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E-grāmata: Pediatric and Congenital Cardiac Care: Volume 1: Outcomes Analysis

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  • Formāts: PDF+DRM
  • Izdošanas datums: 04-Dec-2014
  • Izdevniecība: Springer London Ltd
  • Valoda: eng
  • ISBN-13: 9781447165873
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Pediatric and Congenital Cardiac Care: Volume 1: Outcomes AnalysisPalielināt
  • Formāts: PDF+DRM
  • Izdošanas datums: 04-Dec-2014
  • Izdevniecība: Springer London Ltd
  • Valoda: eng
  • ISBN-13: 9781447165873
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There are growing questions regarding the safety, quality, risk management, and costs of PCC teams, their training and preparedness, and their implications on the welfare of patients and families. This innovative book, authored by an international authorship, will highlight the best practices in improving survival while paving a roadmap for the expected changes in the next 10 years as healthcare undergoes major transformation and reform. An invited group of experts in the field will participate in this project to provide the timeliest and informative approaches to how to deal with this global health challenge. The book will be indispensable to all who treat pediatric cardiac disease and will provide important information about managing the risk of patients with pediatric and congenital cardiac disease in the three domains of: the analysis of outcomes, the improvement of quality, and the safety of patients.

Recenzijas

From the book reviews:

The book emphasizes the importance of past, present, and future longitudinal recordkeeping for pediatric and congenital cardiac disease. The audience includes any individuals interested in pediatric and congenital heart disease, from physicians to statisticians to medical historians. This is an excellent reference for any practitioner involved in pediatric or congenital heart disease. (Shawn Ragbir, Doodys Book Reviews, March, 2015)

