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Correction to Lancet Respir Med 2023; published online Jan 23 https://doi org/10 1016/S2213-2600(22)00492-1

Menzies-Gow A, Wechsler ME, Brightling CE, et al. Long-term safety and efficacy of tezepelumab in people with severe, uncontrolled asthma (DESTINATION): a randomised, placebo-controlled extension study. Lancet Respir Med 2023; published online Jan 23. https://doi.org/10.1016/S2213-2600(22)00492-1 In this Article s appendix, table s7 should have read “n=840” participants in the all tezepelumab group for the pooled NAVIGATOR and SOURCE population and the last line of the legend for figure s2 should have read “(E; data from D were not included; same as the placebo then tezepelumab group)”.

Long-term safety and efficacy of tezepelumab in people with severe, uncontrolled asthma (DESTINATION): a randomised, placebo-controlled extension study

Tezepelumab treatment was well tolerated for up to 2 years and resulted in sustained, clinically meaningful reductions in asthma exacerbations in individuals with severe, uncontrolled asthma. These findings are consistent with previous randomised, placebo-controlled studies and show the long-term safety and sustained efficacy of tezepelumab in individuals with severe, uncontrolled asthma.

Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift?

Usual interstitial pneumonia (UIP) is characterised by a distinctive morphological and radiological appearance that was considered the pathognomonic hallmark of idiopathic pulmonary fibrosis (IPF). However, this peculiar lung remodelling pattern is also seen in other fibrotic interstitial lung diseases, including hypersensitivity pneumonitis, and connective tissue diseases. In this Personal View, we advocate the designation of a UIP pattern as a single, discrete diagnostic entity, amalgamating its primary form and secondary processes in disorders such as hypersensitivity pneumonitis (hypersensitivity pneumonitis with UIP), rheumatoid arthritis (rheumatoid arthritis with UIP), and others.

Tomato flu: misnomer for a common disease? – Authors reply

We thank Saurav Paul and colleagues for their response to our Correspondence.1 Our original Correspondence was written at a time when scarce scientific information was available on this uncommon presentation referred to as tomato flu; hence we included media reports in our references. The main aim of our Correspondence was to increase awareness of this unusual presentation, based on the information available to us at the time; however, we appreciate that discussion of the COVID-19 pandemic in relation to tomato flu might have caused unnecessary concern.

The future of paediatric acute respiratory distress syndrome

Heterogeneity is a familiar concept to paediatric intensive care physicians, because patients, pathologies, and treatments vary both within the paediatric intensive care unit (PICU) and within a given disease process. Paediatric acute respiratory distress syndrome (ARDS) typifies this problem. Children with ARDS vary in terms of age (and therefore lung development), underlying cause (pneumonia, sepsis, or trauma), pre-existing comorbid conditions, and baseline immunological state. There is not one pathway by which ARDS occurs or manifests, as indicated by the identification of hyperinflammatory and hypoinflammatory subtypes in adults and children.

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