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Guide to clinical management of idiopathic pulmonary fibrosis

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Guide to clinical management of idiopathic pulmonary fibrosis/ by Steven D Nathan, A Whitney Brown, Christopher S King.
Author:	Nathan, Steven D.
other author:	Brown, A Whitney.
Published:	Cham :Springer International Publishing : : 2016.,
Description:	xvii, 123 p. :ill. (some col.), digital ; : 24 cm.;
Contained By:	Springer eBooks
Subject:	Pulmonary fibrosis. -
Online resource:	http://dx.doi.org/10.1007/978-3-319-32794-5
ISBN:	9783319327945

Guide to clinical management of idiopathic pulmonary fibrosis
Nathan, Steven D.

Guide to clinical management of idiopathic pulmonary fibrosis[electronic resource] /by Steven D Nathan, A Whitney Brown, Christopher S King. - Cham :Springer International Publishing :2016. - xvii, 123 p. :ill. (some col.), digital ;24 cm.

Overview of idiopathic pulmonary fibrosis -- Clinical presentation and diagnosis -- Diseases that mimic idiopathic pulmonary fibrosis -- Pathogenesis idiopathic pulmonary fibrosis -- Prognosis, clinical course, and monitoring of patients with idiopathic pulmonary fibrosis -- Comorbidities and complications of idiopathic pulmonary fibrosis -- Treatment of idiopathic pulmonary fibrosis -- Non-pharmacologic management of idiopathic pulmonary fibrosis -- The future of idiopathic pulmonary fibrosis.

This clinically focused pocket guide offers a concise yet complete overview of idiopathic pulmonary fibrosis, covering the most recent information on aspects such as pathophysiology, management, treatment, and clinical trials. The text is easily accessible and offers pulmonologists and other health care professionals with an excellent quick reference tool. Full color images and figures enhance and summarize key aspects of the text. Idiopathic pulmonary fibrosis is a condition that affects the alveoli and leads to serious lung damage, and the idiopathic nature of this disease means that the origin or cause is unknown. This disease is relatively rare, affecting 3 in 10,000 people, but it is becoming more common. Physicians should be aware of the early stages and symptoms of this disease so management strategies can be implemented quickly, and the best treatment can be administered.

ISBN: 9783319327945

Standard No.: 10.1007/978-3-319-32794-5doiSubjects--Topical Terms:

1021497
Pulmonary fibrosis.

LC Class. No.: RC776.F5

Dewey Class. No.: 616.24

Guide to clinical management of idiopathic pulmonary fibrosis
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300 $a xvii, 123 p. : $b ill. (some col.), digital ; $c 24 cm.
505 0 $a Overview of idiopathic pulmonary fibrosis -- Clinical presentation and diagnosis -- Diseases that mimic idiopathic pulmonary fibrosis -- Pathogenesis idiopathic pulmonary fibrosis -- Prognosis, clinical course, and monitoring of patients with idiopathic pulmonary fibrosis -- Comorbidities and complications of idiopathic pulmonary fibrosis -- Treatment of idiopathic pulmonary fibrosis -- Non-pharmacologic management of idiopathic pulmonary fibrosis -- The future of idiopathic pulmonary fibrosis.
520 $a This clinically focused pocket guide offers a concise yet complete overview of idiopathic pulmonary fibrosis, covering the most recent information on aspects such as pathophysiology, management, treatment, and clinical trials. The text is easily accessible and offers pulmonologists and other health care professionals with an excellent quick reference tool. Full color images and figures enhance and summarize key aspects of the text. Idiopathic pulmonary fibrosis is a condition that affects the alveoli and leads to serious lung damage, and the idiopathic nature of this disease means that the origin or cause is unknown. This disease is relatively rare, affecting 3 in 10,000 people, but it is becoming more common. Physicians should be aware of the early stages and symptoms of this disease so management strategies can be implemented quickly, and the best treatment can be administered.
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650 1 4 $a Medicine & Public Health. $3 593949
650 2 4 $a Pneumology/Respiratory System. $3 668561
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