Physician characteristics associated with treatment initiation patterns in idiopathic pulmonary fibrosis. (26th September 2019)
- Record Type:
- Journal Article
- Title:
- Physician characteristics associated with treatment initiation patterns in idiopathic pulmonary fibrosis. (26th September 2019)
- Main Title:
- Physician characteristics associated with treatment initiation patterns in idiopathic pulmonary fibrosis
- Authors:
- LaCamera, Peter P
Limb, Susan L
Haselkorn, Tmirah
Morgenthien, Elizabeth A
Stauffer, John L
Wencel, Mark L - Abstract:
- Pirfenidone and nintedanib are oral antifibrotic agents approved for the treatment of idiopathic pulmonary fibrosis (IPF). Real-world data on factors that influence IPF treatment decisions are limited. Physician characteristics associated with antifibrotic therapy initiation following an IPF diagnosis were examined in a sample of US pulmonologists. An online, self-administered survey was fielded to pulmonologists between April 10, 2017, and May 17, 2017. Pulmonologists were included if they spent >20% of their time in direct patient care and had ≥5 patients with IPF receiving antifibrotics. Participants answered questions regarding timing and reasons for considering the initiation of antifibrotic therapy after an IPF diagnosis. A total of 169 pulmonologists participated. The majority (81.7%) considered initiating antifibrotic therapy immediately after IPF diagnosis all or most of the time (immediate group), while 18.3% considered it only some of the time or not at all (delayed group). Pulmonologists in the immediate group were more likely to work in private practice (26.1%), have a greater mean percentage of patients receiving antifibrotic therapy (60.8%), and decide to initiate treatment themselves (31.2%) versus those in the delayed group (16.1%, 30.5%, and 16.1%, respectively). Most pulmonologists consider initiating antifibrotic treatment immediately after establishing an IPF diagnosis all or most of the time versus using a "watch-and-wait" approach. DistinguishingPirfenidone and nintedanib are oral antifibrotic agents approved for the treatment of idiopathic pulmonary fibrosis (IPF). Real-world data on factors that influence IPF treatment decisions are limited. Physician characteristics associated with antifibrotic therapy initiation following an IPF diagnosis were examined in a sample of US pulmonologists. An online, self-administered survey was fielded to pulmonologists between April 10, 2017, and May 17, 2017. Pulmonologists were included if they spent >20% of their time in direct patient care and had ≥5 patients with IPF receiving antifibrotics. Participants answered questions regarding timing and reasons for considering the initiation of antifibrotic therapy after an IPF diagnosis. A total of 169 pulmonologists participated. The majority (81.7%) considered initiating antifibrotic therapy immediately after IPF diagnosis all or most of the time (immediate group), while 18.3% considered it only some of the time or not at all (delayed group). Pulmonologists in the immediate group were more likely to work in private practice (26.1%), have a greater mean percentage of patients receiving antifibrotic therapy (60.8%), and decide to initiate treatment themselves (31.2%) versus those in the delayed group (16.1%, 30.5%, and 16.1%, respectively). Most pulmonologists consider initiating antifibrotic treatment immediately after establishing an IPF diagnosis all or most of the time versus using a "watch-and-wait" approach. Distinguishing characteristics between pulmonologists in the immediate group versus the delayed group included practice setting, percentage of patients receiving antifibrotic therapy, and the decision-making dynamics between the patient and the pulmonologist. … (more)
- Is Part Of:
- Chronic respiratory disease. Volume 16(2019)
- Journal:
- Chronic respiratory disease
- Issue:
- Volume 16(2019)
- Issue Display:
- Volume 16, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 16
- Issue:
- 2019
- Issue Sort Value:
- 2019-0016-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-09-26
- Subjects:
- Antifibrotic therapy -- idiopathic pulmonary fibrosis
Respiratory organs -- Diseases -- Periodicals
616.2005 - Journal URLs:
- http://crd.sagepub.com/ ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/1479973119879678 ↗
- Languages:
- English
- ISSNs:
- 1479-9723
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12712.xml