Science and Research

No Influence on Cardiac Arrhythmia or Heart Rate from Long-Term Treatment with Tiotropium/Olodaterol versus Monocomponents by Holter ECG Analysis in Patients with Moderate-to-Very-Severe COPD

Background: Patients with chronic obstructive pulmonary disease (COPD) and cardiovascular comorbidities may have an increased risk of medication-related cardiac arrhythmias. We therefore performed an analysis of Holter electrocardiogram (ECG) data from two large, long-term, controlled clinical COPD trials to investigate whether tiotropium/olodaterol increased the risk of cardiac arrhythmia and mean heart rate. Methods: We analyzed Holter ECG data from a representative subset of patients (N=506) from the two pooled replicate studies (TONADO 1 and 2) assessing tiotropium/olodaterol 5/5 microg therapy versus tiotropium 5 microg or olodaterol 5 microg monotherapy, inhaled once daily (two single inhalations) using the Respimat((R)) Soft Mist inhaler device. Additionally, major adverse cardiac events (MACE) with tiotropium/olodaterol were assessed versus the respective monotherapies. Results: After 12 weeks of treatment, there was no difference in the number of patients who had an increase or decrease from baseline in 24-hour supraventricular premature beats or ventricular premature beats between tiotropium/olodaterol 5/5 microg combination therapy and its monocomponents. Compared with baseline, a small but statistically significant increase in adjusted mean heart rate was observed for tiotropium 5 microg (+1.6 beats per minute [bpm]; P=0.0010), but no difference was observed for olodaterol 5 microg (+0.3 bpm; P=0.2778) or tiotropium/olodaterol 5/5 microg (-0.1 bpm; P=0.4607). MACE and fatal MACE were limited to 1 to 3 patients across treatment groups. Conclusion: Compared with the compounds given as monotherapy, treatment with tiotropium/olodaterol fixed-dose combination therapy is not associated with medically relevant or statistically significant effects on arrhythmia as assessed by Holter ECG. Based on these findings, there is no evidence to assume a clinically relevant impact on cardiac function from dual tiotropium/olodaterol treatment. Trial Registration: TONADO 1 (ClinicalTrials.gov: NCT01431274); TONADO 2 (ClinicalTrials.gov: NCT01431287).

  • Andreas, S.
  • Bothner, U.
  • de la Hoz, A.
  • Kloer, I.
  • Trampisch, M.
  • Alter, P.

Keywords

  • *Holter ECG
  • *arrhythmia
  • *heart rate
  • *olodaterol
  • *safety
  • *tiotropium
  • payments for presenting from Boehringer Ingelheim, AstraZeneca, Berlin Chemie,
  • Chiesi and Novartis, outside the submitted work. UB, AdlH, IK and MT are
  • employees of Boehringer Ingelheim. PA reports grants from the German Federal
  • Ministry of Education and Research (BMBF) Competence Network Asthma and COPD
  • (ASCONET), AstraZeneca, GlaxoSmithKline, Grifols Deutschland, MSD Sharp & Dohme,
  • Pfizer, Takeda, Boehringer Ingelheim and Novartis Deutschland, grants and
  • non-financial support from Bayer Schering Pharma AG and Chiesi, and grants,
  • personal fees and non-financial support from Novartis Deutschland, outside the
  • submitted work. The authors report no other conflicts of interest in this work.
Publication details
DOI: 10.2147/COPD.S246350
Journal: Int J Chron Obstruct Pulmon Dis
Pages: 1945-1953 
Work Type: Original
Location: UGMLC
Disease Area: COPD
Partner / Member: UMR
Access-Number: 32848380
See publication on PubMed

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