Part I Introduction
1 Introduction
3(6)
Paul R. Barach
Jeffrey P. Jacobs
Peter C. Laussen
Steven E. Lipshultz
2 Introduction: The History of Statistics in Medicine and Surgery
9(18)
Eugene H. Blackstone
3 Introduction: Using Data to Drive Change and Improvement: The Legacy of Florence Nightingale
27(4)
Kathleen Mussatto
Maryanne Kessel
4 Introduction: Quality Improvement and Databases in the Context of Professionalism
31(4)
John E. Mayer Jr.
Part II Nomenclature and Taxonomies
5 Nomenclature for Congenital and Pediatric Cardiac Disease: Historical Perspectives and the International Pediatric and Congenital Cardiac Code
35(16)
Rodney C.G. Franklin
Jeffrey P. Jacobs
Otto N. Krogmann
Marie J. Beland
6 Defining Terms in Lists of Nomenclature
51(12)
Henry L. Walters III
Steven D. Colan
7 Illustrating Terms in Lists of Nomenclature
63(14)
Jorge M. Giroud
Jeffrey P. Jacobs
Diane E. Spicer
James D. St. Louis
Part III Databases
8 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Cardiac Surgery
77(50)
Jeffrey P. Jacobs
9 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Cardiology
127(14)
William B. Drake II
Richard E. Stroup
Allen D. Everett
10 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Anesthesia
141(14)
David F. Vener
11 Databases for Assessing the Outcomes of the Treatment of Patients with Congenital and Pediatric Cardiac Disease: The Perspective of Critical Care
155(8)
Michael G. Gaies
Howard E. Jeffries
Randall Wetzel
Steven M. Schwartz
12 Early Database Initiatives: The Fyler Codes
163(8)
Steven D. Colan
13 The Academic Database: Lessons Learned from the Congenital Heart Surgeons' Society Data Center
171(14)
Christopher A. Caldarone
Jeffrey A. Poynter
William G. Williams
14 Clinical Versus Administrative Data
185(8)
Sara K. Pasquali
J. William Gaynor
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)
193(18)
Ryan R. Davies
16 Databases for Extracorporeal Membrane Oxygenation and Ventricular Assist Devices
211(8)
David S. Cooper
David L.S. Morales
Megan del Corral
Matthew L. Paden
Ravi R. Thiagarajan
17 The United Kingdom National Congenital Heart Disease Audit
219(12)
Rodney C.G. Franklin
David Cunningham
John L. Gibbs
18 The Pediatric Cardiac Care Consortium: The End of an Era and Beginning of a New Mission
231(12)
James D. St. Louis
Lazaros K. Kochilas
19 Pediatric Cardiac Catheterization Databases
243(16)
Joshua P. Kanter
Lisa Bergersen
Sandra Coombs
Thomas J. Forbes
Allen D. Everett
Gerard R. Martin
20 Pediatric Electrophysiology Databases
259(8)
Stephen P. Seslar
John D. Kugler
21 Using Data to Drive Improvement and Build the Science of Nursing
267(20)
Ashley Collins
Jean Anne Connor
Sandra Mott
Patricia Hickey
22 Data Standards of the American College of Cardiology Foundation (ACCF) and the American Heart Association (AHA) and the Universal Pediatric Cardiac Dataset
287(8)
Jeffrey R. Boris
23 Ethical Issues Confronting Outcomes Analysis and Quality Assurance
295(12)
Constantine D. Mavroudis
Jeffrey P. Jacobs
Allison Siegel
Constantine Mavroudis
Part IV Stratification of Complexity
24 Statistical Issues in the Analysis and Interpretation of Outcomes for Congenital Cardiac Surgery
307(12)
Sean M. O'Brien
25 Real Time Monitoring of Risk-Adjusted Surgical Outcomes for Congenital Heart Disease
319(8)
Kate L. Brown
Sonya Crowe
Martin Utley
Christina Pagel
26 Risk Adjustment for Congenital Heart Surgery -1 (RACHS-1) for Evaluation of Mortality in Children Undergoing Cardiac Surgery
327(10)
Ravi R. Thiagarajan
Peter C. Laussen
27 The Aristotle Complexity Score: A Tool to Evaluate Performance in Congenital Heart Surgery
337(26)
Francois Lacour-Gayet
28 Empirically Based Tools for Analyzing Mortality and Morbidity Associated with Congenital Heart Surgery
363(16)
Marshall L. Jacobs
Sara K. Pasquali
Jeffrey P. Jacobs
Sean M. O'Brien
Part V Verification of Data Completeness and Accuracy of Data
29 Verification of Data Completeness and Accuracy
379(16)
David M. Overman
David R. Clarke
Part VI Subspecialty Collaboration
30 Linking Databases
395(8)
Sara K. Pasquali
Marshall L. Jacobs
Jeffrey P. Jacobs
Part VII Longitudinal Follow-Up
31 Use of National Death Registries to Empower Databases in Reporting Longitudinal Follow-Up
403(10)
David L.S. Morales
Farhan Zafar
Jeffrey P. Jacobs
32 Quality of Life: The Need for a National Database
413(22)
Bradley S. Marino
Jeffrey B. Anderson
33 Longitudinal Follow-Up Studies in the Pediatric Heart Network
435(10)
Lynn Mahony
Lynn A. Sleeper
Gail D. Pearson
34 The Value of National Institutes of Health (NIH) Registry-Based Research in Identifying Childhood Cardiac Disease Outcomes: The Pediatric Cardiomyopathy Registry Experience
445(22)
James D. Wilkinson
Joslyn A. Westphal
Samuel W. Ross
Danielle D. Dauphin
Steven E. Lipshultz
Part VIII Public Reporting of Data
35 Public Reporting of Cardiac Data: Pros, Cons, and Lessons for the Future
467(12)
Edward L. Hannan
36 Public Reporting of Pediatric Cardiac Data
479(12)
Vinay Badhwar
J. William Gaynor
Jeffrey P. Jacobs
David M. Shahian
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)
491(16)
Debra Hilton-Kamm
Helen Haskell
Index 507
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