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Pharmacotherapy and Lung Function Decline in Patients with Chronic Obstructive Pulmonary Disease. A Systematic Review

Rationale: Whether pharmacological therapy alters decline in FEV(1) in chronic obstructive pulmonary disease remains controversial. Because pharmacotherapy improves health status, exacerbation rate, and symptoms, it may be unethical to complete placebo-controlled long-term studies aimed at modifying...

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Detalles Bibliográficos
Autores principales: Celli, Bartolome R., Anderson, Julie A., Cowans, Nicholas J., Crim, Courtney, Hartley, Benjamin F., Martinez, Fernando J., Morris, Andrea N., Quasny, Holly, Yates, Julie, Vestbo, Jørgen, Calverley, Peter M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Thoracic Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958521/
https://www.ncbi.nlm.nih.gov/pubmed/32966751
http://dx.doi.org/10.1164/rccm.202005-1854OC
Descripción
Sumario:Rationale: Whether pharmacological therapy alters decline in FEV(1) in chronic obstructive pulmonary disease remains controversial. Because pharmacotherapy improves health status, exacerbation rate, and symptoms, it may be unethical to complete placebo-controlled long-term studies aimed at modifying FEV(1) decline. Objectives: We conducted a systematic review of placebo-controlled pharmacological trials lasting ≥1 year to address the question of whether therapy alters FEV(1) decline. Methods: A literature search for randomized trials that included repeated spirometry with at least one active and one placebo arm was conducted. Articles were excluded if study duration was <1 year, <3 spirometric measurements, or <100 subjects per arm. Study design was assessed using the Jadad score. To combine studies and find the estimated effect, we used random effects methodology to account for both within-study and between-study variation. Measurements and Main Results: There were 33,051 patients in the analysis (active component, n = 21,941; placebo, n = 11,110 in nine studies). The active treatment arms demonstrated a 5.0 ml/yr reduction (95% confidence interval, 0.8–9.1 ml/yr; P < 0.001) in the rate of FEV(1) decline compared with the placebo arms. The relative FEV(1) differences between active and placebo arms were within the range of differences reported for health status and for the exacerbation rate in the same studies. Conclusions: In chronic obstructive pulmonary disease, pharmacotherapy ameliorates rate of lung function decline. The relative benefit observed is within the range of those reported for health status and exacerbations in the same studies. Guidelines should be adjusted according to these findings.