C38 UNDERSTANDING THERAPEUTICS IN IPF: Effect Of Antifibrotic Therapy In Patients With Idiopathic Pulmonary Fibrosis Awaiting Lung Transplantation
Rationale: Idiopathic pulmonary fibrosis (IPF) is a rapidly progressive interstitial lung disease with high mortality. Methods: We conducted a retrospective chart review on 59 subjects with IPF who were listed for lung transplant at our tertiary referral center from September 2014 to October 2016.
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| Veröffentlicht in: | American journal of respiratory and critical care medicine 2017-01, Vol.195 |
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| container_title | American journal of respiratory and critical care medicine |
| container_volume | 195 |
| creator | Dorey-Stein, Z Galli, J Criner, G J |
| description | Rationale: Idiopathic pulmonary fibrosis (IPF) is a rapidly progressive interstitial lung disease with high mortality. Methods: We conducted a retrospective chart review on 59 subjects with IPF who were listed for lung transplant at our tertiary referral center from September 2014 to October 2016. |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1073-449X |
| ispartof | American journal of respiratory and critical care medicine, 2017-01, Vol.195 |
| issn | 1073-449X 1535-4970 |
| language | eng |
| recordid | cdi_proquest_journals_1926867936 |
| source | American Thoracic Society (ATS) Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Journals@Ovid Complete |
| subjects | Mortality Pulmonary fibrosis Transplants & implants |
| title | C38 UNDERSTANDING THERAPEUTICS IN IPF: Effect Of Antifibrotic Therapy In Patients With Idiopathic Pulmonary Fibrosis Awaiting Lung Transplantation |
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