Olfactory loss in people with cystic fibrosis: Community perceptions and impact

Olfaction is a critical sense that augments interpersonal communication, impacts nutritional status, and enables avoidance of certain dangers [1]. Olfactory dysfunction (OD) is common in people with cystic fibrosis (PwCF) and has significant adverse effects. Existing studies demonstrate that OD is present in the majority of adults with CF, with rates of olfactory impairment exceeding 90% in certain reports [2 –4]. OD is associated with increased rates of depression and loneliness, negatively impacts quality-of-life (QOL), and is associated with a greater risk of mortality in the general population [1,5,6].
Source: Journal of Cystic Fibrosis - Category: Respiratory Medicine Authors: Tags: Short Communication Source Type: research