IDIOPATHIC PULMONARY FIBROSIS

IDIOPATHIC PULMONARY FIBROSIS

Editorial:
MOSBY
Año de edición:
Materia
Neumología
ISBN:
978-0-323-54431-3
Páginas:
142
N. de edición:
1
Idioma:
Inglés
Disponibilidad:
Disponible en 10 días

Descuento:

-5%

Antes:

80,07 €

Despues:

76,07 €

1. Introduction
2. Epidemiology of IPF/ILD
3. Mechanisms of Fibrosis
4. Genetics of IPF
5. HRCT in IPF
6. Pathology of IPF
7. Making the Diagnosis of IPF
8. IPF Look-Alikes: Uncharacterized PF, CTD-ILD and cHP
9. Natural History of IPF and Disease Monitoring
10. Biomarkers in IPF
11. Therapeutics (Rx, Rehabilitation, O2, Tx, and Treating Comorbidities: OSA, GERD, PH)

Designed with the practicing clinician in mind, Idiopathic Pulmonary Fibrosis provides a succinct, easy-to-digest overview of this challenging condition in which the cause of thickening lung tissue is unknown. This concise resource by Drs. Kevin K. Brown and Jeff Swigris provides essential information for the physician who sees pulmonary fibrosis patients, including epidemiology, genetics and biomarkers, pathology, diagnosis, disease monitoring, and therapeutics intended to improve the patient’s lifespan and quality of life.

Features:
• Covers the process of making the diagnosis of idiopathic pulmonary fibrosis, as well as IPF look-alikes: uncharacterized PF, CTD-ILD, and cHP.
• Details today’s available therapeutics, including Rx, rehabilitation, O2, Tx, and treating comorbidities: OSA, GERD, and PH.
• Consolidates today’s available information on this timely topic into one convenient resource.

Author
Jeffrey Swigris and Kevin K Brown, MD, National Jewish Health