Pediatric biomedical informatics : computer applications in pediatric research /

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Bibliographic Details
Edition:Second edition.
Imprint:Singapore : Springer, 2016.
Description:1 online resource (x, 450 pages) : illustrations (some color)
Language:English
Series:Translational bioinformatics, 2213-2775 ; volume 10
Translational bioinformatics ; v. 10.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11267510
Hidden Bibliographic Details
Other authors / contributors:Hutton, John J., editor.
ISBN:9789811011047
9811011044
9789811011023
9811011028
Digital file characteristics:text file
PDF
Notes:Includes bibliographical references and index.
Online resource, title from PDF title page (EBSCO, viewed October 13, 2016).
Summary:The book describes the core resources in informatics necessary to support biomedical research programs and how these can best be integrated with hospital systems to receive clinical information that is necessary to conduct translational research. The focus is on the authors' recent practical experiences in establishing an informatics infrastructure in a large research-intensive children's hospital. This book is intended for translational researchers and informaticians in pediatrics, but can also serve as a guide to all institutions facing the challenges of developing and strengthening informatics support for biomedical research. The first section of the book discusses important technical challenges underlying computer-based pediatric research, while subsequent sections discuss informatics applications that support biobanking and a broad range of research programs. Pediatric Biomedical Informatics provides practical insights into the design, implementation, and utilization of informatics infrastructures to optimize care and research to benefit children.
Other form:Printed edition: 9789811011023
Standard no.:10.1007/978-981-10-1104-7
Table of Contents:
  • Foreword; Apps for€Pediatrics: Using Informatics to€Facilitate, Optimize, and€Personalize Care; In Memoriam; Contents; Part I: Core Informatics Resources; Chapter 1: Electronic Health Records in€Pediatrics; 1.1 Current State; 1.1.1 Adoption Rates; 1.1.2 The Pediatric EHR Market; 1.1.3 Vendor Systems; 1.1.4 Homegrown Systems and€Publication Bias; 1.1.5 Pediatric Versus General Environments; 1.1.6 Pediatric Subspecialties Versus€the€General Purpose€EHR; 1.1.7 Data from€Natural Workflow vs. Research, Primary vs. Secondary Use of€Data; 1.2 Workflow and€the€EHR; 1.2.1 Data Entry.
  • 1.2.2 Multiple Job Roles and€Their Interaction with€the€Record1.2.3 Special Pediatric Workflow Issues; 1.3 Special Functional Requirements and€Associated Data; 1.3.1 Growth Monitoring (Including Functions of€Interest Only to€Specialty Care); Basic Growth-Chart Functionality; 1.3.2 Data Found in€Growth Chart; 1.3.3 Special Population Data; 1.4 Drug Dosing; 1.5 Immunization Management; 1.5.1 Decision Support to€Determine Currency of€Immunizations; 1.5.2 Decision Support to€Schedule Immunizations; 1.5.3 Immunization Registries and€Information Exchange; 1.6 Patient Identification.
  • 1.6.1 Newborn-Infant Transition1.6.2 Fetal-Newborn Transition; 1.6.3 Maternal-Fetal/Infant Linking; 1.6.4 Pediatric-Adult Care Linking; 1.7 Developmental Monitoring; 1.7.1 Newborn Screening; 1.7.2 Well-Child Care; 1.8 Terminology Issues in€Pediatric EHRs; 1.9 Pediatric Quality Measurement and€the€EHR; 1.10 Registries and€Population Management Within€the€EHR; 1.11 Conclusion/Summary; References; Chapter 2: Protecting Privacy in€the€Child Health EHR; 2.1 The Information in€an€EHR; 2.1.1 Basic EHR Data Integrity; 2.1.2 Data Entry; 2.2 Privacy Concepts in€Pediatrics; 2.2.1 HIPAA.
  • 2.2.2 HIPAA Business Associate Agreements2.2.3 Pediatric Aspects of€HIPAA; 2.2.4 FERPA; 2.2.5 Release of€Information; 2.2.6 Clinical Data Sharing vs. Financial Data Sharing; 2.2.7 Parental Notification vs. Consent to€Treat; 2.2.8 Mandated Reporting; 2.2.9 The European Data Protection Directive; 2.3 Health Information Privacy in€Adolescent Care; 2.3.1 The Nature of€Adolescent Practice; 2.3.2 Data Access Policies in€the€Adolescent Patient; 2.4 Health Information Privacy and€Mental Health; 2.5 Guardianship Issues (Adoption, Foster Care, Fetal Care); References.
  • Chapter 3: Standards for€Interoperability3.1 Introduction; 3.2 Standards Development Organizations and€Messaging Standards; 3.2.1 ANSI; 3.2.2 HL7; 3.2.3 Committee E31 on€Healthcare Informatics of€ASTM International; 3.2.4 Accredited Standards Committee (ASC) X12; 3.2.5 The National Council for€Prescription Drug Programs (NCPDP); 3.3 Trends Toward Interoperability; 3.3.1 Meaningful Use; 3.3.2 Direct Messaging; 3.3.3 Electronic Prescribing; 3.3.4 Quality Reporting Programs; 3.3.5 Personal Health Records and€Consumer Empowerment; 3.4 HL7 Examples.