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Cystic Fibrosis Foundation invests in Owlstone to develop breath test for Pseudomonas detection<\/h1>E-News<\/a> <\/span><\/span><\/header>\n<\/div><\/section>
\nThe Cystic Fibrosis Foundation has committed up to US$2.3 million (about \u00a31.7 million) in equity investment to Owlstone Medical for the development of a breath test to detect Pseudomonas aeruginosa (PA) infections in people with cystic fibrosis (CF). The Cambridge-based company announced the investment on March 25, 2025, marking a significant step forward in respiratory infection diagnostics for this patient population.<\/h3>\n
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Addressing a critical clinical challenge<\/strong><\/h4>\nPseudomonas aeruginosa represents a significant threat to CF patients, affecting approximately 25% of the population. Once established in the lungs, the pathogen is notoriously difficult to eradicate, making early detection and intervention critical to patient outcomes.<\/p>\n
Current diagnostic approaches rely heavily on sputum culture, which presents substantial challenges. Many children struggle to produce adequate samples, and the effectiveness of modern CF therapies has ironically complicated diagnostics by reducing airway mucus production, making sample collection increasingly difficult even in adult patients.<\/p>\n
The proposed breath test aims to achieve diagnostic accuracy at least comparable to sputum culture tests while offering a non-invasive alternative that could improve monitoring capabilities and early intervention.<\/p>\n<\/div><\/section>
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The Cystic Fibrosis Foundation has committed up to US$2.3 million (about \u00a31.7 million) in equity investment to Owlstone Medical for the development of a breath test to detect Pseudomonas aeruginosa (PA) infections in people with cystic fibrosis (CF). The Cambridge-based company announced the investment on March 25, 2025, marking a significant step forward in respiratory infection diagnostics for this patient population.<\/h3>\n
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Addressing a critical clinical challenge<\/strong><\/h4>\nPseudomonas aeruginosa represents a significant threat to CF patients, affecting approximately 25% of the population. Once established in the lungs, the pathogen is notoriously difficult to eradicate, making early detection and intervention critical to patient outcomes.<\/p>\n
Current diagnostic approaches rely heavily on sputum culture, which presents substantial challenges. Many children struggle to produce adequate samples, and the effectiveness of modern CF therapies has ironically complicated diagnostics by reducing airway mucus production, making sample collection increasingly difficult even in adult patients.<\/p>\n
The proposed breath test aims to achieve diagnostic accuracy at least comparable to sputum culture tests while offering a non-invasive alternative that could improve monitoring capabilities and early intervention.<\/p>\n<\/div><\/section>
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