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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).

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Ethnicity:<br />

The role of ethnicity in the prognosis of IPF contains restricted data. Whites are more<br />

probable to be diagnosed with IPF than blacks (Olson et al., 2007). A previous study on the<br />

unison guidelines proposed higher mortality of whites in contrast to the blacks (Mannino et<br />

al., 1996), while two more current studies of patients recorded for lung transplantation<br />

observed that the survival among both blacks and Hispanics decreased in contrast to the<br />

whites that continued after assimilation of comorbidities and socioeconomic status (Lederer<br />

et al., 2006c, 2006a). It was exhibited by Olson and coworkers that age-assimilated mortality<br />

rates in Hispanics are lower than in white non-Hispanics (Olson et al., 2007).<br />

Smoking status:<br />

The smoking level consequence on the survival is also been inconsistent. It was<br />

observed in older studies that survival benefit in present smokers as compared to the past and<br />

never smokers (King et al., 2001b). The influence of smoking status on IPF in a study<br />

precisely exploring it, exhibited that the survival benefit in present smokers in contrast to the<br />

former smokers on univariate analysis, while after assimilation for disease severity, a<br />

“healthy smoker effect” was demonstrated since this consequence was no longer remarkable<br />

(Antoniou et al., 2008). A selection prejudice was noticed in the healthy smoker effect in<br />

studies of respiratory illnesses, since individuals most fragile to the irritating consequences of<br />

tobacco are more probable to quit smoking, thus focussing on individuals who are “resistant”<br />

to the short-term consequences into the present smokers “healthier” category from a<br />

respiratory point of view (Becklake & Lalloo, 1990). Nonsmokers had a higher survival rate<br />

generally than past smokers and all smokers (present and past).<br />

Dyspnea:<br />

To evaluate the quality of life, disease severity, and prognosis dyspnea scores are<br />

employed in diverse pulmonary diseases. The Medical Research Council chronic dyspnea<br />

score at baseline and the clinical-radiographic-physiologic (CRP) dyspnea score at baseline<br />

and change in score at 6 and 12 months in IPF have exhibited to be remarkable and<br />

autonomous indicators of survival after assimilation for disease seriousness by physiologic<br />

variables (Manali et al., 2008; Collard et al., 2003).<br />

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