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ISSN Approved Journal | | IMPACT FACTOR 8.16 | | eISSN: 2582-5542 | |  Free Crossref DOI 

Fast Publication within 2 days | | Low Article Processing Charges | | Peer Reviewed and Referred Journal

Research and review articles are invited for publication in September 2026 (Volume 27, Issue 3) Submit Paper

Non-cystic fibrosis bronchiectasis: An updated review

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  • Non-cystic fibrosis bronchiectasis: An updated review

Joshua Granados Apú 1, Gabriel Muñoz Jackson 2, María Rebeca Sánchez Calderón 3, Melina Mata Serrano 4, Karina de Los Ángeles Montero Salazar 5 and Daniela Consumi Cordero 6, *

1 Internal Medicine Specialist at San Rafael de Alajuela Hospital, Alajuela, Costa Rica.
2 Internal Medicine Specialist at San Juan de Dios Hospital, San José, Costa Rica.
3 Medical Doctor, at Maximiliano Peralta Jiménez Hospital, Cartago, Costa Rica.
4 Medical Doctor, Independent Researcher, Cartago, Costa Rica.
5 Medical Doctor, Independent Researcher, San José, Costa Rica.
6 Medical Doctor, Independent Researcher, Alajuela, Costa Rica.

Review Article

World Journal of Biology Pharmacy and Health Sciences, 2025, 24(01), 424-432

Article DOI: 10.30574/wjbphs.2025.24.1.0931

DOI url: https://doi.org/10.30574/wjbphs.2025.24.1.0931

Received on 20 September 2025; revised on 26 October 2025; accepted on 29 October 2025

Non-cystic fibrosis bronchiectasis is a chronic and heterogeneous respiratory disease characterized by irreversible dilation of the bronchi, persistent inflammation, and recurrent respiratory infections. Its global prevalence varies widely, from 52.3 to more than 1000 cases per 100,000 individuals, with a progressive increase attributed to improved diagnostic techniques and greater clinical awareness. The condition mainly affects older adults and is currently recognized as the third most frequent chronic inflammatory airway disease, after chronic obstructive pulmonary disease and asthma. The causes are diverse and include post-infectious damage, particularly after tuberculosis or pneumonia, immune deficiencies, autoimmune disorders, congenital malformations, and chronic aspiration.
The pathophysiological basis of the disease is a self-perpetuating cycle of infection and inflammation, driven by chronic bacterial colonization especially by Pseudomonas aeruginosa and neutrophilic inflammation that progressively destroys the bronchial wall. Alterations in the bronchial microbiome and structural remodeling aggravate mucus retention and infection. Clinically, patients present with a persistent productive cough and frequent exacerbations that impair lung function, reduce quality of life, and increase mortality. Diagnosis is established through high-resolution computed tomography, lung function tests, and microbiological cultures. Prognostic indices such as the Bronchiectasis Severity Index, the FACED score, and the E-FACED score allow objective assessment of severity and risk of mortality.
Treatment aims to reduce bacterial load, prevent exacerbations, and improve symptoms through prolonged antibiotic therapy, macrolides, respiratory physiotherapy, and pulmonary rehabilitation. Managing comorbidities and maintaining vaccination coverage are also essential. Despite therapeutic advances, this disease entails a significant physical and psychological burden, requiring a multidisciplinary approach that integrates medical, functional, and psychosocial care to improve adherence, prognosis, and quality of life. 
 

Bronchiectasis; Chronic Inflammation; Bacterial Colonization; Airway Remodeling; Exacerbations; Multidisciplinary Management

https://wjbphs.com/sites/default/files/fulltext_pdf/WJBPHS-2025-0931.pdf

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Joshua Granados Apú, Gabriel Muñoz Jackson, María Rebeca Sánchez Calderón, Melina Mata Serrano, Karina de Los Ángeles Montero Salazar and Daniela Consumi Cordero. Non-cystic fibrosis bronchiectasis: An updated review. World Journal of Biology Pharmacy and Health Sciences, 2025, 24(01), 424-432. Article DOI: https://doi.org/10.30574/wjbphs.2025.24.1.0931.

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