Key result
Short-term administration of high-dose ticagrelor did not alter pulmonary function at rest or during exercise compared to placebo in healthy elderly subjects or those with mild asthma or COPD.
Why the study?
Does ticagrelor alter pulmonary function at rest and during exercise in healthy elderly volunteers and patients with mild asthma or COPD?
RCT (n=30)
Double-blind
crossover
No
Does ticagrelor alter pulmonary function at rest and during exercise in healthy elderly volunteers and patients with mild asthma or COPD?
Short-term, high-dose ticagrelor does not acutely impair pulmonary function or induce bronchospasm in healthy elderly individuals or those with mild asthma/COPD, suggesting ticagrelor-associated dyspnea is not mediated by gross pulmonary mechanical dysfunction.
Ticagrelor does not alter pulmonary function in elderly or asthma/COPD patients; confirms dyspnea is non-pulmonary and supports safe use.
BACKGROUND: Ticagrelor is a direct-acting, reversibly binding, oral P2Y12 platelet inhibitor that reduces thrombotic cardiovascular events in patients with acute coronary syndrome. Dyspnea is one of the most commonly reported adverse events associated with ticagrelor. OBJECTIVE: To determine the effect of ticagrelor on pulmonary function in healthy elderly volunteers and asthma or chronic obstructive pulmonary disease (COPD) patients. METHODS: Two randomized, double-blind, placebo-controlled, two-way crossover, single-center studies were conducted: 1) healthy elderly volunteers (55-75 years; n = 12); 2) patients with mild asthma (n = 11) or mild-to-moderate COPD (n = 7). Subjects were randomized to receive ticagrelor (a single 450 mg dose, 180 mg 12 hours later, twice daily for 2 days, and once on day 4) or placebo, with a 7 day washout. Pulmonary function at rest and during exercise was monitored using similar schedules and assessments across the two studies. RESULTS: Resting pulmonary function parameters, including respiratory rate, minute ventilation, or tidal volume, were similar between ticagrelor and placebo in any cohort. Furthermore, bronchospasm (as determined by spirometry and pulse oximetry), was not observed with either ticagrelor or placebo in any cohort. Perception of breathing was generally similar following ticagrelor or placebo. Exercise performance was not affected, and no clinically relevant differences were seen in pulmonary parameters during exercise for ticagrelor or placebo. There was no apparent relationship between plasma concentrations of ticagrelor and its main metabolite and pulmonary function. Ticagrelor was well tolerated in all cohorts. Study limitations include the use of relatively few subjects without documented coronary artery disease. CONCLUSIONS: Short-term administration of high doses of ticagrelor did not appear to alter pulmonary function at rest and during exercise in subjects at risk of (healthy elderly) or with respiratory impairment (mild asthma or mild-to-moderate COPD).
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Butler et al. (2013) conducted an RCT in Healthy elderly, mild asthma, or mild-to-moderate COPD (n=30). Ticagrelor vs. Placebo was evaluated on Pulmonary function at rest and during exercise. Short-term administration of high-dose ticagrelor did not alter pulmonary function at rest or during exercise compared to placebo in healthy elderly subjects or those with mild asthma or COPD.
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