived limitations of currently available systems. The survey also assessed the level of interest in an ACHD-specific system, and its optimal functions.
RESULTS: Thirty-four centers responded, representing both pediatric and adult institutions that care for patients with ACHD. Of these, 80% reported using a variety of commercially supported electronic medical record products, whereas only 50% employed an ACHD-specific noncommercial database to supplement their institutional system. Comparison of the two systems revealed that most clinical activities are pursued through the institutional electronic medical record system. Research and tracking of clinical activities were the primary uses of ACHD-specific systems, which have several noted limitations. Strong interest in an integrated ACHD-specific system was found among responders.
CONCLUSIONS: There is both an unmet need and a strong interest in an ACHD-oriented electronic health record that could facilitate research, outcome tracking, quality assurance, and inter-institutional collaboration, all functions that are lacking in electronic health systems currently in use.
© 2011 Copyright the Authors. Congenital Heart Disease © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21418535     DOI: 10.1111/j.1747-0803.2011.00498.x

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  3 in total

1.  The TRIVIA Cohort for Surgical Management of Tetralogy of Fallot: Merging Population and Clinical Data for Real-World Scientific Evidence.

Authors:  Samuel Blais; Ariane Marelli; Alain Vanasse; Nagib Dahdah; Adrian Dancea; Christian Drolet; Frederic Dallaire
Journal:  CJC Open       Date:  2020-06-22

2.  Exploring the feasibility of using electronic health records in the surveillance of fetal alcohol syndrome.

Authors:  Craig Hansen; Marvin Adams; Deborah J Fox; Leslie A O'Leary; Jaime L Frías; Heather Freiman; F John Meaney
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2014-02-12

3.  Characteristics of Adults With Congenital Heart Defects in the United States.

Authors:  Michelle Gurvitz; Julie E Dunn; Ami Bhatt; Wendy M Book; Jill Glidewell; Carol Hogue; Angela E Lin; George Lui; Claire McGarry; Cheryl Raskind-Hood; Alissa Van Zutphen; Ali Zaidi; Kathy Jenkins; Tiffany Riehle-Colarusso
Journal:  J Am Coll Cardiol       Date:  2020-07-14       Impact factor: 27.203

  3 in total

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