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Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b). Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).
(DLco) of almost 43% of the predicted value © 2017-2018 All Rights Reserved, No part of this document should be modified/used without prior consent Tutors India - Your trusted mentor since 2001 www.tutorindia.com I UK # +44-1143520021, info@tutorsindia.com Page 94 of 172
- Page 61 and 62: 3.2 Meta-analysis of Randomised Con
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- Page 82: S. no Author; Year 1 Behr et al 7 C
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- Page 90: or temporary cessation of pirfenido
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- Page 111: PaO2, and SaO2; episodes of AE-IPF
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- Page 118 and 119: espectively. However, one study by
- Page 120 and 121: the combined effects of these drugs
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- Page 124 and 125: with respect to background factors
- Page 126 and 127: patient in the intervention group a
- Page 128 and 129: and N-acetylcysteine when combined
- Page 130 and 131: References Abehsera, M., Valeyre, D
- Page 132 and 133: from: http://www.ncbi.nlm.nih.gov/p
- Page 134 and 135: worsening of idiopathic pulmonary f
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- Page 138 and 139: http://www.ncbi.nlm.nih.gov/pubmed/
- Page 140 and 141: Hunninghake, G.W., Colby, T. V., Eg
- Page 142 and 143: Diaz de Leon, A., Cronkhite, J.T.,
- Page 144 and 145: predictors of a diagnosis of idiopa
- Page 146 and 147: ole remains uncertain as anti-inter
- Page 148 and 149: (2007). Occupational exposure and s
- Page 150 and 151: Hillerdal, G., Nöu, E., Osterman,
- Page 152 and 153: Increasing Global Mortality from Id
- Page 154 and 155: pulmonary fibrosis. The New England
- Page 156 and 157: Kim, D.S. (2006). Classification an
- Page 158 and 159: from impaired collagen synthesis by
- Page 160 and 161: and the American Society of Transpl
(DLco) of<br />
almost 43%<br />
of the<br />
predicted<br />
value<br />
© 2017-2018 All Rights Reserved, No part of this document should be modified/used without prior consent<br />
<strong>Tutors</strong> <strong>India</strong> - Your trusted mentor since 2001<br />
www.tutorindia.com I UK # +44-1143520021, info@tutorsindia.com<br />
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