Cardiothoracic Care for Children and Young People (eBook)
240 Seiten
John Wiley & Sons (Verlag)
978-0-470-74852-7 (ISBN)
comprehensive and interprofessional guide aimed at all healthcare
professionals working with children and young people with
Congenital Heart Disease.
Structured around the timeline of the patient's healthcare
journey, this book explores the care of the patient from the point
of presentation and diagnosis (whether that is antenatally, in the
neonatal period or later) until there is a transition in the
patient's healthcare journey either onto adult services, or
in some cases, end of life. It considers all aspects of care that
the child/young person may receive, supported in an evidence based
manner, with chapters written by experts from a variety of
professional groups involved with this patient group.
Kerry Cook is Senior Lecturer in the Children and Young Peoples Nursing Team at the Faculty of Health and Life Sciences at Coventry University. Helen Langton is Professor/Dean of Faculty of Education, Health and Sciences at The University of Derby.
List of Contributors.
Chapter 1 An overview of new ways of working for the 21st
century.
Patient journeys.
E-based learning.
New ways of learning.
Usability and accessibility.
Flexibility.
Cost-effectiveness.
Changes in service and organisational effectiveness.
Interprofessional learning and collaborative practice.
Learning points from other higher education institutions.
Changes in health care.
Congenital Cardiac Services Workshop June 2006.
Advancing roles.
Conclusion.
References.
Chapter 2 Presentation and diagnosis.
Fetal diagnosis of congenital heart disease.
Neonatal presentations.
Unscheduled care.
Late presentations.
Cardiac arrhythmias and sudden death.
Cardiac investigations.
Summary.
References.
Websites.
Chapter 3 Treatment options/management.
Admission and preoperative preparation.
Medical/interventional treatment options.
Introduction to paediatric cardiac surgery.
Summary.
References.
Chapter 4 Impact of heart disease on young people and their
families: an introduction.
How are 'outcomes' measured?
Quality of life - measurement issues.
The infant and toddler with congenital heart disease.
School-age children.
The adult with CHD - long-term physical and social
issues.
The impact on the family.
Diversity and culture.
Conclusion.
References.
Website.
Chapter 5 What are 'communication
skills'?
The changing climate.
Consent.
The 'explanatory' or 'exploratory'
communication style.
An organisational research project.
The templates and the competency in interactive
communication.
Child protection.
Ethical or communication issues?
Adolescents.
Summary.
References.
Chapter 6 Transition to Adult Services .
Preparation.
Logistics.
Psychological aspects of transition.
Support.
Summary.
References.
Websites.
Chapter 7 The information jigsaw.
The beginning of the journey.
Antenatal diagnosis.
The hospital experience.
Family relationships.
The next steps.
Bereavement.
Conclusion.
References.
Further reading.
Index.
"A guide for healthcare professionals who work with children and young people with congenital heart disease that traces the care of the patient from presentation and diagnosis to the transition to adult services." (Book News, December 2009)
Erscheint lt. Verlag | 20.7.2009 |
---|---|
Sprache | englisch |
Themenwelt | Medizinische Fachgebiete ► Innere Medizin ► Kardiologie / Angiologie |
Medizin / Pharmazie ► Medizinische Fachgebiete ► Pädiatrie | |
Medizin / Pharmazie ► Pflege | |
Schlagworte | Krankenpflege • nursing • Pflege |
ISBN-10 | 0-470-74852-4 / 0470748524 |
ISBN-13 | 978-0-470-74852-7 / 9780470748527 |
Haben Sie eine Frage zum Produkt? |
Größe: 2,7 MB
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