Introduction: Chronic obstructive pulmonary disease (COPD) therapy includes a multi-dimensional approach, taking into account both symptoms of the patient and the number of acute exacerbations of COPD (AECOPDs). There are three main pharmaceutical classes currently available including long-acting muscarinic antagonists (LAMA), long-acting beta(2)-agonists (LABA) and inhaled corticosteroids (ICS). COPD is a major risk factor for most cardiovascular diseases, and cardiac comorbidities are very common in COPD patients. Both LAMA and LABA have a considerable impact on cardiac function by stimulating cardiac beta 2-adrenergic receptors or inhibiting the heart M-2 muscarinic receptors. ICS alone or in combination has never been associated with a real cardiovascular risk.Areas covered: This review explores the data published on the safety of COPD therapy and the implications for current pharmacotherapy.Expert opinion: Several studies have confirmed the good safety profile of bronchodilators available both in monotherapy and in association with other bronchodilators of different classes or with ICS despite the device used. Cardiovascular events in clinical trials are generally low and balanced between groups. The actual cardiovascular risk of fixed-dose combinations (FDCs) in an unselected COPD population will need to be investigated through post-marketing surveillance studies and observational studies.

Rogliani, P., Calzetta, L., Matera, M.g., di Daniele, N., Girolami, A., Cazzola, M., et al. (2019). Inhaled therapies and cardiovascular risk in patients with chronic obstructive pulmonary disease. EXPERT OPINION ON PHARMACOTHERAPY, 20(6), 737-750 [10.1080/14656566.2019.1570133].

Inhaled therapies and cardiovascular risk in patients with chronic obstructive pulmonary disease

Rogliani P.
;
Calzetta L.;di Daniele N.;Cazzola M.;
2019-01-01

Abstract

Introduction: Chronic obstructive pulmonary disease (COPD) therapy includes a multi-dimensional approach, taking into account both symptoms of the patient and the number of acute exacerbations of COPD (AECOPDs). There are three main pharmaceutical classes currently available including long-acting muscarinic antagonists (LAMA), long-acting beta(2)-agonists (LABA) and inhaled corticosteroids (ICS). COPD is a major risk factor for most cardiovascular diseases, and cardiac comorbidities are very common in COPD patients. Both LAMA and LABA have a considerable impact on cardiac function by stimulating cardiac beta 2-adrenergic receptors or inhibiting the heart M-2 muscarinic receptors. ICS alone or in combination has never been associated with a real cardiovascular risk.Areas covered: This review explores the data published on the safety of COPD therapy and the implications for current pharmacotherapy.Expert opinion: Several studies have confirmed the good safety profile of bronchodilators available both in monotherapy and in association with other bronchodilators of different classes or with ICS despite the device used. Cardiovascular events in clinical trials are generally low and balanced between groups. The actual cardiovascular risk of fixed-dose combinations (FDCs) in an unselected COPD population will need to be investigated through post-marketing surveillance studies and observational studies.
2019
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/10 - MALATTIE DELL'APPARATO RESPIRATORIO
Settore MED/09 - MEDICINA INTERNA
English
Con Impact Factor ISI
COPD; ICS/LABA; LABA; LABA/LAMA; LAMA; cardiovascular safety; mortality; triple therapy; Administration, Inhalation; Adrenal Cortex Hormones; Adrenergic beta-2 Receptor Agonists; Bronchodilator Agents; Cardiovascular Diseases; Humans; Muscarinic Antagonists; Pulmonary Disease, Chronic Obstructive; Risk Factors
Rogliani, P., Calzetta, L., Matera, M.g., di Daniele, N., Girolami, A., Cazzola, M., et al. (2019). Inhaled therapies and cardiovascular risk in patients with chronic obstructive pulmonary disease. EXPERT OPINION ON PHARMACOTHERAPY, 20(6), 737-750 [10.1080/14656566.2019.1570133].
Rogliani, P; Calzetta, L; Matera, Mg; di Daniele, N; Girolami, A; Cazzola, M; Ora, J
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/217786
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