scholarly journals Parametric Time‐to‐Event Model for Acute Exacerbations in Idiopathic Pulmonary Fibrosis

2020 ◽  
Vol 9 (2) ◽  
pp. 87-95
Author(s):  
Fei Tang ◽  
Benjamin Weber ◽  
Susanne Stowasser ◽  
Julia Korell
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ryo Yamazaki ◽  
Osamu Nishiyama ◽  
Sho Saeki ◽  
Hiroyuki Sano ◽  
Takashi Iwanaga ◽  
...  

AbstractSome patients with idiopathic pulmonary fibrosis (IPF) undergo recurrent acute exacerbations (AEs). This study aimed to elucidate the risk factors for recurrent AEs of IPF (AE-IPF). Consecutive patients with IPF admitted for their first AE-IPF between January 2008 and December 2018 were retrospectively recruited. Of 63 patients admitted for an AE-IPF and discharged alive, 9 (14.3%) developed a recurrence of AE within 1 year. The mean time to recurrence was 233 ± 103 days. Total doses (mg/month and mg/kg/month) of corticosteroids administered over day 1 to 30 after the AE were significantly higher in patients without recurrences of AE-IPF (5185 ± 2414 mg/month, 93.5 ± 44.0 mg/kg/month) than the doses in patients with recurrences (3133 ± 1990 mg/month, 57.2 ± 37.7 mg/kg/month) (p = 0.02 and p = 0.03, respectively). However, no differences were observed between the total doses of corticosteroids administered over days 31 to 60, 61 to 90, 91 to 120, and 151 to 180 after the AE. Furthermore, differences between the administration rates of immunosuppressive and antifibrotic treatments administered to the 2 patient groups were not significant. An increased total dose of corticosteroid administered over day 1 to 30 after an AE-IPF was associated with a decreased risk of subsequent recurrence of AE-IPF within 1 year after the first AE.


Breathe ◽  
2020 ◽  
Vol 16 (3) ◽  
pp. 200086
Author(s):  
Christopher J. Brereton ◽  
Helen E. Jo

An acute exacerbation of idiopathic pulmonary fibrosis (AEIPF) is a potentially fatal complication of an already debilitating disease. Management is currently centred on delivering excellent supportive care and identifying reversible triggers. Despite growing international awareness and collaboration, no effective therapies have been identified. Corticosteroids are often the mainstay of treatment; however, the evidence base for their use is poor. Here, we review our current understanding of the disease process and how to manage it, with a focus on the role of corticosteroid therapy.


2008 ◽  
Vol 177 (12) ◽  
pp. 1397-1397 ◽  
Author(s):  
Wim A. Wuyts ◽  
Michiel Thomeer ◽  
Lieven J. Dupont ◽  
Geert M. Verleden

Respiration ◽  
2013 ◽  
Vol 86 (4) ◽  
pp. 265-274 ◽  
Author(s):  
Katerina M. Antoniou ◽  
Athol U. Wells

Author(s):  
Yutaro Nakamura ◽  
Takafumi Suda

Idiopathic pulmonary fibrosis (IPF) is a parenchymal lung disease characterized by progressive interstitial fibrosis. The clinical course of IPF can be unpredictable and may be punctuated by acute exacerbations. Although much progress is being made in unraveling the mechanisms underlying IPF, effective therapy for improving survival remains elusive. Longitudinal disease profiling, especially in terms of clinical manifestations in a large cohort of patients, should lead to proper management of the patients and development of new treatments for IPF. Appropriate multidisciplinary assessment in ongoing registries is required to achieve this. This review summarizes the current status of the diagnosis and clinical manifestations of IPF.


Author(s):  
Lars Kehler ◽  
Tobias Norajitra ◽  
Julia Ley-Zaporozhan ◽  
Athanasios Giannakis ◽  
Roman Rubtsov ◽  
...  

Author(s):  
Paola Faverio ◽  
Stefania Cerri ◽  
Maria Rosaria Pellegrino ◽  
Giulia Dei ◽  
Enrico Clini ◽  
...  

2011 ◽  
Vol 40 (1) ◽  
pp. 93-100 ◽  
Author(s):  
Eoin P. Judge ◽  
Aurelie Fabre ◽  
Huzaifa I. Adamali ◽  
Jim J. Egan

2017 ◽  
Vol 18 (1) ◽  
Author(s):  
Philip L. Molyneaux ◽  
Michael J Cox ◽  
Athol U. Wells ◽  
Ho Cheol Kim ◽  
Wonjun Ji ◽  
...  

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