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Cystic Fibrosis : A Multi-Organ System Approach / edited by Stephanie Duggins Davis, Margaret Rosenfeld, James Chmiel

Contributor(s): Davis, Stephanie Duggins., editor. | Rosenfeld, Margaret., editor. | Chmiel, James., editor. | SpringerLink (Online service)
Material type: materialTypeLabelE-bookSeries: (Respiratory Medicine,, 2197-7372); (Medicine (Springer-11650)).Publisher: Cham : Springer International Publishing : Imprint: Humana, 2020Edition: 1st ed. 2020.Description: 1 recurso en línea (XVII, 526 páginas) : 36 ilustraciones, 26 ilustraciones a color.ISBN: 9783030423827.Subject: Fibrosis quísticaOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
The Changing Face of CF -- Diagnosing cystic fibrosis -- SECTION I: Pulmonary Manifestations -- Early lung disease -- Pulmonary complications as an adult -- Treating respiratory complications -- Transplant -- SECTION II: Gastrointestinal Manifestations -- Liver disease -- Pancreatic insufficiency and nutritional complications -- SECTION III: Endocrine Manifestations -- Diabetes -- Bone Disease. SECTION IV: Further Comorbidities -- Rheumatologic Manifestations -- Reproductive Issues -- The Impact of CF on the Kidney -- Mental Health.
Abstract: This book provides a comprehensive overview of the multisystem disease, cystic fibrosis, for both pediatric and adult patients. Written by experts in the field, the text outlines the progressive nature of CF as well as the impact of this autosomal recessive disease on the respiratory, gastrointestinal, endocrine, rheumatologic, and renal systems, as well as the patient's mental health. The book begins with a chapter describing the history of cystic fibrosis and how the face of this life-shortening disease has changed over the past several decades. The following chapters elucidate the pathophysiology of how cystic fibrosis impacts each organ system. Current management and therapeutics are detailed with step-by-step guidelines for clinicians. This book is unique in that it highlights the entire person, not just the respiratory system, with detailed inclusion of the patient perspectives throughout, informing practice standards and considerations. This is an ideal guide for pediatric and adult physicians who care for patients with cystic fibrosis, as well as respiratory therapists, physical therapists, nurses, nutritionists, and pharmacists who care for these patients.
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Holdings
Item type Current library Collection Call number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC858.C95 2020 EB (Browse shelf(Opens below)) Acceso electrónico eBook.27062098
Total holds: 0

The Changing Face of CF -- Diagnosing cystic fibrosis -- SECTION I: Pulmonary Manifestations -- Early lung disease -- Pulmonary complications as an adult -- Treating respiratory complications -- Transplant -- SECTION II: Gastrointestinal Manifestations -- Liver disease -- Pancreatic insufficiency and nutritional complications -- SECTION III: Endocrine Manifestations -- Diabetes -- Bone Disease. SECTION IV: Further Comorbidities -- Rheumatologic Manifestations -- Reproductive Issues -- The Impact of CF on the Kidney -- Mental Health.

This book provides a comprehensive overview of the multisystem disease, cystic fibrosis, for both pediatric and adult patients. Written by experts in the field, the text outlines the progressive nature of CF as well as the impact of this autosomal recessive disease on the respiratory, gastrointestinal, endocrine, rheumatologic, and renal systems, as well as the patient's mental health. The book begins with a chapter describing the history of cystic fibrosis and how the face of this life-shortening disease has changed over the past several decades. The following chapters elucidate the pathophysiology of how cystic fibrosis impacts each organ system. Current management and therapeutics are detailed with step-by-step guidelines for clinicians. This book is unique in that it highlights the entire person, not just the respiratory system, with detailed inclusion of the patient perspectives throughout, informing practice standards and considerations. This is an ideal guide for pediatric and adult physicians who care for patients with cystic fibrosis, as well as respiratory therapists, physical therapists, nurses, nutritionists, and pharmacists who care for these patients.

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