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Pediatric and Congenital Cardiac Care

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Cover of 'Pediatric and Congenital Cardiac Care'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction
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    Chapter 2 Introduction: The History of Statistics in Medicine and Surgery
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    Chapter 3 Introduction: Using Data to Drive Change and Improvement: The Legacy of Florence Nightingale
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    Chapter 4 Introduction: Quality Improvement and Databases in the Context of Professionalism
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    Chapter 5 Nomenclature for Congenital and Pediatric Cardiac Disease: Historical Perspectives and the International Pediatric and Congenital Cardiac Code
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    Chapter 6 Defining Terms in Lists of Nomenclature
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    Chapter 7 Illustrating Terms in Lists of Nomenclature
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    Chapter 8 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Cardiac Surgery
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    Chapter 9 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Cardiology
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    Chapter 10 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Anesthesia
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    Chapter 11 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Critical Care
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    Chapter 12 Early Database Initiatives: The Fyler Codes
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    Chapter 13 The Academic Database: Lessons Learned from the Congenital Heart Surgeons’ Society Data Center
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    Chapter 14 Clinical Versus Administrative Data
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    Chapter 15 Databases for Pediatric Cardiac Transplantation: The United Network for Organ Sharing/Scientific Registry of Transplant Recipients (UNOS/SRTR) and the Pediatric Heart Transplant Study (PHTS)
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    Chapter 16 Databases for Extracorporeal Membrane Oxygenation and Ventricular Assist Devices
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    Chapter 17 The United Kingdom National Congenital Heart Disease Audit
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    Chapter 18 The Pediatric Cardiac Care Consortium: The End of an Era and Beginning of a New Mission
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    Chapter 19 Pediatric Cardiac Catheterization Databases
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    Chapter 20 Pediatric Electrophysiology Databases
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    Chapter 21 Using Data to Drive Improvement and Build the Science of Nursing
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    Chapter 22 Data Standards of the American College of Cardiology Foundation (ACCF) and the American Heart Association (AHA) and the Universal Pediatric Cardiac Dataset
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    Chapter 23 Ethical Issues Confronting Outcomes Analysis and Quality Assurance
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    Chapter 24 Statistical Issues in the Analysis and Interpretation of Outcomes for Congenital Cardiac Surgery
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    Chapter 25 Real Time Monitoring of Risk-Adjusted Surgical Outcomes for Congenital Heart Disease
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    Chapter 26 Risk Adjustment for Congenital Heart Surgery -1 (RACHS-1) for Evaluation of Mortality in Children Undergoing Cardiac Surgery
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    Chapter 27 The Aristotle Complexity Score: A Tool to Evaluate Performance in Congenital Heart Surgery
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    Chapter 28 Empirically Based Tools for Analyzing Mortality and Morbidity Associated with Congenital Heart Surgery
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    Chapter 29 Verification of Data Completeness and Accuracy
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    Chapter 30 Linking Databases
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    Chapter 31 Use of National Death Registries to Empower Databases in Reporting Longitudinal Follow-Up
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    Chapter 32 Quality of Life: The Need for a National Database
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    Chapter 33 Longitudinal Follow-Up Studies in the Pediatric Heart Network
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    Chapter 34 The Value of National Institutes of Health (NIH) Registry-Based Research in Identifying Childhood Cardiac Disease Outcomes: The Pediatric Cardiomyopathy Registry Experience
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    Chapter 35 Public Reporting of Cardiac Data: Pros, Cons, and Lessons for the Future
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    Chapter 36 Public Reporting of Pediatric Cardiac Data
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    Chapter 37 Communication Chaos: How Incomplete and Conflicting Information Prevents Improved Outcomes for Patients with Pediatric and Congenital Cardiac Disease (and What We Can Do About It)
Attention for Chapter 37: Communication Chaos: How Incomplete and Conflicting Information Prevents Improved Outcomes for Patients with Pediatric and Congenital Cardiac Disease (and What We Can Do About It)
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Chapter title
Communication Chaos: How Incomplete and Conflicting Information Prevents Improved Outcomes for Patients with Pediatric and Congenital Cardiac Disease (and What We Can Do About It)
Chapter number 37
Book title
Pediatric and Congenital Cardiac Care
Published by
Springer London, November 2015
DOI 10.1007/978-1-4471-6587-3_37
Book ISBNs
978-1-4471-6586-6, 978-1-4471-6587-3
Authors

Debra Hilton-Kamm, Helen Haskell

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