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Authors LaForce C, Derom E, Bothner U, Kloer IM, Trampisch M, Buhl R
Received 4 January 2018
Accepted for publication 22 February 2018
Published 1 June 2018 Volume 2018:13 Pages 1819—1831
DOI https://doi.org/10.2147/COPD.S161489
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Charles Downs
Peer reviewer comments 4
Editor who approved publication: Dr Richard Russell
Introduction: The safety, lung function efficacy, and symptomatic benefits of combined
tiotropium and olodaterol in patients with COPD were established in the 1-year
TONADO® studies (NCT01431274; NCT01431287). As
tiotropium is predominantly excreted by the kidneys, the long-term safety
profile of tiotropium/olodaterol was investigated in patients with renal
impairment in a prespecified safety analysis of the TONADO studies.
Methods: These were 2 replicate, randomized,
double-blind, parallel-group, 52-week Phase III studies that assessed
tiotropium/olodaterol compared with tiotropium or olodaterol alone (all via
Respimat®) in patients with moderate-to-very severe COPD. In
this analysis, renal impairment was defined as mild (creatinine clearance
[CLcr] 60–89 mL/min), moderate (CLcr 30–59 mL/min) or severe (CLcr 15–29
mL/min). Adverse events (AEs) were pooled from both studies.
Results: Of 3,041 patients included in this analysis, 1,333
(43.8%) had mild, 404 (13.3%) had moderate, and 5 (0.2%) had severe renal
impairment; these were distributed equally between treatment groups. Almost
one-quarter of all treated patients (23.4%) had a history of cardiac disorder,
45.6% had hypertension, and 13.3% had glucose metabolism disorders, including
diabetes. AEs with olodaterol, tiotropium, and tiotropium/olodaterol occurred
in 75.1%, 70.8%, and 72.0% of patients with no renal impairment, 75.7%, 74.0%,
and 73.3% with mild renal impairment, and 84.3%, 79.5%, and 79.7% with moderate
renal impairment, respectively. There was no notable effect of renal impairment
on the proportion of patients with an AE, and no differences were observed
between tiotropium/olodaterol versus the monocomponents. There was no
difference in the incidence of major adverse cardiac events, renal and urinary
tract AEs, or potential anticholinergic effects with increasing severity of
renal impairment.
Conclusion: Over half the patients enrolled in the TONADO studies
had renal impairment, and there was a high level of pre-existing cardiovascular
comorbidity. The safety and tolerability of tiotropium/olodaterol is comparable
to the monocomponents, irrespective of the level of renal impairment.
Keywords: COPD, renal
impairment, comorbidities, tiotropium, olodaterol, safety
摘要视频链接:Safety of
tiotropium/olodaterol in patients with COPD and renal impairment