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What is the optimal dose of N-acetylcysteine in adult patients with bronchiectasis?-data from the RIBRON registry
Oscullo, Grace (Hospital Universitari i Politècnic La Fe (València))
Méndez, Raúl (Hospital Universitari i Politècnic La Fe (València))
Olveira, Casilda (Instituto de Investigación Biomédica de Málaga)
Girón, Rosa (Hospital Universitario de la Princesa (Madrid))
García Clemente, Marta (Instituto de Investigación Sanitaria del Principado de Asturias)
Máiz, Luis (Universidad de Alcalá)
Sibila, Oriol (Hospital Clínic i Provincial de Barcelona)
Golpe, Rafael (Hospital Universitario Lucus Augusti (Lugo))
Rodriguez Hermosa, Juan Luis (Universidad Complutense de Madrid)
Barreiro, Esther (Institut Hospital del Mar d'Investigacions Mèdiques)
Prados, Concepción (Hospital Universitario La Paz)
de la Rosa Carrillo, David (Institut de Recerca Sant Pau)
Martínez García, Miguel Ángel (Centro de Investigación Biomédica en Red de Enfermedades Respiratorias)
Rodríguez López, Juan (Hospital Universitario San Agustín (Avilés))
Universitat Autònoma de Barcelona. Departament de Medicina

Fecha: 2025
Resumen: Background: Bronchiectasis is characterized by excessive respiratory secretions, the management of which is clinically significant. Among the available pharmacological treatments, mucolytics play a pivotal role. N-acetylcysteine (N-AC) is the most commonly used mucolytic; however, the optimal dosing regimen remains inadequately defined. The primary aim of the present study is to specifically evaluate the efficacy of 1,200 mg/day of N-AC compared to 600 mg/day in patients with bronchiectasis Methods: This was a retrospective, longitudinal, observational, multi-center study conducted across 43 centers, involving a cohort of 2,461 adult patients diagnosed with bronchiectasis based on a stable clinical state receiving either 600 mg/day of N-AC (n=252) or 1,200 mg/day (n=116), and provided follow-up data were available for 2 years. Propensity score matching (PSM) was employed to balance baseline characteristics between groups. Final outcomes were further adjusted for additional clinically relevant variables. Intergroup differences in intra-group changes were analyzed using a Poisson test. Results: Following PSM, the 1,200 mg/day N-AC group (n=104) demonstrated a statistically significant, fully adjusted reduction in exacerbations (−48. 6%, P=0. 01), hospitalizations (−29. 9%, P=0. 038), and total exacerbation rates (−54. 1%, P=0. 002), compared to the 600 mg/day group (n=219). Furthermore, the proportion of patients with more than 20 cc/day of sputum volume and those with mucopurulent sputum decreased by 24. 3% (P=0. 001) and 8. 5% (P=0. 041), respectively, in the 1,200 mg/day group versus the 600 mg/day group. No statistically significant difference was observed in the rate of Pseudomonas aeruginosa isolation (−0. 9%; P=0. 35). Conclusions: N-AC at a dose of 1,200 mg/day is more effective than 600 mg/day in reducing exacerbations, hospitalizations, and daily sputum volume in patients with bronchiectasis.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades. Creative Commons
Lengua: Anglès
Documento: Article ; recerca ; Versió publicada
Materia: Bronchiectasis ; N-acetylcysteine (N-AC) ; Pseudomonas aeruginosa (PA) ; exacerbations ; hospitalizations
Publicado en: Journal of Thoracic Disease, Vol. 17, Num. 10 (31 2025) , p. 9003-9012, ISSN 2077-6624

DOI: 10.21037/jtd-2025-1159
PMID: 41229849


10 p, 295.8 KB

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Documentos de investigación > Documentos de los grupos de investigación de la UAB > Centros y grupos de investigación (producción científica) > Ciencias de la salud y biociencias > Institut de Recerca Sant Pau
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 Registro creado el 2026-09-21, última modificación el 2026-09-22



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