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Idiopathic Pulmonary Fibrosis

Advances in Diagnostic Tools and Disease Management
BuchGebunden
259 Seiten
Englisch
Springererschienen am08.10.20151st ed. 2016
From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF).mehr
Verfügbare Formate
BuchGebunden
EUR106,99
BuchKartoniert, Paperback
EUR96,29
E-BookPDF1 - PDF WatermarkE-Book
EUR96,29

Produkt

KlappentextFrom epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF).
Details
ISBN/GTIN978-4-431-55581-0
ProduktartBuch
EinbandartGebunden
Verlag
Erscheinungsjahr2015
Erscheinungsdatum08.10.2015
Auflage1st ed. 2016
Seiten259 Seiten
SpracheEnglisch
Gewicht569 g
IllustrationenX, 259 p.
Artikel-Nr.15613983
Rubriken
GenreMedizin

Inhalt/Kritik

Inhaltsverzeichnis
âPart 1.- Definition, epidemiology, and pathogenesis .- Chapter 1: Definition of IPF  (Question: Is the latest classification [ATS/ERS] satisfactory?).- Chapter 2: Epidemiology and risk factors of IPF  (Question: Can we dare to ask, What are the possible causes? ).- Chapter 3: Acute exacerbation of IPF  (Question: The concept was proposed in Japan, but why was it not recognized in western countries?).- Chapter 4: Pathogenesis   (Question: Is abnormal repair of epithelial damage involved in the basic pathogenesis of this disease?) .- Part 2 Diagnosis    .- Chapter 5: Specific serum markers of IPF  (Question: What are the significances of KL-6, SP-A, and SP-D?).- Chapter 6: High-resolution CT of honeycombing and IPF/UIP  (Question: To what extent can honeycomb lung be diagnosed by imaging? To what extent can IPF diagnosis be made by HRCT?).- Chapter 7: Pathology of IPF  (Question: Why does the pathological classification of IIPs vary among pathologists?).- Chapter 8: Differential diagnosis  (Question: What should we particularly keep in mind in the differential diagnosis?) .- Part 3 Management and prognosis    .- Chapter 9 Pharmacotherapy of IPF (antifibrotic compounds)  (Question: Can antifibrotic agents really inhibit fibrosis? How about the development of new therapeutic agents?).- Chapter 10: Pharmacotherapy of IPF (Corticosteroids, immunosuppressants)  (Question: Are these actually effective? Ineffective? Harmful?).- Chapter 11: Non-pharmacological therapy for IPF  (Question: Is respiratory care actually effective?).- Chapter 12: Pharmacotherapy of acute exacerbation of IPF (Corticosteroids, immunosuppressants and direct hemoperfusion with polymyxin B)  (Question: Are high-dose steroid therapy, other immunosuppressant therapy, and PMX therapy [often used in Japan] really effective?) .- Part 4 Topics    .- Chapter 13 :Combined pulmonary fibrosis and emphysema (CPFE)  (Question:Is it an independent disease entity?).- Chapter 14: Common pathways in IPF and lung cancer  (Question: Why is lung cancer associated with IPF at a high frequency?).- Chapter 15 :Acute exacerbation of IIPs after pulmonary resection for lung cancer   (Question: Can acute exacerbation of IPF be predicted preoperatively?)mehr

Autor


Hiroyuki Nakamura, MD, PhD.


Department of Respiratory Medicine,

Tokyo Medical University Ibaraki Medical Center, Japan

Kazutetsu Aoshiba, MD, PhD.


Department of Respiratory Medicine,

Tokyo Medical University Ibaraki Medical Center, Japan